3.9 Article

Porous Silicon-Based Aptasensors: Toward Cancer Protein Biomarker Detection

期刊

ACS MEASUREMENT SCIENCE AU
卷 1, 期 2, 页码 82-94

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsmeasuresciau.1c00019

关键词

Optical Biosensor; PorousSilicon; Aptamer; Anterior Gradient Homologue-2; Cancer Biomarker; Label-Free; Microfluidics; Isotachophoresis

资金

  1. Israel Science Foundation [704/17]
  2. German Research Foundation [SCHE 279/32-1]
  3. National Institutes of Health (NIH) [R21AI156693]
  4. Australian Technion Society
  5. Lorry I. Lokey Center for Life Science and Engineering

向作者/读者索取更多资源

AGR2 protein serves as an attractive biomarker for various types of cancer, including pancreatic cancer, where it is secreted to the pancreatic juice by premalignant lesions. A biosensor based on anti-AGR2 aptamers on nanostructured porous silicon thin film enables sensitive and selective detection of AGR2, with potential for early cancer diagnosis. Various strategies, including isotachophoresis and signal processing techniques, have been employed to enhance the biosensor sensitivity and achieve a limit of detection of 15 nM.
The anterior gradienthomologue-2 (AGR2) protein is an attractivebiomarker for various types of cancer. In pancreatic cancer, it issecreted to the pancreatic juice by premalignant lesions, which wouldbe an ideal stage for diagnosis. Thus, designing assays for the sensitivedetection of AGR2 would be highly valuable for the potential earlydiagnosis of pancreatic and other types of cancer. Herein, we presenta biosensor for label-free AGR2 detection and investigate approachesfor enhancing the aptasensor sensitivity by accelerating the targetmass transfer rate and reducing the system noise. The biosensor isbased on a nanostructured porous silicon thin film that is decoratedwith anti-AGR2 aptamers, where real-time monitoring of the reflectancechanges enables the detection and quantification of AGR2, as wellas the study of the diffusion and target-aptamer binding kinetics.The aptasensor is highly selective for AGR2 and can detect the proteinin simulated pancreatic juice, where its concentration is outnumberedby orders of magnitude by numerous proteins. The aptasensor'sanalytical performance is characterized with a linear detection rangeof 0.05-2 mg mL(-1), an apparent dissociationconstant of 21 & PLUSMN; 1 & mu;M, and a limit of detection of 9.2 & mu;g mL(-1) (0.2 & mu;M), which is attributedto mass transfer limitations. To improve the latter, we applied differentstrategies to increase the diffusion flux to and within the nanostructure,such as the application of isotachophoresis for the preconcentrationof AGR2 on the aptasensor, mixing, or integration with microchannels.By combining these approaches with a new signal processing techniquethat employs Morlet wavelet filtering and phase analysis, we achievea limit of detection of 15 nM without compromising the biosensor'sselectivity and specificity.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

3.9
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据