Electrochemical Study of Lincomycin on Au-PtNPs/nanoPAN/ Chitosan Nanocomposite Membrane and Its Det

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The Au-Pt alloy nanoparticles(Au-PtNPs) were electrochemically deposited on the surface of polyaniline nanotube(nanoPAN) and chitosan(CS) modified glassy carbon electrode(GCE). The electrochemical behavior of lincomycin at Au-PtNPs/nanoPAN/CS modified GCE was investigated by cyclic voltammetry, linear sweep voltammetry and chronocoulometry. Cyclic voltammetric experiments show that lincomycin at the nanocomposite membrane modified electrode exhibited a pair of quasi-reversible redox peaks in pH=6.0 PBS. The membrane could accelerate the electron transfer of lincomycin on the electrode and significantly enhance the peak current. In a range of 3.0―100.0 mg/L, the reductive peak current of lincomycin at 0.42 V was linearly related to its concentration and the linear regression equation was ip,c=0.2703ρ–0.0042(ip,c: μA; ρ: mg/L; r=0.998, n=7) with a detection limit of 1.0 mg/L(S/N =3). Compared with other methods, this method exhibited many advantages such as high sensitivity, selectivity, wide linear range and low detection limit. The method was used to determine the content of lincomycin in injections commercially available with satisfactory results. Some electrochemical parameters involved in the redox reaction of lincomycin, such as parameter of kinetic nα, standard rate constant ks and the number of H+, were also calculated. The electrochemical behavior of lincomycin at Au-PtNPs / nanoPAN / CS modified (GCE). The Au-Pt alloy nanoparticles (Au-PtNPs) were electrochemically deposited on the surface of polyaniline nanotube (nanoPAN) and chitosan (CS) modified glassy carbon electrode GCE was investigated by cyclic voltammetry, linear sweep voltammetry and chronocoulometry. Cyclic voltammetric experiments show that lincomycin at the nanocomposite membrane modified electrode exhibited a pair of quasi-reversible redox peaks in pH = 6.0 PBS. The membrane could accelerate the electron transfer of lincomycin on the electrode and significantly enhance the peak current. In a range of 3.0-100.0 mg / L, the reductive peak current of lincomycin at 0.42 V was linearly related to its concentration and the linear regression equation was ip, c = 0.2703ρ- 0.0042 ( Compared with other methods, this method shows many many such such as high (ip), c: μA; ρ: mg / L; r = 0.998, n = 7) with a detection limit of 1.0 mg / sensitivity, selec tivity, wide linear range and low detection limit. The method was used to determine the content of lincomycin in injections commercially available with satisfactory results. Some electrochemical parameters involved in the redox reaction of lincomycin, such as parameter of kinetic nα, standard rate constant ks and the number of H +, were also calculated.
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