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dc.contributor.author | Biagiotti G. | |
dc.contributor.author | Pisaneschi F. | |
dc.contributor.author | Gammon S. | |
dc.contributor.author | Machetti F. | |
dc.contributor.author | Ligi M. | |
dc.contributor.author | Giambastiani G. | |
dc.contributor.author | Tuci G. | |
dc.contributor.author | Powell E. | |
dc.contributor.author | Piwnica-Worms H. | |
dc.contributor.author | Pranzini E. | |
dc.contributor.author | Paoli P. | |
dc.contributor.author | Cicchi S. | |
dc.contributor.author | Piwnica-Worms D. | |
dc.date.accessioned | 2020-01-15T22:12:07Z | |
dc.date.available | 2020-01-15T22:12:07Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 2050-7518 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/157022 | |
dc.description.abstract | © 2019 The Royal Society of Chemistry. A drug delivery system (DDS) for combined therapy, based on a short oxidized multiwalled carbon nanotube, is reported. It was prepared by exploiting a synthetic approach which allowed loading of two drugs, doxorubicin and metformin, the targeting agent biotin and a radiolabeling tag, to enable labeling with Ga-68 or Cu-64 in order to perform an extensive biodistribution study by PET/CT. The DDS biodistribution profile changes with different administration methods. Once administered at therapeutic doses, the DDS showed a marginal beneficial effect on 4T1 tumor bearing mice, a syngeneic and orthotopic model of triple negative breast cancer, with survival extended by 1 week and 2 days in 20% of the mice. This is encouraging given the aggressiveness of the 4T1 tumor. Furthermore, our DDS was well tolerated, ruling out concerns regarding the toxicity of carbon nanotubes. | |
dc.relation.ispartofseries | Journal of Materials Chemistry B | |
dc.title | Multiwalled carbon nanotubes for combination therapy: A biodistribution and efficacy pilot study | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 16 | |
dc.relation.ispartofseries-volume | 7 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 2678 | |
dc.source.id | SCOPUS20507518-2019-7-16-SID85064645913 |