Tag-Archive for » mephedrone «

Saturday, August 21st, 2010 | Author: Synchronium

Legal Highs

Recently, there have been a few nasty developments in the world of legal highs. I was contacted by this week by GMTV and Radio 5 Live, asking for an interview about the “new” legal high Ivory Wave causing a stir. Unfortunately, I couldn’t give any interviews for various boring reasons and could only give a bit of advice over the phone/email, so I thought I’d write a post about it now I’ve got the time. Also, The UK’s old friend JWH-018 seems to be causing some trouble over the pond, having been linked a couple of deaths in Indiana. Finally, our government have made some more noise about the “problem” of legal highs which makes no difference for a good year or so and will only make matters worse when they manage to cobble some new legislation together eventually.

Ivory Wave

Ivory WaveIvory Wave has been around for at least a year, and before that, it was called Vanilla Sky. Guess what? It’s always been notoriously dodgy. In a quest to pump out the strongest ever “party powder”, its makers sacrificed safety for a marketing angle.

Earlier this year, the Irish government had a number of legal highs analysed including Ivory Wave and found that it contained MDPV (methylenedioxypyrovalerone), and lidocaine. Lidocaine is a local anaesthetic, added to numb your nose, both to dull the pain of snorting the other stuff and to make it more like cocaine. This isn’t news though – a load of similar products around before the cathinone ban contained it. MDPV on the other hand is worrying.

MDPV appears to be a dopamine and noradrenaline reuptake inhibitor, delivering plenty of stimulation but little in the way of euphoria. The vast majority of similar products available before April’s cathinone ban contained either mephedrone (4-methylmethcathinone) or a fluorinated analogue such as 3-fluoroumethcathinone. While these were also very stimulating, they delivered a much loved euphoria as well, so why would the makers of Ivory Wave depart from the norm and go for a subjectively worse compound instead? Because they just weren’t potent enough enough to earn Ivory Wave its reputation as the strongest legal high available.

MDPV

A typical dose of mephedrone or similar analogue for a new user would be around 50 – 100mg, while a typical dose of MDPV is around the 5 – 10mg mark. Sure, at that dose, the effects of MDPV don’t seem like much compared to mephedrone et al, but when people are used to cheap cocaine or the majority of similar legal highs, they rack up their usual sized line and hoover up far more than an equivalent dose of MDPV. As a consequence, users were frequently terrified and unable to sleep for days on end. Well done, Ivory Wave, you truly are the strongest!

On April 16th, 2010, the UK passed legislation banning a huge number of compounds, including mephedrone, all common available derivatives including MDPV and a shitload of theoretical compounds that haven’t been made yet. Despite the original incarnation of Ivory Wave falling under the banning stick, on August 10th, there was a lot of fuss about legal highs including Ivory Wave hospitalising 22 people around the Edinburgh area, so what’s going on?

Charge+Well, firstly, just because MDPV got banned, it doesn’t mean the manufacturers couldn’t stick some new legal chemical in there and call it the same thing. I’m sure you’ve all seen a packet of crisps or a chocolate bar with “New improved recipe!!!!11″ plastered all over the packaging – this is the same sort of thing. Of course, it’s not as innocent as that – these are psychoactive substances we’re talking about – but it’s nothing extraordinary. Products like Charge+ or Beanz pills have changed their ingredients before, so that’s what I expected had happened with Ivory Wave.

That doesn’t appear to be the case. Several websites selling the stuff now claim both that Ivory Wave is no longer for sale in the UK, suggesting it still contains MDPV, and that Ivory Wave found in the UK at the moment is fake. This leaves us with several possible scenarios.

  1. Ivory Wave available in the UK is the same stuff it’s always been, and has been illegally imported.
  2. Ivory Wave available in the UK is fake, but still contains MDPV. If this MDPV had to be illegally sourced or manufactured, it’s more likely to be impure, and these impurities are doing some damage.
  3. Ivory Wave available in the UK is fake, but still a new product with new, legal and dangerous chemicals in, trying to capitalise on the original Ivory Wave’s reputation

At first glance, it looks like we can ignore the first one. If it’s been around for ages, why are we only hearing about it now? Well, before the cathinone ban, Ivory Wave was definitely the strongest, but nowhere near the most enjoyable or popular product, so people tended to steer clear of it. However, when the ban came into effect, and somehow Ivory Wave was still around,  lots of people looking to find a “mephedrone replacement” would have stumbled across it. This spike in popularity makes scenario #1 as plausible as the rest, so for now, it’s anyone’s guess.

If you find any new information making one of these scenarios more likely, please let us all know!

For now, I’d advise anyone to steer clear, especially the stuff in red foil packets as that’s the type most frequently mentioned in the myriad forum posts on the topic.

JWH-018

JWH-018 was the main synthetic cannabinoid found in Spice and similar products in the UK last year. Here’s a couple of posts and comment threads here for some background:

A large number of synthetic cannabinoids (along with GBL, BZP and related piperazines) were banned on December 28th, 2009, but remained legal in the US, where the market has exploded just like it did here before the – the only difference is over there, the most popular brand is K2 rather than Spice.

Well, that was the only difference until very recently. In May, the smoking of K2 was “linked” to two deaths in Indiana – a rather odd situation indeed! It seems there’s no conclusive evidence available to say that K2 actually caused these deaths – it could be the same as all those people that apparently died of mephedrone over here who didn’t actually take it (Eg, Gabbi Price). However, just because we’ve been consistently lied to by the British press, it would be unwise to immediately rule out the other possibility – that K2 is somehow killing these people. As it happens, we’ve also got some more evidence right here on this blog that supports that conclusion: this guy reports vomiting blood after oral ingestion of JWH-018.

Here’s what I think. JWH-018 is safe, at least in the short term, so it’s not responsible for what we’re seeing. I reckon we’ve got a harmful contaminant or impurity left over from the synthesis which is causing all the damage. If there was a bad batch going round, it would also help to explain why those two deaths are both in Indiana, although I’m not sure where that commenter hails from.

Unfortunately, once again, this is all speculation, but it’s speculation based on all the evidence we have available. Fortunately, David Kroll, who’s forgotten more pharmacology than I know, has arrived at that same conclusion – contamination. Be sure to check out his post for links to the original stories, more detail and more speculation.

If you come across any more stories or bad batches, let us know!

For now, I’d advise those in the US to avoid any new brands popping up, avoid K2 in Indiana and, if you’re buying pure JWH-018, avoid it like the plague if it doesn’t exactly resemble the previous batches you’ve bought.

Wednesday, April 14th, 2010 | Author: Synchronium

Following the ACMD’s report on the cathinone derivatives (Part I & Part II), here is the latest amendment to the Misuse of Drugs Act to control them:

Dangerous Drugs, England And Wales
Dangerous Drugs, Scotland
The Misuse of Drugs (Amendment) (England, Wales and Scotland) Regulations 2010

Made
31st March 2010

Laid before Parliament
1st April 2010

Coming into force
16th April 2010

The Secretary of State makes the following Regulations in exercise of the powers conferred by sections 7, 10, 22 and 31 of the Misuse of Drugs Act 1971(1).

In accordance with section 31(3) of that Act the Secretary of State has consulted with the Advisory Council on the Misuse of Drugs.
Citation, commencement, interpretation and extent

1.—(1) These Regulations may be cited as the Misuse of Drugs (Amendment) (England, Wales and Scotland) Regulations 2010 and shall come into force on 16th April 2010.

(2) In these Regulations “the 2001 Regulations” means the Misuse of Drugs Regulations 2001(2).

(3) These Regulations extend to England, Wales and Scotland.
Amendment to the 2001 Regulations

2. The 2001 Regulations shall be amended as follows.

3. In Schedule 1 (which specifies controlled drugs subject to the requirements of regulations 14, 15, 16, 18, 19, 20, 23, 26 and 27)—

(a) in paragraph 1(a), after “methcathinone”, insert—

“4–methylmethcathinone”;

(b) after paragraph 1(l), insert—

“(m) Any compound (not being bupropion, diethylpropion, pyrovalerone or a compound for the time being specified in sub–paragraph (a) above) structurally derived from 2–amino–1–phenyl–1–propanone by modification in any of the following ways, that is to say—

(i) by substitution in the phenyl ring to any extent with alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents, whether or not further substituted in the phenyl ring by one or more other univalent substituents;

(ii) by substitution at the 3–position with an alkyl substituent;

(iii) by substitution at the nitrogen atom with alkyl or dialkyl groups, or by inclusion of the nitrogen atom in a cyclic structure.”.

David Hanson
Minister of State
Home Office
31st March 2010

Let’s take a look at this and try and make some sense of it shall we?

(a) in paragraph 1(a), after “methcathinone”, insert—

“4–methylmethcathinone”;

First off, mephedrone (4-methylmethcathinone) is explicitly mentioned to appear after methcathinone, which is already class B. I suppose we knew that much was going to happen already, so onto the more complicated stuff…

(b) after paragraph 1(l), insert—

“(m) Any compound (not being bupropion, diethylpropion, pyrovalerone or a compound for the time being specified in sub–paragraph (a) above) structurally derived from 2–amino–1–phenyl–1–propanone by modification in any of the following ways, that is to say—

This means that any cathinone derivative described by any of the following paragraphs will also become class B. Like the cannabinoids banned last December, this ban doesn’t list a tonne of individual substances, but instead covers a wide range of actual and theoretical substances by detailing possible alterations to the original cathinone structure. Here they are:

(i) by substitution in the phenyl ring to any extent with alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents, whether or not further substituted in the phenyl ring by one or more other univalent substituents;

This first part covers modifications of the phenyl ring, or “round bit” of the cathinone structure (R4). Unfortunately, this covers a massive range of compounds, including Mephedrone (alkyl), Methedrone (alkoxy), Methylone, Ethylone, Butylone & MDPV (all alkylenedioxy) and flephedrone (halide; also includes the 3-F isomer) .

(ii) by substitution at the 3–position with an alkyl substituent;

This covers the addition of a carbon side chain of any length on the carbon atom just before the nitrogen atom (usually referred to as the alpha carbon).  All the compounds listed in Annex A,  Appendix 1 of the ACMD’s report include a chain of at least one carbon long (alpha methylation), but by not specifying the length of this “alkyl substitute”, this also covers  existing compounds with longer alpha side chains such as pentylone and MDPV as well as any potentially interesting theoretical compounds.

(iii) by substitution at the nitrogen atom with alkyl or dialkyl groups, or by inclusion of the nitrogen atom in a cyclic structure.”

The final nitrogen atom present in cathinone has two available places to add stuff. One or both of these could be a carbon chain (alkyl or dialkyl), or a single carbon chain could form a ring by starting and ending at this nitrogen atom (the “cyclic structure”), which is what this part covers. Examples include ethcathinone (alkyl – a single carbon chain), n,n-dimethylcathinone (dialkyl – two carbon chains) and MDPV (includes the cyclic pyrrolidinyl structure).

I know that’s still quite technical, but hopefully what I’ve written is a little clearer than the original text. Feel free to ask questions in the comments though!

The gist is, all the popular cathinone derivatives mentioned by name above will become class B on Friday 16th, as well as a great deal of the more esoteric ones. One compound not included in this ban is naphyrone, currently marketed as Energy-1 or NRG-1. Unfortunately, I hear it’s rather shit and also not particularly safe, but the ACMD are already looking into banning that for next time. That’s pretty much it for cathinones in the UK then. I feel like we should all go out and get commemorative T-shirts or something… :(

On a more serious note, for those previously law abiding citizens who have developed a psychological addiction to mephedrone, you have two choices: continue buying lower quality stuff at an inflated price from a regular drug dealer or find some help. Luckily, Drug-Forum.com has a great Recovery and Addiction section that you should definitely check out.  You’re also welcome to post your stories and progress in the comments under this post.

