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1.
PLoS One ; 14(1): e0210286, 2019.
Article in English | MEDLINE | ID: mdl-30650158

ABSTRACT

Insurmountable detection challenges will impede the development of many of the next-generation of lab-on-a-chip devices (e.g., point-of-care and real-time health monitors). Here we present the first membrane-based, microfluidic sample preconcentration method that is continuous, quantifiable, simple, and capable of working with any analyte. Forward osmosis rapidly concentrates analytes by removing water from a stream of sample fluid. 10-100X preconcentration is possible in mere minutes. This requires careful selection of the semi-permeable membrane and draw molecule; therefore, the osmosis performance of several classes of membranes and draw molecules were systematically optimized. Proof-of-concept preconcentration devices were characterized based on their concentration ability and fouling resistance. In-silico theoretical modeling predicts the experimental findings and provides an engineering toolkit for future designs. With this toolkit, inexpensive ready-for-manufacturing prototypes were also developed. These devices provide broad-spectrum detection improvements across many analytes and sensing modalities, enabling next-generation lab-on-a-chip devices.


Subject(s)
Lab-On-A-Chip Devices , Animals , Cattle , Computer Simulation , Equipment Design , Glucose/analysis , Humans , Membranes, Artificial , Osmosis , Porosity , Serum Albumin, Bovine/analysis
2.
Lab Chip ; 19(1): 178-185, 2018 12 18.
Article in English | MEDLINE | ID: mdl-30525141

ABSTRACT

Microfluidic flow rate sensors have constraints in both detection limits and dynamic range, and are not often easily integrated into lab-on-chip or wearable sensing systems. We constructed a flow rate sensor that easily couples to the outlet of a microfluidic channel, and measures the flow rate by temporarily shorting periodic droplets generated between two electrodes. The device was tested in a dynamic range as low as 25 nL min-1 and as high as 900 000 nL min-1 (36 000× range). It was tested to continuously operate up to ∼200 hours. The device is also simple to fabricate, requiring inexpensive parts, and is small enough to be integrated into wearable devices. The required input pressure is as low as 370 Pascals. An ultra-low flow rate application was demonstrated for wearable sweat biosensing where sweat generation rates (nL min-1 per gland) were accurately measured in human subjects. The digital nanoliter device provides real-time flow rates for sweat rates and may have other applications for low flow rates in microfluidic devices.


Subject(s)
Clinical Chemistry Tests/instrumentation , Microfluidic Analytical Techniques/instrumentation , Sweat/chemistry , Wearable Electronic Devices , Electrodes , Equipment Design , Female , Humans , Limit of Detection , Linear Models , Male , Monitoring, Ambulatory , Reproducibility of Results
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