Abstract
A quantitative hplc method for the simultaneous determination of lanatoside C and digoxin in Digitalis lanata was developed. The extract of dry leaf powder with 50% MeOH was applied to a Sep-PakC 18 cartridge prior to hplc analysis. The analysis was performed on an octylsilyl bonded silica column, using MeCN-MeOH-H 2 O (20:1:50) and uv detection (220 nm). The quantitation was carried out by the internal standard method. The proposed method is sufficiently precise and relatively simple. Application of this hplc analysis to the determination of lanatoside C and digoxin after fermentation of the leaf powder is also described
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
