Portable Microfluidic Integrated Plasmonic Platform for Pathogen Detection

Timely detection of infectious agents is critical in early diagnosis and treatment of infectious diseases. Conventional pathogen detection methods, such as enzyme linked immunosorbent assay (ELISA), culturing or polymerase chain reaction (PCR) require long assay times and complex and expensive instr...

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Published in:Scientific reports Vol. 5; no. 1; p. 9152
Main Authors: Tokel, Onur, Yildiz, Umit Hakan, Inci, Fatih, Durmus, Naside Gozde, Ekiz, Okan Oner, Turker, Burak, Cetin, Can, Rao, Shruthi, Sridhar, Kaushik, Natarajan, Nalini, Shafiee, Hadi, Dana, Aykutlu, Demirci, Utkan
Format: Journal Article
Language:English
Published: London Nature Publishing Group UK 24.03.2015
Nature Publishing Group
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ISSN:2045-2322, 2045-2322
Online Access:Get full text
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Summary:Timely detection of infectious agents is critical in early diagnosis and treatment of infectious diseases. Conventional pathogen detection methods, such as enzyme linked immunosorbent assay (ELISA), culturing or polymerase chain reaction (PCR) require long assay times and complex and expensive instruments, which are not adaptable to point-of-care (POC) needs at resource-constrained as well as primary care settings. Therefore, there is an unmet need to develop simple, rapid and accurate methods for detection of pathogens at the POC. Here, we present a portable, multiplex, inexpensive microfluidic-integrated surface plasmon resonance (SPR) platform that detects and quantifies bacteria, i.e. , Escherichia coli ( E. coli ) and Staphylococcus aureus ( S. aureus ) rapidly. The platform presented reliable capture and detection of E. coli at concentrations ranging from ~10 5 to 3.2 × 10 7  CFUs/mL in phosphate buffered saline (PBS) and peritoneal dialysis (PD) fluid. The multiplexing and specificity capability of the platform was also tested with S. aureus samples. The presented platform technology could potentially be applicable to capture and detect other pathogens at the POC and primary care settings.
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These authors contributed equally to this work.
ISSN:2045-2322
2045-2322
DOI:10.1038/srep09152