Positron Emission Tomography Based Elucidation of the Enhanced Permeability and Retention Effect in Dogs with Cancer Using Copper-64 Liposomes
Since the first report of the enhanced permeability and retention (EPR) effect, the research in nanocarrier based antitumor drugs has been intense. The field has been devoted to treatment of cancer by exploiting EPR-based accumulation of nanocarriers in solid tumors, which for many years was conside...
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Veröffentlicht in: | ACS nano 2015-07, Vol.9 (7), p.6985-6995 |
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creator | Hansen, Anders E Petersen, Anncatrine L Henriksen, Jonas R Boerresen, Betina Rasmussen, Palle Elema, Dennis R Rosenschöld, Per Munck af Kristensen, Annemarie T Kjær, Andreas Andresen, Thomas L |
description | Since the first report of the enhanced permeability and retention (EPR) effect, the research in nanocarrier based antitumor drugs has been intense. The field has been devoted to treatment of cancer by exploiting EPR-based accumulation of nanocarriers in solid tumors, which for many years was considered to be a ubiquitous phenomenon. However, the understanding of differences in the EPR-effect between tumor types, heterogeneities within each patient group, and dependency on tumor development stage in humans is sparse. It is therefore important to enhance our understanding of the EPR-effect in large animals and humans with spontaneously developed cancer. In the present paper, we describe a novel loading method of copper-64 into PEGylated liposomes and use these liposomes to evaluate the EPR-effect in 11 canine cancer patients with spontaneous solid tumors by PET/CT imaging. We thereby provide the first high-resolution analysis of EPR-based tumor accumulation in large animals. We find that the EPR-effect is strong in some tumor types but cannot be considered a general feature of solid malignant tumors since we observed a high degree of accumulation heterogeneity between tumors. Six of seven included carcinomas displayed high uptake levels of liposomes, whereas one of four sarcomas displayed signs of liposome retention. We conclude that nanocarrier-radiotracers could be important in identifying cancer patients that will benefit from nanocarrier-based therapeutics in clinical practice. |
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The field has been devoted to treatment of cancer by exploiting EPR-based accumulation of nanocarriers in solid tumors, which for many years was considered to be a ubiquitous phenomenon. However, the understanding of differences in the EPR-effect between tumor types, heterogeneities within each patient group, and dependency on tumor development stage in humans is sparse. It is therefore important to enhance our understanding of the EPR-effect in large animals and humans with spontaneously developed cancer. In the present paper, we describe a novel loading method of copper-64 into PEGylated liposomes and use these liposomes to evaluate the EPR-effect in 11 canine cancer patients with spontaneous solid tumors by PET/CT imaging. We thereby provide the first high-resolution analysis of EPR-based tumor accumulation in large animals. We find that the EPR-effect is strong in some tumor types but cannot be considered a general feature of solid malignant tumors since we observed a high degree of accumulation heterogeneity between tumors. Six of seven included carcinomas displayed high uptake levels of liposomes, whereas one of four sarcomas displayed signs of liposome retention. We conclude that nanocarrier-radiotracers could be important in identifying cancer patients that will benefit from nanocarrier-based therapeutics in clinical practice.</description><identifier>ISSN: 1936-0851</identifier><identifier>EISSN: 1936-086X</identifier><identifier>DOI: 10.1021/acsnano.5b01324</identifier><identifier>PMID: 26022907</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Cancer ; Carcinoma - diagnostic imaging ; Carcinoma - veterinary ; Copper Radioisotopes - administration & dosage ; Copper Radioisotopes - pharmacokinetics ; Dogs ; Female ; Heterogeneity ; Imaging ; Liposomes ; Liposomes - chemistry ; Liposomes - pharmacokinetics ; Male ; Multimodal Imaging ; Nanostructure ; Patients ; Permeability ; Polyethylene Glycols - chemistry ; Positron-Emission Tomography ; Radiopharmaceuticals - administration & dosage ; Radiopharmaceuticals - pharmacokinetics ; Tomography, X-Ray Computed ; Tumors</subject><ispartof>ACS nano, 2015-07, Vol.9 (7), p.6985-6995</ispartof><rights>Copyright © American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a407t-ca1857f47255309bb7a285c058eaff103220a991eba9b096708523c44a060943</citedby><cites>FETCH-LOGICAL-a407t-ca1857f47255309bb7a285c058eaff103220a991eba9b096708523c44a060943</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/acsnano.5b01324$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsnano.5b01324$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26022907$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hansen, Anders E</creatorcontrib><creatorcontrib>Petersen, Anncatrine L</creatorcontrib><creatorcontrib>Henriksen, Jonas R</creatorcontrib><creatorcontrib>Boerresen, Betina</creatorcontrib><creatorcontrib>Rasmussen, Palle</creatorcontrib><creatorcontrib>Elema, Dennis R</creatorcontrib><creatorcontrib>Rosenschöld, Per Munck af</creatorcontrib><creatorcontrib>Kristensen, Annemarie T</creatorcontrib><creatorcontrib>Kjær, Andreas</creatorcontrib><creatorcontrib>Andresen, Thomas L</creatorcontrib><title>Positron Emission Tomography Based Elucidation of the Enhanced Permeability and Retention Effect in Dogs with Cancer Using Copper-64 Liposomes</title><title>ACS nano</title><addtitle>ACS Nano</addtitle><description>Since the first report of the enhanced permeability and retention (EPR) effect, the research in nanocarrier based antitumor drugs has been intense. The field has been devoted to treatment of cancer by exploiting EPR-based accumulation of nanocarriers in solid tumors, which for many years was considered to be a ubiquitous phenomenon. However, the understanding of differences in the EPR-effect between tumor types, heterogeneities within each patient group, and dependency on tumor development stage in humans is sparse. It is therefore important to enhance our understanding of the EPR-effect in large animals and humans with spontaneously developed cancer. In the present paper, we describe a novel loading method of copper-64 into PEGylated liposomes and use these liposomes to evaluate the EPR-effect in 11 canine cancer patients with spontaneous solid tumors by PET/CT imaging. We thereby provide the first high-resolution analysis of EPR-based tumor accumulation in large animals. We find that the EPR-effect is strong in some tumor types but cannot be considered a general feature of solid malignant tumors since we observed a high degree of accumulation heterogeneity between tumors. Six of seven included carcinomas displayed high uptake levels of liposomes, whereas one of four sarcomas displayed signs of liposome retention. We conclude that nanocarrier-radiotracers could be important in identifying cancer patients that will benefit from nanocarrier-based therapeutics in clinical practice.</description><subject>Animals</subject><subject>Cancer</subject><subject>Carcinoma - diagnostic imaging</subject><subject>Carcinoma - veterinary</subject><subject>Copper Radioisotopes - administration & dosage</subject><subject>Copper Radioisotopes - pharmacokinetics</subject><subject>Dogs</subject><subject>Female</subject><subject>Heterogeneity</subject><subject>Imaging</subject><subject>Liposomes</subject><subject>Liposomes - chemistry</subject><subject>Liposomes - pharmacokinetics</subject><subject>Male</subject><subject>Multimodal Imaging</subject><subject>Nanostructure</subject><subject>Patients</subject><subject>Permeability</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Positron-Emission Tomography</subject><subject>Radiopharmaceuticals - administration & dosage</subject><subject>Radiopharmaceuticals - pharmacokinetics</subject><subject>Tomography, X-Ray Computed</subject><subject>Tumors</subject><issn>1936-0851</issn><issn>1936-086X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUtr3DAUhUVoyatdZ1e0LBQnV7Jl2ct26jxgoKFMoTtzrZFnFGzJlWTK_In-5mg6k-wKXenC_c4R9xxCrhhcM-DsBlWwaN216IDlvDgh56zOywyq8ueb11mwM3IRwhOAkJUsT8kZL4HzGuQ5-fPogoneWdqMJgSThpUb3cbjtN3RLxj0mjbDrMwa437pehq3mjZ2i1al3aP2o8bODCbuKNo1_a6jtn_Rpu-1itRY-tVtAv1t4pYu9ipPfwRjN3Thpkn7rCzo0kwuuFGHd-Rtj0PQ74_vJVndNqvFfbb8dvew-LzMsAAZM4WsErIvJBcih7rrJPJKKBCVxr5nkHMOWNdMd1h3UJcyhcBzVRQIJdRFfkk-Hmwn737NOsQ2Ha_0MKDVbg4tkyXfhyXy_0AB0oesgITeHFDlXQhe9-3kzYh-1zJo93W1x7raY11J8eFoPnejXr_yL_0k4NMBSMr2yc3eplT-afcM5Bagew</recordid><startdate>20150728</startdate><enddate>20150728</enddate><creator>Hansen, Anders E</creator><creator>Petersen, Anncatrine L</creator><creator>Henriksen, Jonas R</creator><creator>Boerresen, Betina</creator><creator>Rasmussen, Palle</creator><creator>Elema, Dennis R</creator><creator>Rosenschöld, Per Munck af</creator><creator>Kristensen, Annemarie T</creator><creator>Kjær, Andreas</creator><creator>Andresen, Thomas L</creator><general>American Chemical Society</general><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><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20150728</creationdate><title>Positron Emission Tomography Based Elucidation of the Enhanced Permeability and Retention Effect in Dogs with Cancer Using Copper-64 Liposomes</title><author>Hansen, Anders E ; Petersen, Anncatrine L ; Henriksen, Jonas R ; Boerresen, Betina ; Rasmussen, Palle ; Elema, Dennis R ; Rosenschöld, Per Munck af ; Kristensen, Annemarie T ; Kjær, Andreas ; Andresen, Thomas L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a407t-ca1857f47255309bb7a285c058eaff103220a991eba9b096708523c44a060943</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Cancer</topic><topic>Carcinoma - diagnostic imaging</topic><topic>Carcinoma - veterinary</topic><topic>Copper Radioisotopes - administration & dosage</topic><topic>Copper Radioisotopes - pharmacokinetics</topic><topic>Dogs</topic><topic>Female</topic><topic>Heterogeneity</topic><topic>Imaging</topic><topic>Liposomes</topic><topic>Liposomes - chemistry</topic><topic>Liposomes - pharmacokinetics</topic><topic>Male</topic><topic>Multimodal Imaging</topic><topic>Nanostructure</topic><topic>Patients</topic><topic>Permeability</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Positron-Emission Tomography</topic><topic>Radiopharmaceuticals - administration & dosage</topic><topic>Radiopharmaceuticals - pharmacokinetics</topic><topic>Tomography, X-Ray Computed</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hansen, Anders E</creatorcontrib><creatorcontrib>Petersen, Anncatrine L</creatorcontrib><creatorcontrib>Henriksen, Jonas R</creatorcontrib><creatorcontrib>Boerresen, Betina</creatorcontrib><creatorcontrib>Rasmussen, Palle</creatorcontrib><creatorcontrib>Elema, Dennis R</creatorcontrib><creatorcontrib>Rosenschöld, Per Munck af</creatorcontrib><creatorcontrib>Kristensen, Annemarie T</creatorcontrib><creatorcontrib>Kjær, Andreas</creatorcontrib><creatorcontrib>Andresen, Thomas L</creatorcontrib><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><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>ACS nano</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hansen, Anders E</au><au>Petersen, Anncatrine L</au><au>Henriksen, Jonas R</au><au>Boerresen, Betina</au><au>Rasmussen, Palle</au><au>Elema, Dennis R</au><au>Rosenschöld, Per Munck af</au><au>Kristensen, Annemarie T</au><au>Kjær, Andreas</au><au>Andresen, Thomas L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Positron Emission Tomography Based Elucidation of the Enhanced Permeability and Retention Effect in Dogs with Cancer Using Copper-64 Liposomes</atitle><jtitle>ACS nano</jtitle><addtitle>ACS Nano</addtitle><date>2015-07-28</date><risdate>2015</risdate><volume>9</volume><issue>7</issue><spage>6985</spage><epage>6995</epage><pages>6985-6995</pages><issn>1936-0851</issn><eissn>1936-086X</eissn><abstract>Since the first report of the enhanced permeability and retention (EPR) effect, the research in nanocarrier based antitumor drugs has been intense. The field has been devoted to treatment of cancer by exploiting EPR-based accumulation of nanocarriers in solid tumors, which for many years was considered to be a ubiquitous phenomenon. However, the understanding of differences in the EPR-effect between tumor types, heterogeneities within each patient group, and dependency on tumor development stage in humans is sparse. It is therefore important to enhance our understanding of the EPR-effect in large animals and humans with spontaneously developed cancer. In the present paper, we describe a novel loading method of copper-64 into PEGylated liposomes and use these liposomes to evaluate the EPR-effect in 11 canine cancer patients with spontaneous solid tumors by PET/CT imaging. We thereby provide the first high-resolution analysis of EPR-based tumor accumulation in large animals. We find that the EPR-effect is strong in some tumor types but cannot be considered a general feature of solid malignant tumors since we observed a high degree of accumulation heterogeneity between tumors. Six of seven included carcinomas displayed high uptake levels of liposomes, whereas one of four sarcomas displayed signs of liposome retention. We conclude that nanocarrier-radiotracers could be important in identifying cancer patients that will benefit from nanocarrier-based therapeutics in clinical practice.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>26022907</pmid><doi>10.1021/acsnano.5b01324</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Cancer Carcinoma - diagnostic imaging Carcinoma - veterinary Copper Radioisotopes - administration & dosage Copper Radioisotopes - pharmacokinetics Dogs Female Heterogeneity Imaging Liposomes Liposomes - chemistry Liposomes - pharmacokinetics Male Multimodal Imaging Nanostructure Patients Permeability Polyethylene Glycols - chemistry Positron-Emission Tomography Radiopharmaceuticals - administration & dosage Radiopharmaceuticals - pharmacokinetics Tomography, X-Ray Computed Tumors |
title | Positron Emission Tomography Based Elucidation of the Enhanced Permeability and Retention Effect in Dogs with Cancer Using Copper-64 Liposomes |
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