Jump to main content
US EPA
United States Environmental Protection Agency
Search
Search
Main menu
Environmental Topics
Laws & Regulations
About EPA
Health & Environmental Research Online (HERO)
Contact Us
Print
Feedback
Export to File
Search:
This record has one attached file:
Add More Files
Attach File(s):
Display Name for File*:
Save
Citation
Tags
HERO ID
1165442
Reference Type
Journal Article
Title
Development of a simple, rapid and reproducible HPLC assay for the simultaneous determination of hypericins and stabilized hyperforin in commercial St. John's Wort preparations
Author(s)
de Los Reyes, GC; Koda, RT
Year
2001
Is Peer Reviewed?
Yes
Journal
Journal of Pharmaceutical and Biomedical Analysis
ISSN:
0731-7085
EISSN:
1873-264X
Volume
26
Issue
5-6
Page Numbers
959-965
Language
English
PMID
11600308
DOI
10.1016/S0731-7085(01)00449-6
Web of Science Id
WOS:000172247000027
Abstract
A reversed-phase HPLC method was developed and validated for the simultaneous determination of hypericins and stabilized hyperforin in St. John's Wort extract. The sample solution was prepared by extraction of the finely powdered extract with methanol-water (80:20, v/v) containing 5% HP-beta -cyclodextrin, and adjusted to pH 2.5 with orthophosphoric acid. Diluted extract solutions, maintained at 0 degreesC, were injected into a C-18 column. The samples were eluted isocratically using a mobile phase consisting of acetonitrile and 0.3% v/v phosphoric acid (90:10. v/v) at a 1.5 ml/min flow rate with simultaneous fluorescence (315/590 nm, excitation/emission) and UV (273 nm) detection. Quantification of the marker compounds (hypericin, pseudohypericin, hyperforin) was achieved by use of standard curves generated by plotting peak heights versus concentrations. Validation studies demonstrated that this HPLC method is simple, rapid, reliable. and reproducible. The standard curves were linear over the concentration ranges, 0.5-2.5 mug/ml (hypericin), 0.35-1.6 mug/ml (pseudo hype ricin) and 5-50 mug/ml (hyperforin), The intra-day coefficients of variation obtained for hypericin, pseudohypericin and hyperforin were less than or equal to 4.4% less than or equal to 5.4%, and less than or equal to 2.8%, respectively; inter-day CVs were less than or equal to 5.8%, less than or equal to 4.9%, and less than or equal to 2.5%, respectively. This method may be applied for the routine standardization of St. John's Wort products against hyperforin and the hypericins, the putative antidepressant principles in the herbal. (C) 2001 Elsevier Science B.V. All rights reserved.
Keywords
hypericin; pseudohypericin; stabilized hyperforin; reversed-phase HPLC; validation; simultaneous assay
Tags
IRIS
•
Methanol (Non-Cancer)
Search 2012
WOS
Home
Learn about HERO
Using HERO
Search HERO
Projects in HERO
Risk Assessment
Transparency & Integrity