Gabor F, Ertl B, Wirth M, Mallinger R
Institute of Pharmaceutical Technology, University of Vienna, Austria.
J Microencapsul. 1999 Jan-Feb;16(1):1-12. doi: 10.1080/026520499289266.
The effect of manufacturing parameters on the size and drug-loading of ketoprofen-containing biodegradable and biocompatible poly(DL-lactic-co-glycolic acid) (PLGA) microspheres prepared by the solvent evaporation method was investigated. For both drug-free and drug-loaded microspheres, smaller microspheres with a narrower size distribution were obtained when the stirring rate or the volume of the organic phase was increased. Incorporation of ketoprofen was found to increase with increasing volume of the organic phase and decreasing pH of the aqueous phase, but was independent of the acidity and the inherent viscosity of the PLGA used. The biphasic release profile of ketoprofen from the microspheres was dependent on the type of PLGA as well as the size and drug-loading, two parameters governed by the manufacturing process. The first burst effect was found to increase with the drug content, reduction of size of the microspheres and increasing inherent viscosity of the matrix, whereas acidity of the PLGA had no effect on the release of this acidic drug. A vigorous first burst effect was associated with reduced sustained delivery of ketoprofen, the rate of the delayed release phase being dependent on the inherent viscosity of the matrix, the size, the payload and the pH during preparation of the microspheres. Thus, by selection of the manufacturing parameters and the type of PLGA, it is possible to design a controlled drug delivery system for the prolonged release of ketoprofen, improving therapy by possible reduction of time intervals between peroral administration and reduction of local gastrointestinal side effects.
研究了制备参数对采用溶剂蒸发法制备的含酮洛芬的可生物降解且生物相容的聚(DL-乳酸-共-乙醇酸)(PLGA)微球的尺寸和载药量的影响。对于不含药物和含药物的微球,当搅拌速率或有机相体积增加时,可获得尺寸更小且尺寸分布更窄的微球。发现酮洛芬的掺入量随有机相体积的增加和水相pH值的降低而增加,但与所用PLGA的酸度和特性粘度无关。酮洛芬从微球中的双相释放曲线取决于PLGA的类型以及尺寸和载药量,这两个参数由制造工艺决定。发现首次突释效应随药物含量、微球尺寸的减小和基质特性粘度的增加而增加,而PLGA的酸度对这种酸性药物的释放没有影响。强烈的首次突释效应与酮洛芬的持续释放减少有关,延迟释放阶段的速率取决于基质的特性粘度、尺寸、载药量以及微球制备过程中的pH值。因此,通过选择制造参数和PLGA的类型,可以设计一种用于酮洛芬长效释放的控释给药系统,通过可能减少口服给药的时间间隔和减少局部胃肠道副作用来改善治疗效果。