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99mTc‐anti‐epidermal growth factor receptor nanobody for tumor imaging
Nanobodies are important biomolecules for tumor targeting. In this study, we synthesized and labeled anti‐epidermal growth factor receptor (EGFR) nanobody OA‐cb6 with 99mTc(CO)3+ and evaluated its characteristics for targeting the EGFR in the A431 human epidermal carcinoma cell line. Nanobody radiol...
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Published in: | Chemical biology & drug design 2017-04, Vol.89 (4), p.498-504 |
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creator | Piramoon, Majid Hosseinimehr, Seyed Jalal Omidfar, Kobra Noaparast, Zohreh Abedi, Seyed Mohammad |
description | Nanobodies are important biomolecules for tumor targeting. In this study, we synthesized and labeled anti‐epidermal growth factor receptor (EGFR) nanobody OA‐cb6 with 99mTc(CO)3+ and evaluated its characteristics for targeting the EGFR in the A431 human epidermal carcinoma cell line. Nanobody radiolabeling was achieved with high yield and radiochemical purity, and the radioconjugate was stable. Biodistribution results in nude mice exhibited a favorable tumor‐to‐muscle ratio at 4‐hr postinjection, and tumor location was visualized at 4 hr after injection of radiolabeled nanobody. Our result showed that the OA‐cb6‐99mTc‐tricarbonyl radiolabeled nanobody is a promising radiolabeled biomolecule for tumor imaging in cancers with high EGFR overexpression.
This study described the preparation and radiolabeling of anti‐EGFR nanobody, OA‐cb6. The nanobody was labeled using 99mTc‐tricarbonyl. Results showed that radioconjugate had fast blood clearance and a favorable tumor uptake in A431‐xenografted nude mice. |
doi_str_mv | 10.1111/cbdd.12871 |
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This study described the preparation and radiolabeling of anti‐EGFR nanobody, OA‐cb6. The nanobody was labeled using 99mTc‐tricarbonyl. Results showed that radioconjugate had fast blood clearance and a favorable tumor uptake in A431‐xenografted nude mice.</description><identifier>ISSN: 1747-0277</identifier><identifier>EISSN: 1747-0285</identifier><identifier>DOI: 10.1111/cbdd.12871</identifier><language>eng</language><subject>99mTc ; EGFR ; epidermal growth factor receptor ; nanobody ; tumor imaging</subject><ispartof>Chemical biology & drug design, 2017-04, Vol.89 (4), p.498-504</ispartof><rights>2016 John Wiley & Sons A/S.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Piramoon, Majid</creatorcontrib><creatorcontrib>Hosseinimehr, Seyed Jalal</creatorcontrib><creatorcontrib>Omidfar, Kobra</creatorcontrib><creatorcontrib>Noaparast, Zohreh</creatorcontrib><creatorcontrib>Abedi, Seyed Mohammad</creatorcontrib><title>99mTc‐anti‐epidermal growth factor receptor nanobody for tumor imaging</title><title>Chemical biology & drug design</title><description>Nanobodies are important biomolecules for tumor targeting. In this study, we synthesized and labeled anti‐epidermal growth factor receptor (EGFR) nanobody OA‐cb6 with 99mTc(CO)3+ and evaluated its characteristics for targeting the EGFR in the A431 human epidermal carcinoma cell line. Nanobody radiolabeling was achieved with high yield and radiochemical purity, and the radioconjugate was stable. Biodistribution results in nude mice exhibited a favorable tumor‐to‐muscle ratio at 4‐hr postinjection, and tumor location was visualized at 4 hr after injection of radiolabeled nanobody. Our result showed that the OA‐cb6‐99mTc‐tricarbonyl radiolabeled nanobody is a promising radiolabeled biomolecule for tumor imaging in cancers with high EGFR overexpression.
