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Comparison of enzymatic and non-enzymatic glucose sensors based on hierarchical Au-Ni alloy with conductive polymer.
Lee, Won-Chul; Kim, Kwang-Bok; Gurudatt, N G; Hussain, Khalil K; Choi, Cheol Soo; Park, Deog-Su; Shim, Yoon-Bo.
Afiliação
  • Lee WC; Department of Chemistry, Pusan National University, Busan 46241, South Korea.
  • Kim KB; Biomedical System & Technology Group, Korea Institute of Industrial Technology, Cheonan 31056, South Korea.
  • Gurudatt NG; Department of Chemistry, Pusan National University, Busan 46241, South Korea; Endocrinology, Internal Medicine, Gil Medical Center, and Korea Mouse Metabolic Phenotyping Center, Lee Gil Ya Cancer and Diabetes Institute, Gachon University College of Medicine, Incheon 21999, South Korea.
  • Hussain KK; Department of Chemistry, Pusan National University, Busan 46241, South Korea.
  • Choi CS; Endocrinology, Internal Medicine, Gil Medical Center, and Korea Mouse Metabolic Phenotyping Center, Lee Gil Ya Cancer and Diabetes Institute, Gachon University College of Medicine, Incheon 21999, South Korea.
  • Park DS; Institute of BioPhysio Sensor Technology (IBST), Pusan National University, Busan 46241, South Korea. Electronic address: dsupark@pusan.ac.kr.
  • Shim YB; Department of Chemistry, Pusan National University, Busan 46241, South Korea; Institute of BioPhysio Sensor Technology (IBST), Pusan National University, Busan 46241, South Korea. Electronic address: ybshim@pusan.ac.kr.
Biosens Bioelectron ; 130: 48-54, 2019 Apr 01.
Article em En | MEDLINE | ID: mdl-30731345
ABSTRACT
Enzymatic and non-enzymatic amperometric glucose sensors based on nanostructured Au-Ni alloy were prepared and compared in their performance. The hierarchically structured Au-Ni surface was merely used for the non-enzymatic glucose sensor, while glucose oxidase attached poly-3'(benzoic acid) -2,2'5',2'- terthiophene (pTBA) formed on the alloy surface was used as the enzymatic sensor. The fabricated sensor was characterized using surface analysis and electrochemical experiments. In case of the enzymatic sensor, the anodic current of H2O2 generated from the enzyme reaction was used as the analytical signal, while the direct oxidation of glucose was observed on a mere Au-Ni alloy electrode without enzyme immobilization, which shows an excellent catalytic oxidation of glucose even in physiological pH. The potential pulse pretreatment of the sensor surfaces improved the performance, which allowed both the sensors reproducible and reusable (enzymatic sensor coefficient of variation = 1.82%, n = 5, non-enzymatic coefficient of variation = 2.93%). The enzymatic biosensor reveals the advantages of increased sensitivity, selectivity, and stability, compared with the non-enzymatic sensor. The linear range of enzymatic sensor was attained from 1.0 µM to 30.0 mM with a detection limit of 0.29 µM. The reliabilities of the sensors were also demonstrated through the glucose analysis in human blood samples, and the result was compared with the commercially available glucometer.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicemia / Técnicas Biossensoriais / Nanoestruturas / Técnicas Eletroquímicas Limite: Humans Idioma: En Revista: Biosens Bioelectron Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Coréia do Sul

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Glicemia / Técnicas Biossensoriais / Nanoestruturas / Técnicas Eletroquímicas Limite: Humans Idioma: En Revista: Biosens Bioelectron Assunto da revista: BIOTECNOLOGIA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Coréia do Sul