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津蓟咽炎I号合剂定性定量研究
引用本文:张学明,戴学文,王姿婧,刘青,房志仲.津蓟咽炎I号合剂定性定量研究[J].中南药学,2013(9):706-709.
作者姓名:张学明  戴学文  王姿婧  刘青  房志仲
作者单位:[1]天津市蓟县中医院药剂科,天津蓟县301900 [2]天津医科大学药学院药剂学教研室,天津市临床药物关键技术重点实验室,天津300070
摘    要:目的建立中药合剂津蓟咽炎I号的质量控制方法。方法采用薄层色谱法对合剂中金银花所含绿原酸和甘草中所含甘草酸单胺盐进行定性研究;以高效液相色谱法对合剂中含有的腺苷、黄芩苷进行定量研究。结果薄层色谱斑点清晰,阴性样品无干扰;检测腺苷的流动相为0.04mol·L^-1NaH2PO4-乙腈(94:6),流速为1.0mL·min,检测波长为260nm;检测黄芩苷的流动相为甲醇.水(55:45),10%磷酸调整pH至3.3,检测波长280nm,流速1.0mL·min^-1。腺苷进样量在4.5~54.0μg·mL^-1与峰面积呈良好的线性关系,r=0.9997,平均回收率为101.1%,RSD为0.97%(n=9);黄芩苷进样量在10~70μg·mL^-1与峰面积呈良好线性关系,r=0.9996,平均回收率为102.0%,RSD为0.88%(n=9)。结论本方法简便、准确、灵敏度高、专属性和重现性好,可作为该产品的质量控制方法。

关 键 词:津蓟咽炎I号合剂  绿原酸  甘草酸单铵盐  腺苷  黄芩苷  薄层色谱  高效液相色谱法

Qualitative and quantitative method of Jinji Yanyan No.1 mixture
ZHANG Xue-ming,DAI Xue-wen,WANG Zi-jing,LIU Qin,FANG Zhi-zhong.Qualitative and quantitative method of Jinji Yanyan No.1 mixture[J].Central South Pharmacy,2013(9):706-709.
Authors:ZHANG Xue-ming  DAI Xue-wen  WANG Zi-jing  LIU Qin  FANG Zhi-zhong
Institution:1. Department of Pharmacy, Hospital of Tianjin Jixian Chinese Medicine, Jixian Tianjin 301900; 2. Department of Pharmacy, College of Pharmacy, Tianjin Medical University, Tianjin Key Laboratory of Technologies Enabling Development of Clinical Therapeutics and Diagnostics (Theranostics), Tianjin 300070)
Abstract:Objective To establish a method to control the quality of Jinji Yanyan No.1 mixture. Methods Glycyrrhizin in glycyrrhiza uralensis fisch, and chlorogenic acid in onicera japonica thunb were authenticated by thin-layer chromatography. An HPLC method for the determination of adenosine and baicalin in Jinji Yanyan Nod mixture was established. Results The spots on the TLC plate were clear. The negative sample did not interfere. Adenosine was determined with 0.04 tool ~ L- ~NaHzPO4-acetonitrile (94 : 6) as the mobile phase, the flow rate was 1.0 mL ~ min t and the detection wave- length was 260 nm. Baicalin was determined with methanol-water (55 : 45) as the mobile phase which was adjusted to pH 3.3 with 10% H3PO4, The flow rate was 1.0 mL . min^ - 1 and the detection wavelength was 280 nm. Good linearity was obtained at 4.5 -- 54.0 μg . mL^-1 (r = 0.999 7) for adenosine and 10 - 70 μg.mL^-1 (r = 0.999 6) for baicalin. The average recovery was 101.1% (RSD = 0.97%, n = 9) for adenosine and 102.0% (RSD = 0.88%, n = 9) for baicalin. Conclusion The method is specific, accurate and reproducible, and can be used for the quality control of Jinji Yanyan No. 1 mixture.
Keywords:Jinji Yanyan No  1 mixture  chlorogenic acid  glycyrrhizin  adenosine  baicalin  TLC  HPLC
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