Selective induction hyperthermia following transcatheter arterial embolization with a mixture of nano-sized magnetic particles (ferucarbotran) and embolic materials: feasibility study in rabbits
Purpose To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device. Materials and methods Twelve Japanese white rabbits were separated into four groups: those treated with TAE usin...
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Veröffentlicht in: | Japanese journal of radiology 2008-05, Vol.26 (4), p.179-187 |
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container_title | Japanese journal of radiology |
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creator | Takamatsu, Shigeyuki Matsui, Osamu Gabata, Toshifumi Kobayashi, Satoshi Okuda, Miho Ougi, Takahiro Ikehata, Yoshio Nagano, Isamu Nagae, Hideo |
description | Purpose
To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device.
Materials and methods
Twelve Japanese white rabbits were separated into four groups: those treated with TAE using a mixture of ferucarbotran and lipiodol (F-L group); those treated with ferucarbotran and gelatin sponge powder; those treated with saline and lipiodol; and a control group. These four groups received IH. Nine rabbits with renal VX2 carcinoma were separated into three groups: IH after TAE (IH-TAE tumor), TAE without IH (TAE tumor), and no treatment (control tumor). The temperature of the tumor was kept at 45°C for 20 min. The therapeutic effect was pathologically evaluated by TUNEL staining.
Results
In the heating rates of the kidney, the F-L group showed significantly greater values than the group in which iron was not used. In the IH-TAE tumor group, tumors could be selectively heated. In TUNEL staining, the IH-TAE tumor and TAE tumor groups showed significantly greater values of apoptosis rate than in the control tumor group.
Conclusion
IH following TAE with a mixture of ferucarbotran and lipiodol was capable of inducing selective hyperthermia with our device. However, further investigation is needed to confirm its safety and effectiveness in the treatment of malignant neoplasms in humans. |
doi_str_mv | 10.1007/s11604-007-0212-9 |
format | Article |
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To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device.
Materials and methods
Twelve Japanese white rabbits were separated into four groups: those treated with TAE using a mixture of ferucarbotran and lipiodol (F-L group); those treated with ferucarbotran and gelatin sponge powder; those treated with saline and lipiodol; and a control group. These four groups received IH. Nine rabbits with renal VX2 carcinoma were separated into three groups: IH after TAE (IH-TAE tumor), TAE without IH (TAE tumor), and no treatment (control tumor). The temperature of the tumor was kept at 45°C for 20 min. The therapeutic effect was pathologically evaluated by TUNEL staining.
Results
In the heating rates of the kidney, the F-L group showed significantly greater values than the group in which iron was not used. In the IH-TAE tumor group, tumors could be selectively heated. In TUNEL staining, the IH-TAE tumor and TAE tumor groups showed significantly greater values of apoptosis rate than in the control tumor group.
