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Development and evaluation of diltiazem hydrochloride controlled-release pellets by fluid bed coating process

机译:盐酸地尔硫卓控释微丸的流化床包衣工艺开发与评价

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The aim of the present study was to develop controlled-release pellets of diltiazem HCl with ethyl cellulose and hydroxylpropyl methylcellulose phthalate as the release rate retarding polymers by fluid bed coating technique. The prepared pellets were evaluated for drug content, particle size, subjected to Scanning Electron Microscopy (SEM) and Differential Scanning Calori metry (DSC), and evaluated for in vitro release. Stability studies were carried out on the optimized formulations for a period of 3 months. The drug content was in the range of 97%-101%. The mean particle size of the drug-loaded pellets was in the range 700-785 μm. The drug release rate decreased as the concentration of ethyl cellulose increased in the pellet formulations. Among the prepared formulations, FDL10 and FDL11 showed 80% drug release in 16 h, matching with USP dissolution test 6 for diltiazem HCl extended-release capsules. SEM photographs confirmed that the prepared formulations were spherical in nature with a smooth surface. The compatibility between drug and polymers in the drug-loaded pellets was confirmed by DSC studies. Stability studies indicated that the pellets were stable.Keywords: Controlled release, diltiazem HCl, fluid bed coating, multiparticulate dosage forms, sustained release
机译:本研究的目的是通过流化床包衣技术开发盐酸地尔硫卓与乙基纤维素和羟丙基甲基纤维素邻苯二甲酸酯作为缓释速率聚合物的控释药丸。评估所制备的小丸的药物含量,粒径,进行扫描电子显微镜(SEM)和差示扫描量热法(DSC),并评估体外释放。对优化配方进行了3个月的稳定性研究。药物含量在97%-101%的范围内。载药小丸的平均粒度在700-785μm的范围内。随着丸剂中乙基纤维素浓度的增加,药物释放速率降低。在制备的制剂中,FDL10和FDL11在16小时内显示80%的药物释放,与USP地尔硫卓HCl缓释胶囊的溶出度试验6相匹配。 SEM照片证实了所制备的制剂本质上是球形的,具有光滑的表面。 DSC研究证实了载药小丸中药物与聚合物之间的相容性。稳定性研究表明该药丸是稳定的。关键词:控释,盐酸地尔硫卓,流化床包衣,多颗粒剂型,持续释放

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