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作 者:黄勇[1] 石凌云[1] 乔希[1] 王爱民[1] 况时祥[2] 王永林[1]
机构地区:[1]贵阳医学院药学院,贵阳550004 [2]贵阳中医学院附属第二医院,贵阳550001
出 处:《中国药房》2012年第31期2913-2915,共3页China Pharmacy
基 金:贵州省中药现代化科技产业研究开发专项项目(黔科合农字[2006]5023号);贵州省科技计划课题(黔科合计工字[2009]4001);贵阳市科学技术计划项目([2009]筑科计合同字第9-3-04号)
摘 要:目的:优选脑通颗粒成型工艺。方法:以乙醇浓度、糊精用量、阿司帕坦用量为考察因素,以制粒难易程度、口感、外观、粒度、溶化性及其综合评分为评价指标,采用L(934)正交试验优选成型工艺,并考察颗粒的吸湿性。结果:最佳制粒工艺为乙醇浓度85%,糊精用量为45%,阿司帕坦用量为1%,测得临界相对湿度为70%。结论:本试验结果可为脑通颗粒处方组成的确定及生产环境的控制提供理论依据。OBJECTIVE: To optimize the forming technology of Naotong granules. METHODS: The forming technology of Naotong granules was optimized by L9(3^4) orthogonal design with of ethanol concentration, dosage of dextrin and flavoring agent aspartame(APM) as factors using the degree of difficulty in granulating, taste, appearance, particle size and solubility and other comprehensive score as indexes. The hygroscopicity of granules was investigated. RESULTS: The proper forming technology was as follows: the concentration of ethanol was 85%, dosage of dextrin was 45% and APM was 1%, the critical relative humidity was about 70%. CONCLUSION: The study provides theory evidence for formulation process of Naotong granules and the control of production environment.
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