Thursday, April 08th, 2010 | Author: Synchronium

My last two posts have been a bit hard going, so here’s a little something to lighten the mood:

Ok, so now you’re addicted Shaun The Sheep instead of mephedrone.

Although Shaun The Sheep provides me with a cheap, 10 minute euphoria, at least it’s off the ACMD’s radar… for now! Just make sure you only tell your responsible friends about this so our nation’s kids don’t start getting hold of it. That said, you may want to start stockpiling the episodes on DVD before the inevitable.

Also, in case you’re wondering what a couple in their 20′s are doing watching kid’s telly, FUCK YOU, that’s what!

Category: Drugs  | Tags: ACMD, mephedrone, shaun the sheep, tv  | 5 Comments
Wednesday, April 07th, 2010 | Author: Synchronium

This post contains the important annexes from the ACMD’s report on mephedrone and related cathinones. You can read the main body of the report here: The ACMD’s Mephedrone Report Part I. The original pdf is linked to at the end of this post.

I’ll probably write a few comments about the entire report in my next post, whenever that may be. Anyhoo…

Annex A. Recommendation For The Generic Control Of The Cathinone Derivatives

Scope of a generic definition

The ACMD here set out recommendations on the range of compounds that should be included in a generic definition for the control of cathinone derivatives under the Misuse of Drugs Act 1971.

It was proposed that the scope of compounds covered by generic control should be much wider than the 6 ring substituted compounds listed in Table 1 (annex A) and wider than the 10 compounds reported to the EMCDDA since 2006.

The scope should include all cathinone derivatives that have been found in seizures and collected samples together with compounds that have not been encountered but have misuse potential. This includes cathinone derivatives with and without ring substituents and with side chains longer than those usually encountered in the phenethylamine drugs.

The scope should also include any substances known or believed to be pro-drugs, i.e. substances that are metabolised to a known active substance (for example GBL is converted in the body to GHB).

The generic definition should not include those substances already controlled under the Misuse of Drugs Act, i.e. diethylpropion (Class C), cathinone (Class C), methcathinone (Class B) and pyrovalerone (Class C). Finally the definition should not include any substances, e.g. bupropion, that are ingredients of legitimate pharmaceutical products or that have other legitimate uses.

The structure of cathinone derivatives is represented by the generalised structure below:

Figure 1: Generalised structure of cathinone derivatives
where,

R1 = single alkyl group [but not H]
R2 = H or alkyl
R3 = H or alkyl or
[NR2R3] = pyrrolidino or phthalimido or other ring structure
R4 = H (no substituents) or
= one or more of alkyl, alkoxy, alkylenedioxy and halide whether or
not further substituted with an other univalent substituent

The phthalimido group has so far only been encountered in the compound α-phthalimidopropiophenone. This substance has been found in a capsule in combination with 2-fluoromethcathinone and in capsules containing a mixture with 4-methylmethcathinone, N-ethylcathinone, and caffeine.

The reason for adding α-phthalimidopropiophenone is not clear. It may have been added deliberately, perhaps as a pro-drug for cathinone, but there is no information about its pharmacology or metabolism. This substance is also an intermediate in the synthesis of cathinone and N-alkyl derivatives of cathinone. It could therefore be present unintentionally as a residue of an intermediate, the product of a failed chemical synthesis, or even the miss-labelling of an intermediate.

In addition to compounds with the generalised structure in (Figure 1, Annex A) the phenyl ring can be replaced with a naphthyl ring (e.g. Figure 2, Annex A) or with a thiophene ring. The naphthyl analogue of pyrovalerone (Figure 2, Annex A) is available on the Internet and is being retailed as “NRG-1”. These compounds cannot easily be included in a generic definition for the cathinone derivatives having the generalised structure in Figure 1, Annex A, but they could be controlled as named substances or by one or more separate generic definitions. The ACMD intend to review these substances and provide further advice at a later date.

Figure 2: Naphthyl analogue of pyrovalerone

The systematic chemical name for the structure in Figure 2, Annex A is 1-(2-naphthyl)-2-(1-pyrrolidinyl)-1-pentanone and alternative names include naphthylpyrovalerone, naphyrone and O-2482.

Appendix I, of this Annex includes all the cathinone derivatives, with the general structure in Figure 1, Annex A, that have been encountered in seizures and collected samples, substances that are already controlled, ingredients of known pharmaceutical products, substances available via the Internet and substances that are listed in Wikipedia. However, the market for cathinone derivatives is still evolving and new substances will continue to appear.

Many cathinone derivatives are mentioned in patents for pharmaceutical applications but the only known non-controlled cathinone derivative with a marketing authorisation appears to be bupropion, an ingredient of ®Zyban.

Some cathinone derivatives are mentioned in patents for non-pharmaceutical applications.

A structure-based search of the 12th Edition of the Merck Index (1996), carried out previously by Dr Les King, found no contentious compounds.

Interestingly, a recent patent (WO PCT 2010006196) relating to water purification membranes mentions the compound in Figure 3 below, which is closely related to methylone (bk-MDMA). This compound would be included within a generic definition since the term methylenedioxy can have two meanings. However, compounds analogous to those in Figure 3, Annex A are unlikely to have any commercial uses.

Figure 3: 3,4-methylenedioxy-N-methyl-β-keto-amphetamine

Structure Activity Relationships

Cathinone derivatives have a range of effects (e.g. stimulant, empathogen and antidepressant).

The cathinone derivatives without ring substituents (e.g. diethylpropion, methcathinone, buphedrone, N,N-dimethylcathinone) are mostly stimulants.

Most of the cathinone derivatives encountered as legal highs are ring substituted compounds with a secondary amino group (R2 = methyl or ethyl and R3 = hydrogen) or with a cyclic amino group (NR2R3 = pyrrolidino group or phthalimido group). These substances are primarily stimulants, with varying degrees of empathogenic effects (i.e. similar in effects to MDMA). Ring substituents (R4) have included alkyl, alkoxy, methylenedioxy and halide.

The side chain substituent (R1) has mostly been a single alkyl group. However there are examples with allyl (an alkenyl) and propargyl (an alkynyl) groups and also examples with a second alkyl group attached to the same carbon atom as R1, but these compounds are not within the proposed scope.

No haloalkyl substituents (e.g. trifluoromethyl –CF3 as found in piperazine derivatives) in the ring (R4) or on the side chain (R1) have been encountered or reported in the literature. However, replacement of the ring methyl group, as in mephredrone, with a trifluoromethyl group is likely to produce substances with similar activities. It is recommended therefore that haloalkyl substituents be included in the generic definition for ring substituents.

Cathinone derivatives with a primary amino group (i.e. no N-alkyl substituents) are rarely encountered, possibly because of their instability. There are only two known examples, bk-MDA (known to substitute for MDMA in rats) and cathinone (a stimulant).

The NR2R3 amino groups reported in the scientific literature have included alkylamino (R2 = alkyl, R3 = H), dialkylamino (R2 =alkyl, R3 = alkyl), the cyclic pyrrolidino group and a large number of other cyclic amines. However, for the pyrovalerone analogues an increase in size of the nitrogen containing ring from a five-membered pyrrolidine ring to a six-membered piperidine ring resulted in a substantial loss in binding potency. There are also examples of N-allyl, N-propargyl and N-cycloalkyl substituents.

The anti-depressant drug bupropion has a tertiary-butyl group on the nitrogen atom and several other substances investigated for their potential as smoking cessation drugs also have a bulky alkyl group on the nitrogen atom, e.g. tertiary-butyl, iso-propyl or cycloalkyl, or the alkyl amino group is replaced by a cyclic piperidino group (a cyclic amino group with 6 membered ring).

Salts, stereoisomers, esters and ethers

Cathinone derivatives with the generalised structure in Figure 1, Annex A, all have an asymmetric α-carbon atom giving rise to R and S stereoisomers.

With the exception of the phthalimido derivatives, all cathinone derivatives have a basic nitrogen atom and can therefore form salts.

There is no definition of esters and ethers in the Misuse of Drugs Act 1971, but from a chemical perspective esters usually only applies to derivatives of acids with a hydroxyl group, and derivatives of alcohols and phenols. Likewise ethers usually only applies to derivatives of alcohols and phenols. On this basis the cathinone derivatives would not form esters or ethers.

However, keto compounds, R1R2C=O, can form ketals, R1R2C(OR’)2, which arguably might be described as a special form of an ether. Ketals of cathinone derivatives have been discussed on drug forums in the context of a pro-drug and are mentioned in the scientific literature, usually as a means of protecting the keto group during chemical syntheses.

Generic definition for the control of cathinone derivatives

The ACMD have considered a number of options for the control of cathinone derivatives, including listing of named substances, several generic definitions and combinations of these approaches.

Taking into account the ACMD’s consideration of the scope, together with structure activity relationships and prevalence of known cathinone derivatives, the following generic definition is recommended:

Any compound (not being bupropion or a substance for the time being specified in paragraph 2.2) structurally derived from 2-amino-1-phenyl-1-propanone by modification in any of the following ways, that is to say,

  1. by substitution in the phenyl ring to any extent with alkyl, alkoxy, alkylenedioxy, haloalkyl or halide substituents, whether or not further substituted in the phenyl ring by one or more other univalent substituents;
  2. by substitution at the 3-position with an alkyl substituent;
  3. by substitution at the nitrogen atom with alkyl or dialkyl groups, or by inclusion of the nitrogen atom in a cyclic structure.

Notes

  • the parent compound is cathinone
  • “any” is taken to mean one or more

Comments

This is a definition that includes all permutations for the three substitution areas, i.e. in the ring (R4), in the side chain (R1) and on the nitrogen (NR2R3).

  • All the cathinone derivatives would be in the same Class which would result in some anomalies for compounds already controlled.
  • Includes all the compounds in Appendix 1.
  • Includes primary amines without ring substituents (no known examples, except cathinone which is not included within the scope of this definition).
  • Includes ring substituted primary amines (bk-MDA is the only example).
  • The term “cyclic structure” has a very wide scope (e.g. all ring sizes, all heterocyclic nitrogen compounds and structures with ring substituents).

Appendix 1

Cathinone
(Class C)
beta-keto-amphetamine

Note: only encountered in Khat although it has been encountered as the pro-drug, α-phthalimidopropiophenone (see below)

R1 = Me
R2 = H
R3 = H
R4 = H
Cathinone
α-phthalimidopropiophenone

Note: found in products from the Internet

R1 = Me
NR2R3 = phthalimide
R4 = H
α-phthalimidopropiophenone
Methcathinone
(Class B)
Ephedrone
α-methylaminopropiophenone
R1 = Me
R2 = Me
R3 = H
R4 = H
Methcathinone
N,N-Dimethylcathinone
Metamfepramone
Dimethylpropion

Note: encountered in seizures

R1 = Me
R2 = Me
R3 = Me
R4 = H
N,N-Dimethylcathinone
Ethcathinone
Ethylpropion
N-ethylcathinone
2-ethylamino-propiophenone
Sub Coca II

Note: encountered in seizures

R1 = Me
R2 = Et
R3 = H
R4 = H
Ethcathinone
Diethylpropion
(Class C)
Diethylcathinone
Amfepramone
R1 = Me
R2 = Et
R3 = Et
R4 = H
Diethylpropion
α-Pyrrolidinopropiophenone
α-PPP

Note: encountered in Germany

R1 = Me
NR2R3 = Pyrrolidinyl
R4 = H
α-Pyrrolidinopropiophenone
Buphedrone
2-methylamino-1-phenylbutan-1-one

Note: no seizures reported to EMCDDA but is available via the Internet and user reports are on drug forums.

