Nonaqueous emulsion polymerization: A practical synthetic route for the production of molecularly imprinted nanospheres

被引:9
作者
Dvorakova, Gita [1 ,2 ]
Haschick, Robert [3 ]
Klapper, Markus [3 ]
Muellen, Klaus [3 ]
Biffis, Andrea [1 ]
机构
[1] Univ Padua, Dipartimento Sci Chim, I-35131 Padua, Italy
[2] Charles Univ Prague, Dept Phys & Macromol Chem, Prague 12843, Czech Republic
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
关键词
emulsion polymerization; enantioselectivity; molecular imprinting; molecular recognition; propranolol; PRECIPITATION POLYMERIZATION; NANOPARTICLES; MICROSPHERES; MICROGELS; NANOGELS;
D O I
10.1002/pola.26402
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Monodisperse, molecularly imprinted nanospheres were synthesized by nonaqueous (mini)emulsion polymerization using a standard monomer mixture of methacrylic acid and ethylene dimethacrylate containing the drug propranolol as a template. The preparation conditions (solvent, amount of surfactant, and amount of employed template) were extensively varied in order to assess their effect on the properties of the resulting polymer nanoparticles. The molecular recognition capability of the nanospheres was evaluated in batch rebinding experiments, and the effect of the nanosphere preparation conditions as well as of the reaction conditions was investigated. In this way, optimal preparation protocols for molecularly imprinted nanoparticles under nonaqueous conditions with the use of a nonionic emulsifier were identified, which lead to nanospheres with a diameter of around 100 nm having an enhanced capacity of specific template rebinding compared to both nonimprinted nanospheres and to particles obtained by emulsion polymerization in water. Best results were obtained with nanospheres prepared in N,N-dimethylformamide/n-hexane with a high functional monomer to template ratio. The enantioselectivity of the rebinding process was also demonstrated. (c) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013
引用
收藏
页码:267 / 274
页数:8
相关论文
共 35 条
[1]   Molecular imprinting science and technology: a survey of the literature for the years up to and including 2003 [J].
Alexander, C ;
Andersson, HS ;
Andersson, LI ;
Ansell, RJ ;
Kirsch, N ;
Nicholls, IA ;
O'Mahony, J ;
Whitcombe, MJ .
JOURNAL OF MOLECULAR RECOGNITION, 2006, 19 (02) :106-180
[2]  
Biffis A, 2001, MACROMOL CHEM PHYSIC, V202, P163, DOI 10.1002/1521-3935(20010101)202:1<163::AID-MACP163>3.0.CO
[3]  
2-M
[4]   Physical Forms of MIPs [J].
Biffis, Andrea ;
Dvorakova, Gita ;
Falcimaigne-Cordin, Aude .
MOLECULAR IMPRINTING, 2012, 325 :29-82
[5]   Nanoparticle and targeted systems for cancer therapy [J].
Brannon-Peppas, L ;
Blanchette, JO .
ADVANCED DRUG DELIVERY REVIEWS, 2004, 56 (11) :1649-1659
[6]   The first example of molecularly imprinted nanogels with aldolase type I activity [J].
Carboni, Davide ;
Flavin, Kevin ;
Servant, Ania ;
Gouverneur, Veronique ;
Resmini, Marina .
CHEMISTRY-A EUROPEAN JOURNAL, 2008, 14 (23) :7059-7065
[7]   Molecularly Imprinted Microgels as Enzyme Inhibitors [J].
Cutivet, Arnaud ;
Schembri, Carol ;
Kovensky, Jose ;
Haupt, Karsten .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2009, 131 (41) :14699-14702
[8]   Molecularly Imprinted Nanospheres by Nonaqueous Emulsion Polymerization [J].
Dvorakova, Gita ;
Haschick, Robert ;
Chiad, Khalid ;
Klapper, Markus ;
Muellen, Klaus ;
Biffis, Andrea .
MACROMOLECULAR RAPID COMMUNICATIONS, 2010, 31 (23) :2035-2040
[9]   Imprinted nanomaterials: a new class of synthetic receptors [J].
Flavin, Kevin ;
Resmini, Marina .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2009, 393 (02) :437-444
[10]   Poly(divinylbenzene-alt-maleic anhydride) microgels:: Intermediates to microspheres and macrogels in cross-linking copolymerization [J].
Frank, RS ;
Downey, JS ;
Yu, K ;
Stöver, HDH .
MACROMOLECULES, 2002, 35 (07) :2728-2735