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Design space construction of multiple dose-strength tablets utilizing Bayesian estimation based on one set of design-of-experiments

机译:基于一组实验设计的基于贝叶斯估计的多剂剂量片剂的设计空间构造

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摘要

Design spaces for multiple dose strengths of tablets were constructed using a Bayesian estimation method with one set of design of experiments (DoE) of only the highest dose-strength tablet. The lubricant blending process for theophylline tablets with dose strengths of 100, 50, and 25 mg is used as a model manufacturing process in order to construct design spaces. The DoE was conducted using various Froude numbers (X _1) and blending times (X _2) for theophylline 100-mg tablet. The response surfaces, design space, and their reliability of the compression rate of the powder mixture (Y _1), tablet hardness (Y _2), and dissolution rate (Y _3) of the 100-mg tablet were calculated using multivariate spline interpolation, a bootstrap resampling technique, and self-organizing map clustering. Three experiments under an optimal condition and two experiments under other conditions were performed using 50- and 25-mg tablets, respectively. The response surfaces of the highest-strength tablet were corrected to those of the lower-strength tablets by Bayesian estimation using the manufacturing data of the lower-strength tablets. Experiments under three additional sets of conditions of lower-strength tablets showed that the corrected design space made it possible to predict the quality of lower-strength tablets more precisely than the design space of the highest-strength tablet. This approach is useful for constructing design spaces of tablets with multiple strengths.
机译:使用贝叶斯估计方法,通过一组仅最高剂量强度片剂的实验设计(DoE),构造了片剂的多种剂量强度的设计空间。为了构建设计空间,将剂量分别为100、50和25 mg的茶碱片的润滑剂共混过程用作模型制造过程。对于各种茶碱100 mg片剂,使用各种Froude数(X _1)和混合时间(X _2)进行DoE。使用多元样条插值法计算了100 mg片剂的粉末混合物压缩率(Y _1),片剂硬度(Y _2)和溶出度(Y _3)的响应面,设计空间及其可靠性,自举重采样技术和自组织地图聚类。使用50毫克和25毫克片剂分别在最佳条件下进行了3次实验,在其他条件下进行了2次实验。使用低强度片剂的制造数据通过贝叶斯估计将最高强度片剂的响应表面校正为较低强度片剂的响应表面。在另外三组低强度药片的条件下进行的实验表明,校正后的设计空间使预测高强度药片的设计空间比高强度药片的设计空间更为精确。这种方法对于构建具有多种强度的药片的设计空间很有用。

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