Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin

The standard method for the detection of botulinum neurotoxin is currently the mouse bioassay which is considered to be the most reliable method for the detection of the active form of this toxin. Despite this it is a time-consuming and expensive assay to run and as such many alternative assays have...

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Main Authors: Jennifer Halliwell, Alison C. Savage, Nicholas Buckley, Christopher Gwenin
Format: Article
Language:English
Published: Elsevier 2014-12-01
Series:Sensing and Bio-Sensing Research
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214180414000221
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spelling doaj-e3f21f039d1a486e9397ba966e81d98e2020-11-24T23:22:23ZengElsevierSensing and Bio-Sensing Research2214-18042014-12-012C121510.1016/j.sbsr.2014.08.002Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxinJennifer HalliwellAlison C. SavageNicholas BuckleyChristopher GweninThe standard method for the detection of botulinum neurotoxin is currently the mouse bioassay which is considered to be the most reliable method for the detection of the active form of this toxin. Despite this it is a time-consuming and expensive assay to run and as such many alternative assays have recently been proposed. Herein we report the development of two electrochemical assays for the detection of active botulinum neurotoxin in a pharmaceutical sample. Gold electrodes were modified with self-assembled monolayers of the SNARE protein SNAP-25 which is selectively cleaved by active botulinum neurotoxin A. Cyclic voltammetry and electrochemical impedance spectroscopy were performed on the modified working electrodes to observe changes to the layer on addition of the toxin. Both methods were able to distinguish the difference between the presence of the active toxin and a placebo containing the excipients of the pharmaceutical product. The electrochemical impedance spectroscopy assay also allowed for detection of the active toxin at concentrations as low as 25 fg/ml, with results being obtained in under an hour outperforming the mouse bioassay.http://www.sciencedirect.com/science/article/pii/S2214180414000221Electrochemical impedance spectroscopyCyclic voltammetryBotulinum neurotoxinSNAP-25
collection DOAJ
language English
format Article
sources DOAJ
author Jennifer Halliwell
Alison C. Savage
Nicholas Buckley
Christopher Gwenin
spellingShingle Jennifer Halliwell
Alison C. Savage
Nicholas Buckley
Christopher Gwenin
Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
Sensing and Bio-Sensing Research
Electrochemical impedance spectroscopy
Cyclic voltammetry
Botulinum neurotoxin
SNAP-25
author_facet Jennifer Halliwell
Alison C. Savage
Nicholas Buckley
Christopher Gwenin
author_sort Jennifer Halliwell
title Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
title_short Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
title_full Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
title_fullStr Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
title_full_unstemmed Electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
title_sort electrochemical impedance spectroscopy biosensor for detection of active botulinum neurotoxin
publisher Elsevier
series Sensing and Bio-Sensing Research
issn 2214-1804
publishDate 2014-12-01
description The standard method for the detection of botulinum neurotoxin is currently the mouse bioassay which is considered to be the most reliable method for the detection of the active form of this toxin. Despite this it is a time-consuming and expensive assay to run and as such many alternative assays have recently been proposed. Herein we report the development of two electrochemical assays for the detection of active botulinum neurotoxin in a pharmaceutical sample. Gold electrodes were modified with self-assembled monolayers of the SNARE protein SNAP-25 which is selectively cleaved by active botulinum neurotoxin A. Cyclic voltammetry and electrochemical impedance spectroscopy were performed on the modified working electrodes to observe changes to the layer on addition of the toxin. Both methods were able to distinguish the difference between the presence of the active toxin and a placebo containing the excipients of the pharmaceutical product. The electrochemical impedance spectroscopy assay also allowed for detection of the active toxin at concentrations as low as 25 fg/ml, with results being obtained in under an hour outperforming the mouse bioassay.
topic Electrochemical impedance spectroscopy
Cyclic voltammetry
Botulinum neurotoxin
SNAP-25
url http://www.sciencedirect.com/science/article/pii/S2214180414000221
work_keys_str_mv AT jenniferhalliwell electrochemicalimpedancespectroscopybiosensorfordetectionofactivebotulinumneurotoxin
AT alisoncsavage electrochemicalimpedancespectroscopybiosensorfordetectionofactivebotulinumneurotoxin
AT nicholasbuckley electrochemicalimpedancespectroscopybiosensorfordetectionofactivebotulinumneurotoxin
AT christophergwenin electrochemicalimpedancespectroscopybiosensorfordetectionofactivebotulinumneurotoxin
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