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利用原位生成的金纳米团簇进行癌细胞成像

Cancer Cell Imaging Using in Situ Generated Gold Nanoclusters.

作者信息

Chattoraj Shyamtanu, Amin Md Asif, Mohapatra Saswat, Ghosh Surajit, Bhattacharyya Kankan

机构信息

Department of Physical Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata, 700 032, India.

Organic & Medicinal Chemistry Division, CSIR-Indian Institute of Chemical Biology, Jadavpur, Kolkata, 700 032, India.

出版信息

Chemphyschem. 2016 Jan 4;17(1):61-8. doi: 10.1002/cphc.201500731. Epub 2015 Oct 23.

DOI:10.1002/cphc.201500731
PMID:26437799
Abstract

In situ generated fluorescent gold nanoclusters (Au-NCs) are used for bio-imaging of three human cancer cells, namely, lung (A549), breast (MCF7), and colon (HCT116), by confocal microscopy. The amount of Au-NCs in non-cancer cells (WI38 and MCF10A) is 20-40 times less than those in the corresponding cancer cells. The presence of a larger amount of glutathione (GSH) capped Au-NCs in the cancer cell is ascribed to a higher glutathione level in cancer cells. The Au-NCs exhibit fluorescence maxima at 490-530 nm inside the cancer cells. The fluorescence maxima and matrix-assisted laser desorption ionization (MALDI) mass spectrometry suggest that the fluorescent Au-NCs consist of GSH capped clusters with a core structure (Au8-13). Time-resolved confocal microscopy indicates a nanosecond (1-3 ns) lifetime of the Au-NCs inside the cells. This rules out the formation of aggregated Au-thiolate complexes, which typically exhibit microsecond (≈1000 ns) lifetimes. Fluorescence correlation spectroscopy (FCS) in live cells indicates that the size of the Au-NCs is ≈1-2 nm. For in situ generation, we used a conjugate consisting of a room-temperature ionic liquid (RTIL, [pmim][Br]) and HAuCl4. Cytotoxicity studies indicate that the conjugate, [pmim][AuCl4], is non-toxic for both cancer and non-cancer cells.

摘要

原位生成的荧光金纳米簇(Au-NCs)通过共聚焦显微镜用于对三种人类癌细胞进行生物成像,这三种癌细胞分别是肺癌细胞(A549)、乳腺癌细胞(MCF7)和结肠癌细胞(HCT116)。非癌细胞(WI38和MCF10A)中Au-NCs的含量比相应癌细胞中的含量少20 - 40倍。癌细胞中大量存在的谷胱甘肽(GSH)封端的Au-NCs归因于癌细胞中较高的谷胱甘肽水平。Au-NCs在癌细胞内部的荧光最大值在490 - 530 nm处。荧光最大值和基质辅助激光解吸电离(MALDI)质谱表明,荧光Au-NCs由具有核心结构(Au8 - 13)的GSH封端簇组成。时间分辨共聚焦显微镜表明细胞内Au-NCs的寿命为纳秒级(1 - 3 ns)。这排除了形成聚集的金硫醇配合物的可能性,聚集的金硫醇配合物通常具有微秒级(≈1000 ns)的寿命。活细胞中的荧光相关光谱(FCS)表明Au-NCs的尺寸约为1 - 2 nm。对于原位生成,我们使用了由室温离子液体(RTIL,[pmim][Br])和HAuCl4组成的共轭物。细胞毒性研究表明,共轭物[pmim][AuCl4]对癌细胞和非癌细胞均无毒。

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