Relative bioavailability of (+/-)-verapamil hydrochloride administered in tablets and chewing gum.

Acta pharmaceutica Nordica Pub Date : 1990-01-01
L L Christrup, J Bonde, S N Rasmussen, M R Rassing
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引用次数: 0

Abstract

The absorption of verapamil administered orally in chewing gum (23.4-29.7 mg) and perorally in tablets (80 mg) to seven healthy volunteers in a study using an open cross-over design, was compared. Following peroral administration the mean +/- SD AUC/D was (5.4 +/- 1.9) x 10(-3) micrograms ml-1 h per microgram dose and after administration of chewing gum (6.6 +/- 2.3) x 10(-3) micrograms ml-1 h per microgram dose (NS). The AUC ratio of verapamil to the metabolite norverapamil was 1.5 after oral and 0.8 after peroral administration, indicating that a part of the verapamil administered in chewing gum was absorbed through the oral mucosa.

(+/-)-盐酸维拉帕米片剂和口香糖的相对生物利用度。
在一项采用开放式交叉设计的研究中,比较了7名健康志愿者口服维拉帕米口香糖(23.4-29.7毫克)和口服片剂(80毫克)的吸收情况。口服给药后,平均+/- SD AUC/D为(5.4 +/- 1.9)× 10(-3)微克ml-1小时/微克剂量,咀嚼口香糖后为(6.6 +/- 2.3)× 10(-3)微克ml-1小时/微克剂量(NS)。维拉帕米与代谢物诺维拉帕米口服后的AUC比为1.5,经口服后为0.8,说明口香糖中给药的维拉帕米有一部分通过口腔黏膜被吸收。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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