Preparation and in vivo evaluation of multifunctional super(90)Y-labeled magnetic nanoparticles designed for cancer therapy
Two different types of magnetic nanoparticles (MNPs) were synthesized in order to compare their efficiency as radioactive vectors, Fe sub(3)O sub(4)-Naked (80 plus or minus 5 nm) and polyethylene glycol 600 diacid functionalized Fe sub(3)O sub(4) (Fe sub(3)O sub(4)-PEG600) MNPs (46 plus or minus 0.6...
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Veröffentlicht in: | Journal of biomedical materials research. Part A 2015-01, Vol.103 (1), p.126-134 |
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creator | Radovic, Magdalena Calatayud, Maria Pilar Goya, Gerardo Fabian Ibarra, Manuel Ricardo Antic, Bratislav Spasojevic, Vojislav Nikolic, Nadezda Jankovic, Drina Mirkovic, Marija Vranjes-uric, Sanja |
description | Two different types of magnetic nanoparticles (MNPs) were synthesized in order to compare their efficiency as radioactive vectors, Fe sub(3)O sub(4)-Naked (80 plus or minus 5 nm) and polyethylene glycol 600 diacid functionalized Fe sub(3)O sub(4) (Fe sub(3)O sub(4)-PEG600) MNPs (46 plus or minus 0.6 nm). They were characterized based on the external morphology, size distribution, and colloidal and magnetic properties. The obtained specific power absorption value for Fe sub(3)O sub(4)-PEG600 MNPs was 200 W/g, indicated their potential in hyperthermia based cancer treatments. The labeling yield, in vitro stability and in vivo biodistribution profile of super(90)Y-MNPs were compared. Both types of MNPs were super(90)Y-labeled in reproducible high yield (>97%). The stability of the obtained radioactive nanoparticles was evaluated in saline and human serum media in order to optimize the formulations for in vivo use. The biodistribution in Wistar rats showed different pharmacokinetic behaviors of nanoparticles: a large fraction of both injected MNPs ended in the liver (14.58%ID/g for super(90)Y-Fe sub(3)O sub(4)-Naked MNPs and 19.61%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) whereas minor fractions attained in other organs. The main difference between the two types of MNPs was the higher accumulation of super(90)Y-Fe sub(3)O sub(4)-Naked MNPs in the lungs (12.14%ID/g vs. 2.00%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) due to their in vivo agglomeration. The studied radiolabeled magnetic complexes such as super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs constitute a great promise for multiple diagnostic-therapeutic uses combining, for example, MRI-magnetic hyperthermia and regional radiotherapy. copyright 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 126-134, 2015. |
doi_str_mv | 10.1002/jbm.a.35160 |
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They were characterized based on the external morphology, size distribution, and colloidal and magnetic properties. The obtained specific power absorption value for Fe sub(3)O sub(4)-PEG600 MNPs was 200 W/g, indicated their potential in hyperthermia based cancer treatments. The labeling yield, in vitro stability and in vivo biodistribution profile of super(90)Y-MNPs were compared. Both types of MNPs were super(90)Y-labeled in reproducible high yield (>97%). The stability of the obtained radioactive nanoparticles was evaluated in saline and human serum media in order to optimize the formulations for in vivo use. The biodistribution in Wistar rats showed different pharmacokinetic behaviors of nanoparticles: a large fraction of both injected MNPs ended in the liver (14.58%ID/g for super(90)Y-Fe sub(3)O sub(4)-Naked MNPs and 19.61%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) whereas minor fractions attained in other organs. The main difference between the two types of MNPs was the higher accumulation of super(90)Y-Fe sub(3)O sub(4)-Naked MNPs in the lungs (12.14%ID/g vs. 2.00%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) due to their in vivo agglomeration. The studied radiolabeled magnetic complexes such as super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs constitute a great promise for multiple diagnostic-therapeutic uses combining, for example, MRI-magnetic hyperthermia and regional radiotherapy. copyright 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 126-134, 2015.