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乙内酰脲衍生物的生物制药研究。I. 乙内酰脲衍生物的物理化学性质及其肠道吸收

Biopharmaceutical studies on hydantoin derivatives. I. Physico-chemical properties of hydantoin derivatives and their intestinal absorption.

作者信息

Fujioka H, Tan T

出版信息

J Pharmacobiodyn. 1981 Oct;4(10):759-70. doi: 10.1248/bpb1978.4.759.

Abstract

The physico-chemical properties of a series of hydantoin derivatives and their intestinal absorption from solution were studied. The introduction of the benzenesulfonyl group at the 1-position of the hydantoin ring greatly affects the physico-chemical properties: the acid dissociation constants were increased 1000-fold and the partition coefficients were increased 100- to 1000-fold in the chloroform/water system and 10- to 100-fold in the n-octanol/water system. The solubilities of 1-benzenesulfonylhydantoin derivatives increased with increasing pH of the solution at pH more than 5, but the solubilities of the 1- unsubstituted hydantoin derivatives were scarcely dependent on the pH of the solution in the pH 1 to 8 region. The intestinal absorption from solution was found to be caused by the passive transport according to the first-order kinetics. The rate constants of absorption of 1-benzenesulfonylhydantoin derivatives were rather large even under the condition where they were 99% ionized in the solution than that of the corresponding 1-unsubstituted hydantoin derivatives which exist mainly as the unionized from under the same condition. The intestinal absorption from a solution and the partitioning to chloroform produced linear free energy relationships to each other for the 1-benzenesulfonylhydatoin derivatives and for the 1-unsubstituted hydantoin derivatives independently. However when the partition coefficients in the n-octanol/water system were applied, the hydroxyl derivatives were found to deviate from linear relationships. On the basis of the results, a suggestion was made on the in vivo behavior and the bioavailability.

摘要

研究了一系列乙内酰脲衍生物的物理化学性质及其在溶液中的肠道吸收情况。在乙内酰脲环的1位引入苯磺酰基极大地影响了物理化学性质:在氯仿/水体系中,酸解离常数增加了1000倍,分配系数增加了100至1000倍;在正辛醇/水体系中,分配系数增加了10至100倍。1-苯磺酰基乙内酰脲衍生物的溶解度在pH大于5时随溶液pH值的升高而增加,但1-未取代乙内酰脲衍生物的溶解度在pH 1至8范围内几乎不依赖于溶液的pH值。发现溶液中的肠道吸收是由一级动力学的被动转运引起的。即使在溶液中99%离子化的条件下,1-苯磺酰基乙内酰脲衍生物的吸收速率常数也比相应的1-未取代乙内酰脲衍生物大得多,后者在相同条件下主要以非离子形式存在。对于1-苯磺酰基乙内酰脲衍生物和1-未取代乙内酰脲衍生物,溶液中的肠道吸收和分配到氯仿之间分别产生了线性自由能关系。然而,当应用正辛醇/水体系中的分配系数时,发现羟基衍生物偏离了线性关系。基于这些结果,对体内行为和生物利用度提出了建议。

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