Dendrimer-based metal chelates: A new class of magnetic resonance imaging contrast agents
We have developed a new class of magnetic resonance imaging contrast agents with large proton relaxation enhancements and high molecular relaxivities. The reagents are built from the polyamidoamine form of Starburs™ dendrimers in which free amines have been conjugated to the chelator 2‐(4‐isothiocya...
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Veröffentlicht in: | Magnetic resonance in medicine 1994-01, Vol.31 (1), p.1-8 |
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creator | Wiener, Erik Brechbiel, M. W. Brothers, H. Magin, R. L. Gansow, O. A. Tomalia, D. A. Lauterbur, P. C. |
description | We have developed a new class of magnetic resonance imaging contrast agents with large proton relaxation enhancements and high molecular relaxivities. The reagents are built from the polyamidoamine form of Starburs™ dendrimers in which free amines have been conjugated to the chelator 2‐(4‐isothiocyanatobnenzyl)‐6‐methyl‐diethylenetriaminepenta‐acetic acid. The dendrimer gadolinium poly‐chelates have enhancement factors, i.e., the ratlo of the relaxivity per Gd(III) ion to that of Gd(III)‐diethylenetriaminepentaacetic acid, of up to 6. These factors are more than twice those observed for analogous metal‐chelate conjugates formed with serum albumins, polylysine, or dextran. One of the dendrimer‐metal chelate conjugates has 170 gadolinium ions bound, which greatly exceeds the number bound to other macromolecular agents reported In the literature, and has a molecular relaxivity of 5,800 (mM · s)−1, at 25 MHz, 20°C, and pH of 7.4. We observed that these dendrimer‐based agents enhance conventional MR images and 3D time of flight MR angiograms, and that those with molecular weights of 8,508 and 139,000 g/mole have enhancement half lives of 40 ± 10 and 200 ± 100 min, much longer than the 24 ± 4 min measured for Gd(III)‐diethylenetriaminepentaacetic acid. Our results suggest that this new and powerful class of contrast agents have the potential for diverse and extensive application in MR imaging. |
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W. ; Brothers, H. ; Magin, R. L. ; Gansow, O. A. ; Tomalia, D. A. ; Lauterbur, P. C.</creator><creatorcontrib>Wiener, Erik ; Brechbiel, M. W. ; Brothers, H. ; Magin, R. L. ; Gansow, O. A. ; Tomalia, D. A. ; Lauterbur, P. C.</creatorcontrib><description>We have developed a new class of magnetic resonance imaging contrast agents with large proton relaxation enhancements and high molecular relaxivities. The reagents are built from the polyamidoamine form of Starburs™ dendrimers in which free amines have been conjugated to the chelator 2‐(4‐isothiocyanatobnenzyl)‐6‐methyl‐diethylenetriaminepenta‐acetic acid. The dendrimer gadolinium poly‐chelates have enhancement factors, i.e., the ratlo of the relaxivity per Gd(III) ion to that of Gd(III)‐diethylenetriaminepentaacetic acid, of up to 6. These factors are more than twice those observed for analogous metal‐chelate conjugates formed with serum albumins, polylysine, or dextran. One of the dendrimer‐metal chelate conjugates has 170 gadolinium ions bound, which greatly exceeds the number bound to other macromolecular agents reported In the literature, and has a molecular relaxivity of 5,800 (mM · s)−1, at 25 MHz, 20°C, and pH of 7.4. We observed that these dendrimer‐based agents enhance conventional MR images and 3D time of flight MR angiograms, and that those with molecular weights of 8,508 and 139,000 g/mole have enhancement half lives of 40 ± 10 and 200 ± 100 min, much longer than the 24 ± 4 min measured for Gd(III)‐diethylenetriaminepentaacetic acid. Our results suggest that this new and powerful class of contrast agents have the potential for diverse and extensive application in MR imaging.