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Analysis and pharmacokinetic study of polyphyllin H in beagle dog plasma after oral administration of Rhizoma Paridis Extracts by LC‐MS/MS 下载免费PDF全文
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Yan Zhao Xingbin Yang Ru Jiang Xiaoli Sun Wenmin Liu Shengyong Zhang 《Analytical sciences》2006,22(5):747-751
The investigation on capillary electrophoretic enantioseparation of six synthetic compounds containing vicinal diol groups has been undertaken to acquire the optimum conditions using native beta-cyclodextrin (beta-CD) as chiral selector and borate as a background electrolyte. The separation was carried out in an uncoated capillary (58.5 cm x 75 microm i.d., effective length 48.5 cm) and the effects of several important factors were investigated in detail. The results showed that beta-CD as a chiral selector exhibited good enantioselectivity and that the enantioseparation was greatly influenced by the structure of the diols, the borate concentration and the buffer pH. The optimum performance was obtained for the chiral vicinal diols under the conditions of 200 mM borate buffer of pH 9.8 containing 1.7% beta-CD at an applied voltage of 15 kV and a capillary temperature of 20 degrees C. Under the conditions, four diols were baseline separated with fast analysis time and the good theoretical plate numbers (above 10 x 10(4)) and favorable migration-time reproducibilities (RSDs below 3.0%) were obtained. The separation results were satisfactory. 相似文献
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Xingbin Ma Xukun Zhang Hongling Lin A. M. Abd El‐Aty Tsdan Rabah Xiaoxi Liu Zhichao Yu Yanhong Yong Xianghong Ju Yongxin She 《Journal of separation science》2020,43(12):2301-2310
The naturally occurring quercetin flavonoid, dihydroquercetin, is widely distributed in plant tissues and has a variety of biological activities. Herein, a magnetic molecularly imprinted solid‐phase extraction was tailor made for selective determination of dihydroquercetin in Larix griffithiana using high‐performance liquid chromatography. Amino‐functionalized core‐shell magnetic nanoparticles were prepared and characterized using scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometry, and infrared spectroscopy. The polymer had an average diameter of 250 ± 2.56 nm and exhibited good stability and adsorption for template molecule, which is enriched by hydrogen bonding interaction. Multiple factors for extraction, including loading, washing, elution solvents, and extraction time, were optimized. The limit of detection was 1.23 μg/g. The precision determined at various concentration of dihydroquercetin was less than 4% and the mean recovery was between 74.64 and 101.80%. It has therefore been shown that this protocol can be used as an alternative extraction to quantify dihydroquercetin in L. griffithiana and purify quercetin flavonoid from other complex matrices. 相似文献
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The theoretical analysis and experimental results of the wavelength tunability of a tandem optical parametric oscillator (TOPO) based on a single nonlinear crystal are presented.TOPO is a configuration wherein the signal laser is used as a pump laser to generate secondary optical parametric oscillator (OPO).The cascaded parametric interactions are achieved synchronously in a single-grating-period MgO doped periodically poled lithium niobate (PPMgOLN).Tunable multiple-wavelength mid-infrared (mid-IR) lasers are obtained by changing the temperature of the crystal.When the PPMgOLN crystal with a grating period of 31.2 μm is operated at 148 ℃,the dual OPOs generate an identical mid-IR laser of 2.83 μm.The secondary OPO transforms into an optical parametric amplifier,in which different frequency mixing from the signal laser results in the amplification of the idler laser in the first OPO.TOPO is a useful configuration for multiple laser output,broad tuning range,and high-efficiency mid-IR lasers. 相似文献
