a Lek Pharmaceuticals d.d. , Ljubljana , Slovenia.
b Faculty of Pharmacy , University of Ljubljana , Ljubljana , Slovenia.
Drug Dev Ind Pharm. 2018 May;44(5):778-786. doi: 10.1080/03639045.2017.1412459. Epub 2017 Dec 14.
The aim of the present research is to show that the methodology of Design of Experiments can be applied to stability data evaluation, as they can be seen as multi-factor and multi-level experimental designs. Linear regression analysis is usually an approach for analyzing stability data, but multivariate statistical methods could also be used to assess drug stability during the development phase. Data from a stability study for a pharmaceutical product with hydrochlorothiazide (HCTZ) as an unstable drug substance was used as a case example in this paper. The design space of the stability study was modeled using Umetrics MODDE 10.1 software. We showed that a Partial Least Squares model could be used for a multi-dimensional presentation of all data generated in a stability study and for determination of the relationship among factors that influence drug stability. It might also be used for stability predictions and potentially for the optimization of the extent of stability testing needed to determine shelf life and storage conditions, which would be time and cost-effective for the pharmaceutical industry.
本研究旨在表明,实验设计方法可应用于稳定性数据评估,因为它们可以被视为多因素和多层次的实验设计。线性回归分析通常是一种用于分析稳定性数据的方法,但多元统计方法也可用于评估药物在开发阶段的稳定性。本文以含有不稳定药物成分氢氯噻嗪 (HCTZ) 的药物产品的稳定性研究数据为例。使用 Umetrics MODDE 10.1 软件对稳定性研究的设计空间进行建模。我们表明,偏最小二乘模型可用于多维呈现稳定性研究中生成的所有数据,并确定影响药物稳定性的因素之间的关系。它也可用于稳定性预测,并有可能优化确定保质期和存储条件所需的稳定性测试程度,这将对制药行业具有时间和成本效益。