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Centrifugal Microfluidic Platform for Ultrasensitive Detection of Botulinum Toxin

Overview
Journal Anal Chem
Specialty Chemistry
Date 2014 Dec 19
PMID 25521812
Citations 20
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Abstract

We present an innovative centrifugal microfluidic immunoassay platform (SpinDx) to address the urgent biodefense and public health need for ultrasensitive point-of-care/incident detection of botulinum toxin. The simple, sample-to-answer centrifugal microfluidic immunoassay approach is based on binding of toxins to antibody-laden capture particles followed by sedimentation of the particles through a density-media in a microfluidic disk and quantification by laser-induced fluorescence. A blind, head-to-head comparison study of SpinDx versus the gold-standard mouse bioassay demonstrates 100-fold improvement in sensitivity (limit of detection = 0.09 pg/mL), while achieving total sample-to-answer time of <30 min with 2-μL required volume of the unprocessed sample. We further demonstrate quantification of botulinum toxin in both exogeneous (human blood and serum spiked with toxins) and endogeneous (serum from mice intoxicated via oral, intranasal, and intravenous routes) samples. SpinDx can analyze, without any sample preparation, multiple sample types including whole blood, serum, and food. It is readily expandable to additional analytes as the assay reagents (i.e., the capture beads and detection antibodies) are disconnected from the disk architecture and the reader, facilitating rapid development of new assays. SpinDx can also serve as a general-purpose immunoassay platform applicable to diagnosis of other conditions and diseases.

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References
1.
Schaff U, Sommer G . Whole blood immunoassay based on centrifugal bead sedimentation. Clin Chem. 2011; 57(5):753-61. DOI: 10.1373/clinchem.2011.162206. View

2.
Arnon S, Schechter R, Maslanka S, Jewell N, Hatheway C . Human botulism immune globulin for the treatment of infant botulism. N Engl J Med. 2006; 354(5):462-71. DOI: 10.1056/NEJMoa051926. View

3.
OHISHI I . Oral toxicities of Clostridium botulinum type A and B toxins from different strains. Infect Immun. 1984; 43(2):487-90. PMC: 264322. DOI: 10.1128/iai.43.2.487-490.1984. View

4.
Lao U, Mulchandani A, Chen W . Simple conjugation and purification of quantum dot-antibody complexes using a thermally responsive elastin-protein L scaffold as immunofluoresecent agents. J Am Chem Soc. 2006; 128(46):14756-7. DOI: 10.1021/ja065343x. View

5.
Garber E, Venkateswaran K, OBrien T . Simultaneous multiplex detection and confirmation of the proteinaceous toxins abrin, ricin, botulinum toxins, and Staphylococcus enterotoxins a, B, and C in food. J Agric Food Chem. 2010; 58(11):6600-7. DOI: 10.1021/jf100789n. View