Molecularly imprinted polymers（MIPs） were applied as molecular recognition elements to an electro- chemical sensor for cinchonidine（CD）. A kind of MIP was synthesized with cinchonidine as template, modified ro- sin（ethylene glycol maleic rosinate acrylate） containing the skeleton of phenanthrene rings as cross-linker and me- thylacrylic acid as functional monomer. MIP membrane was prepared on a glassy carbon electrode for the determina- tion of CD via free radical polymerization method. Electrochemical impedance spectroscopy（EIS） and cyclic vol- tammetry（CV） were used to characterize the membrane electrochemical behavior in electrode fabrication process. The experimental conditions were discussed. Under optimum conditions, it was found that the response of peak cur- rents was linear to the concentration of CD in a range of 0.013-2.26 mmol/L. The detection limit for CD is 1 μmol/L the relative standard deviation for 100 μmol/L CD is 1.34% and the incubation time is 2 min. The sensor was applied to the determination of CD in urine samples with satisfactory results.
LIU LiTAN Xue-caiZHAO Dan-danWANG LinLEI Fu-houHUANG Zai-yin
A novel third-generation hydrogen peroxide（H2O2） biosensor（Hb/CdS/MWNTs/GCE） was fabricated through hemoglobin（Hb） adsorbed onto the mercaptoacetic acid modified CdS QDs/carboxyl multiwall carbon nanotubes＇（MWNTs） films. Cyclic voltammogram of Hb/CdS/MWNTs/GCE showed a pair of well-defined and quasi-reversible redox peaks with a formal potential（E^0） of-0.230 V（vs. Ag/AgCl） in 0.1 mol/L pH=8.0 phosphate buffer solution（PBS）, which was the characteristic of the Hb heme Fe（Ⅲ）/Fe（Ⅱ） redox couple. The biosensor shows an excellent electrocatalytic activity to the reduction of H2O2. The response time of the designed biosensor to H202 at a potential of-0.30 V was less than 2 s and linear relationships were obtained in the concentration ranges of 2.0×10^-6-2.7×10^-3 mol/L and 2.7×10^-3-7.7×10^-3 mol/L with a detection limit of 3.0×10^-7 mol/L（S/N=3）. The apparent Michaelis-Menten constant Km was estimated to be 1.324 mmol/L that illustrated the excellent biological activity of the fixed Hb.
A novel type of Fe3O4 nanoparticles modified glass carbon electrode（Fe3O4/GCE） was constructed and the electrochemical properties of N-（4-nitro-2-phenoxyphenyl）methanesulfonamide（nimesulide） were studied on the Fe3O4/GCE.In 0.4mol/L HAc-NaAc buffer solution（pH=5.0）,the electrode process of nimesulide was irreversible at bare GCE and Fe3O4/GCE.The Fe3O4/GCE exhibited a remarkable catalytic and enhancement effect on the reduction of nimesulide.The reduction peak potential of nimesulide shifted positively from-0.683 V at bare GCE to-0.625 V at Fe3O4/GCE,and the sensitivity was increased by ca.3 times.Some experimental conditions were optimized.The linear range between the peak current and the concentration of nimesulide was 2.6×10-6 ＂1.0×10-4mol/L（R=0.993） with a detection limit of 1.3×10-7mol/L.This method has been used to determine the content of nimesulide in medical tablets.The recovery was determined to be 96.9% ＂101.9% by means of standard addition method.The method is comparable to UV-Vis spectrometry.
