Relative Bioavailability of Silybin A and Silybin B From 2 Multiconstituent Dietary Supplement Formulations Containing Milk Thistle Extract: A Single-dose Study. Article

Li, Wen-Yi, Yu, Guo, Hogan, Renee M et al. (2018). Relative Bioavailability of Silybin A and Silybin B From 2 Multiconstituent Dietary Supplement Formulations Containing Milk Thistle Extract: A Single-dose Study. . CLINICAL THERAPEUTICS, 40(1), 103-113.e1. 10.1016/j.clinthera.2017.11.013

cited authors

  • Li, Wen-Yi; Yu, Guo; Hogan, Renee M; Mohandas, Rajesh; Frye, Reginald F; Gumpricht, Eric; Markowitz, John S

authors

abstract

  • Purpose

    The purpose of this study was to compare the bioavailability between 2 milk thistle-containing dietary supplements, Product B and IsaGenesis, in healthy volunteers.

    Methods

    Bioavailability between Product B, originally formulated as a powdered capsule, and IsaGenesis, reformulated as a soft gel, were compared by measuring silybin A and silybin B as surrogate pharmacokinetic markers for differences in absorption and bioavailability. For this randomized, open-label, crossover pharmacokinetic study, 12 healthy volunteers consumed a single-dose serving of each supplement separated by at least a 7-day washout period. Serial blood samples were obtained at 0, 0.5, 1, 1.5, 2, 3, 4, 6, and 8 hours and analyzed via LC-MS/MS.

    Findings

    Rapid absorption and elimination of silybin A and silybin B have been observed after oral administration of both Product B and IsaGenesis. However, the absorption rate and extent, as indicated by mean the Cmax and mean plasma AUC, were significantly higher for the IsaGenesis soft gel formulation. The dose-corrected mean Cmax was 365% and 450% greater for silybin A and B, respectively, relative to powdered Product B. The time to Tmax was reached, on average, at least 1 hour earlier with IsaGenesis relative to Product B for both silybin A and silybin B.

    Implications

    The IsaGenesis soft gel formulation provided substantially greater absorption and bioavailability of silybin A and silybin B relative to the powdered Product B supplement. ClinicalTrials.gov Identifier: NCT02529605.

publication date

  • January 1, 2018

published in

keywords

  • Administration, Oral
  • Adult
  • Antioxidants
  • Area Under Curve
  • Biological Availability
  • Capsules
  • Chromatography, Liquid
  • Cross-Over Studies
  • Dietary Supplements
  • Drug Compounding
  • Female
  • Gels
  • Humans
  • Male
  • Plant Extracts
  • Powders
  • Silybin
  • Silybum marianum
  • Silymarin
  • Tandem Mass Spectrometry
  • Therapeutic Equivalency
  • Young Adult

Digital Object Identifier (DOI)

Medium

  • Print-Electronic

start page

  • 103

end page

  • 113.e1

volume

  • 40

issue

  • 1