Method for determining saponin content of SmilaxscobinicaulisC.H.Wringh or its formulation
A technology of smilax smilax and saponin, which is applied in the field of indirect determination of sarsaparilla smilax or its preparations by colorimetry, can solve the problems of quality control, resource evaluation, extraction and separation, unfavorable modernization utilization of Chinese herbal medicines, etc. , to achieve the effect of stable and reliable method, strong reaction specificity and good reproducibility
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Embodiment 1
[0015] Embodiment 1: Maximum Absorption Wavelength Determination
[0016] Precisely draw 1mL of Laxogenin solution into a colorimetric tube, heat in a water bath to evaporate the solvent, add 1mL of vanillin-glacial acetic acid-perchloric acid solution, heat in a water bath at 60°C for 15min, immediately cool in an ice-water bath for 10min after taking it out, and then accurately Add 5.0mL of glacial acetic acid to dilute, shake well, and scan in the range of 400-650nm with a UV-visible spectrophotometer. It is found that both the reference solution and the sample solution have a maximum absorption peak at 450nm and are relatively stable, while the blank solution has only weak absorption here. , the absorption curve is shown in the appendix figure 1 .
Embodiment 2
[0017] Embodiment 2: color reaction temperature is determined
[0018] Precisely draw 1mL of Laxogenin solution into a colorimetric tube, heat in a water bath to evaporate the solvent, add 1mL of vanillin-glacial acetic acid-perchloric acid solution, heat in a water bath at different temperatures for 15min, and immediately cool in an ice-water bath for 10min after taking it out. Accurately add 5.0 mL of glacial acetic acid to dilute, shake well, and scan with a UV-visible spectrophotometer in the range of 400-650 nm. The scanning results are shown in Table 1. It can be seen from Table 1 that when the water bath temperature is 40-60°C, λmax changes little; when the temperature is greater than 70°C, λmax changes greatly; when the temperature is 60°C, the absorbance value (A) is the largest, and the λmax changes the least, Therefore, the color reaction temperature was set at 60°C.
[0019] Table 1 Water bath temperature versus λ max and A influence
[0020] Water bath...
Embodiment 3
[0021] Embodiment 3 stability test
[0022] Accurately draw 0.5mL of the reference solution into the colorimetric tube (make a blank control at the same time), heat in a water bath to evaporate the solvent, add 1.0mL of vanillin-glacial acetic acid-perchloric acid solution, heat in a water bath at 60°C for 15min, take it out immediately Cool in an ice-water bath for 10 minutes, then accurately add 5.0 mL of glacial acetic acid to dilute, shake well, measure the absorbance value A at 450 nm with a UV-visible spectrophotometer, measure A within 0 to 100 minutes, and see the results in figure 2 .
[0023] figure 2 It shows that the absorbance value A of the chromogenic system is unstable within 0-30 minutes; the absorbance value is relatively stable within 30-70 minutes; after more than 70 minutes, A decreases obviously. Therefore, the data measured within 30-70 minutes after color development are reliable.
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