2005
DOI: 10.1590/s1516-93322005000400007
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Avaliação biofarmacotécnica in vitro de formas farmacêuticas sólidas contendo doxiciclina

Abstract: INTRODUÇÃOA absorção de fármacos, a partir de formas farmacêuticas sólidas administradas por via oral, depende de sua liberação e dissolução nas condições fisiológicas e permeabilidade das membranas biológicas que necessitam transpor (Brasil, 2003c; United States, 1997). Com base nestas considerações, pode-se afirmar que a dissolução in vitro é uma etapa relevante para prever o desempenho in vivo do medicamento.

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“…The tablets kinetics of release from SSBI, SSBIII and reference medicine, Rochagan TM , follows the method used for dissolution tests, being the times of collection 10, 30, 45, 60 and 120 minutes. The results were used to calculate the dissolution efficacy (DE) and later compared with the variance analysis (ANOVA) (Aguiar et al, 2005;Anderson et al, 1998;Khan, 1975;Khan, Rhodes, 1972).…”
Section: Kinetic Of In Vitro Releasementioning
confidence: 99%
“…The tablets kinetics of release from SSBI, SSBIII and reference medicine, Rochagan TM , follows the method used for dissolution tests, being the times of collection 10, 30, 45, 60 and 120 minutes. The results were used to calculate the dissolution efficacy (DE) and later compared with the variance analysis (ANOVA) (Aguiar et al, 2005;Anderson et al, 1998;Khan, 1975;Khan, Rhodes, 1972).…”
Section: Kinetic Of In Vitro Releasementioning
confidence: 99%