# Irradiation Enhances the Biomedical Functional Characteristics of Collagen Sponges: A Potential Strategy for Medical Collagen Sponge Modification

**Authors:** Junwei Qin, Hancong Wu, Bifeng Lan, Liucui Yao, Zhenqiang Wu

PMC · DOI: 10.3390/jfb17020103 · 2026-02-21

## TL;DR

This study shows that irradiation improves the properties of collagen sponges, making them more effective for controlling bleeding and wound care.

## Contribution

A novel method using low-dose gamma irradiation to enhance collagen sponges' hemostatic and antibacterial properties is introduced.

## Key findings

- Low-dose gamma irradiation (1–3 kGy) improves mechanical strength, elongation, and biostability of collagen sponges.
- Irradiated sponges show better water absorption, blood cell adsorption, and antibacterial properties than commercial alternatives.
- Spectroscopic analysis confirms chemical bond modifications without loss of crystallinity, and in vivo tests show biocompatibility.

## Abstract

Developing safe and effective hemostatic materials is critical for rapid bleeding control and wound management. However, traditional hemostatic materials using chemical crosslinking often fall short in hemostatic efficiency and carry risks of secondary injury from reagent residues. This study introduced an irradiation-fabricated composite collagen sponge based on fish skin collagen, chitosan, and soluble starch. The sponge was prepared via material solution blending, followed by cobalt-60 gamma irradiation at various doses, with casting and freeze-drying. Its functionality and safety were systematically evaluated. The results show that low-dose gamma irradiation (1–3 kGy) applied to a precursor solution prior to freeze-drying promoted intermolecular crosslinking, improving mechanical strength, elongation, and biostability, while higher doses (6 kGy) slightly reduced crosslinking due to the partial degradation of collagen, chitosan, and starch. With low-dose irradiation, the proposed hemostatic sponges show enhanced water absorption, blood cell adsorption, swelling, and antibacterial properties, indicating effective hemostatic performance. Spectroscopic characterization confirmed chemical bond modifications with no loss of crystallinity. Cytotoxicity and in vivo tests demonstrated biocompatibility and effective hemostatic performance. Compared with the commercial HSD sponge, the irradiated sponges exhibited superior hemostatic efficacy. This study presents that a collagen-based synergistic matrix prepared by gamma-ray irradiation can produce a hemostatic sponge with enhanced absorbency, bioactivity, and antibacterial properties, highlighting its great potential in rapid hemostasis and wound care applications.

## Linked entities

- **Chemicals:** chitosan (PubChem CID 129662530)

## Full-text entities

- **Genes:** Ccs (copper chaperone for superoxide dismutase) [NCBI Gene 84485], Ccs (copper chaperone for superoxide dismutase) [NCBI Gene 12460] {aka Ccsd}, Ccs1 (colon cancer susceptibility 1) [NCBI Gene 110138]
- **Diseases:** HSD (OMIM:143095), thrombosis (MESH:D013927), Cytotoxicity (MESH:D064420), weight loss (MESH:D015431), infection (MESH:D007239), blood coagulation (MESH:D001778), overdose (MESH:D062787), femoral artery injury (MESH:D005264), necrosis (MESH:D009336), inflammation (MESH:D007249), injury to (MESH:D014947), blood loss (MESH:D016063), swelling (MESH:D004487), bleeding (MESH:D006470), Hemolysis (MESH:D006461)
- **Chemicals:** TG (MESH:D013866), sodium citrate (MESH:D000077559), butyl alcohol (MESH:D020001), glycerin (MESH:D005990), penicillin (MESH:D010406), 2,4,6-trinitro-benzene-sulfonic acid (-), NaHCO3 (MESH:D017693), hydrogen peroxide (MESH:D006861), Starch (MESH:D013213), amine (MESH:D000588), hydroxyapatite (MESH:D017886), MTT (MESH:C070243), heme (MESH:D006418), pyrophosphate (MESH:C107241), Dialdehyde starch (MESH:C012880), CO2 (MESH:D002245), acid citrate dextrose (MESH:C002113), DMSO (MESH:D004121), EDC (MESH:C024565), reactive oxygen species (MESH:D017382), PBS (MESH:D007854), Tween 80 (MESH:D011136), hydrogen (MESH:D006859), cobalt-60 (MESH:C000615395), Chitosan (MESH:D048271), NaCl (MESH:D012965), amylose (MESH:D000688), agar (MESH:D000362), chitin (MESH:D002686), polymers (MESH:D011108), streptomycin (MESH:D013307), DPBS (MESH:C012939), pectin (MESH:D010368), polysaccharide (MESH:D011134), nitrogen (MESH:D009584), Al2O3 (MESH:D000537), Water (MESH:D014867), amide (MESH:D000577), NaOH (MESH:D012972), CaCl2 (MESH:D002122), glycolipids (MESH:D006017), HCl (MESH:D006851), acetic acid (MESH:D019342)
- **Species:** Tilapia (genus) [taxon 8126], Oreochromis niloticus (Nile tilapia, species) [taxon 8128], Homo sapiens (human, species) [taxon 9606], Staphylococcus aureus (species) [taxon 1280], Rattus norvegicus (brown rat, species) [taxon 10116], Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Bos taurus (bovine, species) [taxon 9913], Actinopterygii (fishes, superclass) [taxon 7898], Escherichia coli (E. coli, species) [taxon 562], Mus musculus (house mouse, species) [taxon 10090], Ovis aries (domestic sheep, species) [taxon 9940], Sus scrofa (pig, species) [taxon 9823]
- **Cell lines:** CCS-1 — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_B1NU), CCS-6 — Homo sapiens (Human), Human papillomavirus-related endocervical adenocarcinoma, Cancer cell line (CVCL_B1NZ), Tilapia — Oreochromis mossambicus x Oreochromis niloticus (Hybrid tilapia), Spontaneously immortalized cell line (CVCL_R879), L929 — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_AR58)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12941453/full.md

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Source: https://tomesphere.com/paper/PMC12941453