Madan P L, Jani R K, Bartilucci A J
J Pharm Sci. 1978 Mar;67(3):409-11. doi: 10.1002/jps.2600670338.
A new method of preparing gelatin microcapsules of soluble pharmaceuticals is described. Spherical droplets of a gelatin dispersion prepared in the drug solution were produced by the capillary method, and the droplets were congealed rapidly to yield discrete units in the form of a free-flowing powder. The microcapsules obtained were spherical in shape and showed no tendency to form agglomerates. Hardening of the microcapsules resulted in a significant reduction of the release rate without altering the reproducibility. The results indicated that the process of microencapsulation described is simple, reproducible, economical, and amenable to industrial application.
描述了一种制备可溶性药物明胶微胶囊的新方法。通过毛细管法在药物溶液中制备明胶分散液的球形液滴,然后将这些液滴迅速凝固,以得到自由流动粉末形式的离散单元。所获得的微胶囊呈球形,没有形成团聚物的趋势。微胶囊的硬化导致释放速率显著降低,而不改变重现性。结果表明,所述的微囊化过程简单、可重现、经济且适合工业应用。