R1 = Et
R2 = Me
R3 = H
R4 = H
Buphedrone
α-Pyrrolidinobutiophenone
α-PBP

Note: no seizure or user reports but listed on Wikipedia and in a patent

R1 = Et
NR2R3 = Pyrrolidinyl
R4 = H
α-Pyrrolidinobutiophenone
α-Pyrrolidinovalerophenone
α-PVP
α-Pyrrolidinopentiophenone

Note: No seizures reported to EMCDDA, but metabolism study by Germany, as a result of 2 seizures, in Germany and Netherlands.

R1 = n-Pr
NR2R3 = Pyrrolidinyl
R4 = H
α-Pyrrolidinovalerophenone
Mephedrone
4-Methylmethcathinone
4-MMC
Sub Coca I

Note: most frequently encountered cathinone derivative

R1 = Me
R2 = Me
R3 = H
R4 = 4-Me
Mephedrone
4’-methyl-α-pyrrolidinopropiophenone
MPPP

Note: seizure report from Germany

R1 = Me
NR2R3 = Pyrrolidinyl
R4 = 4-Me
4’-methyl-α-pyrrolidinopropiophenone
4’-methyl-α-pyrrolidinobutiophenone
MPBP

Note: seizure report from Germany

R1 = Et
NR2R3 = Pyrrolidinyl
R4 = 4-Me
4’-methyl-α-pyrrolidinobutiophenone
Pyrovalerone
(Class C)
R1 = n-Pr
NR2R3 = Pyrrolidinyl
R4 = Me
Pyrovalerone
4’-methyl-α-pyrrolidinohexiophenone
MPHP

Note: seizure report from Germany

R1 = n-Bu
NR2R3 = Pyrrolidinyl
R4 = Me
4’-methyl-α-pyrrolidinohexiophenone
Methedrone
4-methoxymethcathinone
PMMC
bk-PMMA

Note: encountered in seizures

R1 = Me
R2 = Me
R3 = H
R4 = 4-MeO
Methedrone
4’-Methoxy-α-pyrrolidinopropiophenone
MOPPP

Note: seizure report from Germany

R1 = Me
NR2R3 = Pyrrolidinyl
R4 = 4-MeO
Bupropion
(Zyban – medicinal product in UK)

Note: To be excluded from control. No reports of abuse)

R1 = Me
R2 = t-Bu
R3 = H
R4 = 3-Cl
Bupropion
Flephedrone
4-Fluoromethcathinone
4FMC

Note: encountered in seizures. The 3-fluoro and 2-fluoro isomers have also been found in products from the Internet.

R1 = Me
R2 = Me
R3 = H
R4 = 4-F
(also 2-F and 3-F)
Flephedrone
Methylone
3,4-Methylenedioxymethcathinone
bk-MDMA

Note: encountered in seizures

R1 = Me
R2 = Me
R3 = H
R4 = 3,4-methylenedioxy
Methylone
Ethylone
3,4-methylenedioxyethcathinine
bk-MDEA

Note: encountered in seizures

R1 = Me
R2 = Et
R3 = H
R4 = 3,4-methylenedioxy
Ethylone
3’,4’-methylenedioxy-α-pyrrolidinopropiophenone
MDPPP

Note: seizure reports from Germany and Denmark

R1 = Me
NR2R3 = Pyrrolidinyl
R4 = 3,4-methylenedioxy
3’,4’-methylenedioxy-α-pyrrolidinopropiophenone
Butylone
β-keto-N-methyl-3,4-benzodioxyolylbutanamine
bk-MDBD

Note: seizure reports from 7 countries

R1 = Et
R2 = Me
R3 = H
R4 = 3,4-methylenedioxy
Butylone
3’,4’-Methylenedioxy-α-pyrrolidinobutiophenone

Note: no seizure reports, but mentioned in Wikipedia and in patent

R1 = Et
NR2R3 = Pyrrolidinyl
R4 = 3,4-methylenedioxy
3’,4’-Methylenedioxy-α-pyrrolidinobutiophenone
Pentylone
β-Keto-methylbenzodioxolylpentanamine
bk-Methyl-K
bk-MBDP

Note: no seizure reports, but mentioned in Wikipedia and in patent.

R1 = n-Pr
R2 = Me
R3 = H
R4 = 3,4-methylenedioxy
Pentylone
Methylenedioxypyrovalerone
MDPV

Note: encountered in seizures

R1 = n-Pr
NR2R3 = Pyrrolidinyl
R4 = 3,4-methylenedioxy
Methylenedioxypyrovalerone

Annex B & C

…Aren’t really worth including here. They contain a list of ACMD members and a list of organisations and individuals who submitted evidence included in the report. Go and read it in the original pdf if you want to. Go on! Go and bloody read it!

Annex D. Letter From The Advisory Council On The Misuse Of Drugs To The Home Secretary

22nd December 2009

Dear Home Secretary,

Re: ACMD consideration of mephedrone (and related cathinones)

The ACMD wrote to you in March to explain that it would be pleased to accede to the Government’s priorities that your predecessor set out in her letter of 13 March 2009. Concerning the issue of ‘legal highs’ the ACMD has provided advice on the synthetic cannabinoid receptor agonists (Spice), 1-benzylpiperazine, GBL and 1,4-BD all of which we note will be controlled in the legislation on the 23rd December. In the ACMD’s letter of 30 September 2009 it was explained that we would next provide you with advice on the cathinones.

Despite the difficulties of the last 2 months the ACMD is committed to providing you with advice on the cathinones. Although attention has focused on mephedrone, five other synthetic psychoactive cathinone derivatives are also widely available. The ACMD explained in a previous letter to you that it has concerns about the apparent prevalence and potential harms of these compounds. Much has been made of these compounds in the media over recent weeks; we find it of concern that this may have had the consequence of bringing such drugs to the attention of a wider demographic sooner than may have been the case.

The ACMD understand that mephedrone, amongst other cathinones, is being marketed as a variety of apparently ‘benign’ products e.g. bath salts or plant food. Whilst the potential harms of these drugs are not yet fully known, it is apparent that the selling of such unregulated preparations in a form that they are clearly unintended for could have serious public health implications.

The ACMD is mindful that, after recent events, our statutory membership requirements need to be fulfilled before providing formal advice, according to the requirements of the Misuse of Drugs Act 1971. However, the ACMD would like to assure you that it will seek to provide you with such advice at the earliest possible opportunity on this important issue.

I would be willing to discuss the issue of the cathinones and, more broadly, new psychoactive substances (‘legal highs’) and the timing of advice with you.

Yours sincerely,

Professor Les Iversen
(on behalf of the ACMD)

***

The original (boringly formatted) report can be found here: ACMD-cathinones-report.pdf

Sunday, April 04th, 2010 | Author: Synchronium

MephedroneWhile we were away, what’s left of the ACMD finished their report on mephedrone and structurally similar compounds – one of the final few hurdles before these research chemicals get slapped upside the head with Alan “more insightful than science” Johnson’s banning stick.

Since we’re up to the eyeballs here with a week’s worth of work to catch up on, and this report will have a monstrous impact, I’ll repost it here in full. Kind of. Below is the main body of the report including references. The equally important annexes including recommendations on how to actually ban these substances can be found here: The ACMD’s Mephedrone Report Part II.

I’ve kept page numbers in referring to pages in the original document and included the references, but not included the footnotes. Most of the footnote info has been incorporated in the article somehow though, and if you’re really desperate to read them, you can download the full pdf at the end of part two. Here goes:

Consideration Of The Cathinones

Letter To The Home Secretary From The ACMD

31st March 2010

Dear Home Secretary,

I have pleasure in attaching the Advisory Council on the Misuse of Drugs report on the ‘Consideration of the cathinones’.

The ACMD recommends that the cathinone compounds be brought under control of the Misuse of Drugs Act 1971 in Class B, Schedule I by way of a generic definition. Based on the attached evidence and by analogy with the amphetamines, the ACMD consider that the harms associated with the cathinones most closely equate with other compounds in Class B.

The ACMD also recommend that particular attention is focussed on credible and consistent public health messages that are promulgated both to the public and health professionals – the latter for the purposes of providing advice.

The ACMD is concerned that, particularly in the case of mephedrone, the internet plays a significant part in the marketing, sale and distribution of the drug and social networking sites may also play a role. The ACMD therefore believes that resources should initially be focussed on supply side activities with a concurrent emphasis on educating users of this drug so as to highlight the real dangers of mephedrone and the cathinones.

The ACMD indicated, in its letter to the Home Secretary, of the 22nd December 2009, its concerns about the sale of mephedrone and its plans for review. However, the rapid increase in the use of mephedrone in the UK has been exceptional. This sudden rise in prevalence of what we consider to be a harmful drug has brought to the fore our concerns that we need to consider a range of options for limiting the rapid spread of such substances. The ACMD intend to provide you with further advice on the possible control of ‘legal highs’ concerning recommendations and advice that is broader than the scope of what either this report or that on other individual or classes of compounds will allow.

In addition, I would like to draw your attention to further advice that we will provide on the napthyl analogues of pyrovalerone and other such analogues. The ACMD will meet to discuss other compounds that are not covered by this generic scope in the next few weeks.

Yours faithfully,
Professor Les Iversen FRS

1. Background

1.1. In March 2009 the then Home Secretary requested advice from the ACMD on so called ‘legal highs’. The ACMD have looked at a number of substances to date and provided advice on the piperazines and the synthetic cannabinoids (‘Spice). The ACMD wrote to the Home Secretary in December 2009 (Annex D) setting out the ACMD’s concerns regarding the cathinones and mephedrone in particular, which first came to the ACMDs attention in the summer of 2009. On the 2nd February 2010 the ACMD Chair (Professor Les Iversen) met with the Home Secretary to further discuss the issue and to provide an update.

1.2. The ACMD gathered evidence on the cathinones at a special meeting of the Technical Committee (22nd February 2010) and discussed additional evidence and possible recommendations at a further Technical Committee meeting on the 25th March 2010, and at the ACMD Council meeting on the 29th of March 2010.

2. Introduction

2.1. Cathinone is one of a number of alkaloids which can be extracted from the (fresh) leaves of Catha edulis (khat). It is structurally very similar to amphetamine (1-phenylpropan-2-amine) and represents the β-keto analogue of amphetamine.

2.2. Cathinone (Class C), methcathinone (Class B), diethylpropion (Class C) and pyrovalerone (Class C) are controlled under the Misuse of Drugs Act 1971. The three controlled cathinone derivatives are listed in the United Nations Convention on Psychotropic Substances (1971) and have been reveiwed by the WHO Expert Committee on Drug Dependence (WHO, 1995). However, other derivatives and analogues are not presently controlled (including mephedrone). Notwithstanding the potential harms of the cathinones it is apparent that mephedrone and other cathinones are being sold without any apparent effective regulation.

2.3. The ACMD has communicated its intentions to review the cathinones to the Home Secretary, over recent months, through meetings and correspondence (see the ACMD’s letter of the 22nd Dec 2009 – Annex D). The ACMD has been concerned about the rise in prevalence of the cathinones and potential harms initially through reports from drug services, young people’s treatment services, head teachers, drug surveys, the police and media, among others.

2.4. Other countries (including: Sweden Denmark, Norway, Ireland and Israel) have recently controlled specific cathinones. However, we are not aware of any country that has developed generic legislation to control the cathinones as a class.

