4.7 Article

One-pot synthesis of carboxymethyl-dextran coated iron oxide nanoparticles (CION) for preclinical fMRI and MRA applications

期刊

NEUROIMAGE
卷 238, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2021.118213

关键词

CION; Intravascular; Iron oxide; MRI contrast agent; fMRI; CBV; Angiography

资金

  1. Cross-Disciplinary Fellowship from Human Frontier Science Program (HFSP)
  2. NIH [T32HL069768, RF1MH117053, R01NS091236, R01MH111429, R01MH126518, R41MH113252, P60AA011605, U01AA020023, R01AA025582, P50HD103573, S10-OD026796, S10-MH124745]
  3. Research Foundation Flanders
  4. UNC Summer Undergraduate Research Fellowships
  5. UNC Neuroscience Center Microscopy Core [P30-NS045892]

向作者/读者索取更多资源

Superparamagnetic iron-oxide nanoparticles are effective contrast agents for CBV-MRI applications, with potential for a wide range of functional and structural MRI studies. By developing a simple, cost-effective synthesis method for CION nanoparticles and characterizing their conjugations, this work aims to make CBV-MRI more accessible and affordable for various research applications. The utility of CION in in vivo experiments demonstrates its potential for functional and structural MRI studies, providing a valuable cross-modality research platform for concurrent optical and MRI measurements of CBV.
Superparamagnetic iron-oxide nanoparticles are robust contrast agents for magnetic resonance imaging (MRI) used for sensitive structural and functional mapping of the cerebral blood volume (CBV) when administered intravenously. To date, many CBV-MRI studies are conducted with Feraheme, manufactured for the clinical treatment of iron-deficiency. Unfortunately, Feraheme is currently not available outside the United States due to commercial and regulatory constraints, making CBV-MRI methods either inaccessible or very costly to achieve. To address this barrier, we developed a simple, one-pot recipe to synthesize Carboxymethyl-dextran coated Iron Oxide Nanoparticles, namely, CION , suitable for preclinical CBV-MRI applications. Here we disseminate a stepby-step instruction of our one-pot synthesis protocol, which allows CION to be produced in laboratories with minimal cost. We also characterized different CION-conjugations by manipulating polymer to metal stoichiometric ratio in terms of their size, surface chemistry, and chemical composition, and shifts in MR relaxivity and pharmacokinetics. We performed several proof-of-concept experiments in vivo , demonstrating the utility of CION for functional and structural MRI applications, including hypercapnic CO2 challenge, visual stimulation, targeted optogenetic stimulation, and microangiography. We also present evidence that CION can serve as a cross-modality research platform by showing concurrent in vivo optical and MRI measurement of CBV using fluorescent-labeled CION. The simplicity and cost-effectiveness of our one-pot synthesis method should allow researchers to reproduce CION and tailor the relaxivity and pharmacokinetics according to their imaging needs. It is our hope that this work makes CBV-MRI more openly available and affordable for a variety of research applications.

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