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. 2013 Jun 7;13(6):7492–7504. doi: 10.3390/s130607492

Table 1.

Comparison of the proposed method with other electrochemical methods for determination of NO.

Electrode Linear Range (M) Detection Limit (M) Ks (s−1) Reference
Hb/cyanoethylcellulose-modified glassy carbon electrode 1.12 × 10−6∼4.72 × 10−5 2.0 × 10−8 [39]
poly[N-(2-methacryloyloxyethyl)pyrrolidone]-block-poly[glycidylmethacrylate]/Hb- modifiedglassy carbon electrode 4.5 × 10−7∼10.0 × 10−6 3.2 × 10−7 1.03 ± 0.05 [40]
cytochrome c/sodium dodecylsulfate/polyacrylamide-modified glassycarbon electrode 8.0 × 10−7∼9.5 × 10−5 1.0 × 10−7 1.56 [41]
Hb/gold colloids-modified carbon paste electrode 9.0 × 10−7∼3.0 × 10−4 1.0 × 10−7 3.72 [42]
Hb/poly(diallyldimethyl-ammoniumchloride)- functionalized graphenesheets/room temperature ionicliquid-modified glassy carbon electrode 2.0 × 10−7∼3.26 × 10−5 4.0 × 10−8 [43]
Hb/didodecyldimethylammonium bromide-modified powder microelectrode 1.90 × 10−6∼2.8 × 10−5 2.0 × 10−7 [44]
cytochrome c /polymerized ionic liquid-graphene/BPG electrode 1.05 × 10−6∼1.37 × 10−5 7.0 × 10−7 2.39 [45]
Hb/gold nanoparticles/graphene- modified basal plane graphite electrode 7.2 × 10−7∼7.92 × 10−6 1.2 × 10−8 48 ± 5 This work