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纳曲酮-3-水杨酸盐(纳曲酮的一种前药):在犬类中的合成与药代动力学

Naltrexone-3-salicylate (a prodrug of naltrexone): synthesis and pharmacokinetics in dogs.

作者信息

Hussain M A, Shefter E

机构信息

E. I. du Pont de Nemours & Company, Inc., Medical Products Department, Wilmington, Delaware 19898.

出版信息

Pharm Res. 1988 Feb;5(2):113-5. doi: 10.1023/a:1015944302567.

Abstract

Naltrexone-3-salicylate (3), a prodrug of naltrexone (1), was prepared by a simple procedure from naltrexone-3-acetylsalicylate (2). The plasma (dog and human) hydrolysis half-life of 3 was found to be approximately 30 min. Compound 2 was previously shown to hydrolyze in dog and human plasma with a fast deacetylation step to 3, followed by slower hydrolysis of 3 to 1 (t1/2, approximately 30 min). Oral naltrexone bioavailability was greatly improved (approximately 30-fold) after oral administration of 3 to dogs, similar to the improvement observed after oral administration of 2. The half-life of naltrexone in dogs after oral administration of 3 was similar to that observed after oral administration of 2 (approximately 1 hr).

摘要

纳曲酮-3-水杨酸盐(3)是纳曲酮(1)的前体药物,可通过简单的方法由纳曲酮-3-乙酰水杨酸盐(2)制备得到。发现3在血浆(犬和人)中的水解半衰期约为30分钟。先前已表明化合物2在犬和人血浆中水解,先经过快速脱乙酰化步骤生成3,随后3缓慢水解为1(半衰期约为30分钟)。给犬口服3后,纳曲酮的口服生物利用度大幅提高(约30倍),这与口服2后观察到的改善情况相似。犬口服3后纳曲酮的半衰期与口服2后观察到的半衰期相似(约1小时)。

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