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基于生成式人工智能结构合成方法的药物产品虚拟制剂优化和颗粒工程。

In silico formulation optimization and particle engineering of pharmaceutical products using a generative artificial intelligence structure synthesis method.

机构信息

DigiM Solution LLC, Woburn, MA, USA.

Genentech, Inc., Synthetic Molecule Pharmaceutical Sciences, South San Francisco, CA, USA.

出版信息

Nat Commun. 2024 Nov 7;15(1):9622. doi: 10.1038/s41467-024-54011-9.

Abstract

Pharmaceutical drug dosage forms are critical for ensuring the effective and safe delivery of active pharmaceutical ingredients to patients. However, traditional formulation development often relies on extensive lab and animal experimentation, which can be time-consuming and costly. This manuscript presents a generative artificial intelligence method that creates digital versions of drug products from images of exemplar products. This approach employs an image generator guided by critical quality attributes, such as particle size and drug loading, to create realistic digital product variations that can be analyzed and optimized digitally. This paper shows how this method was validated through two case studies: one for the determination of the amount of material that will create a percolating network in an oral tablet product and another for the optimization of drug distribution in a long-acting HIV inhibitor implant. The results demonstrate that the generative AI method accurately predicts a percolation threshold of 4.2% weight of microcrystalline cellulose and generates implant formulations with controlled drug loading and particle size distributions. Comparisons with real samples reveal that the synthesized structures exhibit comparable particle size distributions and transport properties in release media.

摘要

药物剂型对于确保活性药物成分有效且安全地递送给患者至关重要。然而,传统的制剂开发通常依赖于广泛的实验室和动物实验,这既耗时又昂贵。本文提出了一种生成式人工智能方法,可从示例产品的图像中创建药物产品的数字版本。该方法采用受关键质量属性(如粒径和药物负载)指导的图像生成器来创建可进行数字分析和优化的逼真数字产品变化。本文展示了如何通过两个案例研究验证该方法:一个用于确定在口服片剂产品中形成渗透网络所需的材料量,另一个用于优化长效 HIV 抑制剂植入物中的药物分布。结果表明,生成式 AI 方法可准确预测 4.2%重量的微晶纤维素的渗透阈值,并生成具有控制药物负载和粒径分布的植入物配方。与真实样品的比较表明,合成结构在释放介质中表现出可比的粒径分布和传输特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8344/11544110/15bc9f130908/41467_2024_54011_Fig1_HTML.jpg

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