Arachidonic acid content detecting method in milk and milk products
A technology for the detection of arachidonic acid and its detection method, which is applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve problems affecting the accuracy of detection results, etc., and achieve the effects of improved recovery rate, simple and convenient operation, and short extraction time
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Embodiment 1
[0029] Embodiment 1 The making of arachidonic acid (AA) standard curve
[0030] Chromatographic conditions: flame ionization detector; sample injection temperature: 260°C; detector temperature: 300°C; °C / min to 215°C and hold for 30 minutes. Capillary column: CP-WAX58 or a column with equivalent performance. Carrier gas: high-purity nitrogen, air and hydrogen.
[0031] The n-hexane used in this example is a chromatographically pure reagent. AA standard solution was purchased from sigma with a purity of ≥99.99%. After dissolving the AA methyl ester standard with n-hexane, prepare samples with concentrations of 10ppm, 50ppm, 100ppm, 200ppm, 400ppm, and 800ppm and inject them separately. According to the measured data, draw the standard between the AA content and the detection result curve, the equation is A std = 263.76C, R = 0.9999. Among them, A std Indicates the chromatographic peak area of the standard solution, and C indicates the concentration of the standard solu...
Embodiment 2
[0032] Example 2 Detection of AA content in fatty acid samples
[0033] 1) Accurately weigh 0.5g fatty acid sample, add n-hexane, dissolve the sample with n-hexane, set the volume to 10ml scale, accurately measure 2ml of the solution after constant volume, add 0.5ml anhydrous methanol-potassium hydroxide (4mol / l ) was fully shaken, and left to stand for 20 minutes for esterification reaction, and water was added to the n-hexane solution to 25ml.
[0034] 2) Stand still, and after the organic phase is clarified, take the supernatant, filter, and inject a sample into a gas chromatograph for detection.
[0035] Chromatographic conditions: flame ionization detector; sample injection temperature: 260°C; detector temperature: 300°C; °C / min to 215°C and hold for 30 minutes. Capillary column: CP-WAX58 or a column with equivalent performance. Carrier gas: high-purity nitrogen, air and hydrogen. The result obtained by detection is compared with the standard curve obtained in Example...
Embodiment 3
[0044] Example 3 Detection of AA content in milk powder
[0045]A) Accurately weigh 1.0000g of milk powder sample into a flat-bottomed flask, shake and dissolve with 10ml of 65°C water, add 2ml of 25% ammonia water, shake gently, return to distillation in a water bath at 65°C for 15 minutes, rinse the return distillation tube with 10ml of ethanol, Cool to room temperature. Add it to Mao's ester extraction bottle, and add 2 drops of Congo red indicator. B) After rinsing the flask with 25ml of ether, add it to an ester extraction bottle and shake it 100 times. Then wash the flask twice with 25ml of petroleum ether, and put the washing liquid in an ester extraction bottle, and shake it 50 times. Wash the bottle cap with a mixture of diethyl ether and petroleum ether. After standing for 30 minutes to separate the layers, the organic phase was separated. Repeat the extraction once with 5ml of absolute ethanol, 15ml of ether, and 15ml of petroleum ether, and combine the organic ...
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