A kind of detection method of lactulose in dairy products
A detection method and technology for dairy products, applied in measurement devices, instruments, scientific instruments, etc., can solve the problems of inability to accurately quantify lactulose content, low lactulose sensitivity, and high detection limit, and achieve inhibition of isomerization, The effect of increasing sensitivity and increasing usage
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Embodiment 1
[0044] Example 1: adding the lactulose standard solution to the measured raw fresh milk sample, and mixing to obtain the lactulose spiked sample of this embodiment.
[0045] (1) Sample pretreatment
[0046]Pipette 5.00 mL of lactulose spiked sample into a 50 mL centrifuge tube, add 5.0 mL of water, 2.0 mL of potassium ferrocyanide solution with a concentration of 130 g / L, 2.0 mL of zinc sulfate solution with a concentration of 168 g / L, and 6.0 mL of phosphate buffer (disodium hydrogen phosphate 48 g / L, sodium dihydrogen phosphate 8.6 g / L, magnesium sulfate 1 g / L, adjusted to pH 7.5), each reagent added, need to be vortexed to mix thoroughly. After thorough mixing, centrifuge at 8000 r / min for 5 min at 4 °C, take 1.0 mL of supernatant, add 4.0 mL of phosphate buffer (disodium hydrogen phosphate 48 g / L, sodium dihydrogen phosphate 8.6 g / L, sulfuric acid Magnesium 1 g / L, adjust pH to 7.5), mix well to obtain a dilution. Aspirate 1.00 mL of the diluent, add 200 μL of β-D-galacto...
Embodiment 2
[0060] Prepare pasteurized milk samples.
[0061] (1) Sample pretreatment
[0062] Pipette 5.00 mL of pasteurized milk sample into a 50 mL centrifuge tube, add 5.0 mL of water, 2.0 mL of potassium ferrocyanide solution with a concentration of 130 g / L, 2.0 mL of zinc sulfate solution with a concentration of 168 g / L, and 6.0 mL of phosphate buffer (disodium hydrogen phosphate 48 g / L, sodium dihydrogen phosphate 8.6 g / L, magnesium sulfate 1 g / L, adjusted to pH 7.5), each reagent added, need to be vortexed to mix thoroughly. After mixing, centrifuge at 8000 r / min for 5 min at 4 °C, take 1.0 mL of supernatant, add 4.0 mL of phosphate buffer (48 g / L disodium hydrogen phosphate, 8.6 g / L sodium dihydrogen phosphate, sulfuric acid Magnesium 1 g / L, adjust pH to 7.5), mix well. Aspirate 1.0 mL of the diluent, add 0.2 mL of β-D-galactosidase suspension (enzyme concentration of 40 mg / mL), shake gently, and perform the enzymatic hydrolysis reaction at 50 °C for 1 h.
[0063] Take 0.60 mL...
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