In-Plane Parallel Scanning: A Microarray Technology for Point-of-Care Testing

被引:17
作者
Duer, Reuven [1 ]
Lund, Russell [1 ]
Tanaka, Richard [1 ]
Christensen, Douglas A. [2 ]
Herron, James N. [2 ,3 ]
机构
[1] PLC Diagnost Inc, Thousand Oaks, CA 91360 USA
[2] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
关键词
PROTEIN MICROARRAYS; OPTICAL BIOSENSORS; OVARIAN; IMMUNOSENSOR; IMMUNOASSAYS; IMMOBILIZATION; PERFORMANCE; BIOMARKERS; PLATFORM; SENSORS;
D O I
10.1021/ac101571b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new microarray technology is described for rapid, inexpensive, multiplex diagnostics assays. Referred to as "in-plane parallel scanning" (IPPS), this technology replaces expensive laser scanning with a grid of 100-mu m-wide waveguides embedded in the chip's substrate, enabling real-time quantification of molecular complex formation on the chip's surface. Compared to conventional microarray technology, IPPS has advantages of shorter assay time and lower instrument cost and complexity so that the platform can potentially be used in point-of-care (POC) settings. Two different chip formats are described: a low-density microarray with 10 sensing wells (IPPS-10) and a medium-density one with 100 sensing wells (IPPS-100). Performance was evaluated in two different proof-of-principle immunoassays: interleukin-1 beta (IL-1 beta) and Clostridium difficile toxin A. The two assays gave similar limits of detection of 0.67 and 0.94 pM, respectively. A saturation kinetics model described the sensor response with apparent dissociation constants of 511 pM for IL-1 beta and 6.4.7 nM for C. diflicile toxin A toxoid. The multiplexing capabilities of the IPPS technology were also demonstrated in a multiplex assay for both analytes on the same IPPS-10 chip. Based on these results, the IPPS technology holds promise for translating diagnostic microarrays into near-patient environments.
引用
收藏
页码:8856 / 8865
页数:10
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