Planta Medica International Open 2017; 4(S 01): S1-S202
DOI: 10.1055/s-0037-1608513
Poster Session
Georg Thieme Verlag KG Stuttgart · New York

Development and validation of ultra-performance convergence chromatography method for quality control of Saposhnikoviae Radix

S Kim Hyo
1   K-Herb Research Center, Korea Institute of Oriental Medicine, Daejeon, Korea, Republic of (South)
,
AY Lee
1   K-Herb Research Center, Korea Institute of Oriental Medicine, Daejeon, Korea, Republic of (South)
,
G Choi
1   K-Herb Research Center, Korea Institute of Oriental Medicine, Daejeon, Korea, Republic of (South)
,
C Moon Byeong
1   K-Herb Research Center, Korea Institute of Oriental Medicine, Daejeon, Korea, Republic of (South)
› Author Affiliations
Further Information

Publication History

Publication Date:
24 October 2017 (online)

 

Ultra-performance convergence chromatography (UPC2) is an environmentally friendly analytical method that uses dramatically reduced amounts of organic solvents [1,2]. As the concept of “green chemistry” has grown more widely accepted, UPC2 has become an alternative and complementary method to the HPLC technique [1]. A rapid, sensitive, and environmentally friendly UPC2 method was developed for rapid quantification of four major chromones (cimifugin, 4'-β-D-glucosyl 5-O-methylvisamminol, s-O-glucosylhamaudol and prim-O-glucosylcimifugin) in Saposhnikoviae Radix using a Waters UPC2 Torus Diethylamine column (2.1 mm × 150 mm, 1.7 µm) with a runtime of 6.5 min. This method validated according to the International Conference on Harmonization (ICH) guidelines for the validation of analytical procedures with respect to precision, accuracy, and linearity. The limits of detection of four chromones ranged from 0.01 to 0.03 µg/mL, while the limits of quantitation ranged from 0.02 to 0.10 µg/mL. The four chromones showed good regression (r 2 > 0.999), excellent precision (RSD < 0.60%), and acceptable recoveries (99.48 – 102.89%). Comparison of system performance with conventional HPLC was made with respect to analysis time, efficiency and sensitivity. Quantification of four chromones in 13 commercial samples of Saposhnikoviae Radix was successfully performed using the developed UPC2 method. The identity and authenticity of Saposhnikoviae Radix were successfully monitored by the proposed UPC2 method. This study provided some references for quality control of Saposhnikoviae Radix.

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