Aim To determine five organic acids in Radix Isatidis . Method The extraction method and the column partition chromatographic conditions were studied. Then a capillary zone electrophoretic method was set up for t...Aim To determine five organic acids in Radix Isatidis . Method The extraction method and the column partition chromatographic conditions were studied. Then a capillary zone electrophoretic method was set up for the determination. Results The linear ranges of quinazolinone acid, n anthranilic acid, benzoic acid, salicylic acid, and syringic acid were 5 52-92 0 μg·mL -1 , 5 12-102 μg·mL -1 , 2 28-84 4 μg·mL-1 , 4 78-159 μg·mL -1 , and 1 74-87 0 μg·mL -1 respectively. Conclusion The established method is accurate and simple.展开更多
Objective To develop an efficient method for separating and purifying puerarin from the roots of Pueraria lobata.Methods Separation by fast centrifugal partition chromatography（FCPC）was processed with a biphasic sol...Objective To develop an efficient method for separating and purifying puerarin from the roots of Pueraria lobata.Methods Separation by fast centrifugal partition chromatography（FCPC）was processed with a biphasic solvent system composed of ethyl acetate-n-butanol-water（2：1：3）.The separation conditions were determined as follows：sample loading of 10 mg,flow rate of 2 mL/min,rotation speed of 2200 r/min,ascending mode,and detection wavelength of 254 nm.High speed countercurrent chromatography（HSCCC）was used as a comparative method with the rotation speed of 800 r/min,flow rate of 2.0 mL/min,and sample loading of 10 mg in tail-to-head mode.Results Puerarin was obtained by FCPC with a resolution of 0.90 and a purity above 99%,while a resolution below 0.50 and a purity below 90%by HSCCC.Compared with HSCCC,FCPC has the advantages with higher purity and better resolution.Conclusion FCPC is a powerful method to separate and purify puerarin.展开更多
文摘Aim To determine five organic acids in Radix Isatidis . Method The extraction method and the column partition chromatographic conditions were studied. Then a capillary zone electrophoretic method was set up for the determination. Results The linear ranges of quinazolinone acid, n anthranilic acid, benzoic acid, salicylic acid, and syringic acid were 5 52-92 0 μg·mL -1 , 5 12-102 μg·mL -1 , 2 28-84 4 μg·mL-1 , 4 78-159 μg·mL -1 , and 1 74-87 0 μg·mL -1 respectively. Conclusion The established method is accurate and simple.
基金International Science and Technology cooperation project of Shanghai(No.12120701400,2012)
文摘Objective To develop an efficient method for separating and purifying puerarin from the roots of Pueraria lobata.Methods Separation by fast centrifugal partition chromatography（FCPC）was processed with a biphasic solvent system composed of ethyl acetate-n-butanol-water（2：1：3）.The separation conditions were determined as follows：sample loading of 10 mg,flow rate of 2 mL/min,rotation speed of 2200 r/min,ascending mode,and detection wavelength of 254 nm.High speed countercurrent chromatography（HSCCC）was used as a comparative method with the rotation speed of 800 r/min,flow rate of 2.0 mL/min,and sample loading of 10 mg in tail-to-head mode.Results Puerarin was obtained by FCPC with a resolution of 0.90 and a purity above 99%,while a resolution below 0.50 and a purity below 90%by HSCCC.Compared with HSCCC,FCPC has the advantages with higher purity and better resolution.Conclusion FCPC is a powerful method to separate and purify puerarin.
