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粉末直接压片法制备盐酸丙哌维林片及其稳定性考察
引用本文:欧阳百发,刘春华,金向阳. 粉末直接压片法制备盐酸丙哌维林片及其稳定性考察[J]. 中国药师, 2013, 16(3): 351-354
作者姓名:欧阳百发  刘春华  金向阳
作者单位:康美药业股份有限公司 广东普宁 515300;康美药业股份有限公司 广东普宁 515300 康美药物研究院有限公司;康美药物研究院有限公司
摘    要:
摘 要 目的:优选盐酸丙哌维林片粉末直接压片法最佳制备工艺,并考察其稳定性。方法: 采用粉末直接压片法,以粉末休止角、片剂脆碎度及溶出度为评价指标,制备样品并进行质量考察。结果:所选处方粉末流动性良好,有效成分溶出速率高,各项指标均符合规定。经6个月加速及室温留样考察,样品的外观、含量、有关物质及溶出度均未发生明显变化。结论:优选的处方工艺操作简便、经济、生产周期短,制备的产品质量稳定

关 键 词:盐酸丙哌维林;粉末直接压片法;稳定性;制备工艺
收稿时间:2012-09-10
修稿时间:2012-11-28

Preparation and Stability of Propiverine Hydrochloride Tablets Prepared by Direct Powder Compression
Ouyang Baif,Liu Chunhua and Jin Xiangyang. Preparation and Stability of Propiverine Hydrochloride Tablets Prepared by Direct Powder Compression[J]. China Pharmacist, 2013, 16(3): 351-354
Authors:Ouyang Baif  Liu Chunhua  Jin Xiangyang
Affiliation:Kangmei Pharmaceutical Co. Ltd., Guangdong Puning 515300, China;Kangmei Pharmaceutical Co. Ltd., Guangdong Puning 515300, China; Guangdong Kangmei Pharmaceutical Research Institute Co. Ltd.;Guangdong Kangmei Pharmaceutical Research Institute Co. Ltd.
Abstract:
ABSTRACT Objective: To optimize the preparation process of propiverine hydrochloride tablets by direct powder compression and investigate the stability. Method:The samples were prepared by direct powder compression and the quality was inspected using powder angle of repose, tablet friability and drug dissolution as the evaluation indices. Result:The optimal formula had promising powder fluidity and dissolution rate. The quality of the tablets was accorded with the relative requirements. After accelerated test of 6 months and storage at room temperature, the appearance, content, related substance and dissolution of the samples showed no significant change. Conclusion:The optimal formula and the preparation process are convenient, economical, time-saving and stable.
Keywords:Propiverine hydrochloride   Direct powder compression   Stability   Preparation process
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