A kind of detection method of glycine betaine in aquatic products
A technology of glycine betaine and detection method, applied in the directions of measuring devices, instruments, scientific instruments, etc., can solve the problems of low sensitivity, high detection difficulty, poor detection effect, etc., and achieves the effect of high sensitivity and suitable for popularization and application
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Embodiment 1
[0044] Embodiment 1: a kind of detection method of glycine betaine in aquatic products comprises the following steps:
[0045] 1) Weigh the glycine betaine standard substance and dilute it step by step with acetonitrile solution, and dilute it into 6 different concentrations (10μg / mL, 20μg / mL, 30μg / mL, 60μg / mL, 100μg / mL, 200μg / mL concentrations) Standard solution, these 6 kinds of standard solutions of different concentrations are carried out liquid chromatography detection with high performance liquid chromatography (waters e2695) respectively, measure the chromatographic peak area value corresponding to the standard solution of different concentrations, obtain standard chromatogram, wherein chromatogram The conditions are:
[0046] a) Chromatographic column: a BEH HILIC chromatographic column with a particle size of 2.5 μm and a specification of 4.6×150 mm;
[0047] b) Column temperature: 25°C;
[0048] c) mobile phase: water: acetonitrile (V: V) = 20: 80 mixed solution, i...
Embodiment 2
[0064] Embodiment 2: Other contents are all identical with embodiment 1, and difference is that the chromatographic condition in step 1) and step 4) is:
[0065] a) Chromatographic column: a BEH HILIC chromatographic column with a particle size of 2.5 μm and a specification of 4.6×150 mm;
[0066] b) Column temperature: 20°C;
[0067] c) mobile phase: water: acetonitrile (V: V) = 40: 60 mixed solution, isocratic elution;
[0068] d) Mobile phase flow rate: 0.6mL / min;
[0069] e) Injection volume: 5 μL;
[0070] f) Detector type: fluorescence detector;
[0071] g) Detection wavelength: 195nm.
[0072] And in step 3), after vortexing at room temperature for 30 minutes, centrifuge at 3500r / min for 8 minutes, filter the supernatant, extract repeatedly three times, combine the supernatant, pass the combined supernatant through a 0.22 μm filter membrane to obtain the sample to be tested liquid.
Embodiment 3
[0073] Embodiment 3: other content is all identical with embodiment 1, and difference is that the chromatographic condition in step 1) and step 4) is:
[0074] a) Chromatographic column: a BEH HILIC chromatographic column with a particle size of 2.5 μm and a specification of 4.6×150 mm;
[0075] b) Column temperature: 22°C;
[0076] c) mobile phase: water: acetonitrile (V: V) = 10:90 mixed solution, isocratic elution;
[0077] d) Mobile phase flow rate: 1.0mL / min;
[0078] e) Injection volume: 8 μL;
[0079] f) Detector type: fluorescence detector;
[0080] g) Detection wavelength: 195nm.
[0081] And in step 3), after vortexing at room temperature for 30 minutes, centrifuge at 4500r / min for 6 minutes, filter the supernatant, extract repeatedly three times, combine the supernatant, pass the combined supernatant through a 0.22 μm filter membrane to obtain the sample to be tested liquid.
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