Semi-quantitative rapid detection method for parthenolide
A parthenolide and fast technology, applied in measuring devices, material analysis through observation of the influence on chemical indicators, instruments, etc., can solve the problems of inconvenient inspection and judgment, long time-consuming, high equipment configuration, etc.
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Embodiment 1
[0024] Sample preparation: Take 10 parts of the root bark of Magnolia japonica, add it to a 500ml conical flask, add 100 parts of ethanol, soak at 25-30°C for 2 hours, shake well to get the sample solution for later use.
[0025] Preparation of standard solution: take parthenolide reference substance and prepare standard solution with 0.2% and 0.1% content.
[0026] Detection: Using a 2ul quantitative capillary, take the same volume of sample solution and standard solution, respectively, and point them on the thin-layer chromatography; use ethyl acetate to develop, after completion, dry the thin-layer chromatography plate and put it in iodine / silica gel for 5 minutes , remove the observation spot.
[0027] Conclusion: by attaching figure 1 The results showed that the sample spots and the reference substance spots appeared in the same position, indicating that they contained the target compound; the color of the sample spots was darker than that of the 0.1% standard solution, ...
Embodiment 2
[0029] Sample preparation: Take 10 parts of the dried residue of the root bark of Magnolia japonica after extraction, add it to a 500ml conical flask, add 200 parts of ethanol, soak at 25-30 ° C for 1 hour, shake well to obtain a sample solution for later use.
[0030] Preparation of standard solution: take parthenolide reference substance and prepare standard solution with 0.2% and 0.1% content.
[0031] Detection: Using a 5ul quantitative capillary, take the same volume of sample solution and standard solution, respectively, and point them on TLC; use ethyl acetate to develop, after completion, dry the TLC plate and put it in iodine / silica gel for 5 minutes , remove the observation spot. Conclusion: by attaching figure 2 As a result, it can be seen that the sample spot and the reference substance spot have no spots at the same position, indicating that they do not contain the target compound. It can be judged that the extraction has been completed, and the extraction will...
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