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gIsolation and purification of acetylshikonin and β‐acetoxyisovalerylshikonin from cell suspension cultures of Arnebia euchroma (Royle) Johnston using rapid preparative HPLC*
Author(s) -
Sharma Nandini,
Sharma Upendra Kumar,
Malik Sonia,
Bhushan Shashi,
Kumar Vinod,
Verma Subash Chandra,
Sharma Naina,
Sharma Madhu,
Sinha Arun Kumar
Publication year - 2008
Publication title -
journal of separation science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.72
H-Index - 102
eISSN - 1615-9314
pISSN - 1615-9306
DOI - 10.1002/jssc.200700489
Subject(s) - chromatography , naphthoquinone , high performance liquid chromatography , chemistry , organic chemistry
Shikonin and its derivatives are important red colored naphthoquinone pigments found in a large number of Arnebia species, including A. euchroma , that are responsible for the various pharmacological activities exhibited by the plant. The precise separation of each naphthoquinone is essential for total quality evaluation and bioactivity analysis of herbal formulations of A. euchroma . Furthermore, the overexploitation of this useful plant has resulted in species becoming endangered. With this in mind, a simple and rapid preparative scale HPLC method with single compound recovery for the isolation and purification of two shikonin derivatives ( i. e. acetylshikonin, β‐acetoxyisovalerylshikonin) from cell suspension cultures of A. euchroma is presented. The compounds were separated on a C 18 column within 10 min using acetonitrile/methanol (95:5) as mobile phase in isocratic mode. The isolated compounds were found to be more than 98% pure. The LOD for acetylshikonin and β‐acetoxyisovalerylshikonin was estimated at 0.063 and 0.146 μg/mL, respectively, while the LOQ was found to be 0.209 and 0.487 μg/mL, respectively. The recoveries accomplished for both the shikonin derivatives were in the range of 94.7–96.8%. The repeatability, expressed as %RSD, of acetylshikonin and β‐acetoxyisovalerylshikonin was found to be 1.74 and 1.27, respectively.

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