Silk Microspheres Prepared by Spray‐drying of an Aqueous System

T. Hino, S. Shimabayashi, Atsushi Nakai
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引用次数: 16

Abstract

Scoured silk fibre was dissolved in a solution of calcium chloride in water and ethanol. After dialysis against purified water, theophylline as model drug was added to the solution. Silk microspheres prepared after spray-drying were round but somewhat wrinkled; their diameter was 5 μm (approx.). According to powder X-ray diffractometry, and FTIR and Raman spectroscopy, fibroin and theophylline were amorphous in the microsphere. The microspheres formed gels immediately after soaking in purified water and in Japanese Pharmacopoeia XIII solutions 1 (pH 1.2) and 2 (pH 6.8); the gels dissolved slightly in these aqueous media. In this way we have developed a new drug carrier for sustained release without the use of poisonous organic solvents or glutaraldehyde.
喷雾干燥法制备丝微球
将洗涤后的丝纤维溶解在氯化钙和乙醇溶液中。经纯化水透析后,加入茶碱作为模型药物。喷雾干燥后制备的丝微球呈圆形,但有些褶皱;直径约为5 μm。粉末x射线衍射、红外光谱和拉曼光谱分析表明,丝素和茶碱在微球中呈无定形。微球在纯化水和日本药典XIII溶液1 (pH 1.2)和2 (pH 6.8)中浸泡后立即形成凝胶;凝胶在这些水介质中略有溶解。通过这种方法,我们开发了一种不使用有毒有机溶剂或戊二醛的缓释药物载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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