A sample-to-answer quantitative platform for point-of-care testing of biochemical markers in whole blood

•A sample-to-answer quantitative platform was designed with good portability, low cost, rapidity, and high sensitivity.•Our platform achieved sample-to-answer total bilirubin and direct bilirubin quantitation in whole blood for the first time.•Our platform exhibited a good consistency with the autom...

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Veröffentlicht in:Sensors and actuators. B, Chemical Chemical, 2020-04, Vol.308, p.127750, Article 127750
Hauptverfasser: Xu, Huan, Xia, Anyue, Luo, Jie, Gao, Mingxuan, Liao, Renkuan, Li, Fake, Zhong, Qiu, Zhang, Wenqing, Wang, Yang, Cui, Jinhui, Fu, Weiling, Chang, Kai, Gan, Mingzhe, Jiang, Wenbin, Chen, Ming
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Sprache:eng
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Zusammenfassung:•A sample-to-answer quantitative platform was designed with good portability, low cost, rapidity, and high sensitivity.•Our platform achieved sample-to-answer total bilirubin and direct bilirubin quantitation in whole blood for the first time.•Our platform exhibited a good consistency with the automatic clinical chemistry analyzer. Point-of-care quantitative detection of biochemical markers has broad applications in resource-limited settings. However, current challenges including difficulty in sample preparation and limitation in result quantitation make point-of-care detection platforms failed to achieve fully sample-to-answer detection or meet the clinical quantitative demands. Here, we developed a novel point-of-care platform to realize fully sample-to-answer biochemical marker quantitation in whole blood. Our platform integrated a plasma separation module and a detection module. The plasma separation module contained a plasma separation strip could rapidly separate the plasma from whole blood samples by lateral flow. The detection module generated a colorimetric signal which could be quantified by the smartphone ambient light sensor (ALS) in an equipment-free manner. As a proof-of-concept, two hepatobiliary disease-associated markers, total bilirubin (TBil) and direct bilirubin (DBil), were detected from whole blood to quantitative result. The quantitative performance for clinical samples was highly consistent with the well-established clinical chemistry analyzer. Our platform exhibited remarkable advantages of significant portability (< 40 g), low cost (< $5), rapidity (< 5 min), instrument-free, high sensitivity (< 1 μM), and accuracy (89.5 % for TBil, 94.7 % for DBil), which showed up a great potential for biochemical markers detection in resource-limited settings.
ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2020.127750