Juliana Guerra Pinto

Dr. Juliana Guerra Pinto

Faculdade de ciências da Saúde, Universidade do Vale do Paraíba, São José dos Campos, São Paulo, Brazil
orcid

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 January 2022 in Photodiagnosis and Photodynamic Therapy
Verified
Journal Article
Closed access
IRIsabelle de Paula Ribeiro
Isabelle de Paula Ribeiro
Juliana Guerra PintoJuliana Guerra Pinto
Juliana Guerra Pinto
BSBeatriz Müller Nunes Souza
Beatriz Müller Nunes Souza
AMAlejandro Guillermo Miñán
Alejandro Guillermo Miñán
JFJuliana Ferreira-Srixino
Juliana Ferreira-Srixino

27 March 2018 in Journal of Biomaterials Science, Polymer Edition
Verified
Journal Article
Closed access
JCJanicy Arantes Carvalho
Janicy Arantes Carvalho
AAAlexandro Silva Abreu
Alexandro Silva Abreu
VFVitória Tonini Porto Ferreira
Vitória Tonini Porto Ferreira
EGErika Peterson Gonçalves
Erika Peterson Gonçalves
ATAntonio Claudio Tedesco
Antonio Claudio Tedesco
ASAndreza Ribeiro Simioni
Andreza Ribeiro Simioni
Gelatin nanoparticles have recently been receiving considerable attention because they offer a good option as release systems due to their low cost, biocompatibility, biodegradability and its application in several types of formulations. This study aim was to evaluate the potential application of gelatin nanoparticles entrapping a photosensitizer in Photodynamic Therapy. Gelatin nanoparticles were studied by steady-state techniques and the biological activity evaluated by in vitro MTT assay. The particles were spherical in shape exhibiting a 273 nm diameter with a low tendency to aggregate. The loading efficiency was 76%. Photosensitizer photophysical properties were shown to be preserved after GN encapsulation. The cells viability obtaining 85% cells death compared with control. The results demonstrate that gelatin nanoparticles can be successfully applied for photosensitizers encapsulation or other active drugs and be used as an optimal medium for a variety of bioactive materials, which can also be encapsulated by the proposed method.

7 April 2016 in Lasers in Medical Science
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Journal Article
Closed access
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Juliana Guerra PintoJuliana Guerra Pinto
Juliana Guerra Pinto
LFLetícia Correa Fontana
Letícia Correa Fontana
MOMarco Antonio de Oliveira
Marco Antonio de Oliveira
CKCristina Kurachi
Cristina Kurachi
LRLeandro Raniero
Leandro Raniero
JFJuliana Ferreira-Srixino
Juliana Ferreira-Srixino

1 June 2019 in Future Microbiology
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Journal Article
Closed access
MFMirian Aa Freitas
Mirian Aa Freitas
APAndré Hc Pereira
André Hc Pereira
Juliana Guerra PintoJuliana Guerra Pinto
Juliana Guerra Pinto
ACAdriana Casas
Adriana Casas
JFJuliana Ferreira-Srixino
Juliana Ferreira-Srixino
Staphylococcus aureus are multiresistant pathogens that causes superficial and systemic infections. Antimicrobial photodynamic therapy (APDT) is an alternative in the treatment of diseases caused b...

1 June 2017 in Photodiagnosis and Photodynamic Therapy
Verified
Journal Article
Closed access
Juliana Guerra PintoJuliana Guerra Pinto
Juliana Guerra Pinto
JMJaciara Fagundes de Souza Martins
Jaciara Fagundes de Souza Martins
APAndré Henrique Correia Pereira
André Henrique Correia Pereira
JMJosane Mittmann
Josane Mittmann
LRLeandro Raniero
Leandro Raniero
JFJuliana Ferreira-Srixino
Juliana Ferreira-Srixino

4 May 2022 in Antibiotics
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Journal Article
Open access
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LGLívia Mara Alves Figueiredo Godoi
Lívia Mara Alves Figueiredo Godoi
MGMaíra Terrra Garcia
Maíra Terrra Garcia
Juliana Guerra PintoJuliana Guerra Pinto
Juliana Guerra Pinto
JFJuliana Ferreira-Srixino
Juliana Ferreira-Srixino
EFEliseu Gabriel Faustino.
Eliseu Gabriel Faustino.
Juliana JunqueiraJuliana Junqueira
Juliana Junqueira
Antimicrobial photodynamic therapy (aPDT) is considered a promising alternative strategy to control Acinetobacter baumannii infections. In this study, we evaluated the action of aPDT mediated by a new photosensitizer derivative from chlorin e-6 (Fotoenticine—FTC) on A. baumannii, comparing its effects with methylene blue (MB). For this, aPDT was applied on A. baumannii in planktonic growth, biofilms, and burn infections in Galleria mellonella. The absorption of FTC and MB by bacterial cells was also evaluated using microscopic and spectrophotometric analysis. The results of planktonic cultures showed that aPDT reduced the number of viable cells compared to the non-treated group for the reference and multidrug-resistant A. baumannii strains. These reductions varied from 1.4 to 2 log10 CFU for FTC and from 2 log10 CFU to total inhibition for MB. In biofilms, aPDT with MB reduced 3.9 log10 CFU of A. baumannii, whereas FTC had no effect on the cell counts. In G. mellonella, only MB-mediated aPDT had antimicrobial activity on burn injuries, increasing the larvae survival by 35%. Both photosensitizers were internalized by bacterial cells, but MB showed a higher absorption compared to FTC. In conclusion, MB had greater efficacy than FTC as a photosensitizer in aPDT against A. baumannii.