</description><identifier>ISSN: 0740-3194</identifier><identifier>EISSN: 1522-2594</identifier><identifier>DOI: 10.1002/mrm.1910310102</identifier><identifier>PMID: 8121264</identifier><identifier>CODEN: MRMEEN</identifier><language>eng</language><publisher>Baltimore: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Biological and medical sciences ; cascade polymers ; contrast agents ; Contrast Media ; Contrast media. Radiopharmaceuticals ; dendrimers ; Female ; Magnetic Resonance Imaging ; Medical sciences ; Molecular Structure ; Organometallic Compounds - chemistry ; Pentetic Acid - analogs & derivatives ; Pentetic Acid - chemistry ; Pharmacology. Drug treatments ; Polyamines - chemistry ; Rats ; Rats, Inbred F344</subject><ispartof>Magnetic resonance in medicine, 1994-01, Vol.31 (1), p.1-8</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4732-eb2e3fbb94581ebcb51a1b0957015a444580a93be86903d1805c492c6c255f433</citedby><cites>FETCH-LOGICAL-c4732-eb2e3fbb94581ebcb51a1b0957015a444580a93be86903d1805c492c6c255f433</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmrm.1910310102$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmrm.1910310102$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,4024,27923,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3874219$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8121264$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wiener, Erik</creatorcontrib><creatorcontrib>Brechbiel, M. W.</creatorcontrib><creatorcontrib>Brothers, H.</creatorcontrib><creatorcontrib>Magin, R. L.</creatorcontrib><creatorcontrib>Gansow, O. A.</creatorcontrib><creatorcontrib>Tomalia, D. A.</creatorcontrib><creatorcontrib>Lauterbur, P. C.</creatorcontrib><title>Dendrimer-based metal chelates: A new class of magnetic resonance imaging contrast agents</title><title>Magnetic resonance in medicine</title><addtitle>Magn. Reson. Med</addtitle><description>We have developed a new class of magnetic resonance imaging contrast agents with large proton relaxation enhancements and high molecular relaxivities. The reagents are built from the polyamidoamine form of Starburs™ dendrimers in which free amines have been conjugated to the chelator 2‐(4‐isothiocyanatobnenzyl)‐6‐methyl‐diethylenetriaminepenta‐acetic acid. The dendrimer gadolinium poly‐chelates have enhancement factors, i.e., the ratlo of the relaxivity per Gd(III) ion to that of Gd(III)‐diethylenetriaminepentaacetic acid, of up to 6. These factors are more than twice those observed for analogous metal‐chelate conjugates formed with serum albumins, polylysine, or dextran. One of the dendrimer‐metal chelate conjugates has 170 gadolinium ions bound, which greatly exceeds the number bound to other macromolecular agents reported In the literature, and has a molecular relaxivity of 5,800 (mM · s)−1, at 25 MHz, 20°C, and pH of 7.4. We observed that these dendrimer‐based agents enhance conventional MR images and 3D time of flight MR angiograms, and that those with molecular weights of 8,508 and 139,000 g/mole have enhancement half lives of 40 ± 10 and 200 ± 100 min, much longer than the 24 ± 4 min measured for Gd(III)‐diethylenetriaminepentaacetic acid. Our results suggest that this new and powerful class of contrast agents have the potential for diverse and extensive application in MR imaging.</description><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>cascade polymers</subject><subject>contrast agents</subject><subject>Contrast Media</subject><subject>Contrast media. Radiopharmaceuticals</subject><subject>dendrimers</subject><subject>Female</subject><subject>Magnetic Resonance Imaging</subject><subject>Medical sciences</subject><subject>Molecular Structure</subject><subject>Organometallic Compounds - chemistry</subject><subject>Pentetic Acid - analogs & derivatives</subject><subject>Pentetic Acid - chemistry</subject><subject>Pharmacology. Drug treatments</subject><subject>Polyamines - chemistry</subject><subject>Rats</subject><subject>Rats, Inbred F344</subject><issn>0740-3194</issn><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1v1DAQhi0EKkvhyg3JB8Qty_griblVC22RWpAQH4KLZXsnSyBxWk9Wbf99jXa1iBOnkWaed8Z-GHsuYCkA5Osxj0thBSgBAuQDthBGykoaqx-yBTQaKiWsfsyeEP0CAGsbfcSOWiGFrPWCfX-LaZ37EXMVPOGajzj7gcefOPgZ6Q0_4QlveBw8EZ86PvpNwrmPPCNNyaeIvC-9Pm14nNKcPc3cbzDN9JQ96vxA-Gxfj9mX03efV-fVxcez96uTiyrqRskKg0TVhWC1aQWGGIzwIoA1DQjjtS5t8FYFbGsLai1aMFFbGesojem0Usfs1W7vVZ6ut0izG3uKOAw-4bQl19SqBVnXBVzuwJgnooyduyof9_nOCXB_XLri0v11WQIv9pu3YcT1Ad_LK_OX-7mn6IcuFx09HTDVNloKWzC7w276Ae_-c9Rdfrr85wnVLtvTjLeHrM-_Xd2oxrhvH87cD3nafgWzcufqHmtRmvg</recordid><startdate>199401</startdate><enddate>199401</enddate><creator>Wiener, Erik</creator><creator>Brechbiel, M. W.</creator><creator>Brothers, H.