2015•ZhongcaoyaoRequires access

Simultaneous quantification of nine constituents in Ziziphi Spinosae Semen by HPLC-MS

Qiaoyu Zhang

Open publisher page 2 citations

Abstract

Objective To develop an HPLC-MS/MS method for the determination of jujuboside A, jujuboside B, spinosin, betulinic acid, betulin, rutin, apigenin, hesperidin, and naringin in Ziziphi Spinosae Semen. Methods Analysis was performed on a Sapphire C18 column(150 mm × 4.6 mm, 5 μm) eluted with acetonitrile and 0.1% methanoic acid solution containing 1 mmol/L ammonium acetate in a gradient program. The flow rate was 1 m L/min, the injection volume was 10 μL, and the column temperature was 30 ℃. The multiple-reaction monitoring scanning(MRM) was employed for the quantification with switching electrospray ion source polarity in negative mode. The ion spray voltage was set at-4 500 V and the turbo spray temperature was maintained at 650 ℃. Results The regression equations showing linear relationships between peak areas and contents of each compound were obtained. The average recoveries of the compounds ranged from 98.04% to 101.5% and the precision in terms of RSD was in the range of 0.03%—0.74%. Conclusion The method is simple, rapid, and sensitive. It could be used as a quantitative determination method for the nine components in Ziziphi Spinosae Semen.

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What this paper is about

Objective To develop an HPLC-MS/MS method for the determination of jujuboside A, jujuboside B, spinosin, betulinic acid, betulin, rutin, apigenin, hesperidin, and naringin in Ziziphi Spinosae Semen. Methods Analysis was performed on a Sapphire C18 column(150 mm × 4.6 mm, 5 μm) eluted with acetonitrile and 0.1% methanoic acid solution containing 1 mmol/L ammonium acetate in a gradient program. The flow rate was 1 m L/min, the injection volume was 10 μL, and the column temperature was 30 ℃. The multiple-reaction monitoring scanning(MRM) was employed for the quantification with switching electrospray ion source polarity in negative mode. The ion spray voltage was set at-4 500 V and the turbo spray temperature was maintained at 650 ℃. Results The regression equations showing linear relationships between peak areas and contents of each compound were obtained. The average recoveries of the compounds ranged from 98.04% to 101.5% and the precision in terms of RSD was in the range of 0.03%—0.74%. Conclusion The method is simple, rapid, and sensitive. It could be used as a quantitative determination method for the nine components in Ziziphi Spinosae Semen.

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Available abstract

Objective To develop an HPLC-MS/MS method for the determination of jujuboside A, jujuboside B, spinosin, betulinic acid, betulin, rutin, apigenin, hesperidin, and naringin in Ziziphi Spinosae Semen. Methods Analysis was performed on a Sapphire C18 column(150 mm × 4.6 mm, 5 μm) eluted with acetonitrile and 0.1% methanoic acid solution containing 1 mmol/L ammonium acetate in a gradient program. The flow rate was 1 m L/min, the injection volume was 10 μL, and the column temperature was 30 ℃. The multiple-reaction monitoring scanning(MRM) was employed for the quantification with switching electrospray ion source polarity in negative mode. The ion spray voltage was set at-4 500 V and the turbo spray temperature was maintained at 650 ℃. Results The regression equations showing linear relationships between peak areas and contents of each compound were obtained. The average recoveries of the compounds ranged from 98.04% to 101.5% and the precision in terms of RSD was in the range of 0.03%—0.74%. Conclusion The method is simple, rapid, and sensitive. It could be used as a quantitative determination method for the nine components in Ziziphi Spinosae Semen.

Key concepts: Chromatography, Chemistry, Ammonium acetate, High-performance liquid chromatography, Hesperidin, Medicine, Alternative medicine, Pathology

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