2.5. The ACMD is aware of the collation of data on mephedrone by Europol and the EMCDDA in the form of a joint report under Article 5.1 of Council Decision 2005/387/JHA. The ACMD wrote to the UK focal point (the Reitox NFP) that would be providing information as requested by Article 5 of the Decision.

2.6. This report is compiled from oral and written evidence considered at the meetings (paragraph 2.3) above. A full citation of the evidence received and considered is provided in Section 10 and submitting individuals and organisations are given in Annex C.

3. Chemistry And Pharmacology

Chemistry

(White, 2010)

3.1. Cathinone (2-amino-1-phenyl propanone) is one of a number of alkaloids which can be extracted from the (fresh) leaves of Catha edulis (khat). However, the ACMD understands that most of the cathinones seized, and those that have been tested, are synthetic in origin.

3.2. Cathinone is structurally very similar to amphetamine (1-phenylpropan-2-amine), differing only in the functionality present at the β-carbon. Cathinone possesses a ketone oxygen at the β-carbon; cathinone can therefore be considered as the ‘β-keto analogue’ of amphetamine (see Figures 1 and 2).

Figure 1: The structural similarity between amphetamine (left) and cathinone (right)

3.3. Structural modifications to the 1-phenylpropan-2-amine (amphetamine) backbone have produced a range of different compounds, many of which are closely related structurally to amphetamine; these are known as the ‘amphetamines’. In a similar manner, the molecular architecture of 2-amino-1-phenyl propanone (cathinone) can be altered to produce a series of different compounds which are closely structurally related to cathinone. Together these are known as the ‘cathinones’ or ‘cathinone derivatives’.

3.4. The N-methyl derivative known as methcathinone or ephedrone is the cathinone analogue of methylamphetamine, while 3,4-methylene-dioxymethcathinone (methylone) is the cathinone analogue of MDMA (ecstasy); 4-methylmethcathinone (mephedrone) has no commonly used amphetamine equivalent.

3.5. The basic cathinone structure (see Figure 2) can be altered in a number of predictable ways, such as the inclusion of additional functionality to the aromatic ring (ring substitution, R4), N-alkylation (or inclusion of the nitrogen atom in a ring structure, R2 and R3), and variation of the (typically alkyl) α-carbon substituent (R1). Multiple modifications may of course be present in a single derivative; cathinones are all usually N-alkylated (or the nitrogen is incorporated into a ring structure, typically pyrrolidine) and many also bear ring substituents.

Figure 2: Generic sites for structural variation of cathinone, detailing α and β positions

(The generic cathinone backbone (see Figure 2) possesses a chiral centre (the α-carbon atom if R1≠H); cathinone and its derivatives can therefore exist as stereoisomers, the potencies of which may be markedly different. Although it is the S-enantiomer of cathinone which is found in the fresh leaves of Catha edulis, the chirality of the cathinones is not determined during routine forensic analysis of seizures. There is, however, no evidence to suggest that the synthetic cathinones currently available are enantiopure; it is instead likely that they are supplied as racemic mixtures. The qualitative or quantitative differences between the enantiomers of the non-controlled cathinones is not known.)

3.6. The genesis of synthetic cathinone chemistry is rooted in the synthesis of cathinone over 120 years ago. Since this time, many synthetic cathinones have been reported, the vast majority of which have not been used in a medicinal setting. However, a handful of cathinones, such as diethylpropion, bupropion and pyrovalerone have been used in pharmaceutical preparations, and the properties of novel cathinones (such as napthylpyrovalerone (Meltzer et al., 2006)) is still an area of active research.

3.7. Bupropion (page 42) is used medically as an antidepressant and an aid to smoking cessation and is a prescribed drug, marketed under the trade name Zyban®. Although it is a ring substituted cathinone no samples of Bupropion have been encountered in forensic analysis of seizures in the UK, and there is no evidence for its misuse.

3.8. The misuse of selected synthetic cathinones is not new; methcathinone (ephedrone), originally used as an antidepressant in the former Soviet Union in the 1930’s, went on to be used recreationally there (especially during the 1970s and 1980s) and in the USA (1990s). The emergence of six synthetic cathinones in Germany was reported between 1997 and 2004. All six substances bear an α-pyrrolidino functionality and are therefore closely related to pyrovalerone (page 41).

3.9. More recently, there have been an increasing number of reports of other synthetic cathinones encountered within the European Union. Although many of these compounds are simply β-keto analogues of well-known amphetamines, the presence of the ketone functionality often circumvents any control measures which may already be in place for the related amphetamine congeners. Since 2006, the following cathinones have been reported in the European Union (see Table 1; for the position of the substituents R1 to R4, see Figure 2). According to data from UK forensic providers, since January 2006 six of these have been encountered in the UK (emboldened in Table 1).

Table 1: Some of the non-controlled cathinones encountered in the European Union since 2006 (excluding reports of pyrovalerone derivatives from 1997-2004). those in bold type have been encountered in the UK.

Name Common name R1 R2 R3 R4
N,N-dimethylcathinone - Me Me Me H
Ethcathinone - Me Et H H
4-Methylmethcathinone Mephedrone Me Me H 4-Me
Bk-PMMA Methedrone Me Me H 4-MeO
4-Fluoromethcathinone Flephedrone Me Me H 4-F
3-Fluoromethcathinone - Me Me H 3-F
bk-MDMA Methylone Me Me H 3,4-methylenedioxy
bk-MDEA Ethylone Me Et H 3,4-methylenedioxy
bk-MBDB Butylone Et Me H 3,4-methylenedioxy
Methylenedioxypyrovalerone MDPV (corrected by me) n-Pr pyrrolidinyl 3,4-methylenedioxy

3.10. Of the total number of cathinone derivatives encountered by UK forensic providers, by far the most commonly encountered is 4-methylmethcathinone (mephedrone) (89% of seizures). However, data from the Forensic Science Service indicate that cathinones accounted for a very small fraction of Police seizures submitted in 2009. Tentative data also indicate a rapid rise in the number of cathinone submissions during 2009, with a concomitant decrease in the number of piperazine submissions.

3.11. Data from UK forensic providers suggest that the cathinones are normally submitted as either white or brown powders (the freebase forms of the cathinones are unstable and readily decompose; the cathinones are normally encountered as the hydrochloride salts.); data from January 2006 to mid-February 2010 indicate that, of all cathinone derivatives submitted, 95% were in powder form, 4% being submitted as tablets or capsules.

3.12. Purity data for the cathinones are not available from UK forensic providers, since it is not usually determined during routine forensic analysis. However, cathinones are normally advertised as being of ‘high purity’, typically >95%. Some adulterants, including benzocaine, lignocaine, caffeine and paracetamol, have been detected in a small proportion of seizures of the cathinones. Some submissions have been adulterated with controlled drugs such as cocaine, ketamine, amphetamine and 1-benzylpiperazine (BZP), although these are rarely encountered.

3.13. There are currently no colorimetric field tests available to identify all of the cathinone derivatives, although some chemical tests, such as the Simon’s test and Chen test may be used to give an indication of the presence of a small number of the cathinones. More specific field tests based on immunoassay technology are not yet available.

3.14. As with the amphetamines, both systematic (IUPAC) and non-standard nomenclature is common in cathinone chemistry. Often, the assimilation of a common structural motif is reflected in non-standard nomenclature. Thus, structural incorporation of the ‘2-methylamino-1-phenyl-1-propanone’ fragment, which is also known as methcathinone or ‘ephedrone’, is often indicated in nomenclature; 4-methylmethcathinone is ‘mephedrone’ and 4-fluoromethcathinone is ‘flephedrone’. The use of acronyms is also widespread; 3,4-methylenedioxypyrovalerone is known as ‘MDPV’, whilst α-pyrrolidinopropiophenone, one of a number of α-pyrrolidino cathinones, is simply known as α-PPP. As a consequence of the β-keto substituent, it is also common practice for widely accepted amphetamine acronyms to be augmented with the prefix ‘bk’. For example, 3,4-methylenedioxymethcathinone (methylone), the cathinone analogue of MDMA, is often referred to as ‘bk-MDMA’. Mephedrone [2-(methylamino)-1-(4-methylphenyl)-1-propanone] is the most commonly used cathinone derivative and forms the focus of this report.

Pharmacology

3.15. As with the amphetamines, the cathinones act as central nervous system stimulants, although the potencies of the cathinones are generally lower then their amphetamine congeners, probably because the increased polarity conferred on a cathinone by the presence of a β-keto group reduces their ability to cross the blood-brain barrier.

3.16. Several cathinones have been used as active pharmaceutical ingredients (API). Bupropion has been used as an antidepressant, and as an aid to stop smoking cigarettes. Diethylpropion (Amfepramone) and pyrovalerone have both been proposed as appetite suppressants, although they are not currently in clinical use. 4-methylmethcathinone (mephedrone), the most commonly encountered synthetic cathinone derivative in the UK, has never been used as an API or patented as a potential API.

3.17. Little data are available on either the pharmacokinetics or pharmacodynamics of the cathinones. Research on the metabolism of the ring-substituted cathinones bk-MBDB and bk-MDEA has implicated N-dealkylation, demethylenation followed by O-methylation and β-keto reduction as major metabolic pathways (Zaitsu et al., 2009).

3.18 The effects of cathinones bearing ring-substituents in human subjects are reportedly similar to those of cocaine, amphetamine and MDMA (Table 2; CairScotland, 2010). Self reported subjective effects of ring-substituted cathinones include:

  • Feelings of empathy (openness, love, closeness, sociability, well-being);
  • Stimulation / alertness / rushing;
  • Euphoria / mood lift / appreciation of music; and,
  • Awareness of senses.

3.19.  Studies of the effects of cathinones on monoamine neurotransmission in rat brain confirm their mechanisms of action to be similar to those of the amphetamines. Both groups of drugs bind to monoamine transporters for dopamine, serotonin and noradrenaline (norepinephrine) in brain and promote release of these monoamines (Cozzi et al., 1999; Nagai et al., 2007). As with the different amphetamines, individual cathinone derivatives vary in their relative potencies as inhibitors of the three monoamine transporters – summarised in Table 2. There are no published data on the effects of mephedrone on monoamine transporters, but it may be expected to be intermediate in its profile between methcathinone and methylone.

Table 2: Actions of selected drugs on monoamine transporters

Dopamine Serotonin Noradrenaline
Amphetamine +++ + ++++
MDMA ++ +++ +++
Cathinone +++ ++ +++
Methcathinone +++ + +++
Methylone ++ +++ ++++
Mephedrone ? ? ?

Data from Cozzi et al., (1999) and Nagai et al., (2007). Values are depicted as relative affinities since the studies did not use the same units. + = low affinity; ++++ = highest affinity

3.20. It is notable that the cathinones examined were potent inhibitors of the noradrenaline (norepinephrine) transporter (NET). This helps to explain the strong sympathomimetic actions of cathinones – due to their ability to promote release of noradrenaline from the sympathetic nerves in various peripheral organs, notably the heart and vascular system.

3.21. Cathinone and methcathinone are amphetamine-like behavioural stimulants. When administered to experimental animals they cause hyperactivity, with methcathinone being approximately 10 times more potent than cathinone (Feyissa and Kelly, 2008; Glennon et al., 1987)

3.22 When administered in vivo to rats trained to recognise and to distinguish the subjective effects of amphetamine, the animals cross-generalised completely to methcathinone (i.e. they were unable to recognise this substances as having different effects from amphetamine). Methylone, however, showed only weak cross generalization to amphetamine, but cross generalized completely to MDMA in rats trained to recognize this as the discriminative stimulus (Dal Cason et al.,1997).

