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Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography

We describe the development and application of intravital confocal micro-videography to visualize entrance, distribution, and clearance of drugs within various tissues and organs. We use a Nikon A1R confocal laser scanning microscope system attached to an upright ECLIPSE FN1. The Nikon A1R allows si...

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Autores principales: Matsumoto, Yu, Nomoto, Takahiro, Cabral, Horacio, Matsumoto, Yoko, Watanabe, Sumiyo, Christie, R. James, Miyata, Kanjiro, Oba, Makoto, Ogura, Tadayoshi, Yamasaki, Yuichi, Nishiyama, Nobuhiro, Yamasoba, Tatsuya, Kataoka, Kazunori
Formato: Texto
Lenguaje:English
Publicado: Optical Society of America 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018094/
https://www.ncbi.nlm.nih.gov/pubmed/21258542
http://dx.doi.org/10.1364/BOE.1.001209
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author Matsumoto, Yu
Nomoto, Takahiro
Cabral, Horacio
Matsumoto, Yoko
Watanabe, Sumiyo
Christie, R. James
Miyata, Kanjiro
Oba, Makoto
Ogura, Tadayoshi
Yamasaki, Yuichi
Nishiyama, Nobuhiro
Yamasoba, Tatsuya
Kataoka, Kazunori
author_facet Matsumoto, Yu
Nomoto, Takahiro
Cabral, Horacio
Matsumoto, Yoko
Watanabe, Sumiyo
Christie, R. James
Miyata, Kanjiro
Oba, Makoto
Ogura, Tadayoshi
Yamasaki, Yuichi
Nishiyama, Nobuhiro
Yamasoba, Tatsuya
Kataoka, Kazunori
author_sort Matsumoto, Yu
collection PubMed
description We describe the development and application of intravital confocal micro-videography to visualize entrance, distribution, and clearance of drugs within various tissues and organs. We use a Nikon A1R confocal laser scanning microscope system attached to an upright ECLIPSE FN1. The Nikon A1R allows simultaneous four channel acquisition and speed of 30 frames per second while maintaining high resolution of 512 × 512 scanned points. The key techniques of our intravital imaging are (1) to present a flat and perpendicular surface to the objective lens, and (2) to expose the subject with little or no bleeding to facilitate optical access to multiple tissues and organs, and (3) to isolate the subject from the body movement without compressing the blood vessels, and (4) to insert a tail vein catheter for timed injection without moving the subject. Ear lobe dermis tissue was accessible without surgery. Liver, kidney, and subcutaneous tumor were accessed following exteriorization through skin incision. In order to image initial extravasations of compounds into tissue following intravenous injection, movie acquisition was initialized prior to drug administration. Our technique can serve as a powerful tool for investigating biological mechanisms and functions of intravenously injected drugs, with both spatial and temporal resolution.
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spelling pubmed-30180942011-01-21 Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography Matsumoto, Yu Nomoto, Takahiro Cabral, Horacio Matsumoto, Yoko Watanabe, Sumiyo Christie, R. James Miyata, Kanjiro Oba, Makoto Ogura, Tadayoshi Yamasaki, Yuichi Nishiyama, Nobuhiro Yamasoba, Tatsuya Kataoka, Kazunori Biomed Opt Express Microscopy We describe the development and application of intravital confocal micro-videography to visualize entrance, distribution, and clearance of drugs within various tissues and organs. We use a Nikon A1R confocal laser scanning microscope system attached to an upright ECLIPSE FN1. The Nikon A1R allows simultaneous four channel acquisition and speed of 30 frames per second while maintaining high resolution of 512 × 512 scanned points. The key techniques of our intravital imaging are (1) to present a flat and perpendicular surface to the objective lens, and (2) to expose the subject with little or no bleeding to facilitate optical access to multiple tissues and organs, and (3) to isolate the subject from the body movement without compressing the blood vessels, and (4) to insert a tail vein catheter for timed injection without moving the subject. Ear lobe dermis tissue was accessible without surgery. Liver, kidney, and subcutaneous tumor were accessed following exteriorization through skin incision. In order to image initial extravasations of compounds into tissue following intravenous injection, movie acquisition was initialized prior to drug administration. Our technique can serve as a powerful tool for investigating biological mechanisms and functions of intravenously injected drugs, with both spatial and temporal resolution. Optical Society of America 2010-10-21 /pmc/articles/PMC3018094/ /pubmed/21258542 http://dx.doi.org/10.1364/BOE.1.001209 Text en ©2010 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 Microscopy
Matsumoto, Yu
Nomoto, Takahiro
Cabral, Horacio
Matsumoto, Yoko
Watanabe, Sumiyo
Christie, R. James
Miyata, Kanjiro
Oba, Makoto
Ogura, Tadayoshi
Yamasaki, Yuichi
Nishiyama, Nobuhiro
Yamasoba, Tatsuya
Kataoka, Kazunori
Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
title Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
title_full Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
title_fullStr Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
title_full_unstemmed Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
title_short Direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
title_sort direct and instantaneous observation of intravenously injected substances using intravital confocal micro-videography
topic Microscopy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018094/
https://www.ncbi.nlm.nih.gov/pubmed/21258542
http://dx.doi.org/10.1364/BOE.1.001209
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