HPLC法同时测定人工蛹虫草不同部位中5种核苷类成分的含量
x

请在关注微信后,向客服人员索取文件

篇名: HPLC法同时测定人工蛹虫草不同部位中5种核苷类成分的含量
TITLE:
摘要: 目的:建立同时测定人工蛹虫草不同部位中5种核苷类成分含量的方法。方法:采用高效液相色谱法。色谱柱为Inert- Sustain C18,流动相为甲醇 -0.02 mol/L 磷酸二氢钾溶液(梯度洗脱),流速为0.6 mL/min,检测波长为254 nm,柱温为30 ℃。结果:  尿苷、肌苷、鸟苷、腺苷和虫草素检测进样量线性范围分别为0.568~3.408 μg(r=0.999 9)、0.284~1.704 μg(r=0.999 9)、0.264~1.584 μg(r=0.999 9)、0.232~1.392 μg(r=0.999 9)、1.672~10.032 μg(r=0.999 8);精密度、稳定性、重复性试验的RSD<3.0%;加样回收率分别为98.2%~103.9%(RSD=1.97%,n=9)、96.2%~101.6%(RSD=1.76%,n=9)、96.7%~102.0% (RSD=1.94%,n=9)、95.1%~99.4%(RSD=1.43%,n=9)和95.6%~101.3%(RSD=1.82%,n=9)。结论:该方法操作简便,精密度、稳定性、重复性好,可用于人工蛹虫草中5种核苷类成分含量的同时测定,蛹虫草不同部位中所含核苷类成分含量不同。
ABSTRACT: OBJECTIVE: To establish a method for simultaneous determination of 5 nucleoside from different parts of cultured Cordyceps militaris. METHODS: HPLC method was adopted. The determination was performed on InertSustain C18 column with mobile phase consisting of methanol-0.02 mol/L monobasic potassium phosphate solution (gradient elution) at the flow rate of 0.6 mL/min. The detection wavelength was set at 254 nm, the column temperature was 30 ℃. RESULTS: The linear ranges of uridine, inosine, guanosine, adenosine and cordycepin were 0.568-3.408 μg(r=0.999 9), 0.284-1.704 μg(r=0.999 9),0.264-1.584 μg(r=0.999 9),0.232-1.392 μg(r=0.999 9) and 1.672-10.032 μg(r=0.999 8), respectively. RSDs of precision, stability and repeatability tests were all lower than 3.0%. The recoveries were 98.2%-103.9%(RSD=1.97%,n=9), 96.2%-101.6%(RSD=1.76%,n=9),96.7%-102.0%(RSD=1.94%,n=9),95.1%-99.4%(RSD=1.43%,n=9) and 95.6%-101.3%(RSD=1.82%,n=9). CONCLUSIONS: The method is simple, precise, stable and repeatable, and can be used for simultaneous determination of 5 nucleoside from cultured C. militaris, the content of nucleosides are different in different parts of C. militaris.
期刊: 2017年第28卷第9期
作者: 张勇,卓宝松,刘宝岩,康文艺
AUTHORS: ZHANG Yong,ZHUO Baosong,LIU Baoyan,KANG Wenyi
关键字: 人工蛹虫草;核苷类;高效液相色谱法;含量测定
KEYWORDS: Cultured Cordyceps militaris; Nucleoside; HPLC; Content determination
阅读数: 323 次
本月下载数: 3 次

* 注:未经本站明确许可,任何网站不得非法盗链资源下载连接及抄袭本站原创内容资源!在此感谢您的支持与合作!