1. Academic Validation
  2. Single dose oral pharmacokinetic profile rubraxanthone in mice

Single dose oral pharmacokinetic profile rubraxanthone in mice

  • Heliyon. 2022 Mar 14;8(3):e09104. doi: 10.1016/j.heliyon.2022.e09104.
Meri Susanti 1 Riski Darmianti 1 Yahdiana Harahap 2 Afrizal Itam 3 Dachriyanus Hamidi 1
Affiliations

Affiliations

  • 1 Faculty of Pharmacy, Universitas Andalas, Padang, West Sumatra, 25163, Indonesia.
  • 2 Faculty of Pharmacy, Universitas Indonesia, Depok, West Java, Indonesia.
  • 3 Department of Chemistry, FMIPA, Universitas Andalas, Padang, West Sumatra, 25163, Indonesia.
Abstract

Rubraxanthone is a main active constituent of kandis (Garcinia cowa Roxb), has showed many biological activity including antimicrobial, anti hypercholesterolemic, antiplatelet, antioxidant, cytotoxic, and anti-inflammatory properties. To the best of our knowledge, no reports on the pharmacokinetics (PK) of this rubraxanthone have been published. The PK of rubraxanthone in mice was examined after a single oral dose of 700 mg/kg rubraxanthone suspension in virgin coconut oil. Plasma samples were collected at different time points and further analyzed using validated chromatographic method. Pharmacokinetic parameters were calculated from observed plasma concentration-time profile. The maximum concentration of rubraxanthone in plasma was discovered in 1.5 h. The peak plasma concentration (Cmax) was 4.267 μg/mL, and the area under the curve (AUCt0-t ) was 560.99 μg h/L, with a 6.72-hour terminal half-life (T1/2). The volume of distribution (Vd/F) was 1200.19 mL/kg and 1123.88 mL/h/kg clearance (Cl/F).

Keywords

Bioanalysis; Pharmacokinetic; Rubraxanthone; UHPLC; Validation.

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