In vitro and in vivo correlation of injectable lipid-based nanomedicines: From dissolution to protein coronas

Lipid-based nanomedicines (LBNMs) represent a transformative frontier in improving drug bioavailability and achieving spatiotemporally precise delivery of therapeutic agents. However, establishing robust <i>in vitro-in vivo</i> correlation (IVIVC) for LBNMs remains a significant challenge due to the complexity of their interactions with biological systems after administration. Conventional IVIVC approaches, often relying on simplistic <i>in vitro</i> dissolution models, frequently fail to recapitulate dynamic physiological processes, leading to discrepancies between predicted and actual <i>in vivo</i> performance. Recent advancements in understanding protein coronas-mediated phenomena have revolutionized nanomedicines research by unraveling how adsorbed biomolecules at the nanoparticle interface dictate physiological processes such as immune system interplay and biodistribution. This review systematically evaluates the state-of-the-art models for IVIVC of LBNMs and the emerging roles of protein coronas in bridging the gap between <i>in vitro</i> characterization and <i>in vivo</i> behavior, emphasizing the necessity of integrating protein coronas analysis into IVIVC frameworks.

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Publication Details

Journal
Materials Today Bio
Published
2025-10-09
DOI
https://doi.org/10.1016/j.mtbio.2025.102393
Citations
2
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
1.19
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article

In vitro and in vivo correlation of injectable lipid-based nanomedicines: From dissolution to protein coronas

Xiying Wu, Junji Wang, Xiaoyi Wang, Huan Wang et al.
2 citations
Materials Today Bio
Nanoparticle-Based Drug Delivery
1.19
article

In vitro and in vivo correlation of injectable lipid-based nanomedicines: From dissolution to protein coronas

Xiying Wu, Junji Wang, Xiaoyi Wang, Huan Wang, Ying Lü
article en
2 citations

Abstract

Lipid-based nanomedicines (LBNMs) represent a transformative frontier in improving drug bioavailability and achieving spatiotemporally precise delivery of therapeutic agents. However, establishing robust <i>in vitro-in vivo</i> correlation (IVIVC) for LBNMs remains a significant challenge due to the complexity of their interactions with biological systems after administration. Conventional IVIVC approaches, often relying on simplistic <i>in vitro</i> dissolution models, frequently fail to recapitulate dynamic physiological processes, leading to discrepancies between predicted and actual <i>in vivo</i> performance. Recent advancements in understanding protein coronas-mediated phenomena have revolutionized nanomedicines research by unraveling how adsorbed biomolecules at the nanoparticle interface dictate physiological processes such as immune system interplay and biodistribution. This review systematically evaluates the state-of-the-art models for IVIVC of LBNMs and the emerging roles of protein coronas in bridging the gap between <i>in vitro</i> characterization and <i>in vivo</i> behavior, emphasizing the necessity of integrating protein coronas analysis into IVIVC frameworks.

Materials Today BioVol. 35
Institute of Process Engineering (CN), Shanghai Skin Disease Hospital (CN)
Openalex Percentile: Top 19%
Nanoparticle-Based Drug Delivery
1.19
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In vitro and in vivo correlation of injectable lipid-based nanomedicines: From dissolution to protein coronas — Xiying Wu, Junji Wang, et al. · Materials Today Bio (2025) | TGRS Research Map | TGRS