Influence of pinhole size and fiber optic imaging bundle on resolution in confocal endoscopic imaging system

2005 ◽  
Author(s):  
Huayong Ge ◽  
Qiushi Ren ◽  
Baohua Wang ◽  
Wangrong Li
2018 ◽  
Vol 14 (4) ◽  
pp. 267-270
Author(s):  
Tian-xiang Zheng ◽  
Guang-yue Shen ◽  
Zhao-hui Li ◽  
E. Wu ◽  
Xiu-liang Chen ◽  
...  

1997 ◽  
Vol 3 (S2) ◽  
pp. 845-846
Author(s):  
S. Michael Angel ◽  
H. Trey Skinner ◽  
Brian J. Marquardt

Optical fiber probes are routinely used with optical spectrometers to allow measurements to be made on remotely located samples. In most of these systems, however, the optical fibers are used as non-imaging “light pipes” for the transmission of laser light, and luminescence or Raman signals to and from the sample. Thus, while these systems are suitable for remote spectroscopy, they are limited to single-point measurements. In a recent paper, we showed that a small-diameter (i.e., 350 μm) coherent optical fiber bundle can be combined with an AOTF-based imaging spectrometer for fluorescence and Raman spectral micro-imaging with increased flexibility in terms of sample positioning and in-situ capabilities. The previous paper described the operation of the fiber-optic microimaging probe and AOTF imaging system and showed preliminary Raman and fluorescence images for model compounds with 4 μm resolution. We have extended this work to include a discussion of the lateral and vertical spatial resolution of the fiber-optic microprobe in a non-contact proximity-focused configuration.


Blood ◽  
2010 ◽  
Vol 115 (3) ◽  
pp. 443-452 ◽  
Author(s):  
Daniel Lewandowski ◽  
Vilma Barroca ◽  
Frédéric Ducongé ◽  
Jan Bayer ◽  
Jeanne Tran Van Nhieu ◽  
...  

Abstract Few techniques are available to characterize in vivo the early cellular dynamics of long-term reconstitution of hematopoiesis after transplantation of hematopoietic stem cells (HSCs) after lethal irradiation. Using a fiber-optic imaging system, we track the early steps of in vivo recruitment and proliferation of Lin−Sca-1+c-Kit+CD34− (LSKCD34−) HSCs highly enriched in HSCs and transplanted into lethally irradiated mice. Recruitment of the transplanted LSKCD34− hematopoietic cells first occurs in the femoral head and is continuous during 24 hours. Quantification of the fluorescence emitted by the transplanted hematopoietic cells shows that proliferation of LSKCD34− hematopoietic cells in the femoral head was potent 3 days after transplantation. Using a development of this fiber-optic imaging system, we show that the transplanted LSKCD34− hematopoietic cells are associated with vascularized structures as early as 5 hours after transplantation. This early association is dependent on reactive oxygen species (ROS) partly through the regulation of vascular cell adhesion molecule-1 expression on endothelial cells and is followed by a ROS-dependent proliferation of LSKCD34− hematopoietic cells. This new in vivo imaging technique permits the observation of the early steps of hematopoietic reconstitution by HSCs in long bones and shows a new role of ROS in the recruitment of HSCs by bone marrow endothelial cells.


2018 ◽  
Vol 62 (6) ◽  
pp. 60503-1-60503-5
Author(s):  
Jun Zhou ◽  
Meiqi Li ◽  
Bin Liu ◽  
Zhaoyang Wu ◽  
Jing Zhang ◽  
...  

Author(s):  
J.W. Wong ◽  
W.R. Binns ◽  
A.Y. Chengl ◽  
L.Y. Geer ◽  
J.W. Epstein ◽  
...  

2013 ◽  
Vol 144 (5) ◽  
pp. S-403 ◽  
Author(s):  
Hirokazu Higuchi ◽  
Takuya Yoshino ◽  
Minoru Matsuura ◽  
Hiroshi Nakase ◽  
Tsutomu Chiba

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