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A Study of the Hydrophilic Cellulose Matrix: Effect of Indomethacin and a Water-Soluble Additive on Release Mechanisms

机译:亲水性纤维素基质的研究:消炎痛和水溶性添加剂对释放机理的影响

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摘要

The release profile of indomethacin (IM) from a direct compressible matrix containing three hydrophilic cellulose derivatives, methylcellulose (MC25 and MC50), hydroxypropylcellulose (HPC140), and hydroxypropylmethylcellu-lose (HPMC50) was studied. The drug release profile was affected by matrix size, polymer type, drug: polymer ratio and water soluble additive (lactose). An IM zero-order release matrix can be obtained by mixture and direct compression with MC50, HPMC50 and HPC140. The release rate from the MCSO and HPC140 matrix can be modified by replacing MC50 or HPC140 with MC25, and a zero-order release could be obtained even when the amount of replacement with MC2S is up to 35 and 45%, respectively. Lactose up to 10% slightly affected the release profile. IM released from this kind of matrix by a zero-order rate seems to be controlled by the swelling and relaxation of the polymer.
机译:研究了吲哚美辛(IM)从包含三种亲水性纤维素衍生物,甲基纤维素(MC25和MC50),羟丙基纤维素(HPC140)和羟丙基甲基纤维素(HPMC50)的直接可压缩基质中的释放曲线。药物释放曲线受基质尺寸,聚合物类型,药物:聚合物比率和水溶性添加剂(乳糖)的影响。 IM零级释放矩阵可以通过与MC50,HPMC50和HPC140混合并直接压缩来获得。可以通过用MC25替换MC50或HPC140来更改MCSO和HPC140基质的释放速率,即使用MC2S替换的量分别高达35%和45%,也可以获得零级释放。高达10%的乳糖会稍微影响释放曲线。从这种基质以零级速率释放的IM似乎受聚合物的溶胀和松弛控制。

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