Cargo-driven extracellular vesicles as pharmaceutical nanocarriers: A pharmaceutics-oriented comparison of animal exosomes and plant-derived exosome-like nanoparticles
Xu H., Zhang J., Li M.
Narrative Review on Face & Skin, Hip, Systemic / IV, published in Int J Pharm X (2026) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.
- Study type
- Narrative Review
- Journal
- Int J Pharm X (2026)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 42005347
- PMCID
- PMC13087583
- DOI
- 10.1016/j.ijpx.2026.100530
- Citations
- 3
Abstract (original English)
Exosomes and plant-derived exosome-like nanoparticles (PELNs) are increasingly investigated as biologically derived nanocarriers that can couple cargo protection with biointerface-enabled transport. From a pharmaceutics standpoint, their therapeutic performance is often cargo-governed (e.g., microRNAs and proteins) and is ultimately constrained by delivery determinants such as stability, biodistribution, cellular uptake, and intracellular trafficking. In this review, we compare animal-derived exosomes (ADEs) and PELNs through a formulation-centric lens, emphasizing how source-dependent molecular composition shapes critical delivery behaviors and translational feasibility. We reorganize representative preclinical evidence into pharmaceutics-relevant delivery scenarios-including systemic/vascular targeting, blood-brain barrier transport, oral gastrointestinal delivery, and tumor microenvironment modulation-to connect cargo identity with exposure-site interactions and pharmacodynamic outcomes. We further discuss engineering strategies for improving payload control, targeting precision, and dosing accuracy, including endogenous enrichment, exogenous loading, and surface functionalization, while highlighting scale-up and safety considerations introduced by modification. Finally, we delineate translational priorities required to advance exosome-based products toward clinical developm
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is a narrative review: it collects no new patient data and does not systematically appraise evidence quality.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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