BO Hai-mei, TIAN Chun-yu, BO Jian-zhu, et al. Simultaneous Determination of 18 Constituents in Zishen Qinggan Daiping Formula by UPLC-MS/MS Method[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(14): 52-55.
DOI:
BO Hai-mei, TIAN Chun-yu, BO Jian-zhu, et al. Simultaneous Determination of 18 Constituents in Zishen Qinggan Daiping Formula by UPLC-MS/MS Method[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(14): 52-55. DOI: 10.13422/j.cnki.syfjx.2015140052.
Simultaneous Determination of 18 Constituents in Zishen Qinggan Daiping Formula by UPLC-MS/MS Method
Objective: To develop a UPLC-MS/MS method for the simultaneous determination of 18 constituents in Zishen Qinggan Daiping formula. Method: The samples were separated on a Acquity UPLC BEH C18 column (2.1 mm×100 mm
1.7 μm) by a gradient elution with the mobile phase of 0.1% formic acid-water and acetonitrileas at a flow rate of 0.3 mL · min-1. The column temperature was 50 ℃. The sample size was 5 μL. The electrospray ion source was adopted to monitor in the polarity in positive and negative mode. The multiple-reaction monitoring (MRM) was applied in the quantitative analysis. Result: Within 16 min
the 18 constituents (malic acid
citrate acid
gallic acid
oleanolicacid
ursolic acid
2
3
5
4'-tetrahydroxystilbene-2-O-β-D-glucopyranoside
l-deoxynojirimycin
cassiaside
rubrofusarin gentiobioside
cassiaside B
resveratrol
physcion-8-O-β-D-glucopyranoside
aurantio-obtusin
chryso-obtusin
obtusinfolin
emodin
chrysophanol
icaritin) in Zishen Qinggan Daiping formula were completed separated. The regression equations showed a good linear relationship between the peak area and the concentration of each compound. The average recoveries ranged from 98.81% to 100.80%
and the precision ranged between 0.09% and 2.9%. Conclusion: The methodology validation shows that the method can be used for the content determination and quality control of 18 constituents in Zishen Qinggan Daiping formula.
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