Deploying aptameric sensing technology for rapid pandemic monitoring.
Identifieur interne : 000633 ( PubMed/Corpus ); précédent : 000632; suivant : 000634Deploying aptameric sensing technology for rapid pandemic monitoring.
Auteurs : Caleb Acquah ; Michael K. Danquah ; Dominic Agyei ; Charles K S. Moy ; Amandeep Sidhu ; Clarence M. OngkudonSource :
- Critical reviews in biotechnology [ 1549-7801 ] ; 2016.
English descriptors
- KwdEn :
- MESH :
- chemical : Aptamers, Nucleotide.
- genetics : Bacteria, Viruses.
- Biosensing Techniques, Humans, Pandemics.
Abstract
The genome of virulent strains may possess the ability to mutate by means of antigenic shift and/or antigenic drift as well as being resistant to antibiotics with time. The outbreak and spread of these virulent diseases including avian influenza (H1N1), severe acute respiratory syndrome (SARS-Corona virus), cholera (Vibrio cholera), tuberculosis (Mycobacterium tuberculosis), Ebola hemorrhagic fever (Ebola Virus) and AIDS (HIV-1) necessitate urgent attention to develop diagnostic protocols and assays for rapid detection and screening. Rapid and accurate detection of first cases with certainty will contribute significantly in preventing disease transmission and escalation to pandemic levels. As a result, there is a need to develop technologies that can meet the heavy demand of an all-embedded, inexpensive, specific and fast biosensing for the detection and screening of pathogens in active or latent forms to offer quick diagnosis and early treatments in order to avoid disease aggravation and unnecessary late treatment costs. Nucleic acid aptamers are short, single-stranded RNA or DNA sequences that can selectively bind to specific cellular and biomolecular targets. Aptamers, as new-age bioaffinity probes, have the necessary biophysical characteristics for improved pathogen detection. This article seeks to review global pandemic situations in relation to advances in pathogen detection systems. It particularly discusses aptameric biosensing and establishes application opportunities for effective pandemic monitoring. Insights into the application of continuous polymeric supports as the synthetic base for aptamer coupling to provide the needed convective mass transport for rapid screening is also presented.
DOI: 10.3109/07388551.2015.1083940
PubMed: 26381238
Links to Exploration step
pubmed:26381238Le document en format XML
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Danquah</name><affiliation><nlm:affiliation>b Department of Chemical Engineering , Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Agyei, Dominic" sort="Agyei, Dominic" uniqKey="Agyei D" first="Dominic" last="Agyei">Dominic Agyei</name><affiliation><nlm:affiliation>c Centre for Chemistry and Biotechnology, School of Life and Environmental Sciences Deakin University , Geelong-Waurn Ponds , Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Moy, Charles K S" sort="Moy, Charles K S" uniqKey="Moy C" first="Charles K S" last="Moy">Charles K S. Moy</name><affiliation><nlm:affiliation>d Faculty of Engineering and Science , Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Sidhu, Amandeep" sort="Sidhu, Amandeep" uniqKey="Sidhu A" first="Amandeep" last="Sidhu">Amandeep Sidhu</name><affiliation><nlm:affiliation>a Curtin Sarawak Research Institute, Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Ongkudon, Clarence M" sort="Ongkudon, Clarence M" uniqKey="Ongkudon C" first="Clarence M" last="Ongkudon">Clarence M. Ongkudon</name><affiliation><nlm:affiliation>f Biotechnology Research Institute, Universiti Malaysia Sabah, Kota Kinabalu , Sabah, 88400 , Malaysia.</nlm:affiliation></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PubMed</idno><date when="2016">2016</date><idno type="RBID">pubmed:26381238</idno><idno type="pmid">26381238</idno><idno type="doi">10.3109/07388551.2015.1083940</idno><idno type="wicri:Area/PubMed/Corpus">000633</idno><idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">000633</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en">Deploying aptameric sensing technology for rapid pandemic monitoring.</title><author><name sortKey="Acquah, Caleb" sort="Acquah, Caleb" uniqKey="Acquah C" first="Caleb" last="Acquah">Caleb Acquah</name><affiliation><nlm:affiliation>a Curtin Sarawak Research Institute, Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Danquah, Michael K" sort="Danquah, Michael K" uniqKey="Danquah M" first="Michael K" last="Danquah">Michael K. Danquah</name><affiliation><nlm:affiliation>b Department of Chemical Engineering , Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Agyei, Dominic" sort="Agyei, Dominic" uniqKey="Agyei D" first="Dominic" last="Agyei">Dominic Agyei</name><affiliation><nlm:affiliation>c Centre for Chemistry and Biotechnology, School of Life and Environmental Sciences Deakin University , Geelong-Waurn Ponds , Australia.