4. Epidemiology Of Cathinone Use And Methods Of Use

Availability and use

4.1. Many of the cathinone compounds, particularly mephedrone, can be purchased from many different sources, and are readily available over the internet. Although the provenance of the substances is often not clear, several suppliers source compounds from China (Ramsey, 2010; UK Border Agency, 2010). Exercises at Heathrow targeting air courier traffic from China for delivery to UK domestic addresses gave rise to seizures of mephedrone. Claims of manufacture in a number of other countries are made on the internet.

4.2. Intelligence from Australia Customs and Border Protection Service has identified China and the UK as being the principal source of mephedrone. However, it is likely that in the case of the UK, this represents transit of the drugs and not necessarily production in the apparent country of origin.

4.3. Mephedrone and other cathinones are predominantly sold over the internet and in ‘head shops’. Websites selling cathinone based compounds – generally mephedrone – normally exhibit a disclaimer that the compounds ‘are not for human consumption’. Instead, they are sold as research chemicals, ‘novelty bath salts’ (3-fluoromethcathinone) or, more commonly, as plant food/plant growth regulators (Sumnall, 2009). However, none of the cathinones has any recognized efficacy as a plant fertilizer nor would they suitably function as bath salts.

4.4. Slang terms for some of the cathinones include Bubble(s), miaow, meow meow, 4-MMC, Mcat, sub-coca, toot and Top Cat.

4.5. Cathinones (generally mephedrone) are usually sold as white or brown powders, sometimes as capsules, or more rarely as pills, and are often advertised as being of ‘high’ purity (> 95%). CairScotland (2010) report that ‘Bubbles’ was originally sold in capsules, but now more often in 1g bags. Reports suggest varying prices: around £10-15/g if purchased from ‘headshops’, clubs or dealers (Druglink, 2010; Linell, 2010).

4.6. Self-reported dosages range from 5 mg or less (for MDPV) to 200 mg or more (for mephedrone), with some mephedrone users reporting ‘re-dosing’ (bingeing) to prolong the euphoric experience, leading to 1-2g being consumed in a session. The cathinones are sometimes used in conjunction with alcohol or controlled substances; co-abused substances include cocaine, cannabis, ketamine and MDMA. Studies of polysubstance use with the cathinones are not available, however, it should be noted that polydrug use is increasingly a feature of UK illegal consumption patterns more generally.

4.7. The reason for the apparent emergence and sudden increase in mephedrone use in the UK in 2009 is unclear. However, interviews with users and community workers (Newcombe, 2010; Measham et al., 2010, NME, 2010) suggest that the unavailability and/or low purity of cocaine and MDMA in 2009 (Hand and Rishiraj, 2009) have contributed to the increase in mephedrone use. In addition, the cathinones are presently a legal alternative to other drugs and are widely available from internet websites.

4.8 Mephedrone powder may be snorted (insufflated) (sometimes by keying – approximately 5-8 keys per gram (Linell, 2010)). The drug may also be swallowed – often after wrapping in tissue paper (bombing or dabbing) or, more rarely, injected (CairScotland, 2010; Linell, 2010; McVean, 2009; Measham et al., 2010).

4.9. Reports from users presenting at hospital A&E units are that mephedrone is taken in staggered doses (Wood pers. comm.).

4.10. Emergent research with mephedrone users suggests that they may appear to develop tolerance quickly and as a consequence tend to consume higher doses more frequently.

4.11. Evidence from the Bailiwick of Guernsey Customs report an increase in the prevalence of mephedrone from seizures and this has superseded the seizures of ‘Toot’ (identified predominantly as Butylone and methylone) (McVean, 2009 and 2010). It is reported that mephedrone and ‘Toot’ are being injected by users and has become popular among users of heroin (McVean, 2009 and 2010).

Prevalence and reported data

4.12. There are little published data on the prevalence of the cathinones; most available data are from self reported surveys of particular demographics.

4.13. Since many of the cathinones are not controlled, they are not included in the ‘stimulant’ group of substances in the British Crime Survey (BCS). However, we understand that the BCS will now include a specific question on mephedrone – interim data should be available to the ACMD after 6 months of the question becoming part of the survey.

4.14. The Mixmag survey (Winstock, 2010) is a cross sectional, self reported, self nominating, survey of over 2,000 UK individuals using the online website “Don’t Stay In” for the dance magazine Mixmag. The most recent survey included a question on mephedrone. Of self reported drug use, mephedrone was the fourth most commonly used drug in the last month (Cannabis (any), ecstasy (any) and cocaine powder ranked higher in terms of % use in the last month). The survey data show that 41.7% of respondents indicated they had ever used mephedrone, 33.6% in the previous month. These data suggest that the use of mephedrone is a new phenomenon since lifetime and past month prevalence is so similar in this survey. The synthetic cathinone methylone had been tried by 7.5% of respondents in the last month and 10.8% in their lifetime. Also other surveys of drug use show no reported mephedrone use amongst similar groups of young adults surveyed in bars and clubs in 2004-8 (Measham and Moore, 2009).

4.15. Data from the National Poisons Information Service (NPIS) show that telephone inquiries and TOXBASE accesses relating to cathinones increased sharply over the latter part of 2009 into 2010 (Thomas, 2010). NPIS enquiries more commonly involved males (2:1 sex ratio) and fitted an age profile similar to those taking MDMA with the greater proportion being in the 10-19 and 20-29 age groups, compared to cocaine which has a greater proportion of enquiries concerning the 20-29 and 30-39 age groups.

4.16. The most up to date information regarding visits to the FRANK website relating to the cathinones page are presented in Table 3. The number of visits has more than doubled in the past six months and has shown a month on month increase since September 2009 when the page was first published. This is mirrored by similar increases in calls to the talk to FRANK helpline.

Table 3: Visits to selected pages of the FRANK website between September 2009 and February 2010*.

FRANK website visits Cathinones % of visits Cannabis % of visits Cocaine % of visits Ecstasy % of visits
Sept-09 (page published 18/09/09) 255,765 9,366 3.7% 58185 22.7% 36925 14.4% 22541 8.8%
Oct-09 376,751 33,167 8.8% 72470 19.2% 47140 12.5% 35745 9.5%
Nov-09 444,069 47,954 10.8% 80246 18.1% 48489 10.9% 33167 7.5%
Dec-09 314,236 54,299 17.3% 53141 16.9% 38570 12.3% 28691 9.1%
Jan-10 358,537 66,236 18.5% 81986 22.9% 53736 15.0% 37910 10.6%
Feb-10 378,576 80,969 21.4% 51319 13.6% 53736 14.2% 38028 10.0%

*percentages are of total visits to individual drug webpages on FRANK website.

4.17. ‘Google Insights for search’ is a tool that allows search volume patterns, specifically using the Google search engine, to be compared across regions, categories, time frames, and properties. ‘Google Insights for search’ has been used in this instance to determine the proportion of searches, using Google, to search for the word ‘mephedrone’ since January 2009 to March 2010 in the UK (England region only). It can be seen from Figure 1 that there is a rising trend in the searches, although the month of March 2010 includes only partial data at this time. Please note that some months overlap due to the way in which the data is collated (weekly rather monthly).

Figure 1: Relative number of searches on Google for the term ‘mephedrone’.

4.18. Data provided by the Forensic Science Service (FSS) of police seizures show that the cathinone derivatives account for only a small proportion of total drug seizures. Although the cathinones are not illegal they generally present as ‘white powders’ (predominantly mephedrone – 89% of cathinone seizures).

5. Physical Harms (Toxicity, Dependency And Mental Health)

Acute toxicity

5.1. Most data regarding the harms of the cathinones (mephedrone in particular) are self-reported and there are very few clinical data available.

5.2. Wood et al., (2009) report the first case of sympathomimetic toxicity related to mephedrone (4-MMC) confirmed by toxicological screening where no other drugs or alcohol were detected.

5.3. Data from Guys and St Thomas’ hospital toxicology (Dargan and Wood, pers. comm.) over the last year show that from a total of 1600-1800 cases, of which 40% are due to recreational drugs, 25 of which presented with toxicity due to self reported mephedrone use (Table 4). Of these 25 cases cases, 80% were male with a mean age of 28.5y (SD ± 8.0 y). Reported clinical symptoms are shown in Table 5, clinical examination data are shown in Table 6.

Table 4: Cases of toxicity in individuals presenting due to self reported mephedrone use to Guys and St Thomas’ hospital

Number
January – March 2009 2
April – June 2009 0
July – September 2009 8
October – December 2009 5
January 2010 – 22nd February 2010 10

Table 5: Reported Clinical symptoms for cases of toxicity in individuals presenting due to self reported mephedrone use to Guys and St Thomas’ hospital

% presentations (n=25)
Agitation 52
Palpitations 20
Seizure 12
Vomiting 12
Sweating 12
Headache 4
Discoloration of the skin 0
Cool peripheries 0

Table 6: Clinical examination for cases of toxicity in individuals presenting due to self reported mephedrone use to Guys and St Thomas’ hospital

% presentations (n=25)
Tachycardia >100bpm 48%
Tachycardia >140bpm 16%
Hypertension (>160mmHg) 16%
GCS ≤ 8/15 16%
Bruxism 4%
Hyper-reflexia 4%

5.4. The clinical management of those cases at Guys and St Thomas’ was that:

  • Four (16%) required benzodiazepines for management of agitation
  • Twenty (80%) discharged from ED/observation ward
  • Five admitted to hospital
  • Four to general medical ward
  • One to ICU (for other drug toxicity: GBL)

5.5. Various user reports and clinical observations indicate that mephedrone abuse can cause a number of adverse side effects. Table 7 summarises self reported side effects of mephedrone in terms of increasing severity.

Table 7: Self reported side effects of mephedrone

Modest severity Moderate severity Most severe
Reduced appetite Insomnia Strong desire to re-dose, craving to recapture initial euphoric rush
Dry mouth Nausea (27%)* Uncomfortable changes in body temperature (sweating/chills) (67%)*
Pupil dilation Trismus and Bruxism Increased blood pressure and heart rate, palpitations (43%)*
Unusual body sensations Skin rashes serious vasoconstriction in extremities, cold or blue fingers (15%*)
Change in body temperature regulation Nystagmus and dilated pupils high doses can cause hallucinations and psychosis
Pain and swelling in nose and throat, nose bleeds, sinusitis (when insufflated)
Impaired short term memory, poor concentration
Dizziness, light headidness, vertigo (51%)*
Headache

*Data from Mixmag survey n=>2,000 (Winstock, 2010)

5.6. When taken in large quantities self-reported experiences by ‘psychonaut’ users described vivid hallucinations during 3 day binges of mephedrone (Linell, 2010). However, the quantities reportedly consumed are not likely to mirror those of most users.

5.7. The ACMD has received anecdotal reports from members of the public that when taken in conjunction with other drugs e.g. amphetamines the effects can be quite marked and lead to personality changes, paranoia and sometimes violent episodes.

