Talita Katiane De Brito Pinto

Dr. Talita Katiane De Brito Pinto

Health technology innovation laboratory (LAIS), Natal, Rio Grande do Norte, Brazil
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Research Focus & Metrics

Academic Career Length

7Years (2020-Present)

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

Representative Publications

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1 February 2020 in International Journal of Nanomedicine
Verified
Journal Article
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Talita Katiane De Brito PintoTalita Katiane De Brito Pinto
Talita Katiane De Brito Pinto
RVRony Viana
Rony Viana
Claudia Jassica Gonçalves MorenoClaudia Jassica Gonçalves Moreno
Claudia Jassica Gonçalves Moreno
JBJefferson da Silva Barbosa
Jefferson da Silva Barbosa
FJFrancimar Junior
Francimar Junior
Hugo Alexandre Oliveira RochaHugo Alexandre Oliveira Rocha
Hugo Alexandre Oliveira Rocha
Background: Chagas disease, also known as American Trypanosomiasis, is caused by the protozoan Trypanosoma cruzi. It is occurring in Americas, including USA and Canada, and Europe and its current treatment involves the use of two drugs as follows: benznidazole (BNZ) and nifurtimox, which present high toxicity and low efficacy during the chronic phase of the disease, thus promoting the search for more effective therapeutic alternatives. Amongst them xylan, a bioactive polysaccharide, extracted from corn cob. Methods: Ultraviolet-visible spectroscopy, Fourier transform infrared spectroscopy (FITR), Raman spectroscopy, energy-dispersive X-ray spectroscopy (EDS), scanning electron microscopy, atomic force microscopy, plasma optical emission spectroscopy (ICP-OES), dynamic light scattering (DLS) have been used to characterize the silver-xylan nanoparticles (NX). Their cytotoxicity was evaluated with 3-bromo(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium (MTT) test. MTT and flow cytometry were used to ascertain the anti-Trypanosoma cruzi activity. Results: UV-Vis spectroscopy gave plasmon resonance ranging between 400 and 450 nm while FITC and Raman spectroscopy proved nano interface functionalized with xylan. ICP-OES data showed NX with xylan (81%) and silver (19%). EDS showed NX consisting of carbon (59.4%), oxygen (26.2%) and silver (4.8%) main elements. Spherical NX of 55 nm average size has been depicted with SEM and AFM, while DLS showed 102 ± 1.7 nm NX. The NX displayed negligible cytotoxicity (2000 μg/mL). NX (100 μg/mL) was more effective, regardless of experiment time, in affecting the ability of parasites to reduce MTT than BZN (100 μg/mL). In addition, NX (100 μg/mL) induced death of 95% of parasites by necrosis. Conclusion: This is the first time silver nanoparticles are presented as an anti-Trypanosoma cruzi agent and the data point to the potential application of NX to new preclinical studies in vitro and in vivo.

Talita Katiane De Brito PintoTalita Katiane De Brito Pinto
Talita Katiane De Brito Pinto
Aliete Cunha OliveiraAliete Cunha Oliveira
Aliete Cunha Oliveira
AMAna Isabela Lopes Sales Moioli
Ana Isabela Lopes Sales Moioli
JDJane Francinete Dantas
Jane Francinete Dantas
RCRosângela Maria Morais da Costa
Rosângela Maria Morais da Costa
Ricardo ValentimRicardo Valentim
Ricardo Valentim
(1) Background: Maternal syphilis (MS) and congenital syphilis (CS) are serious public health problems worldwide due to their high morbidity and mortality rates. (2) Objective: Evaluating the applicability of Clinical Protocols and Treatment Guidelines on case incidence trends in Brazil and Portugal. (3) Methods: The review was done through bibliographic research in two public databases and government websites from both countries, published between 2007 and 2022. All guidelines that contained CS and MS were selected. (4) Results and discussion: After evaluation, we found that Brazil and Portugal have adequate protocols for screening and treating congenital and maternal syphilis. (5) Conclusion: The results suggest that CS and MS incidence are notably higher in Brazil than in Portugal due to economic, cultural, and social disparities and the differences in territory size. Therefore, these demographic and socioeconomic factors could strongly influence efforts to fight against syphilis and thus control the infection.

AMAna Isabela Lopes Sales Moioli
Ana Isabela Lopes Sales Moioli
Leonardo J. Galvão-LimaLeonardo J. Galvão-Lima
Leonardo J. Galvão-Lima
Talita Katiane De Brito PintoTalita Katiane De Brito Pinto
Talita Katiane De Brito Pinto
PHPablo Holanda
Pablo Holanda
RSRodrigo D. Silva
Rodrigo D. Silva
Ricardo ValentimRicardo Valentim
Ricardo Valentim
Since the COVID-19 pandemic emerged, vaccination has been the core strategy to mitigate the spread of SARS-CoV-2 in humans. This paper analyzes the impact of COVID-19 vaccination on hospitalizations and deaths in the state of Rio Grande do Norte, Brazil. We analyzed data from 23,516 hospitalized COVID-19 patients diagnosed between April 2020 and August 2021. We excluded the data from patients hospitalized through direct occupancy, unknown outcomes, and unconfirmed COVID-19 cases, resulting in data from 12,635 patients cross-referenced with the immunization status during hospitalization. Our results indicated that administering at least one dose of the immunizers was sufficient to significantly reduce the occurrence of moderate and severe COVID-19 cases among patients under 59 years. Considering the partially or fully immunized patients, the mean age is similar between the analyzed groups, despite the occurrence of comorbidities and higher than that observed among not immunized patients. Thus, immunized patients present lower Unified Score for Prioritization (USP) levels when diagnosed with COVID-19. Our data suggest that COVID-19 vaccination significantly reduced the hospitalization and death of elderly patients (60+ years) after administration of at least one dose. Comorbidities do not change the mean age of moderate/severe COVID-19 cases and the days required for the hospitalization of these patients.

