Determination of Microwave-Assisted Extraction of Chinese Cut Crude Drugs(6) Comparison of the Determination of Linarin from Between Microwave-Assisted Extraction and Chinese Pharmacopeia Method
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Determination of Microwave-Assisted Extraction of Chinese Cut Crude Drugs(6) Comparison of the Determination of Linarin from Between Microwave-Assisted Extraction and Chinese Pharmacopeia Method
Chinese Journal of Experimental Traditional Medical FormulaeVol. 18, Issue 24, Pages: 94-96(2012)
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Published:2012
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FANG Jing, YANG Hong-jun, FU Mei-hong, et al. Determination of Microwave-Assisted Extraction of Chinese Cut Crude Drugs(6) Comparison of the Determination of Linarin from Between Microwave-Assisted Extraction and Chinese Pharmacopeia Method[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(24): 94-96.
DOI:
FANG Jing, YANG Hong-jun, FU Mei-hong, et al. Determination of Microwave-Assisted Extraction of Chinese Cut Crude Drugs(6) Comparison of the Determination of Linarin from Between Microwave-Assisted Extraction and Chinese Pharmacopeia Method[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(24): 94-96.DOI:
Determination of Microwave-Assisted Extraction of Chinese Cut Crude Drugs(6) Comparison of the Determination of Linarin from Between Microwave-Assisted Extraction and Chinese Pharmacopeia Method
比较微波协助提取法与药典法提取蒙花苷优势。 方法: 采用Dikma Diamonsil C18色谱柱(4.6 mm×150 mm
5 μm)
流动相甲醇-水-冰醋酸(26∶23∶1)
检测波长334 nm
柱温30 ℃
流速1 mL·min-1。 结果: 微波提取时间15 min
提取温度100 ℃
提取溶剂50%乙醇。蒙花苷在0.04~1.2 μg呈良好线性关系(r=0.999 9)
平均回收率100.13%(n=6)。 结论: 微波提取法较药典法提取蒙花苷更简便快速、准确
为一种符合环保绿色理念的含量测定方法
可用于检测野菊花饮片中蒙花苷含量。
Abstract
Objective:To establish a microwave-assisted extraction method for the extraction of the linarin from Chrysanthemun indicum. Comparison of the determination of linarin from C. indicum between microwave-assisted extraction and Chinese pharmacopeia method was made. Method: Dikma Diamonsil C18 column(4.6 mm×150 mm
5 μm)was used. The mobile phase cousisted of methanol-water-acetic acid (26∶23∶1).The temperature of column was kept at 30 ℃. The flow rate was 1.0 mL·min-1 and the detection wave-length was at 334 nm. Result: Microwave extractive time was 15 min
the temperature was 100 ℃
the extraction solvent was 50% ethanol. The calibration curve was in good linearity within the range from 0.04 to 1.2 μg(r=0.999 9). The average recovery was 100.13%(n=6). Conclusion: The method is simple
rapid
as well as precise and reliable
and can be used for the determination of linarin from C. indicum.
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