Sensitive multiplex detection of serological liver cancer biomarkers using SERS-active photonic crystal fiber probe

Sensitive multiplex detection of serological liver cancer biomarkers using SERS-active photonic crystal fiber probe
Title:
Sensitive multiplex detection of serological liver cancer biomarkers using SERS-active photonic crystal fiber probe
Other Titles:
Journal of Biophotonics
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Publication Date:
21 August 2013
Citation:
Dinish, U. S., Balasundaram, G., Chang, Y. T. and Olivo, M. (2013), Sensitive multiplex detection of serological liver cancer biomarkers using SERS-active photonic crystal fiber probe. J. Biophoton.. doi: 10.1002/jbio.201300084
Abstract:
Surface Enhanced Raman Scattering (SERS) spectroscopy possesses the most promising advantage of multiplex detection for biosensing applications, which is achieved due to the narrow ‘fingerprint’ Raman spectra from the analyte molecules. We developed an ultrasensitive platform for the multiplex detection of cancer biomarkers by combining SERS technique with hollow core photonic crystal fiber (HCPCF). Axially aligned air channels inside the HCPCF provide an excellent platform for optical sensing using SERS. In addition to the flexibility of optical fibers, HCPCF provides better light confinement and a larger interaction length for the guided light and the analyte, resulting in an improvement in sensitivity to detect low concentration of bio-analytes at extremely low sample volume. Herein, for the first time, we demonstrate the sensitive multiplex detection of biomarkers immobilized inside the HCPCF using antibody conjugated SERS-active nanoparticles (SERS nanotags). As a proof-of-concept for targeted multiplex detection, initially we carried out the sensing of epidermal growth factor receptor (EGFR) biomarker in oral squamous carcinoma cell lysate using three different SERS nanotags. Subsequently, we also achieved simultaneous detection of hepatocellular carcinoma (HCC) biomarkers-alpha fetoprotein (AFP) and alpha-1- antitrypsin (A1AT) secreted in the supernatant from Hep3b cancer cell line. Using SERS-HCPCF sensing platform, we could successfully demonstrate the multiplex detection in an extremely low sample volume of ~20nL. In future, this study may lead to sensitive biosensing platform for the low concentration detection of biomarkers in an extremely low sample volume of body fluids to achieve early diagnosis of multiple diseases.
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PublisherCopyrights
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ISSN:
1864-063X
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