Method for detecting lenthionine and mushroom alcohol
A technology for mushroom alcohol and lentinol, which is applied in the field of detection of mushroom alcohol and mushroom alcohol, can solve the problems of unsuitability for standardized application, complicated pretreatment method, low sensitivity, etc., and achieves shortening sampling time, reducing loss of effective components, and good repeatability. Effect
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Embodiment 1
[0052] Lentinin and mushroom alcohol content determination in embodiment 1 mushroom fresh product
[0053] The fresh product was subjected to high-speed grinding and homogenization, and evenly mixed to obtain the pulverized sample to be tested. Accurately weighed 3 parts of 5 g of the pulverized sample to be tested, and added 10 μL of o-dichlorobenzene standard solution with a concentration of 100 μg / mL respectively to obtain the sample to be tested. Test samples. The sample was heated at 50°C for 30 minutes, extracted at 50°C for 30 minutes using a headspace solid-phase microextraction device, the heating and extraction shaking speed was 500 rpm, and analyzed at the inlet of 220°C for 5 minutes, and then the gas phase Chromatography-mass spectrometry analysis: the sample and the internal standard of o-dichlorobenzene are simultaneously detected by mass spectrometry, and the contents of lentinin and mushroom alcohol in the sample are quantified by calculating the respective pe...
Embodiment 2
[0054] Lentinin and mushroom alcohol in the fresh product of embodiment 2 shiitake mushrooms add recovery test
[0055] The fresh product is homogenized by high-speed grinding, and evenly mixed to obtain the pulverized sample to be tested. Accurately weigh 3 parts of 5g pulverized sample to be tested, and accurately add lentinin standard solution and mushroom alcohol standard solution to each sample. It is 10μg / mL; meanwhile, prepare a blank sample without adding standard substance. After standing still, add 10 μL o-dichlorobenzene standard solution with a concentration of 100 μg / mL to all the samples to obtain the samples to be tested. The sample was heated at 50°C for 30 minutes, extracted at 50°C for 30 minutes using a headspace solid-phase microextraction device, the heating and extraction shaking speed was 500 rpm, and analyzed at the inlet of 220°C for 5 minutes, and then the gas phase Chromatography-mass spectrometry analysis: the sample and the internal standard of o-...
Embodiment 3
[0056] Determination of Lentinin and Mushroom Alcohol Content in Embodiment 3 Chrysanthemum chrysanthemum, Flower mushroom dry product
[0057] Dried mushrooms or flower mushrooms are ground at high speed and evenly mixed to obtain a pulverized sample to be tested (the particle size of the "crushed sample to be tested" is not greater than 355 μm), each accurately weighed 3 parts of 1g after pulverized Place the sample to be tested in a 20mL headspace vial, add 5mL of water, and vortex to mix. Add 10 μL o-dichlorobenzene standard solution with a concentration of 100 μg / mL to obtain the sample to be tested. The sample was heated at 50°C for 30 minutes, extracted at 50°C for 30 minutes using a headspace solid-phase microextraction device, the heating and extraction shaking speed was 500 rpm, and analyzed at the inlet of 220°C for 5 minutes, and then the gas phase Chromatography-mass spectrometry analysis: the sample and the internal standard of o-dichlorobenzene are simultaneous...
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Abstract
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