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作 者:林靖然[1] 邓少东[1] 肖凤霞[1] 林励[1] 邓韬[1] 张旭倩[1]
出 处:《中国实验方剂学杂志》2013年第16期175-178,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技部"十二五"科技支撑计划项目(2011BAI01B02);广东省科技计划项目(2012A030100005);茂名市科技重大专项项目(2012A01002)
摘 要:目的:建立UPLC测定大鼠肝微粒体中柚皮苷和柚皮素含量的方法,并初步考察二者于不同时间点的代谢情况。方法:采用UPLC色谱系统,ACQUITY BEH C18色谱柱(3.0 mm×100 mm,1.7μm),流动相甲醇-0.1%乙酸水溶液梯度洗脱,流速0.5 mL.min-1,柱温30℃,检测波长283,289 nm,内标为槲皮素,进样量3μL。结果:柚皮苷及柚皮素均与槲皮素分离良好且无内源性干扰。生物样品中柚皮苷和柚皮素的线性范围分别为3.814~38.143(r=0.999 2),3.586~35.857 mg.L-1(r=0.999 6);柚皮苷的方法回收率95.43%~97.95%,绝对回收率97.33%~98.18%;柚皮素的方法回收率95.27%~99.31%,绝对回收率97.71%~99.73%;柚皮素在体外肝微粒体中的I相代谢较柚皮苷显著。结论:该方法快速、灵敏、准确,可用于大鼠肝微粒中柚皮苷和柚皮素的含量测定。Objective : To establish a method for determining the content of naringin and naringenin in rat liver microsomes by UPLC, and preliminary investigation in vitro metabolism of two ingredients at different times points. Method: Determination was performed on UPLC chromatographic system, ACQUITY BEH C18 column (3.0 mm × 100 mm, 1.7 μm) with a mobile phase of methanol-0. 1% acetic acid and gradient elution at a flow rate of 0.5 mL -min-1, detection wavelength was 283, 289 nm, column temperature was 30 ℃ , with quercetin as an internal standard, injection volume was 3 μm. Result: Naringin, naringenin and internal standard quercetin had good separation degree and no endogenous interference. The linear range of naringin and naringenin were 3. 814-38. 143 (r =0. 999 2) , 3. 586-35. 857 mg ·L-1 (r =0. 999 6) , respectively. Method recoveries of naringin ranged from 95.43% to 97.95% and absolute recoveries ranged from 97.33% to 98.18%. Method recoveries of naringenin ranged from 95.27% to 99.31% and absolute recoveries ranged from 97.71% to 99.73%. I phase metabolism of naringenin in in vitro liver microsomes was more significant than naringin. Conclusion: This method was rapid, sensitive and accurate, it could be used for determination of naringin and naringenin in rat liver microsomes.
关 键 词:柚皮苷 柚皮素 大鼠 肝微粒体 超高效液相色谱法
分 类 号:R945[医药卫生—微生物与生化药学]
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