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基于 AgS 量子点和碲纳米棒的自组装纳米平台,用于在 HO 激活的近红外-II 荧光成像引导下进行联合化学-光热治疗。

A self-assembled nanoplatform based on AgS quantum dots and tellurium nanorods for combined chemo-photothermal therapy guided by HO-activated near-infrared-II fluorescence imaging.

机构信息

Britton Chance Center for Biomedical Photonics at Wuhan National Laboratory for Optoelectronics, Hubei Bioinformatics and Molecular Imaging Key Laboratory, Department of Biomedical Engineering, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, Hubei 430074, PR China.

Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei 430022, PR China.

出版信息

Acta Biomater. 2022 Mar 1;140:547-560. doi: 10.1016/j.actbio.2021.12.013. Epub 2021 Dec 16.

Abstract

A nanoplatform based on AgS quantum dots (QDs) and tellurium nanorods (TeNRs) was developed for combined chemo-photothermal therapy guided by HO-activated near-infrared (NIR)-II fluorescence imaging. Polypeptide PCAGRD-modified TeNRs and AgS QDs were co-encapsulated in 4T1 cell membrane to prepare a nanoplatform (CCM@AT). AgS QDs and TeNRs in the CCM@AT were used as a fluorescence probe and photosensitizer, and a chemotherapeutic prodrug and quenching agent to quench the fluorescence of AgS QDs, respectively. After the CCM@AT was specifically targeted to the tumor site, the TeNRs were dissolved by the high concentration of HO at the tumor site to light up the fluorescence of AgS QDs for NIR-II fluorescence imaging. In addition, the generated toxic TeO molecules decreased ATP production by selective cancer chemotherapy, which is beneficial for photothermal therapy. The elevated temperature due to photothermal therapy in turn promoted the chemical reaction in chemotherapy. In vitro and in vivo toxicity results showed that the CCM@AT possesses high biocompatibility. Compared to single photothermal therapy and chemotherapy, the synergistic chemo-photothermal therapy can effectively suppress the growth of 4T1 tumor. This all-in-one nanoplatform provides a boulevard for the combination therapy of tumors guided by NIR-II fluorescence imaging. STATEMENT OF SIGNIFICANCE: NIR-II fluorescence imaging shows the characteristics of low tissue absorption, reflection, and scattering, which can greatly reduce the influence of autofluorescence in vivo. However, the non-negligible effect of autofluorescence is still observed in fluorescence imaging in vivo. Therefore, there is an urgent need to develop a strategy of controlled release of fluorescence for accurate imaging and tumor therapy. Here, AgS quantum dots (QDs) with NIR-II fluorescence emission and good photothermal conversion efficiency are used as a fluorescence probe and photosensitizer, and tellurium nanorods (TeNRs) are used as a chemotherapeutic prodrug and quenching agent to quench the fluorescence of AgS QDs. This multiple nanoplatform provides an inspiration for the combination therapy of tumor guided by NIR-II fluorescence imaging.

摘要

基于 AgS 量子点 (QDs) 和碲纳米棒 (TeNRs) 的纳米平台被开发用于 HO 激活的近红外 (NIR)-II 荧光成像引导的联合化学-光热治疗。聚多肽 PCAGRD 修饰的 TeNRs 和 AgS QDs 被共包封在 4T1 细胞膜中以制备纳米平台 (CCM@AT)。CCM@AT 中的 AgS QDs 和 TeNRs 分别用作荧光探针和光敏剂,以及化疗前药和猝灭剂以猝灭 AgS QDs 的荧光。CCM@AT 被特异性靶向肿瘤部位后,TeNRs 在肿瘤部位被高浓度的 HO 溶解以点亮 AgS QDs 的荧光用于 NIR-II 荧光成像。此外,生成的有毒 TeO 分子通过选择性癌症化疗降低了 ATP 的产生,这有利于光热治疗。光热治疗引起的温度升高反过来又促进了化疗中的化学反应。体外和体内毒性结果表明 CCM@AT 具有高生物相容性。与单一光热治疗和化疗相比,协同化学-光热治疗可以有效抑制 4T1 肿瘤的生长。这种一体化纳米平台为 NIR-II 荧光成像引导的肿瘤联合治疗提供了一个途径。

意义声明

NIR-II 荧光成像是一种新的活体成像方法,它展示了低组织吸收、反射和散射的特点,可以大大降低体内自发荧光的影响。然而,在体内荧光成像中仍观察到不可忽视的自发荧光效应。因此,迫切需要开发一种控制荧光释放的策略,以实现准确的成像和肿瘤治疗。在这里,具有近红外-II 荧光发射和良好光热转换效率的 AgS 量子点 (QDs) 被用作荧光探针和光敏剂,碲纳米棒 (TeNRs) 被用作化疗前药和猝灭剂以猝灭 AgS QDs 的荧光。这种多纳平台为 NIR-II 荧光成像引导的肿瘤联合治疗提供了启示。

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