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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id-langga.887012019-10-10T02:32:55Z http://repository.unair.ac.id/88701/ PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata RETNO IKAYANTI, 051514153013 RM300-666 Drugs and their actions 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%. 2019 Thesis NonPeerReviewed text id http://repository.unair.ac.id/88701/1/TF.%2021-19%20Ika%20p%20abstrak.pdf text id http://repository.unair.ac.id/88701/2/TF.%2021-19%20Ika%20p%20daftar%20isi.pdf text id http://repository.unair.ac.id/88701/3/TF.%2021-19%20Ika%20p%20daftar%20pustaka.pdf text id http://repository.unair.ac.id/88701/4/TF.%2021-19%20Ika%20p.pdf RETNO IKAYANTI, 051514153013 (2019) PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata. Thesis thesis, Universitas Airlangga. http://lib.unair.ac.id |
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RM300-666 Drugs and their actions RETNO IKAYANTI, 051514153013 PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata |
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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%. |
format |
Theses and Dissertations NonPeerReviewed |
author |
RETNO IKAYANTI, 051514153013 |
author_facet |
RETNO IKAYANTI, 051514153013 |
author_sort |
RETNO IKAYANTI, 051514153013 |
title |
PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata |
title_short |
PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata |
title_full |
PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata |
title_fullStr |
PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata |
title_full_unstemmed |
PENGEMBANGAN DAN VALIDASI METODE KLTKT-DENSITOMETRI UNTUK PENETAPAN KADAR ANDROGRAFOLIDA DALAM FRAKSI ETIL ASETAT DAN SEDIAAN TABLET Andrographis paniculata |
title_sort |
pengembangan dan validasi metode kltkt-densitometri untuk penetapan kadar andrografolida dalam fraksi etil asetat dan sediaan tablet andrographis paniculata |
publishDate |
2019 |
url |
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 |
_version_ |
1681152549788319744 |