ZnO–Graphene Oxide Nanocomposite for Paclitaxel Delivery and Enhanced Toxicity in Breast Cancer Cells
dc.bibliographicCitation.articleNumber | 3770 | |
dc.bibliographicCitation.firstPage | 3770 | |
dc.bibliographicCitation.issue | 16 | |
dc.bibliographicCitation.journalTitle | Molecules | |
dc.bibliographicCitation.volume | 29 | |
dc.contributor.author | Madeo, Lorenzo Francesco | |
dc.contributor.author | Schirmer, Christine | |
dc.contributor.author | Cirillo, Giuseppe | |
dc.contributor.author | Asha, Ayah Nader | |
dc.contributor.author | Ghunaim, Rasha | |
dc.contributor.author | Froeschke, Samuel | |
dc.contributor.author | Wolf, Daniel | |
dc.contributor.author | Curcio, Manuela | |
dc.contributor.author | Tucci, Paola | |
dc.contributor.author | Iemma, Francesca | |
dc.contributor.author | Büchner, Bernd | |
dc.contributor.author | Hampel, Silke | |
dc.contributor.author | Mertig, Michael | |
dc.date.accessioned | 2024-10-25T06:53:18Z | |
dc.date.available | 2024-10-25T06:53:18Z | |
dc.date.issued | 2024 | |
dc.description.abstract | A ZnO-Graphene oxide nanocomposite (Z-G) was prepared in order to exploit the biomedical features of each component in a single anticancer material. This was achieved by means of an environmentally friendly synthesis, taking place at a low temperature and without the involvement of toxic reagents. The product was physicochemically characterized. The ZnO-to-GO ratio was determined through thermogravimetric analysis, while scanning electron microscopy and transmission electron microscopy were used to provide insight into the morphology of the nanocomposite. Using energy-dispersive X-ray spectroscopy, it was possible to confirm that the graphene flakes were homogeneously coated with ZnO. The crystallite size of the ZnO nanoparticles in the new composite was determined using X-ray powder diffraction. The capacity of Z-G to enhance the toxicity of the anticancer drug Paclitaxel towards breast cancer cells was assessed via a cell viability study, showing the remarkable anticancer activity of the obtained system. Such results support the potential use of Z-G as an anticancer agent in combination with a common chemotherapeutic like Paclitaxel, leading to new chemotherapeutic formulations. | eng |
dc.description.version | publishedVersion | eng |
dc.identifier.uri | https://oa.tib.eu/renate/handle/123456789/17239 | |
dc.identifier.uri | https://doi.org/10.34657/16261 | |
dc.language.iso | eng | |
dc.publisher | Basel : MDPI | |
dc.relation.doi | https://doi.org/10.3390/molecules29163770 | |
dc.relation.essn | 1420-3049 | |
dc.rights.license | CC BY 4.0 Unported | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | |
dc.subject.ddc | 540 | |
dc.subject.other | cancer therapy | eng |
dc.subject.other | graphene oxide | eng |
dc.subject.other | nanocomposite | eng |
dc.subject.other | Paclitaxel delivery | eng |
dc.subject.other | zinc oxide nanoparticles | eng |
dc.title | ZnO–Graphene Oxide Nanocomposite for Paclitaxel Delivery and Enhanced Toxicity in Breast Cancer Cells | eng |
dc.type | Article | |
dc.type | Text | |
tib.accessRights | openAccess | |
wgl.contributor | IFWD | |
wgl.subject | Chemie | ger |
wgl.type | Zeitschriftenartikel | ger |
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