Logotipo do repositório
 

Publicação:
Efficacy of photodynamic therapy using TiO2 nanoparticles doped with Zn and hypericin in the treatment of cutaneous Leishmaniasis caused by Leishmania amazonensis

dc.contributor.authorSepúlveda, Alex Arbey Lopera
dc.contributor.authorArenas Velásquez, Angela Maria [UNESP]
dc.contributor.authorPatiño Linares, Irwin Alexander
dc.contributor.authorde Almeida, Leticia [UNESP]
dc.contributor.authorFontana, Carla Raquel [UNESP]
dc.contributor.authorGarcia, Claudia
dc.contributor.authorGraminha, Marcia Aparecida Silva [UNESP]
dc.contributor.institutionEscuela de Física
dc.contributor.institutionFacultad de Ingeniería Grupo GICEI
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2020-12-12T02:36:15Z
dc.date.available2020-12-12T02:36:15Z
dc.date.issued2020-06-01
dc.description.abstractSince Leishmania parasites exhibit resistance outbreaks to drugs conventionally used in medical treatments, research of new antileishmanial compounds or alternative treatment therapies are essential. A focus of interest has been the implementation of light-based therapies such as photodynamic therapy, where inorganic compounds such as titanium dioxide have shown promising results as drug delivery carriers. In this work, nanoparticles of TiO2 doped with Zn (TiO2/Zn) were synthesized through solution combustion route and with hypericin (HY) in order to enhance its photodynamic activity in the visible light region. Scanning (SEM) and transmission (TEM) electron microscopy analyses showed particles of (TiO2/Zn) with sizes smaller than 20 nm and formation of aggregates smaller than 1 μm, whilst electron diffraction spectroscopy (EDS) analysis ensured the presence of Zn in the system. The association of the TiO2/Zn with HY (TiO2/Zn-HY) was further confirmed by fluorescence spectrometry. Measurements of its cellular uptake showed the presence of smaller molecules into promastigotes after 120 min incubation. TiO2/Zn-HY showed good antileishmanial activity (EC50 of 17.5 ± 0.2 μg mL−1) and low cytotoxicity against murine macrophages (CC50 35.2 ± 0.3 μg mL−1) in the visible light (22 mW cm-2; 52.8 J cm-2). Moreover, in the in vivo analysis, TiO2/Zn-HY decreased the parasite load of L. amazonensis - BALB/c infected mice by 43% – 58% after a combination of blue and red light presenting 22 mW cm-2 of intensity and 52.8 J cm-2 of fluency delivered. All together, these data indicate a new combined system of nanoparticles associated with a photosensitizer and PDT as alternative to amphotericin B for the treatment of cutaneous leishmaniasis.en
dc.description.affiliationUniversidad Nacional de Colombia Escuela de Física, Carrera 65 Nro. 59A - 110 Grupo de Cerámicos y Vítreos
dc.description.affiliationInstitución universitaria Pascual Bravo Facultad de Ingeniería Grupo GICEI, calle 73 No. 73 A 226, código postal 050034
dc.description.affiliationUniversidade Estadual Paulista (UNESP) Faculdade de Ciências Farmacêuticas
dc.description.affiliationInstituto de Química de São Carlos Universidade de São Paulo
dc.description.affiliationUnespUniversidade Estadual Paulista (UNESP) Faculdade de Ciências Farmacêuticas
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.identifierhttp://dx.doi.org/10.1016/j.pdpdt.2020.101676
dc.identifier.citationPhotodiagnosis and Photodynamic Therapy, v. 30.
dc.identifier.doi10.1016/j.pdpdt.2020.101676
dc.identifier.issn1873-1597
dc.identifier.issn1572-1000
dc.identifier.scopus2-s2.0-85079880190
dc.identifier.urihttp://hdl.handle.net/11449/201577
dc.language.isoeng
dc.relation.ispartofPhotodiagnosis and Photodynamic Therapy
dc.sourceScopus
dc.subjectCutaneous leishmaniasis
dc.subjectHypericin
dc.subjectLeishmania amazonensis
dc.subjectNanoparticles
dc.subjectPhotodynamic Therapy (PDT)
dc.subjectReactive oxygen species (ROS)
dc.subjectTitanium
dc.titleEfficacy of photodynamic therapy using TiO2 nanoparticles doped with Zn and hypericin in the treatment of cutaneous Leishmaniasis caused by Leishmania amazonensisen
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublicationa83d26d6-5383-42e4-bb3c-2678a6ddc144
relation.isDepartmentOfPublication.latestForDiscoverya83d26d6-5383-42e4-bb3c-2678a6ddc144
unesp.author.lattes5168319315634298[5]
unesp.author.orcid0000-0002-9135-3690[5]
unesp.departmentAnálises Clínicas - FCFpt

Arquivos