Methylenedioxypyrovalerone

From Wikipedia, the free encyclopedia
Jump to: navigation, search
Methylenedioxypyrovalerone
MDPV.svg
MDPV 3d.gif
Clinical data
Routes of
administration		 Oral, insufflation, intravenous, rectal, vaporization
Legal status
Legal status
  • AU: S9 (Prohibited)
  • CA: Schedule I
  • DE: Anlage II (Prohibited)
  • UK: Class B
  • US: Schedule I
  • Illegal in Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia, France, Hungary, Ireland, Finland, Italy, Latvia, Luxembourg, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Sweden, Turkey[1]
Pharmacokinetic data
Metabolism Hepatic
Excretion Primarily urine (renal)
Identifiers
CAS Number 687603-66-3 YesY
24622-62-6 (HCl)
PubChem (CID) 20111961
ChemSpider 16788110 YesY
UNII E7LD6JMR0L N
ECHA InfoCard 100.222.786
Chemical and physical data
Formula C16H21NO3
Molar mass 275.343 g/mol (freebase)
3D model (Jmol) Interactive image
Chirality Racemic mixture
 NYesY (what is this?)  (verify)

Methylenedioxypyrovalerone (MDPV) is a stimulant of the cathinone class which acts as a norepinephrine-dopamine reuptake inhibitor (NDRI).[2] It was first developed in the 1960s by a team at Boehringer Ingelheim.[3] MDPV remained an obscure stimulant until around 2004 when it was reportedly sold as a designer drug. Products labeled as bath salts containing MDPV were previously sold as recreational drugs in gas stations and convenience stores in the United States, similar to the marketing for Spice and K2 as incense.[4]

Appearance[edit]

The hydrochloride salt exists as a very fine, hygroscopic, crystalline powder that tends to clump to itself, resembling something like powdered sugar. Its color can range from pure white to a yellowish-tan and has a slight odor that strengthens as it colors. Impurities are likely to consist of either pyrrolidine or alpha-dibrominated alkylphenones from either excess pyrrolidine or incomplete amination, respectively, during synthesis. These impurities likely account for its discoloration and fishy (pyrrolidine) or bromine-like odor, which worsens upon exposure to air, moisture, or bases.[5]

Pharmacology[edit]

Methylenedioxypyrovalerone has no record of FDA approved medical use.[6] MDPV has been shown to produce robust reinforcing effects and compulsive self-administration in rats, though this had already been provisionally established by a number of documented cases of misuse and addiction in humans, before the animal tests had been carried out.[7][8]

MDPV is the 3,4-methylenedioxy ring-substituted analog of the compound pyrovalerone, developed in the 1960s, which has been used for the treatment of chronic fatigue and as an anorectic, but caused problems of abuse and dependence.[9]

Other drugs with a similar chemical structure include α-pyrrolidinopropiophenone (α-PPP), 4'-methyl-α-pyrrolidinopropiophenone (M-α-PPP), 3',4'-methylenedioxy-α-pyrrolidinopropiophenone (MDPPP) and 1-phenyl-2-(1-pyrrolidinyl)-1-pentanone (α-PVP).

Effects[edit]

MDPV acts as a stimulant and has been reported to produce effects similar to those of cocaine, methylphenidate, and amphetamines.[10]

The primary psychological effects have a duration of roughly 3 to 4 hours, with after effects such as tachycardia, hypertension, and mild stimulation lasting from 6 to 8 hours.[10] High doses have been observed to cause intense, prolonged panic attacks in stimulant-intolerant users,[10] and there are anecdotal reports of psychosis from sleep withdrawal and addiction at higher doses or more frequent dosing intervals.[10] It has also been repeatedly noted for inducing irresistable cravings to re-administer.[10][11]

Reported modalities of intake include oral consumption, insufflation, smoking, rectal and intravenous use. It is supposedly active at 3–5 mg, with typical doses ranging between 5–20 mg.[10]

Metabolism[edit]

MDPV undergoes CYP450 2D6, 2C19, 1A2,[12] and COMT phase 1 metabolism (liver) into methylcatechol and pyrrolidine, which in turn are glucuronated (uridine 5'-diphospho-glucuronosyl-transferase) allowing it to be excreted by the kidneys, with only a small fraction of the metabolites being excreted into the stools.[13] No free pyrrolidine will be detected in the urine.[14]

Molecularly, this is seen as demethylenation of methylenedioxypyrovalerone (CYP2D6), followed by methylation of the aromatic ring via catechol-O-methyl transferase. Then hydroxylation of both the aromatic ring and side chain takes place followed by an oxidation of the pyrrolidine ring to the corresponding lactam, with subsequent detachment and ring opening to the corresponding carboxylic acid.[15]

