Evidence map›Paper›PMID 39264000›Full record

ArticleSmall (Weinheim an der Bergstrasse, Germany)2025

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

Seo-Hyeon Bae, Hosam Choi, Jisun Lee, Min-Ho Kang, Seong-Ho Ahn, Yu-Sun Lee, Huijeong Choi, Sohee Jo, Yeeun Lee, Hyo-Jung Park and 18 more

Abstract read
In one paragraph

Article in Small (Weinheim an der Bergstrasse, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed.

  1. Dual pKa Lipid Nanoparticles for Lung-tropic mRNA Delivery and pH-Programmed Endosomal Escape.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

Seo-Hyeon BaeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Hosam ChoiDepartment of Biotechnology, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Jisun LeeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Min-Ho KangDepartment of Biotechnology, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Seong-Ho AhnDepartment of Artificial Intelligence, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Yu-Sun LeeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Huijeong ChoiDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Sohee JoDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Yeeun LeeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Hyo-Jung ParkDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Seonghyun LeeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Subin YoonDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Gahyun RohDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Seongje ChoDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Youngran ChoDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Dahyeon HaDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Soo-Yeon LeeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Eun-Jin ChoiDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Ayoung OhDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Jungmin KimDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Sowon LeeDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Jungmin HongDepartment of Chemistry, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Nakyung LeeDepartment of Chemistry, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Minyoung LeeSchool of Chemical and Biological Engineering, Institute of Chemical Processes, Seoul National University, Seoul, 08826, Republic of Korea.
Jungwon ParkSchool of Chemical and Biological Engineering, Institute of Chemical Processes, Seoul National University, Seoul, 08826, Republic of Korea.
Dong-Hwa JeongDepartment of Artificial Intelligence, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Kiyoun LeeDepartment of Chemistry, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.
Jae-Hwan NamDepartment of Medical and Biological Sciences, The Catholic University of Korea, Bucheon, 14662, Republic of Korea.ORCID 0000-0002-0974-4343

Funding

Ministry of Food and Drug Safety 22213MFDS421Ministry of Food and Drug Safety RS-2023-00217074Ministry of Science and ICT, South Korea 2023R1A2C1004182National Research Foundation of Korea
6 · The paper itself

Abstract

Since 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.

Indexed as

LipidsMachine LearningmRNA VaccinesNanoparticlesRNA, MessengerAnimalsLiposomesMiceLipid NanoparticlesLipidsLiposomesmRNA VaccinesRNA, Messengerlipid nanoparticles (LNPs)machine learning (ML) techniquesmRNA expression efficiencymRNA vaccinesstructural optimization

Identifiers

PMID39264000
PMCPMC11855220

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.