A multiscale modeling framework for transport of PEGylated lipid nanoparticle through the extracellular matrix
- 1Purdue University
Abstract
Lipid nanoparticles (LNPs) are one of the leading platforms for delivering nucleic acid therapeutics, yet their efficacy is limited by physicochemical interactions with the extracellular matrix (ECM) that trap the particles before they reach target cells. PEGylated nanoparticles mitigate these interactions by forming a protective steric layer on their surfaces. However, there is a lack of a predictive tool that gives mechanistic insights about how PEG surface density governs the underlying interaction and results in enhanced diffusive transport of LNPs through the ECM. Here, we present a multiscale hierarchical computational framework that couples all-atom constant pH molecular dynamics (CpHMD) with a highly coarse-grained model of the complete LNP within a crosslinked hyaluronic acid (HA) network. These atomistic simulations resolve the free energy of interaction between the LNP surface and HA chains across varying PEG lipid compositions, and integrate these free energy profiles to inform the coarse-grained simulations of LNP transport through the matrix. This work highlights that even a slightly PEGylated surface depletes the near-contact shell between the LNP and HA chains, which disrupts their adhesive interactions. These protective PEG layers produce a sharp, non-linear enhancement in LNP diffusivities, with just 1% PEG increasing the diffusivity nearly eight-fold relative to bare LNPs, which remain trapped in the matrix structures. This work provides a quantitative estimate of how PEG surface density governs LNP transport through the ECM, which offers predictive guidance for engineering LNP surface properties in target-specific drug delivery.
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BibTeX
@misc{nakate2026multiscale,
title = {{A multiscale modeling framework for transport of PEGylated lipid nanoparticle through the extracellular matrix}},
author = {P. Nakate and K. J. Colston and S. T. Schneebeli and A. M. Ardekani},
howpublished = {bioRxiv},
year = {2026},
month = sep,
doi = {10.64898/2026.09.09.750406},
url = {https://www.biorxiv.org/content/10.64898/2026.09.09.750406v1},
note = {CC BY-NC-ND},
}
RIS
TY - UNPB
TI - A multiscale modeling framework for transport of PEGylated lipid nanoparticle through the extracellular matrix
AU - P. Nakate
AU - K. J. Colston
AU - S. T. Schneebeli
AU - A. M. Ardekani
PY - 2026
DA - 2026/09/09
PB - bioRxiv
DO - 10.64898/2026.09.09.750406
UR - https://www.biorxiv.org/content/10.64898/2026.09.09.750406v1
AB - Lipid nanoparticles (LNPs) are one of the leading platforms for delivering nucleic acid therapeutics, yet their efficacy is limited by physicochemical interactions with the extracellular matrix (ECM) that trap the particles before they reach target cells. PEGylated nanoparticles mitigate these interactions by forming a protective steric layer on their surfaces. However, there is a lack of a predictive tool that gives mechanistic insights about how PEG surface density governs the underlying interaction and results in enhanced diffusive transport of LNPs through the ECM. Here, we present a multiscale hierarchical computational framework that couples all-atom constant pH molecular dynamics (CpHMD) with a highly coarse-grained model of the complete LNP within a crosslinked hyaluronic acid (HA) network. These atomistic simulations resolve the free energy of interaction between the LNP surface and HA chains across varying PEG lipid compositions, and integrate these free energy profiles to inform the coarse-grained simulations of LNP transport through the matrix. This work highlights that even a slightly PEGylated surface depletes the near-contact shell between the LNP and HA chains, which disrupts their adhesive interactions. These protective PEG layers produce a sharp, non-linear enhancement in LNP diffusivities, with just 1% PEG increasing the diffusivity nearly eight-fold relative to bare LNPs, which remain trapped in the matrix structures. This work provides a quantitative estimate of how PEG surface density governs LNP transport through the ECM, which offers predictive guidance for engineering LNP surface properties in target-specific drug delivery.
ER -