Application of screen printing electrode in the determination of 5-hydroxytryptamine
A technology of screen printing electrodes and serotonin, applied in the direction of electrochemical variables of materials, can solve the problem of high cost and achieve the effect of high selectivity and sensitivity
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Embodiment 1
[0029] Embodiment 1: at first choose PVC substrate clean and dry heat-resistant, then print electrode lead wire, then dry substrate, print carbon electrode and counter electrode with the carbon ink that contains colloidal gold particle and dry (colloidal gold content is every ml carbon ink containing 0.01μg colloidal gold), printed Ag / AgCl electrodes and dried, and finally printed the insulating layer with insulating paste and cured. Take 20 μL of 10% nafion solution and coat it on the surface of the carbon electrode, and wait for the solvent to evaporate to obtain a sensitive film.
Embodiment 2
[0030] Embodiment 2: firstly select the substrate to clean and dry heat-resistant, then print the electrode leads, then dry the substrate, print carbon electrodes and counter electrodes with the carbon ink containing colloidal gold particles and dry, (colloidal gold content is per ml carbon ink containing 100 μg colloidal gold) to print the Ag / AgCl electrode and dry it, and finally use the insulating paste to print the insulating layer and cure it. Take 0.1 μL of 0.2% nafion solution and coat it on the surface of the carbon electrode, and evaporate the solvent to obtain a sensitive film.
Embodiment 3
[0031] Example 3: First select the substrate to clean and dry heat-resistant, then print electrode leads, then dry the substrate, print carbon electrodes and counter electrodes and dry, print Ag / AgCl electrodes and dry, and finally use insulating paste The insulating layer is printed and cured.
[0032] 80 KM mice were divided into four groups of high reserpine (2 mg / kg), medium (0.5 mg / kg), low (0.25 mg / kg) and blank, 20 in each group. After intraperitoneal injection of reserpine injection, 4 mice were taken from each cage at 0, 2, 3, 5, and 9 hours respectively, and 100 μL of blood was taken, and diluted with 0.05 mol / L phosphate buffer (pH 7.0) 5 times, for the test solution 1. The brain was decapitated and homogenized with 1ml of 0.05mol / L phosphate buffer (pH 7.0). After the protein was measured, the volume was adjusted with the above buffer, which was the test solution 2. And at the same time, their depressive behavior was scored.
[0033] Insert the electrode made in...
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