Dalmont Helene, Pinprayoon Orawan, Saunders Brian R
Biomaterials Research Group, Materials Science Centre, School of Materials, The University of Manchester, Grosvenor Street, Manchester M1 7HS, UK.
Langmuir. 2008 Mar 18;24(6):2834-40. doi: 10.1021/la703597a. Epub 2008 Feb 22.
pH-responsive microgel dispersions contain cross-linked polymer particles that swell when the pH approaches the pKa of the ionic monomer incorporated within the particles. In recent work from our group, it was demonstrated that the mechanical properties of degenerated intervertebral discs (IVDs) could be restored to normal values by injection of pH-responsive microgel dispersions (Saunders, J. M.; Tong, T.; LeMaitre, C.; Freemont, A. J.; Saunders, B. R. Soft Matter 2007, 3, 486). These dispersions change from a fluid to a gel with increasing pH. The present work investigates the pH-dependent properties of dispersions of microgel particles containing MAA (methacrylic acid) and also the effects of added Ca2+. Two microgels are discussed: microgel A is poly(EA/MAA/AM) (EA and AM are ethyl acrylate and allyl methacrylate), and microgel B is poly(EA/MAA/BDDA) (butanediol diacrylate). The pH-dependent particle properties investigated include hydrodynamic diameters and electrophoretic mobilities. The critical coagulation concentrations (CCC) of dilute dispersions and the elastic modulus (G') of concentrated, gelled microgel dispersions were also investigated. In the absence of added Ca2+, the particle swelling and G' were smallest and largest, respectively, for microgel A. The changes in hydrodynamic diameter and mobility with pH were explained in terms of a core-shell swelling mechanism. Added Ca2+ was found to significantly decrease the CCCs, extents of particle swelling, and magnitude of the electrophoretic mobility. This was attributed to the ionic cross-linking of neighboring RCOO- groups by Ca2+. It is suggested that the formation of ionic cross-links is inefficient within the microgel particles because of the presence of covalent cross-links that oppose the large-scale conformational rearrangement of neighboring RCOO- groups. The effect of Ca2+ on the properties of the gelled dispersions is important from the viewpoint of potential application in vivo. Rheological studies of the gelled microgel dispersions showed that added Ca2+ did not have a specific influence on G'. The differences observed in the presence of Ca2+ were attributed to ionic strength effects (screening). The key parameter that controls G' of the gelled microgel dispersions is pH. The results from this work suggest that the elasticity of the gels would be slightly reduced in vivo as a consequence of the high ionic strength present.
pH响应性微凝胶分散体包含交联聚合物颗粒,当pH接近颗粒内所含离子单体的pKa时,这些颗粒会膨胀。在我们小组最近的工作中,已证明通过注射pH响应性微凝胶分散体可将退变椎间盘(IVD)的力学性能恢复到正常值(桑德斯,J.M.;童,T.;勒梅特,C.;弗里蒙特,A.J.;桑德斯,B.R.《软物质》2007年,第3卷,486页)。随着pH升高,这些分散体从流体转变为凝胶。本工作研究了含有甲基丙烯酸(MAA)的微凝胶颗粒分散体的pH依赖性性质以及添加Ca2+的影响。讨论了两种微凝胶:微凝胶A是聚(丙烯酸乙酯/甲基丙烯酸/烯丙基甲基丙烯酸酯)(EA和AM分别是丙烯酸乙酯和烯丙基甲基丙烯酸酯),微凝胶B是聚(丙烯酸乙酯/甲基丙烯酸/丁二醇二丙烯酸酯)。所研究的pH依赖性颗粒性质包括流体动力学直径和电泳迁移率。还研究了稀分散体的临界聚沉浓度(CCC)和浓凝胶化微凝胶分散体的弹性模量(G')。在不添加Ca2+的情况下,微凝胶A的颗粒膨胀最小,G'最大。根据核壳膨胀机制解释了流体动力学直径和迁移率随pH的变化。发现添加Ca2+会显著降低CCC、颗粒膨胀程度和电泳迁移率的大小。这归因于Ca2+对相邻RCOO-基团的离子交联作用。由于存在阻碍相邻RCOO-基团大规模构象重排的共价交联,因此认为离子交联在微凝胶颗粒内效率不高。从体内潜在应用的角度来看,Ca2+对凝胶化分散体性质的影响很重要。对凝胶化微凝胶分散体的流变学研究表明,添加Ca2+对G'没有特定影响。在存在Ca2+的情况下观察到的差异归因于离子强度效应(屏蔽)。控制凝胶化微凝胶分散体G'的关键参数是pH。这项工作的结果表明,由于体内存在高离子强度,凝胶的弹性会略有降低。