药品
药物开发
纳米技术
活性成分
生物制药
文件夹
剂型
试验药物
生化工程
制药工业
药物制剂
药理学
医学
材料科学
业务
工程类
生物技术
临床试验
内科学
财务
生物
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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