Ensaios toxicológicos dermais, pré-clínicos e clínicos fase i, com o hidrogel do extrato alcoólico das cascas do caule de anacardium occidentale linn.

• Ano de defesa: 2011
• Autor(a) principal: Cunha, Mônica Lorena Dias Meirelles da
• Tipo de documento: Dissertação
• Tipo de acesso: Acesso aberto
• Idioma: por
• Instituição de defesa: Universidade Federal da Paraí­ba; BR; Farmacologia; Programa de Pós-Graduação em Produtos Naturais e Sintéticos Bioativos; UFPB
• Palavras-chave em Português: Anacardium occidentale Linn; Ensaios toxicológicos dermais pré-clínicos e clínicos fase I; Dermal toxicity tests; Preclinical and clinical phase I; CIENCIAS BIOLOGICAS::FARMACOLOGIA
• Link de acesso: https://repositorio.ufpb.br/jspui/handle/tede/6864

The study aimed to perform toxicological tests and preclinical dermal clinical phase I, the hydrogel obtained from the hydroalcoholic extract from the bark of Anacardium occidentale Linn. The dermal preclinical studies have assessed the primary irritation of the skin - acute (single dose) and acute eye irritation (single dose) and in both experiments were used rabbits albino, New Zealand, healthy adults, numbering 12, with 6 males and 6 females (control and treated) for a dose of 0.5 g of the hydrogel obtained from the alcoholic extract of Anacardium occidentale Linn. The evaluation of primary irritation of the skin demonstrated that the hydrogel from the stem bark of Anacardium occidentale Linn is not irritating to the skin of rabbits tested in our laboratory, since only 25% of the rabbits showed barely perceptible erythema in the initial phase of the experiment (first time), and no degree of swelling was observed in rabbits throughout the experiment. In relation to the simple eye irritation, the hydrogel from the stem bark of Anacardium occidentale Linn also did not showed irritant effect, because only 33,3% and 8,3% rabbits showed, respectively, conjunctival redness and swelling in the first 24 hours after application of test substance. Did not present any change in level of the iris and cornea, in any animal throughout the experiment. To investigate the clinical phase I toxicity in humans, hydrogel from the stem bark of Anacardium occidentale Linn, we selected 28 volunteers, clinically healthy, aged between 18 and 25. Study participants were divided into two groups, male and female, with 14 participants each, and treated daily, on the night shift, via dermal, with the hydrogel from the stem bark of Anacardium occidentale Linn by a period of 4 weeks. The volunteers were tested before the start of the study and eight weeks after the study, haematological (CBC) and biochemical (glucose, urea, creatinine, total cholesterol, AST, ALT, alkaline phosphatase), in order to detect possible changes arising from the use of hydrogel in patients, as well as compare the results before and after the study. There was no evidence values changed for both hematology and for biochemical variables between times and groups. During treatment with the hydrogel from the stem bark of Anacardium occidentale Linn, Some adverse reactions were observed in participants: tingling, redness, and stinging, but the number of volunteers affected was small, and the reported symptoms occurred during the first weeks of the study and did not require specific treatment and disappeared spontaneously. Only 3,5% of the female volunteers reported feeling oily skin in three weeks of the study. In contrast, 10,7% (first week) and 3,5% (second week) of male volunteers reported skin feeling soft, "cleaner". These results suggest and the low toxicity of the product and indicate that this herbal formulation can be used by the population, the dose and route of administration tested.