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机构地区:[1]天津大学药物科学与技术学院,天津市300072
出 处:《中国药房》2008年第3期183-185,共3页China Pharmacy
摘 要:目的:研究当归超微粉直接压片成型的工艺。方法:采用混料均匀设计法,以片重差异、脆碎度为限制条件,以硬度、崩解度的综合评分为指标建立回归方程,求出综合最优解,对当归超微粉片处方进行优化。用DPS软件进行数据运算。结果:最佳处方为应用粉末直接压片法制备片剂,其硬度可达到75N,崩解时间为10.24min,且片面光滑无缺。结论:该工艺处方合理、成型性好,可为工业化生产提供理论依据。OBJECTIVE: To study the direct powder compression technology of Angelica micropowder. METHODS: The formula of Angelica micropowder was optimized by mixture uniform design with tablet weight variation and friability as re strictive conditions, and a regression equation was established based on the comprehensive grading on the hardness and disintegration to figure out the optimal solution. DPS software was applied in the calculation, RESULTS: Prepared by the direct powder compression technology, the optimal formula of Angelica micropowder was obtained as follows: the hardness of the optimized tablet could reach as high as 75 N and the disintegrating time was about 10.24 min, with smooth and intact surface. CONCLUSION: The technology is reasonable in formulation and satisfactory in molding, and it can serve as theoretical basis for the production of Angelica tablets.
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