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Various techniques have been used to measure changes in the cell volume, including light scattering, 15) total internal reflection fluorescence, 16) confocal fluorescence microscopy,(17) laser scanning reflection microscopy,(18) and interference filter methods.
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By means of infrared radiation, either in the NIR or in the MIR ranges, camera-based or scanning based reflection mode imaging can be performed.
Laser scanning confocal reflection and fluorescence endoscopes have been developed that provide 3D cellular resolution in tissues [ 2, 3].
Tablets were scanned in reflection mode on a benchtop NIRS.
The full width of half maximum of the phi scan of (111) reflection and omega scan of (200) reflection of CZO films is as low as the value of about 5° and 6°, respectively.
Plaque biofilms formed in vivo on human enamel were subjected to a number of different chemical conditions while under observation by confocal laser scanning microscopy in reflection mode.
The reflection scanning through the time-of-flight analysis and signal processing enabled a detailed 3D imaging of the sample.
The developed composites were analyzed by Fourier transform infrared spectroscopy-attenuated total reflection, scanning electron microscopy, transmission electron microscopy, contact angle measurement, determination of salt rejection and water permeate flux capabilities.
Specific NBT/BCIP stainings were detected with 633 nm laser wavelength reflection scanning [ 63].
The proposed endoscopic system works as a reflection scanning fluorescence microscope [ 28].
The same sample was scanned in the reflection and transmission geometry respectively 2θ = 0.2→2θ = 120° and 2θ = 0.2→2θ = 90° by the anomalous diffractometer.
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