A siphonage flow and thread-based low-cost platform enables quantitative and sensitive assays. Issue 2 (18th November 2014)

• Record Type: Journal Article
• Authors: Lu, Fang; Mao, Qingqing; Wu, Rui; Zhang, Shenghai; Du, Jianxiu; Lv, Jiagen
• Is Part Of: Lab on a chip. Volume 15:Issue 2(2015)
• Page Start: 495
• Page End: 503
• Publication Date: 2014-11-18
• Subjects: Miniature electronic equipment -- Periodicals; Combinatorial chemistry -- Periodicals; Biotechnology -- Periodicals; 543.0813
• DOI: 10.1039/c4lc01248h
• Languages: English
• ISSNs: 1473-0197

Abstract

Abstract : A pump-free siphonage flow microfluidic platform is demonstrated for quantitative and sensitive detection in the form of a thread-based device and sensor. Abstract : For pump-free, material abundant, portable, and easy-to-operate low-cost microfluidics, a siphonage flow microfluidic thread-based analytical device (S-μTAD) platform enabling quantitative and sensitive assays was designed. Renewable and continuous siphonage flow allowed replicate sampling and detection on one channel/device, obviating some possible inconsistencies among channels or devices. Y-shaped channels were fabricated with polyester cotton blend thread, due to its greater chemiluminescent sensitivity in comparison with that of cotton and polyester threads. S-μTAD sensors for glucose and uric acid were fabricated by using oxidase-immobilized cotton thread as the sample arm of the channels. The acceptable reproducibility and high sensitivity, demonstrated by the relative standard deviations of less than 5% in all cases and the detection limits of 4 × 10 −8 mol L −1 for hydrogen peroxide, 1 × 10 −7 mol L −1 for glucose, and 3 × 10 −6 mol L −1 for uric acid, demonstrated the feasibility of the S-μTAD for quantitative assays. Good agreements between S-μTAD/sensor results and hospital results for blood glucose and uric acid assays indicated the capability of S-μTAD/sensors for the analysis of real samples. These findings proved the utility of siphonage for low-cost microfluidics and the suitability of our S-μTAD design for quantitative assays.