Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation

Haiming Sun,1,* Xiaohui Chen,2,* Dan Chen,1 Mingyan Dong,1 Xinning Fu,1 Qian Li,1 Xi Liu,1 Qingzhi Wu,1 Tong Qiu,1 Tao Wan,1 Shipu Li11State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and Biomedical Materials and Engineering Center, Wuhan University of Technology, W...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Sun H, Chen X, Chen D, Dong M, Fu X, Li Q, Liu X, Wu Q, Qiu T, Wan T, Li S
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://doaj.org/article/42077606d74249e9a99a8e2cbda42f2d
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:42077606d74249e9a99a8e2cbda42f2d
record_format dspace
spelling oai:doaj.org-article:42077606d74249e9a99a8e2cbda42f2d2021-12-02T02:31:47ZInfluences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation1176-91141178-2013https://doaj.org/article/42077606d74249e9a99a8e2cbda42f2d2012-07-01T00:00:00Zhttp://www.dovepress.com/influences-of-surface-coatings-and-components-of-fept-nanoparticles-on-a10332https://doaj.org/toc/1176-9114https://doaj.org/toc/1178-2013Haiming Sun,1,* Xiaohui Chen,2,* Dan Chen,1 Mingyan Dong,1 Xinning Fu,1 Qian Li,1 Xi Liu,1 Qingzhi Wu,1 Tong Qiu,1 Tao Wan,1 Shipu Li11State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and Biomedical Materials and Engineering Center, Wuhan University of Technology, Wuhan, China; 2Department of Prosthetics, School of Stomatology, Wuhan University, Wuhan, China*Both authors contributed equally to this workAbstract: Malignant gliomas are primary brain tumors with high rates of morbidity and mortality; they are the fourth most common cause of cancer death. Novel diagnostic and therapeutic techniques based on nanomaterials provide promising options in the treatment of malignant gliomas. In order to evaluate the potential of FePt nanoparticles (NPs) for malignant glioma therapy, FePt NPs with different surface coatings and components were tunably synthesized using oleic acid/oleylamine (OA/OA) and cysteines (Cys) as the capping agents, respectively. The samples were characterized using X-ray diffraction, transmission electron microscopy (TEM), X-ray photon spectroscopy, Fourier transform infrared spectroscopy, atomic absorption spectrum, and zeta potential. The influence of the surface coatings and components of the FePt NPs on the proliferation of glioma cells was assessed through MTT assay and TEM observation using three typical glioma cell lines (glioma U251 cells, astrocytoma U87 cells, and neuroglioma H4 cells) as in vitro models. The results showed that the proliferation of glioma cells was significantly suppressed by lipophilic FePt-OA/OA NPs in a time- and/or dose-dependent manner, while no or low cytotoxic effects were detected in the case of hydrophilic FePt-Cys NPs. The IC50 value of FePt-OA/OA NPs on the three glioma cell lines was approximately 5–10 µg mL-1 after 24 hours’ incubation. Although the cellular uptake of FePt NPs was confirmed regardless of the surface coatings and components of the FePt NPs, the suppression of FePt NPs on glioma cell proliferation was dominantly determined by their surface coatings rather than their components. Therefore, these results demonstrate that, through engineering of the surface coating, FePt NPs can potentially be developed as novel therapeutic agents for malignant gliomas.Keywords: FePt nanoparticles, surface coatings, compositions, glioma cells, proliferationSun HChen XChen DDong MFu XLi QLiu XWu QQiu TWan TLi SDove Medical PressarticleMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol 2012, Iss default, Pp 3295-3307 (2012)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
Sun H
Chen X
Chen D
Dong M
Fu X
Li Q
Liu X
Wu Q
Qiu T
Wan T
Li S
Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation
description Haiming Sun,1,* Xiaohui Chen,2,* Dan Chen,1 Mingyan Dong,1 Xinning Fu,1 Qian Li,1 Xi Liu,1 Qingzhi Wu,1 Tong Qiu,1 Tao Wan,1 Shipu Li11State Key Laboratory of Advanced Technology for Materials Synthesis and Processing and Biomedical Materials and Engineering Center, Wuhan University of Technology, Wuhan, China; 2Department of Prosthetics, School of Stomatology, Wuhan University, Wuhan, China*Both authors contributed equally to this workAbstract: Malignant gliomas are primary brain tumors with high rates of morbidity and mortality; they are the fourth most common cause of cancer death. Novel diagnostic and therapeutic techniques based on nanomaterials provide promising options in the treatment of malignant gliomas. In order to evaluate the potential of FePt nanoparticles (NPs) for malignant glioma therapy, FePt NPs with different surface coatings and components were tunably synthesized using oleic acid/oleylamine (OA/OA) and cysteines (Cys) as the capping agents, respectively. The samples were characterized using X-ray diffraction, transmission electron microscopy (TEM), X-ray photon spectroscopy, Fourier transform infrared spectroscopy, atomic absorption spectrum, and zeta potential. The influence of the surface coatings and components of the FePt NPs on the proliferation of glioma cells was assessed through MTT assay and TEM observation using three typical glioma cell lines (glioma U251 cells, astrocytoma U87 cells, and neuroglioma H4 cells) as in vitro models. The results showed that the proliferation of glioma cells was significantly suppressed by lipophilic FePt-OA/OA NPs in a time- and/or dose-dependent manner, while no or low cytotoxic effects were detected in the case of hydrophilic FePt-Cys NPs. The IC50 value of FePt-OA/OA NPs on the three glioma cell lines was approximately 5–10 µg mL-1 after 24 hours’ incubation. Although the cellular uptake of FePt NPs was confirmed regardless of the surface coatings and components of the FePt NPs, the suppression of FePt NPs on glioma cell proliferation was dominantly determined by their surface coatings rather than their components. Therefore, these results demonstrate that, through engineering of the surface coating, FePt NPs can potentially be developed as novel therapeutic agents for malignant gliomas.Keywords: FePt nanoparticles, surface coatings, compositions, glioma cells, proliferation
format article
author Sun H
Chen X
Chen D
Dong M
Fu X
Li Q
Liu X
Wu Q
Qiu T
Wan T
Li S
author_facet Sun H
Chen X
Chen D
Dong M
Fu X
Li Q
Liu X
Wu Q
Qiu T
Wan T
Li S
author_sort Sun H
title Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation
title_short Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation
title_full Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation
title_fullStr Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation
title_full_unstemmed Influences of surface coatings and components of FePt nanoparticles on the suppression of glioma cell proliferation
title_sort influences of surface coatings and components of fept nanoparticles on the suppression of glioma cell proliferation
publisher Dove Medical Press
publishDate 2012
url https://doaj.org/article/42077606d74249e9a99a8e2cbda42f2d
work_keys_str_mv AT sunh influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT chenx influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT chend influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT dongm influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT fux influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT liq influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT liux influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT wuq influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT qiut influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT want influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
AT lis influencesofsurfacecoatingsandcomponentsoffeptnanoparticlesonthesuppressionofgliomacellproliferation
_version_ 1718402403582083072