Method for quickly detecting biogenic amine
A technology for biogenic amines to be detected, applied in the field of chromatographic analysis, can solve the problems of complex operation, long time-consuming instrument analysis methods, high cost, etc., and achieve the effect of rapid development and convenient and fast semi-quantitative detection
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Embodiment 1
[0023] Prepare putrescine solutions with mass concentrations of 5mg / L, 10mg / L, 15mg / L, 20mg / L, and 25mg / L with 0.1M hydrochloric acid, take 1mL each of the standard solution and the wine sample to be tested, and adjust the pH with 2M NaOH When the value reaches 9.4-10.0, add 1 mL of dansyl chloride derivative (5 mg / L acetone), shake and mix. Place it at 60°C for 30 minutes (shake 3-8 times during the period).
[0024] Use a micro-spotter to spot 10 μL of a sample on a 10cm×10cm chromatographic material polyamide film, place the polyamide sheet that has been blown-dried after spotting with the smooth side outward, and the polyamide side inward, tie it with a rubber band, and put it vertically into the airtight Develop upward in a developing cylinder filled with a saturated developing agent (xylene: glacial acetic acid = 10:1), and the equilibrium solvent in the developing cylinder is obtained by mixing and standing the developing agent in the closed developing cylinder. Chroma...
Embodiment 2
[0026] Prepare histamine solutions with mass concentrations of 5mg / L, 10mg / L, 15mg / L, 20mg / L, and 25mg / L with 0.1M hydrochloric acid, take 1mL each of the standard solution and the beer sample to be tested, and adjust the pH with 2M NaOH value to 9.4, add 1mL dansyl chloride derivative (5mg / L acetone), shake and mix. Placed at 65°C for 25 minutes (shaking 5 times during the period).
[0027] Use a micro-spotter to spot 5 μL of a sample on a 10cm×10cm chromatographic material polyamide film, place the smooth side of the blow-dried polyamide sheet after spotting, and the polyamide side inward, tie it with a rubber band, and put it vertically into the airtight Develop upward in a developing cylinder equipped with a saturated developing agent (xylene: glacial acetic acid = 10: 1), stop chromatography when the leading edge of the developing agent is 0.8 cm away from the top of the film, evaporate the solvent, and display under a 254 nm ultraviolet detection lamp. color. The unfol...
Embodiment 3
[0029] Use 0.1M hydrochloric acid to prepare tyramine solutions with mass concentrations of 5mg / L, 10mg / L, 15mg / L, 20mg / L, and 25mg / L, take 1mL each of the standard solution and the liquor sample to be tested, and adjust the pH with 2M NaOH value to 10.0, add 1mL dansyl chloride derivative (5mg / L acetone), shake and mix. Placed at 58°C for 35 minutes (shaking 3 times during the period).
[0030] Use a micro-spotter to spot 12 μL of a sample on a 10cm×10cm chromatographic material polyamide film, place the smooth side of the blow-dried polyamide sheet after spotting, and the polyamide side inward, tie it with a rubber band, and put it vertically into an airtight container. Develop upward in a developing cylinder equipped with a saturated developing agent (xylene: glacial acetic acid = 10: 1), stop chromatography when the front of the developing agent is 1 cm away from the top of the film, evaporate the solvent, and develop color under a 280nm ultraviolet detection lamp . The ...
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