| Literature DB >> 31765118 |
Juliana Coatrini Soares1,2, Andrey Coatrini Soares1,2, Valquiria Cruz Rodrigues1, Matias Eliseo Melendez3, Alexandre Cesar Santos3, Eliney Ferreira Faria3, Rui M Reis3,4,5, Andre Lopes Carvalho3, Osvaldo N Oliveira1.
Abstract
Diagnosis of prostate cancer via PCA3 biomarker detection is promising to be much more efficient than with the prostatic specific antigens currently used. In this study, we present the first electrochemical and impedance-based biosensors that are capable of detecting PCA3 down to 0.128 nmol/L. The biosensors were made with a layer of PCA3-complementary single-stranded DNA (ssDNA) probe, immobilized on a layer-by-layer (LbL) film of chitosan (CHT) and carbon nanotubes (MWCNT). They are highly selective to PCA3, which was confirmed in impedance measurements and with polarization-modulated infrared reflection absorption spectroscopy (PM-IRRAS). Using information visualization methods, we could also distinguish between cell lines expressing the endogenous PCA3 long noncoding RNA (lncRNA) from cells that did not contain detectable levels of this biomarker. Since the methods involved in fabrication the biosensors are potentially low cost, one may hope to deploy PCA3 tests in any laboratory of clinical analyses and even for point-of-care diagnostics.Entities:
Keywords: DNA; EIS; PCA3; biosensors; impedance spectroscopy; prostate cancer
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Year: 2019 PMID: 31765118 DOI: 10.1021/acsami.9b19180
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229