scholarly journals Influence of various herbal irrigants as a final rinse on the adherence of Enterococcus faecalis by fluorescence confocal laser scanning microscope

2013 ◽  
Vol 16 (4) ◽  
pp. 352 ◽  
Author(s):  
Hannah Rosaline ◽  
D Kandaswamy ◽  
D Gogulnath ◽  
MI Rubin
Keyword(s):  
Enterococcus Faecalis ◽  
Laser Scanning ◽  
Confocal Laser Scanning Microscope ◽  
Confocal Laser Scanning ◽  
Confocal Laser ◽  
Scanning Microscope ◽  
Laser Scanning Microscope

scholarly journals ENTEROCOCCUS FAECALIS CAUSE FOR PERSISTING INFECTION A CONFOCAL ANALYSIS

2013 ◽  
Vol 03 (04) ◽  
pp. 057-062
Author(s):  
Rahul Halkai ◽  
Mithra N. Hegde ◽  
Kiran Halkai
Keyword(s):  
Enterococcus Faecalis ◽  
Root Canal ◽  
Laser Scanning ◽  
Confocal Laser Scanning Microscope ◽  
Confocal Laser Scanning ◽  
Confocal Laser ◽  
Extreme Conditions ◽  
Scanning Microscope ◽  
Laser Scanning Microscope ◽  
Root Dentin

Abstract Aim: to know ability of Enterococcus faecalis invasion into root dentin. Methodology: Forty single rooted human intact teeth were selected, after access opening and canal debridement, all the samples were subjected for gamma sterilization to ensure complete absence of microorganisms, then exposed to Enterococcus faecalis broth, broth is placed with the help of micro pipette into root canal and also at the same time apical 1/3 of tooth were immersed into broth for 8 weeks, biomechanical preparation, obturation and coronal sealing done using GIC followed by examination under confocal laser scanning microscope after splitting the teeth samples into two halfs buccolingually. Results: This study shows invasion of Enterococcus faecalis upto 160 μm deep in to root dentin. Conclusion: penetration and survival of Enterococcus faecalis deep into dentin in extreme conditions may be the possible reason for persisting infection after root canal treatment.

3-D imaging of cells using a confocal laser scanning microscope and digital image processing

1988 ◽  
Vol 46 ◽  
pp. 96-97
Author(s):  
Thomas M. Jovin ◽  
Michel Robert-Nicoud ◽  
Donna J. Arndt-Jovin ◽  
Thorsten Schormann
Keyword(s):  
Laser Scanning ◽  
Confocal Laser Scanning Microscope ◽  
Laser Scanning Microscopy ◽  
Confocal Laser Scanning ◽  
Confocal Laser ◽  
Scanning Microscope ◽  
Laser Scanning Microscope ◽  
Biochemical Processes ◽  
Adjacent Structures

Light microscopic techniques for visualizing biomolecules and biochemical processes in situ have become indispensable in studies concerning the structural organization of supramolecular assemblies in cells and of processes during the cell cycle, transformation, differentiation, and development. Confocal laser scanning microscopy offers a number of advantages for the in situ localization and quantitation of fluorescence labeled targets and probes: (i) rejection of interfering signals emanating from out-of-focus and adjacent structures, allowing the “optical sectioning” of the specimen and 3-D reconstruction without time consuming deconvolution; (ii) increased spatial resolution; (iii) electronic control of contrast and magnification; (iv) simultanous imaging of the specimen by optical phenomena based on incident, scattered, emitted, and transmitted light; and (v) simultanous use of different fluorescent probes and types of detectors.We currently use a confocal laser scanning microscope CLSM (Zeiss, Oberkochen) equipped with 3-laser excitation (u.v - visible) and confocal optics in the fluorescence mode, as well as a computer-controlled X-Y-Z scanning stage with 0.1 μ resolution.

A confocal laser scanning microscope designed for indicators with ultraviolet excitation wavelengths

1994 ◽  
Vol 266 (1) ◽  
pp. C303-C310 ◽  
Author(s):  
E. Niggli ◽  
D. W. Piston ◽  
M. S. Kirby ◽  
H. Cheng ◽  
D. R. Sandison ◽  
...  
Keyword(s):  
Heart Muscle ◽  
Laser Scanning ◽  
Muscle Cells ◽  
Confocal Laser Scanning Microscope ◽  
Confocal Laser Scanning ◽  
Confocal Laser ◽  
Scanning Microscope ◽  
Dual Emission ◽  
Laser Scanning Microscope ◽  
Heart Muscle Cells

In this paper we describe the modifications necessary to upgrade, at affordable cost, a commercially available confocal laser scanning microscope for use with ultraviolet (UV) excitation. The optical problems associated with these modifications are described in detail, and easy solutions to solve them are suggested. The optical resolution of the instrument was tested with fluorescent beads and was found to be close to diffraction limited. The light losses due to lateral chromatic aberration were assessed in a thick fluorescent specimen and were found to be comparable to those usually observed with visible light. For a more visual example of the resolution of this instrument, isolated ventricular heart muscle cells were loaded with the fluorescent Ca2+ indicator indo 1. This allowed us to visualize subcellular structural detail and to illustrate the optical sectioning capability of the UV confocal microscope when recording indo 1 emission. Dual-emission line scans were used to perform ratiometric time-resolved detection of Ca2+ transients in voltage-clamped heart muscle cells loaded with the salt form of indo 1. The system presented in this paper should significantly broaden the range of fluorescent indicators that can be used in confocal microscopy.

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