Navarro Fabián H, Gómez Jorge E, Espinal José H, Sandoval Junior E
Department of Chemistry, Universidad del Valle, Cali, Colombia.
Department of Chemistry, Universidad del Valle, Cali, Colombia.
Anal Chim Acta. 2016 Dec 15;948:104-112. doi: 10.1016/j.aca.2016.10.023. Epub 2016 Oct 19.
In the present study, porous silica particles as well as impervious fused-silica wafers and capillary tubes were modified with hydrophilic polymers (hydroxylated polyacrylamides and polyacrylates), using a surface-confined grafting procedure based on atom transfer radical polymerization (ATRP) which was also surface-initiated from α-bromoisobutyryl groups. Initiator immobilization was achieved by hydrosilylation of allyl alcohol on hydride silica followed by esterification of the resulting propanol-bonded surface with α-bromoisobutyryl bromide. Elemental analysis, IR and NMR spectroscopies on silica micro-particles, atomic force microscopy, ellipsometry and profilometry on fused-silica wafers, as well as CE on fused-silica tubes were used to characterize the chemically modified silica substrate at different stages. We studied the effect of monomer concentration as well as cross-linker on the ability of the polymer film to reduce electroosmosis and to prevent protein adsorption (i. e., its non-fouling capabilities) and found that the former was rather insensitive to both parameters. Surface deactivation towards adsorption was somewhat more susceptible to monomer concentration and appeared also to be favored by a low concentration of the cross-linker. The results show that hydrophilic polyacrylamide and polyacrylate coatings of controlled thickness can be prepared by ATRP under very mild polymerization conditions (aqueous solvent, room temperature and short reaction times) and that the coated capillary tubes exhibit high efficiencies for protein separations (0.3-0.6 million theoretical plates per meter) as well as long-term hydrolytic stability under the inherently harsh conditions of capillary isoelectric focusing. Additionally, there was no adsorption of lysozyme on the coated surface as indicated by a complete recovery of the basic enzyme. Furthermore, since polymerization is confined to the inner capillary surface, simple precautions (e.g., solution filtration) during the surface modification process are sufficient to prevent capillary clogging.
在本研究中,使用基于原子转移自由基聚合(ATRP)的表面受限接枝程序,对多孔二氧化硅颗粒以及不透水的熔融石英晶片和毛细管进行了亲水性聚合物(羟基化聚丙烯酰胺和聚丙烯酸酯)改性,该程序也是从α-溴异丁酰基进行表面引发的。通过烯丙醇在氢化物二氧化硅上的硅氢加成反应,然后将所得的丙醇键合表面与α-溴异丁酰溴进行酯化反应,实现引发剂的固定化。对二氧化硅微粒进行元素分析、红外光谱和核磁共振光谱分析,对熔融石英晶片进行原子力显微镜、椭偏仪和轮廓仪分析,以及对熔融石英管进行毛细管电泳分析,以表征不同阶段化学改性的二氧化硅基质。我们研究了单体浓度以及交联剂对聚合物膜降低电渗和防止蛋白质吸附能力(即其抗污染能力)的影响,发现前者对这两个参数相当不敏感。表面对吸附的失活对单体浓度更敏感一些,并且似乎也受到低浓度交联剂的青睐。结果表明,在非常温和的聚合条件下(水性溶剂、室温及短反应时间),通过ATRP可以制备出厚度可控的亲水性聚丙烯酰胺和聚丙烯酸酯涂层,并且涂覆的毛细管柱在毛细管等电聚焦固有苛刻条件下,对蛋白质分离具有高效率(每米0.3 - 0.6百万理论塔板数)以及长期的水解稳定性。此外,如碱性酶完全回收所示,溶菌酶在涂覆表面上没有吸附。此外,由于聚合作用局限于毛细管内表面,在表面改性过程中采取简单的预防措施(例如溶液过滤)就足以防止毛细管堵塞。