Development of piezoelectric immunosensors for competitive and direct determination of atrazine

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F03%3A00008696" target="_blank" >RIV/00216224:14310/03:00008696 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00000493:G41__/03:25150

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Development of piezoelectric immunosensors for competitive and direct determination of atrazine

Popis výsledku v původním jazyce

The improved highly sensitive piezoelectric immunosensor has been developed. The gold electrodes of the piezoelectric quartz crystals were modified with self-assembled layer of cysteamine and carboxyderivative of atrazine was covalently attached after activation with O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (TSTU). The competitive immunoassay for atrazine was developed using anti-atrazine monoclonal antibody (MAb) D6F3. The limit of detection for atrazine was 0.025 ng/ml, the total time of analysis being 25 min. The repeated use of the immunosensors was possible after regeneration using pepsin at pH 2.0. The direct immunosensor for atrazine was constructed by oriented immobilization of anti-atrazine MAb to Protein A covalentlyattached to the gold surface activated with 3,3'-dithio-bis(propionic acid N-hydroxysuccinimide ester) (DTSP). The MAb-Protein A complex was stabilized by cross-linking with dimethyl pimelimidate. Thus developed immunosensor was able to s

Název v anglickém jazyce

Development of piezoelectric immunosensors for competitive and direct determination of atrazine

Popis výsledku anglicky

The improved highly sensitive piezoelectric immunosensor has been developed. The gold electrodes of the piezoelectric quartz crystals were modified with self-assembled layer of cysteamine and carboxyderivative of atrazine was covalently attached after activation with O-(N-succinimidyl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (TSTU). The competitive immunoassay for atrazine was developed using anti-atrazine monoclonal antibody (MAb) D6F3. The limit of detection for atrazine was 0.025 ng/ml, the total time of analysis being 25 min. The repeated use of the immunosensors was possible after regeneration using pepsin at pH 2.0. The direct immunosensor for atrazine was constructed by oriented immobilization of anti-atrazine MAb to Protein A covalentlyattached to the gold surface activated with 3,3'-dithio-bis(propionic acid N-hydroxysuccinimide ester) (DTSP). The MAb-Protein A complex was stabilized by cross-linking with dimethyl pimelimidate. Thus developed immunosensor was able to s

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CE - Biochemie

OECD FORD obor

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Projekt

Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

Návaznosti

P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Rok uplatnění

2003

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Sensors and Actuators B Chemical

ISSN

0925-4005

e-ISSN

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Svazek periodika

91

Číslo periodika v rámci svazku

1

Stát vydavatele periodika

NL - Nizozemsko

Počet stran výsledku

9

Strana od-do

333-341

Kód UT WoS článku

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EID výsledku v databázi Scopus

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