Your browser doesn't support javascript.
loading
An electricity- and instrument-free infectious disease sensor based on a 3D origami paper-based analytical device.
Chen, Chung-An; Yuan, Hao; Chen, Chiao-Wen; Chien, Yuh-Shiuan; Sheng, Wang-Huei; Chen, Chien-Fu.
Affiliation
  • Chen CA; Institute of Applied Mechanics, National Taiwan University, Taipei 106, Taiwan. stevechen@ntu.edu.tw.
  • Yuan H; Institute of Applied Mechanics, National Taiwan University, Taipei 106, Taiwan. stevechen@ntu.edu.tw.
  • Chen CW; Institute of Applied Mechanics, National Taiwan University, Taipei 106, Taiwan. stevechen@ntu.edu.tw.
  • Chien YS; Institute of Applied Mechanics, National Taiwan University, Taipei 106, Taiwan. stevechen@ntu.edu.tw.
  • Sheng WH; Division of Infectious Diseases, Department of Internal Medicine, National Taiwan University Hospital, Taipei 100, Taiwan.
  • Chen CF; Institute of Applied Mechanics, National Taiwan University, Taipei 106, Taiwan. stevechen@ntu.edu.tw.
Lab Chip ; 21(10): 1908-1915, 2021 05 18.
Article in En | MEDLINE | ID: mdl-34008628
ABSTRACT
Infectious diseases cause millions of deaths annually in the developing world. Recently, microfluidic paper-based analytical devices (µPADs) have been developed to diagnose such diseases, as these tests are low cost, biocompatible, and simple to fabricate. However, current µPADs are difficult to use in resource-limited areas due to their reliance on external instrumentation to measure and analyze the test results. In this work, we propose an electricity and external instrumentation-free µPAD sensor based on the colorimetric enzyme-linked immunosorbent assay (ELISA) for the diagnosis of infectious disease (3D-tPADs). Designed based on the principle of origami, the proposed µPAD enables the sequential steps of the colorimetric ELISA test to be completed in just ∼10 min. In addition, in order to obtain an accurate ELISA result without using any instrument, we have integrated an electricity-free "timer" within the µPAD that can be controlled by the buffer viscosity and fluid path volume to indicate the appropriate times for washing and color development steps, which can avoid false positive or false negative results caused by an extended or shortened amount of washing and development times. Due to the low background noise and high positive signal intensity of the µPAD, positive and negative detection results can be distinguished by just the naked eye. Furthermore, the ELISA result can be semi-quantified by comparing the results shown on the µPAD with a color chart diagram with a detection limit of HIV type 1(HIV-1) p24 antigen as low as 0.03 ng mL-1. These results demonstrate the proposed sensor can perform infectious disease diagnosis without external instrumentation or electricity, extending the application of the µPAD test for on-site detection and use in resource-limited settings.
Subject(s)

Full text: 1 Collection: 01-internacional Health context: 2_ODS3 Database: MEDLINE Main subject: Communicable Diseases / Microfluidic Analytical Techniques Limits: Humans Language: En Journal: Lab Chip Year: 2021 Document type: Article

Full text: 1 Collection: 01-internacional Health context: 2_ODS3 Database: MEDLINE Main subject: Communicable Diseases / Microfluidic Analytical Techniques Limits: Humans Language: En Journal: Lab Chip Year: 2021 Document type: Article