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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| Veröffentlicht in: | Scientific reports Jg. 5; H. 1; S. 9152 |
|---|---|
| Hauptverfasser: | , , , , , , , , , , , , |
| Format: | Journal Article |
| Sprache: | Englisch |
| Veröffentlicht: |
London
Nature Publishing Group UK
24.03.2015
Nature Publishing Group |
| Schlagworte: | |
| ISSN: | 2045-2322, 2045-2322 |
| Online-Zugang: | Volltext |
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| Zusammenfassung: | 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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| Bibliographie: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally to this work. |
| ISSN: | 2045-2322 2045-2322 |
| DOI: | 10.1038/srep09152 |