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Title: [Formulation optimization of panax notoginsenoside orally fast disintegration tablets]. Author: Wang Z, Wei L, Chen T. Journal: Zhongguo Zhong Yao Za Zhi; 2008 Jul; 33(14):1676-80. PubMed ID: 18841763. Abstract: OBJECTIVE: To optimize the formulation of panax notoginsenoside orally fast disintegrating tablets. METHOD: Mannitol, microcrystalline cellulose (PH 102) and lactose 80 were used as diluent. A polynomial regression algorithm was used to evaluate the relationship between the controlling factor, compacting pressure and diluent ratio, and disintegration time, tensile strength of tablets. Optimum formulation and process parameters could be determined by contrast the contour plot of tensile strength to that of disintegration time. RESULT: The disintegration time and tensile strength of panax notoginsenoside oral disintegrating tablets were good, and the taste was satisfactory. CONCLUSION: Panax notoginsenoside oral disintegrating tablets achieve the goal of design and this method can be fairly used in formulation screening.[Abstract] [Full Text] [Related] [New Search]