不同剂型盐酸昂丹司琼透皮贴剂的制备及体外评价

Karima Abd allatif, Jameela Ali Hasian
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引用次数: 0

摘要

本研究旨在以丙二醇20%w/w为增塑剂,以不同类型的聚合物乙基纤维素和聚乙烯吡罗烷酮k30按3:0.5,3:1,3:2,2:1,1:1的比例制备盐酸昂丹西琼透皮贴剂(OSH)。对制备的透皮贴片进行物理性能评价。用差示扫描量热法(DSC)研究了药物与赋形剂之间的相容性,其中药物与聚合物之间没有相互作用。从统计学研究来看,各制剂间差异有统计学意义p<0.05。透皮贴剂的体外释放研究是通过在椎间盘上使用桨来进行的。P2、P4剂型的OSH释放曲线符合Korsmeyer - Peppas模型,P1、P3、P5剂型的Higuchi模型。最佳处方P6在12 h内对盐酸昂丹司琼的释放量为96.47%,释放曲线符合Higuchi模型,相关系数(r2 = 0.9815)。
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Preparation and in Vitro Evaluation for Different Types of Ondansetron Hydrochloride Transdermal Patches
This research aims to develop transdermal patches of Ondansetron hydrochloride (OSH) with different types of polymers, ethyl cellulose and, polyvinyl pyrrolidone k30 in a ratio (3:0.5,3:1,3:2,2:1,1:1) with propylene glycol 20%w/w as a plasticizer. Prepared transdermal patches were evaluated for physical properties. The compatibility between the drug and excipients was studied by Differential scanning calorimetry (DSC), where there is no interaction between the drug and polymers. From the statistical study, there is a statistical difference between all the prepared formulations p<0.05. In-vitro Release study of transdermal patches was performed by using a paddle over the disc. The release profile of OSH followed Korsmeyer - Peppas Model in P2, P4 formulations and, Higuchi Model in P1, P3, P5 formulations. The best formulation P6 carrying EC:PVP in ratio1:1 released 96.47% of ondansetron hydrochloride during 12 h. The release profile of P6 followed the Higuchi model and correlation coefficient  (r2 = 0.9815)
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