Intravenous Application of Fluorescein for Confocal Laser Scanning Microscopy: Evaluation of Contrast Dynamics and Image Quality with Increasing Injection-to-Imaging Time

2008 ◽  
Vol 21 (01) ◽  
Author(s):  
V Becker ◽  
S von Delius ◽  
M Bajbouj ◽  
A Karagianni ◽  
RM Schmid ◽  
...  
Keyword(s):  
Image Quality ◽  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Imaging Time ◽  
Intravenous Application

Intravenous application of fluorescein for confocal laser scanning microscopy: evaluation of contrast dynamics and image quality with increasing injection-to-imaging time

2008 ◽  
Vol 68 (2) ◽  
pp. 319-323 ◽  
Author(s):  
Valentin Becker ◽  
Stefan von Delius ◽  
Monther Bajbouj ◽  
Artemisia Karagianni ◽  
Roland M. Schmid ◽  
...  
Keyword(s):  
Image Quality ◽  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Imaging Time ◽  
Intravenous Application

Optimal fluorescein dose for intravenous application in miniprobe-based confocal laser scanning microscopy in pigs

2010 ◽  
Vol 4 (1-2) ◽  
pp. 108-113 ◽  
Author(s):  
Valentin Becker ◽  
Frank J. van den Broek ◽  
Anna M. Buchner ◽  
Evelien Dekker ◽  
Michael B. Wallace ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Intravenous Application

A new protocol for live imaging of mammalian retina ex vivo by confocal laser scanning microscopy

2009 ◽  
Author(s):  
Isabella Panfoli ◽  
Daniela Calzia ◽  
Silvia Ravera ◽  
Giovanni Candiano ◽  
Angela Bachi ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Ex Vivo ◽  
Live Imaging ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Mammalian Retina

ACTIVATED SLUDGE FLOC CHARACTERIZATION BY CONFOCAL LASER SCANNING MICROSCOPY

2012 ◽  
Vol 11 (3) ◽  
pp. 669-674 ◽  
Author(s):  
Szabolcs Szilveszter ◽  
Botond Raduly ◽  
Szilard Bucs ◽  
Beata Abraham ◽  
Szabolcs Lanyi ◽  
...  
Keyword(s):  
Activated Sludge ◽  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser

Cellular Uptake Study of Antimycotic-Loaded Carriers Using Imaging Flow Cytometry and Confocal Laser Scanning Microscopy

2020 ◽  
Vol 128 (6) ◽  
pp. 799-808
Author(s):  
R. A. Verkhovskii ◽  
E. V. Lengert ◽  
M. S. Saveleva ◽  
A. A. Kozlova ◽  
V. V. Tuchin ◽  
...  
Keyword(s):  
Flow Cytometry ◽  
Confocal Laser Scanning Microscopy ◽  
Cellular Uptake ◽  
Laser Scanning ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Uptake Study ◽  
Imaging Flow Cytometry

scholarly journals Bacterial Colonization and Proliferation in Furcal Perforations Repaired by Different Materials: A Confocal Laser Scanning Microscopy Study

2021 ◽  
Vol 11 (8) ◽  
pp. 3403
Author(s):  
Shlomo Elbahary ◽  
Sohad Haj Yahya ◽  
Cemre Koç ◽  
Hagay Shemesh ◽  
Eyal Rosen ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Bacterial Colonization ◽  
Microscopy Study ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser ◽  
Repair Material ◽  
Dentinal Tubules

Following furcal perforation, bacteria may colonize the defect and cause inflammation and periodontal destruction. This study used confocal laser scanning microscopy (CLSM) to evaluate Enterococcus faecalis colonization and proliferation in furcal perforations repaired with different materials. Furcal perforations created in 55 extracted human mandibular molars were repaired using either MTA-Angelus, Endocem, or Biodentine and coronally subjected to E. faecalis suspension for 21 days. The specimens were then stained using a LIVE/DEAD Viability Kit and visualized by CLSM. The minimum and maximum depths of bacterial penetration into the dentinal tubules were 159 and 1790 μM, respectively, with a mean of 713 μM. There were significantly more live than dead bacteria inside the dentinal tubules (p = 0.0023) in all groups, and all three repair materials exhibited a similarly sized stained area (p = 0.083). However, there were significant differences in the numbers of dead bacteria at the circumference of the perforation defect (p = 0.0041), with a significantly higher ratio of live to dead bacteria in the MTA-Angelus group (p = 0.001). Following perforation repair, bacteria may colonize the interface between the repair material and dentin and may penetrate through the dentinal tubules. The type of repair material has a significant effect on the viability of the colonizing bacteria.

Simultaneous immunofluorescence and histology in pemphigus vulgaris using ex vivo confocal laser scanning microscopy

2021 ◽  
Author(s):  
Işın Sinem Bağcı ◽  
Rui Aoki ◽  
Gabriela Vladimirova ◽  
Miklós Sárdy ◽  
Thomas Ruzicka ◽  
...  
Keyword(s):  
Confocal Laser Scanning Microscopy ◽  
Laser Scanning ◽  
Ex Vivo ◽  
Pemphigus Vulgaris ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Scanning Microscopy ◽  
Confocal Laser
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