氯喹和甲哌辛两种抗疟药剂型的药理学基础。

E Minker, Z Matejka
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引用次数: 0

摘要

口服或肠外给药后,氯喹和甲哌辛出现在胃壁,抑制胃排空。测定其在胃壁的浓度,发现其与施用途径有关。当氯喹和甲哌辛避开胃进入时,在给定剂量的胃壁中积累的比例较小。这两种药物的副作用,即抑制胃运动,可以通过肠外和十二指肠给药来最小化;后者可通过肠溶片实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacological basis of dosage form of two antimalarials: chloroquine and mepacrine.

Chloroquine and mepacrine appear in the stomach wall and inhibit gastric emptying in the rat after oral or parenteral administration. Measuring their concentration in the stomach wall, it was found that it depended upon on the route of application. A smaller proportion of a given dose accumulated in the stomach wall when chloroquine and mepacrine were introduced by avoiding the stomach. The side effect of the two drugs, the inhibition of gastric motility, could be minimized by not only parenteral but also duodenal administration; the latter could be realized by enteric-coated tablets.

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