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刊物信息

期刊名称:药物分析杂志
主管单位:中国科学技术协会
主办单位:中国药学会
承办:中国食品药品检定研究院
主编:金少鸿
地址:北京天坛西里2号
邮政编码:100050
电话:010-67012819,67058427
电子邮箱:ywfx@nifdc.org.cn
国际标准刊号:ISSN 0254-1793
国内统一刊号:CN 11-2224/R
邮发代号:2-237
 

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HPLC法同时测定小儿柴桂退热颗粒中葛根素、大豆苷、黄芩苷、大豆苷元、桂皮醛、黄芩素的含量

Simultaneous determination of puerarin, daidzin, baicalin, daidzein, cinnamaldehyde and baicalein in Xiaoer Chaigui Tuire Keli by HPLC

分类号:
出版年·卷·期(页码):2014,34 (6):0-0
DOI: 10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------

目的: HPLC法同时测定小儿柴桂退热颗粒中葛根素、大豆苷、黄芩苷、大豆苷元、桂皮醛、黄芩素的含量。 方法: 采用Agilent ZORBAX SB-C18色谱柱(250 mm×4.6 mm,5 μm),以乙腈(A)-0.1%磷酸水溶液(B)为流动相梯度洗脱(0~5 min,93%B;5~20 min,93%B→89%B;20~23 min,89%B→85%B;23~30 min,85%B→83%B;30~ 35 min,83%B→77%B;35~50 min,77%B→52%B;50~53 min,52%B→15%B;53~55 min,15%B),流速1.0 mL·min-1,检测波长250 nm(0~35 min,测定葛根素和大豆苷)、270 nm(35~48 min,测定黄芩苷和大豆苷元)、290 nm(48~50.5 min,测定桂皮醛)、278 nm(50.5~55 min,测定黄芩素),柱温40 ℃。 结果: 葛根素、大豆苷、黄芩苷、大豆苷元、桂皮醛、黄芩素进样量分别在0.01240~2.480、0.004208~ 0.8416、0.005503~1.101,0.002132~0.4264、0.0007120~0.1424、0.0007980~0.1597 μg范围内与峰面积均有较好的线性关系,平均加样回收率均在99.0%~101.2%范围内,RSD均小于1.3%。 结论: 经方法学验证,本法可用于小儿柴桂退热颗粒中葛根素、大豆苷、黄芩苷、大豆苷元、桂皮醛、黄芩素的含量测定,为小儿柴桂退热颗粒全面的质量控制提供科学依据。

-----英文摘要:---------------------------------------------------------------------------------------

Objective: To simultaneously determine puerarin,d aidzin,baicalin,daidzein,cinnamaldehyde and baicalein in Xiaoer Chaigui Tuire Keli by HPLC. Methods: HPLC experiments were performed on Agilent ZORBAX SB-C18(250 mm×4.6 mm,5 μm),eluted with acetonitrile (A) - 0.1% phosphoric acid (B) as the mobile phases in gradient mode(0-5 min,93%B;5-20 min,93%B→89%B;20-23 min,89%B→85%B;23-30 min,85%B→83%B;30-35 min,83%B→77%B;35-50 min,77%B→52%B;50-53 min,52%B→15%B;53- 55 min,15%B).The detection wavelength was set as follows:0-35 min,250 nm for puerarin and daidzin;35-48 min,270 nm for baicalin and daidzein;48-50.5 min,290 nm for cinnamaldehyde;50.5-55 min,278 nm for baicalein.The column temperature was at 40 ℃. Results: The good linearity with peak areas was achieved in the range of 0.01240-2.480 μg for puerarin,0.004208-0.8416 μg for daidzin,0.005503-1.101 μg for baicalin,0.002132-0.4264 μg for daidzein,0.000712-0.1424 μg for cinnamaldehyde,0.000798-0.1597 μg for baicalein.The average recoveries were between 99.04% and 101.2% with RSD less than 1.3%. Conclusion: The method can be used in determination of Xiaoer Chaigui Tuire Keli,puerarin,daidzin,baicalin,daidzein,cinnamaldehyde,baicalein for the comprehensive quality control by method validation,which can be used for the overall assessment of the quality of Xiaoer Chaigui Tuire Keli.

-----参考文献:---------------------------------------------------------------------------------------

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