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Tytuł artykułu

Rapid method for rhaponticin and deoxyrhaponticin separation and determination by TLC in Rheum rhaponticum L. and Rheum undulatum L.

Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The study describes the solvent extraction procedure and improved version of TLC method for the determination of rhaponticin and deoxyrhaponticin in rhizomes and petioles of two species of Rheum L. genus. Extracts from underground parts and petioles of plant were separated on thin layers of silica using a mixture of dichloromethane-95% ethanol-methanol (8:1:1). The bands of rhaponticin and deoxyrhaponticin were satisfactorily separated from the remaining extract components permitting their densitometric quantitative and qualitative determination. The concentration of these compounds in Rheum undulatum was higher than in Rheum rhaponticum. The amount of rhaponticin and deoxyrhaponticin ranged between 0.3 and 31.5 mg/g.
Rocznik
Strony
127--134
Opis fizyczny
Bibliogr. 15 poz., rys., tab.
Twórcy
  • Medical University of Lublin Chair and Department of Pharmaceutical Botany Lublin Poland
autor
  • Medical University of Lublin Department of Physical Chemistry, Chair of Chemistry Lublin Poland
autor
  • Medical University of Lublin Chair and Department of Pharmaceutical Botany Lublin Poland
autor
  • Medical University of Lublin Department of Physical Chemistry, Chair of Chemistry Lublin Poland
Bibliografia
  • [1] P. Lanckage, R.J. Pyrce, Phytochem. 16, 1193–1198 (1977)
  • [2] Z. Kerem, G. Regev-Shoshani, M.A. Flaishman, L. Silvan, J. Nat. Prod. 66, 1270–1272 (2003)
  • [3] M. Man, Y. Chan. Biochem. Pharmacol. 63, 99–104 (2002)
  • [4] H. Matsuda, S. Tewtrakul, T. Morikawa, M. Yoyshikawa, Med. Chem. 12(18), 4871–4876 (2004)
  • [5] K. A. Roupe, G. L. Hems, S. C. Halls, J.A. Yanez, N.M. Davies, J. Pharm. Sci. 8, 374–386 (2007)
  • [6] L. Fremont, Life Sci. 66, 663–673 (2000)
  • [7] G.I. Nonaka, M. Minami, I. Nishioka, Chem Pharm. Bull. 25, 2300–2305 (1977)
  • [8] L. Gracza, Arch. Pharm. 317, 374–377 (1984)
  • [9] S.K. Ko, C.G. Shin, H.S. Lee, S.T. Han, B.O. Im, S.H. Chung, Korean J. Pharmacog. 35, 171–174 (2004)
  • [10] T.A. Aburiat, Phytochem. 55, 407–410 (2000)
  • [11] M.Y. Yoo, K.S. Oh, I.W. Lee, H.W. Seo, G.H. Yon, D.Y. Kwon, Y.S. Kim, S.Y. Ryu, Phytother. Res. 21, 186–189 (2007)
  • [12] X. Shang, Z. Yuan, Analytical Letters 35, 985–993 (2002)
  • [13] X. Shang, Z. Yuan, Analitica Chimica Acta 456, 183–188 (2002)
  • [14] M. Hennenberg and P. Horak, Acta Pol. Pharm. 16, 189–196 (1959)
  • [15] L. Csupor, Arch. Pharmaz. 304, 32–35 (1971)
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-2051e9ac-5c04-4b3c-aae9-b0bd6c30cd41
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