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使用有序金纳米蜂窝阵列通过表面增强拉曼散射对癌症相关生物标志物进行多重测定。

Multiplexing determination of cancer-associated biomarkers by surface-enhanced Raman scattering using ordered gold nanohoneycomb arrays.

作者信息

Li Li, Liu Chang, Cao Xiaowei, Tan Lianqiao, Lu Wenbo

机构信息

State Key Laboratory of Bioelectronics, School of Biological Science & Medical Engineering, Southeast University, Nanjing 210096, PR China.

出版信息

Bioanalysis. 2017 Oct;9(20):1561-1572. doi: 10.4155/bio-2016-0237. Epub 2017 Oct 26.

Abstract

AIM

Here, a multiplex surface-enhanced Raman scattering (SERS) based assay for simultaneous quantitation of carcinoembryonic antigen (CEA) and α-fetoprotein (AFP) was developed.

METHODS

SERS tags of nanostars and SERS substrates of nanobowl arrays were functionalized with labeling and capturing antibodies, respectively. In presence of antigens, SERS tags, antigens and SERS substrates formed sandwich structure.

RESULTS

The SERS-based technique showed a wide linear range from 0.5 to 100 ng/ml and detection limits were 0.41 and 0.35 ng/ml for CEA and AFP in phosphate-buffered saline buffer, respectively. Analysis results of clinical serum samples using this technique were similar to that shown in phosphate-buffered saline buffer. The LODs were 0.44 and 0.40 ng/ml for CEA and AFP, respectively. Conclusion: The precision and stability of this analysis technique were satisfactory, meanwhile, no obvious cross-reactivity could be found. What's more, it also suggested that this novel multiplex SERS-based technique could be a simple, specific, reliable, sensitive and multiplexed tool for important diagnostic and prognostic applications.

摘要

目的

在此,开发了一种基于多重表面增强拉曼散射(SERS)的检测方法,用于同时定量癌胚抗原(CEA)和甲胎蛋白(AFP)。

方法

分别用标记抗体和捕获抗体对纳米星的SERS标签和纳米碗阵列的SERS底物进行功能化。在存在抗原的情况下,SERS标签、抗原和SERS底物形成夹心结构。

结果

基于SERS的技术在0.5至100 ng/ml范围内显示出较宽的线性范围,在磷酸盐缓冲盐溶液中,CEA和AFP的检测限分别为0.41和0.35 ng/ml。使用该技术对临床血清样本的分析结果与在磷酸盐缓冲盐溶液中显示的结果相似。CEA和AFP的检测限分别为0.44和0.40 ng/ml。结论:该分析技术的精密度和稳定性令人满意,同时未发现明显的交叉反应性。此外,这也表明这种基于SERS的新型多重技术可以成为用于重要诊断和预后应用的简单、特异、可靠、灵敏且多重的工具。

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