Title :
Quantitative immunophenotyping of circulating tumor cells in blood using microfluidic screening chip integrated with hyperspectral microscope
Author :
Horton, A.P. ; Kumar, K. ; Liu, H. ; Cheng, L. ; Lane, N. ; Taylor, E. ; Garner, H.R. ; Uhr, J.W. ; Zhan, X.J.
Author_Institution :
Univ. of Texas at Austin, Austin, TX, USA
Abstract :
An effective screening test for the early diagnosis of cancer is high on the agenda of oncologists, since early detection increases treatment options and patient prognosis. Using microfluidics and Hyperspectral Imaging Microscopy, we demonstrate the ability to capture and immunophenotype circulating tumor cells (CTCs), which are shed by carcinomas at an early stage and signify the presence of cancer in a patient. The technology presented demonstrates the potential for optofluidic microsystems in advanced point-of-care applications and is envisioned to aid disease prognosis, treatment selection, response monitoring, and development of novel therapies.
Keywords :
bioMEMS; biomedical optical imaging; blood; cancer; cell motility; micro-optomechanical devices; optical microscopy; blood; cancer diagnosis; carcinoma; disease prognosis; effective screening test; integrated hyperspectral imaging microscopy; microfluidic screening chip; microfluidics; optofluidic microsystems; patient prognosis; point-of-care applications; quantitative immunophenotype circulating tumor cells; response monitoring; therapies; treatment selection; Blood; Cancer detection; Diseases; Hyperspectral imaging; Medical treatment; Microfluidics; Microscopy; Patient monitoring; Testing; Tumors; Circulating tumor cell; hyperspectral analysis; microfluidics;
Conference_Titel :
Solid-State Sensors, Actuators and Microsystems Conference, 2009. TRANSDUCERS 2009. International
Conference_Location :
Denver, CO
Print_ISBN :
978-1-4244-4190-7
Electronic_ISBN :
978-1-4244-4193-8
DOI :
10.1109/SENSOR.2009.5285561