# Effect of a Localized Oxygen-Releasing Hydrogel Sheet on Early-Stage Infarct Evolution in a Rat Photothrombotic Stroke Model: A Preliminary Study

**Authors:** Kunhee Han, Hyeong-Joong Yi, Hyoung-Joon Chun, Min Kyun Na, Simon Song, Kyung Min Park, Kyu-Sun Choi

PMC · DOI: 10.3390/gels12020159 · 2026-02-12

## TL;DR

A hydrogel sheet that releases oxygen was tested in rats with stroke, showing early promise in reducing brain damage.

## Contribution

A novel oxygen-releasing hydrogel sheet was tested for early-stage stroke treatment in a rat model.

## Key findings

- The hydrogel sheet reduced infarct burden at 24 hours compared to controls.
- No significant differences were observed at 72 hours or in MRI and gene expression outcomes.
- The treatment was well-tolerated with no adverse effects on body weight or perioperative status.

## Abstract

Ischemic stroke triggers hypoxia, inflammation, and oxidative stress. Local oxygen delivery may prevent secondary injuries. Herein, we implanted a catalase-incorporated thiolated gelatin-based oxygen-releasing hydrogel sheet in a rat model of photothrombosis to evaluate early infarct attenuation and feasibility. Male Sprague–Dawley rats were allocated to four groups (n = 6/group): control at 24 h (G1), with hydrogel sheet at 24 h (G2), control at 72 h (G3), and with hydrogel sheet at 72 h (G4). Focal ischemia was induced with Rose Bengal and targeted illumination through a 6.0-mm cranial defect. A hydrogel sheet was applied to the cortex after surgery. The infarct burden was assessed by 2,3,5-triphenyltetrazolium chloride (TTC) staining and magnetic resonance imaging (MRI), while mRNA expression levels of tumor necrosis factor-α (TNF-α), brain-derived neurotrophic factor (BDNF), and superoxide dismutase (SOD) were measured by quantitative reverse transcription PCR. Body weight was monitored as a safety measure. At 24 h, TTC showed a significant infarct reduction in G2 compared with G1. At 72 h, infarct measures did not differ significantly between G4 and G3. MRI and gene expression analyses did not show statistically significant between-group differences and are presented as exploratory outcomes. Weight and perioperative status were similar across groups, indicating short-term tolerability. The hydrogel sheet was associated with reduced TTC-defined infarct burden at 24 h in this model; confirmatory studies will require larger, powered cohorts, longer follow-up with functional testing, and in vivo oxygen release profiling to optimize dose, placement, and exposure time.

## Linked entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 7124], BDNF (brain derived neurotrophic factor) [NCBI Gene 627], SOD1 (superoxide dismutase 1) [NCBI Gene 6647]
- **Chemicals:** Rose Bengal (PubChem CID 25473), 2,3,5-triphenyltetrazolium chloride (PubChem CID 9283)
- **Diseases:** ischemic stroke (MONDO:1060198)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** TNF (tumor necrosis factor) [NCBI Gene 280943] {aka TNF-a, TNF-alpha, TNFa}, glyceraldehyde-3-phosphate dehydrogenase [NCBI Gene 108351137], Sod2 [NCBI Gene 104973000], Bdnf (brain-derived neurotrophic factor) [NCBI Gene 24225], CAT (catalase) [NCBI Gene 531682], BDNF (brain derived neurotrophic factor) [NCBI Gene 617701], Sod2 (superoxide dismutase 2) [NCBI Gene 24787] {aka MnSOD}, Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}, Cat (catalase) [NCBI Gene 24248] {aka CS1, Cas1, Cat01, Catl, Cs-1}, Gapdh (glyceraldehyde-3-phosphate dehydrogenase) [NCBI Gene 24383] {aka BARS-38, Gapd}
- **Diseases:** photothrombotic lesion (MESH:D009059), Infarct (MESH:D007238), Photothrombotic Stroke (MESH:D020521), ischemia (MESH:D007511), Neurological deficits (MESH:D009461), tissue injury (MESH:D017695), hypoxia (MESH:D000860), analgesia (MESH:D000699), cranial defect (MESH:D003389), inflammation (MESH:D007249), injury to (MESH:D014947), death (MESH:D003643), brain herniation (MESH:D001927), hyperoxia (MESH:D018496), behavioral abnormalities (MESH:D001523), ischemic brain (MESH:D020520), Ischemic stroke (MESH:D002544), ischemic (MESH:D002545), ischemic injury (MESH:D017202), cytotoxicity (MESH:D064420), bone defect (MESH:D001847), neuroinflammation (MESH:D000090862), edema (MESH:D004487)
- **Chemicals:** water (MESH:D014867), isoflurane (MESH:D007530), Rose Bengal (MESH:D012395), alcohol (MESH:D000438), tramadol (MESH:D014147), povidone-iodine (MESH:D011206), formalin (MESH:D005557), ROS (MESH:D017382), pO2 (MESH:C093415), DuraGen (-), hydrogen peroxide (MESH:D006861), 2,3,5-triphenyltetrazolium chloride (MESH:C009591), Oxygen (MESH:D010100), thiol (MESH:D013438), peroxide (MESH:D010545), nitrogen (MESH:D009584)
- **Species:** Bos taurus (bovine, species) [taxon 9913], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** TTC at 72, S305C

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940068/full.md

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Source: https://tomesphere.com/paper/PMC12940068