SOLVENT EFFECTS ON THE REACTIVITIES OF AN AMPEROMETRIC GLUCOSE SENSOR

被引:31
|
作者
IWUOHA, EI [1 ]
SMYTH, MR [1 ]
LYONS, MEG [1 ]
机构
[1] UNIV DUBLIN TRINITY COLL,PHYS CHEM LAB,DUBLIN 2,IRELAND
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1995年 / 390卷 / 1-2期
关键词
AMPEROMETRY; REACTIVITY; ORGANIC PHASE BIOSENSORS; SOLVENT EFFECTS; GLUCOSE SENSOR;
D O I
10.1016/0022-0728(95)03906-W
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Reactivities of organic phase biosensors containing 5.1 pmol cm(-2) glucose oxidase (GOx) on glassy carbon (GC) or Pt electrode surfaces (0.071 cm(2) in area) were evaluated in acetonitrile, acetone, butan-2-ol, tetrahydrofuran and 0.1 M phosphate buffer (pa 7.0). Each of the organic media contained 10% v/v of water. Ferrocenemonocarboxylic acid was used as a soluble electron transfer mediator for the detection of glucose in these solvents. Tafel analyses of the cyclic voltammograms (CVs) of the electrocatalytic reaction gave Tafel slopes of between 103 and 129 mV decade(-1), which are in good agreement with the theoretical value of 118 mV decade(-1). Constant-potential amperometric studies an GOx-modified rotating Pt disc electrodes (RDEs) were carried out at 0.45 V, a potential dictated by the limiting catalytic currents I-K Of the CV experiments. The apparent turnover rate constant K-cat' of GOx in the biosensor and its catalytic efficiency k(cat)'/K-m' were estimated from the results of the RDE experiments. Changing from the aqueous buffer to organic media produced a drastic decrease in k(cat)', which is more than two orders of magnitude lower in butan-2-ol. This sensor characteristic is related to the lower solvent-dependent diffusibility of glucose in the sensor for the organic systems vis-g-vis phosphate buffer. The normalized catalytic efficiencies, (k(cat)'/K-m')(org) (solv)/(K-cat'/K-m')(buffer) show an enhancement of biosensor efficiency on changing from phosphate buffer to polar organic solvents. The K-cat'/K-m' values are indicators of the degree of activation of the biosensor's electrocatalytic reaction. Greater stabilization of the transition state of the electroenzymatic process by organic phases relative to phosphate buffer was ascertained from the normalized catalytic efficiency. The enhanced catalytic efficiency of the organic phase sensors is attributed solely to the activation of the catalytic reaction of GOx and beta-D-glucose.
引用
收藏
页码:35 / 45
页数:11
相关论文
共 50 条
  • [1] A multilayered amperometric glucose sensor
    Garjonyte, R
    Malinauskas, A
    BULLETIN OF ELECTROCHEMISTRY, 2003, 19 (12): : 529 - 534
  • [2] Recent Aspects of Amperometric Glucose Sensor
    Dong, Shaojun
    ANALYTICAL SCIENCES, 1991, 7 : 1427 - 1430
  • [3] Digital fabrication of an amperometric glucose sensor
    Du, Xiaosong
    Motley, Joshua
    Herman, Gregory S.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248
  • [4] ON SOLVENT DEPENDENCE OF SUBSTITUENT EFFECTS ON REACTIVITIES
    RITCHIE, CD
    LEWIS, ES
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1962, 84 (04) : 591 - &
  • [5] SOLVENT EFFECTS ON REACTIVITIES OF ORGANOMETALLIC COMPOUNDS
    GUTMANN, V
    COORDINATION CHEMISTRY REVIEWS, 1976, 18 (02) : 225 - 255
  • [6] A Cheap Amperometric and Optical Sensor for Glucose Determination
    Scavetta, E.
    Ballarin, B.
    Tonelli, D.
    ELECTROANALYSIS, 2010, 22 (04) : 427 - 432
  • [7] Construction of Mediated Amperometric Bienzyme Glucose Sensor
    SUN Chang-qing
    DU Wen-yuant
    GAO Qian and XU Hong-ding (Department of chemistry
    ChemicalResearchinChineseUniversities, 1996, (01) : 16 - 21
  • [8] AN AMPEROMETRIC GLUCOSE SENSOR WITH COMBINED ENZYME LAYERS
    WEISS, T
    CAMMANN, K
    HORMONE AND METABOLIC RESEARCH, 1988, 20 : 23 - 25
  • [9] Construction of mediated amperometric bienzyme glucose sensor
    Sun, CQ
    Du, WY
    Gao, Q
    Xu, HD
    CHEMICAL RESEARCH IN CHINESE UNIVERSITIES, 1996, 12 (01) : 16 - 21
  • [10] KINETICS OF AN AMPEROMETRIC GLUCOSE SENSOR WITH A SOLUBLE MEDIATOR
    YOKOYAMA, K
    TAMIYA, E
    KARUBE, I
    JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 273 (1-2): : 107 - 117