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Brillouin spectroscopy as a new method of screening for increased CSF total protein during bacterial meningitis
Bacterial meningitis is a disease of pronounced clinical significance, especially in the developing world. Immediate treatment with antibiotics is essential, and no single test can provide a conclusive diagnosis. It is well established that elevated total protein in cerebrospinal fluid (CSF) is asso...
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Published in: | Journal of biophotonics 2015-05, Vol.8 (5), p.408-414 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Bacterial meningitis is a disease of pronounced clinical significance, especially in the developing world. Immediate treatment with antibiotics is essential, and no single test can provide a conclusive diagnosis. It is well established that elevated total protein in cerebrospinal fluid (CSF) is associated with bacterial meningitis. Brillouin spectroscopy is a widely used optical technique for noninvasive determination of the elastic moduli of materials. We found that elevated protein levels in CSF alter the fluid elasticity sufficiently to be measurable by Brillouin spectroscopy, with model healthy and diseased fluids distinguishable to marked significance (P = 0.014), which increases with sample concentration by dialysis.
Typical raw output of a 2‐stage VIPA Brillouin spectrometer: inelastically scattered Brillouin peaks (arrows) and elastically scattered incident radiation (center cross).
Brillouin spectroscopy is a noninvasive emerging optical method for the detection of mechanical properties of materials, including fluids. For the first time, we show the feasibility of this technique for biofluid tissue diagnostics. Elevated protein concentrations in mock diseased cerebrospinal fluid are differentiated to a high degree of accuracy, while requiring no sample destruction, modification, or preparation. |
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ISSN: | 1864-063X 1864-0648 |
DOI: | 10.1002/jbio.201400047 |