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崩解剂加入方式对流化床湿法制粒片剂特性的影响

Effect of mode of incorporation of disintegrants on the characteristics of fluid-bed wet-granulated tablets.

作者信息

Khattab I, Menon A, Sakr A

机构信息

College of Pharmacy, University of Cincinnati Medical Center, OH 45267-0004.

出版信息

J Pharm Pharmacol. 1993 Aug;45(8):687-91. doi: 10.1111/j.2042-7158.1993.tb07089.x.

Abstract

A full factorial experimental design was employed to investigate the effects of mode of disintegrant incorporation and concentration in wet-granulated paracetamol tablets manufactured by top-spray fluid-bed. Disintegrants (croscarmellose sodium, sodium starch glycolate, or crospovidone) were incorporated either intragranularly, extragranularly, or distributed equally between the two phases. The results were analysed by a general quadratic equation and response surfaces generated. On examining the results for dissolution studies the combined mode resulted in significantly faster dissolution rates than did the extragranular mode which, in turn, was superior to the intragranular mode of inclusion. These results were reflected in the disintegration studies where the combined mode exhibited the shortest disintegration times for all the disintegrants. Tablet crushing strength was not affected by the mode of incorporation of concentration of the disintegrants. Main as well as interaction effects between the types, mode of incorporation and percent disintegrant employed were significant (P < 0.05) for disintegration time and percent release at 15 min. Croscarmellose sodium exhibited the shortest while crospovidone displayed significantly (P < 0.05) longer disintegration times. Formulations containing crospovidone did not meet official compendial (USP XXII) requirements of 80% in 30 min. In general, croscarmellose sodium and sodium starch glycolate were found to be less sensitive to the mode of incorporation than crospovidone.

摘要

采用全因子实验设计,研究了在顶喷流化床制粒的对乙酰氨基酚片中崩解剂加入方式和浓度的影响。崩解剂(交联羧甲基纤维素钠、淀粉乙醇酸钠或交联聚维酮)以颗粒内加入、颗粒外加或在两相之间均匀分布的方式加入。通过一般二次方程分析结果并生成响应面。在考察溶出度研究结果时,混合加入方式导致的溶出速率明显快于颗粒外加方式,而颗粒外加方式又优于颗粒内加入方式。这些结果在崩解研究中也有体现,混合加入方式下所有崩解剂的崩解时间最短。片剂的抗压强度不受崩解剂加入方式和浓度的影响。崩解剂的类型、加入方式和用量百分比之间的主要效应以及相互作用效应,对于崩解时间和15分钟时的释放百分比均具有显著意义(P < 0.05)。交联羧甲基纤维素钠的崩解时间最短,而交联聚维酮的崩解时间则明显更长(P < 0.05)。含有交联聚维酮的制剂不符合官方药典(USP XXII)规定的30分钟内释放80%的要求。总体而言,交联羧甲基纤维素钠和淀粉乙醇酸钠对加入方式的敏感性低于交联聚维酮。

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