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

被引:18
作者
Ereku, Luck Tosan [1 ]
Mackay, Ruth E. [2 ]
Craw, Pascal [3 ]
Naveenathayalan, Angel [2 ]
Stead, Thomas [1 ]
Branavan, Manorharanehru [1 ]
Balachandran, Wamadeva [1 ]
机构
[1] Brunel Univ London, CEDPS, Ctr Elect Syst Res Elect & Comp Engn, Kingston Lane, Uxbridge UB8 3PH, Middx, England
[2] Brunel Univ London, CEDPS, Mech Aerosp & Civil Engn, Kingston Lane, Uxbridge UB8 3PH, Middx, England
[3] CSIRO, Oceans & Atmosphere Flagship, Hobart, Tas 7001, Australia
基金
英国医学研究理事会; 英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
RPA; Point of care; DNA extraction; Isothermal amplification; Multiplexed cartridge; NUCLEIC-ACID AMPLIFICATION; RECOMBINASE POLYMERASE AMPLIFICATION; TECHNOLOGIES; PLATFORM;
D O I
10.1016/j.ab.2018.02.010
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:84 / 88
页数:5
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