5.8. Some of the adverse effects reported for methylone (Table 8 ) are similar to those reported for MDMA (ecstasy) (ACMD, 2009)

Table 8: Self reported side effects of methylone

Modest to moderate severity Most severe
Increase in heart rate and blood pressure Insomnia
General change in consciousness (as with most psychoactives) Hyperthermia and sweating
Pupil dilation, can lead to blurred vision Dizziness, confusion
Difficulty in focusing, restlessness Depersonalization, hallucinations, paranoia, fear (with high doses)
Change in perception of time Unwanted life-changing spiritual experiences
Slight increase in body temperature Gastrointestinal discomfort, nausea and vomiting
Muscle tension and aching Skin rashes common
Trismus and bruxism Hangover may include exhaustion, depression, disorientation, headache, amnesia

5.9. It is notable that several commonly reported side effects reflect the sympathomimetic actions of the cathinones. The NPIS is another important, independent source of information collected from telephone enquiries made by health professionals managing people presenting after mephedrone exposure and website visits. The most commonly reported clinical effects included tachycardia, palpitations, agitation, anxiety, palpitations and mydriasis. Chest pain, breathlessness, nausea, vomiting, headache, hypertension, confusion, hallucinations, peripheral vasoconstriction and convulsions have also been reported in some cases (Thomas, 2010). It is notable how closely the NPIS data match those provided from other sources.

5.10. Data from clinical examination confirms that tachycardia is a common symptom of mephedrone ingestion. Severe cases of cardiovascular toxicity or conditions such as hypopyrexia due to use of cathinones have not been reported (Dargan and Wood, pers. comm.). The majority of presentations have been recent and during the winter months, it is not known if the number of presentations due to conditions such as hypopyrexia will change during warmer weather.

5.11. Users also report severe vasoconstriction of extremities, leading to bluing of fingers or hands. It is worth noting that hyperpyrexia and vascular collapse are among the most dangerous life-threatening side effects of amphetamine misuse. Some of the acute adverse side effects induced by methylamphetamine include (ACMD, 2005):

  • Insomnia
  • Increased physical activity
  • Decreased appetite
  • Increased respiration
  • Hyperthermia
  • Increased heart rate and blood pressure
  • Irregular heart beat
  • Cardiovascular collapse and death (in overdose)
  • Confusion
  • Anxiety
  • Tremors

Cases of death where cathinones have been implicated

5.12. There have been at least 18 deaths in England where cathinones have been implicated. Currently, seven of these have provided positive results for the presence of mephedrone at post mortem. To date, in one case the coroner concluded that the death was “natural” and that an inquest was not required. The remaining cases are awaiting inquest.

5.13. There have been at least seven deaths in Scotland where cathinones have been suspected. Of these, one has been confirmed as the result of the “adverse effects of methadone and mephedrone”. Another case is probable, but underlying health issues contributed to the death and it awaits formal confirmation by the relevant Procurator Fiscal. The presence of mephedrone has been confirmed in a third case.

5.14. One case on Guernsey has provided positive post mortem toxicology results for mephedrone and is awaiting inquest.

5.15. One suspected case in Wales and a further case in Northern Ireland are awaiting toxicology and inquest.

5.16. The UK number of cases are subject to several caveats:

  • Not all suspected cases may have been identified;
  • That mephedrone may have been involved in a death cannot be confirmed until the relevant coroner or Procurator Fiscal has concluded her/his inquest or other formal inquiry; and,
  • The presence of mephedrone in post mortem toxicology does not necessarily imply that it caused or contributed to a death.

5.17. Mephedrone has been linked to the death of an 18-year old girl in Sweden (Gustaffsson and Escher, 2009). The report (December 2008) indicates that she had taken mephedrone and smoked cannabis. The woman was observed to first become sick and then unconscious. Forensic autopsy showed severe brain swelling, preceded by respiratory and circulatory arrest. No other sedatives, narcotics or alcohol were detected in the blood.

Chronic toxicity

5.18. There are so far no reports of the potential harmful effects of the long term use of mephedrone and related cathinones because the substances have only been used in recent months in the UK.

Dependence

5.19. Reports from a case study of mephedrone use (Linell, 2010) suggest that users can become regular users rapidly, although they are generally not in a ‘state of dependency’. However, this conclusion contrasts with the same report whereby users knew people who became daily users. Some users have reported developing cravings for mephedrone, methylone and MDPV after use. Arguing again by analogy with amphetamines, it is clear that the chronic use of amphetamines can lead to dependence, and a downward cycle of bingeing and periods of recovery associated with depression (ACMD, 2005), therefore it is likely that mephedrone use carries a similar risk of dependency.

5.20. Dargan and Wood (2010) report a single case of dependency on mephedrone in Glasgow where the individual had been using the drug for 18 months.

5.21. Data are not available on the number of individuals in treatment services related to the cathinones. However, the evidence suggests that the number is likely to be very small at the time of writing.

6. Societal Harms

Prevalence

6.1. The current prevalence of mephedrone and the related cathinones is not accurately known. Reports from drugs agencies, drug researchers, criminal justice, public health (Talk to FRANK) and education professionals suggest that mephedrone use appears to be very widespread and is growing. From emergence to current levels of usage, commentators have suggested that the rise in mephedrone use is unprecedented. Namely within a year it has risen from a very low baseline to become popular amongst adolescents and adults.

Young people

6.2. Media reports from the 8th March indicate that secondary school children were missing classes due to the use of the drug mephedrone causing sickness. The DCSF minister of State for Schools and Learners has written to schools. In the letter it makes clear that they do have the power to confiscate inappropriate items including a substance that they believe to be mephedrone (or any other drug, whatever its legal status); in line with the school’s behaviour policy and that such items do not need to be returned.

6.3. Mephedrone is sold by online retailers for an average price of £10/g. Given that users take approximately one gram over the course of a session, this makes the drug relatively cheap compared with other intoxicants, as well as being more easily available than alcohol and cigarettes for under 18 year olds who have access to the internet or a high street ‘head shop’.

6.4. There is some evidence that use has escalated following media reports. For example, Google Trends (which collates Google searches) shows that UK Google searches have increased from a very low base in the last twelve months (see paragraph 4.17), with peaks which coincide with media coverage of mephedrone use and deaths where mephedrone might be implicated. The most popular Google search term is for the words “buy mephedrone online”, with four of the top five search terms containing the words “buy” and “mephedrone”. Furthermore online mephedrone retailers have reported an increase in sales following media coverage (The Guadian, 2009)

Anti-social behaviour / acquisitive crime

6.5. The ACMD has been presented with two recent cases where mephedrone users have reported that their use was funded by acquisitive crime (robbery and burglary). At present there remains only limited evidence of a relationship between mephedrone and anti-social behaviour; mainly related to the open dealing and consumption of mephedrone. Notwithstanding the legal implications, the dealing in unspecified white powders for the purposes of intoxication can amount to a public nuisance with a detrimental impact on public confidence.

Organised crime

6.6. There are indications that criminal groups are becoming involved in the supply of mephedrone to the public in the UK (SOCA, 2010). At present the mephedrone retail trade operates mainly through internet importation and distribution and ‘head shops’. However, there are reports of some UK drug suppliers selling mephedrone in dance clubs and at street level either as well as, or instead of cocaine and MDMA, due to mephedrone’s relatively low price, high purity and easy availability. Reports from Guernsey, where importation is currently banned (and prices are reported to be considerably higher), suggest that a street trade in mephedrone has developed. Reports from Guernsey customs officials note that supply is through illegal drug suppliers and incidences of violence have emerged associated with the street trade in mephedrone (McVean, 2010).

Stockpiling

6.7. It is reported that some users are planning to buy large quantities of mephedrone to ‘stockpile’ for future use and future sale should regulation be introduced (Measham et al., 2010; ACPO, pers. comm.). This could lead to an illegal supply of mephedrone coming on to the market should it be controlled under the Misuse of Drugs Act 1971.

Consumption patterns

6.8. It is of concern that there are reports that users of mephedrone have a tendency to re-dose (or ‘fiending’) and for some individuals the consumption of mephedrone is alone at home (Newcombe, 2010; Linnell, 2010). Together these two features of mephedrone consumption patterns may expose users to increased risks such as overdose or cardiovascular problems.

7. Current controls

Present UK controls

7.1. Cathinone (Class C), methcathinone (Class B), diethylpropion (Class C) and pyrovalerone (Class C) are controlled under the Misuse of Drugs Act 1971. However, other derivatives and analogues are not presently controlled (including mephedrone).

7.2. Although paragraph 1(c) of Part 1 (Schedule 2) of the Misuse of Drugs Act 1971 offers some scope for the control of substances which are structurally related to the phenethylamine backbone, it is primarily concerned with ring-substituted amphetamine-like compounds. Specifically, no mention is made of the presence of any substituents (other than hydrogen) at the β-carbon of the phenethylamine backbone (recall that the cathinones all possess a β-ketone oxygen; see Figure 1).

7.3. Irrespective of whether controls for the cathinones are implemented under the Misuse of Drugs Act 1971, the rapidity and easy availability of mephedrone and other cathinones (including websites set up so that vendors that can deliver to individual addresses) does raise the question of whether other legislation and regulation should be available.

International Control

7.4. Some of the substituted cathinones could conceivably be considered as being ‘structurally similar’ to cathinone and methcathinone, which are both already listed in Schedule 1 of the United Nations Convention on Psychotropic Substances 1971. It is therefore possible that some cathinones could be controlled through the implementation of analogue control where such control mechanisms exist.

7.5. Denmark controls a number of cathinones, including mephedrone, methylone and MDPV. Mephedrone has been controlled in Sweden since December 2008; the Swedish authorities have indicated that they also intend to classify MDPV and butylone. Mephedrone is controlled (as a medicinal product) in Finland, and it is anticipated that it will shortly be controlled in Germany, since the German Federal Cabinet made a decision to subordinate a number of materials to the Betäubungsmittelgesetz in January 2009. Methylone is also controlled in the Netherlands.

8. Public Health

8.1. The FRANK campaign (see also paragraph 4.16) provides information on the potential risks of taking cathinone compounds and there was also a recent campaign to highlight the dangers of ‘legal highs’ (‘Crazy Chemist’).

8.2. Lifeline have produced an information leaflet that provides harm reduction advice specific to mephedrone and answers frequently asked questions from users or potential users (Lifeline, 2010). The ACMD is also aware that CairScotland have produced and distributed information leaflets warning of the dangers of these substances (CairScotland, 2010).

8.3. Other than the above there is presently a limited amount of public health information regarding mephedrone and the cathinones. Although recent media profile has presented much apparent public health information it is not always credible or consistent.

9. Conclusions And Recommendations

9.1. Although the current prevalence of mephedrone and related cathionones is relatively low in the UK, use appears to have grown rapidly in the past year.

9.2. The ACMD would like to emphasise that mephedrone and the related cathinones are likely to be harmful to users and in tandem with control mechanisms there should be a credible and comprehensive public health campaign. The messages promulgated by FRANK provide a good basis upon which this should be built.
Control and regulation

9.3. The ACMD consider that the harms associated with mephedrone and the cathinones are commensurate with the amphetamines and therefore those substances in Class B; therefore the ACMD recommend that the cathinones be controlled as Class B substances under the Misuse of Drugs Act 1971.

9.4. The ACMD recommend that, excluding the four compounds already controlled (see paragraph 2.2) and the API Bupropion, the cathinones should be controlled by a generic definition under the Misuse of Drugs Act 1971 – see Annex A, p31, and in schedule 1 of the Misuse of Drugs Regulations 2001.

9.5. The naphthyl analogue of pyrovalerone is now advertised on the Internet and is being retailed as “NRG-1”. The ACMD intend to review these substances and provide further advice at a later date.

9.6. The ACMD recommend that the government implement appropriate additional controls and regulation of the cathinones (which would include mephedrone) through, for example:

  • Import controls
  • Serious Organised Crime Agency (SOCA)

9.7 The ACMD understand that to implement import controls is not administratively burdensome and would stop non-EU imports; where it is understood much of the importated cathinones originate from. The ACMD also believe that SOCA have a role in informing suppliers of the cathinones of the implementation of import controls, trading standards and, if implemented, forthcoming control under the Misuse of Drugs Act 1971.

