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Assessing Physical Stability Risk Using the Amorphous Classification System (ACS) Based on Simple Thermal Analysis

机译:基于简单的热分析,使用非晶分类系统(ACS)评估物理稳定性风险

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The purpose of this study is to develop a classification system utilizing milligram amounts of the compound for physical stability ranking of amorphous pharmaceuticals, which can be used as an early risk assessment tool for amorphous solid dispersion formulations. Simple thermal analysis utilizing a differential scanning calorimeter is used to characterize amorphous pharmaceuticals with respect to their molecular mobility and configurational entropy. Molecular mobility and configurational entropy are considered as two critical factors in determining the physical stability of amorphous phases. Theoretical arguments and numerical simulations suggest that the fragility strength parameter is a good indicator of the molecular mobility below T-g, and the heat capacity change at Tg is a good indicator of the configurational entropy. Using these two indicators, 40 structurally diverse pharmaceuticals with known physical stability were analyzed. Four classes of compounds are defined with class I being the most stable and class IV the least stable. The proposed amorphous classification system and methodology for estimating molecular mobility and configurational entropy provides an easily accessible framework to conduct early risk assessments related to physical stability challenges in developing amorphous formulations.
机译:本研究的目的是开发利用毫克量的化合物的分类系统,用于无定形药物的物理稳定性排名,其可用作无定形固体分散制剂的早期风险评估工具。利用差示扫描量热计的简单热分析用于表征其分子迁移率和配置熵的无定形药物。分子迁移率和配置熵被认为是确定无定形阶段的物理稳定性的两个关键因素。理论争论和数值模拟表明,脆性强度参数是低于T-G的分子迁移率的良好指标,并且Tg的热容量变化是配置熵的良好指标。使用这两种指示器,分析了具有已知物理稳定性的结构各种药物。使用四种类化合物,用A类是最稳定的,最不稳定的等级。拟议的无定形分类系统和用于估算分子迁移率和配置熵的方法提供了一种易于访问的框架,用于开展与发展无定形配方中的物理稳定挑战有关的早期风险评估。

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