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Article: Engineering red-emitting multi-functional nanocapsules for magnetic tumour targeting and imaging

TitleEngineering red-emitting multi-functional nanocapsules for magnetic tumour targeting and imaging
Authors
Issue Date2020
Citation
Biomaterials Science, 2020, v. 8, n. 9, p. 2590-2599 How to Cite?
AbstractIn this work we describe the formulation and characterisation of red-emitting polymeric nanocapsules (NCs) incorporating superparamagnetic iron oxide nanoparticles (SPIONs) for magnetic tumour targeting. The self-fluorescent oligomers were synthesised and chemically conjugated to PLGA which was confirmed by NMR spectroscopy, FT-IR spectroscopy and mass spectrometry. Hydrophobic SPIONs were synthesised through thermal decomposition and their magnetic and heating properties were assessed by SQUID magnetometry and calorimetric measurements, respectively. Magnetic nanocapsules (m-NCs) were prepared by a single emulsification/solvent evaporation method. Their in vitro cytotoxicity was examined in CT26 colon cancer cells. The formulated fluorescent m-NCs showed good stability and biocompatibility both in vitro and in vivo in CT 26 colon cancer models. Following intravenous injection, accumulation of m-NCs in tumours was observed by optical imaging. A higher iron content in the tumours exposed to a magnetic field, compared to the contralateral tumours without magnetic exposure in the same animal, further confirmed the magnetic tumour targeting in vivo. The overall results show that the engineered red-emitting m-NCs have great potential as multifunctional nanocarriers for multi-model bioimaging and magnetic-targeted drug delivery.
Persistent Identifierhttp://hdl.handle.net/10722/349426
ISSN
2023 Impact Factor: 5.8
2023 SCImago Journal Rankings: 1.206

 

DC FieldValueLanguage
dc.contributor.authorWang, Julie Tzu Wen-
dc.contributor.authorMartino, Umberto-
dc.contributor.authorKhan, Rehan-
dc.contributor.authorBazzar, Maasoomeh-
dc.contributor.authorSouthern, Paul-
dc.contributor.authorTuncel, Dönüş-
dc.contributor.authorAl-Jamal, Khuloud T.-
dc.date.accessioned2024-10-17T06:58:27Z-
dc.date.available2024-10-17T06:58:27Z-
dc.date.issued2020-
dc.identifier.citationBiomaterials Science, 2020, v. 8, n. 9, p. 2590-2599-
dc.identifier.issn2047-4830-
dc.identifier.urihttp://hdl.handle.net/10722/349426-
dc.description.abstractIn this work we describe the formulation and characterisation of red-emitting polymeric nanocapsules (NCs) incorporating superparamagnetic iron oxide nanoparticles (SPIONs) for magnetic tumour targeting. The self-fluorescent oligomers were synthesised and chemically conjugated to PLGA which was confirmed by NMR spectroscopy, FT-IR spectroscopy and mass spectrometry. Hydrophobic SPIONs were synthesised through thermal decomposition and their magnetic and heating properties were assessed by SQUID magnetometry and calorimetric measurements, respectively. Magnetic nanocapsules (m-NCs) were prepared by a single emulsification/solvent evaporation method. Their in vitro cytotoxicity was examined in CT26 colon cancer cells. The formulated fluorescent m-NCs showed good stability and biocompatibility both in vitro and in vivo in CT 26 colon cancer models. Following intravenous injection, accumulation of m-NCs in tumours was observed by optical imaging. A higher iron content in the tumours exposed to a magnetic field, compared to the contralateral tumours without magnetic exposure in the same animal, further confirmed the magnetic tumour targeting in vivo. The overall results show that the engineered red-emitting m-NCs have great potential as multifunctional nanocarriers for multi-model bioimaging and magnetic-targeted drug delivery.-
dc.languageeng-
dc.relation.ispartofBiomaterials Science-
dc.titleEngineering red-emitting multi-functional nanocapsules for magnetic tumour targeting and imaging-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/d0bm00314j-
dc.identifier.pmid32238997-
dc.identifier.scopuseid_2-s2.0-85084271226-
dc.identifier.volume8-
dc.identifier.issue9-
dc.identifier.spage2590-
dc.identifier.epage2599-
dc.identifier.eissn2047-4849-

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