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Determination of pharmacologically active compounds in root extracts of Cassia alata L. by use of high performance liquid chromatography

Tipo de material: TextoTextoSeries ; Talanta, 74(4), p.896-902, 2008Trabajos contenidos:
  • Fernand, V.E
  • Dinh, D.T
  • Washington, S.J
  • Fakayode, S.O
  • Losso, J.N
  • Van Ravenswaay, R.O
  • Warner, I.M
Tema(s): Recursos en línea: Resumen: Asimple high performance liquid chromatography (HPLC)methodwas developed and validated for the determination of six phenolic compounds, five anthraquinones (rhein, aloe-emodin, emodin, chrysophanol and physcion)and a flavonoid (kaempferol), in root extracts from Cassia alata L. Solid-phase extraction, using C18 cartridges, was used to remove interfering substances from the root extracts. The extracts were analyzed on a C18 column using an isocratic mobile phase which consisted of acetonitrile, methanol, and 10mM aqueous ammonium acetate (25:55:20, v/v). Identification of the analytes was performed by use of standards and on-line mass spectrometric detection using atmospheric pressure chemical ionization. The concentration of the phenolic compounds in the root extracts was determined using HPLC with ultraviolet detection at 260 nm. The limits of detection obtained for the anlytes were in the range of 0.23-4.61 ppm. The overall R.S.D. precision values (intra- and inter-day)for the retention times and peak-areas were lower than 0.16 and 2.10
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Asimple high performance liquid chromatography (HPLC)methodwas developed and validated for the determination of six phenolic compounds, five anthraquinones (rhein, aloe-emodin, emodin, chrysophanol and physcion)and a flavonoid (kaempferol), in root extracts from Cassia alata L. Solid-phase extraction, using C18 cartridges, was used to remove interfering substances from the root extracts. The extracts were analyzed on a C18 column using an isocratic mobile phase which consisted of acetonitrile, methanol, and 10mM aqueous ammonium acetate (25:55:20, v/v). Identification of the analytes was performed by use of standards and on-line mass spectrometric detection using atmospheric pressure chemical ionization. The concentration of the phenolic compounds in the root extracts was determined using HPLC with ultraviolet detection at 260 nm. The limits of detection obtained for the anlytes were in the range of 0.23-4.61 ppm. The overall R.S.D. precision values (intra- and inter-day)for the retention times and peak-areas were lower than 0.16 and 2.10

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