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Application of a quantitative ^1H NMR method for rapid extraction and determination of the content of paeonol in Cynanchum paniculatum 被引量:4
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作者 Xuejiao Li Jianwei Dong +3 位作者 Xiu Gao Guijun Li Junyou Shi Yanqing Zhang 《Journal of Chinese Pharmaceutical Sciences》 CAS CSCD 2020年第6期422-430,共9页
Cynanchum paniculatum(Bunge) Kitagawa is usually used as an herbal medicine for treating many diseases. Paeonol is the main active component, and its content is the key indicator for quality control of C. paniculatum.... Cynanchum paniculatum(Bunge) Kitagawa is usually used as an herbal medicine for treating many diseases. Paeonol is the main active component, and its content is the key indicator for quality control of C. paniculatum. In the present study, we developed a rapid, accurate and precise method for quantitation of paeonol in C. paniculatum using 1 H NMR spectra. The deuterated solvent of methanol-d4 enabled satisfactory separation of the signals to be integrated in 1 H NMR spectrum. H-6(δ 7.78) of 1 H NMR spectrum of C. paniculatum was selected as the feature signal for quantitation, and trimesic acid(TMA) was selected as an internal standard. Validation of the quantitative method was performed in terms of linearity, specificity, repeatability and stability. This is the first time to report quantitative 1 H NMR(qHNMR) applied to determine the content of paeonol in C. paniculatum and showed a wider linearity range than the reported quantitation of paeonol in others. The simple extraction of paeonol from C. paniculatum was rapid and will prompt the application of the developed method. This work implied that qHNMR represented a feasible alternative to HPLC-based methods for quantitation of paeonol in C. paniculatum, and it was suitable for the quality control of C. paniculatum. 展开更多
关键词 Cynanchum paniculatum Quantitative ^1H NMR PAEONOL Quantitative determination
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手性镧系位移试剂识别-核磁共振氢谱法测定保健食品中肉碱对映体含量
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作者 夏金涛 朱松松 +1 位作者 朱芊 江丰 《中国食品卫生杂志》 CSCD 北大核心 2022年第4期730-736,共7页
目的 采用手性镧系位移试剂识别-核磁共振氢谱法(CLSR-1H qNMR)对保健食品中的肉碱对映体进行快速定性、定量分析研究。方法 样品经氘代甲醇溶解,以吡嗪为内标,经过涡旋、超声辅助萃取、离心后,取适量上层清液,加入手性镧系位移试剂Eu(t... 目的 采用手性镧系位移试剂识别-核磁共振氢谱法(CLSR-1H qNMR)对保健食品中的肉碱对映体进行快速定性、定量分析研究。方法 样品经氘代甲醇溶解,以吡嗪为内标,经过涡旋、超声辅助萃取、离心后,取适量上层清液,加入手性镧系位移试剂Eu(thfc)3,直接对待测物进行检测。结果 左旋肉碱的质量浓度线性范围在16.3~4 800μg/mL,相关系数(r)>0.99,检出限(LOD)为24.5 mg/kg,定量限(LOQ)为73.5 mg/kg;右旋肉碱的质量浓度线性范围在10.6~530μg/mL,r>0.99,LOD为27.5 mg/kg,LOQ为82.5 mg/kg。方法的加标回收率为95.9%~114.6%,RSD(n=6)为3.31%~6.12%。对网购宣称具有减肥功效的胶囊、奶茶、咖啡粉、片剂进行检测,均未检测出右旋肉碱。结论 本方法简便、快速、灵敏,25 min内即可完成检测,能够为肉碱对映体各自含量的快速检测提供理论基础。 展开更多
关键词 手性镧系位移试剂 定量核磁共振氢谱 肉碱对映体 保健食品
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Authentic compound-free strategy for simultaneous determination of primary coumarins in Peucedani Radix using offline high performance liquid chromatography–nuclear magnetic resonance spectroscopy–tandem mass spectrometry 被引量:9
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作者 Yao Liu Qingqing Song +7 位作者 Wenjing Liu Peng Li Jun Li Yunfang Zhao Liang Zhang Pengfei Tu Yitao Wang Yuelin Song 《Acta Pharmaceutica Sinica B》 SCIE CSCD 2018年第4期645-654,共10页
Herein, a strategy is proposed for the simultaneous determination of primary coumarins in Peucedani Radix(Chinese name: Qianhu). The methodology consists of three consecutive steps: 1) Semi-preparative LC in combinati... Herein, a strategy is proposed for the simultaneous determination of primary coumarins in Peucedani Radix(Chinese name: Qianhu). The methodology consists of three consecutive steps: 1) Semi-preparative LC in combination with a home-made automated fraction collection module to fragment the universal metabolome standard into ten fractions(Frs. I–X); 2) LC–accurate MS/MS and quantitative1 H NMR spectroscopy conducted in parallel to acquire the qualitative and quantitative data of each fraction; 3) Robust identification and quantification of components by use of LC coupled to multiple reaction monitoring. In this final step, the most significant fractions(Frs. III–X) were pooled to serve as the pseudo-mixed standard solution. Meticulous online parameter optimization was performed to obtain the optimal parameters, including ion transitions and collision energies. Concerns were particularly paid onto pursuing the parameters being capable of monitoring regiospecific isomers, notably praeruptorin E vs. 3′-isovaleryl-4′-angeloylkhellactone. The quantitative performance of the method was validated according to diverse assays. Eleven primary coumarins(1–11) were unambiguously identified and absolutely quantified, even though no external reference compound was used. Above all, the integrated strategy not only provides a feasible pipeline for the quality assessment of Peucedani Radix, but more importantly, shows the potential for authentic compound-free quantitative evaluation of traditional Chinese medicines. 展开更多
关键词 Authentic compoundindependent quantitation Offline LC–NMR–MS/MS Automated fraction collection module quantitative1h NMR Peucedani Radix Regio-specific monitoring
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