9.8. The ACMD notes that the cathinones have no efficacy as plant fertiliser products or as bath salts and could be the subject of a prosecution under the Trade Descriptions legislation.

Public Health

9.9. Directors of public health in PCTs should be tasked with cascading information to raise awareness of the cathinones – symptoms of use and information on where to seek advice – among GP’s, A&E departments, medical directors / advisors and others as appropriate.

9.10. The ACMD recommends that all agencies involved in the health, education and rehabilitation of young persons should disseminate information, in appropriate formats, as provided by the Department of Health and Home Office, as to the risks of using mephedrone (and associated compounds). We include in this Drug Action Teams (and equivalents e.g. DAATs in the Devolved Administrations), Childrens’ Trust Boards, Youth Offending Teams and Schools.

9.11. We recommend that the FRANK webpages related to the cathinones are given due prominence and that supplementary educational material is easily available. The information provided should be credible and consistent.

9.12. In relation to 9.9-9.11 it is important that the risks of mixing these drugs with other substances (including alcohol) are highlighted.

9.13. The ACMD are presently identifying information streams to update ministers and provide information on both emerging drugs of misuse and emerging trends concerning established illegal drugs. The ACMD consider that this work will assist it in advising on ‘legal highs’ in the future. Among other measures, the continuing development of datasets from drug amnesty bins will contribute to providing an early warning of such emerging trends.

9.14. Appropriate treatment advice and provision should be available to those who have developed cathinones-related problems of which health professionals and drugs service providers should be aware.

Research

9.15. Present forensic analytical testing of the cathinones is expensive and a process that can take some time. Currently, there is no simple drug field test available for cathinones. There is an urgent need to develop a simple and reliable field test.

9.16. For the purposes of identification of cathinone derivatives by forensic providers and pathology laboratories, and the development of drug field tests, there is an urgent need to develop and make available a library of reference standards.

9.17. There is presently a lack of data concerning the involvement of the cathinones in drug-related deaths (DRDs). Therefore, we recommend that the Ministry of Justice approach Her Majesty’s Coroners to include, in the case of suspected DRDs, tests for the cathinones.

9.18. The ACMD welcome the collation of a joint report initiated by the European Drug Centre for Drugs and Drud Addiction (EMCDDA) in respect of mephedrone. However, we understand that this review will be limited in scope to mephedrone as an individual compound. The purpose of the present report is to review the broad spectrum of cathinone derivatives already encountered in the UK and to provide advice to ministers at the earliest opportunity. The ACMD will keep under consideration all emerging evidence including the EMCDDA’s forthcoming report(s) and will provide further advice to ministers accordingly.

9.19. There is a need for more basic research to examine the similarities and differences between the cathinones and their amphetamine equivalents.

9.20. We welcome the inclusion of a specific question on mephedrone in the British Crime Survey to develop the knowledge base on prevalence. The ACMD also recommends more social research to inform our understanding of drug trends, motivations for drug use, fluctuations in demand, and policy implications regarding deterrence, displacement and desistence.

9.21. The ACMD would welcome the continuing collation of data sets concerning toxicity, clinical case reports and dependence liability collected from hospital admissions and treatment services.

10. References (Including Written And Oral Evidence

ACMD, 2009. MDMA (‘ecstasy’): a review of its harms and classification under the Misuse of Drugs Act 1971. ISBN 978-1-84726-868-6

ACMD, 2005. Methylamphetamine Review.CairScotland, 2010. Report to the ACMD.

Cozzi, N.V., Sievert, M.K., Shulgin, A.T., Jacobill, P. and Ruoho, A.E. (1999) Inhibition of plasma membrane monoamine transporters by beta-ketoamphetamines. European Journal of Pharmacology. 381: 63-69.

Dal Cason, T.A., Young, R and Glennon R.A. (1997) Cathinone: an investigation of several N-alkyl and methylenedioxy substituted analogs. Pharmacology Biochemistry and Behavior. 58: 1109-1120

Druglink March/April 2009. Mephedrone: The future of drug dealing?

Druglink. January/February 2010. Teenage Kicks. Vol 25. Issue 1.

Druglink. January/February 2010. World Wired Web Vol 25. Issue 1. [Synchronium: This article quotes me. Woo!]

Feyissa, A.M. and Kelly, J.P. (2008) A review of the neuropharmacological properties of khat. Progress in Neuro-Psychopharmacology and Biological Psychiatry. 32: 1147-1166.

Glennon, R.A., Yousif, M., Naiman, N. and Kaliz, P. (1987) Methcathinone: a new and potent amphetamine-like agent. Pharmacology Biochemistry and Behavior. 26: 547-551.

The Guardian, (2009), Mephedrone and the problem with ‘legal highs’, 5th December. Online at: http://www.guardian.co.uk/society/2009/dec/05/mephedrone-problem-legal-highs [accessed 30th March 2010]

Gustaffsson, D. and Escher, C. (2009) Mefedron. Internetdrog som tycks ha kommit för att stanna. (Mephedrone – Internet drug that seems to have come to stay). Läkartidningen. 106: 2769-2771.

Hand, T., Rishiraj, A. (2009) Seizures of Drugs in England and Wales 2008/09. Home Office Statistical Bulletin 16/09. London: Home Office.

Lifeline. 2010. Mephedrone Frequently Asked Questions. www.lifelinepublications.org (publications@lifeline.org.uk)

Linell, M. (2010) Case study: use of mephedrone in a Northern Town. The Lifeline project. Oral evidence to the ACMD.

McVean, C. (2009) The adverse effects of those “Legal High” powders containing cathinone derivatives on the community in Guernsey. States of Gurnsey, Customs and Immigration Service.

McVean, C. (2010) The impact of cathinones on a small island community. States of Gurnsey, Customs and Immigration Service.

Measham, F. and Moore, K. (2009) Repertoires of Distinction: Exploring patterns of weekend polydrug use within local leisure scenes across the English night time economy; Criminology and Criminal Justice, 9: 437-464.

Measham, F., Moore, K., Newcombe, R. and Welch, Z. (2010) Tweaking, bombing, dabbing and stockpiling: the emergence of mephedrone and the perversity of prohibition. Drugs and Alcohol Today. 10: 14-21.

Meltzer, P.C., Butler, D., Deschamps, J.R. and Madras, B.K. (2006) (4-Methylphenyl)-2-pyrrolidin-1-yl-pentan-1-one (Pyrovalerone) analogues: a promising class of monoamine uptake inhibitors. Journal of Medicinal Chemistry. 49: 1420-1432.

Nagai, F., Nonaka, R. and Kamimura, K.S.H. (2007) The effects of non-medically used drugs on monoamine neurotransmission in rat brain. European Journal of Pharmacology. 559: 132-137.

Newcombe, R. (2010) Mephedrone: the use of mephedrone (m-cat, Meow) in Middlesbrough. Manchester: Lifeline Publications & Research.

New Musical Express (2010), Mephedrone – How dangerous is the UK’s favourite new drug, 8th February. Online at: http://www.nme.com/blog/index.php?blog=10&p=7956&more=1 [accessed 30th March 2010]

Ramsey, J. (2010) Analysis of white powders seized by UK border agency at London Heathrow airport. Written evidence to the ACMD.

Serious Organised Crime Agency (SOCA). (2010) Drugs report – Mephedrone.

Sumnall, H. and Wooding, O. (2009) Mephedrone – an update on current knowledge. North West Public Health Observatory, Centre for Public Health, Liverpool John Moores University.

Thomas, S. (2010) Enquiries relating to the cathinones. National Poisons Information Service, Health Protection Agency. Oral evidence to the ACMD.

UK Border Agency (2010) UKBA – Treatment of cathinones at the frontier. Written evidence to the ACMD.

White, M. (2010) Cathinone Derivatives: Chemistry, Prevalence and Legal status. Forensic Science Service. Oral evidence to the ACMD.

Winstock, A. (2010) Results of the 2009/10 Mixmag drug survey. Oral evidence to the ACMD.

World Health Organisation (1995) WHO Expert Committee on Drug Dependence. Twenty-ninth report. WHO Technical Report Series. No.856.

Wood, D.M., Davies, S., Puchnarewicz, M., Button, J., Archer, R., Ramsey, J., Lee, T., Holt, DW. and Dargan, P.I. (2009) Recreational Use of 4-methylmethcathinone (4-MMC) presenting with sympathomimetic toxicity and confirmed by toxicological screening. Clinical Toxicology. 47: 733.

Zaitsu, K., Katagi, M., Kamata, H., Kamata, T., Shima, N., Miki, A., Tsuchihashi, H. and Mori, Y. (2009) Determination of the metabolites of the new designer drugs bk-MBDB and bk-MDEA in human urine. Forensic Science International. 188: 131-139.

Wednesday, January 06th, 2010 | Author: Synchronium

Mephedrone isn’t just another obscure research chemical. Everyone’s at it, all the time. Despite the media scare stories, over 20% of mephedrone users polled on Drugs Forum take more than 10g each month, with just under half of those consuming over 20g.  A lot of replies to that thread also reveal how quickly usage can escalate, meaning those results are probably on the conservative side. “More acceptable than weed”, some have been saying. “Even my non-druggie friends are doing it!”

Mephedrone MoleculeMephedrone has achieved this unusual status thanks to a number of factors. Firstly, it’s an effective stimulant, which is more than can be said for ecstasy and cocaine these days; the former consisting mainly of disagreeable piperazines (due to their cheapness, and until recently, their legal status) rather than MDMA, and the latter being incredibly inpure. Next up is the lack of a comedown that would normally be experienced with other stimulants, especially for new users. This means people can keep taking it for days on end with little to no perceived negative effects. The other major contributor is the price – at around £10 a gram, it undercuts a great many of its illegal counterparts, while often being more effective, or at least more reliable. Other factors include (potentially inaccurate) purity measures, the ease of buying it from the comfort of your own home  with a credit card, rather than handing over a fistful of crumpled notes to a typical drug dealer, and of course its legal status.  Although the majority of users understand that legal doesn’t mean safe, the fact that you can’t be imprisoned alongside murderers, rapists and other violent criminals for possessing it is certainly a plus. Oh, and it’s psychologically addictive – it won’t kill you if you stop taking it, but you might be able to think of nothing else.

Reports of children doing it, entire friendship groups crumbling as a result of compulsive use and the media frenzy have got people understandably worried and calling for this “evil” drug to be banned.

I Disagree.

Why We Shouldn’t Ban Mephedrone

If you haven’t read Top 10 Reasons Why Legal Highs Should Stay Legal, have a quick look now. Here are a few more mephedrone-specific points:

  • Changing the law won’t change demand – we’ve already seen this with the reclassification of cannabis and the massive popularity of the synthetic cannabinoids that just got banned. Also, the decriminalisation of drugs in Portugal has resulted in not only a decline in drug use, but also a decline in drug-related illness and death (HIV from sharing needles, for example), as well as a increase in the number of people seeking treatment for addiction.
  • The current classification system doesn’t work – Our current ABC system is a shambles, as any scientist, or indeed anyone that values evidence, will testify. Currently, one of the safest drugs, MDMA, sits alongside one of the (if not the) most dangerous, heroin. Cannabis, and soon the synthetic cannabinoids, which haven’t killed anyone, are positioned alongside amphetamine, a drug with far more potential dangers and addiction, meanwhile alcohol, which hospitalises over 1200 people a day and costs the NHS several billion pounds a year, remains legal along with tobacco. I would estimate the harms of mephedrone to be similar to amphetamine, if not a little worse, but placing it in class B would give the message that it is as dangerous as cannabis. Placing it in class A wouldn’t be right, as it certainly doesn’t appear to be as dangerous as heroin, but it’s probably worse than MDMA. Placing it in class C would be ridiculous, as it suggests cannabis is more dangerous. It would be impossible to have a sensible think on how to classify it properly without getting a headache.
  • If mephedrone’s popularity persists, more people will die – in the event of an overdose or an idiosyncratic response, people taking illegal drugs are far more likely not to either tell the doctors what they’ve taken or even go to hospital in the first place. That’s not to say that mephedrone will kill a tonne of people, but if no one ever died whilst on mephedrone, that would be pretty weird…

What Should We Do Instead?

