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1.
Braz. J. Pharm. Sci. (Online) ; 58: e20114, 2022. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1403742

RESUMEN

Abstract Curcumin, contained at Turmeric (Curcumalonga), can exert many beneficial pleiotropic activities in the gastrointestinal tract. This study evaluated the antioxidant and anti-inflammatory activity of C. longa on 5-fluorouracil (5-FU)-induced oral mucositis (OM) in hamsters. Phytochemical analysis of crude C. longa extract (CLE) was performed to detect the presence of curcumin by TLC and HPLC. Golden Syrian hamsters were orally pre-treated with CLE (5, 50, or 100mg/kg). Cheek pouch samples were subjected to macroscopic and histopathological evaluation. ELISA was performed to quantify the inflammatory cytokines IL-1ß and TNF-α. Superoxide dismutase (SOD), glutathione (GSH) and malondialdehyde (MDA) levels were assessed by ultraviolet-visible spectroscopy analysis. Behavior analysis was conducted by the open field test. Curcumin content in the CLE was 0.55%m/m ± 0.0161 (2.84%). The group treated with 5mg/kg CLE showed healing evidence with macroscopic absence of ulceration (p<0.05) and microscopic aspect of re-epithelialization, discrete inflammatory infiltrate and absence of edema. Treatment with 5mg/kg CLE significantly increased GSH levels, and reduced MDA levels and SOD activity (p˂0.05), and decreased IL-1ß (p˂0.05) and TNF-α (p˂0.01) levels. A significant reduction in walking distance, ambulation, speed, and rearing was observed for motor activity. Curcumin reduced oxidative stress, inflammation, and motor activity in hamsters with 5-FU-induced OM.


Asunto(s)
Animales , Masculino , Ratas , Estomatitis/patología , Curcumina/análisis , Curcuma/clasificación , Cromatografía Líquida de Alta Presión/métodos , Fitoquímicos/agonistas , Fluorouracilo/administración & dosificación , Inflamación/complicaciones , Antioxidantes/clasificación
2.
Braz. J. Pharm. Sci. (Online) ; 56: e18456, 2020. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1249172

RESUMEN

The aim of this study was evaluate the in vitro antifungal activity of crude extracts from Eugenia uniflora, Libidibia ferrea and Psidium guajava. The extracts were obtained by turbo-extraction using water (AQ) or acetone-water (AC-W) (7:3, v/v) as solvents and lyophilized to obtain the crude extracts (CE). The CE were characterized by UV-Vis, TLC and HPLC. The activity of CEs was investigated against clinical isolates of Candida spp. and the Minimum Inhibitory Concentration (MIC), MIC50 and MIC90 were determinated. The analysis by TLC showed that all CEs presented polyphenols (flavonoids and tannins). The CEs from E. uniflora showed higher amount of polyphenols (30.35 ± 2.15%, AC-W) and the HPLC analysis revealed the tannins in all extracts. The CEs of E. uniflora showed MIC range from 1.9 to 500.0 µg/mL, and lower values of MIC50 and MIC90 against non-albicans Candida isolates. Regarding L. ferrea and P. guajava, the results showing MIC from 3.9 to 1000.0 µg/mL (CE-AQ) against C. albicans. The results demonstrate antifungal performance from CE against various species of Candida spp., suggesting that the herbal species may be use as new potential antifungal agents. Additionally, the polyphenol content can play a pivotal role in the antifungal properties of CE.


Asunto(s)
Técnicas In Vitro/métodos , Extractos Vegetales/efectos adversos , Polifenoles/análisis , Fitoquímicos , Antifúngicos/administración & dosificación , Flavonoides/farmacocinética , Pruebas de Sensibilidad Microbiana/métodos , Cromatografía Líquida de Alta Presión/métodos
3.
Braz. arch. biol. technol ; 61: e18170586, 2018. tab, graf
Artículo en Inglés | LILACS | ID: biblio-974067