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中药大黄多糖中单糖组成的毛细管区带电泳分析 总被引:5,自引:2,他引:5
以1-苯基-3-甲基-5-吡唑啉酮(PMP)为单糖的衍生化试剂,建立毛细管区带电泳(CZE)同时分离分析8种常见还原单糖PMP衍生物的方法。将该方法用于中药大黄多糖(RTP)的单糖组成及其摩尔比率的测定。结果表明,在pH 10.8和150 mmol/L硼砂缓冲溶液、10kV分离电压、25℃柱温的优化条件下,8种单糖衍生物实现了良好的分离,并证实RTP由阿拉伯糖、葡萄糖、半乳糖、葡萄糖醛酸和半乳糖醛酸5种单糖组成,其摩尔比为8.01∶5.01∶30.30∶1.00∶1.56;样品测定回收率为96.4%~105.3%。该方法灵敏、快速、准确,可用于中药RTP的组成分析。 相似文献
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A new capillary electrophoretic method was developed for enantiomeric separation and optical impurity analysis of three synthetic 2,3-dihydroxy-3-phenylpropionate compounds using native beta-cyclodextrin (beta-CD) as chiral selector and borate as a background electrolyte. The separation was carried out in uncoated capillary (58.5 cm x 75 microm I.D., effective length 48.5 cm). The results showed that beta-CD as the chiral selector exhibited good enantioselectivity and the baseline separation was obtained at pH 9.8, 200 mM borate buffer containing 1.7% beta-CD at applied voltage 15 kV and capillary temperature 20 degrees C within 15 min. The precision of each tested compound was less than 1.0% at migration time and 5.0% in corrected peak area and the accuracy of the method was in the range of 98.7-105%. Furthermore, the developed method was successfully applied to the determination of the undesirable trace (2S,3R)-(+)-form impurity in the synthetic (2R,3S)-(-)-2,3-dihydroxy-3-phenylpropionate samples. 相似文献
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Xingbin Yin Changhai Qu Zhaoxia Li Yujing Zhai Sali Cao Longfei Lin Lijun Feng Lei Yan Jian Ni 《Biomedical chromatography : BMC》2013,27(3):343-348
For the first time, a rapid and specific LC‐MS‐MS method has been developed for the analysis of polyphyllin I, polyphyllin II, polyphyllin VI and polyphyllin VII in beagle dog plasma. The method was applied to study the pharmacokinetics of Rhizoma Paridis extracts containing polyphyllin I, polyphyllin II, polyphyllin VI and polyphyllin VII. The analysis was carried out on an Agilent Zorbax XDB‐C18 reversed‐phase column (100 × 2.1 mm, 1.8 µm) by isocratic elution with acetonitrile and water (50:50, v/v). The flow rate was 0.25 mL/min. All analytes including internal standards were monitored by selected reaction monitoring with an electrospray ionization source. Linear responses were obtained for polyphyllin I, polyphyllin II, polyphyllin VI and polyphyllin VII ranging from 10 to 5000 ng/mL. The intra‐and inter‐day precisions (RSDs) were less than 6.66 and 9.15%. The extraction recovery ranged from 95.53 to 104.21% with RSD less than 8.69%. Stability studies showed that polyphyllin I, polyphyllin II, polyphyllin VI and polyphyllin VII were stable in preparation and analytical process. The validated method was successfully used to determine the concentration–time profiles of polyphyllin I, polyphyllin II, polyphyllin VI and polyphyllin VII. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
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One-step synthesis of pure Cu nanowire/carbon nanotube coaxial nanocables with different structures by arc discharge 总被引:1,自引:0,他引:1
Jijun Ding Xingbin Yan Beng Kang Tay Qunji Xue 《Journal of Physics and Chemistry of Solids》2011,72(12):1519-1523
Pure Cu nanowire/carbon nanotube (Cu@C) coaxial nanocables are one-step fabricated by arc discharge. The microstructure and morphology of the Cu@C nanocables are investigated via X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HRTEM). XRD results reveal that the copper carbide nano-crystals were formed in the nanocables and it plays an important role in the growth of the Cu@C nanocables. As-prepared Cu@C nanocables exhibit three different structures, including well-filled Cu@C nanocables, symmetrically trifurcate Cu@C nanocables, and twice capsulated Cu@C nanocables. The fabrication of Cu@C nanocables with different structures offers more opportunities for the development of nanoelectronic devices. The formation mechanisms of Cu@C nanocables with different structures are discussed as well. 相似文献