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FORMULATION AND EVALUATION OF FAST DISSOLVING ORAL FILMS OF PROCHLORPERAZINE MALEATE

机译:马来酸原哌拉嗪快速溶解性口服制剂的研制与评价

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The objective of the present study was to prepare and evaluate fast-dissolving oral films of prochlorperazine maleate (PCM), in order to enhance the bioavailability of the drug and to provide rapid onset of action thereby improving patient compliance. The solubility of the drug was increased by preparing inclusion complex with 2-hydroxypropyl-p-cyciodextrin (2HP|3CD) and then incorporating it into the fast dissolving films. The fast-dissolving films of PCM were prepared by solvent casting method using different film forming polymers such as HPMC E15 and HPMC E5, either as single polymer or combination of the two. The film formulations were evaluated for various physico-chemical parameters. All formulations released more than 85% of the drug within 15 minutes. Formulation F4 showed best in vitro drug release profile. From the ex vivo study it was found that 94.79% of drug permeated through the porcine oral mucosa from the optimized formulation F4 within 60 mins.
机译:本研究的目的是制备和评估马来酸氯丙嗪(PCM)的速溶口腔膜片,以增强药物的生物利用度并提供快速起效的作用,从而改善患者的依从性。通过与2-羟丙基-对-环糊精(2HP | 3CD)制备包合配合物,然后将其掺入快速溶解膜中,可以增加药物的溶解度。通过溶剂流延法使用不同的成膜聚合物(例如HPMC E15和HPMC E5)作为单一聚合物或两者的组合,来制备PCM的快速溶解膜。评价膜制剂的各种物理化学参数。所有制剂在15分钟内释放了超过85%的药物。制剂F4显示出最佳的体外药物释放曲线。从离体研究中发现,有94.79%的药物在60分钟内从优化配方F4透过猪口腔粘膜渗透。

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