Fabrication of a microfluidic platform for investigating dynamic biochemical processes in living samples by FTIR microspectroscopy

被引:39
作者
Birarda, Giovanni [1 ,3 ]
Grenci, Gianluca [2 ]
Businaro, Luca [2 ]
Marmiroli, Benedetta [4 ]
Pacor, Sabrina [5 ]
Vaccari, Lisa [1 ]
机构
[1] Elettra Synchrotron Light Lab, I-34149 Trieste, Italy
[2] CNR, TASC Natl Lab, I-34149 Trieste, Italy
[3] Univ Trieste, Dept Phys, I-34127 Trieste, Italy
[4] Austrian Acad Sci, Inst Biophys & Nanosyst Res, Graz, Austria
[5] Univ Trieste, Dept Life Sci, I-34127 Trieste, Italy
关键词
FTIR microspectroscopy; Living-cells; Microfabrication; Microfluidic; TRANSFORM INFRARED-SPECTROSCOPY; CELLS;
D O I
10.1016/j.mee.2009.11.081
中图分类号
TM [电工技术]; TN [电子技术、通信技术];
学科分类号
0808 ; 0809 ;
摘要
Here we present the optimization of fabrication steps for realizing an infrared-visible microfluidic chip to study single-living cell behaviour in physiological environment by synchrotron radiation FTIR microspectroscopy. We optimized subtractive and additive lithographic processes on CaF(2) substrate, employing X-ARP 3100/10 photoresist both as etching-mask and for the device fabrication. Using prototype microfabricated liquid cells 9 and 5 mu m thick, we measured the response of small groups of THP1 monocytic cells to mechanical compression and chemical stimulation with fMLP using conventional IR globar source, aiming to evaluate biochemical rearrangements of leukocytes during the capillary circulation or recruitment processes. Stimulated monocytes have spectral features recognizable, differentiating them from unstimulated, especially affecting the spectral region 1280-1000 cm(-1), characteristic of nucleic acids and carbohydrates, and specific band ratios, such as proteins on lipids and methylene on methyl. Spectra variations have been correlated with biochemical events such as transcription, synthesis of new-proteins and variations in membrane fluidity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:806 / 809
页数:4
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