A method for detecting the components of an oral liquid for clearing away heat, nourishing yin, promoting blood circulation and removing blood stasis
A technology of promoting blood circulation and removing blood stasis, oral liquid, which is applied in the field of analytical chemistry, can solve the problems of long detection time and easy deviation of measurement results, and achieve the effect of reducing test pressure, shortening test time, and good durability
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Embodiment 1
[0032] Preparation of reference substance solution: refer to the preparation method of reference substance solution in the current quality standards of Mailuoning Injection and Mailuoning Oral Liquid, take appropriate amount of cinnamic acid reference substance and chlorogenic acid reference substance, accurately weigh, add 50% methanol to dissolve and dilute, A mixed solution containing 60 μg of chlorogenic acid and 2 μg of cinnamic acid per 1 mL was prepared.
[0033] Preparation of the test solution: Precisely measure 1 mL of Mailuoning Oral Liquid, put it in a 25 mL volumetric flask, add water to the mark, shake well, filter, and take the continuous filtrate.
[0034] Determination method: Precisely draw 2 μL of the test solution and the reference solution, respectively, and inject them into a high-performance liquid chromatograph. Chromatographic conditions: The chromatographic column is YMC Meteoric Core C18 (100mm×3.0mm, 2.7μm, 8nm), and the column temperature is 35°C ;...
Embodiment 2
[0036] The investigation of embodiment 2 chromatographic column
[0037] The preparation of the reference solution and the test solution is the same as that in Example 1.
[0038] (1), Kromasil C18 (250mm×4.6mm, 5μm) chromatographic column
[0039] Referring to the content determination method of cinnamic acid in Scrophulariaceae under the quality standard content determination of original Mailuoning injection, a Kromasil C18 (250mm×4.6mm, 5μm) chromatographic column was used, with methanol as mobile phase A and 0.1% phosphoric acid as mobile phase B, flow rate 1.0 mL / min, gradient elution was performed using the following gradient elution procedure (Table 1).
[0040] Table 1. Examination of gradient elution procedures
[0041]
[0042] Depend on Figure 4 It can be seen that the peak separation effect is good, but the sample detection time is more than 60 minutes, which is inconsistent with the purpose of shortening the inspection time of the present invention and increa...
Embodiment 3
[0055] Example 3 Gradient investigation
[0056] The preparation of the reference solution and the test solution is the same as that in Example 1. Except for adjusting the gradient elution procedure (see Table 2), the rest are the same as the assay method in Example 1.
[0057] Table 2. Examination of gradient elution procedures
[0058]
[0059] Depend on Figure 8 It can be seen that after adjusting the gradient elution program, the peak time can be shortened, but because the gradient transition is fast, the baseline separation between peaks cannot be completely achieved.
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