盐酸头孢替安酯片的研制及质量研究
投稿时间:2018-12-03  修订日期:2019-06-13  点此下载全文
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作者单位E-mail
贾玮 西安万隆制药股份有限公司 西安
陕西九州制药有限责任公司 西安 
jiaweiys@126.com 
张红侠 陕西九州制药有限责任公司 西安  
冯志强 西安万隆制药股份有限公司 西安  
孙路 西安万隆制药股份有限公司 西安  
中文摘要:目的 研究盐酸头孢替安酯片的制备工艺及质量。方法 以药物的崩解时限和溶出度为主要指标,采用原研片参比单因素考察法对盐酸头孢替安酯片的处方工艺进行优化,并对其质量进行研究。结果 实验确定最优处方:以无水枸橼酸、α-环糊精、微晶纤维素、羟丙纤维素、二氧化硅、硬脂酸镁、薄膜包衣预混剂(胃溶型)为辅料,采用干法制粒制备盐酸头孢替安酯片。盐酸头孢替安酯片各项指标符合日本药局方(JPXV)标准。结论 盐酸头孢替安酯片的制备工艺可行,产品质量具有良好的稳定性。
中文关键词:盐酸头孢替安酯  崩解时限  溶出度  质量研究
 
The Study on Preparation and Quality of Cefotiam Hydrochloride Tablet
Abstract:Objective To study the preparation technology and quality of cefotiam hexetil hydrochloride tablet. Method With the disintegration time limit, and dissolution of drug as the main index, using the original piece of reference of prescription process optimization, the single factor investigation method preparation of cefotiam hexetil hydrochloride and preliminary study on its quality. Results The best prescription was determined by experiments: cefotiam hexetil hydrochloride tablets were prepared by dry granulation with anhydrous citric acid, alpha-cyclodextrin, microcrystalline cellulose, hydroxypropyl cellulose, silica, magnesium stearate and film-coated premix (gastric-soluble). The indexes of ceftiamide hydrochloride tablets conform to the Japanese Pharmaceutical Bureau Prescription (JPXV) standard. Conclusion The preparation technology of cefotiam hexetil hydrochloride tablet is feasible and the product having good stability.
keywords:cefotiam hexetil hydrochloride  disintegration time limited  dissolution rate  quality research
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