RESUMEN

ABSTRACT The stem bark and pods of "jucá" are widely used in Brazilian folk medicine and, despite their therapeutic relevancies, there are insufficient reports about their quality control. Both herbal drugs from the species are rich in tannins, which showed a lot of biological and economic interest. Thus, the purpose of this study was to evaluate the method for quantification of tannins in the stem bark and pods from L. ferrea. The performance of the method was tested against the influence of the most relevant parameters (reaction time; amount of drug; type and amount of precipitationagents; and, concentration of the reagents). The procedure was validated according to the literature. After optimization, the experimental conditions were established as: 30 min of reaction; λ of 760 nm; 1.0 mL of Folin-Ciocalteu; 29% of Na2CO3 (w/v); and, skin powder as complexion agent. The method validation showed that the instrumental response was linear and sensitive to the investigated analyte. The method presented the necessary precision (RSD < 2.19%) and accuracy (96.84%-109.13%), as recommended by the official codex. Moreover, the deliberate introduction of experimental variations showed the stability of the procedure error against external sources (RSD < 2.42%). In conclusion, the data demonstrated the suitability of the method and can be used as anappropriate analytical tool for quality control of herbal drugs from L. ferrea.

4.
Braz. J. Pharm. Sci. (Online) ; 54(4): e17720, 2018. tab, graf
Artículo en Inglés | LILACS | ID: biblio-1001580

RESUMEN

The purpose of this study was to evaluate the safety of Kalanchoe brasiliensis extract, followed by the development of an oil in water emulsion containing the K. brasiliensis leaves extract and evaluating its clinical moisturizing efficacy. The formulations containing sodium acrylates/ Beheneth-25 methacrylate Crosspolymer (and) hydrogenated polydecene (and) lauryl glucoside and 0.5% of extract were prepared. The extract was considered as non-irritating through skin irritant tests. The stability testing was carried out in different conditions for 90 days. The skin hydration was measured by capacitance measurement and transepidermal water loss using biophysical techniques. The results indicate that the formulation containing 0.5% of extract increased the hydration of the stratum corneum up to 5 h after application on the forearm. The transepidermal water loss was reduced when compared to the untreated area and placebo area. Therefore, we can conclude that the increased skin hydration and protection of barrier function can be attributed to the K. brasiliensis extract. This research presents a new raw material from the Brazilian Caatinga biome and shows its possible application in the development of cosmetic products.


Asunto(s)
Agentes Mojantes/farmacología , Kalanchoe/anatomía & histología , Emulsiones , Extractos Vegetales/efectos adversos , Estabilidad de Cosméticos
5.
Artículo en Portugués | LILACS | ID: lil-691778

RESUMEN

O Diabetes mellitus, por tratar-se de uma doença crônica e por apresentar um crescimento acentuado na sociedade brasileira, tornou-se alvo da comunidade científica na busca de novas alternativas terapêuticas. Diversos estudos estão sendo desenvolvidos com o objetivo de comprovar as aparentes propriedades farmacológicas de espécies vegetais empregadas no tratamento desta enfermidade. Sendo assim, a Bauhinia forficata Link, comumente conhecida como pata-de-vaca, figura entre as espécies mais utilizadas para esse fim. Dentre os representantes de Bauhinia, a que apresenta maior número de estudos referentes à atividade hipoglicemiante e antidiabética é a espécie referida. Isto, pois, devido as suas atividades farmacológicas, diversos estudos relatam seus aspectos botânicos, composição química e eficácia. Esse constante interesse em seu estudo se mostra imperioso para sua utilização de forma segura e eficaz, possibilitando o desenvolvimento de formas farmacêuticas para o tratamento de diabetes.


Diabetes mellitus is a chronic disease with an ever-increasing incidence in Brazil and has become the object of scientific research into the search for novel therapeutic alternatives. A number of studies have been developed to demonstrate the pharmacological properties of plant species employed in folk medicine for the treatment of this disease. One such plant is the Brazilian white orchid tree, Bauhinia forficate Link, known locally as pata-de-vaca [cow foot]. Among representatives of the genus Bauhinia, this species has the greatest number of studies addressing its botanical aspects, chemical composition and effectiveness in terms of hypoglycemic and anti-diabetic activity. Studies on this plant are important to the safe, effective development of pharmaceutical products for the treatment of diabetes.


