The effect of radiation dose rate over the formation of protein-based nanoparticles for nanosized delivery of chemo and radiotherapeutics

dc.contributor.authorVARCA, G.H.C.
dc.contributor.authorFAZOLIN, G.N.
dc.contributor.authorFERREIRA, A.H.
dc.contributor.authorOLIVEIRA, J.P.R. de
dc.contributor.authorMARQUES, F.
dc.contributor.authorLUGAO, A.B.
dc.coverageNacionalpt_BR
dc.creator.eventoCONGRESSO BRASILEIRO DE ENGENHARIA E CIÊNCIA DOS MATERIAIS, 23.pt_BR
dc.date.accessioned2019-02-20T20:11:16Z
dc.date.available2019-02-20T20:11:16Z
dc.date.evento04-08 de novembro, 2018pt_BR
dc.description.abstractRecent studies demonstrated the development of papain and bovine serum albumin nanoparticles using gamma radiation (10 kGy) in presence of 20-30% (v/v) ethanol. With the purpose of producing stable and well defined nanocarriers, this work aims to determine the influence of different dose rates over protein nanoparticle formation. For this purpose, papain and BSA nanoparticles were synthetized in phosphate buffer (50 mM, pH 7.2) and ethanol (20-30%, v/v) using a radiation dose of 10 kGy and dose rate of 0.8, 2, 5 and 10 kGy.h-1. After irradiation, samples were evaluated by dynamic light scattering, fluorescence and proteolytic activity to verify the size, secondary structure and monitoring of the enzymatic activity, respectively. For papain nanoparticles it was observed that the dose rate did not influence the particle size formation, however crosslinking evidenced by bityrosine showed that samples irradiated at 0.8 and 5 kGy.h-1 presented higher bityrosine levels. On the other hand, BSA nanoparticles presented different results if compared to papain NPs. Different dose rates caused different and non-linear size increase for each condition, following the order: 5 > 10 > 0.8 > 2 kGy.h-1. However, in terms of crosslinking formation, a linear increase was registered, as at 0.8 kGy.h-1 the smallest signal was achieved, whereas at 10 kGy.h- 1 the highest signal was recorded. In conclusion, BSA nanoparticles were more sensitive to different radiation dose rates than nanopapain. Optimized results in terms of size increase and higher bityrosine levels were observed for the samples irradiated at 5 kGy.h-1, in which nanoparticle formation will occur faster if compared to the synthesis carried out under distinct conditions. As final applications of the system concert their use for the delivery of chemo or radiotherapeutics, the loading of paclitaxel, a well-known chemotherapeutic agent, and radiolabeling with tecntetium- 99m, a radioisotope suitable for biomedical applications, have also been performed with high efficiency, thus demonstrating a proof of concept of such systems.pt_BR
dc.event.siglaCBECiMatpt_BR
dc.format.extent8875-8875pt_BR
dc.identifier.citationVARCA, G.H.C.; FAZOLIN, G.N.; FERREIRA, A.H.; OLIVEIRA, J.P.R. de; MARQUES, F.; LUGAO, A.B. The effect of radiation dose rate over the formation of protein-based nanoparticles for nanosized delivery of chemo and radiotherapeutics. In: CONGRESSO BRASILEIRO DE ENGENHARIA E CIÊNCIA DOS MATERIAIS, 23., 04-08 de novembro, 2018, Foz do Iguaçu, PR. <b>Resumo...</b> p. 8875-8875. Disponível em: http://repositorio.ipen.br/handle/123456789/29677.
dc.identifier.orcidaguardandopt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-1737-3191
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/29677
dc.local.eventoFoz do Iguaçu, PRpt_BR
dc.rightsopenAccesspt_BR
dc.subjectalbumins
dc.subjectblood serum
dc.subjectcattle
dc.subjectcross-linking
dc.subjectdose rates
dc.subjectdrug delivery
dc.subjectfluorescence
dc.subjectlight scattering
dc.subjectnanoparticles
dc.subjectpapain
dc.subjectparticle size
dc.subjectproteins
dc.subjectradiation doses
dc.subjectradiation effects
dc.titleThe effect of radiation dose rate over the formation of protein-based nanoparticles for nanosized delivery of chemo and radiotherapeuticspt_BR
dc.typeResumo de eventos científicospt_BR
dspace.entity.typePublication
ipen.autorGABRIELA NEMESIO FAZOLIN
ipen.autorADEMAR BENEVOLO LUGAO
ipen.autorJUSTINE PAULA RAMOS DE OLIVEIRA
ipen.autorARYEL HEITOR FERREIRA
ipen.autorGUSTAVO HENRIQUE COSTAVARCA
ipen.codigoautor14241
ipen.codigoautor339
ipen.codigoautor8726
ipen.codigoautor12722
ipen.codigoautor8661
ipen.contributor.ipenauthorGABRIELA NEMESIO FAZOLIN
ipen.contributor.ipenauthorADEMAR BENEVOLO LUGAO
ipen.contributor.ipenauthorJUSTINE PAULA RAMOS DE OLIVEIRA
ipen.contributor.ipenauthorARYEL HEITOR FERREIRA
ipen.contributor.ipenauthorGUSTAVO HENRIQUE COSTAVARCA
ipen.date.recebimento19-02pt_BR
ipen.event.datapadronizada2018pt_BR
ipen.identifier.ipendoc25429pt_BR
ipen.notas.internasResumopt_BR
ipen.type.genreResumo
relation.isAuthorOfPublicationc93580c2-7cf1-4cc7-a8ce-84b448cf8136
relation.isAuthorOfPublication99ac24c5-2ae1-465a-a6f2-40b4d9af6af7
relation.isAuthorOfPublicatione31cd2b4-ae29-47a5-aa35-ba3e58cdeb92
relation.isAuthorOfPublication169db0fc-742e-4a4f-9a14-d2d354e3895b
relation.isAuthorOfPublication46f998cf-b207-4854-94c0-dd2def4eec2a
relation.isAuthorOfPublication.latestForDiscovery46f998cf-b207-4854-94c0-dd2def4eec2a
sigepi.autor.atividadeVARCA, G.H.C.:8661:750:Spt_BR
sigepi.autor.atividadeFAZOLIN, G.N.:14241:740:Npt_BR
sigepi.autor.atividadeFERREIRA, A.H.:12722:740:Npt_BR
sigepi.autor.atividadeOLIVEIRA, J.P.R. DE:8726:740:Npt_BR
sigepi.autor.atividadeLUGAO, A.B.:339:740:Npt_BR

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