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Formulation and optimization of Gastric floating matrix tablets of norfloxacin with combination of polymers using Box-Behnken experimental design

机译:使用Box-Behnken实验设计配制和优化诺氟沙星与聚合物结合的胃漂浮基质片

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The purpose of the present study was to develop and optimize gastric floating drug delivery system (GFDDS) containing norfloxacin as a model drug using Box-Behnken design. A 3-factor, 3-level Box-Behnken design was used to derive a second order polynomial equation and construct contour plots to predict responses. The independent variables selected were Compritol ATO 888 (X_1), Poloxamer 188 (X_2) and chitosan (X_3). Fifteen batches were prepared by wet granulation method and evaluated for Floating lag time (FLT), total floating time (TFT) and time required to release 50% of the drug (t_(50)) as dependent variables. Compritol ATO 888 containing tablets were found to be significant for floating properties, poloxamer 188 had a negative effect on floating properties but was found helpful in controlling the release rate of the drug. No significant effect of chitosan on floating properties was observed but it was important for gel formation. The computer optimization process and contour plots predicted the levels of independent variables X_1, X_2, and X_3 (26.33, 9.20 and 15.13 respectively), for maximized response of TFT.
机译:本研究的目的是使用Box-Behnken设计开发和优化以诺氟沙星为模型药物的胃漂浮药物递送系统(GFDDS)。使用三因子,三级Box-Behnken设计来导出二阶多项式方程,并构造轮廓图以预测响应。选择的自变量为Compritol ATO 888(X_1),泊洛沙姆188(X_2)和壳聚糖(X_3)。通过湿法制粒法制备了15个批次,并评估了漂浮滞后时间(FLT),总漂浮时间(TFT)和释放50%药物所需的时间(t_(50))作为因变量。发现含有Compritol ATO 888的片剂对漂浮性能很重要,泊洛沙姆188对漂浮性能有负面影响,但发现有助于控制药物的释放速率。没有观察到壳聚糖对漂浮性能的显着影响,但对凝胶形成很重要。计算机优化过程和轮廓图预测了自变量X_1,X_2和X_3(分别为26.33、9.20和15.13)的水平,以使TFT的响应最大化。

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