Rational Design of Lipid Nanoparticles for Enhanced mRNA Vaccine Delivery via Machine Learning

Author:

Bae Seo‐Hyeon12,Choi Hosam23,Lee Jisun1,Kang Min‐Ho24,Ahn Seong‐Ho5,Lee Yu‐Sun1,Choi Huijeong1,Jo Sohee12,Lee Yeeun12,Park Hyo‐Jung12,Lee Seonghyun12,Yoon Subin12,Roh Gahyun12,Cho Seongje12,Cho Youngran12,Ha Dahyeon12,Lee Soo‐Yeon12,Choi Eun‐Jin12,Oh Ayoung12,Kim Jungmin12,Lee Sowon12,Hong Jungmin3,Lee Nakyung3,Lee Minyoung67,Park Jungwon6789,Jeong Dong‐Hwa5,Lee Kiyoun3,Nam Jae‐Hwan1210ORCID

Affiliation:

1. Department of Medical and Biological Sciences The Catholic University of Korea Bucheon 14662 Republic of Korea

2. Department of Biotechnology The Catholic University of Korea Bucheon 14662 Republic of Korea

3. Department of Chemistry The Catholic University of Korea Bucheon 14662 Republic of Korea

4. Department of Biomedical‐Chemical Engineering The Catholic University of Korea Bucheon 14662 Republic of Korea

5. Department of Artificial Intelligence The Catholic University of Korea Bucheon 14662 Republic of Korea

6. School of Chemical and Biological Engineering Institute of Chemical Processes Seoul National University Seoul 08826 Republic of Korea

7. Center for Nanoparticle Research Institute of Basic Science (IBS) Seoul 08826 Republic of Korea

8. Institute of Engineering Research College of Engineering Seoul National University Seoul 08826 Republic of Korea

9. Advanced Institutes of Convergence Technology Seoul National University Suwon‐si 16229 Republic of Korea

10. SML Biopharm Gwangmyeong 14353 Republic of Korea

Abstract

AbstractSince the coronavirus pandemic, mRNA vaccines have revolutionized the field of vaccinology. Lipid nanoparticles (LNPs) are proposed to enhance mRNA delivery efficiency; however, their design is suboptimal. Here, a rational method for designing LNPs is explored, focusing on the ionizable lipid composition and structural optimization using machine learning (ML) techniques. A total of 213 LNPs are analyzed using random forest regression models trained with 314 features to predict the mRNA expression efficiency. The models, which predict mRNA expression levels post‐administration of intradermal injection in mice, identify phenol as the dominant substructure affecting mRNA encapsulation and expression. The specific phospholipids used as components of the LNPs, as well as the N/P ratio and mass ratio, are found to affect the efficacy of mRNA delivery. Structural analysis highlights the impact of the carbon chain length on the encapsulation efficiency and LNP stability. This integrated approach offers a framework for designing advanced LNPs and has the potential to unlock the full potential of mRNA therapeutics.

Funder

Ministry of Food and Drug Safety

National Research Foundation of Korea

Ministry of Science and ICT, South Korea

Publisher

Wiley

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