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别嘌醇口服和直肠剂型的生物利用度。

Bioavailability of allopurinol oral and rectal dosage forms.

作者信息

Chang S L, Kramer W G, Feldman S, Ballentine R, Frankel L S

出版信息

Am J Hosp Pharm. 1981 Mar;38(3):365-8.

PMID:7223751
Abstract

The bioavailability of allopurinol from orally administered tablets and rectally administered suppositories is reported. Two types of rectal suppositories (cocoa butter and polyethylene glycol) were compounded and contained 300 mg allopurinol (from oral tablets). Five healthy volunteers received 300 mg allopurinol orally from tablets or rectally from suppositories in a randomized, three-way crossover design. Serial blood samples were drawn for 72 hours following administration and were analyzed by high-pressure liquid chromatography for allopurinol and its metabolite, oxipurinol. The interaction between allopurinol and PEG was studied in vitro using a dialysis method. Serum allopurinol levels following oral administration of tablets peaked at 1.5 +/- 0.23 microgram/ml at 5.20 +/- 0.65 hours. Allopurinol was not detectable after administration of cocoa butter/allopurinol suppositories; oxipurinol peaked at 0.34 +/- 0.14 microgram/ml at 13 +/- 11 hours. The bioavailability of allopurinol from the cocoa butter suppository, relative to the tablet, was 5.77 +/- 2.5%. Neither allopurinol nor oxipurinol was detectable (less than 0.1 microgram/ml) in the sera of persons following administration of PEG suppositories. Dialysis studies showed decreased loss of allopurinol from the dialysis sac as PEG concentration increased. The rectal suppositories of allopurinol used in this study did not appear to be an efficient means of administering this drug.

摘要

报告了口服片剂和直肠给药栓剂中别嘌醇的生物利用度。制备了两种类型的直肠栓剂(可可脂和聚乙二醇),均含有300mg别嘌醇(来自口服片剂)。5名健康志愿者按照随机、三交叉设计,分别口服300mg片剂或直肠给予栓剂。给药后72小时内连续采集血样,采用高压液相色谱法分析别嘌醇及其代谢产物氧嘌呤醇。采用透析法体外研究了别嘌醇与聚乙二醇之间的相互作用。口服片剂后血清别嘌醇水平在5.20±0.65小时达到峰值1.5±0.23μg/ml。给予可可脂/别嘌醇栓剂后未检测到别嘌醇;氧嘌呤醇在13±11小时达到峰值0.34±0.14μg/ml。相对于片剂,可可脂栓剂中别嘌醇的生物利用度为5.77±2.5%。给予聚乙二醇栓剂后,受试者血清中未检测到别嘌醇和氧嘌呤醇(低于0.1μg/ml)。透析研究表明,随着聚乙二醇浓度的增加,透析袋中别嘌醇的损失减少。本研究中使用的别嘌醇直肠栓剂似乎不是一种有效的给药方式。

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