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丁丙诺啡透皮制剂用于阿片类药物脱毒的评估。

Evaluation of a transdermal buprenorphine formulation in opioid detoxification.

作者信息

Lanier Ryan K, Umbricht Annie, Harrison Joseph A, Nuwayser Elie S, Bigelow George E

机构信息

Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, Baltimore, MD, USA.

出版信息

Addiction. 2007 Oct;102(10):1648-56. doi: 10.1111/j.1360-0443.2007.01944.x.

Abstract

AIMS

Buprenorphine is marketed in a sublingual formulation for treatment of opioid dependence. A transdermal formulation has been developed that may provide extended relief from opioid withdrawal, reduce required clinic visits and improve adherence, while having less potential for diversion and abuse. This study evaluated the safety and biodelivery (blood levels) of this transdermal buprenorphine formulation (i.e. buprenorphine patch), and its apparent efficacy in suppressing the opioid withdrawal syndrome.

DESIGN

Open-label, first-in-humans trial.

SETTING

A residential research facility.

PARTICIPANTS

Nine physically dependent opioid-users completed the 10-day opioid detoxification study.

INTERVENTION

Each volunteer received a single patch application that remained in place for 3 days. The formulation has shown an average delivery of 1.9 mg/day of buprenorphine over 3 days in pre-clinical evaluation.

MEASURES

Physiological, behavioral, subjective and observer ratings of opioid withdrawal and opioid agonist effects were collected.

FINDINGS

Overall, the patch appeared safe and well tolerated. There were no serious adverse events, and no opioid intoxication following patch application. Oxygen saturation, heart rate, blood pressure, skin temperature and pupil diameter remained well within normal ranges. Buprenorphine blood levels peaked 48 hours after patch application at a concentration of 0.60 ng/ml. Volunteers' self-reports of the presence and severity of withdrawal symptoms were reduced by approximately 50% on the 3 days of patch application. Withdrawal symptoms increased marginally upon patch removal. Administration of opioid rescue medication was eliminated within 6 hours of patch application, and increased slightly upon patch removal.

CONCLUSIONS

The significant biodelivery of buprenorphine and the suppression of the opioid withdrawal syndrome during patch application and its reappearance after patch removal indicate clinically useful pharmacodynamic activity. Transdermal buprenorphine may be a useful opioid detoxification treatment that reduces compliance concerns, and delivers buprenorphine in a formulation less likely to be diverted to illicit use.

摘要

目的

丁丙诺啡有舌下含片剂型用于治疗阿片类药物依赖。已研发出一种透皮剂型,它可能提供更长时间的阿片类药物戒断缓解,减少所需的门诊就诊次数并提高依从性,同时被转移和滥用的可能性较小。本研究评估了这种丁丙诺啡透皮制剂(即丁丙诺啡贴片)的安全性和生物递送(血药浓度),以及其在抑制阿片类药物戒断综合征方面的明显疗效。

设计

开放标签的首例人体试验。

地点

一个住院研究机构。

参与者

九名对阿片类药物产生身体依赖的使用者完成了为期10天的阿片类药物脱毒研究。

干预

每位志愿者接受一次贴片应用,贴片保留3天。该制剂在临床前评估中显示在3天内丁丙诺啡的平均递送量为1.9毫克/天。

测量

收集了阿片类药物戒断和阿片类激动剂效应的生理、行为、主观和观察者评分。

结果

总体而言,贴片看起来安全且耐受性良好。没有严重不良事件,贴片应用后也没有阿片类药物中毒情况。血氧饱和度、心率、血压、皮肤温度和瞳孔直径均保持在正常范围内。丁丙诺啡血药浓度在贴片应用后48小时达到峰值,浓度为0.60纳克/毫升。在贴片应用的3天里,志愿者对戒断症状的存在和严重程度的自我报告减少了约50%。贴片移除后戒断症状略有增加。在贴片应用后6小时内不再需要使用阿片类救援药物,贴片移除后略有增加。

结论

丁丙诺啡显著的生物递送以及贴片应用期间阿片类药物戒断综合征的抑制及其移除后的再次出现表明其具有临床有用的药效学活性。透皮丁丙诺啡可能是一种有用的阿片类药物脱毒治疗方法,可减少对依从性的担忧,并以一种不太可能被转移用于非法用途的制剂形式递送丁丙诺啡。

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