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基质金属蛋白酶 2 靶向递呈载吲哚菁绿金纳米星用于双模成像及光热/光动力协同治疗

Matrix metallopeptidase 2 targeted delivery of gold nanostars decorated with IR-780 iodide for dual-modal imaging and enhanced photothermal/photodynamic therapy.

机构信息

Institute of Nano Biomedicine and Engineering, Shanghai Engineering Research Centre for Intelligent Diagnosis and Treatment Instrument, Department of Instrument Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, 800 Dongchuan RD, Shanghai 200240, PR China; National Center for Translational Medicine, Collaborative Innovational Center for System Biology, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, PR China.

School of Laboratory Medicine and Life Science, Wenzhou Medical University, University Town, Chashan, Wenzhou, Zhejiang 325035, PR China.

出版信息

Acta Biomater. 2019 Apr 15;89:289-299. doi: 10.1016/j.actbio.2019.03.008. Epub 2019 Mar 6.

Abstract

Nanotheranostics has gained increasing interest, as it offers a great potential to realize personalized diagnostics and therapy. In this work, we report a facile approach of the fabrication of gold nanostars (GNS) attached with matrix metalloproteinases (MMP2) polypeptides (Ac-GPLGIAGQ) and IR-780 iodide through bovine serum albumin (BSA) for targeted dual-modal photoacoustic (PA)/near-infrared (NIR) fluorescence imaging and enhanced photothermal therapy (PTT)/photodynamic therapy (PDT) for lung cancer. MMP2 polypeptides served as the targeting ligand, IR-780 iodide functioned as the NIR fluorescence imaging agent as well as PTT/PDT agent, and GNS acted as the carrier of IR-780 molecules and performed PA imaging and PTT. DLS and CCK-8 assay demonstrated that the nanoprobes (GNS@BSA/I-MMP2) exhibited excellent stability and biocompatibility under physiological conditions. Subsequent in vitro studies verified that GNS@BSA/I-MMP2 nanoparticles (NPs) were effectively internalized by A549 cancer cells and exhibited remarkable antitumor efficacy. Furthermore, GNS@BSA/I-MMP2 NPs could specifically target the tumor and significantly suppress the tumor growth, and their antitumor effects were mainly through the synergistic effects of PDT and PTT based on IR-780 and GNS. These findings imply the potential of GNS@BSA/I-MMP2 NPs as a targeting PA/NIR probe in tumor diagnosis and combined therapy with a single light source. STATEMENT OF SIGNIFICANCE: We reported a convenient and facile approach to load IR-780 iodides in gold nanostars (GNS). This material could simultaneously perform near-infrared imaging/photoacoustic imaging and thermotherapy/photodynamic therapy. MMP2 coating on the surface of GNS@BSA/IR-780 promoted the prepared nanoparticles (GNS@BSA/I-MMP2) to target the tumor region. The heat generated by the synergistic effect of the GNS and IR-780 molecules resulted in the high temperature of the GNS@BSA/I-MMP2 NPs, which efficiently suppressed the growth of tumor, and the tumor volume decreased by 93% compared with that in the PBS groups with laser irradiation.

摘要

纳米诊断学越来越受到关注,因为它为实现个性化诊断和治疗提供了巨大的潜力。在这项工作中,我们报告了一种简便的方法,通过牛血清白蛋白(BSA)将金纳米星(GNS)与基质金属蛋白酶(MMP2)多肽(Ac-GPLGIAGQ)和 IR-780 碘化物连接起来,用于靶向双模态光声(PA)/近红外(NIR)荧光成像以及增强光热治疗(PTT)/光动力治疗(PDT)治疗肺癌。MMP2 多肽作为靶向配体,IR-780 碘化物既是 NIR 荧光成像剂,也是 PTT/PDT 剂,GNS 则作为 IR-780 分子的载体,实现 PA 成像和 PTT。DLS 和 CCK-8 测定表明,纳米探针(GNS@BSA/I-MMP2)在生理条件下表现出优异的稳定性和生物相容性。随后的体外研究证实,GNS@BSA/I-MMP2 纳米颗粒(NPs)可被 A549 癌细胞有效内化,并表现出显著的抗肿瘤功效。此外,GNS@BSA/I-MMP2 NPs 可以特异性地靶向肿瘤并显著抑制肿瘤生长,其抗肿瘤作用主要是通过基于 IR-780 和 GNS 的 PDT 和 PTT 的协同作用。这些发现表明,GNS@BSA/I-MMP2 NPs 有望成为肿瘤诊断和基于单光源联合治疗的靶向 PA/NIR 探针。

我们报道了一种简便的方法来装载金纳米星(GNS)中的 IR-780 碘化物。这种材料可以同时进行近红外成像/光声成像和热疗/光动力疗法。GNS@BSA/IR-780 表面的 MMP2 涂层促进了制备的纳米颗粒(GNS@BSA/I-MMP2)靶向肿瘤区域。GNS 和 IR-780 分子协同作用产生的热量导致 GNS@BSA/I-MMP2 NPs 温度升高,有效地抑制了肿瘤的生长,与激光照射下的 PBS 组相比,肿瘤体积减少了 93%。

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