</nlm:affiliation></affiliation></author><author><name sortKey="Moy, Charles K S" sort="Moy, Charles K S" uniqKey="Moy C" first="Charles K S" last="Moy">Charles K S. Moy</name><affiliation><nlm:affiliation>d Faculty of Engineering and Science , Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Sidhu, Amandeep" sort="Sidhu, Amandeep" uniqKey="Sidhu A" first="Amandeep" last="Sidhu">Amandeep Sidhu</name><affiliation><nlm:affiliation>a Curtin Sarawak Research Institute, Curtin University , Sarawak 98009 , Malaysia.</nlm:affiliation></affiliation></author><author><name sortKey="Ongkudon, Clarence M" sort="Ongkudon, Clarence M" uniqKey="Ongkudon C" first="Clarence M" last="Ongkudon">Clarence M. Ongkudon</name><affiliation><nlm:affiliation>f Biotechnology Research Institute, Universiti Malaysia Sabah, Kota Kinabalu , Sabah, 88400 , Malaysia.</nlm:affiliation></affiliation></author></analytic><series><title level="j">Critical reviews in biotechnology</title><idno type="eISSN">1549-7801</idno><imprint><date when="2016" type="published">2016</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Aptamers, Nucleotide</term><term>Bacteria (genetics)</term><term>Biosensing Techniques</term><term>Humans</term><term>Pandemics</term><term>Viruses (genetics)</term></keywords><keywords scheme="MESH" type="chemical" xml:lang="en"><term>Aptamers, Nucleotide</term></keywords><keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Bacteria</term><term>Viruses</term></keywords><keywords scheme="MESH" xml:lang="en"><term>Biosensing Techniques</term><term>Humans</term><term>Pandemics</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The genome of virulent strains may possess the ability to mutate by means of antigenic shift and/or antigenic drift as well as being resistant to antibiotics with time. The outbreak and spread of these virulent diseases including avian influenza (H1N1), severe acute respiratory syndrome (SARS-Corona virus), cholera (Vibrio cholera), tuberculosis (Mycobacterium tuberculosis), Ebola hemorrhagic fever (Ebola Virus) and AIDS (HIV-1) necessitate urgent attention to develop diagnostic protocols and assays for rapid detection and screening. Rapid and accurate detection of first cases with certainty will contribute significantly in preventing disease transmission and escalation to pandemic levels. As a result, there is a need to develop technologies that can meet the heavy demand of an all-embedded, inexpensive, specific and fast biosensing for the detection and screening of pathogens in active or latent forms to offer quick diagnosis and early treatments in order to avoid disease aggravation and unnecessary late treatment costs. Nucleic acid aptamers are short, single-stranded RNA or DNA sequences that can selectively bind to specific cellular and biomolecular targets. Aptamers, as new-age bioaffinity probes, have the necessary biophysical characteristics for improved pathogen detection. This article seeks to review global pandemic situations in relation to advances in pathogen detection systems. It particularly discusses aptameric biosensing and establishes application opportunities for effective pandemic monitoring. Insights into the application of continuous polymeric supports as the synthetic base for aptamer coupling to provide the needed convective mass transport for rapid screening is also presented.</div></front></TEI><pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">26381238</PMID><DateCompleted><Year>2017</Year><Month>02</Month><Day>09</Day></DateCompleted><DateRevised><Year>2017</Year><Month>02</Month><Day>09</Day></DateRevised><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Electronic">1549-7801</ISSN><JournalIssue CitedMedium="Internet"><Volume>36</Volume><Issue>6</Issue><PubDate><Year>2016</Year><Month>Dec</Month></PubDate></JournalIssue><Title>Critical reviews in biotechnology</Title><ISOAbbreviation>Crit. Rev. Biotechnol.</ISOAbbreviation></Journal><ArticleTitle>Deploying aptameric sensing technology for rapid pandemic monitoring.</ArticleTitle><Pagination><MedlinePgn>1010-1022</MedlinePgn></Pagination><Abstract><AbstractText>The genome of virulent strains may possess the ability to mutate by means of antigenic shift and/or antigenic drift as well as being resistant to antibiotics with time. The outbreak and spread of these virulent diseases including avian influenza (H1N1), severe acute respiratory syndrome (SARS-Corona virus), cholera (Vibrio cholera), tuberculosis (Mycobacterium tuberculosis), Ebola hemorrhagic fever (Ebola Virus) and AIDS (HIV-1) necessitate urgent attention to develop diagnostic protocols and assays for rapid detection and screening. Rapid and accurate detection of first cases with certainty will contribute significantly in preventing disease transmission and escalation to pandemic levels. As a result, there is a need to develop technologies that can meet the heavy demand of an all-embedded, inexpensive, specific and fast biosensing for the detection and screening of pathogens in active or latent forms to offer quick diagnosis and early