Synthesis and aqueous solution properties of sterically stabilized pH-responsive polyampholyte microgels

被引:31
作者
Tan, Beng H.
Ravi, P.
Tan, Lie N.
Tam, Kam C.
机构
[1] Nanyang Technol Univ, Sch Mech & Aerosp Engn, Singapore 639798, Singapore
[2] Nanyang Technol Univ, Singapore MIT Alliance, Singapore 639798, Singapore
[3] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 639798, Singapore
关键词
emulsion polymerization; pH-responsive polyampholyte microgel; isoelectric pH; steric stabilization;
D O I
10.1016/j.jcis.2007.01.019
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Emulsion copolymerization of poly(methacrylic acid) and poly(2-(diethylamino)ethyl methacrylate) (PMAA/PDEA) yielded pH-responsive polyampholyte microgels of 200-300 run in diameter. These microgels showed enhanced hydrophilic behavior in aqueous medium at low and high pH, but formed large aggregates of similar to 2500 rim at intermediate pH. To achieve colloidal stability at intermediate pH, a second batch of microgels of identical monomer composition were synthesized, where monomethoxy-capped poly(ethylene glycol)methacrylate (PEGMA) was grafted onto the surface of these particles. Dynamic light-scattering measurements showed that the hydrodynamic radius, R-h, of sterically stabilized microgels was approximately 100 nm at intermediate pH and increased to 120 and 200 run at pH 2 and 10, respectively. Between pH 4 and 6, these microgels possessed mobility close to zero and a negative second virial coefficient, A(2), due to overall charge neutralization near the isoelectric pH. From the R-h, mobility, and A(2), cross-linked MAA-DEA microgels with and without PEGMA retained their polyampholytic properties in solution. By varying the composition of MAA and DEA in the microgel, it is possible to vary the isoelectric point of the colloidal particles. These new microgels are being explored for use in the delivery of DNA and proteins. (C) 2007 Elsevier Inc All rights reserved.
引用
收藏
页码:453 / 463
页数:11
相关论文
共 47 条
[1]   Synthesis and characterization of novel pH-responsive microgels based on tertiary amine methacrylates [J].
Amalvy, JI ;
Wanless, EJ ;
Li, Y ;
Michailidou, V ;
Armes, SP ;
Duccini, Y .
LANGMUIR, 2004, 20 (21) :8992-8999
[2]   Interactions, structural ordering and phase transitions in colloidal dispersions [J].
Arora, AK ;
Tata, BVR .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 1998, 78 (01) :49-97
[3]  
BEKTUROV EA, 1990, MAKROMOL CHEM, V191, P457
[5]  
BROWN W, 1992, DYNAMIC LIGHT SCATTE
[6]   Synthesis of zwitterionic shell cross-linked micelles [J].
Bütün, V ;
Lowe, AB ;
Billingham, NC ;
Armes, SP .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1999, 121 (17) :4288-4289
[7]   AQUEOUS-SOLUTION PROPERTIES OF AMPHOLYTIC COPOLYMERS PREPARED IN MICROEMULSIONS [J].
CORPART, JM ;
CANDAU, F .
MACROMOLECULES, 1993, 26 (06) :1333-1343
[8]   CHARACTERIZATION OF HIGH CHARGE-DENSITY AMPHOLYTIC COPOLYMERS PREPARED BY MICROEMULSION POLYMERIZATION [J].
CORPART, JM ;
SELB, J ;
CANDAU, F .
POLYMER, 1993, 34 (18) :3873-3886
[9]   Exchange of polymer molecules between block copolymer micelles studied by emission spectroscopy. A method for the quantification of unimer exchange rates [J].
Creutz, S ;
vanStam, J ;
Antoun, S ;
DeSchryver, FC ;
Jerome, R .
MACROMOLECULES, 1997, 30 (14) :4078-4083
[10]   Dynamics of poly((dimethylamino)alkyl methacrylate-block-sodium methacrylate) micelles. Influence of hydrophobicity and molecular architecture on the exchange rate of copolymer molecules [J].
Creutz, S ;
van Stam, J ;
De Schryver, FC ;
Jerome, R .
MACROMOLECULES, 1998, 31 (03) :681-689