Dielectrophoretic isolation and detection of cfc-DNA nanoparticulate biomarkers and virus from blood

Authors


  • Colour Online: See the article online to view Figs. 1–4 in colour.

Correspondence: Professor Michael J. Heller, Department of Nanoengineering, University of California San Diego, SME Building, Rm 243J, 9500 Gilman Dr., La Jolla CA 92093-0448, USA

E-mail: mheller@ucsd.edu

Fax: +1-858-534-9553

Abstract

Dielectrophoretic (DEP) microarray devices allow important cellular nanoparticulate biomarkers and virus to be rapidly isolated, concentrated, and detected directly from clinical and biological samples. A variety of submicron nanoparticulate entities including cell free circulating (cfc) DNA, mitochondria, and virus can be isolated into DEP high-field areas on microelectrodes, while blood cells and other micron-size entities become isolated into DEP low-field areas between the microelectrodes. The nanoparticulate entities are held in the DEP high-field areas while cells are washed away along with proteins and other small molecules that are not affected by the DEP electric fields. DEP carried out on 20 μL of whole blood obtained from chronic lymphocytic leukemia patients showed a considerable amount of SYBR Green stained DNA fluorescent material concentrated in the DEP high-field regions. Whole blood obtained from healthy individuals showed little or no fluorescent DNA materials in the DEP high-field regions. Fluorescent T7 bacteriophage virus could be isolated directly from blood samples, and fluorescently stained mitochondria could be isolated from biological buffer samples. Using newer DEP microarray devices, high-molecular-weight DNA could be isolated from serum and detected at levels as low as 8–16 ng/mL.

Ancillary