4.7 Article

Chitosan/PVA Hetero-Composite Hydrogel Containing Antimicrobials, Perfluorocarbon Nanoemulsions, and Growth Factor-Loaded Nanoparticles as a Multifunctional Dressing for Diabetic Wound Healing: Synthesis, Characterization, and In Vitro/In Vivo Evaluation

Journal

PHARMACEUTICS
Volume 14, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics14030537

Keywords

diabetic wound healing; hydrogel; nanoparticle; perfluorocarbon; oxygen delivery; antibacterial; anti-inflammatory; cell growth

Funding

  1. Ministry of Science and Technology, Taiwan [MOST 110-2221-E-008-015]

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A chitosan-based composite hydrogel called PEENPPCH was developed for diabetic wound healing. This hydrogel sustained release of drugs and antibacterial substances, promoted cell growth and had anti-inflammatory effects. It also provided oxygen delivery to alleviate hypoxia conditions. In animal experiments, PEENPPCH significantly improved wound healing in diabetic rats.
Diabetic foot ulcers remain one of the most difficult-to-treat complications of diabetes and may seriously threaten the life of patients since it frequently results in limb loss due to amputation, suggesting that an effective therapeutic strategy is still urgently needed. In this study, a chitosan-based heterogeneous composite hydrogel encapsulating perfluorocarbon emulsions, epidermal growth factor (EGF)-loaded chitosan nanoparticles, and polyhexamethylene biguanide (PHMB) named PEENPPCH was developed for diabetic wound healing. The PEENPPCH could sustainably release EGF and PHMB in an ion-rich environment to exert antibacterial effects and promote cell growth for wound repair. In addition, the PEENPPCH can provide anti-inflammatory effects functioned by its main constituent of chitosan. Moreover, the PEENPPCH can proactively offer oxygen delivery through the incorporation of perfluorocarbon and, therefore, is able to alleviate hypoxia conditions on diabetic wounds. These functionalities enabled a markedly enhanced wound healing efficacy on diabetic rats treated with the P(E)E(NP)PCHs, including thorough re-epithelization, a reduced inflammatory response, faster collagen deposition, and advanced collagen maturation resulting in a 95% of wound closure degree after 15 days that was 12.6% (p < 0.05) higher than the value of the group treated with the commercial dressing HeraDerm. Given the aforementioned advantages, together with the known merits of hydrogels, the developed PEENPPCH is anticipated to be a feasible tool for clinical diabetic wound treatment.

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