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
Hauptverfasser: Radovic, Magdalena, Calatayud, Maria Pilar, Goya, Gerardo Fabian, Ibarra, Manuel Ricardo, Antic, Bratislav, Spasojevic, Vojislav, Nikolic, Nadezda, Jankovic, Drina, Mirkovic, Marija, Vranjes-uric, Sanja
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container_end_page 134
container_issue 1
container_start_page 126
container_title Journal of biomedical materials research. Part A
container_volume 103
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 (&gt;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. 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source Wiley Online Library Journals Frontfile Complete
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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