PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata

Andrographolide is the major active compound of Andrographis paniculata and determined as marker compund of ethyl acetate fractions of A. paniculata products. This fraction has a potential activity as antimalarial and prospective to be developed as phytopharmaceutical products. To ensure the quality...

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Bibliographic Details
Main Author: RETNO IKAYANTI, 051514153013
Format: Theses and Dissertations NonPeerReviewed
Language:Indonesian
Indonesian
Indonesian
Indonesian
Published: 2019
Subjects:
Online Access:http://repository.unair.ac.id/88701/1/TF.%2021-19%20Ika%20p%20abstrak.pdf
http://repository.unair.ac.id/88701/2/TF.%2021-19%20Ika%20p%20daftar%20isi.pdf
http://repository.unair.ac.id/88701/3/TF.%2021-19%20Ika%20p%20daftar%20pustaka.pdf
http://repository.unair.ac.id/88701/4/TF.%2021-19%20Ika%20p.pdf
http://repository.unair.ac.id/88701/
http://lib.unair.ac.id
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Institution: Universitas Airlangga
Language: Indonesian
Indonesian
Indonesian
Indonesian
Description
Summary:Andrographolide is the major active compound of Andrographis paniculata and determined as marker compund of ethyl acetate fractions of A. paniculata products. This fraction has a potential activity as antimalarial and prospective to be developed as phytopharmaceutical products. To ensure the quality, efficacy and safety of the phytopharmaceutical products, a rapid and selective analytical method becomes important for the determination of andrographolide in both the raw materials and products. The purpose of this study was to develop and validate a rapid, inexpensive, and selective High Performance Thin Layer Chromatography (HPTLC) for quantification andrographolide in raw material and tablet ethyl acetate fractions of A. paniculata. This method was performed using silica gel G60 F254 HPTLC plate as stationary phase with mobile phase of chloroform:metanol (90:10 v/v) and detected at 228 nm. The validated method was selective to separate andrographolide from other component with good resolution and retention factor andrographolide was 0.38 ±0.03. The data for calibration plots showed good linear relationship with r2 = 0.998 in the concentration range 67.5-225.0 ppm. The Limit of Detection and Quantification were found 9.6 ng/spot and 28.8 ng/spot, respectively. The recovery method was found between 98.0 and 100.5% and the relative standard deviation method was found between 1.4% and 1.5%.