Evaluation of different strategies for the development of amperometric biosensors for l-lactate

Two strategies were investigated for the development of lactate biosensors based on sol–gel matrixes and polysulfone composite films, both containing l-lactate dehydrogenase (LDH). Firstly, reagentless disposable screen-printed electrodes (SPE's) with Meldola's Blue (MB) and the cofactor N...

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Bibliographic Details
Published inBiosensors & bioelectronics Vol. 22; no. 11; pp. 2663 - 2668
Main Authors Prieto-Simón, Beatriz, Fàbregas, Esteve, Hart, Alan
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 15.05.2007
Elsevier Science
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Summary:Two strategies were investigated for the development of lactate biosensors based on sol–gel matrixes and polysulfone composite films, both containing l-lactate dehydrogenase (LDH). Firstly, reagentless disposable screen-printed electrodes (SPE's) with Meldola's Blue (MB) and the cofactor NAD + inside a sol–gel matrix were prepared. These showed relatively low sensitivities (260 μA/M). Secondly, mediator-modified-polysulfone–graphite composite films deposited over both cylindrical epoxy–graphite and SPE's. These electrodes showed enhanced performance characteristics: improved sensitivity (80 mA/M), detection limit (0.87 μM) and reproducibility (2%). Reagentless electrodes, incorporating NAD + in the polysulfone film, had a decreased sensitivity, although better than that achieved by the sol–gel electrodes. While sol–gel electrodes showed a linear range between 1.25 × 10 −4 and 2.48 × 10 −3 M, the epoxy–graphite composite electrodes based on polysulfone composite films allowed the detection of lactate at a linear range of lower concentrations from 1 × 10 −6 to 1.2 × 10 −5 M. Finally, the performance of the LDH-MB-polysulfone-composite film-based SPE's in a flow system was studied. Short response times were obtained ( t < 30 s). Furthermore, repeatability and reproducibility values were notably improved, especially when working with electrodes covered with a polyamide layer prepared with N-(2-aminoethyl)-piperazine.
Bibliography:ObjectType-Article-1
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ISSN:0956-5663
1873-4235
DOI:10.1016/j.bios.2006.10.034