Conclusion
IH following TAE with a mixture of ferucarbotran and lipiodol was capable of inducing selective hyperthermia with our device. However, further investigation is needed to confirm its safety and effectiveness in the treatment of malignant neoplasms in humans.</description><identifier>ISSN: 0288-2043</identifier><identifier>ISSN: 1867-1071</identifier><identifier>EISSN: 1862-5274</identifier><identifier>EISSN: 1867-108X</identifier><identifier>DOI: 10.1007/s11604-007-0212-9</identifier><identifier>PMID: 18509717</identifier><language>eng</language><publisher>Japan: Springer Japan</publisher><subject><![CDATA[Animals ; Chi-Square Distribution ; Contrast Media - administration & dosage ; Dextrans ; Disease Models, Animal ; Embolization, Therapeutic - methods ; Feasibility Studies ; Ferrosoferric Oxide ; Gelatin Sponge, Absorbable - administration & dosage ; Hemostatics - administration & dosage ; Hyperthermia, Induced ; Imaging ; Iodized Oil - administration & dosage ; Iron - administration & dosage ; Kidney Neoplasms - diagnostic imaging ; Kidney Neoplasms - therapy ; Magnetite Nanoparticles ; Male ; Medicine ; Medicine & Public Health ; Nanoparticles ; Neoplasms, Experimental - diagnostic imaging ; Neoplasms, Experimental - therapy ; Nuclear Medicine ; Original Article ; Oxides - administration & dosage ; Rabbits ; Radiology ; Radiotherapy ; Sodium Chloride - administration & dosage ; Tomography, X-Ray Computed]]></subject><ispartof>Japanese journal of radiology, 2008-05, Vol.26 (4), p.179-187</ispartof><rights>Japan Radiological Society 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-4775e94d21fb7be9c7d48e53754ba9d2eecbdcbb0457d55233e61f45ab137ee93</citedby><cites>FETCH-LOGICAL-c425t-4775e94d21fb7be9c7d48e53754ba9d2eecbdcbb0457d55233e61f45ab137ee93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18509717$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takamatsu, Shigeyuki</creatorcontrib><creatorcontrib>Matsui, Osamu</creatorcontrib><creatorcontrib>Gabata, Toshifumi</creatorcontrib><creatorcontrib>Kobayashi, Satoshi</creatorcontrib><creatorcontrib>Okuda, Miho</creatorcontrib><creatorcontrib>Ougi, Takahiro</creatorcontrib><creatorcontrib>Ikehata, Yoshio</creatorcontrib><creatorcontrib>Nagano, Isamu</creatorcontrib><creatorcontrib>Nagae, Hideo</creatorcontrib><title>Selective induction hyperthermia following transcatheter arterial embolization with a mixture of nano-sized magnetic particles (ferucarbotran) and embolic materials: feasibility study in rabbits</title><title>Japanese journal of radiology</title><addtitle>Radiat Med</addtitle><addtitle>Radiat Med</addtitle><description>Purpose
To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device.
Materials and methods
Twelve Japanese white rabbits were separated into four groups: those treated with TAE using a mixture of ferucarbotran and lipiodol (F-L group); those treated with ferucarbotran and gelatin sponge powder; those treated with saline and lipiodol; and a control group. These four groups received IH. Nine rabbits with renal VX2 carcinoma were separated into three groups: IH after TAE (IH-TAE tumor), TAE without IH (TAE tumor), and no treatment (control tumor). The temperature of the tumor was kept at 45°C for 20 min. The therapeutic effect was pathologically evaluated by TUNEL staining.
Results
In the heating rates of the kidney, the F-L group showed significantly greater values than the group in which iron was not used. In the IH-TAE tumor group, tumors could be selectively heated. In TUNEL staining, the IH-TAE tumor and TAE tumor groups showed significantly greater values of apoptosis rate than in the control tumor group.
Conclusion
