Poyard S, Gorchkov D, Jdanova A, Jaffrezic-Renault N, Martelet C, Soldatkin A, El'Skaya A
Laboratoire de physicochimie des interfaces, UMR 5621 404, Ecole centrale de Lyon, Ecully, France.
C R Acad Sci III. 1996 Apr;319(4):257-62.
Urea-sensitive enzyme field effect transistors (ENFETs) were prepared by cross-linking urease with bovine serum albumin in saturated glutaraldehyde vapor on the sensitive surface of a pH-FET. The linear part of the biosensor dynamic range is between 5 x 10(-5) and 10(-3) M of urea. The influence of pH on the sensor response, stability and reproducibility of the urea sensor were examined. The addition of EDTA, glycerol, sodium azide and dithiothreitol in the storage buffer solution was studied. In these specific storage conditions, an increase of sensor sensitivity and stability was observed, which means that the enzyme is inhibited during the immobilisation procedure and can be partially restored. Furthermore such reagents do not affect the operational characteristics of the sensor when working in serum.
通过在pH场效应晶体管(pH-FET)的敏感表面上,于饱和戊二醛蒸气中使脲酶与牛血清白蛋白交联,制备了对尿素敏感的酶场效应晶体管(ENFET)。生物传感器动态范围的线性部分在尿素浓度为5×10⁻⁵至10⁻³ M之间。研究了pH对尿素传感器响应、稳定性和重现性的影响。考察了在储存缓冲溶液中添加乙二胺四乙酸(EDTA)、甘油、叠氮化钠和二硫苏糖醇的情况。在这些特定的储存条件下,观察到传感器灵敏度和稳定性有所提高,这意味着酶在固定化过程中受到抑制,并且可以部分恢复。此外,当传感器在血清中工作时,这些试剂不会影响其操作特性。