Asunto(s)
Diabetes Mellitus , Fabaceae , Medicamento Fitoterápico , Plantas Medicinales
6.
Artículo en Portugués | LILACS | ID: lil-655407

RESUMEN

Folhas da espécie vegetal Bauhinia forficata Link, popularmente conhecida como pata de vaca, apresentam amplo potencial terapêutico no tratamento do diabetes mellitus. Amostras desta espécie vegetal, obtidas em duas regiões do Brasil (Minas Gerais e Paraná), foram submetidas à caracterização fitoquímica e físico-química (granulometria, perda por dessecação, teor de cinzas e teor de extrativos) para realização de um estudo comparativo entre indivíduos cultivados em regiões distintas, bem como estabelecimento de especificações para seu controle de qualidade. Para a caracterização fitoquímica, extratos metanólicos das amostras foram avaliados através de cromatografia de camada delgada (CCD) para pesquisa das principais classes de metabolitos secundários. Enquanto que, para as análises físico-químicas foram adotadas metodologias farmacopeicas. A análise estatística dos dados realizou-se através dos testes F de Fischer e t de Student. De acordo com a avaliação fitoquímica foi possível observar um perfil similar para ambas as amostras com presença dos seguintes grupos: flavonóides, proantocianidinas, leucoantocianidinas, triterpenos, esteróides, açúcares redutores, além de substâncias antioxidantes com bandas coincidentes às dos compostos flavonoídicos. Por outro lado, as amostras apresentaram algumas propriedades físico-químicas diferentes tais como granulometria e umidade residual em virtude da origem e do processamento adotados pelos fornecedores. Já os valores do teor de cinzas mostraram-se dentro das especificações e não foi observada diferença significativa para o teor de extrativos. Os resultados obtidos neste trabalho contribuíram no processo de identificação e padronização de parâmetros de qualidade para as folhas de B. forficata.


Leaves of the plant species Bauhinia forficata Link, popularly known as pata de vaca, have broad therapeutic potential in treating diabetes mellitus. Aiming to establish specifications for quality control of the specie, samples of plant material obtained from two regions of Brazil (Minas Gerais and Paraná), were subjected to phytochemical and physicochemical characterization (grain size, loss on drying, ash content and extractives). For phytochemical characterization, methanolic extracts of samples were evaluated by thin layer chromatography (TLC) to search the main classes of secondary metabolites. While for the physicochemical analyses were followed Pharmacopoeic procedures. The statistical analysis was performed using the Fisher F test and Student t test. According to phytochemical evaluation was observed one similar profile for both samples with the presence of following groups: flavonoids, proanthocyanidins, leucoanthocyanidins, triterpenes, steroids, sugars, and antioxidants with similar bands of flavonoid compounds. On the other hand, the samples showed some different physicochemical properties such as particle size and content residual moisture because of the origin and processing adopted by suppliers. In turn the values of ash showed to be within specifications and there was no significant difference in the extractive content. The results of this work contributed to the process of identification and standardization of quality parameters for the leaves of B. forficata


Asunto(s)
Bauhinia , Medicamento Fitoterápico , Brasil , Plantas Medicinales
7.
Rev. ciênc. méd., (Campinas) ; 21(1/6): 87-93, 2012. tab, ilus
Artículo en Portugués | LILACS | ID: lil-691084

RESUMEN

Objetivo: Este trabalho objetivou realizar um estudo comparativo de controle de qualidade entre a suspensão de referência de naproxeno sódico, Flanax®, denominada R, e suspensões obtidas de seis farmácias de manipulação na cidade de Natal, Rio Grande do Norte, denominadas A, B, C, D, E e F, com concentrações de 25mg/mL. Realizaram-se ensaios para determinação do teor, pH, homogeneidade, identificação, volume e características organolépticas.Métodos: O método utilizado para o doseamento mostrou precisão, exatidão, linearidade e especificidade.Resultados: As formulações obtidas nas farmácias B, C e E apresentaram teor abaixo das especificações farmacopeicas, enquanto a formulação F apresentou um teor acima do recomendado. Em relação ao pH, as suspensões C, E e F apresentaram valores fora das especificações. Quanto à homogeneidade, as amostras obtidas das farmácias C e E foram reprovadas. Observou-se que a maioria das amostras apresentou volume compatível ao rotulado, exceto a amostra C. Conclusão: Os resultados indicaram a necessidade de uma maior fiscalização pelos órgãos competentes, de forma a garantir a segurança do paciente e a qualidade dos medicamentos produzidos pelas farmácias de manipulação


Asunto(s)
Cromatografía Líquida de Alta Presión , Naproxeno , Preparaciones Farmacéuticas , Control de Calidad , Suspensiones
8.
Braz. j. pharm. sci ; 46(3): 509-513, July-Sept. 2010. tab
Artículo en Inglés | LILACS | ID: lil-564917

RESUMEN

The aim of this study was to evaluate the quality of five different solid formulations of carbamazepine. The reference formulation was Tegretol® 200.00 mg (Novartis) and the others were: generic formulation of carbamazepine 200.00 mg (National Industry), similar formulation of carbamazepine 200.00 mg (National Industry), and two formulations of carbamazepine 200.00 mg acquired from two different compounding pharmacies. The latter consisted of capsules obtained in Natal, the capital city of the Brazilian State of Rio Grande do Norte. The quality of samples was evaluated through physical and physical-chemical tests, including: weight, diameter, thickness, content, dissolution, disintegration, hardness, friability and moisture. The results of friability analysis showed that all formulations met Brazilian and United States Pharmacopeia (USP) specifications. In spite of having a higher hardness compared to the reference, the generic formulation had a lower disintegration time. This could be associated to the presence of crospovidone in its formulation. Results of this study showed that all formulations had dissolutions which were in accordance with Brazilian Pharmacopoeia specifications, and quality control tests. An exception was found for the similar formulation, which had a hardness parameter that exceeded the USP standard. However, this difference was not significant given the similar formulation's satisfactory disintegration time.


O objetivo desse trabalho foi avaliar a qualidade de cinco formulações de carbamazepina na dosagem de 200,00 mg: medicamento referência Tegretol® (Novartis), medicamento genérico (indústria nacional), medicamento similar (indústria nacional) e cápsulas do mesmo medicamento obtidas de duas farmácias de manipulação da cidade do Natal, RN. Os ensaios realizados foram: peso médio, diâmetro, espessura, teor, dissolução, desintegração, dureza, friabilidade e umidade. Foi observado que nenhuma das amostras analisadas apresentou friabilidade superior ao limite máximo determinado pela Farmacopéia Americana (1,5 por cento). O medicamento genérico, apesar de apresentar dureza superior em relação ao medicamento de referência, desintegrou em menor tempo, o que pode estar relacionado à crospovidona presente na formulação. As amostras analisadas atenderam às especificações da Farmacopéia Brasileira no que diz respeito à dissolução. Em geral, os resultados das amostras A, B, C, D e E foram considerados satisfatórios uma vez que atenderam as especificações farmacopéicas. Embora a apresentação similar não tenha atendido ao padrão USP no que diz respeito à dureza, esse dado não se mostrou significativo, uma vez que o tempo de desintegração foi satisfatório.


Asunto(s)
Carbamazepina/farmacología , Diagnóstico/métodos , Química Farmacéutica , Medicamentos Genéricos/uso terapéutico
9.
Braz. arch. biol. technol ; 52(3): 647-652, May-June 2009. ilus, tab
Artículo en Inglés | LILACS | ID: lil-520917

RESUMEN

The purpose of this study was to evaluate the influences from variables of preparation on dry residue and total tannins from macerates of Astronium urundeuva barks. Thus, a 3 ² factorial design was used to study the importance of plant proportion (10, 15 and 20 percent, w/v) and the ethanol concentration (40, 60 and 80 percent, v/v) on the selected response. Mathematical models were fitted according to experimental data. The validated equations were used to generate response surfaces. The analysis of the surfaces showed that the optimum conditions to obtain extractive preparations with high extractive efficiency for tannins were: 10 percent (w/v) of plant with ethanol 40 percent (v/v) as solvent.


O objetivo deste trabalho foi avaliar as influências de variáveis de preparação de macerados das cascas de Astronium urundeuva sobre resíduo seco e teor de taninos totais. Desta forma, um desenho fatorial do tipo 3² foi empregado para avaliar a importância da proporção de planta (10, 15 e 20 por cento; m/v) e da concentração de etanol (40, 60 e 80 por cento; v/v) sobre as respostas eleitas. Modelos matemáticos foram ajustados aos dados experimentais. As equações validadas foram usadas para gerar superfícies de respostas. A análise das superfícies demonstrou que as condições ótimas para obtenção de preparações extrativas com elevada eficiência extrativa de taninos foram: 10 por cento (m/v) para planta e etanol 40 por cento (v/v) como solvente.

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