Just because I don’t think it should be illegal doesn’t mean I think the current situation is perfect. Instead, I think the best thing the government could do to reduce harm is keep it legal, restrict its sale to people over the age of 21 and slap on a tax of something like £15 per gram. This would make it much harder to buy large quantities at a time, especially for kids with little expendable income, and so curb mephedrone’s addictive nature. Obviously, this wouldn’t be the perfect solution, as some teenagers would still be able to get hold of it just like they do with alcohol, but at least less people will be taking it and a lot more money would be available to better fund the NHS, harm reduction methods, education about the drug and scientific research.

Why Mephedrone Won’t Be Classified Immediately

Heh. The government have certainly shot themselves in the foot here. Thanks to the sacking of Dave Nutt and the resignation of three others on the ACMD, the government now lacks the skills to ban it. Dr Les King, one of the resignees, was responsible for a large part of the ban last month, so without people like him, the government can’t do anything for a while. Looks like it’ll be legal for a good year or so yet.

How YOU Can Help

Well, you can’t really do anything about the mephedrone situation, but you can help me out by posting Mephedrone Cat everywhere!

You might save millions of lives by directing them to some of my harm reduction articles. :)

Tuesday, January 05th, 2010 | Author: Synchronium

Mephedrone Cat

Mephedrone Cat knows when enough is enough, and so should you!

Thursday, December 17th, 2009 | Author: Synchronium

Apart from the exponentially expanding list of slang names for mephedrone, there have been a couple of interesting new developments everyone should be aware of.

#1 – Gabrielle Price Died From Bronchopneumonia

Gabi has featured in pretty much every mephedrone-related news story these past few weeks, since she died at a party after consuming mephedrone and ketamine (and probably alcohol as well, although alcohol is so ingrained into our society it wouldn’t occur to anyone to report it). It turns out that Gabi actually died from bronchopneumonia following a group A streptococcal infection. Don’t get me wrong, this is nothing to be cheery about – a teenager still died. I’m just reporting this here because nowhere else will report it, since it’s no longer a story. Actually, if you read about another mephedrone article that mentions this girl, do everyone a favour and leave a link to this blog post in their comments.

This also doesn’t mean mephedrone is safer than we thought. Being on any drug isn’t a good idea if you also have a potentially fatal illness, never mind a cocktail of drugs in a party environment.

#2 – No One Ripped Their Balls Off

This is another piece of bullshit whipped out by the media at every opportunity: apparently, some young gentleman thought he saw centipedes crawling about his person and tore his balls off in (a totally proportionate) response. Turns out, this probably didn’t happen, since the “facts” were obtained from unsubstantiated reports on poor quality forums and chat rooms. Well done, the media!

#3 – West Yorkshire Police Have No Idea What The Fuck They’re Talking About

Here’s what they had to say following a poster launch designed to raise awareness.

“MCAT is a substance which is currently legal, however; it is predominately used for plants and can have quite an adverse effect if consumed by a human.

“We know that this substance is often used by young people, particularly between the ages of 14 to 25. These posters are therefore designed to reach this particular generation and help them to make an informed decision.

“Police and partners in Kirklees will be placing them in various locations frequented by young people and hopefully they will take in the message.

“MCAT is often referred to as a ‘legal high’ and gives the impression that because it’s legal, it is safe. There are number of substances, which are not controlled drugs or illegal which can be abused. We would always advise against ingesting anything into your body which is not for a bone fide medical reason. MCAT in particular has the potential to damage both mental and physical health.

Their first mistake might be hard to spot, but MCAT means “methcathinone” which is NOT mephedrone (4-MMCAT). Their second mistake needs no more explaination or emphasis than a simple emboldening of their own words.

Unbelievable.

Category: Drugs  | Tags: bullshit, media, mephedrone  | 7 Comments
Thursday, December 03rd, 2009 | Author: Synchronium

I don’t know how much people outside “the industry” have heard about mephedrone, but by all accounts, it’s exploded in popularity over the past few months. In the last three months, there’s been at least 50 news stories reposted to Drugs-Forum on the topic, and probably quite a few more that haven’t been picked up. We’ve got reports of teens dying, 11 year olds taking the stuff and a guy ripping his balls off – all the classic examples of the media whipping up an unnecessary (and untrue) shit storm. I’ve also read lots of anecdotes about the drug’s prevalence among students, friendship groups and even dealers of illegal drugs (points for diversification!). Since my articles on JWH-018 have been reasonably popular and stimulated some interesting discussion, I felt it was about time we gave mephedrone the same treatment.

The Basics

Mephedrone is not only cheap and legal, but it’s also incredibly effective. It’s a short-acting stimulant that feels something like a mixture of cocaine and ecstasy. If that wasn’t enough to explain its popularity, then the icing on the cake is the almost complete lack of a comedown the next day when used in moderation. Purities of over 99% make another great selling point when compared with similar illegal drugs.

Mephedrone is a white, crystalline powder with little to no smell. The term “Mephedrone” comes from methyl-ephedrone, describing the chemical structure.  Other names for it include:Mephedrone Powder

  • 4-MethylMethCathinone (methcathinone is another name for ephedrone)
  • 4-MMC
  • 4-MMCAT
  • MCAT (This is incorrect, but people use it anyway)
  • Meow
  • Bubbles (seems to be a brand name for capsules containing it and methylone, another research chemical)

Effects include an initial euphoria, which tapers off to a milder stimulation. Mephedrone does seem to oil social situations rather well and get everyone talking, laughing and having a good time, especially during the initial euphoria. Several users have compared it to cocaine, but some how less jittery and “arrogant”, while others will compare it to a more rushy ecstasy (which has to be a good thing, given the current state of the MDMA market). Actually, the effects seem to depend very much on dose and your chosen route of administration.

The most common ways to get this stuff into your blood are snorting it and eating it. As you can probably imagine, eating it will give a longer, less intense experience, while doing lines of it will give a much shorter, more intense buzz and make you want to keep taking it, but we’ll get to that later. Oh, I should probably mention that snorting it feels not too dissimilar from being raped in the sinuses by a Portuguese Man o’ War, particularly for your first line.

Other reported methods of administration include shoving it up your arse, requiring less than an oral dose and peaking somewhere between an oral or insufflated dose, and intravenously injecting it, which apparently isn’t that great, having a similar effect profile to being snorted with a million times the risk.

Dosage

A single oral dose would typically be between 150 mg and 300 mg, while lines can range from 50 mg to a monster 150 mg rail.

Pharmacology

MephedroneIf only we knew! Unfortunately, no one knows anything for certain, so we’re forced to do a bit of guesswork. If it feels like a cross between MDMA and cocaine, then we can assume that there’s some serotonin and dopamine involvement. The apparent addictiveness of mephedrone (more on that later, srsly), along with talkativeness also points to dopamine pathways, while the similarity of some side effects compared with serotonin depletion (taking too much MDMA or abruptly discontinuing selective serotonin reuptake inhibitors [SSRIs]) points to the serotonin pathways.

I would love some more information on this, so if you ever come across anything in the future, please report back!

Misconceptions

There are a number of misconceptions surrounding mephedrone, which we should clear up:

Legal does not mean safe

While it seems that users can take vast quantities of the stuff and still function,  we don’t know what the long term effects of mephedrone use will entail. A handful of people have died from taking it too. While the number is tiny compared with alcohol, it’s still always a good thing to remember.

Purity isn’t necessarily accurate

Mephedrone bought online will certainly be purer than illegal drugs bought on the street, but claims of 99.9% purity may not be true. Since it’s not sold for human consumption (like everything legal and fun), I’m not sure an accurate purity measure is required. Also, that 0.01% could be some deadly poison. It probably won’t be, but it might!

“Plant Food” might not be mephedrone

Lots of those news stories I’ve mentioned above have listed a million different “street names” for this drug, including “Plant Food”. No one is actually calling it plant food, it’s just how it, and lots of other compounds like it, are sold. If you’ve obtained anything psychoactive packaged as plant food, make sure you know what the hell it is you’re taking!

Side Effects

Side effects can be many and varied, some serious and some not. Mephedrone shares a number of the typical side effects you’d expect to find with any stimulant, such as:

  • Increased heart rate (tachycardia)
  • Raised blood pressure (hypertension)
  • Not wanting to sleep (insomnia)
  • Not wanting to eat (anorexia)
  • Chewing/grinding teeth (bruxism)
  • Moving your eyes loads (nystagmus)

More mephedrone-specific, and so perhaps more serious side effects include

  • Turning blue at the extremities & feeling cold (vasoconstriction)
  • Pains in the chest, throat and nose
  • Nosebleeds when snorted, especially with prolonged or frequent use

The more you use, the more the side effects become apparent and the initial pleasant effects diminish. Also, significant evidence is coming forward suggesting circulation issues are not just vasoconstriction, but something more serious – autoimmune vasculitis, where the immune system attacks your own body. This would seem to account for some of the odd and infrequent side effects, such as bruising or turning blue at the joints. Current reports suggest that this isn’t an issue of a dodgy supply for some people compared with the rest, but rather a small percentage of the population are at risk, probably because of some genetic differences. If you’ve noticed this, stop taking mephedrone! This condition will only get worse the more you consume. Add to that the usual stimulant-induced vasoconstriction, and you could find yourself with some serious problems.

Warning

Mephedrone can be addictive!

  • It’s easy to have several large sessions per week because of the cheapness and lack of comedown. Several people have reported taking over 20g per month.
  • It’s easy to keep taking it, especially when snorted, so a single line can turn into 5g session easily if you lack self control. There have been a few reports of people taking 5-7g over a 48 hour long single session.
  • Tolerance can also develop, so more is required for the same effect.

Safe Usage Tips

Mephedrone is not 100% safe, but then again, nothing is. To make sure you’re as safe as possible, here are a few tips:

  • Don’t buy it in bulk – 80% of people won’t be able to resist the charms of a massive bag of the stuff. Sure, you may save a few quid on the gram, but if your consumption sky-rockets, you’re not saving anything.
  • If you do buy in bulk, limit yourself – it’s all too easy to “just have one more line”, so perhaps let your friend look after your supply for you, or if you’re going out, take a predetermined quantity out with you and stick to it.
  • Don’t snort it if you think there’s any chance you will become addicted to it – this route of administration makes you want to keep on taking it much more than an oral dose, despite the snotty nose and watering eyes.
  • Eat healthily before and after – your body needs a good supply of nutrients, vitamins, etc to stay healthy and replenish your neurotransmitters. Forcing yourself to eat, especially during long binges, is essential. At least munch some vitamin tablets or something.
  • Take some magnesium supplements – this helps relax your muscles and stop all the jaw clenching and chewing that goes with most stimulants.
  • If you’re going to snort it, blow your nose soon after to clear out any powder – drugs aren’t  absorbed from your nostrils, so you want to get rid of it. I’d also suggest giving your nose a wash with either a spray bottle and some water, or by cramming some wet tissue up there with your head tilted back.