</description><identifier>ISSN: 1549-3296</identifier><identifier>EISSN: 1552-4965</identifier><identifier>DOI: 10.1002/jbm.a.35160</identifier><language>eng</language><subject>Biocompatibility ; Biomedical materials ; Cancer ; In vivo testing ; In vivo tests ; Nanoparticles ; Stability ; Surgical implants</subject><ispartof>Journal of biomedical materials research. 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Part A</title><description>Two different types of magnetic nanoparticles (MNPs) were synthesized in order to compare their efficiency as radioactive vectors, Fe sub(3)O sub(4)-Naked (80 plus or minus 5 nm) and polyethylene glycol 600 diacid functionalized Fe sub(3)O sub(4) (Fe sub(3)O sub(4)-PEG600) MNPs (46 plus or minus 0.6 nm). They were characterized based on the external morphology, size distribution, and colloidal and magnetic properties. The obtained specific power absorption value for Fe sub(3)O sub(4)-PEG600 MNPs was 200 W/g, indicated their potential in hyperthermia based cancer treatments. The labeling yield, in vitro stability and in vivo biodistribution profile of super(90)Y-MNPs were compared. Both types of MNPs were super(90)Y-labeled in reproducible high yield (>97%). The stability of the obtained radioactive nanoparticles was evaluated in saline and human serum media in order to optimize the formulations for in vivo use. The biodistribution in Wistar rats showed different pharmacokinetic behaviors of nanoparticles: a large fraction of both injected MNPs ended in the liver (14.58%ID/g for super(90)Y-Fe sub(3)O sub(4)-Naked MNPs and 19.61%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) whereas minor fractions attained in other organs. The main difference between the two types of MNPs was the higher accumulation of super(90)Y-Fe sub(3)O sub(4)-Naked MNPs in the lungs (12.14%ID/g vs. 2.00%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) due to their in vivo agglomeration. The studied radiolabeled magnetic complexes such as super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs constitute a great promise for multiple diagnostic-therapeutic uses combining, for example, MRI-magnetic hyperthermia and regional radiotherapy. copyright 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 126-134, 2015.</description><subject>Biocompatibility</subject><subject>Biomedical materials</subject><subject>Cancer</subject><subject>In vivo testing</subject><subject>In vivo tests</subject><subject>Nanoparticles</subject><subject>Stability</subject><subject>Surgical implants</subject><issn>1549-3296</issn><issn>1552-4965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqNjL1OwzAUhS0EEqUw8QIey5Din9iJR1RBQaoEQxem6sa-hlSOE-KkEuLlSVUegOkcfefTIeSWsyVnTNzvq2YJS6m4ZmdkxpUSWW60Oj_23GRSGH1JrlLaT7JmSszIz1uPHfQw1G2kEB2tIz3Uh5biAcJ4wq2nzRiG2o_RHgEEmsYO-4Vhd-9ZgAoDOtrAR8ShtjRCbKfLqQZM1GGqp8FR3_bUQrTY0-ETe-i-r8mFh5Dw5i_nZPv0uF09Z5vX9cvqYZN1WutMOem8M4ZZcKViDopKCO6ZL_McC5AsL7WTokJVlLwApQ3kshJKeu6cNVbOyeJ02_Xt14hp2DV1shgCRGzHtONacVlKzvQ_VKmYFHmp5C890XC6</recordid><startdate>20150101</startdate><enddate>20150101</enddate><creator>Radovic, Magdalena</creator><creator>Calatayud, Maria Pilar</creator><creator>Goya, Gerardo Fabian</creator><creator>Ibarra, Manuel Ricardo</creator><creator>Antic, Bratislav</creator><creator>Spasojevic, Vojislav</creator><creator>Nikolic, Nadezda</creator><creator>Jankovic, Drina</creator><creator>Mirkovic, Marija</creator><creator>Vranjes-uric, Sanja</creator><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>F28</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20150101</creationdate><title>Preparation and in vivo evaluation of multifunctional super(90)Y-labeled magnetic nanoparticles designed for cancer therapy</title><author>Radovic, Magdalena ; Calatayud, Maria Pilar ; Goya, Gerardo Fabian ; Ibarra, Manuel Ricardo ; Antic, Bratislav ; Spasojevic, Vojislav ; Nikolic, Nadezda ; Jankovic, Drina ; Mirkovic, Marija ; Vranjes-uric, Sanja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p666-5d3dfd990cad850da7b221f0f844e7a30486d32be57817a569a43b253f1ddc9c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Biocompatibility</topic><topic>Biomedical materials</topic><topic>Cancer</topic><topic>In vivo testing</topic><topic>In vivo tests</topic><topic>Nanoparticles</topic><topic>Stability</topic><topic>Surgical implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Radovic, Magdalena</creatorcontrib><creatorcontrib>Calatayud, Maria Pilar</creatorcontrib><creatorcontrib>Goya, Gerardo Fabian</creatorcontrib><creatorcontrib>Ibarra, Manuel Ricardo</creatorcontrib><creatorcontrib>Antic, Bratislav</creatorcontrib><creatorcontrib>Spasojevic, Vojislav</creatorcontrib><creatorcontrib>Nikolic, Nadezda</creatorcontrib><creatorcontrib>Jankovic, Drina</creatorcontrib><creatorcontrib>Mirkovic, Marija</creatorcontrib><creatorcontrib>Vranjes-uric, Sanja</creatorcontrib><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of biomedical materials research. Part A</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Radovic, Magdalena</au><au>Calatayud, Maria Pilar</au><au>Goya, Gerardo Fabian</au><au>Ibarra, Manuel Ricardo</au><au>Antic, Bratislav</au><au>Spasojevic, Vojislav</au><au>Nikolic, Nadezda</au><au>Jankovic, Drina</au><au>Mirkovic, Marija</au><au>Vranjes-uric, Sanja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and in vivo evaluation of multifunctional super(90)Y-labeled magnetic nanoparticles designed for cancer therapy</atitle><jtitle>Journal of biomedical materials research. Part A</jtitle><date>2015-01-01</date><risdate>2015</risdate><volume>103</volume><issue>1</issue><spage>126</spage><epage>134</epage><pages>126-134</pages><issn>1549-3296</issn><eissn>1552-4965</eissn><abstract>Two different types of magnetic nanoparticles (MNPs) were synthesized in order to compare their efficiency as radioactive vectors, Fe sub(3)O sub(4)-Naked (80 plus or minus 5 nm) and polyethylene glycol 600 diacid functionalized Fe sub(3)O sub(4) (Fe sub(3)O sub(4)-PEG600) MNPs (46 plus or minus 0.6 nm). They were characterized based on the external morphology, size distribution, and colloidal and magnetic properties. The obtained specific power absorption value for Fe sub(3)O sub(4)-PEG600 MNPs was 200 W/g, indicated their potential in hyperthermia based cancer treatments. The labeling yield, in vitro stability and in vivo biodistribution profile of super(90)Y-MNPs were compared. Both types of MNPs were super(90)Y-labeled in reproducible high yield (>97%). The stability of the obtained radioactive nanoparticles was evaluated in saline and human serum media in order to optimize the formulations for in vivo use. The biodistribution in Wistar rats showed different pharmacokinetic behaviors of nanoparticles: a large fraction of both injected MNPs ended in the liver (14.58%ID/g for super(90)Y-Fe sub(3)O sub(4)-Naked MNPs and 19.61%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) whereas minor fractions attained in other organs. The main difference between the two types of MNPs was the higher accumulation of super(90)Y-Fe sub(3)O sub(4)-Naked MNPs in the lungs (12.14%ID/g vs. 2.00%ID/g for super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs) due to their in vivo agglomeration. The studied radiolabeled magnetic complexes such as super(90)Y-Fe sub(3)O sub(4)-PEG600 MNPs constitute a great promise for multiple diagnostic-therapeutic uses combining, for example, MRI-magnetic hyperthermia and regional radiotherapy. copyright 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 126-134, 2015.</abstract><doi>10.1002/jbm.a.35160</doi><tpages>9</tpages></addata></record> |
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subjects | Biocompatibility Biomedical materials Cancer In vivo testing In vivo tests Nanoparticles Stability Surgical implants |
title | Preparation and in vivo evaluation of multifunctional super(90)Y-labeled magnetic nanoparticles designed for cancer therapy |
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