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Application of the Solid Dispersion Method to the Controlled Release of Medicine. VII. Release Mechanism of a Highly Water-Soluble Medicine from Solid Dispersion with Different Molecular Weights of Polymer

机译:固体分散法在药物控制释放中的应用。七。高分子不同分子量的固体分散体中高水溶性药物的释放机理

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Solid dispersion films were prepared with a highly water-soluble medicine (oxprenolol hydrochloride (OXP)), four grades of water-insoluble ethylcellulose (EC) having different molecular weights and water-soluble hydroxypropyl cellulose (HPC). The internal structure of the solid dispersion films and the penetration of the dissolution medium into the films were studied to clarify the mechanism of OXP release from the OXP-EC and OXP-EC-HPC solid dispersion systems having various molecular weights of EC. In the OXP-EC system, the release rate of OXP slightly decreased with increasing molecular weight of EC and the mechanism of OXP release was hardly affected by the molecular weight of EC. In the OXP-EC-HPC system, the release rate of OXP markedly decreased with increasing molecular weight of EC. When EC with the lowest molecular weight of the four grades was used, the same mechanism of OXP release was observed as in the OXP-EC system, but it was clear that OXP was released from the films with the two higher-molecular-weight grades of EC through a diffusion-controlled release mechanism. This result can be explained in terms of diffusion of OXP through the quasi-equilibrium swollen gel region formed by rapid hydration of HPC with water penetrating into the solid dispersion film.
机译:固体分散膜是用高度水溶性的药物(盐酸羟丙诺醇(OXP)),具有不同分子量的四种等级的水不溶性乙基纤维素(EC)和水溶性羟丙基纤维素(HPC)制备的。研究了固体分散膜的内部结构和溶解介质向膜中的渗透,以阐明OXP从具有各种EC分子量的OXP-EC和OXP-EC-HPC固体分散体系中释放的机理。在OXP-EC系统中,随着EC分子量的增加,OXP的释放速率略有降低,并且EC的分子量几乎不影响OXP的释放机理。在OXP-EC-HPC系统中,随着EC分子量的增加,OXP的释放速率明显降低。当使用四个级别中分子量最低的EC时,观察到的OXP释放机理与OXP-EC系统中相同,但是很明显,从两个更高分子量级别的膜中释放了OXP。 EC通过扩散控制释放机制。可以用OXP扩散通过HPC迅速水化而形成的准平衡溶胀凝胶区域的扩散来解释这一结果,水渗透到固体分散膜中。

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