协调
潘生丁
产品(数学)
溶解
药理学
医学
化学
工程伦理学
工程类
内科学
哲学
化学工程
数学
几何学
美学
作者
Yasuhiro Tsume,L. J. Ashworth,Marival Bermejo,Vincent Cicale,Jennifer B. Dressman,Masahiro Fushimi,Isabel González‐Álvarez,Pin-Syuan Haung,Corinne Jankovsky,Xiaohong Liu,Xujin Lu,Kazuki Matsui,Sanjaykumar R. Patel,Alejandro Ruiz-Picazo,Changquan Calvin Sun,Naveen K. Thakral,Laurin Zöller
标识
DOI:10.1021/acs.molpharmaceut.4c00878
摘要
Biorelevant dissolution and its concept have been widely accepted and further developed to meaningfully predict the bioperformance of oral drug products. Biorelevant methodologies have been applied to design and optimize oral formulations, to facilitate formulation bridging, and to predict the outcome of bioperformance by coupling the results with modeling. Yet, those methodologies have often been independently customized to align with specific aspects of the oral drug products being developed. Therefore, the evolution of biorelevant dissolution methodologies has taken slightly diverse pathways rather than being standardized like compendial quality control (QC) methodologies. This manuscript presents an effort through the Product Quality Research Institute (PQRI, https://pqri.org) consortium entitled: the standardization of "
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