Cargando…
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...
Autores principales: | , , , , , , , , , , , , |
---|---|
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 |
_version_ | 1782196021061746688 |
---|---|
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. |
format | Text |
id | pubmed-3018094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Optical Society of America |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT matsumotoyu directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT nomototakahiro directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT cabralhoracio directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT matsumotoyoko directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT watanabesumiyo directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT christierjames directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT miyatakanjiro directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT obamakoto directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT oguratadayoshi directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT yamasakiyuichi directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT nishiyamanobuhiro directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT yamasobatatsuya directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography AT kataokakazunori directandinstantaneousobservationofintravenouslyinjectedsubstancesusingintravitalconfocalmicrovideography |