Performance enhanced UV/vis spectroscopic microfluidic sensor for ascorbic acid quantification in human blood

被引:42
作者
Bi, Hongyan [1 ]
Duarte, Carla M. [2 ,3 ]
Brito, Marina [1 ]
Vilas-Boas, Vania [1 ,4 ]
Cardoso, Susana [2 ,3 ]
Freitas, Paulo [1 ]
机构
[1] Int Iberian Nanotechnol Lab INL, Ave Mestre Jose Veiga, P-4715330 Braga, Portugal
[2] INESC MN, Rua Alves Redol,9-1, P-1000029 Lisbon, Portugal
[3] Univ Lisbon, Dept Phys, Inst Super Tecn, P-1000 Lisbon, Portugal
[4] Univ Porto, Fac Pharm, Dept Biol Sci, UCIBIO REQUIMTE,Lab Toxicol, P-4050313 Oporto, Portugal
关键词
Antioxidant analysis; UV/vis spectroscopic sensor; PDMS microfluidic chip; Human blood; Sol-gel; VITAMIN-C; GLUTAMATE MICROSENSORS; HEALTH; IMMOBILIZATION; STABILITY; DISEASE; ENZYMES; PHASE;
D O I
10.1016/j.bios.2016.05.054
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Quantitative analysis of antioxidants in a fast, simple and accurate manner is of great importance in the view of real-time monitoring the health of individuals. Recently, we have developed a UV/vis spectroscopic microfluidic sensor to specifically quantify ascorbic acid based on the immobilization of ascorbate oxidase, a relatively unstable enzyme. In this work, three different strategies for the immobilization of the unstable enzyme, including alumina sol-gel encapsulation, physisorption to PDMS channels with, and without alumina xerogel modification, were compared to build a microsensor. We found that the loading amount of the enzyme is not the determinative factor for the performance of the microfluidic biosensor but the retained activity of the enzyme and diffusion in the microfluidic channel. Taking into account of the two factors, the protocol of adsorbing enzymes to alumina (Al2O3) xerogel modified PDMS surface was demonstrated to be the best for preparing the microfluidic sensor among the utilized protocols. The microsensor prepared under the optimized protocol was further used to quantify ascorbic acid in human blood, where only dozens of microliters of blood (few drops) was required, demonstrating its potential application in clinical diagnosis. The developed strategy is featured with optimized enzymatic activity, simple process of microfluidic platform, low sample consumption, and straightforward spectrophotometry based detection. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:568 / 572
页数:5
相关论文
共 27 条
[1]   Effect of vitamin C on endothelial function in health and disease: A systematic review and meta-analysis of randomised controlled trials [J].
Ashor, Ammar W. ;
Lara, Jose ;
Mathers, John C. ;
Siervo, Mario .
ATHEROSCLEROSIS, 2014, 235 (01) :9-20
[2]   Polymer microfluidic devices [J].
Becker, H ;
Locascio, LE .
TALANTA, 2002, 56 (02) :267-287
[3]   Interference-blind microfluidic sensor for ascorbic acid determination by UV/vis spectroscopy [J].
Bi, Hongyan ;
Fernandes, Ana Carolina ;
Cardoso, Susana ;
Freitas, Paulo .
SENSORS AND ACTUATORS B-CHEMICAL, 2016, 224 :668-675
[4]   Strategy for allosteric analysis based on protein-patterned stationary phase in microfluidic chip [J].
Bi, HY ;
Weng, XX ;
Qu, HY ;
Kong, JL ;
Yang, PY ;
Liu, BH .
JOURNAL OF PROTEOME RESEARCH, 2005, 4 (06) :2154-2160
[5]  
Bsoul SA., 2004, J Contemp Dent Pract, V5, P1, DOI DOI 10.5005/JCDP-5-2-1
[6]   Enhanced proteolytic activity enzymes in photopolymerized of covalently bound sol gel [J].
Dulay, MT ;
Baca, QJ ;
Zare, RN .
ANALYTICAL CHEMISTRY, 2005, 77 (14) :4604-4610
[7]   Measurement of intracellular vitamin C levels in human lymphocytes by reverse phase high perfon-nance liquid chromatography (HPLC) [J].
Emadi-Konjin, P ;
Verjee, Z ;
Levin, AV ;
Adeli, K .
CLINICAL BIOCHEMISTRY, 2005, 38 (05) :450-456
[8]   Vitamin C in Health and Disease: Its Role in the Metabolism of Cells and Redox State in the Brain [J].
Figueroa-Mendez, Rodrigo ;
Rivas-Arancibia, Selva .
FRONTIERS IN PHYSIOLOGY, 2015, 6
[9]   Determination of vitamin C in tropical fruits:: A comparative evaluation of methods [J].
Hernández, Y ;
Lobo, MG ;
González, M .
FOOD CHEMISTRY, 2006, 96 (04) :654-664
[10]   THEORY OF KINETICS OF REACTIONS CATALYZED BY ENZYMES ATTACHED TO INTERIOR SURFACES OF TUBES [J].
KOYAYASHI, T ;
LAIDLER, KJ .
BIOTECHNOLOGY AND BIOENGINEERING, 1974, 16 (01) :99-118