Gamella M, Campuzano S, Reviejo A J, Pingarrón J M
Dpto. Química Analítica, Facultad de CC. Químicas, Universidad Complutense de Madrid, E-28040 Madrid, Spain.
Anal Chim Acta. 2008 Feb 25;609(2):201-9. doi: 10.1016/j.aca.2007.12.036. Epub 2008 Jan 8.
The construction and performance of integrated amperometric biosensors for the determination of glycerol are reported. Two different biosensor configurations have been evaluated: one based on the glycerol dehydrogenase/diaphorase (GDH/DP) bienzyme system, and another using glycerol kinase/glycerol-3-phosphate oxidase/peroxidase (GK/GPOx/HRP). Both enzyme systems were immobilized together with the mediator tetrathiafulvalene (TTF) on a 3-mercaptopropionic acid (MPA) self-assembled monolayer (SAM)-modified gold electrode by using a dialysis membrane. The electrochemical oxidation of TTF at +150mV (vs. Ag/AgCl), and the reduction of TTF(+) at 0mV were used for the monitoring of the enzyme reactions for the bienzyme and trienzyme configurations, respectively. Experimental variables concerning both the biosensors composition and the working conditions were optimized for each configuration. A good repeatability of the measurements with no need of cleaning or pretreatment of the biosensors was obtained in both cases. After 51 days of use, the GDH/DP biosensor still exhibited 87% of the original sensitivity, while the GK/GPOx/HRP biosensor yielded a 46% of the original response after 8 days. Calibration graphs for glycerol with linear ranges of 1.0x10(-6) to 2.0x10(-5) or 1.0x10(-6) to 1.0x10(-5)M glycerol and sensitivities of 1214+/-21 or 1460+/-34microAM(-1) were obtained with GDH/DP and GK/GPOx/HRP biosensors, respectively. The calculated detection limits were 4.0x10(-7) and 3.1x10(-7)M, respectively. The biosensors exhibited a great sensitivity with no significant interferences in the analysis of wines. The biosensors were applied to the determination of glycerol in 12 different wines and the results advantageously compared with those provided by a commercial enzyme kit.
报道了用于测定甘油的集成电流型生物传感器的构建与性能。评估了两种不同的生物传感器配置:一种基于甘油脱氢酶/黄递酶(GDH/DP)双酶系统,另一种使用甘油激酶/甘油-3-磷酸氧化酶/过氧化物酶(GK/GPOx/HRP)。通过使用透析膜,将这两种酶系统与媒介体四硫富瓦烯(TTF)一起固定在3-巯基丙酸(MPA)自组装单层(SAM)修饰的金电极上。分别利用TTF在+150mV(相对于Ag/AgCl)处的电化学氧化以及TTF(+)在0mV处的还原,来监测双酶和三酶配置的酶反应。针对每种配置,对与生物传感器组成和工作条件相关的实验变量进行了优化。在这两种情况下,均获得了良好的测量重复性,且无需对生物传感器进行清洗或预处理。使用51天后,GDH/DP生物传感器仍表现出原始灵敏度的87%,而GK/GPOx/HRP生物传感器在使用8天后产生了原始响应的46%。使用GDH/DP和GK/GPOx/HRP生物传感器分别获得了甘油的校准曲线,线性范围为1.0×10(-6)至2.0×10(-5)或1.0×10(-6)至1.0×10(-5)M甘油,灵敏度分别为1214±21或1460±34μA M(-1)。计算得出的检测限分别为4.0×10(-7)和3.1×10(-7)M。这些生物传感器在葡萄酒分析中表现出极高的灵敏度且无明显干扰。将这些生物传感器应用于12种不同葡萄酒中甘油的测定,并将结果与商业酶试剂盒提供的结果进行了有利比较。