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Preparation of surfactant-free nanoparticles of methacrylic acid copolymers used for film coating

机译:用于薄膜包衣的无表面活性剂的甲基丙烯酸共聚物的纳米粒子的制备

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摘要

The aim of the present study was to prepare surfactant-free pseudolatexes of various methacrylic acid copolymers. These aqueous colloidal dispersions of polymeric materials for oral administration are intended for film coating of solid dosage forms or for direct manufacturing of manoparticles. Nanoparticulate dispersions were produced by an emulsification-diffusion method involving the use of partially water-miscible solvents and the mutual saturation of the aqueous and organic phases prior to the emulsification in order to reduce the initial thermodynamic instability of the emulsion. Because of the self-emulsifying properties of the methacrylic acid copolymers, it was possible to prepare aqueous dispersions of colloidal size containing up to 30% wt/vol of Eudragit RL, RS, and E using 2-butanone or methyl acetate as partially water-miscible solvents, but without any surfactant. However, in the case of the cationic Eudragit E, protonation of the tertiary amine groups by acidification of the aqueous phase was necessary to improve the emulsion stability in the absence of surfactant and subsequently to prevent droplet coalescence during evaporation. In addition, a pseudolatex of Eudragit E was used to validate the coating properties of the formulation for solid dosage forms. Film-coated tablets of quinidine sulfate showed a transparent glossy continuous film that was firmly attached to the tablet. The dissolution profile of quinidine sulfate from the tablets coated with the Eudragit E pseudolatex was comparable to that of tablets coated with an acetonic solution of Eudragit E. Furthermore, both types of coating ensured similar taste masking. The emulsification-evaporation method used was shown to be appropriate for the preparation of surfactant-free colloidal dispersions of the 3 types of preformed methacrylic acid copolymers; the dispersions can subsequently be used for film coating of solid dosage forms.
机译:本研究的目的是制备各种甲基丙烯酸共聚物的不含表面活性剂的假胶乳。这些用于口服的聚合材料的水胶体分散体旨在用于固体剂型的薄膜包衣或直接制造木糖颗粒。通过乳化-扩散方法生产纳米颗粒分散体,该方法包括在乳化之前使用部分与水混溶的溶剂以及水相和有机相的相互饱和,以降低乳液的初始热力学不稳定性。由于甲基丙烯酸共聚物的自乳化特性,可以使用2-丁酮或乙酸甲酯作为部分水,制备胶体大小的水性分散体,其中包含高达30%wt / vol的Eudragit RL,RS和E。可混溶的溶剂,但不含任何表面活性剂。然而,在阳离子Eudragit E的情况下,通过在不存在表面活性剂的情况下提高水乳液的稳定性并随后防止液滴在蒸发过程中的聚结,必须通过水相酸化使叔胺基质子化。另外,使用Eudragit E的假乳胶来验证固体剂型的制剂的包衣性质。薄膜状的硫酸奎尼丁片剂显示出牢固地附着在片剂上的透明光泽连续薄膜。涂有Eudragit E假乳胶的片剂中硫酸奎尼丁的溶出曲线与涂有Eudragit E的丙酮溶液的片剂的溶出度相当。此外,两种类型的包衣均确保相似的掩味。结果表明,所用的乳化-蒸发方法适用于制备三种类型的预制甲基丙烯酸共聚物的无表面活性剂的胶态分散体。该分散体随后可用于固体剂型的薄膜包衣。

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