[金属离子介导的天然小分子无载体水凝胶联合CDT/PDT的抗肿瘤作用]。

Q3 Pharmacology, Toxicology and Pharmaceutics
Wen-Min Pi, Gen Li, Xin-Ru Tan, Zhi-Xia Wang, Xiao-Yu Lin, Hai-Ling Qiu, Fu-Hao Chu, Bo Wang, Peng-Long Wang
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引用次数: 0

摘要

金属离子促进化学动力疗法(CDT)与光动力疗法(PDT)联合应用在增强抗肿瘤作用方面具有广阔的应用前景。本研究将甘草酸(GA)、铜离子(Cu~(2+))和去甲花青素(NCTD)共组装,成功制备了具有优异材料性能的天然小分子无载体水凝胶(NCTD凝胶)。在808 nm激光照射下,NCTD凝胶响应肿瘤微环境(TME),作为高效的Fenton试剂和光敏剂,催化肿瘤内内源性过氧化氢(H_2O_2)转化为氧(O_2)、羟基自由基(·OH,Ⅰ型活性氧)和单线态氧(~ 10_2,Ⅱ型活性氧),同时消耗谷胱甘肽(GSH)稳定活性氧,缓解肿瘤缺氧。体外和体内实验表明,NCTD凝胶具有显著的CDT/PDT协同治疗作用。进一步的安全性评价和代谢试验证实其具有良好的生物相容性和安全性。该新型水凝胶不仅制备简单、安全、经济,而且具有很大的临床转化潜力,为金属离子介导的水凝胶抗肿瘤疗法的研究和开发提供了见解和参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Anti-tumor effect of metal ion-mediated natural small molecules carrier-free hydrogel combined with CDT/PDT].

Metal ion-promoted chemodynamic therapy(CDT) combined with photodynamic therapy(PDT) offers broad application prospects for enhancing anti-tumor effects. In this study, glycyrrhizic acid(GA), copper ions(Cu~(2+)), and norcantharidin(NCTD) were co-assembled to successfully prepare a natural small-molecule, carrier-free hydrogel(NCTD Gel) with excellent material properties. Under 808 nm laser irradiation, NCTD Gel responded to the tumor microenvironment(TME) and acted as an efficient Fenton reagent and photosensitizer, catalyzing the conversion of endogenous hydrogen peroxide(H_2O_2) within the tumor into oxygen(O_2), and hydroxyl radicals(·OH, type Ⅰ reactive oxygen species) and singlet oxygen(~1O_2, type Ⅱ reactive oxygen species), while depleting glutathione(GSH) to stabilize reactive oxygen species and alleviate tumor hypoxia. In vitro and in vivo experiments demonstrated that NCTD Gel exhibited significant CDT/PDT synergistic therapeutic effects. Further safety evaluation and metabolic testing confirmed its good biocompatibility and safety. This novel hydrogel is not only simple to prepare, safe, and cost-effective but also holds great potential for clinical transformation, providing insights and references for the research and development of metal ion-mediated hydrogel-based anti-tumor therapies.

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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