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Dual-force aggregation of magnetic particles enhances label-free quantification of DNA at the sub-single cell level.
Nelson, Daniel A; Strachan, Briony C; Sloane, Hillary S; Li, Jingyi; Landers, James P.
Afiliação
  • Nelson DA; Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22904, USA.
  • Strachan BC; Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22904, USA.
  • Sloane HS; Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22904, USA.
  • Li J; Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22904, USA.
  • Landers JP; Department of Chemistry, University of Virginia, McCormick Road, Charlottesville, VA 22904, USA; Department of Pathology, University of Virginia Health Science Center, Charlottesville, VA 22908, USA; Department of Mechanical Engineering, University of Virginia, Engineer's Way, Charlottesville, VA 22
Anal Chim Acta ; 819: 34-41, 2014 Mar 28.
Article em En | MEDLINE | ID: mdl-24636408
We recently reported the 'pinwheel effect' as the foundation for a DNA assay based on a DNA concentration-dependent aggregation of silica-coated magnetic beads in a rotating magnetic field (RMF). Using a rotating magnet that generated a 5 cm magnetic field that impinged on a circular array of 5mm microwells, aggregation was found to only be effective in a single well at the center of the field. As a result, when multiple samples needed to be analyzed, the single-plex (single well) analysis was tedious, time-consuming and labor-intensive, as each well needed to be exposed to the center of the RMF in a serial manner for consistent well-to-well aggregation. For more effective multiplexing (simultaneous aggregation in 12 wells), we used a circular array of microwells and incorporated 'agitation' as a second force that worked in concert with the RMF to provide effective multiplexed aggregation-based DNA quantitation. The dual-force aggregation (DFA) approach allows for effective simultaneous aggregation in multiple wells (12 demonstrated) of the multi-well microdevice, allowing for 12 samples to be interrogated for DNA content in 140 s, providing a ∼35-fold improvement in time compared to single-plex approach (80 min) and ∼4-fold improvement over conventional fluorospectrometric methods. Furthermore, the increased interaction between DNA and beads provided by DFA improved the limit of detection to 250 fg µL(-1). The correlation between the DFA results and those from a fluorospectrometer, demonstrate DFA as an inexpensive and rapid alternative to more conventional methods (fluorescent and spectrophotometric).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Viral / Células / Imãs Idioma: En Revista: Anal Chim Acta Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: DNA Viral / Células / Imãs Idioma: En Revista: Anal Chim Acta Ano de publicação: 2014 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Holanda