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Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice

BACKGROUND: Near-infrared photoimmunotherapy (NIR-PIT) is a cancer therapy that causes an increase in tumor perfusion, a phenomenon termed the super-enhanced permeability and retention effect. Currently, in vivo treatment efficacy of NIR-PIT is observable days after treatment, but monitoring would b...

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Autores principales: Rosenberg, Adrian, Fujimura, Daiki, Okada, Ryuhei, Furusawa, Aki, Inagaki, Fuyuki, Wakiyama, Hiroaki, Kato, Takuya, Choyke, Peter L., Kobayashi, Hisataka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331766/
https://www.ncbi.nlm.nih.gov/pubmed/32609570
http://dx.doi.org/10.1177/1536012120934965
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author Rosenberg, Adrian
Fujimura, Daiki
Okada, Ryuhei
Furusawa, Aki
Inagaki, Fuyuki
Wakiyama, Hiroaki
Kato, Takuya
Choyke, Peter L.
Kobayashi, Hisataka
author_facet Rosenberg, Adrian
Fujimura, Daiki
Okada, Ryuhei
Furusawa, Aki
Inagaki, Fuyuki
Wakiyama, Hiroaki
Kato, Takuya
Choyke, Peter L.
Kobayashi, Hisataka
author_sort Rosenberg, Adrian
collection PubMed
description BACKGROUND: Near-infrared photoimmunotherapy (NIR-PIT) is a cancer therapy that causes an increase in tumor perfusion, a phenomenon termed the super-enhanced permeability and retention effect. Currently, in vivo treatment efficacy of NIR-PIT is observable days after treatment, but monitoring would be improved by more acute detection of intratumor change. Fluorescence imaging may detect increased tumor perfusion immediately after treatment. METHODS: In the first experiment, athymic nude mouse models bearing unilateral subcutaneous flank tumors were treated with either NIR-PIT or laser therapy only. In the second experiment, mice bearing bilateral flank tumors were treated with NIR-PIT only on the left-sided tumor. In both groups, immediately after treatment, indocyanine green was injected at different doses intravenously, and mice were monitored with the Shimadzu LIGHTVISION fluorescence imaging system for 1 hour. RESULTS: Tumor-to-background ratio of fluorescence intensity increased over the 60 minutes of monitoring in treated mice but did not vary significantly in control mice. Tumor-to-background ratio was highest in the 1 mg kg(−1) and 0.3 mg kg(−1) doses. In mice with bilateral tumors, tumor-to-untreated tumor ratio increased similarly. CONCLUSIONS: Acute changes in tumor perfusion after NIR-PIT can be detected by real-time fluorescence imaging.
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spelling pubmed-73317662020-07-10 Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice Rosenberg, Adrian Fujimura, Daiki Okada, Ryuhei Furusawa, Aki Inagaki, Fuyuki Wakiyama, Hiroaki Kato, Takuya Choyke, Peter L. Kobayashi, Hisataka Mol Imaging Research Article BACKGROUND: Near-infrared photoimmunotherapy (NIR-PIT) is a cancer therapy that causes an increase in tumor perfusion, a phenomenon termed the super-enhanced permeability and retention effect. Currently, in vivo treatment efficacy of NIR-PIT is observable days after treatment, but monitoring would be improved by more acute detection of intratumor change. Fluorescence imaging may detect increased tumor perfusion immediately after treatment. METHODS: In the first experiment, athymic nude mouse models bearing unilateral subcutaneous flank tumors were treated with either NIR-PIT or laser therapy only. In the second experiment, mice bearing bilateral flank tumors were treated with NIR-PIT only on the left-sided tumor. In both groups, immediately after treatment, indocyanine green was injected at different doses intravenously, and mice were monitored with the Shimadzu LIGHTVISION fluorescence imaging system for 1 hour. RESULTS: Tumor-to-background ratio of fluorescence intensity increased over the 60 minutes of monitoring in treated mice but did not vary significantly in control mice. Tumor-to-background ratio was highest in the 1 mg kg(−1) and 0.3 mg kg(−1) doses. In mice with bilateral tumors, tumor-to-untreated tumor ratio increased similarly. CONCLUSIONS: Acute changes in tumor perfusion after NIR-PIT can be detected by real-time fluorescence imaging. SAGE Publications 2020-07-01 /pmc/articles/PMC7331766/ /pubmed/32609570 http://dx.doi.org/10.1177/1536012120934965 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Article
Rosenberg, Adrian
Fujimura, Daiki
Okada, Ryuhei
Furusawa, Aki
Inagaki, Fuyuki
Wakiyama, Hiroaki
Kato, Takuya
Choyke, Peter L.
Kobayashi, Hisataka
Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice
title Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice
title_full Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice
title_fullStr Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice
title_full_unstemmed Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice
title_short Real-Time Fluorescence Imaging Using Indocyanine Green to Assess Therapeutic Effects of Near-Infrared Photoimmunotherapy in Tumor Model Mice
title_sort real-time fluorescence imaging using indocyanine green to assess therapeutic effects of near-infrared photoimmunotherapy in tumor model mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331766/
https://www.ncbi.nlm.nih.gov/pubmed/32609570
http://dx.doi.org/10.1177/1536012120934965
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