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Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats

OBJECTIVE: Fluorophore-labeled contrast imaging agents are moving toward clinical use for a number of applications. The near-infrared dye IRDye 800CW is frequently used in its N-hydroxysuccinamide (NHS) ester form for labeling these agents. Following conjugation or breakdown of a labeled ligand, exc...

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Autores principales: Marshall, Milton V., Draney, Daniel, Sevick-Muraca, Eva M., Olive, D. Michael
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978892/
https://www.ncbi.nlm.nih.gov/pubmed/20376568
http://dx.doi.org/10.1007/s11307-010-0317-x
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author Marshall, Milton V.
Draney, Daniel
Sevick-Muraca, Eva M.
Olive, D. Michael
author_facet Marshall, Milton V.
Draney, Daniel
Sevick-Muraca, Eva M.
Olive, D. Michael
author_sort Marshall, Milton V.
collection PubMed
description OBJECTIVE: Fluorophore-labeled contrast imaging agents are moving toward clinical use for a number of applications. The near-infrared dye IRDye 800CW is frequently used in its N-hydroxysuccinamide (NHS) ester form for labeling these agents. Following conjugation or breakdown of a labeled ligand, excess NHS ester is converted to the carboxylate form. To prepare for clinical use as a near-infrared fluorophore, a toxicity study was conducted on IRDye 800CW carboxylate. METHODS: Male and female Sprague–Dawley rats were given a single intravenous or intradermal administration of IRDye 800CW carboxylate; Indocyanine Green was used as a comparative control. Animals were injected with varying doses of the test and control articles and observed for up to 14 days. Clinical chemistry, hematological, and pharmacokinetic analyses were performed on subgroups of animals. Organs were analyzed for content of the test article. Tissues were analyzed microscopically for pathological changes. RESULTS: Based on hematologic, clinical chemistry, and histopathologic evaluation, single administration of IRDye 800CW carboxylate intravenously at dose levels of 1, 5, and 20 mg/kg or 20 mg/kg intradermally produced no pathological evidence of toxicity. CONCLUSION: A dose of 20 mg/kg was identified as the no observed adverse effect level following IV or ID routes of administration of IRDye 800CW. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11307-010-0317-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-29788922010-12-08 Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats Marshall, Milton V. Draney, Daniel Sevick-Muraca, Eva M. Olive, D. Michael Mol Imaging Biol Research Article OBJECTIVE: Fluorophore-labeled contrast imaging agents are moving toward clinical use for a number of applications. The near-infrared dye IRDye 800CW is frequently used in its N-hydroxysuccinamide (NHS) ester form for labeling these agents. Following conjugation or breakdown of a labeled ligand, excess NHS ester is converted to the carboxylate form. To prepare for clinical use as a near-infrared fluorophore, a toxicity study was conducted on IRDye 800CW carboxylate. METHODS: Male and female Sprague–Dawley rats were given a single intravenous or intradermal administration of IRDye 800CW carboxylate; Indocyanine Green was used as a comparative control. Animals were injected with varying doses of the test and control articles and observed for up to 14 days. Clinical chemistry, hematological, and pharmacokinetic analyses were performed on subgroups of animals. Organs were analyzed for content of the test article. Tissues were analyzed microscopically for pathological changes. RESULTS: Based on hematologic, clinical chemistry, and histopathologic evaluation, single administration of IRDye 800CW carboxylate intravenously at dose levels of 1, 5, and 20 mg/kg or 20 mg/kg intradermally produced no pathological evidence of toxicity. CONCLUSION: A dose of 20 mg/kg was identified as the no observed adverse effect level following IV or ID routes of administration of IRDye 800CW. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11307-010-0317-x) contains supplementary material, which is available to authorized users. Springer-Verlag 2010-04-08 2010 /pmc/articles/PMC2978892/ /pubmed/20376568 http://dx.doi.org/10.1007/s11307-010-0317-x Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Research Article
Marshall, Milton V.
Draney, Daniel
Sevick-Muraca, Eva M.
Olive, D. Michael
Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats
title Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats
title_full Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats
title_fullStr Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats
title_full_unstemmed Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats
title_short Single-Dose Intravenous Toxicity Study of IRDye 800CW in Sprague-Dawley Rats
title_sort single-dose intravenous toxicity study of irdye 800cw in sprague-dawley rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978892/
https://www.ncbi.nlm.nih.gov/pubmed/20376568
http://dx.doi.org/10.1007/s11307-010-0317-x
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