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Quantifying Withanolides in Plasma: Pharmacokinetic Studies and Analytical Methods.

Alex B Speers, Axel Lozano-Ortiz, Amala Soumyanath
Review Nutrients 2024 6 Zitierungen
PubMed DOI CC-BY PDF
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Study Design

Studientyp
narrative_review
Intervention
Quantifying Withanolides in Plasma: Pharmacokinetic Studies and Analytical Methods. variable across 20 studies (4 human, 16 animal); Cmax range humans 0.1-49.5 ng/mL
Vergleichsgruppe
Placebo
Wirkungsrichtung
Positive
Verzerrungsrisiko
Moderate

Abstract

Withania somnifera (common name: ashwagandha; WS) is an Ayurvedic botanical that has become popular for its reputed effects on stress and insomnia. Research into the bioactive compounds responsible for the biological effects of WS has largely focused on withanolides, a group of steroidal lactones commonly found in the Solanaceae family. Until recently, however, it was unclear which, if any, withanolides were present in the plasma after the ingestion of WS products. The aim of this review is to summarize current knowledge regarding the plasma pharmacokinetics of withanolides found in WS and the analytical methods developed to detect them in plasma. Twenty studies (sixteen animal, four human) were identified in which isolated withanolides or withanolide-containing products were administered to animals or humans and quantified in plasma. Withanolides were commonly analyzed using reversed-phase liquid chromatography coupled to mass spectrometry. Plasma concentrations of withanolides varied significantly depending on the substance administered, withanolide dose, and route of administration. Plasma pharmacokinetics of withaferin A, withanolide A, withanolide B, withanoside IV, 12-deoxywithastramonolide, and withanone have been reported in rodents (Cmax range: 5.6-8410 ng/mL), while withaferin A, withanolide A, 12-deoxywithastramonolide, and withanoside IV pharmacokinetic parameters have been described in humans (Cmax range: 0.1-49.5 ng/mL).

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Figures

Tables

Table 5

MethodValidationSpeciesPlasma PreparationVolume Used; Method LC-MS Method (and UV Wavelength if Applicable)Compounds and MRM Transition UsedRef.
WithanolidesInternal Standard
LC-MS/MSNoHuman85 µL; solid phase extraction using Agilent, Bond Elute PLEXA CartridgesColumn: Exsil Mono 100 C18, 3 µm, (100 × 4.6) mmMobile Phase: Acetonitrile and 10 mM ammonium formate in water (70:30) with 0.1% glacial acetic acid MRM mode: Positive ionization modeWithanolide A (488.5/263.2)12-DWS (471.4/263.2)Atorvastatin D5(564.4/445.4)[57]
LC-MS/MSYesHuman380 µL; solid phase extraction using Bond Elute C18 SPE cartridgesColumn: Agilent ZORBAX Eclipse Plus (4.6 × 100 mm, 3.5 µm) C18 columnMobile Phase: 1 mm ammonium formate in water (A) and acetonitrile (B)MRM mode: Positive ionization modeWithaferin A (471.3/281.1)Withanolide A (488.3/471.2)Withanoside V (784.45/443.3) Withanoside IV (800.45/459.3) 12-DWS (488.3/471.2)Fluoxymesterone (337.2/91)[59]
LC-MS/MSYesHumanVolume NR; solid phase extraction using OasisR HLB CartridgesColumn: Acquity UPLC BEH phenyl C18 column 100 × 2.1 mm L.D., 1.7 μmMobile Phase: Formic acid 0.1% in water (A) and in acetonitrile (B)MRM Mode: Positive and negative ESI (negative ion mode for withanoside IV and positive ion mode for withaferin A,withanolide A, and internal standard)Withaferin A (471.1711/94.95)Withanolide A (471.185/263.1045)Withanoside IV (827.4404/763.3592)Taineptine (437.0904/292.0991)[58]
LC-UVNoHumanVolume NR; simple Protein Precipitation (details NR)Column: Reversed-phase C18 columnMobile Phase: Water (A) and acetonitrile (B). UV wavelength: 225 nm.Withaferin A (NR)NR[56]

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