Thermo-sensitive hydrogels from free radical copolymerization of NIPAAm and crosslinking monomer MBA (p(NIPAAm-co-MBA)) using in situ liquid atmospheric DBD plasma are successfully synthesized as revealed by FTIR and solid state 13 C-NMR analysis, despite a rather short polymerization time of 10 min. The addition of MBA crosslinking monomer exerts a positive influence on the p(NIPAAm-co-MBA) copolymerization process, particularly at higher monomer concentrations and incident plasma power as suggested by GPC analysis. The swelling capacity of the p(NIPAAm-co-MBA) hydrogels declines significantly when the MBA concentration increased due to better crosslinking efficiency during the copolymerization process. The decrease in swelling capacity of p(NIPAAm-co-MBA) is also displayed by cryo-SEM analysis as smaller pore sizes and higher pore density of hydrogels were detected. The thermo responsiveness of p(NIPAAm-co-MBA) hydrogels is confirmed by DSC analysis with LCST values similar to the LCTS value of p(NIPAAm) around 32 8C. Enthalpy /J/g : 58,5924 (Endothermic effect) Exo Peak: 32.8140 o C Onset point: 26.5695 o C Enthalpy: 26.4631 J/g Peak: 33.2749 o C Onset point: 30.6265 o C Enthalpy: 69.6224 J/g Peak: 33.5454 o C Onset point: 21.9078 o C Enthalpy: 58.5924 J/g Peak: 33.0978 o C Onset point: 30.6117 o C Enthalpy: 59.0967 J/g Figure 6. DSC thermograms of the p(NIPAAm-co-MBA) hydrogels obtained at 30 W plasma power with (a) 10% NIPAAm with 0.1% MBA, (b) 10% NIPAAm with 1% MBA, (c) 20% NIPAAm with 0.2% MBA, and (d) 20% NIPAAm with 2% MBA (heating rate of 1.5 8C min À1 from 5 to 50 8C).