Understanding the Manufacturing Process of Lipid Nanoparticles for mRNA Delivery Using Machine Learning

IF 1.5 4区 医学 Q4 CHEMISTRY, MEDICINAL Chemical & pharmaceutical bulletin Pub Date : 2024-06-05 DOI:10.1248/cpb.c24-00089
Shinya Sato, Syusuke Sano, Hiroki Muto, Kenji Kubara, Keita Kondo, Takayuki Miyazaki, Yuta Suzuki, Yoshifumi Uemoto, Koji Ukai
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Abstract

Lipid nanoparticles (LNPs), used for mRNA vaccines against severe acute respiratory syndrome coronavirus 2, protect mRNA and deliver it into cells, making them an essential delivery technology for RNA medicine. The LNPs manufacturing process consists of two steps, the upstream process of preparing LNPs and the downstream process of removing ethyl alcohol (EtOH) and exchanging buffers. Generally, a microfluidic device is used in the upstream process, and a dialysis membrane is used in the downstream process. However, there are many parameters in the upstream and downstream processes, and it is difficult to determine the effects of variations in the manufacturing parameters on the quality of the LNPs and establish a manufacturing process to obtain high-quality LNPs. This study focused on manufacturing mRNA-LNPs using a microfluidic device. Extreme gradient boosting (XGBoost), which is a machine learning technique, identified EtOH concentration (flow rate ratio), buffer pH, and total flow rate as the process parameters that significantly affected the particle size and encapsulation efficiency. Based on these results, we derived the manufacturing conditions for different particle sizes (approximately 80 and 200 nm) of LNPs using Bayesian optimization. In addition, the particle size of the LNPs significantly affected the protein expression level of mRNA in cells. The findings of this study are expected to provide useful information that will enable the rapid and efficient development of mRNA-LNPs manufacturing processes using microfluidic devices.

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利用机器学习了解用于 mRNA 运送的脂质纳米粒子的制造过程
脂质纳米颗粒(LNPs)用于抗严重急性呼吸系统综合征冠状病毒 2 的 mRNA 疫苗,可保护 mRNA 并将其输送到细胞中,因此成为 RNA 药物的重要输送技术。LNPs 的生产过程包括两个步骤:上游制备 LNPs,下游去除乙醇(EtOH)和交换缓冲液。一般来说,上游过程使用微流控装置,下游过程使用透析膜。然而,上游和下游工艺的参数很多,很难确定生产参数的变化对 LNPs 质量的影响,也很难建立获得高质量 LNPs 的生产工艺。本研究的重点是使用微流控装置制造 mRNA-LNPs。通过机器学习技术极端梯度提升法(XGBoost),我们发现 EtOH 浓度(流速比)、缓冲液 pH 值和总流速是对粒径和封装效率有显著影响的工艺参数。根据这些结果,我们利用贝叶斯优化法得出了不同粒径(约 80 纳米和 200 纳米)LNPs 的生产条件。此外,LNPs 的粒度对细胞中 mRNA 的蛋白表达水平有显著影响。这项研究的结果有望为利用微流体设备快速高效地开发 mRNA-LNPs 制造工艺提供有用的信息。
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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
132
审稿时长
1.7 months
期刊介绍: The CPB covers various chemical topics in the pharmaceutical and health sciences fields dealing with biologically active compounds, natural products, and medicines, while BPB deals with a wide range of biological topics in the pharmaceutical and health sciences fields including scientific research from basic to clinical studies. For details of their respective scopes, please refer to the submission topic categories below. Topics: Organic chemistry In silico science Inorganic chemistry Pharmacognosy Health statistics Forensic science Biochemistry Pharmacology Pharmaceutical care and science Medicinal chemistry Analytical chemistry Physical pharmacy Natural product chemistry Toxicology Environmental science Molecular and cellular biology Biopharmacy and pharmacokinetics Pharmaceutical education Chemical biology Physical chemistry Pharmaceutical engineering Epidemiology Hygiene Regulatory science Immunology and microbiology Clinical pharmacy Miscellaneous.
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