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Magnetite/dextran-functionalized graphene oxide nanosheets for in vivo positive contrast magnetic resonance imaging
Moradi, S ; Sharif University of Technology | 2015
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- Type of Document: Article
- DOI: 10.1039/c5ra03331d
- Publisher: Royal Society of Chemistry , 2015
- Abstract:
- Superparamagnetic iron oxide (SPIO) nanomaterials are widely used as magnetic resonance imaging (MRI) contrast agents (CAs). These CAs significantly shorten transverse relaxation time (T
2 ) and so decrease the intensity of the T2 -weighted MRI (negative contrast imaging). However, the partial-volume effect is known to be one of the problems in negative contrast MRI. In this work, SPIO nanoparticles were modified by dextran and graphene oxide (GO) nanosheets to achieve a positive contrast MRI with high intensity. This modification resulted in shortening the longitudinal relaxation time (T1 ) of the SPIO nanoparticles (in addition to the T2 shortening). Using FLASH pulse sequence, T1 -weighted positive contrast MRI of Wistar rats revealed that the SPIO/dextran-functionalized GO (SPIO-Dex-FGO) significantly enhanced the contrast to noise ratio (CNR) of the positive contrast MRI as compared to the common clinical positive CA, i.e., Magnevist®. In fact, based on the CNR calculations for in vivo positive contrast images it was found that the SPIO-Dex-FGO could provide the same CNR as Magnevist® at concentrations two orders of magnitudes lower than the concentrations used for Magnevist®. Therefore, SPIO-Dex-FGO can be proposed as a promising substitution for the current CAs such as Magnevist® in T1 -weighted positive contrast MRI, at lower and safer concentrations - Keywords:
- Graphene ; Nanoparticles ; Nanosheets ; Relaxation time ; Contrast to noise ratio ; Graphene oxide nanosheets ; Longitudinal relaxation time ; Magnetic resonance imaging contrast agents ; Partial volume effect ; Superparamagnetic iron oxides ; Transverse relaxation time ; Magnetic resonance imaging
- Source: RSC Advances ; Volume 5, Issue 59 , May , 2015 , Pages 47529-47537 ; 20462069 (ISSN)
- URL: http://pubs.rsc.org/en/Content/ArticleLanding/2015/RA/C5RA03331D#!divAbstract