陈小平, 郭庆东, 石庭森. 二氢埃托啡透皮给药系统的研究J. 药学学报, 1996, 31(10): 770-774.
引用本文: 陈小平, 郭庆东, 石庭森. 二氢埃托啡透皮给药系统的研究J. 药学学报, 1996, 31(10): 770-774.
XP Chen, QD Guo, , TS Shi. STUDIES ON TRANSDERMAL DELIVERY SYSTEM OF DIHYDROETORPHINE HYDROCHLORIDEJ. Acta Pharmaceutica Sinica, 1996, 31(10): 770-774.
Citation: XP Chen, QD Guo, , TS Shi. STUDIES ON TRANSDERMAL DELIVERY SYSTEM OF DIHYDROETORPHINE HYDROCHLORIDEJ. Acta Pharmaceutica Sinica, 1996, 31(10): 770-774.

二氢埃托啡透皮给药系统的研究

STUDIES ON TRANSDERMAL DELIVERY SYSTEM OF DIHYDROETORPHINE HYDROCHLORIDE

  • 摘要: 报道了二氢埃托啡透皮贴片系统(DHE-TDS)的研制情况,并对该系统进行了初步动物实验,结果说明,以PVA,PVP、乳糖等为主要基质制成的DHE-TDS对皮肤的刺激性属轻度,用家兔腹部贴片。测定药库中药物剩余量,结果推知药物释放符合一级原理。大鼠实验证明,DHE-TDS稳定释药时间为用药后4~32h,大鼠扭体实验证明DHE-TDS一次用药,镇痛作用持续时间至少48h。此制剂是否有成瘾性,尚待证明。

     

    Abstract: A transdermal delivery system of dihydroetorphine hydrochloride(DHE-TDS)wasdeveloped.The DHE-TDS mainly composed of polyvinyl alcohol,polyvinyl pyrrolidone and lactose.Tests on rabbits showed only slight skin irritation according to federal hazardous substances act Bygiving DHE-TDS to rabbits, DHE release was shown to be governed by first-order mechanism. WhenDHE-TDS was given to Wistar rats,a relatively stable blood drug concentration was observed from 4~32 h after drug adminstration. Writhing tests showed that one dose of DHE-TDS would maintainthe narcotic action on rats for at least 48 h.

     

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