4.7 Article

An Integrated Amperometric Biosensor for the Determination of Lactose in Milk and Dairy Products

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 58, 期 12, 页码 7141-7148

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jf101173e

关键词

Self-assembled monolayers; enzyme electrodes; lactose; milk

资金

  1. Spanish Ministerio de Educacion y Ciencia [CTQ2009-09351]
  2. Comunidad de Madrid [S2009/PPQ-1642]
  3. Comunidad Autonoma de Madrid
  4. AVANSENS Program

向作者/读者索取更多资源

An integrated amperometric biosensor for the determination of lactose is reported. The bioelectrode design is based on the use of a 3-mercaptopropionic acid (MPA) self-assembled monolayer (SAM)modified gold electrode on which the enzymes beta-galactosidase (beta-Gal), glucose oxidase (GOD), peroxidase (HAP) and the mediator tetrathiafulvalene (TTF) are coimmobilized by a dialysis membrane. beta-Gal catalyzes the hydrolysis of lactose, and the produced glucose is catalytically oxidized to gluconic acid and H2O2, which is reduced in the presence of HAP. This enzyme reaction is mediated by TTF, and the reduction of TTF+ at 0.00 V (vs Ag/AgCl) gives rise to an amperometric signal proportional to the lactose concentration. The biosensor exhibits a good repeatability of the measurement carried out with the same biosensor, a good reproducibility of the responses obtained with different biosensors and a useful lifetime of 28 days. A linear calibration plot was obtained for lactose over the 1.5 x 10(-6) to 1.2 x 10(-4) M concentration range, with a limit of detection of 4.6 x 10(-7) M. The effect of potential interferents (sucrose, lactulose, fructose, arabinose, maltose, galactose, glucose and uric and ascorbic acids) on the biosensor response was evaluated. Furthermore, the bioelectrode exhibits a suitable performance in flow-injection systems in connection with amperometric detection. The developed biosensor was applied to the determination of lactose in milk and other foodstuffs (chocolate, butter, margarine, yogurt, cheese and mayonnaise), and the results obtained were validated by comparison with those provided by using a commercial enzyme test kit.

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