Detection in biological specimens[edit]

MDPV may be quantified in blood, plasma or urine by gas chromatography-mass spectrometry or liquid chromatography-mass spectrometry to confirm a diagnosis of poisoning in hospitalized patients or to provide evidence in a medicolegal death investigation. Blood or plasma MDPV concentrations are expected to be in a range of 10–50 μg/L in persons using the drug recreationally, >50 μg/L in intoxicated patients, and >300 μg/L in victims of acute overdose.[16]

Legality[edit]

In the UK, following the ACMD's report on substituted cathinone derivatives,[11] MDPV is a Class B drug under The Misuse of Drugs Act 1971 (Amendment) Order 2010, making it illegal to sell, buy, or possess without a license.[17][18]

MDPV is specifically listed as a controlled substance in Finland (listed appendix IV substance as of June 28, 2010),[19] Denmark and Sweden. In Sweden a 33-year-old man has been sentenced to six years in prison by an appellate court, Hovrätt, for possession of 250 grams of MDPV that had been acquired prior to criminalization.[20]

Australia[edit]

In Western Australia, MDPV has been banned under the Poisons Act 1964, having been included in Appendix A Schedule 9 of the Poisons Act 1964 as from February 11, 2012. The Director of Public Prosecutions for Western Australia announced that anyone intending to sell or supply MDPV faces a maximum $100,000 fine or 25 years in jail. Users face a $2000 fine or two years' jail. Therefore, anyone caught with MDPV can be charged with possession, selling, supplying or intent to sell or supply.[21]

Canada[edit]

Canadian Health Minister Leona Aglukkaq announced on June 5, 2012 that MDPV would be listed on Schedule I of the Controlled Drugs and Substances Act, which was realized on September 26, 2012.[22]

United States[edit]

In the United States, MDPV is a DEA federally scheduled drug. On October 21, 2011, the DEA issued a temporary one-year ban on MDPV, classifying it as a schedule I substance. Schedule I status is reserved for those substances with a high potential for abuse, no currently accepted use for treatment in the United States and a lack of accepted safety for use of the drug under medical supervision.[23]

Prior to the Federal ban being announced, it was already banned in Louisiana and Florida.[24] On March 24, 2011, Kentucky passed bill HB 121 which makes MDPV, as well as three other cathinones, controlled substances in the state. It also makes it a Class A misdemeanor to sell the drug, and a Class B misdemeanor to possess it.[25]

MDPV is banned in New Jersey under Pamela's Law. The law is named after Pamela Schmidt, a Rutgers University student, murdered in March 2011 by an alleged user of MDPV.[26] A toxicology report later found that no "bath salts" were present in his system.[27]

On May 5, 2011, Tennessee Governor Bill Haslam signed a law making it a crime "to knowingly produce, manufacture, distribute, sell, offer for sale or possess with intent to produce, manufacture, distribute, sell, or offer for sale" any product containing 3,4-Methylenedioxypyrovalerone (MDPV).[28]

On July 6, 2011, the governor of Maine signed a bill establishing fines for possession and penalties for trafficking of MDPV.[29]

On October 17, 2011, an Ohio law banning synthetic drugs took effect barring selling and/or possession of "any material, compound, mixture, or preparation that contains any quantity of the following substances having a stimulant effect on the central nervous system, including their salts, isomers, and salts of isomers" listing ephedrine and pyrovalerone. It also specifically includes MDPV, misspelling the full name as "methyenedioxypyrovalerone".[30]Four days after this Ohio law was passed, the DEA's national emergency ban was implemented.[23]

On December 8, 2011, under the Synthetic Drug Control Act, the US House of Representatives voted to ban MDPV and a variety of other synthetic drugs which had been sold legally in stores.[31]

Documented misuse[edit]

In April 2011, two weeks after they went missing, two men in northwestern Pennsylvania were found dead in a remote location on government land. The official cause of death of both men was hypothermia, but toxicology reports later confirmed that both Troy Johnson, 29, and Terry Sumrow, 28, had ingested MDPV shortly before their deaths. "It wasn't anything to kill them, but enough to get them messed up," the county coroner said. MDPV containers were found in their vehicle along with spoons, hypodermic syringes and marijuana paraphernalia. In April 2011, an Alton, Illinois, woman apparently died from an MDPV overdose.[32] In May 2011, The CDC reported a hospital emergency department (ED) visit after the use of "bath salts" in Michigan. One person was reported dead on arrival at the ED. Associates of the dead person reported that he had used bath salts. His toxicology results revealed high levels of MDPV in addition to marijuana and prescription drugs. The primary factor contributing to death was cited as MDPV toxicity after autopsy was performed.[33] An incident of hemiplegia has been reported.[34]

