1993
DOI: 10.1021/jf00029a031
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Reusable fiber optic immunosensor for rapid detection of imazethapyr herbicide

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Cited by 43 publications
(21 citation statements)
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“…Finally, we anticipate that the optimized displacement method (coupled with QCM) and model for TNT detection can be modified for the detection of other molecules of interest (e.g. imazethapyr [49] or cocaine [50]), provided that an antibody specific for the molecule of interest, and displaying cross reactivity for analogous molecules that typically limit its detection, has been isolated or engineered.…”
Section: Discussionmentioning
confidence: 99%
“…Finally, we anticipate that the optimized displacement method (coupled with QCM) and model for TNT detection can be modified for the detection of other molecules of interest (e.g. imazethapyr [49] or cocaine [50]), provided that an antibody specific for the molecule of interest, and displaying cross reactivity for analogous molecules that typically limit its detection, has been isolated or engineered.…”
Section: Discussionmentioning
confidence: 99%
“…The observed bulk concentration limit of detection for the biotin/streptavidin bioassay is 15 nM, which is on the order of the LOD reported for several de-clad fiber fluorescence sensors. (Anis et al, 1993;Devine et al, 1995;Eenink et al, 1990;Graham et al, 1992;McCormack et al, 1997;Oroszlan et al, 1993;Pandey & Weetall, 1995;Shriver-Lake et al, 1995;Sutherland et al, 1984) However, the measured pathlength of the FOC is only ~ 24 mm for this device compared to the ~ 60 mm pathlength of most cylindrical core de-clad fiber sensor platforms. The de-clad fiber sensor platforms require large fiber cores (~ 600 µm) with low modal surface interaction to increase mechanical strength, and therefore, a long interaction length is necessary.…”
Section: Bsa-biotin/streptavidin-cy Bioassay On the Planar Fiber Optimentioning
confidence: 95%
“…The pioneering research utilizing a de-clad quartz fiber to collect back-coupled fluorescence from immobilized biomolecules was presented by Sutherland et.al, Andrade et.al, and Glass et.al. Biosensors based on receptor proteins (Garden et al, 2004;Rogers et al, 1991;Rogers et al, 1989), antibody-antigen interactions (Anis et al, 1993;Bier et al, 1992;Devine et al, 1995;Eenink et al, 1990;McCormack et al, 1997;Oroszlan et al, 1993;Shriver-Lake et al, 1995;Toppozada et al, 1997;Walczak et al, 1992), sandwich immunoassay (Geng et al, 2006;Kapoor et al, 2004), and oligonucleotides (Abel et al, 1996;Graham et al, 1992;Pandey & Weetall, 1995) have been presented employing the de-clad fiber geometry. However, the declad fiber architecture is limited by the fragile nature of the fiber platform and inefficient fluorescence back-coupling due to the sharp V-number mismatch.…”
Section: Fiber Optic Based Fluorescence Sensorsmentioning
confidence: 99%
“…Enzymatic labels used in immunosensor devices are usually ox i d o reductases such as peroxidase (HRP) or hy d ro ly t i c enzymes such as alkaline phosphatase. Immunosensors can be divided into four classes, depending on the transducer e m p l oye d : p i e zo e l e c t ric [12][13][14], optical [15][16][17], e l e c t rochemical [18,19], or thermometric. The immobilized sensing element can be either an antibody (AB) or an antigen (AG) wich can be chemically modified (hapten).…”
Section: Immunosensorsmentioning
confidence: 99%