摘要

A rapid, sensitive and simple electrophoresis immunoassay was developed using a positive polyelectrolyte multilayer (PEM)-modified cellulose acetate (CA) membrane filter (PEM-CA). C-reactive protein (CRP), a cardiac and inflammation marker, was used as a measurement model. This rapid immunoassay was carried out using electrophoresis to drive the antigen movement, thus allowing local condensation of CRP in the proximity of an antibody-enriched PEM-CA filter. This overcame the diffusion resistance that normally dictates the time required for conventional ELISA. Moreover, electrophoresis could enhance the CRP specificity in a mixed solution of serum proteins because each protein has a unique electrophoretic velocity. The calibration curve for electrophoresis detection had a wide linear range of concentration from 0.013 to 50 nM, with a limit of detection of 33 pM, regardless of the presence of other proteins. The incubation time for antigen-antibody reaction was only 2 min, or about 1/30th of the time required for a conventional ELISA system. We conclude that this electrophoresis detection system should be developed further as a rapid, precise, and simple system for various immunosensors, using PEM-modified membrane filters.