This
Letter describes a new rapid and sensitive immunosensing device
using the pore space of a porous membrane as the reaction space. A
track-etched membrane with uniform cylindrical pores is used as the
base substrate of this device. The capture antibodies are covalently
and densely immobilized inside the membrane pores by the uniform introduction
of poly(acrylic acid) (PAAc) via the plasma graft polymerization technique,
followed by the active ester method. This membrane shows excellent
antibody retention by covalent binding. The detection test was carried
out via a sandwich-type assay, and all reaction steps from the antigen–antibody
reaction to the enzyme reaction were conducted by permeating each
solution into the pores. The detection test showed a signal comparable
to that of the conventional enzyme-linked immunosorbent assay, although
the detection time required in the test was shortened to 35 min. The
reason for achieving both high sensitivity and short detection time
is that the antibody accumulated pore space with high selectivity
and promoted contact between the reactants by solution permeation.
This report is expected to aid the design of systems for membrane-based
devices, which currently have problems associated with sensitivity,
rapidity, selectivity, or amount of sample. We further expect that
this system could be applied to various diagnostic areas, including
point-of-care testing.
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