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1.
Biosens Bioelectron ; 14(10-11): 785-94, 2000 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-10945453

RESUMEN

A fluorescence-based biosensor has been developed for simultaneous analysis of multiple samples for multiple biohazardous agents. A patterned array of antibodies immobilized on the surface of a planar waveguide is used to capture antigen present in samples; bound analyte is then quantified by means of fluorescent tracer antibodies. Upon excitation of the fluorophore by a small diode laser, a CCD camera detects the pattern of fluorescent antibody:antigen complexes on the waveguide surface. Image analysis software correlates the position of fluorescent signals with the identity of the analyte. This array biosensor has been used to detect toxins, toxoids, and killed or non-pathogenic (vaccine) strains of pathogenic bacteria. Limits of detection in the mid-ng/ml range (toxins and toxoids) and in the 10(3)-10(6) cfu/ml range (bacterial analytes) were achieved with a facile 14-min off-line assay. In addition, a fluidics and imaging system has been developed which allows automated detection of staphylococcal enterotoxin B (SEB) in the low ng/ml range.


Asunto(s)
Técnicas Biosensibles , Sustancias Peligrosas/análisis , Fluorescencia , Sensibilidad y Especificidad
2.
Anal Biochem ; 281(1): 123-33, 2000 May 15.
Artículo en Inglés | MEDLINE | ID: mdl-10847619

RESUMEN

A rapid assay for cholera toxin (CT) has been developed using a fluorescence-based biosensor. This sensor was capable of analyzing six samples simultaneously for CT in 20 min with few manipulations required by the operator. The biochemical assays utilized a ganglioside-"capture" format: ganglioside GM1, utilized for capture of analyte, was immobilized in discrete locations on the surface of the optical waveguide. Binding of CT to immobilized GM1 was demonstrated with direct assays (using fluorescently labeled CT) and "sandwich" immunoassays (using fluorescently labeled tracer antibodies). Limits of detection for CT were 200 ng/ml in direct assays and 40 ng/ml and 1 microg/ml in sandwich-type assays performed using rabbit and goat tracer antibodies. Binding of CT to other glycolipid capture reagents was also observed. While significant CT binding was observed to loci patterned with GD1b, Gb3, and Gb4, CT did not bind significantly to immobilized GT1b at the concentrations tested. This is the first description of such a non-antibody-based recognition system in a multi-specific planar array sensor.


Asunto(s)
Técnicas Biosensibles/métodos , Toxina del Cólera/análisis , Gangliósidos/análisis , Anticuerpos Monoclonales/inmunología , Toxina del Cólera/inmunología , Ensayo de Inmunoadsorción Enzimática/métodos , Gangliósidos/inmunología , Glucolípidos/química , Vibrio cholerae/química
3.
Biosens Bioelectron ; 15(11-12): 579-89, 2000.
Artículo en Inglés | MEDLINE | ID: mdl-11213218

RESUMEN

Recently, we demonstrated that an array biosensor could be used with cocktails of fluorescent antibodies to perform three assays simultaneously on a single substrate, and that multiple samples could be analyzed in parallel. We extend this technology to demonstrate the simultaneous analysis of six samples for six different hazardous analytes, including both bacteria and protein toxins. The level of antibody cross-reactivity is explored, revealing a possible common epitope in two of the toxins. A panel of environmental interferents was added to the samples; these interferents neither prevented the detection of the analytes nor caused false-positive responses.


Asunto(s)
Bacterias/aislamiento & purificación , Toxinas Bacterianas/análisis , Técnicas Biosensibles , Monitoreo del Ambiente , Ricina/análisis , Reacciones Cruzadas
4.
Anal Chem ; 71(17): 3846-52, 1999 Sep 01.
Artículo en Inglés | MEDLINE | ID: mdl-10489530

RESUMEN

The array biosensor was fabricated to analyze multiple samples simultaneously for multiple analytes. The sensor utilized a standard sandwich immunoassay format: Antigen-specific "capture" antibodies were immobilized in a patterned array on the surface of a planar waveguide and bound analyte was subsequently detected using fluorescent tracer antibodies. This study describes the analysis of 126 blind samples for the presence of three distinct classes of analytes. To address potential complications arising from using a mixture of tracer antibodies in the multianalyte assay, three single-analyte assays were run in parallel with a multianalyte assay. Mixtures of analytes were also assayed to demonstrate the sensor's ability to detect more than a single species at a time. The array sensor was capable of detecting viral, bacterial, and protein analytes using a facile 14-min assay with sensitivity levels approaching those of standard ELISA methods. Limits of detection for Bacillus globigii, MS2 bacteriophage, and staphylococcal enterotoxin B (SEB) were 10(5) cfu/mL, 10(7) pfu/mL, and 10 ng/mL, respectively. The array biosensor also analyzed multiple samples simultaneously and detected mixtures of the different types of analytes in the multianalyte format.


Asunto(s)
Anticuerpos/análisis , Antígenos Bacterianos/análisis , Antígenos Virales/análisis , Técnicas Biosensibles , Ensayo de Inmunoadsorción Enzimática , Sensibilidad y Especificidad
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