Evidence map›Paper›PMID 42146191›Full record

ArticleACS omega2026

Understanding Size Distributions during Lipid Nanoparticle Manufacturing through Mechanistic Modeling.

Saikat Mukherjee, Sunkyu Shin, Cedric Devos, Aniket Udepurkar, Peter Sagmeister, Bernhardt L Trout, Allan S Myerson, Richard D Braatz

Abstract read
In one paragraph

Article in ACS omega, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Saikat MukherjeeDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Sunkyu ShinDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.
Cedric DevosDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.ORCID https://orcid.org/0000-0002-8154-4872
Aniket UdepurkarDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.ORCID https://orcid.org/0000-0001-9958-412X
Peter SagmeisterDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.ORCID https://orcid.org/0000-0002-4326-1775
Bernhardt L TroutDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.ORCID https://orcid.org/0000-0003-1417-9470
Allan S MyersonDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.ORCID https://orcid.org/0000-0002-7468-8093
Richard D BraatzDepartment of Chemical Engineering, Massachusetts Institute of Technology, 77 Massachusetts Avenue, Cambridge, Massachusetts 02139, United States.ORCID https://orcid.org/0000-0003-4304-3484

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent breakthroughs in messenger RNA (mRNA) therapeutics have highlighted the importance of lipid nanoparticles (LNPs) as delivery vehicles that protect fragile mRNA and facilitate cellular uptake. While manufacturing technologies that rely on self-assembly through mixing, including microfluidic systems and turbulent jet mixers, have enabled scalable production, a first-principles model explaining the fundamental mechanisms responsible for LNP size and its distribution has remained elusive. This has limited predictive process control and optimization. To address this gap, we present here a model based on crystallization of a lipid during turbulent mixing of water-ethanol, employing population balance equations to predict particle size distributions. The model successfully predicts the influence of key operating parameters including total flow rate, flow rate ratio, and lipid concentration, demonstrating favorable comparison with experimental results and enabling the development of predictive manufacturing processes for consistent critical quality attributes. The mechanistic understanding provides the foundation necessary to optimize manufacturing of LNPs used as delivery agents of mRNA vaccines, which extends beyond the current application to the broader field of nucleic acid therapeutics.

Identifiers

PMID42146191
PMCPMC13177254

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.