Interpenetrating polymer networks (IPNs) of poly(N-isopropylacrylamide)/polyurethane (PNIPAAm/PU) and poly(N-isopropylacrylamide)/poly(N-isopropylacrylamide)/poly(acrylic acid) (PNI-PAAm/PAA) were synthesized to investigate the swelling and drug releasing behavior. The presence of methane network in PNIPAAm/PU IPNs improved the mechanical strength, but reduced the swelling and drug releasing rates because of its hydrophobic characteristics. The swelling transition temperatures of PNIPAAm gels were Little affected by the incorporation of PU networks in IPN structures. The drug releasing process was analyzed with a simple exponential expression of time dependent fractional drug release. The swelling and drug releasing behavior of PNIPAAm/PAA IPNs was significantly affected by the variation of PAA. compositions. The drug release process changed from anomalous to dual type via zero-order mode with increasing PAA concentration due to the competitive swelling rates between PNEPAAm and PAA during release process. The releasing rate decreased in the buffer solution of pH 7.4, but increased in that of pH 5.0 with increasing PAA concentration at both 28 and 37 degrees C because the swelling power of PAA in pH 5.0 was much less than that in pH 7.4.