This study described the preparation and radiolabeling of anti‐EGFR nanobody, OA‐cb6. The nanobody was labeled using 99mTc‐tricarbonyl. Results showed that radioconjugate had fast blood clearance and a favorable tumor uptake in A431‐xenografted nude mice.</description><subject>99mTc</subject><subject>EGFR</subject><subject>epidermal growth factor receptor</subject><subject>nanobody</subject><subject>tumor imaging</subject><issn>1747-0277</issn><issn>1747-0285</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNpjYBAyNNAzBAL95KSUFD1DIwtzQyYGTkNzE3NdAyMLUxY429ycg4GruDjLwMDExNTIgpPBy9IyNyT5UcOExLySTCCVWpCZklqUm5ijkF6UX16SoZCWmFySX6RQlJqcWgBi5CXm5Sflp1QqpAE5JaW5QDIzNzE9My-dh4E1LTGnOJUXSnMzGLq5hjh76JZn5qRWxhcUAdUVVcYbGsSDnBoPcmo82Knxzk4uLmCWMTl6AIZuS7A</recordid><startdate>201704</startdate><enddate>201704</enddate><creator>Piramoon, Majid</creator><creator>Hosseinimehr, Seyed Jalal</creator><creator>Omidfar, Kobra</creator><creator>Noaparast, Zohreh</creator><creator>Abedi, Seyed Mohammad</creator><scope/></search><sort><creationdate>201704</creationdate><title>99mTc‐anti‐epidermal growth factor receptor nanobody for tumor imaging</title><author>Piramoon, Majid ; Hosseinimehr, Seyed Jalal ; Omidfar, Kobra ; Noaparast, Zohreh ; Abedi, Seyed Mohammad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-wiley_primary_10_1111_cbdd_12871_CBDD128713</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>99mTc</topic><topic>EGFR</topic><topic>epidermal growth factor receptor</topic><topic>nanobody</topic><topic>tumor imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Piramoon, Majid</creatorcontrib><creatorcontrib>Hosseinimehr, Seyed Jalal</creatorcontrib><creatorcontrib>Omidfar, Kobra</creatorcontrib><creatorcontrib>Noaparast, Zohreh</creatorcontrib><creatorcontrib>Abedi, Seyed Mohammad</creatorcontrib><jtitle>Chemical biology & drug design</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Piramoon, Majid</au><au>Hosseinimehr, Seyed Jalal</au><au>Omidfar, Kobra</au><au>Noaparast, Zohreh</au><au>Abedi, Seyed Mohammad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>99mTc‐anti‐epidermal growth factor receptor nanobody for tumor imaging</atitle><jtitle>Chemical biology & drug design</jtitle><date>2017-04</date><risdate>2017</risdate><volume>89</volume><issue>4</issue><spage>498</spage><epage>504</epage><pages>498-504</pages><issn>1747-0277</issn><eissn>1747-0285</eissn><abstract>Nanobodies are important biomolecules for tumor targeting. In this study, we synthesized and labeled anti‐epidermal growth factor receptor (EGFR) nanobody OA‐cb6 with 99mTc(CO)3+ and evaluated its characteristics for targeting the EGFR in the A431 human epidermal carcinoma cell line. Nanobody radiolabeling was achieved with high yield and radiochemical purity, and the radioconjugate was stable. Biodistribution results in nude mice exhibited a favorable tumor‐to‐muscle ratio at 4‐hr postinjection, and tumor location was visualized at 4 hr after injection of radiolabeled nanobody. Our result showed that the OA‐cb6‐99mTc‐tricarbonyl radiolabeled nanobody is a promising radiolabeled biomolecule for tumor imaging in cancers with high EGFR overexpression.
This study described the preparation and radiolabeling of anti‐EGFR nanobody, OA‐cb6. The nanobody was labeled using 99mTc‐tricarbonyl. Results showed that radioconjugate had fast blood clearance and a favorable tumor uptake in A431‐xenografted nude mice.</abstract><doi>10.1111/cbdd.12871</doi><tpages>7</tpages></addata></record> |
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subjects | 99mTc EGFR epidermal growth factor receptor nanobody tumor imaging |
title | 99mTc‐anti‐epidermal growth factor receptor nanobody for tumor imaging |
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