A total of 107 non-fatal intoxications and 99 analytically confirmed deaths related to MDPV between September 2009 and August 2013 were reported by nine European countries.[1]

Overdose treatment[edit]

Physicians often treat MDPV overdose cases with anxiolytics, such as benzodiazepines, to lessen the drug-induced activity in the brain and body.[35] In some cases, general anesthesia was used because sedatives were ineffective.[36]

Treatment in the emergency department for severe hypertension, tachycardia, agitation, or seizures consists of large doses of lorazepam in 2–4 mg increments every 10–15 minutes intravenously or intramuscularly. If this is not effective, haloperidol is an alternative treatment. It has been found that the use of any beta blockers to treat hypertension in these patients can cause an unopposed peripheral alpha-adrenergic effect with a dangerous paradoxical rise in blood pressure.[37]

References[edit]

  1. ^ a b "EMCDDA–Europol Joint Report on a new psychoactive substance: MDPV (3,4-methylenedioxypyrovalerone)" (PDF). European Monitoring Centre for Drugs and Drug Addiction (EMCDDA). January 2014. 
  2. ^ Simmler, L. D.; Buser, T. A.; Donzelli, M.; Schramm, Y.; Dieu, L-H.; Huwyler, J.; et al. (January 2013). "Pharmacological characterization of designer cathinones in vitro". British Journal of Pharmacology. 168 (2): 458–470. doi:10.1111/j.1476-5381.2012.02145.x. ISSN 0007-1188. PMC 3572571Freely accessible. PMID 22897747. 
  3. ^ Herbert Koppe; Gerhard Ludwig; Karl Zeile (May 1965). "US Patent 3478050 - 1-(3',4'-methylenedioxy-phenyl)-2-pyrrolidino-alkanones-(1)". Boehringer Sohn Ingelheim. 
  4. ^ Anita Slomski (December 2012). "A Trip on "Bath Salts" Is Cheaper Than Meth or Cocaine But Much More Dangerous". JAMA. 308 (23): 2445–2447. doi:10.1001/jama.2012.34423. PMID 23288310. 
  5. ^ Brandt, S. D.; Freeman, S.; Sumnall, H. R.; Measham, F.; Cole, J. (2011). "Analysis of NRG 'legal highs' in the UK: Identification and formation of novel cathinones". Drug Testing and Analysis. 3 (9): 569–75. doi:10.1002/dta.204. PMID 21960541. 
  6. ^ Westphal, F.; Junge, T.; Rösner, P.; Sönnichsen, F.; Schuster, F. (2009). "Mass and NMR spectroscopic characterization of 3,4-methylenedioxypyrovalerone: A designer drug with α-pyrrolidinophenone structure". Forensic Science International. 190 (1–3): 1–8. doi:10.1016/j.forsciint.2009.05.001. PMID 19500924. 
  7. ^ Watterson, L. R.; Kufahl, P. R.; Nemirovsky, N. E.; Sewalia, K.; Grabenauer, M.; Thomas, B. F.; Marusich, J. A.; Wegner, S.; Olive, M. F. (March 2014). "Potent rewarding and reinforcing effects of the synthetic cathinone 3,4-methylenedioxypyrovalerone (MDPV)". Addiction Biology. 19 (2): 165–174. doi:10.1111/j.1369-1600.2012.00474.x. PMC 3473160Freely accessible. PMID 22784198. 
  8. ^ Coppola, M.; Mondola, R. (2012). "3,4-Methylenedioxypyrovalerone (MDPV): Chemistry, pharmacology and toxicology of a new designer drug of abuse marketed online". Toxicology Letters. 208 (1): 12–5. doi:10.1016/j.toxlet.2011.10.002. PMID 22008731. 
  9. ^ Ernst Seeger (October 1964). "US Patent 3314970 - α-Pyrrolidino ketones". Boehringer Ingelheim. 
  10. ^ a b c d e f "Report on MDPV" (PDF). Drugs of Concern. DEA. May 2013. 
  11. ^ a b "Consideration of the Cathinones" (PDF). Advisory Council on the Misuse of Drugs. 31 March 2010. 
  12. ^ Kalapos, Miklós Péter (December 2011). "3,4-methylene-dioxy-pyrovalerone (MDPV) epidemic?". Orvosi Hetilap. 152 (50): 2010–2019. doi:10.1556/OH.2011.29259. PMID 22112374. 
  13. ^ Strano-Rossi, S.; Cadwallader, A. B.; De La Torre, X.; Botrè, F. (2010). "Toxicological determination and in vitro metabolism of the designer drug methylenedioxypyrovalerone (MDPV) by gas chromatography/mass spectrometry and liquid chromatography/quadrupole time-of-flight mass spectrometry". Rapid Communications in Mass Spectrometry. 24 (18): 2706–14. doi:10.1002/rcm.4692. PMID 20814976. 
