Gu Yufan, You Yuxin, Yang Yijia, Liu Xinyi, Yang Luyuan, Li Yanzhu, Zhang Chaoyi, Yang Huan, Sha Ziqi, Ma Youzhen, Pang Yipeng, Liu Yi
Department of Biophysics, School of Life Sciences, Xuzhou Medical University, Xuzhou, Jiangsu 221004, China.
ACS Appl Mater Interfaces. 2024 Sep 25;16(38):50238-50250. doi: 10.1021/acsami.4c08169. Epub 2024 Sep 16.
Damaged skin is susceptible to invasion by harmful microorganisms, especially and , which can delay healing. Epigallocatechin-3-gallate (EGCG) is a natural compound known for effectively promoting wound healing and its potent anti-inflammatory effects. However, its application is limited due to its susceptibility to oxidation and isomerization, which alter its structure. The use of zeolitic imidazolate framework-8 (ZIF-8) can effectively tackle these issues. This study introduces an oxygen (O) and hydrogen peroxide (HO) self-supplying ZIF-8 nanoplatform designed to enhance the bioavailability of EGCG, combining photodynamic therapy (PDT) and chemodynamic therapy (CDT) to improve antibacterial properties and ultimately accelerate wound healing. For this purpose, EGCG and indocyanine green (ICG), a photosensitizer, were successively integrated into a ZIF-8, and coated with bovine serum albumin (BSA) to enhance biocompatibility. The outer layer of this construct was further modified with manganese dioxide (MnO) to promote CDT and calcium peroxide (CaO) to supply HO and O, resulting in the final nanoplatform EGCG-ICG@ZIF-8/BSA-MnO/CaO (EIZBMC). In experiments under 808 nm laser, EIZBMC exhibited synergistic antibacterial effects through PDT and CDT. This combination effectively released reactive oxygen species (ROS), which mediated oxidative stress to inhibit the bacteria. Subsequently, in a murine model of wound infection, EIZBMC not only exerted antibacterial effects through PDT and CDT but also alleviated the inflammatory condition and promoted the regeneration of collagen fibers, which led to accelerated wound healing. Overall, this research presents a promising approach to enhancing the therapeutic efficacy of EGCG by leveraging the synergistic antibacterial effects of PDT and CDT. This multifunctional nanoplatform maximizes EGCG's anti-inflammatory properties, offering a potent solution for promoting infected wound healing.
受损皮肤易受有害微生物侵袭,尤其是[此处原文缺失两种微生物名称],这会延迟伤口愈合。表没食子儿茶素-3-没食子酸酯(EGCG)是一种天然化合物,以有效促进伤口愈合及其强大的抗炎作用而闻名。然而,由于其易氧化和异构化,从而改变其结构,其应用受到限制。使用沸石咪唑酯骨架-8(ZIF-8)可以有效解决这些问题。本研究引入了一种氧(O)和过氧化氢(HO)自供应的ZIF-8纳米平台,旨在提高EGCG的生物利用度,结合光动力疗法(PDT)和化学动力疗法(CDT)以改善抗菌性能并最终加速伤口愈合。为此,将EGCG和一种光敏剂吲哚菁绿(ICG)依次整合到ZIF-8中,并用牛血清白蛋白(BSA)包被以增强生物相容性。该构建体的外层进一步用二氧化锰(MnO)修饰以促进CDT,用过氧化钙(CaO)供应HO和O,从而得到最终的纳米平台EGCG-ICG@ZIF-8/BSA-MnO/CaO(EIZBMC)。在808nm激光照射下的实验中,EIZBMC通过PDT和CDT表现出协同抗菌作用。这种组合有效地释放了活性氧(ROS),其介导氧化应激来抑制细菌。随后,在伤口感染的小鼠模型中,EIZBMC不仅通过PDT和CDT发挥抗菌作用,还减轻了炎症状况并促进了胶原纤维的再生,从而加速了伤口愈合。总体而言,本研究提出了一种通过利用PDT和CDT的协同抗菌作用来提高EGCG治疗效果的有前景的方法。这种多功能纳米平台最大限度地发挥了EGCG的抗炎特性,为促进感染伤口愈合提供了一种有效的解决方案。