4.8 Article

Ternary Complex Coacervate of PEG/TA/Gelatin as Reinforced Bioadhesive for Skin Wound Repair

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 16, 页码 18097-18109

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c00236

关键词

ternary complex; tannic acid; bioadhesive; wound closure; tissue repair

资金

  1. National Natural Science Foundation of China [31670972]
  2. Qingdao Science and Technology Demonstration and Guidance Project the Taishan Scholar Program, China [20-3-4-50 nsh]

向作者/读者索取更多资源

This study introduces a novel bioadhesive composed of tannic acid, polyethylene glycol, and gelatin, fabricated through a simple physical blending method. By optimizing curing parameters and gelatin content, the adhesive strength and comprehensive performance were enhanced, demonstrating excellent wound closure and tissue repair efficacy in a rat skin wound model.
Bioadhesives have attracted more attention in surgery due to their easy operability and abilities of promoting wound closure and tissue healing. However, it is still a great challenge to develop a robust and biocompatible bioadhesive through a facile preparation method. Herein, a ternary complex coacervate comprised of tannic acid (TA), polyethylene glycol (PEG), and gelatin (TPG) is proposed as a novel bioadhesive, which is fabricated by simple physical blending method. The adhesion capacity of TPG was reinforced through programming the cross-linking network of TPG matrix and tailoring the interfacial interactions between matrix and tissue. Curing parameters (pH, temperature, and period) and gelatin content in TPG have crucial impacts on the final comprehensive adhesion performance. The adhesion strength of the optimized formulation, fabricated with 10% (m/m) gelatin (TPG10), was over 3 folds of TPG0 (without gelatin inclusion) after 24 h curing at pH 6 and 37 degrees C. The mechanism of the reinforced comprehensive adhesion was also investigated, suggesting TA provided tough interfacial adhesion, covalent cross-link of TA-gelatin improved mechanical properties, and the hydrogen bonds mediated dynamic cross-link between TA and PEG enabled the bulk matrix to dissipate energy upon deformation. Furthermore, the additional antibacterial activity, biocompatibility, and suitable degradability endowed TPG10 with desirable wound closure and tissue repairing efficacy on rat skin wound model. Such low-cost, readily prepared, and function-efficient bioadhesive could provide a versatile platform for tissue repair and regeneration.

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