PENGEMBANGAN DAN VALIDASI METODE KCKT UNTUK ANALISIS MORAKHALKON A DALAM PLASMA DARAH KELINCI IN VITRO

Artocarpus champeden ethanol extract has been reported as antimalarial and prospect to developed as phytomedicine products which morachalcone A was determined as it’s active marker compund. To support the development of phytomedicine products from Artocarpus champeden especially in bioavailability a...

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Bibliographic Details
Main Author: MICHAEL RAHARJA GANI, 051414153024
Format: Theses and Dissertations NonPeerReviewed
Language:English
English
Published: 2017
Subjects:
Online Access:http://repository.unair.ac.id/66414/1/abstrak.pdf
http://repository.unair.ac.id/66414/2/Tesis%20Michael%20Raharja%20Gani.pdf
http://repository.unair.ac.id/66414/
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Institution: Universitas Airlangga
Language: English
English
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Summary:Artocarpus champeden ethanol extract has been reported as antimalarial and prospect to developed as phytomedicine products which morachalcone A was determined as it’s active marker compund. To support the development of phytomedicine products from Artocarpus champeden especially in bioavailability and clinical study, a selective and sensitive analytical method becomes important for the determination of morachalcone A in blood plasma. The aim of this study was to develop and validate selectivity and sensitivity of HPLC method for determination of morachalcone A in rabbit plasma. This method was performed using a RP-C18 Column (250 x 4.6 mm i.d., 5 μm parcticle size), under isocratic elution with acetonitrile : water (50:50 v/v), detection was carried out at 368 nm and analyses were run at a flow rate of 1,0 mL/min, 4-hydroxychalcone and methanol were used as internal standard and precipitate agent. The results showed that this method was selective and good linearity in range of 3096,774-154.839 ng/mL for morachalcone A in rabbit plasma. LOD and LLOQ were found 89.384 and 154.839 ng/mL, respectively. The mean difference method was found between 2,79-14.33%. The intra-day and inter-day precision were both lower than 15% and recovery from extraction method from morachalcone A and Internal Standard were 80-120%.