Please use this identifier to cite or link to this item: http://ir.swu.ac.th/jspui/handle/123456789/13855
Title: The detection of tuberculosis by loop-mediated isothermal amplification (LAMP) combined with a lateral flow dipstick
Authors: Kaewphinit T.
Santiwatanakul S.
Chansiri K.
Keywords: Developing countries
Electrophoresis
Isotherms
Constant temperature
Fluorescein isothiocyanate
Infectious disease
Lateral flow dipsticks
Loop mediated isothermal amplifications
Mycobacterium tuberculosis
Nested polymerase chain reaction
Toxic substances
Polymerase chain reaction
Issue Date: 2014
Abstract: Tuberculosis (TB) is an airborne infectious disease caused by the bacterium Mycobacterium Tuberculosis (MTB) and is a persistent problem in developing countries. Present methods for its detection include normal or nested Polymerase Chain Reaction (PCR) followed by electrophoresis, real-time PCR, Ziehl- Neelsen staining, and culture assay. These techniques entail various disadvantages such as high cost, long assay time and use of toxic substances. Novel loop-mediated isothermal amplification (LAMP) permits DNA to be amplified rapidly under constant temperature. The combination of LAMP and chromatographic Lateral Flow Dipstick (LAMP-LFD) by using biotinylated LAMP amplicon hybridized with Fluorescein Isothiocyanate (FITC)-labeled probes are allowed to detect MTB without electrophoresis and interpreted within 3-5 min. LAMP-LFD is as highly sensitive as PCR-electrophoresis method. Based on its sensitivity, specificity, rapidity, cost effectiveness, ease of use, and convenience, LAMP-LFD could be suitable for use in early MTB detection. © 2015 by IGI Global. All rights reserved.
URI: https://www.scopus.com/inward/record.uri?eid=2-s2.0-84945397281&doi=10.4018%2f978-1-4666-6363-3.ch013&partnerID=40&md5=a01a43c055c309c6d8f2a3c02fc4dead
http://ir.swu.ac.th/jspui/handle/123456789/13855
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