treatments in order to avoid disease aggravation and unnecessary late treatment costs. Nucleic acid aptamers are short, single-stranded RNA or DNA sequences that can selectively bind to specific cellular and biomolecular targets. Aptamers, as new-age bioaffinity probes, have the necessary biophysical characteristics for improved pathogen detection. This article seeks to review global pandemic situations in relation to advances in pathogen detection systems. It particularly discusses aptameric biosensing and establishes application opportunities for effective pandemic monitoring. Insights into the application of continuous polymeric supports as the synthetic base for aptamer coupling to provide the needed convective mass transport for rapid screening is also presented.</AbstractText></Abstract><AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Acquah</LastName><ForeName>Caleb</ForeName><Initials>C</Initials><AffiliationInfo><Affiliation>a Curtin Sarawak Research Institute, Curtin University , Sarawak 98009 , Malaysia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>b Department of Chemical Engineering , Curtin University , Sarawak 98009 , Malaysia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Danquah</LastName><ForeName>Michael K</ForeName><Initials>MK</Initials><AffiliationInfo><Affiliation>b Department of Chemical Engineering , Curtin University , Sarawak 98009 , Malaysia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Agyei</LastName><ForeName>Dominic</ForeName><Initials>D</Initials><AffiliationInfo><Affiliation>c Centre for Chemistry and Biotechnology, School of Life and Environmental Sciences Deakin University , Geelong-Waurn Ponds , Australia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Moy</LastName><ForeName>Charles K S</ForeName><Initials>CK</Initials><AffiliationInfo><Affiliation>d Faculty of Engineering and Science , Curtin University , Sarawak 98009 , Malaysia.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Sidhu</LastName><ForeName>Amandeep</ForeName><Initials>A</Initials><AffiliationInfo><Affiliation>a Curtin Sarawak Research Institute, Curtin University , Sarawak 98009 , Malaysia.</Affiliation></AffiliationInfo><AffiliationInfo><Affiliation>e Faculty of Health Sciences , Curtin University , Perth 6102 , Australia , and.</Affiliation></AffiliationInfo></Author><Author ValidYN="Y"><LastName>Ongkudon</LastName><ForeName>Clarence M</ForeName><Initials>CM</Initials><AffiliationInfo><Affiliation>f Biotechnology Research Institute, Universiti Malaysia Sabah, Kota Kinabalu , Sabah, 88400 , Malaysia.</Affiliation></AffiliationInfo></Author></AuthorList><Language>eng</Language><PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType><PublicationType UI="D016454">Review</PublicationType></PublicationTypeList><ArticleDate DateType="Electronic"><Year>2015</Year><Month>09</Month><Day>18</Day></ArticleDate></Article><MedlineJournalInfo><Country>England</Country><MedlineTA>Crit Rev Biotechnol</MedlineTA><NlmUniqueID>8505177</NlmUniqueID><ISSNLinking>0738-8551</ISSNLinking></MedlineJournalInfo><ChemicalList><Chemical><RegistryNumber>0</RegistryNumber><NameOfSubstance UI="D052157">Aptamers, Nucleotide</NameOfSubstance></Chemical></ChemicalList><CitationSubset>IM</CitationSubset><MeshHeadingList><MeshHeading><DescriptorName UI="D052157" MajorTopicYN="Y">Aptamers, Nucleotide</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D001419" MajorTopicYN="N">Bacteria</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading><MeshHeading><DescriptorName UI="D015374" MajorTopicYN="Y">Biosensing Techniques</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D006801" MajorTopicYN="N">Humans</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D058873" MajorTopicYN="Y">Pandemics</DescriptorName></MeshHeading><MeshHeading><DescriptorName UI="D014780" MajorTopicYN="N">Viruses</DescriptorName><QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName></MeshHeading></MeshHeadingList><KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Aptamers</Keyword><Keyword MajorTopicYN="N">bioscreening</Keyword><Keyword MajorTopicYN="N">cell culture</Keyword><Keyword MajorTopicYN="N">molecular diagnostics</Keyword><Keyword MajorTopicYN="N">pandemics</Keyword></KeywordList></MedlineCitation><PubmedData><History><PubMedPubDate PubStatus="pubmed"><Year>2015</Year><Month>9</Month><Day>19</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="medline"><Year>2017</Year><Month>2</Month><Day>10</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate><PubMedPubDate PubStatus="entrez"><Year>2015</Year><Month>9</Month><Day>19</Day><Hour>6</Hour><Minute>0</Minute></PubMedPubDate></History><PublicationStatus>ppublish</PublicationStatus><ArticleIdList><ArticleId IdType="pubmed">26381238</ArticleId><ArticleId IdType="doi">10.3109/07388551.2015.1083940</ArticleId></ArticleIdList></PubmedData></pubmed></record>Pour manipuler ce document sous Unix (Dilib)
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