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基于 Croconium 的酸性溶酶体锚定纳米平台用于增强的三模式生物成像和 Fe 触发的肿瘤协同治疗。

Acidic Lysosome-Anchoring Croconium-Based Nanoplatform for Enhanced Triple-Mode Bioimaging and Fe-Triggered Tumor Synergistic Therapy.

机构信息

NMPA Key Laboratory for Research and Evaluation of Drug Metabolism & Guangdong Provincial Key Laboratory of New Drug Screening & Guangdong-Hongkong-Macao Joint Laboratory for New Drug Screening, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.

School of Pharmaceutical Sciences, Southern Medical University, Guangzhou 510515, China.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 4;16(35):46066-46078. doi: 10.1021/acsami.4c09587. Epub 2024 Aug 22.

DOI:10.1021/acsami.4c09587
PMID:39172044
Abstract

Metal-modulated croconium dyes with multimodal-imaging and synergistic therapy in the tumor microenvironment have exhibited great potential in tumor theranostics. However, their unideal structure optimization always weakened the efficacy of near-infrared fluorescence-photoacoustic (NIRF/PA) imaging and photothermal therapy (PTT). Here, we screened croconium dye containing two indole groups with better NIRF/PA imaging and PTT in their family, linked to two morpholine rings, and obtained CR-736, as a lysosome-targeting and Fe-modulated agent. The established CR-736-Fe nanoplatform was accurately delivered to the breast tumor site, released CR-736 and Fe in the lower acidic lysosome microenvironment, and activated pH-responsive NIRF/PA/magnetic resonance imaging and PTT. Furthermore, ferroptosis generated hydroxyl free radicals and lipid peroxide by consuming GSH and HO by dint of the accumulation of Fe in tumor cells, which resulted in the inhibition of the expression of heat shock proteins and the concomitant recovery of PTT. The synergistic therapy of PTT, ferroptosis, and chemodynamics was further optimized to the maximal extent in tumor lysosome acidic microenvironment and proved both in vitro and a mouse tumor model. This study opens a new avenue in designing excellent and unique croconium-based nanoplatforms, synergizing multiple tumor theranostic methods, and further optimizing the theranostic effects in tumor microenvironment.

摘要

金属调节型克罗酮染料在肿瘤微环境中具有多模态成像和协同治疗的作用,在肿瘤治疗学中具有很大的潜力。然而,它们不理想的结构优化往往会削弱近红外荧光-光声(NIRF/PA)成像和光热治疗(PTT)的效果。在这里,我们筛选出了含有两个吲哚基团的克罗酮染料,其在家族中具有更好的近红外荧光/光声(NIRF/PA)成像和光热治疗(PTT)效果,连接了两个吗啉环,并得到了 CR-736,作为溶酶体靶向和 Fe 调节剂。所建立的 CR-736-Fe 纳米平台能够准确地递送到乳腺肿瘤部位,在较低的酸性溶酶体微环境中释放 CR-736 和 Fe,并激活 pH 响应的近红外荧光/光声/磁共振成像和 PTT。此外,铁死亡通过消耗 GSH 和 HO 产生羟基自由基和脂质过氧化物,借助肿瘤细胞中铁的积累,抑制热休克蛋白的表达,并同时恢复 PTT。PTT、铁死亡和化学动力学协同治疗在肿瘤溶酶体酸性微环境中被进一步优化到最大程度,并在体外和小鼠肿瘤模型中得到了证实。这项研究为设计优秀而独特的基于克罗酮的纳米平台、协同多种肿瘤治疗方法以及进一步优化肿瘤微环境中的治疗效果开辟了新的途径。

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