Green tea in transdermal formulation: HPLC method for quality control and in vitro drug release assays

RP-HPLC based analytical method for use in both quality control of green tea in a semisolid formulation and for in vitro drug release assays was developed and validated. The method was precise (CV < 5%), accurate (recovery between 98% and 102%), linear (R² &gt; 0.99), robust, and specific for the determination of epigallocatechin 3-gallate (EGCG), caffeine (CAF), and gallic acid (GA). In a diffusion cell chamber, the release rate of EGCG was 8896.01 µg cm-2. This data showed that EGCG will be able to exert its systemic activity when delivered though the transdermal formulation, due to its good flux rates with the synthetic membrane.

Bibliographic Details

Main Authors:	Alves,Michele Campos, Almeida,Priscila Aparecida de, Polonini,Hudson Caetano, Raposo,Nádia Rezende Barbosa, Ferreira,Anderson de Oliveira, Brandão,Marcos Antônio Fernandes
Format:	Digital revista
Language:	English
Published:	Sociedade Brasileira de Química 2014
Online Access:	http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422014000400024
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