Abstract

Abstract
 Objective: Mangosteen rind (Garcinia mangostana L.) contains secondary metabolites, namely alpha-mangostin which has
 antioxidant activity, as well as antibacterial and anti-aging properties. In order to obtain a maximum amount of alpha-mangostin
 compounds, the maceration method using ethyl acetate was used. To ensure the effectiveness of the mangosteen rind extraction
 process, all of the processes and methods in preparing the extract should be properly controlled, particularly the analytical
 method used in determining the alpha-mangostin level of the extract. The method used should be able to determine the alphamangosteen
 level accurately. This study aimed to test the validation of the analytical method used.
 Method: The parameters for the validation of the analytical method tested in this study include accuracy, precision, range and
 linearity, limit of detection (LOD), limit of quantitation (LOQ) and specificity. In this study, the level of alpha-mangostin in the
 extract was determined using TLC-Spectrodensitometry with the stationary phase of the silica gel plate GF 254 and the mobile
 phase of chloroform and methanol (10:0.1 v/v).
 Result: The results of the study showed that this method has met the acceptance criteria for validation with the accuracy value in
 the range of percent recovery, from 93.85 % to 111.16%; precision with KV <2%; specification with spectrum correlation >0.99;
 linearity with r =0,99372; limit of detection (LOD) of 5.33 ng and limit of quantitation (LOQ) of 11.43 ng.

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