Literature DB >> 27667655

Quantification and biodistribution of iron oxide nanoparticles in the primary clearance organs of mice using T1 contrast for heating.

Jinjin Zhang1, Hattie L Ring1,2, Katie R Hurley2, Qi Shao3, Cathy S Carlson4, Djaudat Idiyatullin1, Navid Manuchehrabadi5, P Jack Hoopes6, Christy L Haynes2, John C Bischof3,5, Michael Garwood1.   

Abstract

PURPOSE: To use contrast based on longitudinal relaxation times (T1 ) or rates (R1 ) to quantify the biodistribution of iron oxide nanoparticles (IONPs), which are of interest for hyperthermia therapy, cell targeting, and drug delivery, within primary clearance organs.
METHODS: Mesoporous silica-coated IONPs (msIONPs) were intravenously injected into 15 naïve mice. Imaging and mapping of the longitudinal relaxation rate constant at 24 h or 1 week postinjection were performed with an echoless pulse sequence (SWIFT). Alternating magnetic field heating measurements were also performed on ex vivo tissues.
RESULTS: Signal enhancement from positive T1 contrast caused by IONPs was observed and quantified in vivo in liver, spleen, and kidney at concentrations up to 3.2 mg Fe/(g tissue wt.) (61 mM Fe). In most cases, each organ had a linear correlation between the R1 and the tissue iron concentration despite variations in intra-organ distribution, degradation, and IONP surface charge. Linear correlation between R1 and volumetric SAR in hyperthermia therapy was observed.
CONCLUSION: The linear dependence between R1 and tissue iron concentration in major organs allows quantitative monitoring of IONP biodistribution in a dosage range relevant to magnetic hyperthermia applications, which falls into the concentration gap between CT and conventional MRI techniques. Magn Reson Med 78:702-712, 2017.
© 2016 International Society for Magnetic Resonance in Medicine. © 2016 International Society for Magnetic Resonance in Medicine.

Entities:  

Keywords:  SWIFT; biodistribution; hyperthermia; iron oxide nanoparticle; primary clearance organs

Mesh:

Substances:

Year:  2016        PMID: 27667655      PMCID: PMC5366089          DOI: 10.1002/mrm.26394

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  34 in total

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6.  Surface charge-mediated rapid hepatobiliary excretion of mesoporous silica nanoparticles.

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Review 7.  Clearance properties of nano-sized particles and molecules as imaging agents: considerations and caveats.

Authors:  Michelle Longmire; Peter L Choyke; Hisataka Kobayashi
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8.  Predictable Heating and Positive MRI Contrast from a Mesoporous Silica-Coated Iron Oxide Nanoparticle.

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9.  Hepatic MR imaging with ferumoxides: a multicenter clinical trial of the safety and efficacy in the detection of focal hepatic lesions.

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2.  Positive contrast from cells labeled with iron oxide nanoparticles: Quantitation of imaging data.

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Journal:  Magn Reson Med       Date:  2017-01-17       Impact factor: 4.668

Review 3.  Magnetic iron oxide nanoparticles for imaging, targeting and treatment of primary and metastatic tumors of the brain.

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4.  Imaging the distribution of iron oxide nanoparticles in hypothermic perfused tissues.

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5.  Establishing the overlap of IONP quantification with echo and echoless MR relaxation mapping.

Authors:  Hattie L Ring; Jinjin Zhang; Nathan D Klein; Lynn E Eberly; Christy L Haynes; Michael Garwood
Journal:  Magn Reson Med       Date:  2017-06-26       Impact factor: 4.668

6.  Improved tissue cryopreservation using inductive heating of magnetic nanoparticles.

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7.  Effect of Iron Oxide Nanoparticles on the Oxidation and Secondary Structure of Growth Hormone.

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8.  Thermal Analyses of Nanowarming-Assisted Recovery of the Heart From Cryopreservation by Vitrification.

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9.  Imaging of a high concentration of iron labeled cells with positive contrast in a rat knee.

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Journal:  Magn Reson Med       Date:  2018-09-21       Impact factor: 4.668

Review 10.  From Nanowarming to Thermoregulation: New Multiscale Applications of Bioheat Transfer.

Authors:  John C Bischof; Kenneth R Diller
Journal:  Annu Rev Biomed Eng       Date:  2018-06-04       Impact factor: 9.590

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