药品
药物开发
纳米技术
活性成分
文件夹
剂型
工作流程
生化工程
药理学
医学
材料科学
计算机科学
业务
工程类
数据库
财务
作者
Akosua B. Anane‐Adjei,Esther Jacobs,Samuel C. Nash,Sean Askin,Ramesh Soundararajan,Mary Kyobula,Jonathan Booth,Andrew D. Campbell
标识
DOI:10.1016/j.ijpharm.2021.121387
摘要
The poor aqueous solubility of many active pharmaceutical ingredients (APIs) dominates much of the early drug development portfolio and poses a major challenge in pharmaceutical development. Polymer-based amorphous solid dispersions (ASDs) are becoming increasingly common and offer a promising formulation strategy to tackle the solubility and oral absorption issues of these APIs. This review discusses the design, manufacture, and utilisation of ASD formulations in preclinical drug development, with a key focus on the pre-formulation assessments and workflows employed at AstraZeneca.
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