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Multifunctional Self-Healing Carbon Dot–Gelatin Bioadhesive: Improved Tissue Adhesion with Simultaneous Drug Delivery, Optical Tracking, and Photoactivated Sterilization

生物粘附 明胶 化学 药物输送 戊二醛 粘附 纳米技术 材料科学 生物物理学 有机化学 生物
作者
Maansi Aggarwal,Harekrishna Panigrahi,Dinesh K. Kotnees,Prolay Das
出处
期刊:Biomacromolecules [American Chemical Society]
卷期号:25 (5): 3178-3189 被引量:8
标识
DOI:10.1021/acs.biomac.4c00313
摘要

Bioadhesives with all-inclusive properties for simultaneous strong and robust adhesion, cohesion, tracking, drug delivery, self-sterilization, and nontoxicity are still farfetched. Herein, a carbon dot (CD) is made to infuse each of the above-desired aspects with gelatin, an inexpensive edible protein. The CD derived through controlled hydrothermal pyrolysis of dopamine and terephthaldehyde retained –NH2, –OH, –COOH, and, most importantly, –CHO functionality on the CD surface for efficient skin adhesion and cross-linking. Facile fabrication of CD–gelatin bioadhesive through covalent conjugation of –CHO of the CD with –NH2 of gelatin through Schiff base formation was accomplished. This imparts remarkable self-healing attributes as well as excellent adhesion and cohesion evident from physicomechanical analysis in a porcine skin model. Improved porosity of the bioadhesive allows loading hemin as a model drug whose disembarkment is tracked with intrinsic CD photoluminescence. In a significant achievement, antibiotic-free self-sterilization of bioadhesive is demonstrated through visible light (white LED, 23 W)-irradiated photosensitization of the CD to produce reactive oxygen species for annihilation of both Gram-positive and Gram-negative bacteria with exceptional efficacy (99.9%). Thus, a comprehensive CD–gelatin bioadhesive for superficial and localized wound management is reported as a promising step for the transformation of the bioadhesive domain through controlled nanotization for futuristic clinical translations.
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