Monteiro Tiago, Rodrigues Patrícia R, Gonçalves Ana Luisa, Moura José J G, Jubete Elena, Añorga Larraitz, Piknova Barbora, Schechter Alan N, Silveira Célia M, Almeida M Gabriela
Centro de Investigação Interdisciplinar Egas Moniz (CiiEM), Instituto Superior de Ciências da Saúde Egas Moniz, Campus Universitário, Quinta da Granja, 2829-511 Caparica, Portugal; UCIBIO, REQUIMTE, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Monte Caparica, Portugal.
UCIBIO, REQUIMTE, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, 2829-516 Monte Caparica, Portugal.
Talanta. 2015 Sep 1;142:246-51. doi: 10.1016/j.talanta.2015.04.057. Epub 2015 Apr 27.
In this paper we aim to demonstrate, as a proof-of-concept, the feasibility of the mass production of effective point of care tests for nitrite quantification in environmental, food and clinical samples. Following our previous work on the development of third generation electrochemical biosensors based on the ammonia forming nitrite reductase (ccNiR), herein we reduced the size of the electrodes' system to a miniaturized format, solved the problem of oxygen interference and performed simple quantification assays in real samples. In particular, carbon paste screen printed electrodes (SPE) were coated with a ccNiR/carbon ink composite homogenized in organic solvents and cured at low temperatures. The biocompatibility of these chemical and thermal treatments was evaluated by cyclic voltammetry showing that the catalytic performance was higher with the combination acetone and a 40°C curing temperature. The successful incorporation of the protein in the carbon ink/solvent composite, while remaining catalytically competent, attests for ccNiR's robustness and suitability for application in screen printed based biosensors. Because the direct electrochemical reduction of molecular oxygen occurs when electroanalytical measurements are performed at the negative potentials required to activate ccNiR (ca.-0.4V vs Ag/AgCl), an oxygen scavenging system based on the coupling of glucose oxidase and catalase activities was successfully used. This enabled the quantification of nitrite in different samples (milk, water, plasma and urine) in a straightforward way and with small error (1-6%). The sensitivity of the biosensor towards nitrite reduction under optimized conditions was 0.55 A M(-1) cm(-2) with a linear response range 0.7-370 μM.
在本文中,我们旨在作为概念验证,证明大规模生产用于环境、食品和临床样品中亚硝酸盐定量的有效即时检测的可行性。继我们之前关于基于氨形成亚硝酸盐还原酶(ccNiR)的第三代电化学生物传感器的开发工作之后,在此我们将电极系统的尺寸缩小为小型化形式,解决了氧干扰问题,并在实际样品中进行了简单的定量分析。具体而言,碳糊丝网印刷电极(SPE)涂覆有在有机溶剂中均质化并在低温下固化的ccNiR/碳墨复合材料。通过循环伏安法评估了这些化学和热处理的生物相容性,结果表明丙酮和40°C固化温度的组合具有更高的催化性能。蛋白质成功掺入碳墨/溶剂复合材料中,同时保持催化活性,证明了ccNiR的稳健性及其适用于丝网印刷型生物传感器。由于在激活ccNiR所需的负电位(相对于Ag/AgCl约为-0.4V)下进行电分析测量时会发生分子氧的直接电化学还原,因此成功使用了基于葡萄糖氧化酶和过氧化氢酶活性偶联的氧清除系统。这使得能够以直接的方式且误差较小(1-6%)对不同样品(牛奶、水、血浆和尿液)中的亚硝酸盐进行定量。在优化条件下,生物传感器对亚硝酸盐还原的灵敏度为0.55 A M(-1) cm(-2),线性响应范围为0.7-370 μM。