Gender-related differences in pharmacokinetics, tissue distribution, and excretion of 20(R)-25-methoxyl-dammarane-3β,12β,20-triol and its metabolite in rats and anti-ovarian cancer evaluation

J Pharm Biomed Anal. 2018 Sep 5:158:327-338. doi: 10.1016/j.jpba.2018.06.010. Epub 2018 Jun 7.

Abstract

Our previous study suggests a well-defined pharmacological activity of 20(R)-25-methoxyl-dammarane-3β,12β,20-triol (AD-1) and its metabolite 20(R)-dammarane-3β,12β,20,25-tetrol (AD-2). The current study aims to investigate the gender-related differences in pharmacokinetics, tissue distribution, and excretion of AD-1 and its metabolite in both male and female rats. A sensitive and rapid ultra-performance liquid chromatography tandem mass spectrometric (UPLC-MS/MS) method was developed for the simultaneous determination of AD-1 and AD-2 levels in plasma, various tissues, bile, urine, and feces. The results showed that AD-1 and its metabolite were rapidly distributed and eliminated from rat plasma; linear dynamics (r ≥ 0.8042) was observed in the dose range of 10-40 mg/kg. Compared with male rats, AD-1 and AD-2 were eliminated slowly from the plasma of female rats, and significant gender-related differences were observed in the pharmacokinetics as well as tissue distribution, however, long-term accumulation was not observed. Gender also significantly influenced excretion via urine and feces, but this effect was not observed in the bile excretion study. In rats, AD-1 and its metabolite were highly distributed in female genital organs, which implied that AD-1 and AD-2 might have a great potential for the treatment of ovarian cancer. Therefore, this study first investigated the in vitro activity of AD-1 and AD-2 for ovarian cancer. The results indicated that AD-1, AD-2, and Mitomycin C (Mito C) obviously inhibited the growths of ovarian cancer cells (HO-8910 and OVCAR(R)-3). At 40, 80 μM, AD-1, AD-2 reduced growth of two ovarian Cancer cells by 80%, were more effective than Mito C, and AD-1 showed stronger anti-ovarian cancer cell activity than AD-2. The results provide a theoretical basis for the future studies of AD-1 and AD-2 in ovarian cancer.

Keywords: Excretion; Gender-related differences; Ovarian cancer; Pharmacokinetics; Tissue distribution.

Publication types

  • Validation Study

MeSH terms

  • Administration, Oral
  • Animals
  • Antineoplastic Agents / analysis*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / therapeutic use
  • Body Fluids / chemistry
  • Cell Line, Tumor
  • Cell Proliferation / drug effects
  • Chromatography, High Pressure Liquid / instrumentation
  • Chromatography, High Pressure Liquid / methods
  • Drug Evaluation, Preclinical
  • Feces / chemistry
  • Female
  • Ginsenosides / analysis*
  • Ginsenosides / metabolism
  • Ginsenosides / pharmacokinetics
  • Ginsenosides / therapeutic use
  • Humans
  • Kidney / metabolism*
  • Male
  • Ovarian Neoplasms / drug therapy*
  • Ovary / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Renal Elimination
  • Sensitivity and Specificity
  • Sex Factors
  • Tandem Mass Spectrometry / instrumentation
  • Tandem Mass Spectrometry / methods
  • Tissue Distribution

Substances

  • 20(R)-25-methoxyldammarane-3beta,12beta,20-triol
  • Antineoplastic Agents
  • Ginsenosides