Pei Yuxin, Fan Fengfeng, Wang Xinxin, Feng Weiwei, Hou Yong, Pei Zhichao
Shanxi Key Laboratory of Natural Products & Chemical Biology, College of Chemistry & Pharmacy, Northwest A&F University, Yangling 712100, Shaanxi, China.
Polymers (Basel). 2017 Sep 24;9(10):469. doi: 10.3390/polym9100469.
To fabricate molecularly imprinted polymer nanospheres via click reaction, five different clickable compounds were synthesized and two types of click reactions (azide-alkyne and thiol-yne) were explored. It was found that molecularly imprinted polymer nanospheres could be successfully synthesized via thiol-yne click reaction using 3,5-diethynyl-pyridine (1) as the monomer, tris(3-mercaptopropionate) (tri-thiol, 5) as the crosslinker, and hypericin as the template (MIP⁻NSHs). The click polymerization completed in merely 4 h to produce the desired MIP⁻NSHs, which were characterized by FTIR, SEM, DLS, and BET, respectively. The reaction conditions for adsorption capacity and selectivity towards hypericin were optimized, and the MIP⁻NSHs synthesized under the optimized conditions showed a high adsorption capacity (Q = 6.03 μmol•g-1) towards hypericin. The imprinting factors of MIP⁻NSHs towards hypericin, protohypericin, and emodin were 2.44, 2.88, and 2.10, respectively.
为了通过点击反应制备分子印迹聚合物纳米球,合成了五种不同的可点击化合物,并探索了两种类型的点击反应(叠氮化物-炔烃和硫醇-炔烃)。研究发现,以3,5-二乙炔基吡啶(1)为单体、三(3-巯基丙酸酯)(三硫醇,5)为交联剂、金丝桃素为模板,通过硫醇-炔烃点击反应能够成功合成分子印迹聚合物纳米球(MIP⁻NSHs)。点击聚合反应仅需4小时即可完成,生成所需的MIP⁻NSHs,分别通过傅里叶变换红外光谱(FTIR)、扫描电子显微镜(SEM)、动态光散射(DLS)和比表面积分析仪(BET)对其进行表征。优化了对金丝桃素的吸附容量和选择性的反应条件,在优化条件下合成的MIP⁻NSHs对金丝桃素表现出高吸附容量(Q = 6.03 μmol•g-1)。MIP⁻NSHs对金丝桃素、原金丝桃素和大黄素的印迹因子分别为2.44、2.88和2.10。