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1.包头市第三医院药剂科,内蒙古 包头 014040
2.包头市中心医院药剂科,内蒙古 包头 014040
3.内蒙古医科大学药学院,呼和浩特 010110
4.内蒙古自治区新药筛选工程研究中心,呼和浩特 010110
Received:23 June 2025,
Revised:2025-08-19,
Accepted:27 August 2025,
Published:15 October 2025
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陈佳惠,罗琼,赵俊立,等.多指标定量联合化学计量学评价不同产地苦参质量[J].中国药房,2025,36(19):2404-2408.
CHEN Jiahui,LUO Qiong,ZHAO Junli,et al.Multivariate quantitative combined with chemometrics for evaluating the quality of Sophora flavescens from different producing areas[J].ZHONGGUO YAOFANG,2025,36(19):2404-2408.
陈佳惠,罗琼,赵俊立,等.多指标定量联合化学计量学评价不同产地苦参质量[J].中国药房,2025,36(19):2404-2408. DOI: 10.6039/j.issn.1001-0408.2025.19.08.
CHEN Jiahui,LUO Qiong,ZHAO Junli,et al.Multivariate quantitative combined with chemometrics for evaluating the quality of Sophora flavescens from different producing areas[J].ZHONGGUO YAOFANG,2025,36(19):2404-2408. DOI: 10.6039/j.issn.1001-0408.2025.19.08.
目的
2
建立不同产地苦参中多指标成分的含量测定方法,并结合化学计量学方法评价不同产地样品的质量。
方法
2
以不同产地的13批苦参(编号K1~K13)为检测样品,采用高效液相色谱-串联三重四极杆质谱(HPLC-MS/MS)法测定苦参中苦参碱、氧化苦参碱、甜菜碱、金雀花碱、
N
-甲基金雀花碱、槐定碱、染料木苷、高丽槐素、苦参酮、芒柄花素、苦参醇Ⅰ、降苦参酮12种成分的含量。色谱分离采用Shim-pack GIST-HP C
18
色谱柱,以甲醇为流动相A、0.1%甲酸水为流动相B进行梯度洗脱,体积流量为0.25 mL/min,柱温为35 ℃,进样量为3 μL;质谱采用电喷雾离子源,在正、负离子电离模式下扫描,通过多反应监测模式,分段采集数据。运用逼近理想解排序(TOPSIS)与灰色关联度分析(GRA)法对不同产地的13批苦参进行比较分析和综合评价。
结果
2
含量测定方法学考察符合相关规定。12种成分的含量分别为490.66~1 231.00、11 088.10~18 021.50、7.91~25.38、903.97~1 713.64、336.08~1 485.54、1 065.33~2 075.50、27.52~71.80、109.36~517.83、6 034.55~10 632.73、21.26~145.35、814.84~1 911.32、1 040.87~3 446.37 μg/g。TOPSIS结果显示,欧氏贴近度排名前7位的样品依次为K6、K12、K11、K3、K5、K10、K13;GRA结果显示,相对关联度排名前7位的样品依次为K12、K11、K10、K6、K13、K5、K3。
结论
2
所建立的HPLC-MS/MS法快速准确、灵敏度高、稳定可靠,结合化学计量学方法可用于苦参的质量控制和评价;样品K3、K5、K6(产地河北),K10(产地四川),K11~K13(产地山西)等的综合质量相对较好。
OBJECTIVE
2
To establish a content determination method for multiple components in
Sophora flavescens
from different origins and to evaluate its quality by combining with chemometrics.
METHODS
2
Thirteen batches (No. K1-K13) of
S. flavescens
from different origins were selected as test samples. A high-performance liquid chromatography-tandem triple quadrupole mass spectrometry (HPLC-MS/MS) method was established to determine the contents of 12 components, including matrine, oxymatrine, betaine, cytisine,
N
-methylcytisine, sophoridine, genistein, sophoricoside, sophorone, formononetin, sophorolone Ⅰ and norkurarinone in
S. flavescens
. Chromatographic separation was performed on a Shim-pack GIST-HP C
18
column with a mobile phase consisting of methanol (A) and water containing 0.1% formic acid (B), using gradient elution at a flow rate of 0.25 mL/min, column temperature of 35 ℃, and an injection volume of 3 μL. Mass spectrometry was conducted using an electrospray ionization source with positive and negative ion scanning. Data were collected in segments using the multiple reaction monitoring mode. Technique for order preference by similarity to ideal solution (TOPSIS) and grey relational analysis (GRA) methods were employed to compare and comprehensively evaluate the 13 batches of
S. flavescens
from different origins.
RESULTS
2
The methodological validation for the content determination met the relevant regulatory requirements. The contents of the 12 components were 490.66-1 231.00, 11 088.10- 18 021.50, 7.91-25.38, 903.97-1 713.64, 336.08-1 485.54, 1 065.33-2 075.50, 27.52-71.80, 109.36-517.83, 6 034.55-10 632.73, 21.26-145.35, 814.84-1 911.32, 1 040.87-3 446.37 μg/g), respectively. TOPSIS results showed that the top 7 samples in Euclidean distance ranking were K6, K12, K11, K3, K5, K10, K13. The GRA results showed that the top 7 samples in the relative correlation ranking were K12, K11, K10, K6, K13, K5, K3.
CONCLUSIONS
2
The established HPLC-MS/MS method is rapid, accurate, highly sensitive, stable and reliable. Combined with chemometrics methods, it can be used for the quality control and evaluation of
S. flavescens
. The comprehensive quality of samples K3, K5, K6
(from Hebei), K10 (from Sichuan), K11-K13 (from Shanxi), etc. is relatively superior.
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