Gogu P K, Jithan A V
Vaagdevi College of Pharmacy, Ramnagar, Hanamkonda - 506 001, India.
Indian J Pharm Sci. 2010 May;72(3):346-52. doi: 10.4103/0250-474X.70481.
The objective of the present study was to prepare and characterize in vitro and in vivo performance of a sustained release microsphere formulation of 4-chlorocurcumin, a novel curcumin analogue. A spray dried technique with ethylcellulose as the polymer was used in the preparation of these microspheres. Microspheres were characterized for drug content, particle size and shape, in vitro drug release and the drug-polymer interaction. To assess in vivo performance, both pharmacokinetics and hepatoprotective activity were investigated. Results were compared with an equivalent i.v. solution. The microspheres of 4-chlorocurcumin with ethylcellulose were successfully prepared using a spray-dried technique. These microspheres were able to sustain the release of the drug both in vitro as well as in vivo. Microspheres offered better pharmacokinetic and hepatoprotective properties to the drug compared to its solution form.
本研究的目的是制备一种新型姜黄素类似物4-氯姜黄素的缓释微球制剂,并对其体外和体内性能进行表征。这些微球的制备采用喷雾干燥技术,以乙基纤维素为聚合物。对微球的药物含量、粒径和形状、体外药物释放以及药物-聚合物相互作用进行了表征。为了评估体内性能,研究了药代动力学和肝保护活性。将结果与等效的静脉注射溶液进行比较。使用喷雾干燥技术成功制备了含有乙基纤维素的4-氯姜黄素微球。这些微球在体外和体内都能够持续释放药物。与溶液形式相比,微球为药物提供了更好的药代动力学和肝保护特性。