Publication
Targeting canine mammary tumours via gold nanoparticles functionalized with promising Co(II) and Zn(II) compounds
dc.contributor.author | Raposo, L. R. | |
dc.contributor.author | Roma-Rodrigues, C. | |
dc.contributor.author | Jesus, J. | |
dc.contributor.author | Martins, Luisa | |
dc.contributor.author | Pombeiro, Armando | |
dc.contributor.author | Baptista, P. V. | |
dc.contributor.author | Fernandes, A. R. | |
dc.date.accessioned | 2017-12-05T10:22:57Z | |
dc.date.available | 2017-12-05T10:22:57Z | |
dc.date.issued | 2017-12 | |
dc.description.abstract | Background: Despite continuous efforts, the treatment of canine cancer has still to deliver effective strategies. For example, traditional chemotherapy with doxorubicin and/or docetaxel does not significantly increase survival in dogs with canine mammary tumors (CMTs). Aims: Evaluate the efficiency of two metal compounds [Zn(DION)2]Cl (TS262, DION = 1,10- phenanthroline-5,6-dione) and [CoCl(H2O)(DION)2][BF4] (TS265) and novel nanovectorizations designed to improve the anti-cancer efficacy of these compounds in a new CMT derived cell line (FR37-CMT). Materials and methods: FR37-CMT cells were exposed to different concentrations of TS262 and TS265 and two new nanoparticle systems and cellular viability was determined. These nanosystems are composed of polyethylene-glycol, bovine-serum-albumin and TS262 or TS265 (NanoTS262 or NanoTS265, respectively). Results: In FR37-CMT, TS262 and TS265 displayed IC50 values well below those displayed by doxorubicin and cisplatin. The nanovectorizations further decreased the IC50 values. Discussion: TS262 and TS265 proved to be effective against FR37-CMT cells and more effective than of doxorubicin and cisplatin. The Nanosystems efficiently delivered the cytotoxic cargo inducing a significant reduction of cell viability in FR37-CMT cell line when compared to the free compounds. Conclusions: TS262 and TS265 are compounds with potential in the treatment of CMTs. NanoTS262 and NanoTS265 demonstrate that such simple nanovectorization via gold nanoparticles shows tremendous potential as anti-cancer formulations, which may easily be expanded to suit other cargo. | pt_PT |
dc.description.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | RAPOSO, L. R.; [et al] – Targeting canine mammary tumours via gold nanoparticles functionalized with promising Co(II) and Zn(II) compounds. Veterinary and Comparative Oncology. ISSN 1476-5810. Vol. 15, N.º 4 (2017), pp. 1537-1542 | pt_PT |
dc.identifier.doi | 10.1111/vco.12298 | pt_PT |
dc.identifier.issn | 1476-5810 | |
dc.identifier.issn | 1476-5829 | |
dc.identifier.uri | http://hdl.handle.net/10400.21/7645 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Wiley | pt_PT |
dc.relation | POCI-01-0145-FEDER-007728 | pt_PT |
dc.relation | TRANSCRIPTOME AND PROTEOME PROFILING OF CANINE MAMMARY TUMORS: DOG AS A GENETIC MODEL FOR UNREVEALING MAMMARY CANCER MOLECULAR SIGNATURES | |
dc.relation.publisherversion | http://onlinelibrary.wiley.com/doi/10.1111/vco.12298/epdf | pt_PT |
dc.subject | canine mammary tumours | pt_PT |
dc.subject | cisplatin | pt_PT |
dc.subject | doxorubicin | pt_PT |
dc.subject | FR37-CMT | pt_PT |
dc.subject | gold nanoparticles | pt_PT |
dc.subject | nanotechnology | pt_PT |
dc.title | Targeting canine mammary tumours via gold nanoparticles functionalized with promising Co(II) and Zn(II) compounds | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.awardTitle | TRANSCRIPTOME AND PROTEOME PROFILING OF CANINE MAMMARY TUMORS: DOG AS A GENETIC MODEL FOR UNREVEALING MAMMARY CANCER MOLECULAR SIGNATURES | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT/5876/UID%2FMulti%2F04378%2F2013/PT | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT//SFRH%2FBD%2F70202%2F2010/PT | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT/5876/UID%2FQUI%2F00100%2F2013/PT | |
oaire.awardURI | info:eu-repo/grantAgreement/FCT/5876/UID%2FDTP%2F04138%2F2013/PT | |
oaire.citation.endPage | 1542 | pt_PT |
oaire.citation.issue | 4 | pt_PT |
oaire.citation.startPage | 1537 | pt_PT |
oaire.citation.title | Veterinary and Comparative Oncology | pt_PT |
oaire.citation.volume | 15 | pt_PT |
oaire.fundingStream | 5876 | |
oaire.fundingStream | 5876 | |
oaire.fundingStream | 5876 | |
person.familyName | Martins | |
person.familyName | Pombeiro | |
person.givenName | Luisa | |
person.givenName | Armando | |
person.identifier | 637885 | |
person.identifier.ciencia-id | E218-E297-A4EA | |
person.identifier.ciencia-id | 8311-38FA-CEFB | |
person.identifier.orcid | 0000-0002-5403-9352 | |
person.identifier.orcid | 0000-0001-8323-888X | |
person.identifier.rid | G-6210-2011 | |
person.identifier.rid | I-5945-2012 | |
person.identifier.scopus-author-id | 8650947800 | |
person.identifier.scopus-author-id | 7006067269 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.identifier | http://doi.org/10.13039/501100001871 | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
project.funder.name | Fundação para a Ciência e a Tecnologia | |
rcaap.rights | closedAccess | pt_PT |
rcaap.type | article | pt_PT |
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