2012
DOI: 10.1016/j.snb.2012.01.031
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β-Cyclodextrin/Fe3O4 hybrid magnetic nano-composite modified glassy carbon electrode for tryptophan sensing

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Cited by 97 publications
(41 citation statements)
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“…Therefore, this strategy may implicate great promises for the fabrication of other electrochemical sensors. Au-NPs/GCE DPV 2.5 8.0 × 10 −8 [10] Boron doped diamond nanowire modified silicon substrate DPV 11 5 × 10 −7 [34] PAA modified GC DPV 6 5.2 × 10 −6 [35] ERGO/GCE DPV 6.5 0.1 × 10 −6 [14] MWCNT/CoSal-modified carbon paste electrode DPV 4 1.0 × 10 −7 [36] ß-CD-MNPs/GCE DPV 7 5.0 × 10 −7 [9] CS-CNDs/GCE DPV 9 9.0 × 10 −8 Present work …”
Section: Discussionmentioning
confidence: 99%
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“…Therefore, this strategy may implicate great promises for the fabrication of other electrochemical sensors. Au-NPs/GCE DPV 2.5 8.0 × 10 −8 [10] Boron doped diamond nanowire modified silicon substrate DPV 11 5 × 10 −7 [34] PAA modified GC DPV 6 5.2 × 10 −6 [35] ERGO/GCE DPV 6.5 0.1 × 10 −6 [14] MWCNT/CoSal-modified carbon paste electrode DPV 4 1.0 × 10 −7 [36] ß-CD-MNPs/GCE DPV 7 5.0 × 10 −7 [9] CS-CNDs/GCE DPV 9 9.0 × 10 −8 Present work …”
Section: Discussionmentioning
confidence: 99%
“…On the other hand, electrochemical method of determination is less expensive, more convenient, easy in handling, as well as with high sensitivity and selectivity. Several studies have been conducted in this area [8][9][10][11][12][13][14]. The results of such studies have revealed that the voltammetric response of the electrochemical process is not satisfactory due to slow heterogeneous electron transfer on the electrode surface and consequent high overpotentials of the electrochemical oxidation [15,16].…”
mentioning
confidence: 99%
“…As shown in Scheme 1, 6-TsO-b-CD was prepared by two steps with reference to our previously reported protocol [19]. First, ptoluenesulfonyl imidazole (Ts-Im) was generated by reacting imidazole with p-toluenesulfonyl chloride in dried CH 2 Cl 2 .…”
Section: Preparationmentioning
confidence: 99%
“…Magnetic nanoparticles Fe 3 O 4 were synthesized based on the reported co-precipitating Fe 2þ and Fe 3þ ions in ammonia solution under hydrothermal conditions [19,20], as shown in Scheme 1. 67 mg of FeCl 2 4H 2 O and FeCl 3 6H 2 O in 1:2 M ratio were dissolved in 200 mL redistilled water with the concentration of iron ions at 0.30 M. Precipitation was generated by adding 25% NH 4 OH solution into Fe 2þ and Fe 3þ solution at 25 C under vigorous stirring.…”
Section: Preparation Of Fe 3 O 4 Magnetic Nanoparticlesmentioning
confidence: 99%
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