Tesis
Desenvolvimento e validação de método analítico para determinação de teor de ácido gálico e catequina no fitoterápico sanativo® por cromatografia líquida de alta eficiência
Date
2012-02-27Registration in:
BEZERRA, Beatriz Pinheiro. Desenvolvimento e validação de método analítico para determinação de teor de ácido gálico e catequina no fitoterápico sanativo® por cromatografia líquida de alta eficiência. 2012. 140 f. Dissertação (Mestrado em Bioanálises e Medicamentos) - Universidade Federal do Rio Grande do Norte, Natal, 2012.
Author
Bezerra, Beatriz Pinheiro
Institutions
Abstract
The herbal medicine Sanativo® is produced by the Pernambucano Laboratory
since 1888 with indications of healing and hemostasis. It is composed of a fluid
extract about Piptadenia colubrina, Schinus terebinthifolius, Cereus peruvianus and
Physalis angulata. Among the plants in their composition, S. terebinthifolius and P.
colubrina have in common phenolic compounds which are assigned most of its
pharmacological effects. The tannins, gallic acid and catechin were selected as
markers for quality control. The aim of this study was the development and validation
of analytical method by HPLC/UV/DAD for the separation and simultaneous
quantification of gallic acid (GAC) and catechin (CTQ) in Sanativo®. The
chromatographic system was to stationary phase, C-18 RP column, 4,6 x 150 mm (5
mm) under a temperature of 35 ° C, detection at 270 and 210 nm. The mobile phase
consisted of 0.05% trifluoroacetic acid and methanol in the proportions 88:12 (v/v), a
flow rate of 1 ml/min. The analytical method presented a retention factor of 0.30 and
1.36, tail factor of 1.8 and 1.63 for gallic acid and catechin, respectively, resolution of
18.2, and theoretical plates above 2000. The method validation parameters met the
requirements of Resolution n º 899 of May 29, 2003, ANVISA. The correlation
coefficient of linear regression analysis for GAC and CTQ from the standard solution
was 0.9958 and 0.9973 and when performed from the Sanativo® 0.9973 and 0.9936,
the matrix does not interfere in the range 70 to 110 %. The limits of detection and
quantification for GAC and CQT were 3.25 and 0.863, and 9.57 and 2.55 mg/mL,
respectively. The markers, GAC and CQT, showed repetibility (coefficient of variation
of 0.94 % and 2.36 %) and satisfactory recovery (100.02 ± 1.11 % and 101.32 ± 1.36
%). The method has been characterized selective and robust quantification of GAC
and CTQ in the Sanativo® and was considered validated