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大鼠直肠给药后吗啡生物利用度提高。

Enhanced bioavailability of morphine after rectal administration in rats.

作者信息

Katagiri Y, Itakura T, Naora K, Kanba Y, Iwamoto K

机构信息

Department of Pharmacy, Shimane Medical University Hospital, Izumo, Japan.

出版信息

J Pharm Pharmacol. 1988 Dec;40(12):879-81. doi: 10.1111/j.2042-7158.1988.tb06293.x.

Abstract

Plasma morphine levels and the area under the plasma concentration-time curve (AUC) after i.v. (10 mg kg-1), p.o. (100 mg kg-1) and rectal (unrestricted or restricted to 1.5 cm from the anus, 10 mg kg-1) administration of morphine hydrochloride were determined in 10 or 11-week-old male Wistar rats to compare bioavailability of morphine after the rectal dosage with that after oral administration. The AUC value after oral administration (15 micrograms min mL-1), which was normalized by the dose, was only one-tenth of that after i.v. dosing (151 micrograms min mL-1). In contrast, the AUC after rectal administration (unrestricted, 133 micrograms min mL-1; restricted, 142 micrograms min mL-1) was almost comparable with that after i.v. administration. From the comparison of these AUC values, the extent of systemic availability of morphine after rectal (unrestricted or restricted) and p.o. administration was estimated to be approximately 90 and 10%, respectively.

摘要

在10或11周龄雄性Wistar大鼠中,测定静脉注射(10mg/kg)、口服(100mg/kg)和直肠给药(无限制或距肛门1.5cm限制,10mg/kg)盐酸吗啡后的血浆吗啡水平及血浆浓度-时间曲线下面积(AUC),以比较直肠给药后与口服给药后吗啡的生物利用度。口服给药后经剂量归一化的AUC值(15μg·min/mL)仅为静脉给药后(151μg·min/mL)的十分之一。相比之下,直肠给药后(无限制,133μg·min/mL;受限,142μg·min/mL)的AUC与静脉给药后几乎相当。通过比较这些AUC值,估计直肠给药(无限制或受限)和口服给药后吗啡的全身可利用程度分别约为90%和10%。

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