Isolation of circulating tumor cells using photoacoustic flowmetry and two phase flow

被引:1
作者
O'Brien, Christine M. [1 ]
Rood, Kyle D. [1 ]
Gupta, Sagar K. [1 ]
Mosley, Jeffrey D. [1 ]
Goldschmidt, Benjamin S. [1 ]
Sharma, Nikhilesh [1 ]
Sengupta, Shramik [1 ]
Viator, John A. [1 ]
机构
[1] Univ Missouri, Biol Engn Dept, Columbia, MO 65211 USA
来源
PHOTONS PLUS ULTRASOUND: IMAGING AND SENSING 2011 | 2011年 / 7899卷
关键词
circulating tumor cells; separation; slug; flowmetry; photoacoustics; CAPTURE;
D O I
10.1117/12.875324
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
Melanoma is the deadliest form of skin cancer, yet current diagnostic methods are inadequately sensitive. Patients must wait until secondary tumors form before malignancy can be diagnosed and treatment prescribed. Detection of cells that have broken off the original tumor and flow through the blood or lymph system can provide data for diagnosing and monitoring cancer. Our group utilizes the photoacoustic effect to detect metastatic melanoma cells, which contain the pigmented granule melanin. As a rapid laser pulse irradiates melanoma, the melanin undergoes thermo-elastic expansion and ultimately creates a photoacoustic wave. Thus, melanoma patient's blood samples can be enriched, leaving the melanoma in a white blood cell (WBC) suspension. Irradiated melanoma cells produce photoacoustic waves, which are detected with a piezoelectric transducer, while the optically transparent WBCs create no signals. Here we report an isolation scheme utilizing two-phase flow to separate detected melanoma from the suspension. By introducing two immiscible fluids through a t-junction into one flow path, the analytes are compartmentalized. Therefore, the slug in which the melanoma cell is located can be identified and extracted from the system. Two-phase immiscible flow is a label free technique, and could be used for other types of pathological analytes.
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页数:9
相关论文
共 26 条
[1]   Highly efficient circulating tumor cell isolation from whole blood and label-free enumeration using polymer-based microfluidics with an integrated conductivity sensor [J].
Adams, Andre A. ;
Okagbare, Paul I. ;
Feng, Juan ;
Hupert, Matuesz L. ;
Patterson, Don ;
Goettert, Jost ;
McCarley, Robin L. ;
Nikitopoulos, Dimitris ;
Murphy, Michael C. ;
Soper, Steven A. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2008, 130 (27) :8633-8641
[2]  
[Anonymous], 2010, Cancer Facts Figures 2010
[3]   Counting particles by means of optoacoustics: Potential limits in real solutions [J].
Autrey, T ;
Egerev, S ;
Foster, NS ;
Fokin, A ;
Ovchinnikov, O .
REVIEW OF SCIENTIFIC INSTRUMENTS, 2003, 74 (01) :628-631
[4]   Generation of monodisperse alginate microbeads and in situ encapsulation of cell in microfluidic device [J].
Choi, Chang-Hyung ;
Jung, Jae-Hoon ;
Rhee, Young Woo ;
Kim, Dong-Pyo ;
Shim, Sang-Eun ;
Lee, Chang-Soo .
BIOMEDICAL MICRODEVICES, 2007, 9 (06) :855-862
[5]   Circulating tumor cells, disease progression, and survival in metastatic breast cancer [J].
Cristofanilli, M ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Matera, J ;
Miller, MC ;
Reuben, JM ;
Doyle, GV ;
Allard, WJ ;
Terstappen, LWMM ;
Hayes, DF .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :781-791
[6]   10-YEAR RESULTS OF A RANDOMIZED CLINICAL-TRIAL COMPARING RADICAL MASTECTOMY AND TOTAL MASTECTOMY WITH OR WITHOUT RADIATION [J].
FISHER, B ;
REDMOND, C ;
FISHER, ER ;
BAUER, M ;
WOLMARK, N ;
WICKERHAM, DL ;
DEUTSCH, M ;
MONTAGUE, E ;
MARGOLESE, R ;
FOSTER, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1985, 312 (11) :674-681
[7]  
Galanzha EI, 2009, NAT NANOTECHNOL, V4, P855, DOI [10.1038/nnano.2009.333, 10.1038/NNANO.2009.333]
[8]  
Garstecki P, 2006, LAB CHIP, V6, P693
[9]   Effect of geometry on droplet formation in the squeezing regime in a microfluidic T-junction [J].
Gupta, Amit ;
Kumar, Ranganathan .
MICROFLUIDICS AND NANOFLUIDICS, 2010, 8 (06) :799-812
[10]  
Gutierrez-Juarez G., 2009, LASER SURG IN PRESS