Suppr超能文献

含丁丙诺啡的治疗方法:在阿片类药物成瘾管理中的地位。

Buprenorphine-containing treatments: place in the management of opioid addiction.

作者信息

Robinson Susan E

机构信息

Department of Pharmacology and Toxicology, and Institute for Drug and Alcohol Studies, Virginia Commonwealth University, Richmond, Virginia 23298-0613, USA.

出版信息

CNS Drugs. 2006;20(9):697-712. doi: 10.2165/00023210-200620090-00001.

Abstract

Although the synthetic opioid buprenorphine has been available clinically for almost 30 years, its use has only recently become much more widespread for the treatment of opioid addiction. The pharmacodynamic and pharmacokinetic profiles of buprenorphine make it unique in the armamentarium of drugs for the treatment of opioid addiction. Buprenorphine has partial mu-opioid receptor agonist activity and is a kappa-opioid receptor antagonist; hence, it can substitute for other micro-opioid receptor agonists, yet is less apt to produce overdose reactions or dysphoria. On the other hand, buprenorphine can block the effects of opioids such as heroin (diamorphine) and morphine, and can even precipitate withdrawal in individuals physically dependent upon these drugs. Buprenorphine has significant sublingual bioavailability and a long half-life, making administration on a less than daily basis possible. Furthermore, its discontinuation is associated with only a mild withdrawal syndrome. Clinical trials have demonstrated that sublingual buprenorphine is effective in both maintenance therapy and detoxification of individuals addicted to opioids. The introduction of a sublingual formulation combining naloxone with buprenorphine further reduces the risk of diversion to illicit intravenous use. Because of its relative safety and lower risk of illegal diversion, buprenorphine has been made available in several countries for treating opioid addiction in the private office setting, greatly enhancing treatment options for this condition.

摘要

尽管合成阿片类药物丁丙诺啡已在临床上应用近30年,但直到最近它在治疗阿片类药物成瘾方面的应用才变得更为广泛。丁丙诺啡的药效学和药代动力学特性使其在治疗阿片类药物成瘾的药物库中独具特色。丁丙诺啡具有部分μ-阿片受体激动活性,且是κ-阿片受体拮抗剂;因此,它可以替代其他微阿片受体激动剂,同时不太容易产生过量反应或烦躁不安。另一方面,丁丙诺啡可以阻断海洛因(二乙酰吗啡)和吗啡等阿片类药物的作用,甚至能使对这些药物产生身体依赖的个体出现戒断症状。丁丙诺啡具有显著的舌下生物利用度和较长的半衰期,使得不必每日给药成为可能。此外,停用它只会引发轻微的戒断综合征。临床试验表明,舌下含服丁丙诺啡在维持治疗和使阿片类药物成瘾者戒毒方面均有效。将纳洛酮与丁丙诺啡联合制成的舌下制剂进一步降低了被转用于非法静脉注射的风险。由于其相对安全性以及非法转移的风险较低,丁丙诺啡已在多个国家被用于在私人诊所环境中治疗阿片类药物成瘾,极大地增加了针对这种病症的治疗选择。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验