Optical clearing agent for enhanced imaging dorsal blood vessels in nude mice

Author(s):  
Xiangyu Niu ◽  
Huabin He ◽  
Buhong Li
2016 ◽  
Vol 5 (2) ◽  
Author(s):  
Olga Zhernovaya ◽  
Valery V. Tuchin ◽  
Martin J. Leahy

AbstractThe results of a feasibility study of the application of PEG-300 and fructose as two independent optical clearing agents for the reduction of light scattering in biological tissues are presented.An OCT system operating at 1300 nm was used to study optical clearing effects. InThe intradermal injection of fructose in combination with the intravenous injection of PEG-300 led to a rapid optical clearing effect. In the experiments on miceThe experiments on mice have clearly demonstrated that intradermal and intravenous injections of optical clearing agents enhanced light transport through the skin and blood vessels.


2008 ◽  
Vol 13 (2) ◽  
pp. 021106 ◽  
Author(s):  
Dan Zhu ◽  
Jing Zhang ◽  
Han Cui ◽  
Zongzhen Mao ◽  
Pengcheng Li ◽  
...  

2009 ◽  
Vol 78 (3) ◽  
pp. 379-385 ◽  
Author(s):  
Wen-jian Zhang ◽  
Lian-qiu Wu ◽  
Hong-lin Liu ◽  
Li-ya Ye ◽  
Yu-ling Xin ◽  
...  

2013 ◽  
Vol 2 (1) ◽  
Author(s):  
Jing Wang ◽  
Rui Shi ◽  
Yang Zhang ◽  
Dan Zhu

AbstractVarious optical imaging techniques have shown a great potential for monitoring angiogenesis, development of blood vessels, and even tumor transfer, but they suffer from the limited imaging depth in tissue. Although the mouse ear provides an available window, the residual scattering of ear skin still influences the imaging quality. The proposed tissue optical clearing technique presents a new opportunity to decrease the scattering of skin, and enhance the imaging contrast or imaging depth of optical methods. The purpose of this study is to develop an innovative ear skin optical clearing agent (ESOCA) for improving the transparency of the mouse ear.The ESOCA was topically applied on the ear skin of BALB/c miceThe transmittance of mice ear was enhanced by 111.0±8.2% at 633 nm after application of ESOCA. The cutaneous blood vessels and blood flow could be distinguished more clearly with LSCI technique. In addition, the calculated CNR values of speckle contrast images showed a great enhancement compared with the initial (control) values.In summary, topical application of an innovative ESOCA permits the vessel structure and flow distribution information of cutaneous blood vessels to be imaged by LSCI with higher contrast, which will be significant for tumor studies in the future.


2012 ◽  
Author(s):  
Yasunori Tome ◽  
Naotoshi Sugimoto ◽  
Shuya Yano ◽  
Masashi Momiyama ◽  
Hiroki Maehara ◽  
...  

1999 ◽  
Vol 5 (S2) ◽  
pp. 496-497
Author(s):  
C. D. Bucana ◽  
S. Yano ◽  
D. Reynolds ◽  
K. Dunner ◽  
I. J. Fidler

This study was conducted to compare the immunohistochemical and morphometric characteristics of blood vessels in brain metastasis with blood vessels of the adjacent uninvolved brain tissue. This is based on the hypothesis that new vessels formed in the tumor express antigens that are not expressed in blood vessels of the adult brain parenchyma. Thus, a panel of antibodies known to react with mouse endothelial cells at various stages of differentiation or stimulation was tested on frozen sections of experimental brain metastasis. Intratumoral microvessel density which has been reported to reflect the intensity of tumor angiogenesis was inapplicable to experimental brain metastasis therefore other parameters were measured.Brain metastasis was produced in nude mice following intracarotid injection of tumor cells. Three human tumors and three murine tumors were injected into the carotid artery of nude mice. The animals were sacrificed when they were moribund, the brains were embedded in OCT and frozen in liquid nitrogen. Some animals were injected with bromodeoxyuridine (BrdU) 1 h before they were necropsied. Immunohistochemistry was performed using antibodies directed to the following antigens: CD31, CD34, MECA-32, endoglin, ICAM-1, ICAM-2, and BrdU. Antibodies to leukocyte antigens, F4/80 and CD3 were also tested to determine the amount of host cells infiltrating the tumors. SEM of immunogold labeled preparations determined the cellular localization of some antigens.


2014 ◽  
Vol 8 (6) ◽  
pp. 1723-1726 ◽  
Author(s):  
NALI ZHANG ◽  
GUOJUN ZHANG ◽  
YOUGUANG ZHENG ◽  
TONGBING WANG ◽  
HONGLEI WANG

2009 ◽  
Vol 33 (11) ◽  
pp. 986-990 ◽  
Author(s):  
Zhang Xi ◽  
Yuan Qing-Xi ◽  
Yang Xin-Rong ◽  
Li Hai-Qing ◽  
Chen Yu ◽  
...  

2020 ◽  
Author(s):  
Miguel A. Gama Sosa ◽  
Rita De Gasperi ◽  
Gissel M. Perez ◽  
Patrick R. Hof ◽  
Gregory A. Elder

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