Formulation, Optimization, and Evaluation of Bioadhesive Xanthan Gum Based Buccal Patch for Sustained Delivery of Ropinirole Hydrochloride

IF 0.4 Q4 PHARMACOLOGY & PHARMACY
Kalyani Kayande
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引用次数: 0

Abstract

Introduction: Parkinson’s disease is a neurological disorder in which there is a gradual loss of brain cells that make and store dopamine. Ropinirole hydrochloride (ROPH) is an anti-Parkinson’s drug which undergoes extensively first-pass metabolism, with oral bioavailability 45%. Aim: The study aimed to formulation, optimization, and evaluation of ROPH buccal patch using xanthan gum (XG). Materials and Methods: Solvent casting method was used to prepare mucoadhesive buccal patch ROPH using XG as a mucoadhesive polymer, polyvinylpyrrolidone K90 as a film former and polycarbophil and hydroxypropyl methylcellulose K4M as a release retardant. Results and Discussion: The dissolution studies showed sustained release of drug about 97.86% for 8 h following Korsmeyer-Peppas model (r2=0.989, n = 0.199). The optimization of all prepared batches was carried out by 32 factorial designs, the optimized batch F3 showed acceptable physicochemical properties and having swelling index 286.10%, mucoadhesive strength 26.90 g, tensile strength 0.04±0.01 N/mm2, and in vitro drug release 97.86%. Ex vivo permeability was carried out using sheep buccal mucosa and it was found to be increased by five folds than that of formulation without penetration enhancer. After histopathological evaluation cellular membrane was found to be intact and did not show any signs of necrosis. Conclusion: Thus, an attempt to formulate a stable mucoadhesive buccal patch was made. The in vitro studies have shown that this is a potential drug delivery system for ROPH with good stability and release profile.
生物胶粘剂黄原胶口腔贴剂的配方、优化及评价
引言:帕金森病是一种神经系统疾病,产生和储存多巴胺的脑细胞逐渐丧失。盐酸Ropinirole(ROPH)是一种抗帕金森病药物,经过广泛的首过代谢,口服生物利用度为45%。目的:以黄原胶(XG)为原料,对ROPH口腔贴片的配方、优化及评价进行研究。材料与方法:采用溶剂浇铸法,以XG为粘膜粘附聚合物,聚乙烯吡咯烷酮K90为成膜剂,聚羧甲基纤维素和羟丙基甲基纤维素K4M为缓释剂,制备口腔粘膜粘附贴片ROPH。结果与讨论:根据Korsmeyer-Peppas模型(r2=0.989,n=0.199),溶出度研究显示药物在8h内持续释放约97.86%。通过32个析因设计对所有制备的批次进行了优化,优化的批次F3显示出可接受的理化性质,溶胀指数为286.10%,粘膜粘附强度为26.90g,拉伸强度为0.04±0.01N/mm2,体外释药率为97.86%。用绵羊颊粘膜进行体外渗透性试验,发现其比不含渗透促进剂的制剂增加了5倍。组织病理学评估后,发现细胞膜完好无损,没有任何坏死迹象。结论:为研制一种稳定的口腔粘膜粘附贴片进行了尝试。体外研究表明,这是一种潜在的ROPH给药系统,具有良好的稳定性和释放特性。
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来源期刊
Asian Journal of  Pharmaceutics
Asian Journal of Pharmaceutics PHARMACOLOGY & PHARMACY-
自引率
0.00%
发文量
47
期刊介绍: Character of the publications: -Pharmaceutics and Pharmaceutical Technology -Formulation Design and Development -Drug Discovery and Development Interface -Manufacturing Science and Engineering -Pharmacokinetics, Pharmacodynamics, and Drug Metabolism -Clinical Pharmacology, General Medicine and Translational Research -Physical Pharmacy and Biopharmaceutics -Novel Drug delivery system -Biotechnology & Microbiological evaluations -Regulatory Sciences
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