A microfluidic dialysis device for complex biological mixture SERS analysis

被引:20
作者
Perozziello, Gerardo [1 ]
Candeloro, Patrizio [1 ]
Gentile, Francesco [1 ]
Coluccio, Maria Laura [1 ]
Tallerico, Marco [2 ]
De Grazia, Antonio [2 ]
Nicastri, Annalisa [3 ]
Perri, Angela Mena [3 ]
Parrotta, Elvira [3 ]
Pardeo, Francesca [1 ]
Catalano, Rossella [1 ]
Cuda, Giovanni [3 ]
Di Fabrizio, Enzo [1 ,2 ]
机构
[1] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med, BioNEM Lab, I-88100 Catanzaro, Italy
[2] KAUST, Thuwal 239556900, Saudi Arabia
[3] Magna Graecia Univ Catanzaro, Dept Expt & Clin Med, Prot Lab, I-88100 Catanzaro, Italy
关键词
Microfluidic filtering; Complex mixture analysis; SERS analysis; RAMAN-SPECTROSCOPY; MASS-SPECTROMETRY; IN-VITRO; SEPARATION; CELLS; MICRODIALYSIS; SURFACES; SYSTEM; CHIP;
D O I
10.1016/j.mee.2015.02.015
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
In this paper, we present a microfluidic device fabricated with a simple and inexpensive process allowing rapid filtering of peptides from a complex mixture. The polymer microfluidic device can be used for sample preparation in biological applications. The device is fabricated by micromilling and solvent assisted bonding, in which a microdialysis membrane (cut-off of 12-14 kDa) is sandwiched in between an upper and a bottom microfluidic chamber. An external frame connects the microfluidic device to external tubes, microvalves and syringe pumps. Bonding strength and interface sealing are pneumatically tested. Microfluidic protocols are also described by using the presented device to filter a sample composed of specific peptides (MW 1553.73 Da, at a concentration of 1.0 ng/mu l) derived from the BRCA1 protein, a tumor-suppressor molecule which plays a pivotal role in the development of breast cancer, and albumin (MW 66.5 kDa, at a concentration of 35 mu g/mu l), the most represented protein in human plasma. The filtered samples coming out from the microfluidic device were subsequently deposited on a SERS (surface enhanced Raman scattering) substrate for further analysis by Raman spectroscopy. By using this approach, we were able to sort the small peptides from the bigger and highly concentrated protein albumin and to detect them by using a label-free technique at a resolution down to 1.0 ng/mu l. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:37 / 41
页数:5
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