Method for detecting related substances in tauroursodeoxycholic acid
A technology of tauroursodeoxycholic acid and related substances, which is applied in the field of high-performance liquid chromatography-evaporative light scattering detection method, can solve the problems of low sensitivity, low accuracy, and interference of components to be measured, and achieve a reduction in chromatographic The effect of peak broadening behavior, good specificity and accuracy, and improved quality controllability
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Embodiment 1
[0046] The determination of embodiment 1 chromatographic column
[0047] Preliminary mobile phase: mobile phase A-mobile phase B;
[0048] Mobile phase A is 50mmol / L ammonia water (adjust the pH to 3.5 with formic acid), and mobile phase B is acetonitrile;
[0049] The column temperature is 40°C;
[0050] The flow rate is 1.0ml / min;
[0051] Evaporative light scattering detector, drift tube temperature is 115°C, carrier gas flow rate is 2.5L / min;
[0052] The test solution: take an appropriate amount of tauroursodeoxycholic acid raw material, and prepare a solution of about 10 mg / ml to obtain the product;
[0053] System Suitability Solution: Take Tauroursodeoxycholic Acid, Tauro-7-ketocholic Acid, Taurochenodeoxycholic Acid, Taurocholic Acid, Cholic Acid, Ursodeoxycholic Acid, 7-Ketocholic Acid Appropriate amounts of cholelithic acid, chenodeoxycholic acid, and cholelithic acid reference substances were prepared into a mixed solution containing about 250 μg / ml of each com...
Embodiment 2
[0058] The selection of embodiment 2 mobile phases
[0059] Accurately measure tauroursodeoxycholic acid reference solution 1 (2.5 μg / ml) or tauroursodeoxycholic acid reference solution 2 (5.0 μg / ml) and system suitability solution respectively, under different mobile phase conditions Next, inject into the high performance liquid chromatograph and record the chromatogram. Investigate the effects of different types and concentrations of buffer salts and different pH regulators on component separation (the number of system suitability solution peaks) and detection sensitivity. The results are shown in Table 2:
[0060] Table 2 buffer salt selection results
[0061]
[0062] Column: The chromatographic column number is the same as in Table 1.
[0063] The above results show that: using 2.5mmol / L to 50mmol / L ammonium salt buffer and adjusting the pH value to the range of 2.5 to 3.5 with formic acid, acetic acid or trifluoroacetic acid can obtain higher sensitivity and ensure ...
Embodiment 3
[0077] Embodiment 3 Determination of Evaporative Light Scattering Detector Conditions
[0078] Chromatographic conditions:
[0079] Chromatographic column: with the chromatographic column 3 in embodiment 1;
[0080] Mobile phase: the same as buffer salt 6 in Example 2;
[0081] Gradient elution conditions:
[0082]
[0083] Flow rate: 1.0ml / min;
[0084] The injection volume is 10 μl;
[0085] Investigate the influence of evaporative light scattering detector conditions, drift tube temperature in the range of 70-115 °C, and carrier gas flow rate in the range of 2.5-4.0 L / min, take 10 μg / ml tauroursodeoxycholic acid reference solution 10 μl respectively Inject into a liquid chromatograph, record the chromatogram, and investigate the sensitivity of tauroursodeoxycholic acid response under different conditions. Other chromatographic conditions are as above, and the results are shown in Table 7.
[0086] Table 7 Effect of evaporative light scattering detector conditions on...
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