4.5 Article

RPA using a multiplexed cartridge for low cost point of care diagnostics in the field

Journal

ANALYTICAL BIOCHEMISTRY
Volume 547, Issue -, Pages 84-88

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ab.2018.02.010

Keywords

RPA; Point of care; DNA extraction; Isothermal amplification; Multiplexed cartridge

Funding

  1. UKCRC Translational Infection Research (TIR) Initiative - Medical Research Council [G0901608]
  2. Biotechnology and Biological Sciences Research Council
  3. National Institute for Health Research on behalf of the Department of Health
  4. Chief Scientist Office of the Scottish Government Health Directorates
  5. Wellcome Trust
  6. Medical Research Council [G0901608] Funding Source: researchfish
  7. MRC [G0901608] Funding Source: UKRI

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A point of care device utilising Lab-on-a-Chip technologies that is applicable for biological pathogens was designed, fabricated and tested showing sample in to answer out capabilities. The purpose of the design was to develop a cartridge with the capability to perform nucleic acid extraction and purification from a sample using a chitosan membrane at an acidic pH. Waste was stored within the cartridge with the use of sodium polyacrylate to solidify or gelate the sample in a single chamber. Nucleic acid elution was conducted using the RPA amplification reagents (alkaline pH). Passive valves were used to regulate the fluid flow and a multiplexer was designed to distribute the fluid into six microchambers for amplification reactions. Cartridges were produced using soft lithography of silicone from 3D printed moulds, bonded to glass substrates. The isothermal technique, RPA is employed for amplification. This paper shows the results from two separate experiments: the first using the RPA control nucleic acid, the second showing successful amplification from Chlamydia Trachomatis. Endpoint analysis conducted for the RPA analysis was gel electrophoresis that showed 143 base pair DNA was amplified successfully for positive samples whilst negative samples did not show amplification. End point analysis for Chlamydia Trachomatis samples was fluorescence detection that showed successful detection of 1 copy/4 and 10 copies/4 spiked in a MES buffer.

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