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1.
Exp Parasitol ; 236-237: 108257, 2022.
Article in English | MEDLINE | ID: mdl-35398101

ABSTRACT

We performed a biological evaluation of antileishmanial activity, in silico ADME-Tox profile, and molecular docking of riparins A-F. The antileishmanial activity was evaluated in Leishmania major promastigotes, whereas the cytotoxic activity was tested on murine macrophages. Computational parameters were predicted by in silico analysis. Molecular docking was performed with 18 L. major molecular targets. Riparins, especially RipC and RipE, showed cytotoxic activity in vitro toward L. major promastigotes and a high selectivity index. Riparins showed small differences in their physicochemical properties, such as polarity and aqueous solubility. LogP was an important parameter for the differences in the antileishmanial activity between the molecules. In molecular docking, the ligands displayed Ki < 1 µM for LmNMT and LmLEI. Significant molecular interactions were observed with residues from the active site and adjacent regions of such enzymes. Thus, riparins have the potential for application in antileishmanial therapy.


Subject(s)
Antiprotozoal Agents , Leishmania major , Animals , Antiprotozoal Agents/chemistry , Antiprotozoal Agents/toxicity , Ligands , Macrophages , Mice , Molecular Docking Simulation
2.
Biosci. j. (Online) ; 37: e37077, Jan.-Dec. 2021. ilus, tab
Article in English | LILACS | ID: biblio-1361400

ABSTRACT

Leishmaniasis are a group of parasitic zoonoses provoked by protozoa from Leishmania genus and belonging to the group of neglected tropical diseases. The search and development for new drugs is necessary not only to investigate the activity against only the parasite, but also to investigate the possible synergistic effect of new drugs with the immune response of the host. In the present review, macrophages are pointed out as potential targets of the investigation of new antileishmanial drugs, and some methodologies in order to assess their activation as response to Leishmania-infected cells are presented. Macrophages are an important role in the cellular immune response, since they are cells from mononuclear phagocytic system, the first line of defense of the host, against parasites from Leishmania genus. Phagocytic capacity, lysosomal activity, increase of nitric oxide and intracellular calcium levels are parameters regarding assessment of macrophages activation which allow them to be more hostile in order to solve the infection and lead the patient to cure. In this context, we bring 19 substances already investigated and that activate macrophages, what makes them promising in the antileishmanial treatment. Therefore, assessment of macrophages activation, are important tools for discovery of immunomodulatory compounds which have potential to act in synergism with host immune response. Such compounds might be promising as monotherapy in the treatment of leishmaniasis, as well as being used as adjuvants in vaccines and/or in combination with conventional drugs.


Subject(s)
Leishmaniasis/drug therapy , Immunomodulation , Macrophage Activation/immunology
3.
AAPS PharmSciTech ; 21(8): 302, 2020 Nov 04.
Article in English | MEDLINE | ID: mdl-33146782

ABSTRACT

The dental intracanal disinfection is crucial to achieve the success of endodontic treatment, avoiding the maintenance of endodontic infections. Chlorhexidine digluconate can act as an irrigating agent for it. However, it can cause tissue irritation in high concentrations. Therefore, combinations with other antimicrobial agents and more efficient therapeutic alternatives are studied, which make it possible to administer drugs more safely and with minimal adverse effects. Thus, the objective of this study was the development of a microemulsion containing chlorhexidine digluconate and essential oil of Lippia sidoides to be used for disinfection of dental root canals and to evaluate its profile of substantivity and antimicrobial activity. The microemulsions were obtained through phase diagrams, using the spontaneous formation method. We completed a physical-chemical characterization and evaluate the stability of the microemulsions, in addition to the substantivity profile in a bovine root dentin model, and in vitro antibacterial effect on Enterococcus faecalis. A method for quantifying chlorhexidine was developed using UV-Vis spectroscopy. The microemulsions showed acid pH, conductivity above 1.3 µScm-1, and dispersion index similar to water. The microemulsions showed antimicrobial inhibition halos similar to the commercial gel conventionally used, but with four times more substantivity to dentinal tissues. Microemulsions were obtained as a therapeutic alternative to formulations available on the market, presenting themselves as a system with great potential for the administration of drugs for disinfection of root canals.


