Dergi makalesi Açık Erişim

Paper and Flexible Substrates as Materials for Biosensing Platforms to Detect Multiple Biotargets

Shafiee, Hadi; Asghar, Waseem; Inci, Fatih; Yuksekkaya, Mehmet; Jahangir, Muntasir; Zhang, Michael H.; Durmus, Naside Gozde; Gurkan, Umut Atakan; Kuritzkes, Daniel R.; Demirci, Utkan


MARC21 XML

<?xml version='1.0' encoding='UTF-8'?>
<record xmlns="http://www.loc.gov/MARC21/slim">
  <leader>00000nam##2200000uu#4500</leader>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Asghar, Waseem</subfield>
    <subfield code="u">Stanford Univ, Sch Med, Canary Ctr Stanford Canc Early Detect, Demirci Bioacoust MEMS Med BAMM Lab, Palo Alto, CA 94304 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Inci, Fatih</subfield>
    <subfield code="u">Stanford Univ, Sch Med, Canary Ctr Stanford Canc Early Detect, Demirci Bioacoust MEMS Med BAMM Lab, Palo Alto, CA 94304 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Yuksekkaya, Mehmet</subfield>
    <subfield code="u">Harvard Univ, Brigham &amp; Womens Hosp, Sch Med,Div Biomed Engn,Dep Med, Demirci Bioacoust MEMS Med BAMM Lab,Div Renal Med, Boston, MA 02115 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Jahangir, Muntasir</subfield>
    <subfield code="u">Harvard Univ, Brigham &amp; Womens Hosp, Sch Med,Div Biomed Engn,Dep Med, Demirci Bioacoust MEMS Med BAMM Lab,Div Renal Med, Boston, MA 02115 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Zhang, Michael H.</subfield>
    <subfield code="u">Harvard Univ, Brigham &amp; Womens Hosp, Sch Med,Div Biomed Engn,Dep Med, Demirci Bioacoust MEMS Med BAMM Lab,Div Renal Med, Boston, MA 02115 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Durmus, Naside Gozde</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Gurkan, Umut Atakan</subfield>
    <subfield code="u">Harvard Univ, Brigham &amp; Womens Hosp, Sch Med,Div Biomed Engn,Dep Med, Demirci Bioacoust MEMS Med BAMM Lab,Div Renal Med, Boston, MA 02115 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Kuritzkes, Daniel R.</subfield>
    <subfield code="u">Harvard Univ, Sch Med, Brigham &amp; Womens Hosp, Div Infect Dis, Cambridge, MA 02138 USA</subfield>
  </datafield>
  <datafield tag="700" ind1=" " ind2=" ">
    <subfield code="a">Demirci, Utkan</subfield>
  </datafield>
  <datafield tag="909" ind1="C" ind2="4">
    <subfield code="p">SCIENTIFIC REPORTS</subfield>
    <subfield code="v">5</subfield>
  </datafield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="a">user-tubitak-destekli-proje-yayinlari</subfield>
  </datafield>
  <datafield tag="540" ind1=" " ind2=" ">
    <subfield code="a">Creative Commons Attribution</subfield>
    <subfield code="u">http://www.opendefinition.org/licenses/cc-by</subfield>
  </datafield>
  <datafield tag="024" ind1=" " ind2=" ">
    <subfield code="a">10.1038/srep08719</subfield>
    <subfield code="2">doi</subfield>
  </datafield>
  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Paper and Flexible Substrates as Materials for Biosensing Platforms to Detect Multiple Biotargets</subfield>
  </datafield>
  <datafield tag="100" ind1=" " ind2=" ">
    <subfield code="a">Shafiee, Hadi</subfield>
    <subfield code="u">Harvard Univ, Brigham &amp; Womens Hosp, Sch Med,Div Biomed Engn,Dep Med, Demirci Bioacoust MEMS Med BAMM Lab,Div Renal Med, Boston, MA 02115 USA</subfield>
  </datafield>
  <datafield tag="909" ind1="C" ind2="O">
    <subfield code="o">oai:zenodo.org:76631</subfield>
    <subfield code="p">user-tubitak-destekli-proje-yayinlari</subfield>
  </datafield>
  <datafield tag="650" ind1="1" ind2="7">
    <subfield code="2">opendefinition.org</subfield>
    <subfield code="a">cc-by</subfield>
  </datafield>
  <datafield tag="260" ind1=" " ind2=" ">
    <subfield code="c">2015-01-01</subfield>
  </datafield>
  <datafield tag="856" ind1="4" ind2=" ">
    <subfield code="u">https://aperta.ulakbim.gov.trrecord/76631/files/bib-2ba50ae0-6ddc-4a7f-8d82-3c4a76c31895.txt</subfield>
    <subfield code="z">md5:f5ea698803345da28a4cc0a3bf8c3a5e</subfield>
    <subfield code="s">263</subfield>
  </datafield>
  <datafield tag="542" ind1=" " ind2=" ">
    <subfield code="l">open</subfield>
  </datafield>
  <controlfield tag="005">20210316044152.0</controlfield>
  <controlfield tag="001">76631</controlfield>
  <datafield tag="980" ind1=" " ind2=" ">
    <subfield code="a">publication</subfield>
    <subfield code="b">article</subfield>
  </datafield>
  <datafield tag="520" ind1=" " ind2=" ">
    <subfield code="a">The need for sensitive, robust, portable, and inexpensive biosensing platforms is of significant interest in clinical applications for disease diagnosis and treatment monitoring at the point-of-care (POC) settings. Rapid, accurate POC diagnostic assays play a crucial role in developing countries, where there are limited laboratory infrastructure, trained personnel, and financial support. However, current diagnostic assays commonly require long assay time, sophisticated infrastructure and expensive reagents that are not compatible with resource-constrained settings. Although paper and flexible material-based platform technologies provide alternative approaches to develop POC diagnostic assays for broad applications in medicine, they have technical challenges integrating to different detection modalities. Here, we address the limited capability of current paper and flexible material-based platforms by integrating cellulose paper and flexible polyester films as diagnostic biosensing materials with various detection modalities through the development and validation of new widely applicable electrical and optical sensing mechanisms using antibodies and peptides. By incorporating these different detection modalities, we present selective and accurate capture and detection of multiple biotargets including viruses (Human Immunodeficieny Virus-1), bacteria (Escherichia coli and Staphylococcus aureus), and cells (CD4(+) T lymphocytes) from fingerprick volume equivalent of multiple biological specimens such as whole blood, plasma, and peritoneal dialysis effluent with clinically relevant detection and sensitivity.</subfield>
  </datafield>
</record>
16
4
görüntülenme
indirilme
Görüntülenme 16
İndirme 4
Veri hacmi 1.1 kB
Tekil görüntülenme 16
Tekil indirme 4

Alıntı yap