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1.内蒙古医科大学药学院,呼和浩特 010110
2.内蒙古自治区新药筛选工程研究中心,呼和浩特 010110
3.内蒙古医科大学附属医院药物临床试验机构,呼和浩特 010110
讲师,硕士。研究方向:中蒙药质量控制。E-mail:804142815@qq.com
教授。研究方向:药物分析。E-mail:whuanyun999@163.com
收稿日期:2023-07-03,
修回日期:2023-11-16,
录用日期:2023-11-23,
纸质出版日期:2023-12-30
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孙丽君,李君,王秋桐,等.蒙药材山苦荬的成分鉴别及7种成分含量测定方法建立 [J].中国药房,2023,34(24):3006-3011.
SUN Lijun,LI Jun,WANG Qiutong,et al.Method establishment of component identification and content determination of 7 components in Mongolian medicine Ixeris chinensis[J].ZHONGGUO YAOFANG,2023,34(24):3006-3011.
孙丽君,李君,王秋桐,等.蒙药材山苦荬的成分鉴别及7种成分含量测定方法建立 [J].中国药房,2023,34(24):3006-3011. DOI: 10.6039/j.issn.1001-0408.2023.24.09.
SUN Lijun,LI Jun,WANG Qiutong,et al.Method establishment of component identification and content determination of 7 components in Mongolian medicine Ixeris chinensis[J].ZHONGGUO YAOFANG,2023,34(24):3006-3011. DOI: 10.6039/j.issn.1001-0408.2023.24.09.
目的
2
建立鉴别山苦荬的化学成分以及7种成分(绿原酸、木犀草素、槲皮素、芦丁、原儿茶酸、异绿原酸A、木犀草苷)的含量测定方法。
方法
2
采用高效液相色谱-四极杆/静电场轨道阱高分辨质谱技术对山苦荬的化学成分进行鉴定,采用高效液相色谱串联三重四极杆质谱技术测定山苦荬中绿原酸等7种成分的含量。
结果
2
从山苦荬药材中共鉴别出45个成分,包括20个有机酸类成分、13个黄酮类成分、4个脂肪酸类成分、4个氨基酸成分、3个核苷类成分和1个香豆素类成分。绿原酸、木犀草素、槲皮素、芦丁、原儿茶酸、异绿原酸A、木犀草苷检测质量浓度的线性范围分别为503.00~25 150.00、42.00~2 100.00、5.05~252.50、20.05~1 002.50、25.10~1 255.00、750.00~37 500.00、196.00~9 800.00 ng/mL(
r
≥0.999 2),精密度、稳定性、重复性试验的RSD均小于3.00%(
n
=6),平均加样回收率为96.72%~105.84%(RSD均小于4.00%,
n
=6)。3批山苦荬中绿原酸等7种成分的含量范围分别为1 145.77~3 261.25、23.75~97.90、0.92~2.12、1.06~23.18、9.35~21.85、833.25~1 045.58、199.56~1 869.78 μg/g。
结论
2
本研究所建立的鉴别和定量方法快速、简便,可用于山苦荬药材化学成分的鉴别和绿原酸等7种成分的含量测定。
OBJECTIVE
2
To establish the methods to identify the chemical components of
Ixeris chinensis
, and determine the contents of 7 components (chlorogenic acid, luteolin, quercetin, rutin, protocatechuic acid, isochlorogenic acid A, luteoloside).
METHODS
2
HPLC-Q-Exactive-MS was used to identify the chemical comp
onents of
I. chinensis
. The contents of 7 components in
I. chinensis
, including chlorogenic acid,
were determined by HPLC-MS/MS.
RESULTS
2
A total of 45 components were identified in
I. chinensis
, including 20 organic acids, 13 flavonoids, 4 fatty acids, 4 amino acids, 3 nucleosides, and 1 coumarin. The linear range of chlorogenic acid, luteolin, quercetin, rutin, protocatechuic acid, isochlorogenic acid A and luteoloside were 503.00- 25 150.00, 42.00-2 100.00, 5.05-252.50, 20.05-1 002.50, 25.10-1 255.00, 750.00-37 500.00, 196.00-9 800.00 ng/mL (
r
≥0.999 2), respectively. RSDs of precision, stability and reproducibility tests were all less than 3.00% (
n
=6), and average recovery ranged from 96.72% to 105.84% (all RSD<4.00%,
n
=6). The contents of 7 components in 3 batches of
I. chinensis
were 1 145.77- 3 261.25, 23.75-97.90, 0.92-2.12, 1.06-23.18, 9.35-21.85, 833.25-1 045.58, 199.56-1 869.78 μg/g, respectively.
CONCLUSIONS
2
The established methods for identification and content determination are rapid and simple, and can be used for the identification of chemical components and the content determination of 7 components in
I.
c
hinensis
.
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