In vitro and in vivo evaluation of the metabolism and pharmacokinetics of sebacoyl dinalbuphine

Li Heng Pao, Cheng Huei Hsiong, Oliver Yoa Pu Hu, Jhi Jung Wang, Shung Tai Ho

研究成果: 雜誌貢獻文章

11 引文 斯高帕斯(Scopus)

摘要

A diester prodrug of nalbuphine, sebacoyl dinalbuphine (SDN), and its long-acting formulation are currently being developed to prolong the duration of nalbuphine. A comparative in vitro hydrolysis study was conducted for SDN in rat, rabbit, dog, and human blood. Both SDN and nalbuphine in blood or plasma were measured by high-performance liquid chromatography. The hydrolysis rates of SDN in blood were ranked as follows: rat > rabbit > human > dog. The rapid formation of nalbuphine in the blood accounted for almost 100% of the prodrug, which supported the contention that nalbuphine is the major metabolite after SDN hydrolysis. The hydrolysis profiles of SDN were similar both in plasma and in red blood cells when compared in the blood. In vitro release results of SDN long-acting formulation showed that the rate-limited step of SDN hydrolysis to nalbuphine in blood is the penetration of SDN from oil into the blood. After intravenous administration of SDN in sesame oil into rats, nalbuphine quickly appeared in plasma and, thereafter, exhibited monoexponential decay. Pharmaceutical dosage forms affecting the drug disposition kinetics were demonstrated after intravenous administration. The AUC of nalbuphine was significantly higher and clearance was significantly lower, without changes in the t1/2 of nalbuphine after intravenous dosing of SDN in sesame oil when compared with that of intravenous dosing with nalbuphine HCl in rats. Overall, these results suggest that SDN fulfilled the original pro-soft drug design in which the prodrug can rapidly metabolize to nalbuphine, and no other unexpected compounds were apparent in the blood.
原文英語
頁(從 - 到)395-402
頁數8
期刊Drug Metabolism and Disposition
33
發行號3
DOIs
出版狀態已發佈 - 三月 1 2005
對外發佈Yes

ASJC Scopus subject areas

  • Pharmacology
  • Pharmaceutical Science

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