  14. ^ Michaelis, W.; Russel, J. H.; Schindler, O. (1970). "Metabolism of pyrovalerone hydrochloride". Journal of Medicinal Chemistry. 13 (3): 497–503. doi:10.1021/jm00297a036. PMID 5441133. 
  15. ^ Meyer, M. R.; Du, P.; Schuster, F.; Maurer, H. H. (2010). "Studies on the metabolism of the α-pyrrolidinophenone designer drug methylenedioxy-pyrovalerone (MDPV) in rat and human urine and human liver microsomes using GC-MS and LC-high-resolution MS and its detectability in urine by GC-MS". Journal of Mass Spectrometry. 45 (12): 1426–42. doi:10.1002/jms.1859. PMID 21053377. 
  16. ^ Baselt RC (2014). Disposition of toxic drugs and chemicals in man. Seal Beach, Ca.: Biomedical Publications. pp. 1321–1322. ISBN 978-0-9626523-9-4. 
  17. ^ "A change to the Misuse of Drugs Act 1971 : Control of mephedrone and other cathinone derivatives". Home Office. 16 April 2010. 
  18. ^ "The Misuse of Drugs Act 1971 (Amendment) Order 2010". Home Office. 12 April 2010. 
  19. ^ Suomen valtioneuvosto (28 June 2010). "Finlex: huumausaineina pidettävistä aineista, valmisteista ja kasveista annetun valtioneuvoston asetuksen liitteen IV muuttamisesta". Oikeusministeriö (in Finnish). Oikeusministeriö. Retrieved January 25, 2011. 
  20. ^ "Hovrätten skärper straff i MDPV-dom". Norrköpings Tidningar (in Swedish). 4 June 2010. 
  21. ^ "Emerging drug, MDPV banned in WA". Government of Western Australia. 8 February 2012. 
  22. ^ "'Bath salts' drug ingredient banned in Canada". CBC News. 26 September 2012. 
  23. ^ a b "Chemicals Used in "Bath Salts" Now Under Federal Control and Regulation" (Press release). Drug Enforcement Administration (DEA). 21 October 2011. 
  24. ^ Allen, Greg (8 February 2011). "Florida Bans Cocaine-Like 'Bath Salts' Sold in Stores". NPR. 
  25. ^ Beshear, Steve (23 March 2011). "Gov. Beshear signs law banning new synthetic drugs" (Press release). Commonwealth of Kentucky. 
  26. ^ Rowe, Amy (2 September 2011). "Governor bans bath salts after student's death". Daily Targum. 
  27. ^ David, Giambusso (2 September 2011). "Cranford man charged with murdering girlfriend; Toxicology report shows no trace of 'bath salts'". Nj.com. 
  28. ^ "State of Tennessee Public Chapter No. 169 House Bill No. 457" (PDF). State of Tennessee. 18 April 2011. 
  29. ^ "New law sets fine at $350 for 'bath salts' possession". Portland Press Herald. 7 July 2011. 
  30. ^ "Ohio Amendment to Controlled Substances Act HB 64". Ohio General Assembly Archives. 17 October 2011. 
  31. ^ Kreider, Randy (8 December 2011). "House Votes to Ban 'Spice,' 'Bath Salts'". ABC News. 
  32. ^ Wilson, Todd (12 May 2011). "Illinois lawmakers target bath salts used as a drug". Chicago Tribune. 
  33. ^ "Emergency Department Visits After Use of a Drug Sold as "Bath Salts" --- Michigan, November 13, 2010--March 31, 2011". Morbidity and Mortality Weekly Report. 60 (19). Centers for Disease Control and Prevention (CDC). May 2011. pp. 624–627. PMID 21597456. 
  34. ^ Boshuisen, K.; Arends, J. E.; Rutgers, D. R.; Frijns, C. J. (8 May 2012). "A young man with hemiplegia after inhaling the bath salt "Ivory Wave"". Neurology. 78 (19): 1533–1534. doi:10.1212/WNL.0b013e3182553c70. PMID 22539576. 
  35. ^ Salter, Jim; Suhr, Jim (6 April 2011). "Synthetic drugs sent thousands to ER". NBC News. 
  36. ^ Goodnough, Abby; Zezima, Katie (16 July 2011). "An Alarming New Stimulant, Legal in Many States". New York Times. 
  37. ^ ""Bath Salts" Health Care Provider Fact Sheet" (PDF). Michigan Department of Community Health. 30 April 2012. 

External links[edit]

Retrieved from "https://en.wikipedia.org/w/index.php?title=Methylenedioxypyrovalerone&oldid=754542583"