首页> 外文期刊>Indian journal of pharmaceutical sciences. >Effect of Different Polymer Concentration on Drug Release Rate and Physicochemical Properties of Mucoadhesive Gastroretentive Tablets
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Effect of Different Polymer Concentration on Drug Release Rate and Physicochemical Properties of Mucoadhesive Gastroretentive Tablets

机译:不同聚合物浓度对粘膜胃滞留片药物释放速率和理化性质的影响

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摘要

Mucoadhesive tablets have emerged as potential candidates for gastroretentive drug delivery providing controlled release along with prolonged gastric residence time. Gastroretentive mucoadhesive tablets could result in increased bioavailability due to prolonged gastric residence time. A hydrophilic matrix system was developed as mucoadhesion is achievable on appropriate wetting and swelling of the polymers used. The polymers were so chosen so as to provide a balance between swelling, mucoadhesion and drug release. The polymers chosen were hydroxypropyl methylcellulose K4M, chitosan, and Carbopol 934. The concentrations of these polymers used has a great impact on the physicochemical properties of the resulting formulation. The tablets were formulated using wet granulation method and tranexamic acid was used as the model drug. The prepared tablets were characterized for size, shape, appearance, hardness, friability, weight variation, swelling, mucoadhesion and in vitro drug release. Several batches of tablets were prepared by varying the ratio of hydroxypropyl methylcellulose K4M and Chitosan. The batches having a greater ratio of chitosan showed higher rate of swelling, greater erosion, less mucoadhesion and faster release rate of the drug whereas the batches having greater ratio of hydroxypropyl methylcellulose K4M showed lesser rate of swelling, less erosion, better mucoadhesion and a smaller drug release rate. The level of carbopol was kept constant in all the batches.
机译:粘膜黏附片已经成为胃固性药物递送的潜在候选者,其提供了控释以及延长的胃停留时间。胃滞留性粘膜粘连片可能会由于胃停留时间延长而导致生物利用度增加。开发了亲水性基质体系,因为在适当润湿和溶胀所用聚合物时可以实现粘膜粘附。选择聚合物以便在溶胀,粘膜粘附和药物释放之间提供平衡。选择的聚合物是羟丙基甲基纤维素K4M,壳聚糖和Carbopol934。所用这些聚合物的浓度对所得制剂的物理化学性质有很大的影响。使用湿法制粒法配制片剂,并使用氨甲环酸作为模型药物。所制备的片剂的尺寸,形状,外观,硬度,易碎性,重量变化,溶胀,粘膜粘附和体外药物释放具有特征。通过改变羟丙基甲基纤维素K4M和壳聚糖的比例来制备几批片剂。壳聚糖比例较高的批次显示出更高的溶胀率,更大的侵蚀,更少的粘膜粘附性和更快的药物释放速率,而羟丙基甲基纤维素K4M比例较大的批次显示出更低的溶胀率,更少的侵蚀性,更好的粘膜粘附性和更小的体积药物释放速率。在所有批次中,卡波普的含量均保持恒定。

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