Abstract

The irregular deep chronic wound is a grand challenge to be healed due to multiple factors including slow angiogenesis that causing regenerated tissue failure. The narrow gap of deep wounds could hinder and slow down normal wound healing. Thus, the current study aimed to develop a polymerised genipin-crosslinked gelatin (gelipin) hydrogel (GNP_GH) as a potential biodegradable filler for the abovementioned limitations. Briefly, GNP_GH bioscaffolds have been developed successfully within three-minute polymerisation at room temperature (22–24 °C). The physicochemical and biocompatibility of GNP_GH bioscaffolds were respectively evaluated. Amongst GNP_GH groups, the 0.1%GNP_GH10% displayed the highest injectability (97.3 ± 0.6%). Meanwhile, the 0.5%GNP_GH15% degraded within more than two weeks with optimum swelling capacity (108.83 ± 15.7%) and higher mechanical strength (22.6 ± 3.9 kPa) than non-crosslinked gelatin hydrogel 15% (NC_GH15%). Furthermore, 0.1%GNP_GH15% offered higher porosity (>80%) and lower wettability (48.7 ± 0.3) than NC_GH15%. Surface and cross-section SEM photographs displayed an interconnected porous structure for all GNP_GH groups. The EDX spectra and maps represented no major changes after GNP modification. Moreover, no toxicity effect of GNP_GH against dermal fibroblasts was shown during the biocompatibility test. In conclusion, the abovementioned findings indicated that gelipin has excellent physicochemical properties and acceptable biocompatibility as an acellular rapid treatment for future use in irregular deep cutaneous wounds.

Highlights

  • Skin is the most extensive protective layer in the human body that natively hinders the penetration of external pathogens

  • Three different ratios of GNP-crosslinked gelatin hydrogel (GNP_GH) (0.1%GNP_GH10%; 0.1%GNP_GH15% and 0.5%GNP_GH15%), which were polymerised within three minutes at room temperature (22–24 ◦C), were successfully fabricated

  • The three-minute selection for the polymerisation time was selected in the current study to ensure the clinician/surgeon has enough time to apply them on skin wounds before polymerisation

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Summary

Introduction

Skin is the most extensive protective layer in the human body that natively hinders the penetration of external pathogens. Any deterioration of anatomical skin structure due to traumatic injuries, burns and abrasion, causes the loss of its integrity and stability. A tissue-engineered skin substitute (TESS) is a gold standard tissue engineering product. It presents less painful procedures and reduces post-operative interventions. The currently available TESS can not fully resemble native skin due to inadequate angiogenesis and low mechanical integrity. There is a high potential to develop a smart three-dimensional (3D) bioscaffold as an acellular skin substitute to expedite wound closure and tissue regeneration

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