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Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy

We validate specific binding activity of a fluorescence-labeled peptide to colorectal dysplasia in living mice using a miniature, flexible, fiber microendoscope that passes through the instrument channel of an endoscope. The microendoscope delivers excitation light at 473 nm through a fiber-optic bu...

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Detalles Bibliográficos
Autores principales: Elahi, Sakib F., Miller, Sharon J., Joshi, Bishnu, Wang, Thomas D.
Formato: Texto
Lenguaje:English
Publicado: Optical Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072136/
https://www.ncbi.nlm.nih.gov/pubmed/21483619
http://dx.doi.org/10.1364/BOE.2.000981
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author Elahi, Sakib F.
Miller, Sharon J.
Joshi, Bishnu
Wang, Thomas D.
author_facet Elahi, Sakib F.
Miller, Sharon J.
Joshi, Bishnu
Wang, Thomas D.
author_sort Elahi, Sakib F.
collection PubMed
description We validate specific binding activity of a fluorescence-labeled peptide to colorectal dysplasia in living mice using a miniature, flexible, fiber microendoscope that passes through the instrument channel of an endoscope. The microendoscope delivers excitation light at 473 nm through a fiber-optic bundle with outer diameter of 680 µm to collect en face images at 10 Hz with 4 µm lateral resolution. We applied the FITC-labeled peptide QPIHPNNM topically to colonic mucosa in genetically engineered mice that spontaneously develop adenomas. More than two-fold greater fluorescence intensity was measured from adenomas compared to adjacent normal-appearing mucosa. Images of adenomas showed irregular morphology characteristic of dysplasia.
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spelling pubmed-30721362011-04-11 Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy Elahi, Sakib F. Miller, Sharon J. Joshi, Bishnu Wang, Thomas D. Biomed Opt Express Endoscopes, Catheters and Micro-Optics We validate specific binding activity of a fluorescence-labeled peptide to colorectal dysplasia in living mice using a miniature, flexible, fiber microendoscope that passes through the instrument channel of an endoscope. The microendoscope delivers excitation light at 473 nm through a fiber-optic bundle with outer diameter of 680 µm to collect en face images at 10 Hz with 4 µm lateral resolution. We applied the FITC-labeled peptide QPIHPNNM topically to colonic mucosa in genetically engineered mice that spontaneously develop adenomas. More than two-fold greater fluorescence intensity was measured from adenomas compared to adjacent normal-appearing mucosa. Images of adenomas showed irregular morphology characteristic of dysplasia. Optical Society of America 2011-03-28 /pmc/articles/PMC3072136/ /pubmed/21483619 http://dx.doi.org/10.1364/BOE.2.000981 Text en ©2011 Optical Society of America http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 Unported License, which permits download and redistribution, provided that the original work is properly cited. This license restricts the article from being modified or used commercially.
spellingShingle Endoscopes, Catheters and Micro-Optics
Elahi, Sakib F.
Miller, Sharon J.
Joshi, Bishnu
Wang, Thomas D.
Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
title Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
title_full Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
title_fullStr Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
title_full_unstemmed Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
title_short Targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
title_sort targeted imaging of colorectal dysplasia in living mice with fluorescence microendoscopy
topic Endoscopes, Catheters and Micro-Optics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3072136/
https://www.ncbi.nlm.nih.gov/pubmed/21483619
http://dx.doi.org/10.1364/BOE.2.000981
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