Subject(s)
Anti-Infective Agents, Local/administration & dosage , Chlorhexidine/analogs & derivatives , Lippia/chemistry , Oils, Volatile/administration & dosage , Root Canal Irrigants/administration & dosage , Anti-Bacterial Agents/administration & dosage , Chlorhexidine/administration & dosage , Dental Pulp Cavity/drug effects , Disinfection , Enterococcus faecalis/drug effects , Enterococcus faecalis/isolation & purification , Humans , Microbial Sensitivity Tests
4.
Antimicrob Agents Chemother ; 64(12)2020 11 17.
Article in English | MEDLINE | ID: mdl-32928735

ABSTRACT

In this study, we demonstrated the potential associative effect of combining conventional amphotericin B (Amph B) with gallic acid (GA) and with ellagic acid (EA) in topical formulations for the treatment of cutaneous leishmaniasis in BALB/c mice. Preliminary stability tests of the formulations and in vitro drug release studies with Amph B, GA, Amph B plus GA, EA, and Amph B plus EA were carried out, as well as assessment of the in vivo treatment of BALB/c mice infected with Leishmania major After 40 days of infection, the animals were divided into 6 groups and treated twice a day for 21 days with a gel containing Amph B, GA, Amph B plus GA, EA, or Amph B plus EA, and the negative-control group was treated with the vehicle. In the animals that received treatment, there was reduction of the lesion size and reduction of the parasitic load. Histopathological analysis of the treatments with GA, EA, and combinations with Amph B showed circumscribed lesions with the presence of fibroblasts, granulation tissue, and collagen deposition, as well as the presence of activated macrophages. The formulations containing GA and EA activated macrophages in all evaluated parameters, resulting in the activation of cells of the innate immune response, which can generate healing and protection. GA and EA produced an associative effect with Amph B, which makes them promising for use with conventional Amph B in the treatment of cutaneous leishmaniasis.


Subject(s)
Amphotericin B , Antiprotozoal Agents , Ellagic Acid , Leishmania major , Leishmaniasis, Cutaneous , Amphotericin B/pharmacology , Amphotericin B/therapeutic use , Animals , Antiprotozoal Agents/pharmacology , Antiprotozoal Agents/therapeutic use , Ellagic Acid/pharmacology , Leishmaniasis, Cutaneous/drug therapy , Mice , Mice, Inbred BALB C
5.
Rev. enferm. UFPI ; 6(3): 37-44, jul.-set.2017. tab
Article in Portuguese | BDENF - Nursing | ID: biblio-1033941

ABSTRACT

Objetivo: identificar fatores associados à pressão arterial elevada em docentes de um Instituto Federal de Educação, ciência e Tecnologia do Piauí. Metodologia: trata-se de estudo transversal, com 150 docentes, os dados foram coletados entre março e abril de 2015, através de um questionário, seguido da verificação de pressão arterial. Para análise dos dados foram utilizados os testes de qui-quadrado e exato de Fisher. A pesquisa foi aprovada pelo comitê de ética e pesquisa, com número de CAAE: 38967414.3.0000.5209. Resultados: 25,3% dos indivíduos apresentaram níveis pressóricos altos, 65,3% eram do sexo masculino, as faixas etárias mais frequentes foram 30-39 anos (34,7%) e 40-49 anos (34,7%). Houve associação estatisticamente significativa entre a hipertensão e os fatores: sexo (p=0,0001), faixa de idade (p=0,0483), estado civil (p=0,0218), cor da pele autodeclarada (p=0,0051), cardiopatia (p=0,036), uso de bebida alcoólica (p=0,036), índice de massa corporal - IMC (p<0,05) e circunferência abdominal (p=0,004). Conclusão: foi possível identificar fatores que estão relacionados à hipertensão em docentes de um Instituto Federal do Piauí. Recomenda-se aos docentes a adequação do estilo de vida para uma melhor qualidade de vida.


Objective: to identify factors associated with high blood pressure in teachers of a Federal Institute of Education, Science and Technology of Piauí. Methodology: it is cross-sectional study. The participants of the studywere 150 teachers. The data collection period was from March to April 2015. The data collection instrument was a questionnaire followed by blood pressure check of teachers. For analysis, we used chi-square and Fisher exact tests. The study was approved by the Research Ethics Committee, with number of CAAE: 38967414.3.0000.5209. Results: 25.3% of the individuals presented high blood pressure levels, 65.3% of the teachers were male, the most frequent age groups were 30-39 years (34.7%) and 40-49 years (34.7%). There was a statistically significant association between hypertension and factors: sex (p=0.0001), age group (p=0.0483), marital status (p=0.0218), self-reported skin color (p=0.0051), heart disease (p=0.036), alcohol use (p=0.036), body mass index -BMI (p<0.05) and waist circumference (p=0.004). Conclusion: it was possible to identify factors that are related to hypertension in teachers of a Federal Institute of Piauí. It is recommended that teachers adequacy theirlifestyle for a better quality of life.


