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...
Main Authors: | , , , |
---|---|
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 |
id |
doaj-e3f21f039d1a486e9397ba966e81d98e |
---|---|
record_format |
Article |
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 |
_version_ |
1725568224655835136 |