Method for rapidly identifying and detecting manuka honey
A manuka honey, identification and detection technology, which is applied to measuring devices, instruments, scientific instruments, etc., can solve the problems of shoddy charging and adulteration, and achieve improved accuracy, sensitivity and high accuracy and high sensitivity. Effect
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Embodiment 1
[0051] The investigation and establishment of embodiment 1 liquid chromatography, mass spectrometry method
[0052] Standards and reagents used in this embodiment are: 3,5-dimethoxybenzoic acid methyl ester-4-diglucoside purity is greater than 99%; Experimental acetonitrile (chromatographically pure) is purchased from German Merck company; Formic acid (chromatographically pure) Pure) from TEDIA, USA.
[0053] Accurately weigh an appropriate amount of standard substance, make a 1.0mg / mL standard stock solution with water, and store it in the refrigerator at 4°C. Dilute with acetonitrile water (1:9v / v) to a working solution with a concentration of 100μg / ml.
[0054] 1. Establishment of liquid chromatography conditions
[0055] A small amount of formic acid was added during liquid phase analysis.
[0056] The high performance liquid chromatography conditions are as follows:
[0057] Column: Dikma Diamonsil Plus C 18 150*4.6mm chromatographic column;
[0058] Mobile phase: A...
Embodiment 2
[0075] Determination of 3,5-dimethoxybenzoic acid methyl ester-4-diglucoside content in the honey of embodiment 2
[0076] 1. Content analysis of 3,5-dimethoxybenzoic acid methyl ester-4-diglucoside in manuka honey
[0077] Accurately weigh 1.0 g of the melted sample (accurate to 0.01 g) into a quantitative bottle, dilute to 10.0 mL with water, vortex until dissolved, take an appropriate amount of supernatant to filter the membrane, and prepare for sample analysis.
Embodiment 3
[0082] Example 3 Methodological investigation of methyl 3,5-dimethoxybenzoate-4-diglucoside as a characteristic marker of manuka honey
[0083] The standard stock solution was diluted with acetonitrile water (1:9v / v) into the standard working solution, and the contents were 1.0μg / mL, 5.0μg / mL, 10.0μg / mL, 20.0μg / mL, 50.0μg / mL and 100.0μg / mL standard solution, determined according to the following conditions, and quantified by the external standard method.
[0084] (1) High performance liquid chromatography separation conditions are as follows,
[0085] Column: Dikma Diamonsil Plus C 18 150*4.6mm chromatographic column;
[0086] Mobile phase: A is 0.1% (v / v) formic acid aqueous solution, B is acetonitrile;
[0087] Flow rate: 0.8mL / min;
[0088] Gradient elution program: 0-2min 70%A, 2-12min 70-10%A, 12-15min 10%A, 15-16min10-90%A, 16-18min 70%A;
[0089] Column temperature: 25°C;
[0090] Injection volume: 25 μL.
[0091] (2) The mass spectrometry detection selects a he...
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