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Title: | Electrochemical paper-based peptide nucleic acid biosensor for detecting human papillomavirus |
Authors: | Teengam P. Siangproh W. Tuantranont A. Henry C.S. Vilaivan T. Chailapakul O. |
Keywords: | Biosensors Cell culture Chemical detection DNA Electrochemical impedance spectroscopy Graphene Ink jet printing Ketones Nucleic acids Oligonucleotides Peptides Polyaniline Polymerase chain reaction Probes Voltammetry acpcPNA Electrochemical biosensor ELectrochemical detection Electrochemical DNA biosensors Electrochemical signals Electrostatic attractions Human papillomavirus Square wave voltammetry Electrochemical electrodes anthraquinone graphene nucleic acid polyaniline pyrrolidine derivative pyrrolidinyl peptide nucleic acid unclassified drug peptide nucleic acid virus DNA amino terminal sequence Article biosensor controlled study electrochemical detection electrochemical impedance spectroscopy electron transport Human papillomavirus type 16 hybridization limit of detection limit of quantitation nonhuman paper based electrochemical biosensor polymerase chain reaction potentiometry priority journal reproducibility square wave voltammetry static electricity uterine cervix cancer virus detection chemistry electrochemical analysis electrode genetic procedures human Human papillomavirus type 16 isolation and purification nucleic acid hybridization tumor cell line Electrodes Ink Jet Printing Nucleic Acids Peptides Biosensing Techniques Cell Line, Tumor DNA, Viral Electrochemical Techniques Electrodes Human papillomavirus 16 Humans Nucleic Acid Hybridization Peptide Nucleic Acids |
Issue Date: | 2017 |
Abstract: | A novel paper-based electrochemical biosensor was developed using an anthraquinone-labeled pyrrolidinyl peptide nucleic acid (acpcPNA) probe (AQ-PNA) and graphene-polyaniline (G-PANI) modified electrode to detect human papillomavirus (HPV). An inkjet printing technique was employed to prepare the paper-based G-PANI-modified working electrode. The AQ-PNA probe baring a negatively charged amino acid at the N-terminus was immobilized onto the electrode surface through electrostatic attraction. Electrochemical impedance spectroscopy (EIS) was used to verify the AQ-PNA immobilization. The paper-based electrochemical DNA biosensor was used to detect a synthetic 14-base oligonucleotide target with a sequence corresponding to human papillomavirus (HPV) type 16 DNA by measuring the electrochemical signal response of the AQ label using square-wave voltammetry before and after hybridization. It was determined that the current signal significantly decreased after the addition of target DNA. This phenomenon is explained by the rigidity of PNA-DNA duplexes, which obstructs the accessibility of electron transfer from the AQ label to the electrode surface. Under optimal conditions, the detection limit of HPV type 16 DNA was found to be 2.3 nM with a linear range of 10–200 nM. The performance of this biosensor on real DNA samples was tested with the detection of PCR-amplified DNA samples from the SiHa cell line. The new method employs an inexpensive and disposable device, which easily incinerated after use and is promising for the screening and monitoring of the amount of HPV-DNA type 16 to identify the primary stages of cervical cancer. © 2016 Elsevier B.V. |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13158 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85006381853&doi=10.1016%2fj.aca.2016.11.071&partnerID=40&md5=4887fe3094bb3cda5164e64c3f5e950a |
ISSN: | 32670 |
Appears in Collections: | Scopus 1983-2021 |
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