# Injectable Thermosensitive Composite Hydrogels for Sustained Nanoparticle Delivery and Enhanced Wound Healing

**Authors:** Yiting Qiu, Zhiyun Cheng, Meiyan Liu, Dagui Zhang, Xia Gao, Longxiang Feng, Xianxiang Xu, Haoyang You, Xunxun Wu, Yong Diao

PMC · DOI: 10.3390/gels12030191 · 2026-02-25

## TL;DR

A new injectable hydrogel was developed to deliver nanoparticles for faster wound healing by reducing oxidative stress and promoting tissue regeneration.

## Contribution

A thermosensitive hydrogel was created for sustained delivery of sinomenine–gallic acid nanoparticles to enhance wound healing.

## Key findings

- The hydrogel enables sustained SGNP release for up to 24 hours and shows good hemocompatibility.
- In vitro tests showed improved keratinocyte migration and proliferation.
- In mice, the hydrogel accelerated wound closure and improved tissue regeneration.

## Abstract

Wound healing is frequently compromised by excessive oxidative stress, prolonged inflammation, and inadequate tissue regenerative capacity. To address these challenges, a thermosensitive and injectable composite hydrogel based on Pluronic F127 (F127), phosphatidylcholine (PC), and L-lysine (Lys) was developed for the sustained delivery of sinomenine–gallic acid nanoparticles (SGNPs) and the acceleration of wound repair. The hydrogel undergoes a rapid sol–gel transition at physiological temperatures through physical interactions, enabling excellent injectability and in situ gelation. The optimized composite hydrogel exhibited improved mechanical properties, enhanced structural stability, and a uniform porous microarchitecture. The F127−Lys−PCF127−Lys−PC@SGNPs hydrogel showed superior overall stability and hemocompatibility while enabling the sustained release of SGNPs for up to 24 h. Benefiting from the incorporation of SGNPs, the composite hydrogel displayed enhanced antioxidant activity, effectively scavenging free radicals and alleviating cellular oxidative stress. In vitro experiments demonstrated that the hydrogel promoted keratinocyte migration and proliferation. Furthermore, in a murine full-thickness skin wound model, treatment with F127−Lys−PCF127−Lys−PC@SGNPs significantly accelerated wound closure and facilitated re-epithelialization, angiogenesis, and collagen deposition. Collectively, this multifunctional thermosensitive hydrogel provides a promising platform for advanced wound dressings that integrate sustained delivery, antioxidant protection, and tissue regeneration.

## Linked entities

- **Chemicals:** Pluronic F127 (PubChem CID 24751), L-lysine (PubChem CID 5962)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** PC (pyruvate carboxylase) [NCBI Gene 5091] {aka PCB}, SPATS2L (spermatogenesis associated serine rich 2 like) [NCBI Gene 26010] {aka DNAPTP6, SGNP}
- **Diseases:** infection (MESH:D007239), injury to (MESH:D014947), cytotoxicity (MESH:D064420), weight (MESH:D015431), hemolysis (MESH:D006461), inflammation (MESH:D007249), skin abrasions (MESH:D012871), Swelling (MESH:D004487)
- **Chemicals:** Pluronic (MESH:D020442), Triton X-100 (MESH:D017830), Sinomenine (MESH:C009271), Gallic acid (MESH:D005707), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (-), streptomycin (MESH:D013307), gold (MESH:D006046), ABTS (MESH:C002502), EDTA (MESH:D004492), kaempferol (MESH:C006552), propidium iodide (MESH:D011419), eosin (MESH:D004801), phospholipid (MESH:D010743), PBS (MESH:D007854), F127 (MESH:C078661), phosphoric acid (MESH:C030242), H&amp;E (MESH:D006371), H2O2 (MESH:D006861), penicillin (MESH:D010406), Calcein-AM (MESH:C085925), PC (MESH:D010713), DCFH-DA (MESH:C029569), L-lysine (MESH:D008239), isoflurane (MESH:D007530), PEO-PPO-PEO (MESH:C116176), ROS (MESH:D017382), acetonitrile (MESH:C032159), DTG (MESH:C562325), saline (MESH:D012965), nitrogen (MESH:D009584), K2S2O8 (MESH:C009007), KBr (MESH:C039004), water (MESH:D014867), hematoxylin (MESH:D006416), CO2 (MESH:D002245), alkaloid (MESH:D000470)
- **Species:** Glycine max (soybean, species) [taxon 3847], Sinomenium acutum (species) [taxon 152363], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** HaCaT — Homo sapiens (Human), Spontaneously immortalized cell line (CVCL_0038), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Figures

12 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13025013/full.md

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Source: https://tomesphere.com/paper/PMC13025013