1. Academic Validation
  2. Effects of graphene oxide incorporation via non-covalent interfacial interactions on the properties of small intestinal submucosa

Effects of graphene oxide incorporation via non-covalent interfacial interactions on the properties of small intestinal submucosa

  • RSC Adv. 2026 Jan 19;16(5):4032-4044. doi: 10.1039/d5ra09329e.
Mianshu Hu 1 Xiuyun Chuan 1 Yiting Wang 2 Wenyue Cheng 3 Yun Yan 4 Wenbin Zhang 4 Kun Zhang 2 Jinsong Han 2 Jian Zhang 3
Affiliations

Affiliations

  • 1 Key Laboratory of Orogenic Belts and Crustal Evolution, School of Earth and Space Sceiences, Peking University Beijing 100871 China [email protected] [email protected].
  • 2 Peking University Third Hospital Beijing 100191 China.
  • 3 Naval Medical University, Shanghai Changzheng Hospital Shanghai 200003 China.
  • 4 College of Chemistry and Molecular Engineering, Peking University Beijing 100871 China.
Abstract

To investigate the modifying effect of graphene oxide (GO) on small intestinal submucosa (SIS), GO-SIS biocomposite films were fabricated via a non-covalent coating strategy. Structural analyses confirmed the non-covalent interactions between GO and SIS Collagen fibers and the preservation of SIS's native fibrous structure. The GO-SIS biocomposite film showed significantly improved hydrophilicity (contact angle: 71.3 ± 1.0°, p < 0.001; water absorption: 159.00 ± 5.60%, p < 0.01) compared to the SIS film. It also exhibited superior mechanical properties under both dry and wet conditions, with significantly higher tensile strength (dry: 24.46 ± 0.99 MPa; wet: 10.16 ± 0.37 MPa) and elongation at break (dry: 11.41 ± 0.55%; wet: 21.26 ± 0.65%) than the SIS film (p < 0.001 for all comparisons). After in vitro degradation, the GO-SIS biocomposite film showed better morphological stability compared to the SIS film. At 4, 8, 16, 24, 48, and 72 hours, the in vitro degradation of the GO-SIS biocomposite film was significantly slower than that of the SIS film. Furthermore, at 4, 8, 16, and 24 hours, the tensile strength and elongation at break of the degraded GO-SIS biocomposite film were significantly higher than those of the degraded SIS film. Biocompatibility assessment indicated no impact on L929 fibroblast viability or proliferation, along with favorable hemocompatibility. Collectively, the non-covalent incorporation of GO effectively enhances the hydrophilicity and mechanical performance of the GO-SIS biocomposite film and slows down its in vitro degradation, offering a promising strategy for the design of advanced tissue repair Materials.

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