Tat Peptide Directs Enhanced Clearance and Hepatic Permeability of Magnetic Nanoparticles
Superparamagnetic nanoparticles have a number of important biomedical applications, serving as MR contrast agents for imaging specific molecular targets, as reagents for cell labeling and cell tracking, and for the isolation of specific classes of cells. We have determined the physical and biologica...
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Veröffentlicht in: | Bioconjugate chemistry 2002-03, Vol.13 (2), p.264-268 |
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creator | Wunderbaldinger, Patrick Josephson, Lee Weissleder, Ralph |
description | Superparamagnetic nanoparticles have a number of important biomedical applications, serving as MR contrast agents for imaging specific molecular targets, as reagents for cell labeling and cell tracking, and for the isolation of specific classes of cells. We have determined the physical and biological properties of MION-47 and amino-CLIO, nanoparticles which serve as precursors for the synthesis of targeted MR contrast agents, and Tat-CLIO, a nanoparticle used as a cell labeling reagent. Blood half-lives for MION-47 and amino-CLIO were 682 ± 34 and 655 ± 37 min, respectively. The attachment of 9.7 tat peptides per crystal to amino-CLIO resulted in a reduction in blood half-life to 47 ± 6 min. MION-47, amino-CLIO, and Tat-CLIO were present in highest concentrations in liver and spleen and lymph nodes, where concentrations for all three nanoparticles ranged from 8.80 to 6.11% of injected dose per gram. Twenty-four hours after the intravenous injection of amino-CLIO, the nanoparticle was concentrated in cells surrounding hepatic blood vessels (endothelial and Kupffer cells), in a fashion similar to that obtained with other nanoparticle preparations. In contrast, Tat-CLIO was present as numerous discrete foci of intense fluorescence throughout the parenchyma. Using the peptide as a component of future nanoparticles, it might be possible to design sensors for the detection of macromolecules present in intracellular compartments. |
doi_str_mv | 10.1021/bc015563u |
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We have determined the physical and biological properties of MION-47 and amino-CLIO, nanoparticles which serve as precursors for the synthesis of targeted MR contrast agents, and Tat-CLIO, a nanoparticle used as a cell labeling reagent. Blood half-lives for MION-47 and amino-CLIO were 682 ± 34 and 655 ± 37 min, respectively. The attachment of 9.7 tat peptides per crystal to amino-CLIO resulted in a reduction in blood half-life to 47 ± 6 min. MION-47, amino-CLIO, and Tat-CLIO were present in highest concentrations in liver and spleen and lymph nodes, where concentrations for all three nanoparticles ranged from 8.80 to 6.11% of injected dose per gram. Twenty-four hours after the intravenous injection of amino-CLIO, the nanoparticle was concentrated in cells surrounding hepatic blood vessels (endothelial and Kupffer cells), in a fashion similar to that obtained with other nanoparticle preparations. In contrast, Tat-CLIO was present as numerous discrete foci of intense fluorescence throughout the parenchyma. Using the peptide as a component of future nanoparticles, it might be possible to design sensors for the detection of macromolecules present in intracellular compartments.</description><identifier>ISSN: 1043-1802</identifier><identifier>EISSN: 1520-4812</identifier><identifier>DOI: 10.1021/bc015563u</identifier><identifier>PMID: 11906263</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Amino Acid Sequence ; Animals ; Cells, Cultured ; Drug Carriers - chemistry ; Drug Carriers - pharmacokinetics ; Female ; Gene Products, tat - chemistry ; Gene Products, tat - pharmacokinetics ; Humans ; Liver - metabolism ; Magnetics ; Mice ; Mice, Inbred BALB C ; Nanotechnology ; Particle Size ; Permeability ; Tissue Distribution</subject><ispartof>Bioconjugate chemistry, 2002-03, Vol.13 (2), p.264-268</ispartof><rights>Copyright © 2002 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a415t-6846bfbaea8233a97d7bb03029b631409a5056a5302b85e6824492709cd67f593</citedby><cites>FETCH-LOGICAL-a415t-6846bfbaea8233a97d7bb03029b631409a5056a5302b85e6824492709cd67f593</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bc015563u$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bc015563u$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,777,781,2752,27057,27905,27906,56719,56769</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11906263$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wunderbaldinger, Patrick</creatorcontrib><creatorcontrib>Josephson, Lee</creatorcontrib><creatorcontrib>Weissleder, Ralph</creatorcontrib><title>Tat Peptide Directs Enhanced Clearance and Hepatic Permeability of Magnetic Nanoparticles</title><title>Bioconjugate chemistry</title><addtitle>Bioconjugate Chem</addtitle><description>Superparamagnetic nanoparticles have a number of important biomedical applications, serving as MR contrast agents for imaging specific molecular targets, as reagents for cell labeling and cell tracking, and for the isolation of specific classes of cells. We have determined the physical and biological properties of MION-47 and amino-CLIO, nanoparticles