纳米传感器
微流控
全血
生物传感器
生物标志物
探测器
循环肿瘤细胞
纳米技术
注意事项
医学
材料科学
实验室晶片
计算机科学
生物医学工程
癌症
色谱法
化学
生物
病理
免疫学
电信
生物化学
转移
遗传学
作者
Eric Stern,Aleksandar Vacic,Nitin K. Rajan,Jason M. Criscione,Jason Y. Park,B. Ilic,David Mooney,Mark A. Reed,Tarek M. Fahmy
标识
DOI:10.1038/nnano.2009.353
摘要
Label-free nanosensors can detect disease markers to provide point-of-care diagnosis that is low-cost, rapid, specific and sensitive1,2,3,4,5,6,7,8,9,10,11,12,13. However, detecting these biomarkers in physiological fluid samples is difficult because of problems such as biofouling and non-specific binding, and the resulting need to use purified buffers greatly reduces the clinical relevance of these sensors. Here, we overcome this limitation by using distinct components within the sensor to perform purification and detection. A microfluidic purification chip simultaneously captures multiple biomarkers from blood samples and releases them, after washing, into purified buffer for sensing by a silicon nanoribbon detector. This two-stage approach isolates the detector from the complex environment of whole blood, and reduces its minimum required sensitivity by effectively pre-concentrating the biomarkers. We show specific and quantitative detection of two model cancer antigens from a 10 µl sample of whole blood in less than 20 min. This study marks the first use of label-free nanosensors with physiological solutions, positioning this technology for rapid translation to clinical settings. A biosensor containing a microfluidic purification chip that supplies a downstream nanoribbon-detector can detect disease biomarkers in samples of whole blood.
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