Predicting liposome formulations by the integrated machine learning and molecular modeling approaches

IF 10.7 1区 医学 Q1 PHARMACOLOGY & PHARMACY Asian Journal of Pharmaceutical Sciences Pub Date : 2023-05-01 DOI:10.1016/j.ajps.2023.100811
Run Han , Zhuyifan Ye , Yunsen Zhang , Yaxin Cheng , Ying Zheng , Defang Ouyang
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引用次数: 3

Abstract

Liposome is one of the most widely used carriers for drug delivery because of the great biocompatibility and biodegradability. Due to the complex formulation components and preparation process, formulation screening mostly relies on trial-and-error process with low efficiency. Here liposome formulation prediction models have been built by machine learning (ML) approaches. The important parameters of liposomes, including size, polydispersity index (PDI), zeta potential and encapsulation, are predicted individually by optimal ML algorithm, while the formulation features are also ranked to provide important guidance for formulation design. The analysis of key parameter reveals that drug molecules with logS [-3, -6], molecular complexity [500, 1000] and XLogP3 (≥2) are priority for preparing liposome with higher encapsulation. In addition, naproxen (NAP) and palmatine HCl (PAL) represented the insoluble and water-soluble molecules are prepared as liposome formulations to validate prediction ability. The consistency between predicted and experimental value verifies the satisfied accuracy of ML models. As the drug properties are critical for liposome particles, the molecular interactions and dynamics of NAP and PAL liposome are further investigated by coarse-grained molecular dynamics simulations. The modeling structure reveals that NAP molecules could distribute into lipid layer, while most PAL molecules aggregate in the inner aqueous phase of liposome. The completely different physical state of NAP and PAL confirms the importance of drug properties for liposome formulations. In summary, the general prediction models are built to predict liposome formulations, and the impacts of key factors are analyzed by combing ML with molecular modeling. The availability and rationality of these intelligent prediction systems have been proved in this study, which could be applied for liposome formulation development in the future.

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通过集成机器学习和分子建模方法预测脂质体配方
脂质体具有良好的生物相容性和生物降解性,是应用最广泛的药物载体之一。由于配方成分和制备过程复杂,配方筛选大多依赖于试错过程,效率较低。在这里,脂质体配方预测模型已经通过机器学习(ML)方法建立。通过最优ML算法分别预测脂质体的重要参数,包括大小、多分散指数(PDI)、ζ电位和包封率,同时对配方特征进行排序,为配方设计提供重要指导。关键参数分析表明,logS[-3,-6]、分子复杂度[5001000]和XLogP3(≥2)的药物分子是制备高包封度脂质体的优先选择。此外,以萘普生(NAP)和盐酸巴马汀(PAL)为代表的不溶性和水溶性分子被制备为脂质体制剂,以验证预测能力。预测值与实验值的一致性验证了ML模型令人满意的准确性。由于药物性质对脂质体颗粒至关重要,因此通过粗粒分子动力学模拟进一步研究了NAP和PAL脂质体的分子相互作用和动力学。模拟结构表明,NAP分子可以分布在脂质体的脂质层中,而PAL分子大多聚集在脂质体内部水相中。NAP和PAL完全不同的物理状态证实了药物性质对脂质体制剂的重要性。总之,建立了预测脂质体配方的通用预测模型,并将ML与分子模型相结合,分析了关键因素的影响。本研究证明了这些智能预测系统的有效性和合理性,可用于脂质体制剂的开发。
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来源期刊
Asian Journal of Pharmaceutical Sciences
Asian Journal of Pharmaceutical Sciences Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
18.30
自引率
2.90%
发文量
11
审稿时长
14 days
期刊介绍: The Asian Journal of Pharmaceutical Sciences (AJPS) serves as the official journal of the Asian Federation for Pharmaceutical Sciences (AFPS). Recognized by the Science Citation Index Expanded (SCIE), AJPS offers a platform for the reporting of advancements, production methodologies, technologies, initiatives, and the practical application of scientific knowledge in the field of pharmaceutics. The journal covers a wide range of topics including but not limited to controlled drug release systems, drug targeting, physical pharmacy, pharmacodynamics, pharmacokinetics, pharmacogenomics, biopharmaceutics, drug and prodrug design, pharmaceutical analysis, drug stability, quality control, pharmaceutical engineering, and material sciences.
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