期刊
SENSORS
卷 21, 期 8, 页码 -出版社
MDPI
DOI: 10.3390/s21082683
关键词
bacteria; Salmonella typhimurium; white light reflectance spectroscopy; immunosensor
资金
- program of Industrial Scholarships of Stavros Niarchos Foundation
This study presented an optical biosensor based on white light reflectance spectroscopy for detecting Salmonella typhimurium lipopolysaccharide and bacteria in drinking water. The sensor chip, with a simple structure, employed a competitive immunoassay configuration for rapid detection of extremely low concentrations of Salmonella LPS and bacteria. With short analysis time and small size, this immunosensor could have broad applications in bacteria detection in drinking water.
Biosensors represent an attractive approach for fast bacteria detection. Here, we present an optical biosensor for the detection of Salmonella typhimurium lipopolysaccharide (LPS) and Salmonella bacteria in drinking water, based on white light reflectance spectroscopy. The sensor chip consisted of a Si die with a thin SiO2 layer on top that was transformed into a biosensor through the immobilization of Salmonella LPS. The optical setup included a reflection probe with seven 200 mu m fibers, a visible and near-infrared light source, and a spectrometer. The six fibers at the reflection probe circumference were coupled with the light source and illuminated the biosensor chip vertically, whereas the central fiber collected the reflected light and guided it to the spectrometer. A competitive immunoassay configuration was adopted for the analysis. Accordingly, a mixture of LPS or bacteria solution, pre-incubated for 15 min, with an anti-Salmonella LPS antibody was pumped over the chip followed by biotinylated secondary antibody and streptavidin for signal enhancement. The binding of the free anti-Salmonella antibody to chip-immobilized LPS led to a shift of the reflectance spectrum that was inversely related to the analyte concentration (LPS or bacteria) in the calibrators or samples. The total assay duration was 15 min, and the detection limits achieved were 4 ng/mL for LPS and 320 CFU/mL for bacteria. Taking into account the low detection limits, the short analysis time, and the small size of the chip and instrumentation employed, the proposed immunosensor could find wide application for bacteria detection in drinking water.
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