The use of micronized cellulose disintegrants as insoluble swellable matrices for sustained-release tablets.

Drug design and delivery Pub Date : 1991-07-01
H Nakagami, M Nada
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Abstract

Five cellulose disintegrants--low-substituted hydroxypropylcellulose (L-HPC), microcrystalline cellulose (MCC), carboxymethylcellulose (CMC), cross-linked NaCMC (C.L.NaCMC), and CaCMC-were evaluated as directly compressed matrices for sustained-release (SR) tablets in vitro, using procainamide hydrochloride as a model drug. Coarser particles (14-19 microns) of the jet mill ground disintegrants, as well as intact disintegrants, provided rapidly disintegrating tablets with fast drug release but finer particles (2.5-3.5 microns) provided matrix-type SR tablets. The SR tablets based on non-ionic polymers (L-HPC and MCC) did not disintegrate at any pH; those based on anionic polymers (C.L.NaCMC and CaCMC) did not disintegrate at pH 1.2, but they disintegrated gradually from the exterior in water and in a pH 6.8 medium. We conclude that the particle size and concentration of the cellulose disintegrants are determinant factors in the formulation of SR matrices.

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用微粉纤维素崩解剂作为缓释片的不溶性溶胀基质。
以盐酸普鲁卡因酰胺为模型药物,对低取代羟丙基纤维素(L-HPC)、微晶纤维素(MCC)、羧甲基纤维素(CMC)、交联NaCMC (C.L.NaCMC)和cacmc这5种纤维素崩解剂作为直接压缩基质用于体外缓释片(SR)的评价。射流磨碎崩解剂颗粒粗(14 ~ 19微米)和完整崩解剂颗粒细(2.5 ~ 3.5微米),崩解片剂快速释放,基质型SR片剂快速释放。基于非离子聚合物(L-HPC和MCC)的SR片在任何pH下均不崩解;阴离子聚合物(c.l.c acmc和CaCMC)在pH为1.2时不发生分解,但在水和pH为6.8的介质中从外部逐渐分解。我们得出结论,纤维素崩解剂的粒径和浓度是SR基质配方的决定因素。
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