Recognition of 5-fluorouracil by thermosensitive magnetic surface molecularly imprinted microspheres designed using a computational approach

被引:12
|
作者
Zhang, Li [1 ]
Chen, Lin [2 ,3 ]
Zhang, Huan [2 ,4 ]
Yang, Yongzhen [2 ,3 ]
Liu, Xuguang [2 ,4 ]
机构
[1] Shanxi Dayi Hosp, Dept Urol, Taiyuan 030032, Peoples R China
[2] Taiyuan Univ Technol, Minist Educ, Key Lab Interface Sci & Engn Adv Mat, Taiyuan 030024, Peoples R China
[3] Taiyuan Univ Technol, Res Ctr Adv Mat Sci & Technol, Taiyuan 030024, Peoples R China
[4] Taiyuan Univ Technol, Dept Appl Chem, Coll Chem & Chem Engn, Taiyuan 030024, Peoples R China
基金
中国国家自然科学基金;
关键词
drug delivery systems; molecular recognition; theory and modeling; DRUG-DELIVERY; CARBON MICROSPHERE; SUSTAINED-RELEASE; BISPHENOL-A; POLYMERS; HYPERTHERMIA; TEMPERATURE; DERIVATIVES; ANTICANCER; SEPARATION;
D O I
10.1002/app.45468
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Thermosensitive magnetic surface molecularly imprinted polymer microspheres based on thermosensitive monomer n-isopropylacrylamide (NIPAM) are applied for the recognition of 5-fluorouracil (5-FU). A computational analysis is used to predict the interaction sites between 5-FU and NIPAM, the stoichiometry of the synthesis procedure, and the affinity of imprinted cavities toward 5-FU. Due to hydrogen bond interactions, a stable complex configuration of 5-FU and NIPAM shows a binding energy of -46.50 kJ/mol confirming the suitability of imprinting 5-FU into thermosensitive polymer network. After optimization, the appropriate stoichiometry of 5-FU to NIPAM is set to 1:4 during the preparation process. The simulated imprinted cavities show affinity toward 5-FU, with a binding energy of -112.24 kJ/mol. A preliminary experimental evaluation for the drug recognition of thermosensitive magnetic surface molecularly imprinted polymer microspheres is made, obtaining an adsorption capacity of 21.72 mg/g at 25 degrees C. Pseudo-second-order kinetics well describes the adsorption process. (c) 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 45468.
引用
收藏
页数:9
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