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用于成像引导的靶向线粒体光热/光动力/化疗联合治疗诱导免疫原性细胞死亡的双重刺激响应胶束。

Dual Stimuli-Responsive Micelles for Imaging-Guided Mitochondrion-Targeted Photothermal/Photodynamic/Chemo Combination Therapy-Induced Immunogenic Cell Death.

机构信息

Department of Biochemistry and Molecular Biology, Binzhou Medical University, YanTai, ShanDong, 264003, People's Republic of China.

Department of Physiology and Pathophysiology, School of Basic Medicine, Qingdao University, QingDao, ShanDong, 266071, People's Republic of China.

出版信息

Int J Nanomedicine. 2023 Aug 2;18:4381-4402. doi: 10.2147/IJN.S410047. eCollection 2023.

DOI:10.2147/IJN.S410047
PMID:37551273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10404442/
Abstract

INTRODUCTION

As the special modality of cell death, immunogenic cell death (ICD) could activate immune response. Phototherapy in combination with chemotherapy (CT) is a particularly efficient tumor ICD inducing method that could overcome the defects of monotherapies.

METHODS

In this study, new dual stimuli-responsive micelles were designed and prepared for imaging-guided mitochondrion-targeted photothermal/photodynamic/CT combination therapy through inducing ICD. A dual-sensitive methoxy-polyethylene glycol-SS-poly(L-γ-glutamylglutamine)-SS-IR780 (mPEG-SS-PGG-SS-IR780) polymer was synthesized by grafting IR780 with biodegradable di-carboxyl PGG as the backbone, and mPEG-SS-PGG-SS-IR780/paclitaxel micelles (mPEG-SS-PGG-SS-IR780/PTXL MCs) were synthesized by encapsulating PTXL in the hydrophobic core.

RESULTS

In-vivo and -vitro results demonstrated that the three-mode combination micelles inhibited tumor growth and enhanced the therapeutic efficacy of immunotherapy. The dual stimuli-responsive mPEG-SS-PGG-SS-IR780/PTXL MCs were able to facilitate tumor cell endocytosis of nanoparticles. They were also capable of promoting micelles disintegration and accelerating PTXL release. The mPEG-SS-PGG-SS-IR780/PTXL MCs induced mitochondrial dysfunction by directly targeting the mitochondria, considering the thermo- and reactive oxygen species (ROS) sensitivity of the mitochondria. Furthermore, the mPEG-SS-PGG-SS-IR780/PTXL MCs could play the diagnostic and therapeutic roles via imaging capabilities.

CONCLUSION

In summary, this study formulated a high-efficiency nanoscale platform with great potential in combined therapy for tumors through ICD.

摘要

简介

作为细胞死亡的特殊形式,免疫原性细胞死亡(ICD)能够激活免疫反应。光疗联合化疗(CT)是一种特别有效的诱导肿瘤 ICD 的方法,可以克服单药治疗的缺陷。

方法

本研究设计并制备了新型双刺激响应性胶束,通过诱导 ICD 实现成像引导的靶向线粒体光热/光动力/CT 联合治疗。通过将具有生物降解性的二羧酸基 PGG 接枝到可降解的聚合物上作为主链,合成了一种双敏感的甲氧基聚乙二醇-SS-聚(L-γ-谷氨酰-谷氨酸)-SS-IR780(mPEG-SS-PGG-SS-IR780)聚合物,并将紫杉醇(PTXL)包裹在疏水性内核中制备 mPEG-SS-PGG-SS-IR780/PTXL 胶束(mPEG-SS-PGG-SS-IR780/PTXL MCs)。

结果

体内和体外实验结果表明,三模式联合胶束抑制肿瘤生长并增强免疫治疗的疗效。双刺激响应性 mPEG-SS-PGG-SS-IR780/PTXL MCs 能够促进肿瘤细胞对纳米颗粒的内吞作用。它们还能够促进胶束的解体并加速 PTXL 的释放。mPEG-SS-PGG-SS-IR780/PTXL MCs 通过直接靶向线粒体,考虑到线粒体的热和活性氧(ROS)敏感性,导致线粒体功能障碍。此外,mPEG-SS-PGG-SS-IR780/PTXL MCs 可以通过成像能力发挥诊断和治疗作用。

结论

总之,本研究通过 ICD 为肿瘤联合治疗制定了一种具有高效能的纳米级平台,具有很大的潜力。

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