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碳酸钙包裹的金纳米星实现肿瘤触发的药物释放用于近红外光动力/光热联合抗肿瘤治疗。

Tumor-triggered drug release from calcium carbonate-encapsulated gold nanostars for near-infrared photodynamic/photothermal combination antitumor therapy.

作者信息

Liu Yanlei, Zhi Xiao, Yang Meng, Zhang Jingpu, Lin Lingnan, Zhao Xin, Hou Wenxiu, Zhang Chunlei, Zhang Qian, Pan Fei, Alfranca Gabriel, Yang Yuming, de la Fuente Jesús M, Ni Jian, Cui Daxiang

机构信息

Institute of Nano Biomedicine and Engineering, Key Laboratory for Thin Film and Micro fabrication of the Ministry of Education, Department of Instrument Science and Engineering, School of Electronic Information and Electrical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China.

School of Biomedical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China.

出版信息

Theranostics. 2017 Apr 10;7(6):1650-1662. doi: 10.7150/thno.17602. eCollection 2017.

Abstract

Different stimulus including pH, light and temperature have been used for controlled drug release to prevent drug inactivation and minimize side-effects. Herein a novel nano-platform (GNS@CaCO/ICG) consisting of calcium carbonate-encapsulated gold nanostars loaded with ICG was established to couple the photothermal properties of gold nanostars (GNSs) and the photodynamic properties of indocyanine green (ICG) in the photodynamic/photothermal combination therapy (PDT/PTT). In this study, the calcium carbonate worked not only a drug keeper to entrap ICG on the surface of GNSs in the form of a stable aggregate which was protected from blood clearance, but also as the a pH-responder to achieve highly effective tumor-triggered drug release locally. The application of GNS@CaCO/ICG for and therapy achieved the combined antitumor effects upon the NIR irradiation, which was superior to the single PDT or PTT. Meanwhile, the distinct pH-triggered drug release performance of GNS@CaCO/ICG implemented the tumor-targeted NIR fluorescence imaging. In addition, we monitored the bio-distribution and excretion pathway of GNS@CaCO/ICG based on the NIR fluorescence from ICG and two-photon fluorescence and photoacoustic signal from GNSs, and the results proved that GNS@CaCO/ICG had a great ability for tumor-specific and tumor-triggered drug release. We therefore conclude that the GNS@CaCO/ICG holds great promise for clinical applications in anti-tumor therapy with tumor imaging or drug tracing.

摘要

不同的刺激因素,包括pH值、光和温度,已被用于控制药物释放,以防止药物失活并将副作用降至最低。在此,我们构建了一种新型纳米平台(GNS@CaCO/ICG),它由负载吲哚菁绿(ICG)的碳酸钙包裹金纳米星组成,用于在光动力/光热联合疗法(PDT/PTT)中结合金纳米星(GNSs)的光热特性和吲哚菁绿(ICG)的光动力特性。在本研究中,碳酸钙不仅作为药物载体,以稳定聚集体的形式将ICG捕获在GNSs表面,防止其被血液清除,还作为pH响应剂,实现局部高效的肿瘤触发药物释放。GNS@CaCO/ICG用于光动力和光热疗法,在近红外(NIR)照射下实现了联合抗肿瘤效果,优于单一的PDT或PTT。同时,GNS@CaCO/ICG独特的pH触发药物释放性能实现了肿瘤靶向近红外荧光成像。此外,我们基于ICG的近红外荧光以及GNSs的双光子荧光和光声信号监测了GNS@CaCO/ICG的生物分布和排泄途径,结果证明GNS@CaCO/ICG具有很强的肿瘤特异性和肿瘤触发药物释放能力。因此,我们得出结论,GNS@CaCO/ICG在肿瘤成像或药物追踪的抗肿瘤治疗临床应用中具有巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/064b/5436518/c19d6cce10ad/thnov07p1650g001.jpg

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