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葡萄糖修饰的金纳米簇:一种用于快速识别表达葡萄糖转运蛋白受体的癌细胞的膜电位无关荧光探针。

Glucose decorated gold nanoclusters: A membrane potential independent fluorescence probe for rapid identification of cancer cells expressing Glut receptors.

作者信息

Singh Sanjay

机构信息

Division of Biological and Life Sciences, School of Arts and Sciences, Central Campus, Ahmedabad University, Navrangpura, Ahmedabad 380009, Gujarat, India.

出版信息

Colloids Surf B Biointerfaces. 2017 Jul 1;155:25-34. doi: 10.1016/j.colsurfb.2017.03.052. Epub 2017 Apr 1.

Abstract

The effective nanomedicines require nanoparticles to attach or adhere to the cell surface, which is dictated by several parameters of nanoparticles such as shape, size, charge, and composition. However, these parameters lead to the membrane potential dependent non-specific delivery of therapeutic or imaging nanosystems into cancer cells. This leads to significant complications and results into the serious impediment to effective treatment of cancer. Cancer cells are known to metabolize high amount of glucose in order to support their rapid proliferation and expansion. Recently, gold nanoclusters (AuNCs) have emerged as an excellent fluorescent nanoprobe for bio-imaging and related applications in cancer treatment. Therefore, taking cues from these studies, we have developed two types of gold nanoclusters, BSA-coated (BSA-AuNCs) and glucose coated gold nanoclusters (Glu-AuNCs) and investigated their mechanism of internalization in cell culture model systems of cancerous and noncancerous cells. Our study demonstrates that Glu-AuNCs are not internalized by HaCaT cells but selectively taken up by A431 cells through Glut-1 receptors, but their uptake was cell membrane potential independent. However, BSA-AuNCs showed more internalization in A431 than HaCaT cells, but their uptake was cell membrane potential dependent.

摘要

有效的纳米药物需要纳米颗粒附着或黏附于细胞表面,这取决于纳米颗粒的几个参数,如形状、大小、电荷和组成。然而,这些参数导致治疗性或成像纳米系统依赖膜电位非特异性地递送至癌细胞中。这会导致严重的并发症,并严重阻碍癌症的有效治疗。已知癌细胞为了支持其快速增殖和扩张会代谢大量葡萄糖。最近,金纳米团簇(AuNCs)已成为用于生物成像及癌症治疗相关应用的出色荧光纳米探针。因此,借鉴这些研究,我们开发了两种类型的金纳米团簇,即牛血清白蛋白包被的(BSA-AuNCs)和葡萄糖包被的金纳米团簇(Glu-AuNCs),并在癌细胞和非癌细胞的细胞培养模型系统中研究了它们的内化机制。我们的研究表明,Glu-AuNCs不会被HaCaT细胞内化,而是通过Glut-1受体被A431细胞选择性摄取,但其摄取与细胞膜电位无关。然而,BSA-AuNCs在A431细胞中的内化比在HaCaT细胞中更多,但其摄取与细胞膜电位有关。

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