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谷胱甘肽响应型半导体聚合物作为用于近红外二区成像引导的化疗-光热疗法的纳米诊疗平台

GSH-Responsive Semiconducting Polymer as a Nanotheranostic Platform for NIR-II Imaging-Guided Chemo-Photothermal Therapy.

作者信息

Wang Ben, Zhang Yujing, Ji Yuquan, Yang Guangzhao, Zhang Xiaolong, Zhou Yi, Yu Siyang, Yin Haotong, Zhou Hui, Yin Chao, Fan Quli

机构信息

State Key Laboratory of Flexible Electronics (LoFE), Jiangsu Key Laboratory of Smart Biomaterials and Theranostic Technology, Institute of Advanced Materials (IAM), Jiangsu National Synergetic Innovation Center for Advanced Materials (SICAM), School of Materials Science and Engineering, Nanjing University of Posts and Telecommunications, 9 Wenyuan Road, Nanjing, 210023, China.

出版信息

Macromol Rapid Commun. 2025 May;46(10):e2401098. doi: 10.1002/marc.202401098. Epub 2025 Feb 22.

Abstract

The development of multifunctional nanotheranostic platforms with stimuli-responsive capabilities holds significant potential for enhancing cancer diagnosis and treatment. Herein, a glutathione (GSH)-responsive semiconducting polymer (SP) nanotheranostic system, SP/DOX-SS-PEG nanoparticles (NPs), is presented, designed for combined near-infrared II (NIR-II) fluorescence imaging (FI) and chemo-photothermal therapy. The amphiphilic SP (SP-SS-PEG) is synthesized through a multi-step reaction sequence, including Suzuki coupling, amidation, and thiol-disulfide exchange reactions, and subsequently encapsulates the anticancer drug doxorubicin (DOX) through self-assembly, resulting in the formation of GSH-responsive SP/DOX-SS-PEG NPs. These SP/DOX-SS-PEG NPs exhibit high photothermal stability and significant GSH-triggered DOX release. In vitro studies demonstrate that SP/DOX-SS-PEG NPs display enhanced cellular uptake and robust cytotoxicity against 4T1 cancer cells under 808 nm laser irradiation. Upon intravenous injection in tumor-bearing mice, NIR-II FI reveals efficient tumor accumulation and prolonged retention of the NPs. In vivo anti-tumor efficacy studies indicate that SP/DOX-SS-PEG NPs combined with 808 nm laser irradiation achieve the most significant inhibition of tumor growth, with minimal systemic toxicity. Taken together, these findings highlight the promising potential of SP/DOX-SS-PEG NPs as a multifunctional platform for precision cancer theranostics, integrating efficient NIR-II imaging, GSH-triggered drug release, and dual chemo-photothermal therapy.

摘要

具有刺激响应能力的多功能纳米诊疗平台的发展在增强癌症诊断和治疗方面具有巨大潜力。在此,我们展示了一种谷胱甘肽(GSH)响应型半导体聚合物(SP)纳米诊疗系统,即SP/DOX-SS-PEG纳米颗粒(NPs),其设计用于近红外二区(NIR-II)荧光成像(FI)和化学-光热疗法的联合应用。两亲性SP(SP-SS-PEG)通过多步反应序列合成,包括铃木耦合、酰胺化和硫醇-二硫键交换反应,随后通过自组装封装抗癌药物阿霉素(DOX),从而形成GSH响应型SP/DOX-SS-PEG NPs。这些SP/DOX-SS-PEG NPs表现出高光热稳定性和显著的GSH触发的DOX释放。体外研究表明,在808 nm激光照射下SP/DOX-SS-PEG NPs对4T1癌细胞具有增强的细胞摄取和强大的细胞毒性。在荷瘤小鼠静脉注射后,NIR-II FI显示NPs在肿瘤中有效积累并长时间滞留。体内抗肿瘤疗效研究表明,SP/DOX-SS-PEG NPs与808 nm激光照射联合使用对肿瘤生长的抑制作用最为显著,且全身毒性最小。综上所述,这些发现突出了SP/DOX-SS-PEG NPs作为一种多功能平台用于精准癌症诊疗的潜力,该平台整合了高效的NIR-II成像、GSH触发的药物释放以及化学-光热联合治疗。

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