详细信息
Preparation of core-shell molecular imprinting polymer for lincomycin A and its application in chromatographic column ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Preparation of core-shell molecular imprinting polymer for lincomycin A and its application in chromatographic column
作者:Wang, Zi[1];Cao, Xuejun[1]
机构:[1]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Dept Bioengn, Shanghai 200237, Peoples R China
年份:2015
卷号:50
期号:7
起止页码:1136
外文期刊名:PROCESS BIOCHEMISTRY
收录:;EI(收录号:20151900821903);WOS:【SCI-EXPANDED(收录号:WOS:000356749300014)】;
语种:英文
外文关键词:Molecular imprinting; Separation; Core-shell; Chromatography; Purification; Lincomycin
摘要:Lincomycin A is one main component of lincomycin, and the separation of lincomycin A from analogues B, C, D by organic solvent extraction has the problems of environmental pollution and multi-step process. Molecular imprinting polymer (MIP) could separate the target product from their structure analogues. In this paper, methyl methacrylate (MMA) was used as monomer in seed core and acrylamide (AM) was used as shell functional monomer. Core-shell MIP for lincomycin A was prepared using lincomycin A as template molecule, ethylene glycol dimethacrylate (EGDMA) as cross-linker and the ammonium persulfate (APS) as the initiator. The structure of MIP was characterized. Lincomycin A purification condition was explored and optimized. The result revealed that the maximal adsorption capacity was 62.66 mg/g, which reached equilibrium within 6 h. The selectivity coefficients of MIP and non-imprinted polymer (NIP) for lincomycin A related to lincomycin B were 3.14 and 1.08. In addition, MIP obtained a good purification result by column chromatography, and the recovery and purity of lincomycin A reached 97.57% and 93.3%, respectively. (C) 2015 Elsevier Ltd. All rights reserved.
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