Qian Zheng-Ming, Li Chun-Hong, Song Yue-Lin, Zhou Miao-Xia, Li Wen-Jia
Key Laboratory of State Administration of Traditional Chinese Medicine, Sunshine Lake Pharma Co., LTD, Dongguan, Guangdong, China.
Modern Research Center for Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
J Chromatogr Sci. 2019 Apr 1;57(4):381-384. doi: 10.1093/chromsci/bmz007.
In this study, determination of adenosine in Cordyceps was accomplished by an online pressurized liquid extraction HPLC, and a poroshell column was employed for rapid HPLC separation. The Cordyceps sample powder was filled into a hollow guard column and extracted by thermal and pressurized water (75°C, 150 bar) for 3 min. Chromatographic separation was conducted on a poroshell 120 SB-Aq (4.6 × 50 mm, 2.7 μm) column and gradient elution was performed by water and methanol at a flow rate of 1.5 mL/min. The detection wavelength was set at 260 nm. The total measurement time including sample extraction and separation was <6 min. The calibration curve of adenosine was Y = 4.502 × 106X + 1.731 × 104, which showed good linearity (r2 > 0.9993) within tested range (4.03-80.5 μg/mL). The intra- and inter-day precisions of adenosine were 0.24% and 0.94%, respectively, and the recoveries of adenosine was 96.1% (relative standard deviation, 4.49%). The validated method was then applied to determinate adenosine in six batches of Cordyceps, and the contents of adenosine were 0.28-0.48 mg/g. The developed method is beneficial for the quality control of Cordyceps.
在本研究中,采用在线加压液体萃取高效液相色谱法测定冬虫夏草中的腺苷,并使用核壳柱进行高效液相色谱快速分离。将冬虫夏草样品粉末装入空心保护柱,用热水(75℃,150 bar)萃取3分钟。在核壳120 SB-Aq(4.6×50 mm,2.7μm)柱上进行色谱分离,以水和甲醇为流动相进行梯度洗脱,流速为1.5 mL/min。检测波长设定为260 nm。包括样品萃取和分离在内的总测定时间<6分钟。腺苷的校准曲线为Y = 4.502×106X + 1.731×104,在测试范围(4.03 - 80.5μg/mL)内显示出良好的线性(r2>0.9993)。腺苷的日内和日间精密度分别为0.24%和0.94%,回收率为96.1%(相对标准偏差为4.49%)。然后将该验证方法应用于测定六批冬虫夏草中的腺苷,腺苷含量为0.28 - 0.48 mg/g。所建立的方法有利于冬虫夏草的质量控制。