VALIDASI METODE ANALISA PENETAPAN KADAR EPIGALOKATEKIN GALAT DENGAN KROMATOGRAFI CAIR KINERJA TINGGI

Authors

  • Nining Sugihartini
  • Achmad Fudholi
  • Suwidjiyo Pramono
  • Sismindari Sismindari

DOI:

https://doi.org/10.12928/pharmaciana.v4i2.1567

Keywords:

Epigallocatechin gallate, Validation, HPLC

Abstract

High Performance Liquid Chromatography (HPLC) was one of analytical methods
commonly used to determine the concentration of epigallocatechin gallate (EGCG) on green tea
extract. The method must be validated in order to fit to its purpose. The aim of this research was to
prove that the used method has selectifity, liniearity, precise, accurate and know limit of detection
(LOD) and limit of quantification (LOQ) is acceptable. The selectivity of analytical method was
determined by calculating the resolution value between two peak. Data from 10 μg/mL and
100 μg/mL with 5 replicates would give precition and accuration. Precition was known from CV
value and accuration was known from recovery value in each concentration. Liniearity was known
from regression linear between concentration and wide area of peak. From regresion linear could
calculate LOD and LOQ. Research show that method of analyse have selectificity with
Rs= 2.27>1.5; liniearity with r= 0.99; precision with CV 8.74% at concentration 200 µg/mL and
3.74% at concentration 500 µg/mL; accuration with recovery 99.76% at concentration 200 µg/mL
and 100.52% at concentration 500 µg/mL and the value of LOD is 33.28 μg/mL and LOQ is
110.93 μg/mL.

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Published

2014-11-01

Issue

Vol. 4 No. 2 (2014): Pharmaciana

Section

Analytical Pharmacy and Medicinal Chemistry

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