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作 者:黄鲛[1,2] 易进海[1] 刘玉红[1] 黄志芳[1] 陈燕[1] 刘云华[1]
机构地区:[1]四川省中医药科学院,成都610041 [2]成都中医药大学,成都611137
出 处:《中国实验方剂学杂志》2013年第16期59-62,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家重点基础研究发展计划(973计划)项目(2009CB522804)
摘 要:目的:建立HPLC测定天南星、半夏、白附子中8种核苷成分含量的方法。方法:采用Phenomenex Luna PFP(2)柱(4.6 mm×250 mm,5μm),以甲醇-水为流动相,梯度洗脱,流速0.8 mL.min-1,柱温35℃,检测波长260 nm。结果:尿嘧啶、次黄嘌呤、黄嘌呤、尿苷、肌苷、鸟苷、胸苷、腺苷进样量分别在0.004 34~0.434μg(r=0.999 9),0.002 34~0.234μg(r=0.999 9),0.004 07~0.407μg(r=0.999 7),0.010 90~1.090μg(r=0.999 9),0.002 01~0.201μg(r=0.999 9),0.00732~0.732μg(r=0.999 9),0.001 22~0.122μg(r=0.999 7),0.002 07~0.207μg(r=0.999 9)有良好的线性关系;平均回收率分别为104.2%(RSD 2.1%),98.7%(RSD 2.4%),103.7%(RSD 3.0%),99.4%(RSD 1.4%),101.8%(RSD 2.0%),102.9%(RSD 1.9%),98.3%(RSD 2.8%),102.3%(RSD 2.7%)。结论:方法简便、准确、快速,结果可靠,为测定天南星、半夏、白附子中8种核苷成分提供依据。Objective: To establish an HPLC method for simultaneous determination of eight nucleosides in Rhizoma Arisaema, Rhizoma Pinellie and Rhizoma Typhonii. Method: The chromatographic separation was achieved on a Phenomenex Luna PFP (2) (4.6 mm × 250 mm, 5 μm) column with methanol-water solution as mobile phase ( gradient elution). The flow rate was 0.8 mL -min-I, the column temperature was maintained at 35 ℃ and the detective wavelength was set at 260 nm. Result: The linear ranges of uracil, hypoxanthine, xanthine, uridine, inosine, guanosine, thymidine and adenosine were 0. 004 34-0. 434 μg (r =0. 999 9), 0. 002 34- 0.234 μg (r =0.999 9), 0.004 07-0.407 μg (r =0.999 7), 0.010 90-1.090 μg (r =0.999 9), 0.002 01- 0.201 μg (r=0.999 9), 0.007 32-0.732μg (r =0.999 9), 0.001 22-0. 122 μg (r =0.999 7), 0.002 07- 0.207 μg ( r = 0. 999 9 ) respectively. The average recoveries of the eight nucleosides were 104.2% , 98.7% , 103.7%, 99.4%, 101.8%, 102.9%, 98.3%, 102.3% and RSDs were 2.1%, 2.4%, 3.0%, 1.4%, 2.0%, 1.9%, 2.8%, 2.7% respectively. Conclusion: The method is simple, accurate and rapid. It can be used for determination of nucleosides in Rhizoma Arisaema, Rhizoma Pinellie and Rhizoma Typhonii.
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