PUBLICATION
Characterization of flow direction in microchannels and zebrafish blood vessels by scanning fluorescence correlation spectroscopy
- Authors
- Pan, X., Yu, H., Shi, X., Korzh, V., and Wohland, T.
- ID
- ZDB-PUB-070310-12
- Date
- 2007
- Source
- Journal of Biomedical Optics 12(1): 014034-014044 (Journal)
- Registered Authors
- Korzh, Vladimir
- Keywords
- none
- MeSH Terms
-
- Equipment Failure Analysis
- Blood Flow Velocity/physiology*
- Spectrometry, Fluorescence/instrumentation*
- Spectrometry, Fluorescence/methods
- Microcirculation/physiology*
- Equipment Design
- Microscopy, Confocal/instrumentation*
- Microscopy, Confocal/methods
- Animals
- Reproducibility of Results
- Zebrafish
- Sensitivity and Specificity
- Microscopy, Fluorescence/instrumentation*
- Microscopy, Fluorescence/methods
- Microfluidics/instrumentation*
- Microfluidics/methods
- PubMed
- 17343509 Full text @ J. Biomed. Opt.
Citation
Pan, X., Yu, H., Shi, X., Korzh, V., and Wohland, T. (2007) Characterization of flow direction in microchannels and zebrafish blood vessels by scanning fluorescence correlation spectroscopy. Journal of Biomedical Optics. 12(1):014034-014044.
Abstract
The investigation of flow profiles in microstructures and tissues by fluorescence correlation spectroscopy (FCS) has been a challenging topic in the past decade. Due to its inherent optical configuration, a circular focused laser beam, FCS is unable to resolve microfluidic flow directions. Earlier schemes reported the use of two laser beams or the use of nonsymmetrical laser foci to break the symmetry of the measurement system. This, however, is difficult to combine with confocal systems since it would require modifications that interfere with the imaging capabilities. We propose a method called line-scan FCS to measure different flow angles in microchannels and tissues. This method is implemented on a combined laser scanning confocal microscopy (LSCM) and FCS system that enables uncompromised imaging and spectroscopy measurements. We demonstrate that by scanning the laser beam with a defined speed and direction we can measure flow direction with the current system at an optimal resolution of at least 3 mum. The combination system is assessed by measuring flow profiles in a microchannel with and without obstruction. To extend the technique to live tissue measurements we demonstrate that line-scan FCS can determine the flow direction in zebrafish small blood vessels in a label-free approach.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping