Tecnologias de produção e controle de qualidade da matéria-prima vegetal, obtida a partir das folhas de Poincianella pyramidalis (TUL.) L. P. QUEIROZ

Detalhes bibliográficos
Ano de defesa: 2017
Autor(a) principal: Oliveira, Agna Hélia de
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal da Paraíba
Brasil
Farmacologia
Programa de Pós-Graduação em Desenvolvimento e Inovação Tecnológica em Medicamentos
UFPB
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: https://repositorio.ufpb.br/jspui/handle/123456789/11240
Resumo: Poincianella pyramidalis (Tul.) L. P. QUEIROZ is an endemic species of the caatinga biome, popularly known as "catingueira". Used in traditional medicine for the treatment of gastritis, colic, diarrhea, asthma, bronchitis, diabetes, inflammation, besides presenting cicatrizant activity. Due to this variety of medicinal uses, the species has great potential for the development of a herbal medicine. The present work had as main objectives, to standardize dry extracts, obtained by the sprinkling process, to develop and validate analytical methodology by HPLC for quantification of canferol and quercetin and to carry out an accelerated stability study of binary mixtures of dry extract with different pharmaceutical excipients. Dry extracts were obtained by spraying in Mini Spray Dryer, LabPlant, SD-05, employing the following operating parameters: air inlet temperature (160, 170 and 180 ° C), feed flow rate (4, 6 and 8 mL / min) and drying adjuvant ratio colloidal silicon dioxide (10, 15 and 20%). A 23+1 factorial design associated with MSR was applied to evaluate the effects of the process parameters on canferol and quercetin contents and to define the best operating conditions (T = 160ºC, TF = 4mL / min and% of drying adjuvant = 10 %). The simultaneous quantification of the two flavonoids was performed by HPLC in the following chromatographic conditions: ? = 370 nm, methanol: 1% phosphoric acid (47:53 v / v), pH = 3.1, 1.2 mL flow / min and Phenomenex® C18 column (250 mm x 4.6 mm x 5µ). The accelerated stability study of the binary mixtures (1: 1) of the dry extract with microcrystalline cellulose, maltodextrin, starch and lactose was carried out in a B.O.D incubator under temperature control for 180 days at a temperature of 40 ± 2 ° C. The results obtained showed that the levels of canferol and quercetin were significantly affected by the process conditions. The analytical method was linear in the range of 0.4-7.6 µg / mL for both analytes, R2 = 0.9999 and 0.9996, for canferol and quercetin, respectively. The biomarkers presented better stability in the mixtures with starch and different degradation kinetics for each excipient studied.