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批次间和批次内变异性对证明半固体制剂等效微观结构所需样本量的影响。

Influence of Inter- and Intra-Batch Variability on the Sample Size Required for Demonstration of Equivalent Microstructure of Semisolid Dosage Forms.

作者信息

Xu Zhengguo, Mangas-Sanjuán Víctor, Merino-Sanjuán Matilde, Merino Virginia, García-Arieta Alfredo

机构信息

Departamento de Farmacia y Tecnología Farmacéutica y Parasitología, Facultad de Farmacia, Universitat de València, Av. Vicente Andrés Estellés s/n, Burjassot, 46100 Valencia, Spain.

Instituto Interuniversitario de Investigación de Reconocimiento Molecular y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, 46100 Valencia, Spain.

出版信息

Pharmaceutics. 2020 Nov 28;12(12):1159. doi: 10.3390/pharmaceutics12121159.

Abstract

Inter- and intra-batch variability of the quality attributes contribute to the uncertainty for demonstrating equivalent microstructure of post-approval changes and generic/hybrids of semisolid topical products. Selecting a representative sample size to describe accurately the in vitro properties of semisolids and to reach enough statistical power to demonstrate similarity between two semisolid topical products is currently challenging. The objective of this work is to establish the number of batches and units per batch to be compared based on different inter-batch and intra-batch variability to demonstrate equivalence in the physical characteristics of the products that ensure a similar microstructure of the semisolid. This investigation shows that the minimum number of batches to be compared of each product is 3 and the minimum number of units per batch could be 6 in the case of low intra- and inter-batch variability. If the products are not identical, i.e., 2.5-5% differences that are expected due to differences in the manufacturing process or the suppliers of excipients, 12 units and 6 batches are needed. If intra- or inter-batch variability is larger than 10%, the number of batches and/or the number of units needs to be increased. As the interplay between inter- and intra-batch variability is complex, the sample size required for each combination of inter- and intra-batch variability and expected difference between products can be obtained in the attached tables.

摘要

质量属性的批次间和批次内变异性导致了在证明批准后变更以及半固体局部用产品的仿制药/混合药具有等效微观结构时的不确定性。选择具有代表性的样本量以准确描述半固体的体外性质,并获得足够的统计效力来证明两种半固体局部用产品之间的相似性,目前具有挑战性。本研究的目的是根据不同的批次间和批次内变异性确定要比较的批次数量和每批的单位数量,以证明产品物理特性的等效性,确保半固体具有相似的微观结构。本研究表明,在批次内和批次间变异性较低的情况下,每种产品要比较的最小批次数量为3,每批的最小单位数量可以为6。如果产品不相同,即由于生产工艺或辅料供应商的差异预期会有2.5-5%的差异,则需要12个单位和6个批次。如果批次内或批次间变异性大于10%,则需要增加批次数量和/或单位数量。由于批次间和批次内变异性之间的相互作用很复杂,批次间和批次内变异性的每种组合以及产品之间预期差异所需的样本量可在附表中获得。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/09a1/7760601/485b9cdbacf8/pharmaceutics-12-01159-g001.jpg

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