Biocompatibility and proteomic profiling of DMSA-coated iron nanocubes in a human glioblastoma cell line.
- Publisher:
- TAYLOR & FRANCIS LTD
- Publication Type:
- Journal Article
- Citation:
- Nanomedicine (Lond), 2024, 19, (4), pp. 303-323
- Issue Date:
- 2024-02
Open Access
Copyright Clearance Process
- Recently Added
- In Progress
- Open Access
This item is open access.
Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author | Ulanova, M | |
dc.contributor.author |
Gloag, L https://orcid.org/0000-0001-7548-1521 |
|
dc.contributor.author | Kim, C-K | |
dc.contributor.author | Bongers, A | |
dc.contributor.author | Kim Duong, HT | |
dc.contributor.author | Gooding, JJ | |
dc.contributor.author | Tilley, RD | |
dc.contributor.author | Sachdev, PS | |
dc.contributor.author | Braidy, N | |
dc.date.accessioned | 2024-11-22T02:28:40Z | |
dc.date.available | 2024-11-22T02:28:40Z | |
dc.date.issued | 2024-02 | |
dc.identifier.citation | Nanomedicine (Lond), 2024, 19, (4), pp. 303-323 | |
dc.identifier.issn | 1743-5889 | |
dc.identifier.issn | 1748-6963 | |
dc.identifier.uri | http://hdl.handle.net/10453/182056 | |
dc.description.abstract | Background: Superparamagnetic iron core iron oxide shell nanocubes have previously shown superior performance in magnetic resonance imaging T2 contrast enhancement compared with spherical nanoparticles. Methods: Iron core iron oxide shell nanocubes were synthesized, stabilized with dimercaptosuccinic acid (DMSA-NC) and physicochemically characterized. MRI contrast enhancement and biocompatibility were assessed in vitro. Results: DMSA-NC showed a transverse relaxivity of 122.59 mM-1·s-1 Fe. Treatment with DMSA-NC did not induce cytotoxicity or oxidative stress in U-251 cells, and electron microscopy demonstrated DMSA-NC localization within endosomes and lysosomes in cells following internalization. Global proteomics revealed dysregulation of iron storage, transport, transcription and mRNA processing proteins. Conclusion: DMSA-NC is a promising T2 MRI contrast agent which, in this preliminary investigation, demonstrates favorable biocompatibility with an astrocyte cell model. | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | TAYLOR & FRANCIS LTD | |
dc.relation.ispartof | Nanomedicine (Lond) | |
dc.relation.isbasedon | 10.2217/nnm-2023-0304 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 0306 Physical Chemistry (incl. Structural), 1004 Medical Biotechnology, 1007 Nanotechnology | |
dc.subject.classification | Nanoscience & Nanotechnology | |
dc.subject.classification | 3206 Medical biotechnology | |
dc.subject.classification | 4003 Biomedical engineering | |
dc.subject.classification | 4018 Nanotechnology | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Iron | |
dc.subject.mesh | Magnetite Nanoparticles | |
dc.subject.mesh | Glioblastoma | |
dc.subject.mesh | Proteomics | |
dc.subject.mesh | Ferric Compounds | |
dc.subject.mesh | Cell Line | |
dc.subject.mesh | Contrast Media | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Succimer | |
dc.subject.mesh | Cell Line | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Glioblastoma | |
dc.subject.mesh | Iron | |
dc.subject.mesh | Ferric Compounds | |
dc.subject.mesh | Succimer | |
dc.subject.mesh | Contrast Media | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Proteomics | |
dc.subject.mesh | Magnetite Nanoparticles | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Iron | |
dc.subject.mesh | Magnetite Nanoparticles | |
dc.subject.mesh | Glioblastoma | |
dc.subject.mesh | Proteomics | |
dc.subject.mesh | Ferric Compounds | |
dc.subject.mesh | Cell Line | |
dc.subject.mesh | Contrast Media | |
dc.subject.mesh | Magnetic Resonance Imaging | |
dc.subject.mesh | Succimer | |
dc.title | Biocompatibility and proteomic profiling of DMSA-coated iron nanocubes in a human glioblastoma cell line. | |
dc.type | Journal Article | |
utslib.citation.volume | 19 | |
utslib.location.activity | England | |
utslib.for | 0306 Physical Chemistry (incl. Structural) | |
utslib.for | 1004 Medical Biotechnology | |
utslib.for | 1007 Nanotechnology | |
pubs.organisational-group | University of Technology Sydney | |
pubs.organisational-group | University of Technology Sydney/Faculty of Science | |
utslib.copyright.status | open_access | * |
dc.rights.license | This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0). To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/ | |
dc.date.updated | 2024-11-22T02:28:35Z | |
pubs.issue | 4 | |
pubs.publication-status | Published | |
pubs.volume | 19 | |
utslib.citation.issue | 4 |
Abstract:
Background: Superparamagnetic iron core iron oxide shell nanocubes have previously shown superior performance in magnetic resonance imaging T2 contrast enhancement compared with spherical nanoparticles. Methods: Iron core iron oxide shell nanocubes were synthesized, stabilized with dimercaptosuccinic acid (DMSA-NC) and physicochemically characterized. MRI contrast enhancement and biocompatibility were assessed in vitro. Results: DMSA-NC showed a transverse relaxivity of 122.59 mM-1·s-1 Fe. Treatment with DMSA-NC did not induce cytotoxicity or oxidative stress in U-251 cells, and electron microscopy demonstrated DMSA-NC localization within endosomes and lysosomes in cells following internalization. Global proteomics revealed dysregulation of iron storage, transport, transcription and mRNA processing proteins. Conclusion: DMSA-NC is a promising T2 MRI contrast agent which, in this preliminary investigation, demonstrates favorable biocompatibility with an astrocyte cell model.
Please use this identifier to cite or link to this item:
Download statistics for the last 12 months
Not enough data to produce graph