which serve as precursors for the synthesis of targeted MR contrast agents, and Tat-CLIO, a nanoparticle used as a cell labeling reagent. Blood half-lives for MION-47 and amino-CLIO were 682 ± 34 and 655 ± 37 min, respectively. The attachment of 9.7 tat peptides per crystal to amino-CLIO resulted in a reduction in blood half-life to 47 ± 6 min. MION-47, amino-CLIO, and Tat-CLIO were present in highest concentrations in liver and spleen and lymph nodes, where concentrations for all three nanoparticles ranged from 8.80 to 6.11% of injected dose per gram. Twenty-four hours after the intravenous injection of amino-CLIO, the nanoparticle was concentrated in cells surrounding hepatic blood vessels (endothelial and Kupffer cells), in a fashion similar to that obtained with other nanoparticle preparations. In contrast, Tat-CLIO was present as numerous discrete foci of intense fluorescence throughout the parenchyma. Using the peptide as a component of future nanoparticles, it might be possible to design sensors for the detection of macromolecules present in intracellular compartments.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Cells, Cultured</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Carriers - pharmacokinetics</subject><subject>Female</subject><subject>Gene Products, tat - chemistry</subject><subject>Gene Products, tat - pharmacokinetics</subject><subject>Humans</subject><subject>Liver - metabolism</subject><subject>Magnetics</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Nanotechnology</subject><subject>Particle Size</subject><subject>Permeability</subject><subject>Tissue Distribution</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0MFO3DAQBmALFcEWOPQFUC5F6iEwtmMnOVZbKEi7gLSLtPRijZMJBLJJaicSvH292hW9cPIvz6cZ6WfsG4dzDoJf2AK4UlqOe2zClYA4ybj4EjIkMuYZiEP21fsXAMh5Jg7YIec5aKHlhD0ucYjuqR_qkqJftaNi8NFl-4xtQWU0bQjdJkbYltE19TjUReBuTWjrph7eo66K5vjU0mZwi23XowuxIX_M9itsPJ3s3iP2cHW5nF7Hs7vfN9OfsxgTroZYZ4m2lUXCTEiJeVqm1oIEkVsteQI5KlAaVfixmSKdiSTJRQp5Ueq0Urk8Ymfbvb3r_o7kB7OufUFNgy11ozcpV1ImAgL8sYWF67x3VJne1Wt074aD2fRoPnoM9nS3dLRrKv_LXXEBxFtQ-4HePuboXo1OZarM8n5hVgudzlezP0YH_33rsfDmpRtdGzr55PA_UwuHRQ</recordid><startdate>20020301</startdate><enddate>20020301</enddate><creator>Wunderbaldinger, Patrick</creator><creator>Josephson, Lee</creator><creator>Weissleder, Ralph</creator><general>American Chemical Society</general><scope>BSCLL</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>20020301</creationdate><title>Tat Peptide Directs Enhanced Clearance and Hepatic Permeability of Magnetic Nanoparticles</title><author>Wunderbaldinger, Patrick ; Josephson, Lee ; Weissleder, Ralph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a415t-6846bfbaea8233a97d7bb03029b631409a5056a5302b85e6824492709cd67f593</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Cells, Cultured</topic><topic>Drug Carriers - chemistry</topic><topic>Drug Carriers - pharmacokinetics</topic><topic>Female</topic><topic>Gene Products, tat - chemistry</topic><topic>Gene Products, tat - pharmacokinetics</topic><topic>Humans</topic><topic>Liver - metabolism</topic><topic>Magnetics</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Nanotechnology</topic><topic>Particle Size</topic><topic>Permeability</topic><topic>Tissue Distribution</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wunderbaldinger, Patrick</creatorcontrib><creatorcontrib>Josephson, Lee</creatorcontrib><creatorcontrib>Weissleder, Ralph</creatorcontrib><collection>Istex</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>Bioconjugate chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wunderbaldinger, Patrick</au><au>Josephson, Lee</au><au>Weissleder, Ralph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tat Peptide Directs Enhanced Clearance and Hepatic Permeability of Magnetic Nanoparticles</atitle><jtitle>Bioconjugate chemistry</jtitle><addtitle>Bioconjugate Chem</addtitle><date>2002-03-01</date><risdate>2002</risdate><volume>13</volume><issue>2</issue><spage>264</spage><epage>268</epage><pages>264-268</pages><issn>1043-1802</issn><eissn>1520-4812</eissn><abstract>Superparamagnetic nanoparticles have a number of important biomedical applications, serving as MR contrast agents for imaging specific molecular targets, as reagents for cell labeling and cell tracking, and for the isolation of specific classes of cells. 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In contrast, Tat-CLIO was present as numerous discrete foci of intense fluorescence throughout the parenchyma. Using the peptide as a component of future nanoparticles, it might be possible to design sensors for the detection of macromolecules present in intracellular compartments.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>11906263</pmid><doi>10.1021/bc015563u</doi><tpages>5</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Cells, Cultured Drug Carriers - chemistry Drug Carriers - pharmacokinetics Female Gene Products, tat - chemistry Gene Products, tat - pharmacokinetics Humans Liver - metabolism Magnetics Mice Mice, Inbred BALB C Nanotechnology Particle Size Permeability Tissue Distribution |
title | Tat Peptide Directs Enhanced Clearance and Hepatic Permeability of Magnetic Nanoparticles |
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