Qualitative and Quantitative Analysis of Salviaflaside in Prunella vulgaris by TLC and HPLC
Limei Lin
Abstract
Limei Lin
Abstract
Objective:To establish an effective TLC and HPLC method for qualitative and quantitative analysis of salviaflaside in P.vulgaris which can be used to be one of the quality control of P.vulgaris.Method: Salviaflaside was identified by TLC in P.vulgaris and different parts from P.vulgaris;salviaflaside was determined by RP-HPLC.Chromatography conditions were Agilent Eclipse XDB-C18(4.6 mm×250 mm,5μm) column with mobile phase of acetonitrile-1.0% acetic acid(16∶84),UV detection wavelength was set at 319 nm and the column temperature was set at 30 ℃ with the flow rate of 1.0 mL · min-1;the sample injection was 10 μL.Result: The TLC sports developed were fairly clear only in flower spike with no interference;good linearity of salviaflaside was obtained in the range of 0.032 667-0.653 34 μg(r=0.999 9).The recovery of salviaflaside was 99.18% and RSD was 0.25%.The content of salviaflaside was more than 0.1‰.Conclusion: Salviaflaside was characteristic compound in flower spike of P.vulgaris.The method is simple,reliable and accurate,which can be applied as the quantity control method of P.vulgaris.
A significance statement is not available in the OpenAlex record.
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 establish an effective TLC and HPLC method for qualitative and quantitative analysis of salviaflaside in P.vulgaris which can be used to be one of the quality control of P.vulgaris.Method: Salviaflaside was identified by TLC in P.vulgaris and different parts from P.vulgaris;salviaflaside was determined by RP-HPLC.Chromatography conditions were Agilent Eclipse XDB-C18(4.6 mm×250 mm,5μm) column with mobile phase of acetonitrile-1.0% acetic acid(16∶84),UV detection wavelength was set at 319 nm and the column temperature was set at 30 ℃ with the flow rate of 1.0 mL · min-1;the sample injection was 10 μL.Result: The TLC sports developed were fairly clear only in flower spike with no interference;good linearity of salviaflaside was obtained in the range of 0.032 667-0.653 34 μg(r=0.999 9).The recovery of salviaflaside was 99.18% and RSD was 0.25%.The content of salviaflaside was more than 0.1‰.Conclusion: Salviaflaside was characteristic compound in flower spike of P.vulgaris.The method is simple,reliable and accurate,which can be applied as the quantity control method of P.vulgaris.
Key concepts: Chromatography, Prunella vulgaris, High-performance liquid chromatography, Chemistry, Content determination, Medicine, Traditional Chinese medicine, Alternative medicine