Substance

ID:217

Names and Identifiers
Synonyms
MethadonMethadone(+/-)-MethadoneDL-Methadone hydrochloridedl-Methadone(+/-)-Methadone hydrochlorideMethadone HCLPhenadone hydrochlorideMethadone hydrochloride
Brand Name
HeptanonMethadone HCL IntensolMoheptanAlthose hydrochlorideAmidonBiscuitsDolofin hydrochlorideDolophineDolophine HCLKetalgin hydrochlorideMethadone MMethaquaioneWestadoneAdolanAlgidonDoloheptonKetalginDolophin hydrochlorideMephenonPhenadonePhyseptonePolamidoneMecodinMethadoseMiadonePolamidonTussolDepridolDiaminon hydrochlorideFenadonFenadoneHeptadonHeptadoneDiaminonDolliesDollyDolophinAdanonButalgin(+/-)-TussalAdanon hydrochlorideAlgolysinAlgovetinAmidone
IUPAC Traditional name
methadone
IUPAC name
6-(dimethylamino)-4,4-diphenylheptan-3-one
Registration numbers
CAS Number
PubChem SID
PubChem CID
Properties
Physical Property
Hydrophobicity(logP)
3.93 [HANSCH,C ET AL. (1995)]
Molecule Details
Drug Groups
approved
Description
A synthetic opioid that is used as the hydrochloride. It is an opioid analgesic that is primarily a mu-opioid agonist. It has actions and uses similar to those of morphine. It also has a depressant action on the cough center and may be given to control intractable cough associated with terminal lung cancer. Methadone is also used as part of the treatment of dependence on opioid drugs, although prolonged use of methadone itself may result in dependence. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1082-3)
Indication
For the treatment of dry cough, drug withdrawal syndrome, opioid type drug dependence, and pain.
Pharmacology
Methadone is a synthetic opioid analgesic with multiple actions quantitatively similar to those at morphine, the most prominent of which involve the central nervous system and organs composed of smooth muscle. However, Methadone is more active and more toxic than morphine. Methadone is indicated for relief of severe pain, for detoxification treatment of narcotic addiction, and for temporary maintenance treatment of narcotic addiction. The principal actions of therapeutic value are analgesia and sedation and detoxification or temporary maintenance in narcotic addiction. The Methadone abstinence syndrome, although qualitatively similar to that of morphine, differs in that the onset is slower, the course is more prolonged, and the symptoms are less severe.
Toxicity
In severe overdosage, particularly by the intravenous route, apnea, circulatory collapse, cardiac arrest, and death may occur.
Affected Organisms
Humans and other mammals
Biotransformation
Hepatic. Cytochrome P450 enzymes, primarily CYP3A4, CYP2B6, and CYP2C19 and to a lesser extent CYP2C9 and CYP2D6, are responsible for conversion of methadone to EDDP and other inactive metabolites, which are excreted mainly in the urine.
Absorption
Well absorbed following oral administration. The bioavailability of methadone ranges between 36 to 100%.
Half Life
24-36 hours
Protein Binding
In plasma, methadone is predominantly bound to α1-acid glycoprotein (85% to 90%).
Elimination
The elimination of methadone is mediated by extensive biotransformation, followed by renal and fecal excretion.
Unmetabolized methadone and its metabolites are excreted in urine to a variable degree.
Distribution
* 1.0 to 8.0 L/kg
Clearance
* 1.4 to 126 L/h
References
• Kell MJ: Utilization of plasma and urine methadone concentrations to optimize treatment in maintenance clinics: I. Measurement techniques for a clinical setting. J Addict Dis. 1994;13(1):5-26. [Pubmed]
• Eap CB, Buclin T, Baumann P: Interindividual variability of the clinical pharmacokinetics of methadone: implications for the treatment of opioid dependence. Clin Pharmacokinet. 2002;41(14):1153-93. [Pubmed]
• Joseph H, Stancliff S, Langrod J: Methadone maintenance treatment (MMT): a review of historical and clinical issues. Mt Sinai J Med. 2000 Oct-Nov;67(5-6):347-64. [Pubmed]
• Connock M, Juarez-Garcia A, Jowett S, Frew E, Liu Z, Taylor RJ, Fry-Smith A, Day E, Lintzeris N, Roberts T, Burls A, Taylor RS: Methadone and buprenorphine for the management of opioid dependence: a systematic review and economic evaluation. Health Technol Assess. 2007 Mar;11(9):1-171, iii-iv. [Pubmed]
• Donny EC, Brasser SM, Bigelow GE, Stitzer ML, Walsh SL: Methadone doses of 100 mg or greater are more effective than lower doses at suppressing heroin self-administration in opioid-dependent volunteers. Addiction. 2005 Oct;100(10):1496-509. [Pubmed]
External Links
Molecular Spectra
No Data Available
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References
• Kell MJ: Utilization of plasma and urine methadone concentrations to optimize treatment in maintenance clinics: I. Measurement techniques for a clinical setting. J Addict Dis. 1994;13(1):5-26. Pubmed
• Joseph H, Stancliff S, Langrod J: Methadone maintenance treatment (MMT): a review of historical and clinical issues. Mt Sinai J Med. 2000 Oct-Nov;67(5-6):347-64. Pubmed
• Connock M, Juarez-Garcia A, Jowett S, Frew E, Liu Z, Taylor RJ, Fry-Smith A, Day E, Lintzeris N, Roberts T, Burls A, Taylor RS: Methadone and buprenorphine for the management of opioid dependence: a systematic review and economic evaluation. Health Technol Assess. 2007 Mar;11(9):1-171, iii-iv. Pubmed
• Eap CB, Buclin T, Baumann P: Interindividual variability of the clinical pharmacokinetics of methadone: implications for the treatment of opioid dependence. Clin Pharmacokinet. 2002;41(14):1153-93. Pubmed
• Donny EC, Brasser SM, Bigelow GE, Stitzer ML, Walsh SL: Methadone doses of 100 mg or greater are more effective than lower doses at suppressing heroin self-administration in opioid-dependent volunteers. Addiction. 2005 Oct;100(10):1496-509. Pubmed