Literature DB >> 17402032

HPCL Separation and quantitative determination of valepotriates from Valeriana kilimandascharica.

S F Dossaji1, H Becker.   

Abstract

Valepotriates, mainly isovaltrate and valtrate, have been separated and quantitatively estimated by reversed-phase HPLC in the leaves, flowers, stems and rhizomes of VALERIANA KILIMANDASCHARICA. The isovaltrate/valtrate concentration reaches a maximum of 5.89% in the leaves, 3.84% in the flowers, 3.17% in the stems and 5.15% in the rhizomes. A micro Bondapak C (18) column using MeOH-H (2)O mixtures as eluant is suitable for a baseline separation of isovaltrate, valtrate, acevaltrate and baldrinal at UV 254 nm in 15 min and didrovaltrate and IVHD-valtrat at UV 208 nm in 10 min. Relative standard deviation for quantitative determinations is approximately 1.5% for valepotriate contents of 1%. This method is adaptable for routine analysis of crude extracts.

Entities:  

Year:  1981        PMID: 17402032     DOI: 10.1055/s-2007-971496

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  2 in total

1.  Further investigations of valepotriates in the Valerianaceae.

Authors:  S Chavadej; H Becker; F Weberling
Journal:  Pharm Weekbl Sci       Date:  1985-08-23

2.  In vitro mutagenicity of valepotriates.

Authors:  W von der Hude; M Scheutwinkel-Reich; R Braun; W Dittmar
Journal:  Arch Toxicol       Date:  1985-02       Impact factor: 5.153

  2 in total

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