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负载阿霉素的荧光金纳米簇对乳腺癌细胞的选择性杀伤:共聚焦显微镜与荧光共振能量转移

Selective Killing of Breast Cancer Cells by Doxorubicin-Loaded Fluorescent Gold Nanoclusters: Confocal Microscopy and FRET.

作者信息

Chattoraj Shyamtanu, Amin Asif, Jana Batakrishna, 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), Fax.

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

出版信息

Chemphyschem. 2016 Jan 18;17(2):253-9. doi: 10.1002/cphc.201500982. Epub 2015 Dec 4.

Abstract

Fluorescent gold nanoclusters (AuNCs) capped with lysozymes are used to deliver the anticancer drug doxorubicin to cancer and noncancer cells. Doxorubicin-loaded AuNCs cause the highly selective and efficient killing (90 %) of breast cancer cells (MCF7) (IC50 =155 nm). In contrast, the killing of the noncancer breast cells (MCF10A) by doxorubicin-loaded AuNCs is only 40 % (IC50 =4500 nm). By using a confocal microscope, the fluorescence spectrum and decay of the AuNCs were recorded inside the cell. The fluorescence maxima (at ≈490-515 nm) and lifetime (≈2 ns), of the AuNCs inside the cells correspond to Au10-13 . The intracellular release of doxorubicin from AuNCs is monitored by Förster resonance energy transfer (FRET) imaging.

摘要

用溶菌酶包覆的荧光金纳米团簇(AuNCs)将抗癌药物阿霉素递送至癌细胞和非癌细胞。负载阿霉素的AuNCs可高效、高选择性地杀死90%的乳腺癌细胞(MCF7)(半数抑制浓度[IC50]=155纳米)。相比之下,负载阿霉素的AuNCs对非癌性乳腺细胞(MCF10A)的杀伤率仅为40%(IC50=4500纳米)。通过共聚焦显微镜记录细胞内AuNCs的荧光光谱和衰减情况。细胞内AuNCs的荧光最大值(约490 - 515纳米)和寿命(约2纳秒)对应于Au10 - 13。通过荧光共振能量转移(FRET)成像监测阿霉素从AuNCs的细胞内释放情况。

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