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用于增强糖尿病伤口愈合中光免疫疗法的胸腺五肽整合自组装纳米平台。

Thymopentin-integrated self-assembling nanoplatform for enhanced photo-immunotherapy in diabetic wound healing.

作者信息

Wang Runze, Cheng Wenting, Tian Hailong, Dong Mengchao, He Weifeng, Wang Xie, Zou Yingying

机构信息

Department of Pathology and Pathophysiology, School of Basic Medicine, Kunming Medical University, Kunming 650500, China.

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu 610041, China.

出版信息

J Colloid Interface Sci. 2025 Dec;699(Pt 2):138264. doi: 10.1016/j.jcis.2025.138264. Epub 2025 Jun 22.

Abstract

Diabetic wounds represent a significant clinical challenge owing to infection, oxidative stress, and immune dysregulation. In this study, a multifunctional photoimmunotherapy nanoplatform (I-P-T NPs) was developed through the self-assembly of the near-infrared photosensitizer IR820, the immunomodulatory agent thymopentin (TP5), and the antioxidant phloretin (Phl) via intermolecular hydrogen bonding and hydrophobic interactions. This nanoplatform integrates photothermal therapy (PTT), immune modulation, and reactive oxygen species scavenging to address the infection-oxidation-immunosuppression triad in diabetic wounds. The I-P-T NPs exhibited robust photothermal conversion under 808 nm irradiation, generating localized hyperthermia with antibacterial effects. In vitro experiments demonstrated that I-P-T NPs promoted M2 macrophage polarization, reduced oxidative stress, enhanced endothelial and keratinocyte migration, and suppressed pro-inflammatory cytokine release. Additionally, the nanoplatform displayed potent antibacterial activity against both Gram-positive and Gram-negative bacteria. In a streptozotocin-induced diabetic mouse model with infected wounds, topical application of I-P-T NPs combined with photothermal treatment accelerated wound closure, enhanced re-epithelialization and collagen deposition, and mitigated inflammation. The self-assembled design improved the solubility of Phl and enabled spatiotemporally controlled delivery of multiple therapeutic components. No significant systemic toxicity was observed, confirming the biocompatibility of I-P-T NPs. This study presents a novel nanoplatform that synergistically combines photothermal sterilization, TP5-mediated immune regulation, and Phl-driven antioxidant effects, offering a promising strategy for managing complex diabetic wounds. This modular design highlights the potential for translating multifunctional nanotherapies into clinical applications for the treatment of chronic wounds.

摘要

由于感染、氧化应激和免疫失调,糖尿病伤口是一个重大的临床挑战。在本研究中,通过近红外光敏剂IR820、免疫调节剂胸腺五肽(TP5)和抗氧化剂根皮素(Phl)通过分子间氢键和疏水相互作用自组装,开发了一种多功能光免疫治疗纳米平台(I-P-T NPs)。该纳米平台整合了光热疗法(PTT)、免疫调节和活性氧清除功能,以解决糖尿病伤口中的感染-氧化-免疫抑制三联征。I-P-T NPs在808 nm照射下表现出强大的光热转换能力,产生具有抗菌作用的局部高温。体外实验表明,I-P-T NPs促进M2巨噬细胞极化,降低氧化应激,增强内皮细胞和角质形成细胞迁移,并抑制促炎细胞因子释放。此外,该纳米平台对革兰氏阳性菌和革兰氏阴性菌均显示出强大的抗菌活性。在链脲佐菌素诱导的感染伤口糖尿病小鼠模型中,局部应用I-P-T NPs并结合光热处理可加速伤口闭合,增强上皮再形成和胶原蛋白沉积,并减轻炎症。自组装设计提高了Phl的溶解度,并实现了多种治疗成分的时空控制递送。未观察到明显的全身毒性,证实了I-P-T NPs的生物相容性。本研究提出了一种新型纳米平台,该平台将光热杀菌、TP5介导的免疫调节和Phl驱动的抗氧化作用协同结合,为管理复杂的糖尿病伤口提供了一种有前景的策略。这种模块化设计突出了将多功能纳米疗法转化为慢性伤口治疗临床应用的潜力。

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