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›› 2012, Vol. 12 ›› Issue (1): 31-37.

• 反应与分离 • 上一篇    下一篇

舒必利分子印迹聚合物的制备及其吸附性能

张薇 佘旭辉 范华均 江子滔 巫坤宏 王李平   

  1. 广东药学院基础学院 广东药学院药科学院 广东药学院药科学院 广东药学院药科学院 广东药学院药科学院
  • 收稿日期:2011-12-15 修回日期:2012-02-06 出版日期:2012-02-20 发布日期:2012-02-20
  • 通讯作者: 张薇

Preparation of Molecularly Imprinted Polymer for Sulpiride and Its Adsorption Characteristics

ZHANG Wei SHE Xu-hui FAN Hua-jun JIANG Zi-tao WU Kun-hong WANG Li-ping   

  1. School of Basic Courses, Guangdong Pharmaceutical University College of Pharmacy, Guangdong Pharmaceutical University College of Pharmacy, Guangdong Pharmaceutical University College of Pharmacy, Guangdong Pharmaceutical University College of Pharmacy, Guangdong Pharmaceutical University
  • Received:2011-12-15 Revised:2012-02-06 Online:2012-02-20 Published:2012-02-20
  • Contact: ZHANG Wei

摘要: 以舒必利(SUL)为模板分子,甲基丙烯酸(MAA)为功能单体,乙二醇二甲基丙烯酸酯为交联剂,采用本体聚合法合成了舒必利的分子印迹聚合物(MIP),采用静态平衡和等温吸附实验研究了影响MIP性能的各种因素及吸附机理. 结果表明,当SUL为0.3 mmol时,制备其MIP的优化条件为:乙腈溶剂用量6 mL, SUL与MAA的摩尔比为1:4,以甲醇-乙酸(9:1, j)溶液为洗脱剂洗脱;该聚合物结构均匀、疏松,对SUL具有较好吸附性能,最大吸附容量为79.12 mmol/g,印迹因子为3.76;初步认为其吸附机理是SUL分子结构中的N-甲基吡咯烷、酰胺和苯磺酰胺基团上的氨基与MAA自组装形成的吸附识别位点空穴;该MIP能识别SUL及其结构类似物阿米舒必利和泰必利,特异性吸附率分别为68.35%, 66.72%和58.8%.

关键词: 舒必利, 分子印迹聚合物, 吸附, 选择性

Abstract: Using sulpiride (SUL) as template, methacrylic acid (MAA) as function monomer, and ethyleneglycol dimethacrylate (EDMA) as cross linker, a molecularly imprinted polymer (MIP) was synthesized by bulk polymerization. Static adsorption and isothermal adsorption experiments were performed to study the influential factors on adsorption properties of the MIP to SUL by UV, FT-IR and SEM analysis. Adsorption mechanism of the MIP was also analyzed. The results showed that its best imprinting effect on SUL was observed when the volume of acetonitrile was 6 mL, molar ratio of SUL to MAA 1 to 4, and methanol-acetic acid (9:1, j) used as eluting agent. The MIP offered uniform, loose and porous structure with 79.12 mmol/g of maximum adsorption capacity and 3.76 of imprinted factor for SUL. The main recognition sites of MIP were cavities caused by three types of amino groups on amide, benzsulfamide and 1-methylpyrrolidine in molecular structure. The MIP had better specific adsorption and exhibited good recognition and selectivity to SUL and its analogues such as amisulpride and tiapride. Their specific adsorption rates were respectively 68.35%, 66.72% and 58.8%. Thus, the MIP could be used in separation and analysis for SUL drugs.

Key words: sulpiride, molecularly imprinted polymer, adsorption, selectivity

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