Academician Workstation, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China; School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin 150090, China.
Academician Workstation, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2021 Jul 15;1178:122767. doi: 10.1016/j.jchromb.2021.122767. Epub 2021 May 26.
In this work, a novel strategy was developed for separation and enrichment of sibiskoside by dummy molecular imprinting technology and magnetic separation technology. The structural analogue geniposide was selected as the dummy template, using 4-vinylpyridine as the functional monomer, ethylene glycol dimethacrylate as the cross-linking agent, and acetonitrile as the porogen. The molecularly imprinted layer was formed on the surface of the magnetic carrier to prepare dummy template molecularly imprinted polymers (DMIPs) with a core-shell structure. The DMIPs were characterized by scanning electron microscope (SEM), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA) and Vibration sample magnetometer (VSM). The results of adsorption kinetics experiments and isothermal adsorption experiments showed that DMIPs can reach adsorption equilibrium in a short period of time and the maximum adsorption capacity can reach 14.67 mg/g. The imprinting factor was 2.08. Compared with the andrographolide, polydatin, arbutin, caffeic acid, neohesperidin dihydrochalcone and quercetin, DMIPs have good adsorption capacity for the sibiskoside. And the reusability was better. After the adsorption of DMIPs, the purity of sibiskoside in the crude extracts from Sibiraea angustata increased to 78%. It provided a basis for the further development and utilization of Sibiraea angustata as well as the separation and enrichment of monoterpenes.
本工作采用虚拟分子印迹技术和磁分离技术开发了一种分离和富集西贝母苷的新策略。选择京尼平苷作为结构类似物作为虚拟模板,以 4-乙烯基吡啶为功能单体,乙二醇二甲基丙烯酸酯为交联剂,乙腈为致孔剂。在磁性载体表面形成分子印迹层,制备具有核壳结构的虚拟模板分子印迹聚合物(DMIPs)。通过扫描电子显微镜(SEM)、傅里叶变换红外光谱(FT-IR)、热重分析(TGA)和振动样品磁强计(VSM)对 DMIPs 进行了表征。吸附动力学实验和等温吸附实验结果表明,DMIPs 可以在短时间内达到吸附平衡,最大吸附量可达 14.67mg/g。印迹因子为 2.08。与穿心莲内酯、虎杖苷、熊果苷、咖啡酸、新橙皮苷二氢查尔酮和槲皮素相比,DMIPs 对西贝母苷具有良好的吸附能力。且重复使用性更好。DMIPs 吸附后,从窄叶鲜卑花粗提物中西贝母苷的纯度提高到 78%。为进一步开发利用窄叶鲜卑花以及单萜的分离富集提供了依据。