Establishment method of fingerprint spectrum of blood-enriching motherwort pills and quality detection method
A technology for fingerprint and method establishment, applied in the field of traditional Chinese medicine analysis and detection, can solve the problems of single quality control standard, difficult to accurately assess the quality of tonifying blood and Yimu preparations, weak and other problems, achieve a good linear relationship, ensure quality and clinical efficacy, peak good effect
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Embodiment 1
[0045] The optimization of embodiment 1 chromatographic conditions
[0046] In the method of establishing fingerprints, because the chemical components in different Chinese medicinal materials vary widely, the elution conditions of fingerprints of different medicinal materials and preparations have no reference value to each other, and small changes in the mobile phase ratio will affect the fingerprints. It has a great impact, such as affecting the resolution and peak shape of characteristic peaks. In order to make the characteristic peaks in the fingerprints have better resolution and peak shape, the selection of gradient elution conditions is very important. In this embodiment, the mobile phase and detection wavelength are mainly investigated and optimized.
[0047] 1. Selection of mobile phase
[0048] Take an appropriate amount of Buxue Yimu pills, pulverize them, accurately weigh about 3.0g into a 50mL measuring bottle, add 10mL of water and sonicate for 10min, then add ...
Embodiment 2
[0055] The optimization of embodiment 2 Buxue Yimu pills test solution preparation method
[0056] In the establishment method of the fingerprint, in order to make the operation more convenient and time-consuming, and to make each characteristic peak in the fingerprint have better resolution and peak shape, and to reasonably control the detection time of the fingerprint, It is very important to investigate and optimize the preparation method of the test product. In this embodiment, the extraction sample amount, extraction solvent and extraction time are mainly investigated and optimized.
[0057] This optimization is detected under the chromatographic conditions determined in Example 1.
[0058] 1. Investigation on the amount of extracted samples
[0059] Take an appropriate amount of Buxue Yimu Pills, crush them, and accurately weigh three different samples of 3g, 1g, and 0.5g into a 50mL measuring bottle, add 10mL of water and sonicate for 10min, then add 40mL of acetonitri...
Embodiment 3
[0073] Embodiment 3 methodological investigation
[0074] Preparation of reference solution:
[0075] Precisely weigh 7.96mg of motherwort, 13.03mg of calycosin glucoside, 3.53mg of rutin, 4.88mg of ferulic acid, and 2.71mg of ligustilide reference substance, place them in 6 measuring bottles, add methanol to prepare the mass concentration 796.0, 1303.0, 353.0, 488.0, 2710.0 μg / mL single reference substance stock solution in sequence. Another appropriate amount of the above-mentioned 5 kinds of reference substance stock solutions was taken respectively, and added to a 10mL measuring bottle, and the mass concentrations of leonurine, calycosin glucoside, rutin, ferulic acid, and ligustilide were respectively 7.96, 5.47, 35.30, 58.56, 100.27μg / mL mixed reference solution.
[0076] Preparation of the test solution:
[0077] Determining the preferred test solution preparation method according to Example 2 to prepare the Buxue Yimu Pill test solution.
[0078] 1. System adaptabili...
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