The applications of machine learning to predict the forming of chemically stable amorphous solid dispersions prepared by hot-melt extrusion

IF 5.2 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Junhuang Jiang , Anqi Lu , Xiangyu Ma , Defang Ouyang , Robert O. Williams III
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引用次数: 4

Abstract

Amorphous solid dispersion (ASD) is one of the most important strategies to improve the solubility and dissolution rate of poorly water-soluble drugs. As a widely used technique to prepare ASDs, hot-melt extrusion (HME) provides various benefits, including a solvent-free process, continuous manufacturing, and efficient mixing compared to solvent-based methods, such as spray drying. Energy input, consisting of thermal and specific mechanical energy, should be carefully controlled during the HME process to prevent chemical degradation and residual crystallinity. However, a conventional ASD development process uses a trial-and-error approach, which is laborious and time-consuming. In this study, we have successfully built multiple machine learning (ML) models to predict the amorphization of crystalline drug formulations and the chemical stability of subsequent ASDs prepared by the HME process. We utilized 760 formulations containing 49 active pharmaceutical ingredients (APIs) and multiple types of excipients. By evaluating the built ML models, we found that ECFP-LightGBM was the best model to predict amorphization with an accuracy of 92.8%. Furthermore, ECFP-XGBoost was the best in estimating chemical stability with an accuracy of 96.0%. In addition, the feature importance analyses based on SHapley Additive exPlanations (SHAP) and information gain (IG) revealed that several processing parameters and material attributes (i.e., drug loading, polymer ratio, drug's Extended-connectivity fingerprints (ECFP) fingerprints, and polymer's properties) are critical for achieving accurate predictions for the selected models. Moreover, important API's substructures related to amorphization and chemical stability were determined, and the results are largely consistent with the literature. In conclusion, we established the ML models to predict formation of chemically stable ASDs and identify the critical attributes during HME processing. Importantly, the developed ML methodology has the potential to facilitate the product development of ASDs manufactured by HME with a much reduced human workload.

Abstract Image

机器学习在预测热熔挤压制备的化学稳定的非晶固体分散体形成中的应用
非晶态固体分散体(ASD)是提高难溶性药物溶解度和溶出率的最重要策略之一。作为一种广泛使用的制备ASD的技术,热熔挤出(HME)提供了各种好处,包括无溶剂工艺、连续制造以及与基于溶剂的方法(如喷雾干燥)相比的有效混合。在HME过程中,应仔细控制由热能和特定机械能组成的能量输入,以防止化学降解和残留结晶度。然而,传统的ASD开发过程使用试错方法,这既费力又耗时。在这项研究中,我们成功地建立了多个机器学习(ML)模型,以预测结晶药物制剂的非晶化以及通过HME工艺制备的后续ASD的化学稳定性。我们使用了760种配方,其中含有49种活性药物成分(API)和多种赋形剂。通过评估所建立的ML模型,我们发现ECFP LightGBM是预测非晶化的最佳模型,准确率为92.8%。此外,ECFP XGBoost在估计化学稳定性方面最好,准确率达96.0%。此外,基于SHapley加法运算(SHAP)和信息增益(IG)的特征重要性分析表明,几个加工参数和材料属性(即药物负载量、聚合物比例、药物的扩展连接性指纹(ECFP)指纹和聚合物性质)对于实现对所选模型的准确预测至关重要。此外,还确定了与非晶化和化学稳定性相关的重要API亚结构,其结果与文献基本一致。总之,我们建立了ML模型来预测化学稳定ASD的形成,并确定HME加工过程中的关键属性。重要的是,所开发的ML方法有可能促进HME制造的ASD的产品开发,大大减少人力工作量。
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来源期刊
International Journal of Pharmaceutics: X
International Journal of Pharmaceutics: X Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.60
自引率
0.00%
发文量
32
审稿时长
24 days
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