Methadone is a synthetic opioid, used medically as an analgesic and in the treatment of narcotic addiction.
On September 11, 1941 Bockmühl and Ehrhart filed an application for a patent for a synthetic substance they called Hoechst 10820 or polamidon and whose structure had no relation to morphine or the opioid alkaloids (Bockmühl and Ehrhart, 1949). Although chemically unlike morphine or heroin, methadone also acts on the opioid receptors and thus produces many of the same effects. Chemically, methadone is the simplest of the opioids.
Methadone was introduced into the United States in 1947 by Eli Lilly and Company as an analgesic (They gave it the trade name Dolophine,® which is now registered to Roxane Laboratories). Since then, it has been best known for its use in treating narcotic addiction, though it is also used in managing chronic pain due to its long duration of action and very low cost. In late 2004, the cost of a one-month supply of methadone was $20, as compared to an equivalent analgesic amount of Demerol at $120. The old name Dolophine comes from the German Dolphium. The name derives from the Latin dolor which means "pain" and phine which means "end".
Methadone (as Dolophine) was first manufactured in the USA by Mallinckrodt pharmaceuticals, a St. Louis-based subsidiary of the Tyco International corporation. Mallinckrodt held the patent up until the early 1990s. Today a number of pharmaceutical companies produce and distribute methadone. However, the major producer remains Mallinckrodt. Mallinckrodt sells bulk methadone to most of the producers of generic preparations and also distributes its own brand name product in the form of tablets, dispersable tablets and oral concentrate under the name Methadose in the United States.
Generally, one will only hear "dolophine" used by older addicts who used the product in the 1960s and 1970s. Medical professionals who believe that dolophine is the generic name for methadone, when actually it is the reverse, may also use the old brand name. A persistent but untrue urban legend claims that the trade name "Dolophine" was coined in tribute to Adolf Hitler by its German creators, and it is sometimes even claimed that the drug was originally named "adolphine" or "adolophine". The claim is still presented as fact by Church of Scientology literature Buttnor, Al. "The Drug Problem: How It CAN be Solved". Freedom Magazine (vol. 4, iss. 1) p. 15. Retrieved Apr. 7, 2006. and was repeated by actor and vocal Scientologist Tom Cruise in a 2005 Entertainment Weekly interview. However, as the magazine pointed out, this isn't true: the name "Dolophine" was in fact created after the war by the American branch of Eli Lilly http://www.exchangesupplies.org/publications/methadone_briefing/section1.html, and the name "Adolphine" (never an actual name of the drug) was created in the United States in the early 1970s.http://www.indro-online.de/discovery.pdf (PDF format)
Current research shows methadone has a unique affinity for the NMDA (N-methyl-D-aspartic acid) brain receptor. Some researchers propose that NMDA may regulate psychic dependence and tolerance by exhibiting opioid antagonist-like activity. Withdrawal symptoms are generally less acutely severe than those of morphine and heroin at equivalent doses, but are significantly more prolonged.
Methadone is considered to be generally effective in management of heroin addiction and harm reduction (e.g., reduction of HIV rates from needle sharing). At proper dosing, methadone usually reduces the appetite for and need to take heroin. However, some heroin addicts report more difficulty in quitting methadone than heroin. While there is much debate over the treatment schedule and duration required, treatment at a methadone maintenance clinic is intended to be for an indefinite duration. Many factors determine the treatment dose schedule, and some follow the philosophy that methadone maintenance treatment is not curative for heroin addiction.
In recent years, methadone has gained popularity among physicians for the treatment of other medical problems, such as chronic pain. The increased usage comes as doctors search for an opioid drug that can be dosed less frequently than short-acting drugs like morphine or hydrocodone. Methadone, with its long half-life (and thus long duration of effect) and oral bioavailability, is a common second-choice drug for pain that doesn't respond to weaker agonists.
Methadone also is tied to an increasing number of drug overdose deaths in the United States, more than any other prescription narcotic painkiller.
According to the National Center for Health Statistics. medical examiners listed methadone as contributing to 2,992 deaths in 2003, up from 790 in 1999. Approximately 82 percent of those deaths were listed as accidental, and most involved methadone in combination with other drugs.
However, many of those who died accidentally were prescribed too much or were prescribed methadone with other drugs in dangerous combinations, according to a 2006 series in The Charleston Gazette.*
Buprenorphine has also been used in the treatment of narcotic addiction. It is interesting to note that, in USA, Buprenorphine products are in Schedule III of the United States Controlled Substances Act, which allows for their use on an outpatient basis, unlike methadone and LAAM. In the UK and many other countries, however, not only buprenorphine and methadone but also diamorphine (heroin) and other opioids may be used for outpatient treatment of opiate addiction, and treatment is generally provided in much less heavily regulated environments than in the United States. A study from Austria indicated that oral morphine provides better results than oral methadone, and studies of heroin maintenance have indicated that a low background dose of methadone combined with heroin maintenance may significantly improve outcomes for less-responsive patients.
Another close relative of methadone is dextropropoxyphene, first marketed in 1957 under the trade name of Darvon. Oral analgesic potency is one-half to one-third that of codeine, with 65 mg approximately equivalent to about 600 mg of aspirin. Dextropropoxyphene is prescribed for relief of mild to moderate pain. Bulk dextropropoxyphene is in Schedule II of the United States Controlled Substances Act, while preparations containing it are in Schedule IV. More than 100 tons of dextropropoxyphene are produced in the United States annually, and more than 25 million prescriptions are written for the products. This narcotic is associated with a number of toxic side effects and is among the top 10 drugs reported by medical examiners in recreational drug use deaths.
Analgesics | Opioids | Schedule II controlled substances
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