</creator><creator>Magin, R. L.</creator><creator>Gansow, O. A.</creator><creator>Tomalia, D. A.</creator><creator>Lauterbur, P. C.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Williams & Wilkins</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199401</creationdate><title>Dendrimer-based metal chelates: A new class of magnetic resonance imaging contrast agents</title><author>Wiener, Erik ; Brechbiel, M. W. ; Brothers, H. ; Magin, R. L. ; Gansow, O. A. ; Tomalia, D. A. ; Lauterbur, P. C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4732-eb2e3fbb94581ebcb51a1b0957015a444580a93be86903d1805c492c6c255f433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>cascade polymers</topic><topic>contrast agents</topic><topic>Contrast Media</topic><topic>Contrast media. Radiopharmaceuticals</topic><topic>dendrimers</topic><topic>Female</topic><topic>Magnetic Resonance Imaging</topic><topic>Medical sciences</topic><topic>Molecular Structure</topic><topic>Organometallic Compounds - chemistry</topic><topic>Pentetic Acid - analogs & derivatives</topic><topic>Pentetic Acid - chemistry</topic><topic>Pharmacology. Drug treatments</topic><topic>Polyamines - chemistry</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wiener, Erik</creatorcontrib><creatorcontrib>Brechbiel, M. W.</creatorcontrib><creatorcontrib>Brothers, H.</creatorcontrib><creatorcontrib>Magin, R. L.</creatorcontrib><creatorcontrib>Gansow, O. A.</creatorcontrib><creatorcontrib>Tomalia, D. A.</creatorcontrib><creatorcontrib>Lauterbur, P. C.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wiener, Erik</au><au>Brechbiel, M. W.</au><au>Brothers, H.</au><au>Magin, R. L.</au><au>Gansow, O. A.</au><au>Tomalia, D. A.</au><au>Lauterbur, P. C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dendrimer-based metal chelates: A new class of magnetic resonance imaging contrast agents</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn. Reson. Med</addtitle><date>1994-01</date><risdate>1994</risdate><volume>31</volume><issue>1</issue><spage>1</spage><epage>8</epage><pages>1-8</pages><issn>0740-3194</issn><eissn>1522-2594</eissn><coden>MRMEEN</coden><abstract>We have developed a new class of magnetic resonance imaging contrast agents with large proton relaxation enhancements and high molecular relaxivities. The reagents are built from the polyamidoamine form of Starburs™ dendrimers in which free amines have been conjugated to the chelator 2‐(4‐isothiocyanatobnenzyl)‐6‐methyl‐diethylenetriaminepenta‐acetic acid. The dendrimer gadolinium poly‐chelates have enhancement factors, i.e., the ratlo of the relaxivity per Gd(III) ion to that of Gd(III)‐diethylenetriaminepentaacetic acid, of up to 6. These factors are more than twice those observed for analogous metal‐chelate conjugates formed with serum albumins, polylysine, or dextran. One of the dendrimer‐metal chelate conjugates has 170 gadolinium ions bound, which greatly exceeds the number bound to other macromolecular agents reported In the literature, and has a molecular relaxivity of 5,800 (mM · s)−1, at 25 MHz, 20°C, and pH of 7.4. We observed that these dendrimer‐based agents enhance conventional MR images and 3D time of flight MR angiograms, and that those with molecular weights of 8,508 and 139,000 g/mole have enhancement half lives of 40 ± 10 and 200 ± 100 min, much longer than the 24 ± 4 min measured for Gd(III)‐diethylenetriaminepentaacetic acid. Our results suggest that this new and powerful class of contrast agents have the potential for diverse and extensive application in MR imaging.</abstract><cop>Baltimore</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8121264</pmid><doi>10.1002/mrm.1910310102</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological and medical sciences cascade polymers contrast agents Contrast Media Contrast media. Radiopharmaceuticals dendrimers Female Magnetic Resonance Imaging Medical sciences Molecular Structure Organometallic Compounds - chemistry Pentetic Acid - analogs & derivatives Pentetic Acid - chemistry Pharmacology. Drug treatments Polyamines - chemistry Rats Rats, Inbred F344 |
title | Dendrimer-based metal chelates: A new class of magnetic resonance imaging contrast agents |
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