2011
DOI: 10.1016/j.bios.2011.04.035
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Paper based point-of-care testing disc for multiplex whole cell bacteria analysis

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Cited by 192 publications
(93 citation statements)
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“…1.2c), adopting folding techniques [119] and microplate paper platforms [120]. NP-based detection has been demonstrated with metabolites [109,111,113,117,121,147], bacterial agents [112] in disease diagnosis such as HIV [119], malaria [115], tuberculosis [120] and in environmental monitoring [114,118]. To multiplex the assay, monodisperse latex can be coupled with fluorescent and coloured dyes, and para/magnetic components.…”
Section: Colloidal Nanoparticles (Nps)mentioning
confidence: 99%
See 1 more Smart Citation
“…1.2c), adopting folding techniques [119] and microplate paper platforms [120]. NP-based detection has been demonstrated with metabolites [109,111,113,117,121,147], bacterial agents [112] in disease diagnosis such as HIV [119], malaria [115], tuberculosis [120] and in environmental monitoring [114,118]. To multiplex the assay, monodisperse latex can be coupled with fluorescent and coloured dyes, and para/magnetic components.…”
Section: Colloidal Nanoparticles (Nps)mentioning
confidence: 99%
“…These devices were demonstrated by using porous materials such as nitrocellulose and cellulose depending on the sensing application. Other 2D paper networks involved integrating the inlets of a number of lateral flow assays [112] (Fig. 1.2c), adopting folding techniques [119] and microplate paper platforms [120].…”
Section: Colloidal Nanoparticles (Nps)mentioning
confidence: 99%
“…[1][2][3][4][5][6][7][8][9] Among them, paper-based POC devices are a special category due to the advantages of being simple, rapid, on-site, and cost-effective; they have been widely used in home health care and medical testing, [10][11][12] even environmental monitoring. [13][14][15] The lateral flow immunochromatographic assay, also called lateral flow test, is one of the simplest and most popular formats of paper-based POC devices and can be used to detect specific substances, including small molecules, [15][16][17][18] large proteins, [19][20][21] and even whole pathogens, 10 in a sample by using an immunological reaction. However, most of these tests are based on qualitative colorimetry, which is not sufficient in many cases.…”
Section: Introductionmentioning
confidence: 99%
“…Owing to its capability of rapid, label-free, cost-effective detection of molecular interaction with kinetics information [1][2][3], surface plasmon resonance (SPR)-based optical sensors have been demonstrated in the past decade to be a powerful tool not only for the measurement of molecular binding kinetics and binding affinity, but also for quantitative analysis of genetic and proteomic biomarkers. The detection of analytes by SPR relies on the successful immobilization of biomolecular recognition probes, such as antibody, aptamer and molecular imprinted polymer at the metal-media interface [4][5][6].…”
mentioning
confidence: 99%