4.7 Article

Hybrid Hydrogel Loaded with Chlorhexidine??-CD-MSN Composites as Wound Dressing

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INTERNATIONAL JOURNAL OF NANOMEDICINE
卷 18, 期 -, 页码 1725-1740

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DOVE MEDICAL PRESS LTD
DOI: 10.2147/IJN.S401705

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mesoporous silica; cyclodextrin; pH -responsive; antibacterial property; wound healing

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In this study, pH-sensitive CHX subset of CD-MSN@HA@GelMA hydrogels were constructed, which enable ultra-long-acting drug release and sustained antibacterial properties. The combination of beta-CD and MSN gradually releases active molecules, making them ideal anti-infection materials for wound dressing.
Background: Much attention has been paid to sustained drug release and anti-infection in wound management. Hydrogels, which are biocompatible materials, are promising tools for controlled drug release and infective protection during wound healing. However, hydrogels also demonstrate limitations in the highly efficient treatment of wounds because of the diffusion rate. In this work, we explored pH-sensitive hydrogels that enable ultra-long-acting drug release and sustained antibacterial properties. Methods: We constructed a hybrid gelatin methacrylate (GelMA) system with sustainable antibacterial properties combining hyaluronic acid (HA)-coated mesoporous silica nanoparticles (MSN), which loaded host-guest complexes of chlorhexidine (CHX) with beta-cyclodextrins (beta-CD) (CHX subset of CD-MSN@HA@GelMA). The release mechanism of CHX was explored using UV-vis spectra after intermittent diffusion of CHX. The hybrid hydrogels were characterized, and the drug content in terms of the release profile, bacterial inhibition, and in vivo experiments were investigated. Results: Except for dual protection from both hydrogels, MSN in the HA improved the drug loading efficiency to promote the local drug concentration. It showed that complicated CHX-loaded MSN releases CHX more gradually and over a longer duration than CHX-loaded MSNs. This demonstrated a 12-day CHX release time and antibacterial activity, primarily attributable to the capacity of beta-CD to form an inclusion complex with CHX. Meanwhile, in vivo experiments revealed that the hydrogels safely promote skin wound healing and enhance therapeutic efficacy.Conclusion: We constructed pH-sensitive CHX subset of CD-MSN@HA@GelMA hydrogels that enable ultra-long-acting drug release and sustained antibacterial properties. The combination of beta-CD and MSN would be better suited to release a reduced rate of active molecules over time (slow delivery), making them great candidates for wound dressing anti-infection materials.

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