Quantitative analysis of notoginsenoside R_1 in Radix Notoginseng by HPLC gradient elution mode
Xing Li
Abstract
Xing Li
Abstract
OBJECTIVE:To quantitate analyze notoginsenoside R 1 in Radix Notoginseng by HPLC gradient elution mode.METHODS:The chromatographic conditions included column Sphericorb NH 2,mobile phase of acetonitrile methanol water(gradient concentration 55∶30∶15→70∶20∶10),and detector UV 210 nm.RESULTS:The linear range and the limit of detection for notoginsenoside R 1 were within 5~40 μg·ml -1 ( r = 0.999 4 )and above 0.6 μg·ml -1 of by measuring the peak area,respectively.The method was accurate (mean recovery= 102.6 %, RSD = 1.43 %).CONCLUSIONS:The method was proved to be simple and rapid. [
OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
OBJECTIVE:To quantitate analyze notoginsenoside R 1 in Radix Notoginseng by HPLC gradient elution mode.METHODS:The chromatographic conditions included column Sphericorb NH 2,mobile phase of acetonitrile methanol water(gradient concentration 55∶30∶15→70∶20∶10),and detector UV 210 nm.RESULTS:The linear range and the limit of detection for notoginsenoside R 1 were within 5~40 μg·ml -1 ( r = 0.999 4 )and above 0.6 μg·ml -1 of by measuring the peak area,respectively.The method was accurate (mean recovery= 102.6 %, RSD = 1.43 %).CONCLUSIONS:The method was proved to be simple and rapid. [
Key concepts: Chromatography, Gradient elution, Radix (gastropod), High-performance liquid chromatography, Chemistry, Elution, Detection limit, Acetonitrile