Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents

Combinatorial chemistry and high-throughput screening have become standard tools for discovering new drug candidates with suitable pharmacological properties. Now, those same technologies are starting to be applied to the problem of discovering novel in vivo imaging agents. Important differences in...

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Main Authors: Robert J. Gillies, John M. Hoffman, Kit S. Lam, Anne E. Menkens, David R. Piwnica-Worms, Daniel C. Sullivan, Ralph Weissleder
Format: Article
Language:English
Published: SAGE Publishing 2005-04-01
Series:Molecular Imaging
Online Access:https://doi.org/10.1162/15353500200505115
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author Robert J. Gillies
John M. Hoffman
Kit S. Lam
Anne E. Menkens
David R. Piwnica-Worms
Daniel C. Sullivan
Ralph Weissleder
author_facet Robert J. Gillies
John M. Hoffman
Kit S. Lam
Anne E. Menkens
David R. Piwnica-Worms
Daniel C. Sullivan
Ralph Weissleder
author_sort Robert J. Gillies
collection DOAJ
description Combinatorial chemistry and high-throughput screening have become standard tools for discovering new drug candidates with suitable pharmacological properties. Now, those same technologies are starting to be applied to the problem of discovering novel in vivo imaging agents. Important differences in the biological and pharmacological properties needed for imaging agents, compared to those for a therapeutic agent, require new screening methods that emphasize those characteristics, such as optimized residence time and tissue specificity, that make for a good imaging agent candidate.
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institution DOAJ
issn 1536-0121
language English
publishDate 2005-04-01
publisher SAGE Publishing
record_format Article
series Molecular Imaging
spelling doaj-art-45c9ed255d7047c5844fbcd5792da7472025-08-20T02:43:12ZengSAGE PublishingMolecular Imaging1536-01212005-04-01410.1162/1535350020050511510.1162_15353500200505115Meeting Report: High-Throughput Technologies for In Vivo Imaging AgentsRobert J. Gillies0John M. Hoffman1Kit S. Lam2Anne E. Menkens3David R. Piwnica-Worms4Daniel C. Sullivan5Ralph Weissleder6University of ArizonaNational Cancer InstituteUniversity of California—DavisNational Cancer InstituteWashington UniversityNational Cancer InstituteHarvard UniversityCombinatorial chemistry and high-throughput screening have become standard tools for discovering new drug candidates with suitable pharmacological properties. Now, those same technologies are starting to be applied to the problem of discovering novel in vivo imaging agents. Important differences in the biological and pharmacological properties needed for imaging agents, compared to those for a therapeutic agent, require new screening methods that emphasize those characteristics, such as optimized residence time and tissue specificity, that make for a good imaging agent candidate.https://doi.org/10.1162/15353500200505115
spellingShingle Robert J. Gillies
John M. Hoffman
Kit S. Lam
Anne E. Menkens
David R. Piwnica-Worms
Daniel C. Sullivan
Ralph Weissleder
Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents
Molecular Imaging
title Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents
title_full Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents
title_fullStr Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents
title_full_unstemmed Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents
title_short Meeting Report: High-Throughput Technologies for In Vivo Imaging Agents
title_sort meeting report high throughput technologies for in vivo imaging agents
url https://doi.org/10.1162/15353500200505115
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