Thermogelation of polymer nanoassemblies: promising platforms for injectable biomaterials in medical applications
Han B., van der Vlies AJ., Hasegawa U.
Narrative Review on Hip, published in Nanomedicine (Lond) (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
- Nanomedicine (Lond) (2026)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 41696938
- PMCID
- PMC12962701
- DOI
- 10.1080/17435889.2026.2627319
Abstract (original English)
Thermally induced gelling systems, or thermogels, represent an important class of injectable biomaterials that remain liquid prior to administration but undergo a sol - gel transition upon heating to body temperature, thereby providing a minimally invasive alternative to conventional hydrogels. These materials are typically composed of amphiphilic block copolymer micelles that assemble into macroscopic hydrogel networks. This review highlights the design principles and gelation mechanisms of micelle‑derived thermogels, including mesophase transitions, aggregation mediated by thermosensitive outer shells, and percolated network formation through controlled assembly of patchy micelles with multiple thermosensitive-binding domains. We discuss how polymer composition, block length, and end‑group chemistry dictate critical gelation temperature and concentration, mechanical properties, and long‑term stability. Recent advances in biomedical applications are then introduced, spanning localized drug delivery, vascular embolization, tissue engineering, and cell transplantation. Finally, we outline key challenges for clinical translation, emphasizing the needs for rational design strategies and predictive modeling to accelerate the development of next‑generation thermogels. Literature search: PubMed, SciFinder, and Google Scholar, up to November 2025.
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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