Department of Pharmaceutical Technology, Graduate School of Medicine and Pharmaceutical Science for Research, University of Toyama, 2630 Sugitani, Toyama-shi, Toyama 930-0194, Japan.
Department of Pharmaceutical Technology, Graduate School of Medicine and Pharmaceutical Science for Research, University of Toyama, 2630 Sugitani, Toyama-shi, Toyama 930-0194, Japan; Formulation Development Department, Development & Planning Division, Nichi-Iko Pharmaceutical Co., Ltd., 205-1, Shimoumezawa, Namerikawa-shi, Toyama 936-0857, Japan.
Int J Pharm. 2020 Mar 15;577:119083. doi: 10.1016/j.ijpharm.2020.119083. Epub 2020 Jan 24.
Our aim was to understand better the causal relationships between material attributes (MAs), process parameters (PPs), and critical quality attributes (CQAs) using an originally created large dataset and regularized linear regression models. In this study, we focused on the following three points: (1) creation of a dataset comprising several tablet production methods, (2) the influence of interaction terms of MAs and/or PPs, and (3) comparison of regularized linear regression models with partial least squares (PLS) regression. First, we prepared 44 kinds of tablets using direct compression and five kinds of granulation methods. We then measured 12 MAs and two model CQAs (tensile strength and disintegration time of tablet). Principal component analysis showed that the constructed dataset comprised a wide variety of particles. We applied regularized linear regression models, such as ridge regression, LASSO and Elastic Net (ENET), and PLS to our dataset to predict CQAs from the MAs and PPs. As a result of external validation, the prediction performance of the models was sufficiently high, although ENET was slightly better than the other methods. Moreover, in almost all cases, the models with interaction terms showed higher predictive ability than those without interaction terms, indicating that the interaction terms of MAs and/or PPs have a strong influence on CQAs. ENET also allowed the selection of critical factors that strongly affect CQAs. The results of this study will help to understand systematically knowledge obtained in pharmaceutical development.
我们的目的是使用原始创建的大型数据集和正则化线性回归模型更好地理解物质属性(MAs)、工艺参数(PPs)和关键质量属性(CQAs)之间的因果关系。在这项研究中,我们主要关注以下三个方面:(1)创建一个包含多种片剂生产方法的数据集,(2)MA 和/或 PP 的交互项的影响,(3)正则化线性回归模型与偏最小二乘(PLS)回归的比较。首先,我们使用直接压缩法和五种制粒方法制备了 44 种片剂。然后,我们测量了 12 个 MA 和两个模型 CQA(片剂的拉伸强度和崩解时间)。主成分分析表明,构建的数据集包含了各种各样的颗粒。我们将正则化线性回归模型(如岭回归、LASSO 和弹性网(ENET)以及 PLS)应用于我们的数据集,以从 MA 和 PP 预测 CQA。经过外部验证,模型的预测性能足够高,尽管 ENET 略优于其他方法。此外,在几乎所有情况下,具有交互项的模型都比没有交互项的模型具有更高的预测能力,这表明 MA 和/或 PP 的交互项对 CQA 有很强的影响。ENET 还允许选择对 CQA 有强烈影响的关键因素。本研究的结果将有助于系统地了解药物开发中获得的知识。