Preparation of molecularly imprinted polypyrrole peroxide/gold nanoparticles modified electrode and its application in electrochemical recognition of cysteine enantiomers
A technology for peroxidizing polypyrrole and modifying electrodes is applied in the fields of biotechnology and electrochemical research, and can solve the problems of less imprinting sites, increasing L-cysteine, and low recognition efficiency of chiral substances in molecularly imprinted chiral sensors. , to achieve the effect of simple and easy preparation method and improved recognition efficiency
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Embodiment 1
[0024] a. Prepare a mixed solution including 0.12mM chloroauric acid and 0.1M potassium chloride, and reduce the chloroauric acid under different constant potential time conditions to obtain nano-gold modified electrodes.
[0025] b. Put the nano-gold modified electrode prepared in step a into the pre-prepared mixed solution including 2mM L-cysteine, 0.1M pyrrole, and 0.1M potassium chloride for 10min, in the potential range of –0.6~0.8V The method of cyclic voltammetry is used to polymerize the monomer pyrrole. After the polymerization, in the phosphate buffer solution, the cyclic voltammetry is used to dedope in the potential range of 0-1.6V, and the molecularly imprinted polypyrrole peroxide / nano gold is obtained. Modified electrodes.
[0026] c. Prepare a phosphate buffer solution containing 1mM L- / D-cysteine, insert the molecularly imprinted polypyrrole peroxide / nano-gold modified electrode prepared in step b into the electrode containing L- / D-cysteine After standing in ...
Embodiment 2
[0029] The preparation process of the molecularly imprinted polypyrrole peroxide / gold nanometer modified electrode and the recognition method for cysteine are the same as those in Example 1.
[0030] In order to examine the effect of the thickness of the molecularly imprinted membrane on the recognition efficiency of L- / D-cysteine in step b, cyclic voltammetry polymerization was used for 5 cycles, 10 cycles, 15 cycles, 20 cycles, and 25 cycles for the final recognition effect, the result is figure 2 As shown, the thickness of the molecularly imprinted membrane is closely related to the number of polymerization circles. Although the doping amount will increase as the thickness of the film increases, but when the number of polymerization circles exceeds 15, the too thick film will make it difficult for the template molecules to escape. Reduced recognition efficiency.
Embodiment 3
[0032] The preparation process of the molecularly imprinted polypyrrole peroxide / gold nanometer modified electrode and the recognition method for cysteine are the same as those in Example 1.
[0033] In order to examine the influence of the enrichment time on the recognition efficiency of L- / D-cysteine in step c, the influence of the enrichment time of 6min, 8min, 10min, 12min and 14min on the final recognition was used respectively, and the results are as follows image 3 As shown, as the enrichment time increases, the target molecules will enter the cavity of the imprinted membrane. When the enrichment time is 10 min, the recognition efficiency reaches the highest. As the enrichment time is longer than 10 min, more target molecules It will be adsorbed on the surface of the membrane and reduce the separation efficiency.
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