IH following TAE with a mixture of ferucarbotran and lipiodol was capable of inducing selective hyperthermia with our device. However, further investigation is needed to confirm its safety and effectiveness in the treatment of malignant neoplasms in humans.</description><subject>Animals</subject><subject>Chi-Square Distribution</subject><subject>Contrast Media - administration & dosage</subject><subject>Dextrans</subject><subject>Disease Models, Animal</subject><subject>Embolization, Therapeutic - methods</subject><subject>Feasibility Studies</subject><subject>Ferrosoferric Oxide</subject><subject>Gelatin Sponge, Absorbable - administration & dosage</subject><subject>Hemostatics - administration & dosage</subject><subject>Hyperthermia, Induced</subject><subject>Imaging</subject><subject>Iodized Oil - administration & dosage</subject><subject>Iron - administration & dosage</subject><subject>Kidney Neoplasms - diagnostic imaging</subject><subject>Kidney Neoplasms - therapy</subject><subject>Magnetite Nanoparticles</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Nanoparticles</subject><subject>Neoplasms, Experimental - diagnostic imaging</subject><subject>Neoplasms, Experimental - therapy</subject><subject>Nuclear Medicine</subject><subject>Original Article</subject><subject>Oxides - administration & dosage</subject><subject>Rabbits</subject><subject>Radiology</subject><subject>Radiotherapy</subject><subject>Sodium Chloride - administration & dosage</subject><subject>Tomography, X-Ray Computed</subject><issn>0288-2043</issn><issn>1867-1071</issn><issn>1862-5274</issn><issn>1867-108X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp1kc1u1DAUhS1ERaeFB2CDLDYti4Dt2HHCrqr4kyqxANaRf25mXCX2YDuU6eP1yXDISJWQ2NhHut8590oHoZeUvKWEyHeJ0obwqsiKMMqq7gna0LZhlWCSP0Ubwtq2YoTXp-gspVtSFG-bZ-iUtoJ0ksoNevgGI5jsfgF23s5FBY93hz3EvIM4OYWHMI7hzvktzlH5ZFQZZIhYxfI6NWKYdBjdvfprvXN5hxWe3O88R8BhwF75UCV3DxZPaushO4P3xezMCAlfDhBno6IOS_obrLw9BpqCrxvSezyASk670eUDTnm2h3Itjkprl9NzdDIUCF4c_3P04-OH79efq5uvn75cX91UhjORKy6lgI5bRgctNXRGWt6CqKXgWnWWARhtjdaEC2mFYHUNDR24UJrWEqCrz9HFmruP4ecMKfeTSwbGUXkIc-o7UZydYKKQr_8hb8McfTmuL43UsulqViC6QiaGlCIM_T66ScVDT0m_1Nuv9faLXOrtlxNeHYNnPYF9dBz7LABbgVRGfgvxcfP_U_8AdUS2aw</recordid><startdate>20080501</startdate><enddate>20080501</enddate><creator>Takamatsu, Shigeyuki</creator><creator>Matsui, Osamu</creator><creator>Gabata, Toshifumi</creator><creator>Kobayashi, Satoshi</creator><creator>Okuda, Miho</creator><creator>Ougi, Takahiro</creator><creator>Ikehata, Yoshio</creator><creator>Nagano, Isamu</creator><creator>Nagae, Hideo</creator><general>Springer Japan</general><general>Springer Nature B.V</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>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20080501</creationdate><title>Selective induction hyperthermia following transcatheter arterial embolization with a mixture of nano-sized magnetic particles (ferucarbotran) and embolic materials: feasibility study in rabbits</title><author>Takamatsu, Shigeyuki ; Matsui, Osamu ; Gabata, Toshifumi ; Kobayashi, Satoshi ; Okuda, Miho ; Ougi, Takahiro ; Ikehata, Yoshio ; Nagano, Isamu ; Nagae, Hideo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-4775e94d21fb7be9c7d48e53754ba9d2eecbdcbb0457d55233e61f45ab137ee93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Chi-Square Distribution</topic><topic>Contrast Media - administration & dosage</topic><topic>Dextrans</topic><topic>Disease Models, Animal</topic><topic>Embolization, Therapeutic - methods</topic><topic>Feasibility Studies</topic><topic>Ferrosoferric Oxide</topic><topic>Gelatin Sponge, Absorbable - administration & dosage</topic><topic>Hemostatics - administration & dosage</topic><topic>Hyperthermia, Induced</topic><topic>Imaging</topic><topic>Iodized Oil - administration & dosage</topic><topic>Iron - administration & dosage</topic><topic>Kidney Neoplasms - diagnostic imaging</topic><topic>Kidney Neoplasms - therapy</topic><topic>Magnetite Nanoparticles</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Nanoparticles</topic><topic>Neoplasms, Experimental - diagnostic imaging</topic><topic>Neoplasms, Experimental - therapy</topic><topic>Nuclear Medicine</topic><topic>Original Article</topic><topic>Oxides - administration & dosage</topic><topic>Rabbits</topic><topic>Radiology</topic><topic>Radiotherapy</topic><topic>Sodium Chloride - administration & dosage</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takamatsu, Shigeyuki</creatorcontrib><creatorcontrib>Matsui, Osamu</creatorcontrib><creatorcontrib>Gabata, Toshifumi</creatorcontrib><creatorcontrib>Kobayashi, Satoshi</creatorcontrib><creatorcontrib>Okuda, Miho</creatorcontrib><creatorcontrib>Ougi, Takahiro</creatorcontrib><creatorcontrib>Ikehata, Yoshio</creatorcontrib><creatorcontrib>Nagano, Isamu</creatorcontrib><creatorcontrib>Nagae, Hideo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Nursing & Allied Health Database (ProQuest)</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Biological Sciences</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Japanese journal of radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takamatsu, Shigeyuki</au><au>Matsui, Osamu</au><au>Gabata, Toshifumi</au><au>Kobayashi, Satoshi</au><au>Okuda, Miho</au><au>Ougi, Takahiro</au><au>Ikehata, Yoshio</au><au>Nagano, Isamu</au><au>Nagae, Hideo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selective induction hyperthermia following transcatheter arterial embolization with a mixture of nano-sized magnetic particles (ferucarbotran) and embolic materials: feasibility study in rabbits</atitle><jtitle>Japanese journal of radiology</jtitle><stitle>Radiat Med</stitle><addtitle>Radiat Med</addtitle><date>2008-05-01</date><risdate>2008</risdate><volume>26</volume><issue>4</issue><spage>179</spage><epage>187</epage><pages>179-187</pages><issn>0288-2043</issn><issn>1867-1071</issn><eissn>1862-5274</eissn><eissn>1867-108X</eissn><abstract>Purpose
To evaluate the possibility of selective hyperthermia following transcatheter arterial embolization (TAE) with ferucarbotran using a newly developed inductive heating (IH) device.
Materials and methods
Twelve Japanese white rabbits were separated into four groups: those treated with TAE using a mixture of ferucarbotran and lipiodol (F-L group); those treated with ferucarbotran and gelatin sponge powder; those treated with saline and lipiodol; and a control group. These four groups received IH. Nine rabbits with renal VX2 carcinoma were separated into three groups: IH after TAE (IH-TAE tumor), TAE without IH (TAE tumor), and no treatment (control tumor). The temperature of the tumor was kept at 45°C for 20 min. The therapeutic effect was pathologically evaluated by TUNEL staining.
Results
In the heating rates of the kidney, the F-L group showed significantly greater values than the group in which iron was not used. In the IH-TAE tumor group, tumors could be selectively heated. In TUNEL staining, the IH-TAE tumor and TAE tumor groups showed significantly greater values of apoptosis rate than in the control tumor group.
Conclusion
IH following TAE with a mixture of ferucarbotran and lipiodol was capable of inducing selective hyperthermia with our device. However, further investigation is needed to confirm its safety and effectiveness in the treatment of malignant neoplasms in humans.</abstract><cop>Japan</cop><pub>Springer Japan</pub><pmid>18509717</pmid><doi>10.1007/s11604-007-0212-9</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Chi-Square Distribution Contrast Media - administration & dosage Dextrans Disease Models, Animal Embolization, Therapeutic - methods Feasibility Studies Ferrosoferric Oxide Gelatin Sponge, Absorbable - administration & dosage Hemostatics - administration & dosage Hyperthermia, Induced Imaging Iodized Oil - administration & dosage Iron - administration & dosage Kidney Neoplasms - diagnostic imaging Kidney Neoplasms - therapy Magnetite Nanoparticles Male Medicine Medicine & Public Health Nanoparticles Neoplasms, Experimental - diagnostic imaging Neoplasms, Experimental - therapy Nuclear Medicine Original Article Oxides - administration & dosage Rabbits Radiology Radiotherapy Sodium Chloride - administration & dosage Tomography, X-Ray Computed |
title | Selective induction hyperthermia following transcatheter arterial embolization with a mixture of nano-sized magnetic particles (ferucarbotran) and embolic materials: feasibility study in rabbits |
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