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首页> 外文期刊>Journal of the Chilean Chemical Society >DESIGN AND DEVELOPMENT OF MONTELUKAST SODIUM FAST DISSOLVING FILMS FOR BETTER THERAPEUTIC EFFICACY
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DESIGN AND DEVELOPMENT OF MONTELUKAST SODIUM FAST DISSOLVING FILMS FOR BETTER THERAPEUTIC EFFICACY

机译:孟鲁司特钠快速溶解膜的设计和开发以提高疗效

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The oral route is most popular route for the administration of therapeutic agents because of the low cost of therapy and ease of administration lead to high levels of patient compliance. The most popular oral solid dosage forms are tablets and capsules. Many patients find it difficult to swallow tablets and hard gelatin capsules particularly pediatric and geriatric patients and do not take their medicines as prescribed. The objective of this research was to prepare fast dissolving oral thin film (FDOTF) containing Montelukast sodium is indicated for the prophylaxis and chronic treatment of asthma to enhance convenience and compliance to the elderly and pediatric patients for better therapeutic efficacy. The present investigation was undertaken with the objective of formulating of the montelukast sodium fast dissolving oral thin films allowing fast reproducible drug dissolution in oral cavity thus bypassing first pass metabolism. The film were prepared by using polymers such as hydroxypropyl methyl cellulose (HPMC) and Maltodextrin, plasticizer such as PEG 400, by a solvent casting method. They were evaluated for physical characteristics such as thickness, uniformity of weight, folding endurance, drug content, surface ph, percentage elongation and tensile strength, drug polymers compatibility by FTIR study, scanning electron microscopy and in vitro drug release. The formulations were subjected to disintegration, in-vitro drug release test. The in vitro disintegration time of the optimized batch F4 was found to be 20 sec. The optimized batch was found to be stable for 1 month under specified stability conditions.
机译:口服途径是用于治疗剂的最流行的途径,因为治疗成本低并且易于施用导致高水平的患者依从性。最受欢迎的口服固体剂型是片剂和胶囊剂。许多患者发现难以吞咽药片和硬明胶胶囊,尤其是小儿和老年患者,并且不按处方服用药物。这项研究的目的是制备包含孟鲁司特钠的快速溶解口腔薄膜(FDOTF),用于预防和慢性治疗哮喘,以增强老年人和儿科患者的便利性和依从性,从而获得更好的治疗效果。进行本研究的目的是配制孟鲁司特钠速溶口腔薄膜,从而使药物在口腔中快速可重现溶解,从而绕过首过代谢。通过使用溶剂流延法,使用诸如羟丙基甲基纤维素(HPMC)和麦芽糊精,增塑剂诸如PEG 400的聚合物来制备膜。通过FTIR研究,扫描电子显微镜和体外药物释放,对它们的物理特性进行了评估,例如厚度,重量均匀性,耐折性,药物含量,表面酸碱度,延伸百分比和拉伸强度,药物聚合物相容性。将制剂进行崩解,体外药物释放测试。发现优化批次F4的体外崩解时间为20秒。发现优化的批次在指定的稳定性条件下稳定1个月。

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