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A combination of ultrasonic‐assisted extraction with RRLC‐QQQ method for the determination of artemisinin in the Chinese herb <i>Artemisia annua</i> L.

Xiao WangInstitute of Chinese Material Medical, China Academy of Chinese Medical Sciences, 16 Dongzhimennei Street, Beijing 100700, ChinaXian‐En ZhaoShandong Analysis and Test Center, Shandong Academy of Sciences, 19 Keyuan Street, Jinan, Shandong 250014, ChinaBin YangInstitute of Chinese Material Medical, China Academy of Chinese Medical Sciences, 16 Dongzhimennei Street, Beijing 100700, ChinaHongjing DongShandong Analysis and Test Center, Shandong Academy of Sciences, 19 Keyuan Street, Jinan, Shandong 250014, ChinaDahui LiuInstitute of Chinese Material Medical, China Academy of Chinese Medical Sciences, 16 Dongzhimennei Street, Beijing 100700, ChinaLuqi HuangInstitute of Chinese Material Medical, China Academy of Chinese Medical Sciences, 16 Dongzhimennei Street, Beijing 100700, China
2011en
ABI

Аннотация

INTRODUCTION: Artemisinin, the primary active ingredient of the Chinese herb Artemisia annua L., is known to have considerable anti-malaria properties. However, rapid, sensitive and selective method for the determination of artemisinin in it is not currently available. OBJECTIVE: To develop and validate an efficient method for extraction and analysis of artemisinin from the plant samples of Artemisia annua L. by rapid resolution liquid chromatography triple quadrupole mass spectrometry (RRLC-QQQ). METHODOLOGY: Following ultrasound-assisted extraction (USE), RRLC-QQQ was utilised to separate and determine artemisinin from the plant sample of Artemisia annua L. The LC separation, QQQ-MS detection and multiple reaction monitoring (MRM) mode were optimised, and the method validation concluding selectivity, calibration, accuracy and precision, and recovery were also evaluated. RESULTS: LC separation was performed with an isocratic elution of 20% of methanol-water (10 mmol/L ammonium acetate, pH 4.0) on a C(18) column. The triple quadrupole MS detection was carried out under MRM mode of precursor ion [M + H]+ → fragment ions m/z 265.1 and m/z 247.2. The limits of detection and quantitation of artemisinin were 0.20 and 0.75 ng/mL, respectively. The intra- and inter-day precisions did not exceed 3.71%, and the deviation of the intra- and inter-day mean values did not exceed ±7.50. The average recoveries for artemisinin ranged from 92.45 to 103.8% with an RSD from 2.47 to 2.79%. CONCLUSION: The developed RRLC-QQQ assay is an efficient method for separation and determination of artemisinin from the plant samples of Artemisia annua L.

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