Liquid chromatography and enzyme electrode combining device and application thereof
A technology of liquid chromatography and enzyme electrode, which is applied in the direction of measuring devices, electrochemical variables of materials, instruments, etc., can solve problems such as the complex composition of traditional Chinese medicine ingredients, achieve application prospects and good effects, improve the quality of Chinese medicinal materials, and strengthen the research on active ingredients Effect
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Embodiment 1
[0046] like figure 1 Shown is a liquid chromatography-enzyme electrode combination device, which includes a chromatographic separation unit, a detector, an organic solvent removal unit, an activity evaluation unit and a computer 12, and the chromatographic separation unit adopts a high performance liquid chromatography separation system or an ultra-high pressure For the liquid chromatography separation system, the detector is a single-wavelength ultraviolet detector, a diode array detector or a fluorescence detector. The chromatographic separation unit includes a mobile phase storage tank 1, a chromatographic pump 2, an injection valve 3 and a liquid chromatography column 4 connected to each other through pipelines in sequence, and the liquid phase chromatographic column 4 is connected to the detector 5 through pipelines . The organic solvent removal unit includes a nitrogen cylinder, a nitrogen pump 7, a heating tube 8 and an evaporation tube 6, the nitrogen cylinder adopts ...
Embodiment 2
[0048] A liquid chromatography-enzyme electrode combination method for online analysis of the activity of traditional Chinese medicine components, the method uses the liquid chromatography-enzyme electrode combination device of Example 1 to perform the operations comprising the following steps:
[0049] 1) Preparation of mobile phase
[0050] Water is used as the aqueous phase, and methanol is used as the organic phase. Take deionized pure water and chromatographic methanol, pass through microporous membranes with a pore size of 0.45μ, respectively, and place the filtrates in solvent bottles for the aqueous phase and the organic phase, respectively, for later use.
[0051] 2) Pretreatment of samples to be tested
[0052] Take the dried Atractylodes macrocephala, crush it, weigh 0.6 g, put it in a 25 mL volumetric flask, add 20 mL of methanol, ultrasonically extract for 20 minutes, take it out, put it at room temperature, add chromatographic methanol to the scale, shake well, ...
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