Method for detecting ponceaux 2R in food
A detection method, food technology, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problems of easy blockage of capillary, interference of analysis and measurement, large residual current, etc., and achieve simplified sample processing procedures, reduced solvent consumption, and high selectivity Effect
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Embodiment 1
[0017] Example 1: Detection of Ponceau 2R in commercially available chili powder
[0018] 1. Determine the testing standard
[0019] A. Qualitative testing standards:
[0020] Take the Ponceau 2R standard product dissolved in ultrapure water, and then dissolve it in a volumetric flask to prepare a standard stock solution with a concentration of 0.5-2.0 mg / mL. Dilute the Ponceau 2R standard stock solution with ultrapure water to prepare The standard solution with a concentration range of 0.1-15μg / mL, after filtration with a 0.45μm filter membrane, the chromatographic column is XDB-C18 (150mm×4.6mmi.d.5μm); mobile phase A: 0.005mol / L ammonium acetate NH 4 Ac+0.06% triethylamine aqueous solution, adjust the pH to 8 with 0.1mol / L glacial acetic acid, B: chromatographically pure acetonitrile CH 3CN; Elution gradient: t=0 minutes, 10% B; t=2 minutes, 10% B; t=15 minutes, 90% B; t=17 minutes, 10% B; flow rate 1.0mL / min, detection wavelength Under the chromatographic analysis condi...
Embodiment 2
[0029] Example 2: Detection of Ponceau 2R in commercially available hard candies
[0030] 1, determine the standard of detection: its qualitative detection, quantitative detection standard are with embodiment 1
[0031] 2. Sample processing
[0032] Accurately weigh 2g of the sample, put it into a 200mL beaker, dissolve it in hot ultrapure water at 70°C, dilute it with ultrapure water, and put it in a 25mL volumetric flask. Take 6mL of the diluted solution and centrifuge at 6000r / min for 20min, and absorb the supernatant 3mL spare.
[0033] The weak anion solid-phase extraction column is first activated with the chromatographically pure methanol, and then activated with 3mL ultrapure water. Wash the solid-phase extraction column with water and 3mL of methanol solvent, enter the air-dried extraction column for 30 seconds, and finally use 3mL of chromatographically pure methanol containing 2% pure ammonia water for elution, and collect the eluate. The eluting solution was blo...
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