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Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study

A new concept for cancer screening has been preliminarily investigated. A cancer targeting agent loaded with a near-infrared (NIR) dye was topically applied on the tissue to highlight cancer-suspect locations and guide optical coherence tomography (OCT) imaging, which was used to further investigate...

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Autores principales: Iftimia, Nicusor, Iyer, Arun K., Hammer, Daniel X., Lue, Niyom, Mujat, Mircea, Pitman, Martha, Ferguson, R. Daniel, Amiji, Mansoor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Optical Society of America 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255336/
https://www.ncbi.nlm.nih.gov/pubmed/22254178
http://dx.doi.org/10.1364/BOE.3.000178
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author Iftimia, Nicusor
Iyer, Arun K.
Hammer, Daniel X.
Lue, Niyom
Mujat, Mircea
Pitman, Martha
Ferguson, R. Daniel
Amiji, Mansoor
author_facet Iftimia, Nicusor
Iyer, Arun K.
Hammer, Daniel X.
Lue, Niyom
Mujat, Mircea
Pitman, Martha
Ferguson, R. Daniel
Amiji, Mansoor
author_sort Iftimia, Nicusor
collection PubMed
description A new concept for cancer screening has been preliminarily investigated. A cancer targeting agent loaded with a near-infrared (NIR) dye was topically applied on the tissue to highlight cancer-suspect locations and guide optical coherence tomography (OCT) imaging, which was used to further investigate tissue morphology at the micron scale. A pilot study on ApcMin mice has been performed to preliminarily test this new cancer screening approach. As a cancer-targeting agent, poly(epsilon-caprolactone) microparticles (PCLMPs), labeled with a NIR dye and functionalized with an RGD (argenine-glycine-aspartic acid) peptide, were used. This agent recognizes the α(ν)β(3) integrin receptor (ABIR), which is over-expressed by epithelial cancer cells. The contrast agent was administered topically in vivo in mouse colon. After incubation, the animals were sacrificed and fluorescence-guided high resolution optical coherence tomography (OCT) imaging was used to visualize colon morphology. The preliminary results show preferential staining of the abnormal tissue, as indicated by both microscopy and laser-induced fluorescence imaging, and OCT’s capability to differentiate between normal mucosal areas, early dysplasia, and adenocarcinoma. Although very preliminary, the results of this study suggest that fluorescence-guided OCT imaging might be a suitable approach for cancer screening. If successful, this approach could be used by clinicians to more reliably diagnose early stage cancers in vivo.
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spelling pubmed-32553362012-01-17 Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study Iftimia, Nicusor Iyer, Arun K. Hammer, Daniel X. Lue, Niyom Mujat, Mircea Pitman, Martha Ferguson, R. Daniel Amiji, Mansoor Biomed Opt Express Optical Coherence Tomography A new concept for cancer screening has been preliminarily investigated. A cancer targeting agent loaded with a near-infrared (NIR) dye was topically applied on the tissue to highlight cancer-suspect locations and guide optical coherence tomography (OCT) imaging, which was used to further investigate tissue morphology at the micron scale. A pilot study on ApcMin mice has been performed to preliminarily test this new cancer screening approach. As a cancer-targeting agent, poly(epsilon-caprolactone) microparticles (PCLMPs), labeled with a NIR dye and functionalized with an RGD (argenine-glycine-aspartic acid) peptide, were used. This agent recognizes the α(ν)β(3) integrin receptor (ABIR), which is over-expressed by epithelial cancer cells. The contrast agent was administered topically in vivo in mouse colon. After incubation, the animals were sacrificed and fluorescence-guided high resolution optical coherence tomography (OCT) imaging was used to visualize colon morphology. The preliminary results show preferential staining of the abnormal tissue, as indicated by both microscopy and laser-induced fluorescence imaging, and OCT’s capability to differentiate between normal mucosal areas, early dysplasia, and adenocarcinoma. Although very preliminary, the results of this study suggest that fluorescence-guided OCT imaging might be a suitable approach for cancer screening. If successful, this approach could be used by clinicians to more reliably diagnose early stage cancers in vivo. Optical Society of America 2011-12-19 /pmc/articles/PMC3255336/ /pubmed/22254178 http://dx.doi.org/10.1364/BOE.3.000178 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 Optical Coherence Tomography
Iftimia, Nicusor
Iyer, Arun K.
Hammer, Daniel X.
Lue, Niyom
Mujat, Mircea
Pitman, Martha
Ferguson, R. Daniel
Amiji, Mansoor
Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
title Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
title_full Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
title_fullStr Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
title_full_unstemmed Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
title_short Fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
title_sort fluorescence-guided optical coherence tomography imaging for colon cancer screening: a preliminary mouse study
topic Optical Coherence Tomography
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3255336/
https://www.ncbi.nlm.nih.gov/pubmed/22254178
http://dx.doi.org/10.1364/BOE.3.000178
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