Ott Sonja, Niessner Reinhard, Seidel Michael
Chair for Analytical Chemistry and Institute of Hydrochemistry, Technische Universität München, Munich, Germany.
J Sep Sci. 2011 Aug;34(16-17):2181-92. doi: 10.1002/jssc.201100208. Epub 2011 Jul 7.
Macroporous epoxy-based monolithic columns were used for immunofiltration of bacteria. The prepared monolithic polymer support is hydrophilic and has large pore sizes of 21 μm without mesopores. A surface chemistry usually applied for immobilization of antibodies on glass slides is successfully transferred to monolithic columns. Step-by-step, the surface of the epoxy-based monolith is hydrolyzed, silanized, coated with poly(ethylene glycol diamine) and activated with the homobifunctional crosslinker di(N-succinimidyl)carbonate for immobilization of antibodies on the monolithic columns. The functionalization steps are characterized to ensure the coating of each monolayer. The prepared antibody-immobilized monolithic column is optimized for immunofiltration to enrich Staphylococcus aureus as an important food contaminant. Different kinds of geometries of monolithic columns, flow rates and elution buffers are tested with the goal to get high recoveries in the shortest enrichment time as possible. An effective capture of S. aureus was achieved at a flow rate of 7.0 mL/min with low backpressures of 20.1±5.4 mbar enabling a volumetric enrichment of 1000 within 145 min. The bacteria were quantified by flow cytometry using a double-labeling approach. After immunofiltration the sensitivity was significantly increased and a detection limit of the total system of 42 S. aureus/mL was reached.
大孔环氧基整体柱用于细菌的免疫过滤。制备的整体聚合物载体具有亲水性,孔径为21μm且无中孔。通常用于在载玻片上固定抗体的表面化学方法成功地转移到了整体柱上。逐步地,对环氧基整体柱的表面进行水解、硅烷化处理,用聚(乙二醇二胺)包被,并用同双功能交联剂二(N-琥珀酰亚胺基)碳酸酯活化,以便在整体柱上固定抗体。对功能化步骤进行表征以确保每个单层的包被。制备的固定抗体的整体柱针对免疫过滤进行了优化,以富集作为重要食品污染物的金黄色葡萄球菌。测试了不同几何形状的整体柱、流速和洗脱缓冲液,目标是在尽可能短的富集时间内获得高回收率。在流速为7.0 mL/min、背压低至20.1±5.4 mbar的条件下实现了对金黄色葡萄球菌的有效捕获,从而在145分钟内实现了1000倍的体积富集。使用双标记方法通过流式细胞术对细菌进行定量。免疫过滤后,灵敏度显著提高,整个系统的检测限达到42个金黄色葡萄球菌/mL。