Talita Katiane De Brito PintoTalita Katiane De Brito Pinto
Talita Katiane De Brito Pinto
TLThaísa Lima
Thaísa Lima
Aliete Cunha OliveiraAliete Cunha Oliveira
Aliete Cunha Oliveira
ANAndré Noronha
André Noronha
CBCintia Brito
Cintia Brito
Ricardo ValentimRicardo Valentim
Ricardo Valentim
(1) Introduction: Syphilis is a sexually transmitted infection (STI) that constitutes a serious public health problem in Brazil and worldwide; (2) Methods: This was a descriptive and exploratory study that sought to analyze and compare the characteristics of Brazilian health systems with a new platform (Salus) developed by the Laboratory of Technological Innovation in Health in the scope of notification and management of disease data, including syphilis. In addition, this analysis aimed to assess whether Salus fully meets the necessary data management fields and can be indicated as a tool to improve health management in the context of syphilis in Brazil. (3) Results: In this study, the Salus functionalities were demonstrated and compared with the current Brazilian systems by discovering the existing gaps in the evaluated systems. The gaps found may explain the delay in meeting demands, the difficulty of making routine therapeutic follow-ups, in addition to interference with the vital purpose of follow-up in the epidemiological surveillance of diseases. As a result, Salus demonstrates functionalities that surpass all others and meet case management demands in a superior way to the systems currently used in the country. (4) Conclusions: The Brazilian health information systems related to the response to syphilis do not fulfill the purpose for which they were developed. Instead, they contribute to the fragmentation of health data and information, delays in diagnosis, incomplete case management, and loss of data due to inconsistencies and inadequate reporting. In addition, they are systems without interconnection, which do not articulate epidemiological surveillance actions with primary health care. All these factors may be obscuring accurate data on syphilis in Brazil, resulting in high and unnecessary public spending and late care for users of the Unified Health System (SUS).

Verified
Journal Article
Open access
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Claudia Jassica Gonçalves MorenoClaudia Jassica Gonçalves Moreno
Claudia Jassica Gonçalves Moreno
HFHenriqueta Monalisa Farias
Henriqueta Monalisa Farias
RMRafael de Lima Medeiros
Rafael de Lima Medeiros
Talita Katiane De Brito PintoTalita Katiane De Brito Pinto
Talita Katiane De Brito Pinto
JOJohny Olivera
Johny Olivera
MSMarcelo Sousa Silva
Marcelo Sousa Silva
Leishmanolysin, also known as major promastigote protease (PSP) or gp63, is the most abundant surface glycoprotein of Leishmania spp., and has been extensively studied and recognized as the main parasite virulence factor. Characterized as a metalloprotease, gp63 can be powerfully inactivated in the presence of a metal chelator. In this study, we first used the structural parameters of a 7-hydroxycoumarin derivative, L1 compound, to evaluate the theoretical–computational experiments against gp63, comparing it with an available metal chelator already described. The methodology followed was (i) analysis of the three-dimensional structure of gp63 as well as its active site, and searching the literature and molecular databases for possible inhibitors; (ii) molecular docking simulations and investigation of the interactions in the generated protein–ligand complexes; and (iii) the individual energy of the gp63 amino acids that interacted most with the ligands of interest was quantified by ab initio calculations using Molecular Fraction with Conjugated Caps (MFCC). MFCC still allowed the final quantum balance calculations of the protein interaction to be obtained with each inhibitor candidate binder. L1 obtained the best energy quantum balance result with −2 eV, followed by DETC (−1.4 eV), doxycycline (−1.3 eV), and 4-terpineol (−0.6 eV), and showed evidence of covalent binding in the enzyme active site. In vitro experiments confirmed L1 as highly effective against L. amazonensis parasites. The compound also exhibited a low cytotoxicity profile against mammalian RAW and 3T3 cells lines, presenting a selective index of 149.19 and 380.64 µM, respectively. L1 induced promastigote forms’ death by necrosis and the ultrastructural analysis revealed disruption in membrane integrity. Furthermore, leakage of the contents and destruction of the parasite were confirmed by Spectroscopy Dispersion analysis. These results together suggested L1 has a potential effect against L. amazonensis, the etiologic agent of diffuse leishmaniasis, and the only one that currently does not have a satisfactory treatment.

GBGabriel M. C. Barros
Gabriel M. C. Barros
Dionísio Dias Aires de CarvalhoDionísio Dias Aires de Carvalho
Dionísio Dias Aires de Carvalho
ACAgnaldo S. Cruz
Agnaldo S. Cruz
EMEllen K. L. Morais
Ellen K. L. Morais
AMAna Isabela Lopes Sales Moioli
Ana Isabela Lopes Sales Moioli
Ricardo ValentimRicardo Valentim
Ricardo Valentim
The improvement of laboratory diagnosis is a critical step for the reduction of syphilis cases around the world. In this paper, we present the development of an impedance-based method for detecting T. pallidum antigens and antibodies as an auxiliary tool for syphilis laboratory diagnosis. We evaluate the voltammetric signal obtained after incubation in carbon or gold nanoparticle-modified carbon electrodes in the presence or absence of Poly-L-Lysine. Our results indicate that the signal obtained from the electrodes was sufficient to distinguish between infected and non-infected samples immediately (T0′) or 15 min (T15′) after incubation, indicating its potential use as a point-of-care method as a screening strategy.
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