Please use this identifier to cite or link to this item: http://bura.brunel.ac.uk/handle/2438/16622
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dc.contributor.authorEreku, LT-
dc.contributor.authorMackay, RE-
dc.contributor.authorCraw, P-
dc.contributor.authorNaveenathayalan, A-
dc.contributor.authorStead, T-
dc.contributor.authorBranavan, M-
dc.contributor.authorBalachandran, W-
dc.date.accessioned2018-07-23T11:45:54Z-
dc.date.available2018-02-12-
dc.date.available2018-07-23T11:45:54Z-
dc.date.issued2018-
dc.identifier.citationAnalytical Biochemistry, 2018, 547 pp. 84 - 88en_US
dc.identifier.issn0003-2697-
dc.identifier.issnhttp://dx.doi.org/10.1016/j.ab.2018.02.010-
dc.identifier.urihttp://bura.brunel.ac.uk/handle/2438/16622-
dc.description.abstractA 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.en_US
dc.description.sponsorshipMedical Research Councilen_US
dc.format.extent84 - 88-
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectRPAen_US
dc.subjectPoint of careen_US
dc.subjectDNA extractionen_US
dc.subjectIsothermal amplificationen_US
dc.subjectMultiplexed cartridgeen_US
dc.titleRPA using a multiplexed cartridge for low cost point of care diagnostics in the fielden_US
dc.typeArticleen_US
dc.identifier.doihttp://dx.doi.org/10.1016/j.ab.2018.02.010-
dc.relation.isPartOfAnalytical Biochemistry-
pubs.publication-statusPublished-
pubs.volume547-
Appears in Collections:Dept of Mechanical and Aerospace Engineering Research Papers

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