Infinite Coordination Polymer Polydopamine Nanocomposites Dual-Pathway Multistep Induction of Long-Term Hyperimmunity Combined With Photothermal-Chemo Synergistic Therapy Colorectal Cancer

IF 13.9 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xiaojiang Zhang, Yujie Zhang, Pengqian Wang, Feiyu Shi, Siyuan Du, Zhe Zhang, Daocheng Wu, Junjun She, Ya Wang
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Abstract

To improve the long-term therapeutic efficacy of colorectal cancer, we propose a synergistic treatment strategy involving dual-pathway, multistep induction of long-term hyperimmunity combined with photothermal-chemotherapy. To implement this strategy, infinite coordination polymer nanoparticles (SN38-Mn(II)-EGCG ICP NPs) were prepared by coordinating SN38, EGCG, and Mn2+. These nanoparticles were then coated with polydopamine (PDA) and grafted with folate-PEG-thiol (FA-PEG-SH) onto their surfaces, producing tumor-targeting folate-modified PDA infinite coordination polymer nanocomposites (ICP@FA-PDA nanocomposites). These nanocomposites exhibit a particle size of 94.9 ± 1.6 nm with a high drug loading capacity (83.3% ± 1.5%), drug release under acidic conditions while maintaining stability in physiological environments. Furthermore, each component within the nanocomposites serves multiple functions. Notably, the incorporation of multiple components triggers a powerful antitumor immune effect and establishes enduring immune memory through a dual-pathway and multistep approach, which is produced with the activation of the cGAS-STING pathway and immunogenic cell death (ICD) by a four-component multistep process. Under a low-dose regimen, this approach induces dual-pathway hyperimmunity effect and generates ultra-long immunological memory, marked by a ninefold increase in CD8+ T cell infiltration, a fourfold increase in CD4+ T lymphocytes, a fourfold reduction in Treg cells, and a fivefold increase in memory T cells. The remarkable therapy efficacy is achieved by hyperimmunity effect combination of SN38 and EGCG chemotherapy and photothermal therapy. In vivo studies demonstrated that mice treated with ICP@FA-PDA nanocomposites achieved complete eradication of cancer within 21 days, with no recurrence observed within 60 days. These nanocomposites hold significant promise and potential for future clinical translation.

Abstract Image

无限配位聚合物聚多巴胺纳米复合材料双途径多步骤诱导长期高免疫联合光热化疗协同治疗结直肠癌
为了提高结直肠癌的长期治疗效果,我们提出了双途径、多步骤诱导长期高免疫联合光热化疗的协同治疗策略。为了实现这一策略,通过SN38、EGCG和Mn2+的配位,制备了无限配位聚合物纳米粒子SN38- mn (II)-EGCG ICP NPs。然后在这些纳米颗粒表面涂覆聚多巴胺(PDA),并在其表面接枝叶酸-聚乙二醇-硫醇(FA-PEG-SH),制备肿瘤靶向叶酸修饰的聚乙二醇-聚乙二醇无限配位聚合物纳米复合材料(ICP@FA-PDA纳米复合材料)。这些纳米复合材料的粒径为94.9±1.6 nm,具有较高的载药量(83.3%±1.5%),在酸性条件下可释放药物,同时在生理环境中保持稳定性。此外,纳米复合材料中的每个组件都具有多种功能。值得注意的是,多种成分的结合可触发强大的抗肿瘤免疫效应,并通过双途径和多步骤方法建立持久的免疫记忆,这是通过四组分多步骤过程激活cGAS-STING途径和免疫原性细胞死亡(ICD)而产生的。在低剂量方案下,该方法诱导双通路超免疫效应并产生超长免疫记忆,其特征是CD8+ T细胞浸润增加9倍,CD4+ T淋巴细胞增加4倍,Treg细胞减少4倍,记忆T细胞增加5倍。SN38联合EGCG化疗及光热治疗的高免疫效应取得显著的治疗效果。体内研究表明,用ICP@FA-PDA纳米复合材料治疗的小鼠在21天内完全根除了癌症,60天内没有复发。这些纳米复合材料在未来的临床翻译中具有重要的前景和潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
17.40
自引率
0.00%
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审稿时长
7 weeks
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