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纳米颗粒大小和细胞类型对局部表面等离子体共振生物传感器高灵敏度细胞检测的影响。

Effects of nanoparticle size and cell type on high sensitivity cell detection using a localized surface plasmon resonance biosensor.

机构信息

Department of Electronic Engineering, City University of Hong Kong, Kowloon, Hong Kong; Center for Biosystems, Neuroscience, and Nanotechnology, City University of Hong Kong, Kowloon, Hong Kong; Department of Electronic Information Engineering, Tianjin University, Tianjin 300072, China.

Department of Biology and Chemistry, City University of Hong Kong, Kowloon, Hong Kong; Center for Biosystems, Neuroscience, and Nanotechnology, City University of Hong Kong, Kowloon, Hong Kong.

出版信息

Biosens Bioelectron. 2014 May 15;55:141-8. doi: 10.1016/j.bios.2013.11.075. Epub 2013 Dec 10.

Abstract

A localized surface plasmon resonance (LSPR) effect was used to distinguish cell concentration on ordered arrays of Au nanoparticles (NPs) on glass substrates. Human-derived retinal pigment epithelial RPE-1 cells with flatter bodies and higher confluency were compared with breast cancer MCF-7 cells. Nanosphere lithography was used to form Au NPs with average diameters of 500 and 60 nm in order to compare cell detection range, resonance peak shift, and cell concentration sensitivity. A larger cell concentration range was detected on the larger 500 nm Au NPs compared to 60 nm Au NPs (8.56 × 10(3)-1.09 × 10(6) vs. 3.43 × 10(4)-2.73 × 10(5)cells/ml). Resonance peak shift could distinguish RPE-1 from MCF-7 cells on both Au NPs. RPE-1 cells consistently displayed larger resonance peak shifts compared to MCF-7 cells until the detection became saturated at higher concentration. For both types of cells, higher concentration sensitivity in the range of ~10(4)-10(6)cells/ml was observed on 500 nm compared to 60 nm Au NPs. Our results show that cells on Au NPs can be detected in a large range and at low concentration. Optimal cell sensing can be achieved by altering the dimensions of Au NPs according to different cell characteristics and concentrations.

摘要

利用局域表面等离子体共振(LSPR)效应来区分玻璃基底上有序排列的金纳米粒子(Au NPs)上的细胞浓度。与乳腺癌 MCF-7 细胞相比,我们比较了具有更扁平形状和更高融合度的人源性视网膜色素上皮 RPE-1 细胞。采用纳米球光刻法形成平均直径为 500nm 和 60nm 的 Au NPs,以比较细胞检测范围、共振峰位移和细胞浓度灵敏度。与 60nm Au NPs 相比,较大的 500nm Au NPs 上检测到的细胞浓度范围更大(8.56×10(3)-1.09×10(6) vs. 3.43×10(4)-2.73×10(5)cells/ml)。共振峰位移可以区分 Au NPs 上的 RPE-1 和 MCF-7 细胞。与 MCF-7 细胞相比,RPE-1 细胞的共振峰位移始终更大,直到在更高浓度下检测达到饱和。对于这两种类型的细胞,在 500nm Au NPs 上观察到的 ~10(4)-10(6)cells/ml 范围内的浓度灵敏度更高,而在 60nm Au NPs 上的灵敏度较低。我们的结果表明,可以在较大的浓度范围内和较低的浓度下检测 Au NPs 上的细胞。通过根据不同的细胞特性和浓度改变 Au NPs 的尺寸,可以实现最佳的细胞感应。

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