Echinacea purpurea (L.) Moench, a top selling botanical medicine, is currently of considerable interest due to immunomodulatory, anti-inflammatory, antiviral and cannabinoid receptor 2 (CB2) binding activities of its alkylamide constituents. The purpose of these studies was to comprehensively profile the alkylamide (alkamide) content of E. purpurea root, and to compare yields of alkylamide constituents resulting from various ethanolic extraction procedures commonly employed by the dietary supplements industry. To accomplish this goal, a high performance liquid chromatographyelectrospray ionization mass spectrometry (HPLC-ESI-MS) method was validated for quantitative analysis of several E. purpurea alkylamides. Using this method, at least 15 alkylamides were identified and it was shown that fresh and dry E. purpurea extracts prepared from equivalent amounts (dry weight) of roots, with exceptions, exhibited similar yield of specific alkylamides. However, the amount of total dissolved solids in the dry extract was higher (by 38%) than the fresh extract. Two extracts prepared from dried roots at different ratios of root:solvent (1:5 w:v and 1:11 w:v) were similar in yield of total dissolved solids, but, there were differences in quantities of specific alkylamides extracted using these two root:solvent ratios. In addition, the important bioactive dodecatetraenoic acid isobutylamides are fully extracted from dry E. purpurea root in 2 days, suggesting that the manufacturing practice of macerating Echinacea extracts for weeks may be unnecessary for optimal alkylamide extraction. Finally, the identification of a new alkylamide has been proposed. These results demonstrate the differences of the described extractions and utility of the analytical methods used to determine the wide-ranging individual alkylamide content of commonly consumed Echinacea extracts.
Background: Taraxacum officinale (L.) Weber (Asteraceae) has been extensively employed as a diuretic in traditional folk medicine and in modern phytotherapy in Europe, Asia, and the Americas without prior clinical trial substantiation. Objectives: In this pilot study, a high-quality fresh leaf hydroethanolic extract of the medicinal plant T. officinale (dandelion) was ingested by volunteers to investigate whether an increased urinary frequency and volume would result. Design: Volume of urinary output and fluid intake were recorded by subjects. Baseline values for urinary frequency and excretion ratio (urination volume:fluid intake) were established 2 days prior to dandelion dosing (8 mL TID) and monitored throughout a 1-day dosing period and 24 hours postdosing. Results: For the entire population (n ¼ 17) there was a significant ( p < 0.05) increase in the frequency of urination in the 5-hour period after the first dose. There was also a significant ( p < 0.001) increase in the excretion ratio in the 5-hour period after the second dose of extract. The third dose failed to change any of the measured parameters. Conclusions: Based on these first human data, T. officinale ethanolic extract shows promise as a diuretic in humans. Further studies are needed to establish the value of this herb for induction of diuresis in human subjects.
Drug screening for antimalarials uses heme biocrystallization inhibition methods as an alternative to parasite cultures, but they involve complex processes and cannot detect artemisinin-like molecules. The described method detects heme-binding compounds by mass spectrometry, using dissociation of the drug-heme adducts to evaluate putative antiplasmodial activity. Applied to a chemical library, it showed a good hit-to-lead ratio and is an efficient early stage screening for complex mixtures like natural extracts.
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