TY - JOUR
T1 - RPA using a multiplexed cartridge for low cost point of care diagnostics in the field
AU - Ereku, Luck Tosan
AU - Mackay, Ruth E
AU - Craw, Pascal
AU - Naveenathayalan, Angel
AU - Stead, Thomas
AU - Branavan, Manorharanehru
AU - Balachandran, Wamadeva
N1 - Crown Copyright © 2018. Published by Elsevier Inc. All rights reserved.
PY - 2018/4/15
Y1 - 2018/4/15
N2 - 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/μL and 10 copies/μL spiked in a MES buffer.
AB - 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/μL and 10 copies/μL spiked in a MES buffer.
KW - Chitosan/chemistry
KW - Chlamydia trachomatis/genetics
KW - Hydrogen-Ion Concentration
KW - Lab-On-A-Chip Devices
KW - Membranes, Artificial
KW - Nucleic Acid Amplification Techniques/instrumentation
KW - Nucleic Acids/analysis
KW - Point-of-Care Systems
U2 - 10.1016/j.ab.2018.02.010
DO - 10.1016/j.ab.2018.02.010
M3 - Article
C2 - 29447855
SN - 0003-2697
VL - 547
SP - 84
EP - 88
JO - Analytical Biochemistry
JF - Analytical Biochemistry
ER -