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[软性隐形眼镜中的药物动力学。I. 体外研究]

[Drug kinetics in soft contact lenses. I. In vitro studies].

作者信息

Rybakova E G, Avetisov S E, Badun G A, Krasnianskiĭ A V

出版信息

Vestn Oftalmol. 1995 Oct-Dec;111(4):21-4.

PMID:8604532
Abstract

The in vitro kinetics (specifically, absorption and desorption) of drugs belonging to various pharmacological groups (atropine sulfate, gentamicin sulfate, dexamethasone, lecozyme, and poludan) in soft contact lenses (low-hydrophilic with 40% aqueous content and highly hydrophilic with 74% aqueous content. 0.2 and 0.7 mm thick) was studied by radiometry, as were the effects of chemical structure of a drug, hydrophilic properties and thickness of soft contact lenses, and temperature of solution on these processes.

摘要

采用放射测量法研究了不同药理组药物(硫酸阿托品、硫酸庆大霉素、地塞米松、胰酶和保妥丹)在软性隐形眼镜(含水量40%的低亲水性和含水量74%的高亲水性,厚度分别为0.2和0.7毫米)中的体外动力学(具体为吸收和解吸),以及药物化学结构、软性隐形眼镜的亲水特性和厚度、溶液温度对这些过程的影响。

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