A Microfluidic Paper-Based Origami Nanobiosensor for Label-Free, Ultrasensitive Immunoassays

Adv Healthc Mater. 2016 Jun;5(11):1326-35. doi: 10.1002/adhm.201501038. Epub 2016 Apr 28.

Abstract

Microfluidic paper-based analytical devices (μPADs) represent a promising platform technology for point-of-care diagnosis. Highly sensitive, rapid, and easy-to-perform immunoassays implemented on μPADs are desirable to fulfill the promise of the μPAD technology. This article reports the first microfluidic paper-based origami nanobiosensor (origami μPAD), which integrates zinc oxide nanowires (ZnO NWs) and electrochemical impedance spectroscopy (EIS) biosensing mechanism, for label-free, ultrasensitive immunoassays. The EIS mechanism features simple and label-free assay operations which take less than 25 min to be finished, while the ZnO NWs allow covalent bonding for immobilizing probe proteins and improve the biosensing performance with such features as high surface-area-to-volume ratios and high sensitivity to surface binding. The calibration of the device reveals an ultralow limit of detection (LOD) of 60 fg mL(-1) (>100 times lower than those of existing μPADs) for rabbit immunoglobulin G in phosphate-buffered saline. The detection of human immunodeficiency virus p24 antigen in human serum with a low LOD of 300 fg mL(-1) (>33 times lower than that of a commercial p24 antigen test kit) is also demonstrated. This novel μPAD design offers ultrahigh sensitivity, short assay time, and ease of operation, and thus possesses significant potential for low-cost, rapid molecular diagnosis of early-stage diseases.

Keywords: biosensors; disease diagnosis; electrochemical impedance spectroscopy; human immunodeficiency virus; paper-based microfluidics; zinc oxide nanowires.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biosensing Techniques
  • Calibration
  • Early Diagnosis
  • HIV / immunology
  • HIV Infections / diagnosis
  • HIV Infections / immunology
  • HIV Infections / virology
  • Humans
  • Immunoassay / methods*
  • Microfluidic Analytical Techniques / methods*
  • Microfluidics / methods*
  • Paper
  • Sensitivity and Specificity