File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Microwave-assisted synthesis of SPION-reduced graphene oxide hybrids for magnetic resonance imaging (MRI)

TitleMicrowave-assisted synthesis of SPION-reduced graphene oxide hybrids for magnetic resonance imaging (MRI)
Authors
KeywordsBiomedical imaging
Contrast agents
Ultrasmall superparamagnetic iron oxide nanoparticles
Issue Date2019
Citation
Nanomaterials, 2019, v. 9, n. 10, article no. 1364 How to Cite?
AbstractMagnetic resonance imaging (MRI) is a useful tool for disease diagnosis and treatment monitoring. Superparamagnetic iron oxide nanoparticles (SPION) show good performance as transverse relaxation (T2) contrast agents, thus facilitating the interpretation of the acquired images. Attachment of SPION onto nanocarriers prevents their agglomeration, improving the circulation time and efficiency. Graphene derivatives, such as graphene oxide (GO) and reduced graphene oxide (RGO), are appealing nanocarriers since they have both high surface area and functional moieties that make them ideal substrates for the attachment of nanoparticles. We have employed a fast, simple and environmentally friendly microwave-assisted approach for the synthesis of SPION-RGO hybrids. Different iron precursor/GO ratios were used leading to SPION, with a median diameter of 7.1 nm, homogeneously distributed along the RGO surface. Good relaxivity (r2*) values were obtained in MRI studies and no significant toxicity was detected within in vitro tests following GL261 glioma and J774 macrophage-like cells for 24 h with SPION-RGO, demonstrating the applicability of the hybrids as T2-weighted MRI contrast agents.
Persistent Identifierhttp://hdl.handle.net/10722/349359

 

DC FieldValueLanguage
dc.contributor.authorLlenas, Marina-
dc.contributor.authorSandoval, Stefania-
dc.contributor.authorCosta, Pedro M.-
dc.contributor.authorOró-Solé, Judith-
dc.contributor.authorLope-Piedrafita, Silvia-
dc.contributor.authorBallesteros, Belén-
dc.contributor.authorAl-Jamal, Khuloud T.-
dc.contributor.authorTobias, Gerard-
dc.date.accessioned2024-10-17T06:58:01Z-
dc.date.available2024-10-17T06:58:01Z-
dc.date.issued2019-
dc.identifier.citationNanomaterials, 2019, v. 9, n. 10, article no. 1364-
dc.identifier.urihttp://hdl.handle.net/10722/349359-
dc.description.abstractMagnetic resonance imaging (MRI) is a useful tool for disease diagnosis and treatment monitoring. Superparamagnetic iron oxide nanoparticles (SPION) show good performance as transverse relaxation (T2) contrast agents, thus facilitating the interpretation of the acquired images. Attachment of SPION onto nanocarriers prevents their agglomeration, improving the circulation time and efficiency. Graphene derivatives, such as graphene oxide (GO) and reduced graphene oxide (RGO), are appealing nanocarriers since they have both high surface area and functional moieties that make them ideal substrates for the attachment of nanoparticles. We have employed a fast, simple and environmentally friendly microwave-assisted approach for the synthesis of SPION-RGO hybrids. Different iron precursor/GO ratios were used leading to SPION, with a median diameter of 7.1 nm, homogeneously distributed along the RGO surface. Good relaxivity (r2*) values were obtained in MRI studies and no significant toxicity was detected within in vitro tests following GL261 glioma and J774 macrophage-like cells for 24 h with SPION-RGO, demonstrating the applicability of the hybrids as T2-weighted MRI contrast agents.-
dc.languageeng-
dc.relation.ispartofNanomaterials-
dc.subjectBiomedical imaging-
dc.subjectContrast agents-
dc.subjectUltrasmall superparamagnetic iron oxide nanoparticles-
dc.titleMicrowave-assisted synthesis of SPION-reduced graphene oxide hybrids for magnetic resonance imaging (MRI)-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.3390/nano9101364-
dc.identifier.scopuseid_2-s2.0-85073408335-
dc.identifier.volume9-
dc.identifier.issue10-
dc.identifier.spagearticle no. 1364-
dc.identifier.epagearticle no. 1364-
dc.identifier.eissn2079-4991-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats