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刘焕

作品数:3 被引量:39H指数:2
供职机构:北京大学药学院天然药物学系更多>>
发文基金:国家自然科学基金国家科技支撑计划更多>>
相关领域:医药卫生更多>>

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Determination of 8,2′-diprenylquercetin 3-methyl ether in plasma by UPLC-MS-MS and its pharmacokinetic application in rats
2017年
8,2'-Diprenylquercetin 3-methyl ether with significant anti-breast cancer activity is the main constituent of Tibetan medicine Sinopodophylli Fructus. In the present study, we developed and validated a rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method for the determination of 8,2'-diprenylquercetin 3-methyl ether in rat plasma. 8-Prenylkaempferol was used as the internal standard. The separation was carried out using Waters ACQUITY UPLC BEH C18 column (2.1 mm×100 ram, 1.7 μm) with a mobile phase consisting of acetonitrile and 0.1% formic acid in water on a gradient program at a flow rate of 0.4 mL'min-1 and temperature of 30 ℃. Triple quadrupole mass spectrometric detection in negative ion mode was used for multiple-reaction monitoring of the transitions at m/z 451.30→177.25 and m/z 353.25→298.15 for 8,2'-diprenylquercetin 3-methyl ether and 8-prenylkaempferol, respectively. The calibration curves were linear within the concentration range 0.1-2000 ng/mL (r = 0.9954). The recoveries were 103%-115%, and the results were consistent across low, middle and high concentration levels. The intra- and inter-day precisions were within 15%, and the bias was between --6%-15%. This method was simple, rapid and sensitive, which could be applied to the determination of 8,2'-diprenylquercetin 3-methyl ether in plasma and pharmacokinetic study in rats. Pharmacokinetic test indicated that the peak plasma concentration occurred in 2 h after the female rats were intragastrically administered with 8,2'-diprenylquercetin 3-methyl ether at the dose of 100 mg/kg, and the biological half-life was 6.79 h. The blood drug concentration maintained equal amount for 20 h, which was conducive to the in vivo effects of drugs.
刘焕范珊珊张雯张驿帆李腾尚明英刘广学徐风蔡少青
关键词:UPLC-MS/MSPHARMACOKINETIC
五指毛桃的质量标准研究被引量:28
2017年
目的控制五指毛桃Fici Hirtae Radix药材质量,制订药材质量标准。方法通过植物形态、产地、历史沿革、功效、近年研究结果等的全面查考,修正《中国药典》1977年版五指毛桃药材的基原错误;采用性状、显微、薄层鉴别不同来源的商品药材;采用HPLC法测定药材中指标成分的量;按《中国药典》2010年版附录方法检测各检查项。结果五指毛桃药材基原并非极简榕Ficus simplicissima Lour.,而是粗叶榕Ficus hirta Vahl。20批五指毛桃商品药材中除规定药用部位粗叶榕的根外,有约40%非药用部位的茎枝样品;不同部位性状、显微特征及薄层色谱区别明显。药材中补骨脂素量为0.00848%~0.150%,佛手柑内酯为0.005 87%~0.026 3%,根类样品2种指标成分量显著高于非药用部位的茎枝样品。药材水分量为4.73%~8.27%,总灰分为2.58%~4.37%,酸不溶性灰分为0.054%~0.710%,醇溶性浸出物为6.23%~8.34%。结论修正《中国药典》1977年版五指毛桃药材基原错误,规范其药用部位为粗叶榕的根。建立的五指毛桃药材的质量标准可全面、有效地控制药材质量,为临床合理、有效、安全用药提供参考。
马雅静刘焕史晶晶尚明英李耀利刘广学徐风蔡少青
关键词:五指毛桃补骨脂素佛手柑内酯
桂枝汤中9种主要成分含量的测定和不同煎煮方式的比较研究被引量:11
2016年
目的:建立同时测定桂枝汤中9种主要成分含量的方法,比较传统煎煮和煎药机煎煮对桂枝汤中上述成分含量的影响。方法:采用高效液相色谱法。色谱柱为Agilent Zorbax SB C18,流动相为乙腈-0.1%磷酸(梯度洗脱),流速为1.0 ml/min,检测波长为230 nm(芍药内酯苷、芍药苷、甘草苷)、254 nm(桂皮醛、甘草酸)、280 nm(没食子酸、香豆素、桂皮酸、2-甲氧基桂皮醛),柱温为25℃,进样量为10μl。结果:没食子酸、芍药内酯苷、芍药苷、甘草苷、香豆素、桂皮酸、桂皮醛、2-甲氧基桂皮醛和甘草酸检测质量浓度线性范围分别为0.410 2~210.0(r=0.999 9)、0.994 0~254.5(r=0.999 9)、1.636 0~1 675.0(r=0.999 9)、0.988 3~506.0(r=0.999 6)、0.987 3~31.59(r=0.999 5)、0.486 8~124.6(r=0.999 5)、2.458 0~314.6(r=0.999 5)、0.034 3~1.096(r=0.999 8)、1.711 0~219.0μg/ml(r=0.999 7);精密度、稳定性、重复性试验的RSD〈5%,加样回收率分别为93.56%~103.19%(RSD=4.00%,n=9)、101.51%~107.32%(RSD=2.21%,n=9)、95.08%~103.76%(RSD=2.87%,n=9)、100.82%~105.73%(RSD=1.85%,n=9)、85.08%~89.12%(RSD=1.40%,n=9)、92.31%~99.12%(RSD=2.71%,n=9)、99.17%~102.32%(RSD=1.24%,n=9)、100.15%~103.98%(RSD=1.18%,n=9)、99.93%~102.61%(RSD=1.03%,n=9)。煎药机煎煮所得总有效成分含量为4 565μg/g,传统煎煮所得总有效成分含量为2 742μg/g。结论:该方法操作简便、稳定、重复性好,可用于桂枝汤中9种主要成分含量的同时测定,其中没食子酸、芍药内酯苷和2-甲氧基桂皮醛的含量测定为桂枝汤中首次报道。煎药机煎煮所得总有效成分含量高于传统煎煮所得总有效成分。
袁鹏飞刘焕尚明英徐风刘广学蔡少青李兰芳姜廷良
关键词:桂枝汤高效液相色谱法
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