RESUMO
This study compared eight major ginsenosides (Rg1, Rg2, Rf, Re, Rd, Rc, Rb1 and Rb2) between Panax sokpayensis and Panax bipinnatifidus collected from Sikkim Himalaya, India. High-performance liquid chromatographic analysis revealed that all major ginsenosides were present in the rhizomes of P. sokpayensis except ginsenoside Rc, whereas ginsenoside Rf, Rc and Rb2 were not detected in P. bipinnatifidus.
Assuntos
Ginsenosídeos/análise , Panax/química , Cromatografia Líquida de Alta Pressão/métodos , Ginsenosídeos/química , Índia , Rizoma/química , Siquim , Especificidade da EspécieRESUMO
A hyphenated accelerated solvent extraction (ASE) technique coupled with centrifugal partition chromatography (CPC), ultra high performance liquid chromatography (UPLC), and mass spectrometry (MS) was established. The CPC fractions were prepared using the hyphenated technique. Subsequently, tyrosinase inhibitory activities of the CPC fractions were experimentally evaluated, and the activities of individual components were calculated theoretically. This new approach was applied to saponin fractions obtained from 10.0g of raw Panax bipinnatifidus Seem. via a biphasic solvent system of ethyl acetate/n-butanol/methanol/water (2:3:2:5, v/v/v/v). The CPC fractions monitoring was performed using an online UPLC/PDA system at 5-min intervals. The tyrosinase inhibitory activities of all fractions were analysed using the fluorescence method. Mathematical calculations indicated that the inhibition rates of the ginsenosides Rh1, Rh2, Rg1, Rg2, and chikusetsusaponin L5 were all above 50.00%, showing potential for further development. The results were confirmed by comparison with authentic standards.