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[混悬液基质(层压板)的填充剂控释]

[Filler-controlled release from suspension matrices (laminates)].

作者信息

Lippold B C, Kurka P

机构信息

Institut für Pharmazeutische Technologie, Universität Düsseldorf, BRD.

出版信息

Pharmazie. 1987 Nov;42(11):729-31.

PMID:3438337
Abstract

The release from a matrix (polyethylenmineral oilgel, Plastibase) with drug (bupranolol) in suspension can be controlled by a controlling layer of the same material which is saturated with the drug. Thus, after a burst period zero order release is reached from the laminate, before square root t-kinetics predominate. The duration of constant release may be extended with fillers in the controlling layer (glass beads, d less than 20 microns). Increasing the thickness of the controlling layer increases both duration of constant release and time to reach it, the latter to a lower extent.

摘要

悬浮于基质(聚乙烯 - 矿物油凝胶,塑性基质)中的药物(布普萘洛尔)的释放可通过同一材料的控释层来控制,该控释层已被药物饱和。因此,在一个突释期后,层压板达到零级释放,在此之前平方根t动力学占主导。控释层中的填充剂(玻璃珠,直径小于20微米)可延长恒速释放的持续时间。增加控释层的厚度会增加恒速释放的持续时间及其达到的时间,后者增加幅度较小。

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