Optofluidic characterization of marine algae using a microflow cytometer

被引:73
作者
Hashemi, Nastaran [1 ]
Erickson, Jeffrey S. [1 ]
Golden, Joel P. [1 ]
Ligler, Frances S. [1 ]
机构
[1] USN, Res Lab, Ctr Bio Mol Sci & Engn, Washington, DC 20375 USA
来源
BIOMICROFLUIDICS | 2011年 / 5卷 / 03期
关键词
band-pass filters; biological techniques; bioMEMS; bio-optics; fluorescence; light scattering; marine pollution; microchannel flow; microorganisms; molecular biophysics; optical fibres; optical filters; photomultipliers; proteins; FLOW-CYTOMETRY; SHEATH FLOW; PHYTOPLANKTON; FLUORESCENCE; PATTERNS; CLIMATE; DIATOM;
D O I
10.1063/1.3608136
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The effects of global warming, pollution in river effluents, and changing ocean currents can be studied by characterizing variations in phytoplankton populations. We demonstrate the design and fabrication of a Microflow Cytometer for characterization of phytoplankton. Guided by chevron-shaped grooves on the top and bottom of a microfluidic channel, two symmetric sheath streams wrap around a central sample stream and hydrodynamically focus it in the center of the channel. The lasers are carefully chosen to provide excitation light close to the maximum absorbance wavelengths for the intrinsic fluorophores chlorophyll and phycoerythrin, and the excitation light is coupled to the flow cytometer through the use of an optical fiber. Fluorescence and light scatter are collected using two multimode optical fibers placed at 90-degree angles with respect to the excitation fiber. Light emerging from these collection fibers is directed through optical bandpass filters into photomultiplier tubes. The cytometer measured the optical and side scatter properties of Karenia b., Synechococcus sp., Pseudo-Nitzchia, and Alexandrium. The effect of the sheath-to-sample flow-rate ratio on the light scatter and fluorescence of these marine microorganisms was investigated. Reducing the sample flow rate from 200 mu L/min to 10 mu L/min produced a more tightly focused sample stream and less heterogeneous signals. (C) 2011 American Institute of Physics. [doi:10.1063/1.3608136]
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页数:9
相关论文
共 30 条
[1]   Life cycle, size reduction patterns, and ultrastructure of the pennate planktonic diatom Pseudo-nitzschia delicatissima (Bacillariophyceae) [J].
Amato, A ;
Orsini, L ;
D'Alelio, D ;
Montresor, M .
JOURNAL OF PHYCOLOGY, 2005, 41 (03) :542-556
[2]   Reorganization of North Atlantic marine copepod biodiversity and climate [J].
Beaugrand, G ;
Reid, PC ;
Ibañez, F ;
Lindley, JA ;
Edwards, M .
SCIENCE, 2002, 296 (5573) :1692-1694
[3]   Flow cytometric discrimination of various phycobilin-containing phytoplankton groups in a hypertrophic reservoir [J].
Becker, A ;
Meister, A ;
Wilhelm, C .
CYTOMETRY, 2002, 48 (01) :45-57
[4]  
DAVISON SM, 2006, P COMSOL MULTIPHYSIC
[5]   High frequency monitoring reveals phytoplankton dynamics [J].
Dubelaar, GBJ ;
Geerders, PJF ;
Jonker, RR .
JOURNAL OF ENVIRONMENTAL MONITORING, 2004, 6 (12) :946-952
[6]   CytoBuoy: a step forward towards using flow cytometry in operational oceanography [J].
Dubelaar, GBJ ;
Gerritzen, PL .
SCIENTIA MARINA, 2000, 64 (02) :255-265
[7]   FISH and chips: Marine bacterial communities analyzed by flow cytometry based on microfluidics [J].
Gerdts, G ;
Luedke, G .
JOURNAL OF MICROBIOLOGICAL METHODS, 2006, 64 (02) :232-240
[8]   CAROTENOID FLUORESCENCE [J].
GILLBRO, T ;
COGDELL, RJ .
CHEMICAL PHYSICS LETTERS, 1989, 158 (3-4) :312-316
[9]   Multi-wavelength microflow cytometer using groove-generated sheath flow [J].
Golden, Joel P. ;
Kim, Jason S. ;
Erickson, Jeffrey S. ;
Hilliard, Lisa R. ;
Howell, Peter B. ;
Anderson, George P. ;
Nasir, Mansoor ;
Ligler, Frances S. .
LAB ON A CHIP, 2009, 9 (13) :1942-1950
[10]   An integrated flow-cell for full sample stream control [J].
Hairer, G. ;
Vellekoop, M. J. .
MICROFLUIDICS AND NANOFLUIDICS, 2009, 7 (05) :647-658