Subject(s)
Humans , Faculty , Risk Factors , Hypertension
6.
Braz. j. pharm. sci ; 52(2): 251-264, Apr.-June 2016. tab, graf
Article in English | LILACS | ID: lil-794999

ABSTRACT

ABSTRACT This study aimed to obtain and characterize a microemulsion (ME) containing phenobarbital (PB). The PB was incorporated in the proportion of 5% and 10% in a microemulsion system containing Labrasol(r), ethanol, isopropyl myristate and purified water. The physicochemical characterization was performed and the primary stability of the ME was evaluated. An analytical method was developed using spectrophotometry in UV  = 242 nm. The kinetics of the in vitro release (Franz model) of the ME and the emulsion (EM) containing PB was evaluated. The incorporation of PB into ME at concentrations of 5 and 10% did not change pH and resistance to centrifugation. There was an increase in particle size, a decrease of conductivity and a change in the refractive index in relation to placebo ME. The ME remained stable in preliminary stability tests. The analytical method proved to be specific, linear, precise, accurate and robust. Regarding the kinetics of the in vitro release, ME obtained an in vitro release profile greater than the EM containing PB. Thus, the obtained ME has a potential for future transdermal application, being able to compose a drug delivery system for the treatment of epilepsy.


RESUMO O objetivo deste trabalho foi obter e caracterizar uma microemulsão (ME) contendo fenobarbital (FEN). O FEN foi incorporado na proporção de 5% e 10% em um sistema microemulsionado composto por labrasol(r), etanol, miristato de isopropila e água purificada. Foi realizada a caracterização físico-química e avaliada a estabilidade preliminar da ME. Desenvolveu-se um método analítico por espectrofotometria em UV  = 242 nm. Foi avaliada a cinética de liberação in vitro (em modelo de Franz) da ME e da emulsão (EM) contendo FEN. A incorporação do FEN em ME nas concentrações de 5 e 10% não alterou o pH e a resistência à centrifugação. Houve aumento do tamanho da partícula, redução da condutividade e alteração do índice de refração em relação à ME placebo. A ME manteve-se estável nos ensaios de estabilidade preliminar. O método analítico demonstrou ser específico, linear, preciso, exato e robusto. Na cinética de liberação in vitro, a ME obteve um perfil de liberação in vitro superior a EM contendo FEN. Desta forma, a ME obtida tem potencial para uma futura aplicação transdérmica, podendo compor um sistema de liberação de fármacos para tratamento da epilepsia.


Subject(s)
Phenobarbital/pharmacokinetics , Emulsions/analysis , Quality Control , Spectrophotometry, Ultraviolet/methods , Kinetics , Nanotechnology/methods , Drug Liberation/drug effects
7.
Pharmacol Biochem Behav ; 131: 6-12, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25620677

ABSTRACT

This study aimed to evaluate a microemulsion system (ME) containing phenobarbital in epilepsy model induced by pilocarpine in rats and to oxidative stress and histologic lesions in hippocampus. The microemulsion was applied to the shaved back of Wistar rats. The animals were divided into the following groups: control group (P400); ME50 40mg/kg, topically-t.p.; ME100, 40mg/kg, t.p.; EM50, 40mg/kg, t.p.; phenobarbital solution 40mg/kg (PS), oral. After 60min, behavioral changes were evaluated for 1h in the model of epileptical crisis induced by pilocarpine. Phenobarbital in microemulsion was able to increase the latency for status epilepticus (SE) (p<0.05), decrease the number of epileptical crisis (ME50: p<0.001; ME100: p<0.01) and decrease mortality rate by 80% compared to P400. In EM50 and PS groups, deaths were decreased by 53.3% and 100% respectively. The ME50 and ME100 groups were able to reduce oxidative stress in experimental animals when compared to the P400. The microemulsion was still capable of reducing neuronal damage in the hippocampal areas. The results of this study come in an innovative way, demonstrating the ability of transdermal ME50 and ME100 to reduce pilocarpine-induced epileptical crisis, oxidative stress, besides neuronal damages.


Subject(s)
Anticonvulsants/administration & dosage , Antioxidants/administration & dosage , Phenobarbital/administration & dosage , Pilocarpine/pharmacology , Seizures/drug therapy , Administration, Cutaneous , Animals , Anticonvulsants/therapeutic use , Antioxidants/therapeutic use , Disease Models, Animal , Emulsions/administration & dosage , Female , Hippocampus/drug effects , Lipid Peroxidation/drug effects , Oxidative Stress/drug effects , Phenobarbital/therapeutic use , Rats , Rats, Wistar , Seizures/chemically induced
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