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Development of a keratinocyte-specific microgel-based wound dressing with the ability of wound exudate retention, thereby enhancing the wound healing process. To this end, a microgel of chitosan, glycerin and heparin was developed. Specifically, 1-ethyl-3-(3-dimethyl-aminopropyl) carbodiimide and N-hydroxysuccinimide were used to conjugate chitosan (CTSC) and heparin (HP) to glycerin (GL), forming polymeric microgel (CTSC-HP-GL) in water. The effect of the microgel on the properties of the dressing was examined by using Fourier-transform infrared spectroscopy, X-ray diffraction, and differential scanning calorimetry. The non-leaching property of the microgel was also analyzed to ensure its safety profile on skin under the in vivo condition. Additionally, the biocompatibility and cell adherence efficiency of CTSC-HP-GL to mouse fibroblast and human keratinocyte cells were examined using colony formation and in vitro wound scratch assays, respectively. The in vivo adherence, acute inflammation, and granulation effects were tested in a mouse wound model. The CTSC-HP-GL microgel showed nanosized crystalline and amorphous structures with significant improvements in their thermal properties compared to the raw GL. Moreover, the glucosamine (-NH2) group in the HP was successfully incorporated into the microgel, and the microgel was non-leaching, with the potential to keep its properties after contacting skin. Furthermore, the microgel was found to be non-cytotoxic and showed improved cell adherence to both mouse fibroblast and human keratinocyte cells as well as wound healing in a mouse model. Consequently, this study presents a novel non-leaching wound microgel that could be an effective regenerative dressing material for improving wound healing.
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