High performance liquid chromatography analysis method and detection method of impurities in telmisartan medicine
A technology of high-performance liquid chromatography and analysis method, which is applied in the field of high-performance liquid chromatography analysis method and the detection of impurities in telmisartan medicine, can solve the problems of high detection cost, difficult detection process, time-consuming reagent consumption, etc., and achieve Change the effect of many operation steps, shorten analysis time, and simple operation
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preparation example 1
[0047] Accurately weigh telmisartan and impurity A, impurity B, impurity C, impurity E, impurity F, impurity G, impurity H, impurity I, add 0.005mol / L sodium hydroxide methanol solution to prepare a solution, wherein , the mass concentration of telmisartan is 0.5 mg / mL; the respective mass concentrations of impurity A, impurity B, impurity C, impurity E, impurity F, impurity G, impurity H and impurity I in the solution are 5 μg / mL respectively.
Embodiment 1
[0049] The solution in the preparation example 1 is analyzed with high performance liquid chromatography, and the record chromatogram, the chromatographic condition of described high performance liquid chromatography is as follows:
[0050] Chromatographic column: 150mm×4.6μm 5μm C18, column temperature 35℃
[0051] Wavelength: 230nm
[0052] Injection volume: 10μL
[0053] Flow rate: 1.0mL / min
[0054] The first mobile phase: add 2.0g potassium dihydrogen phosphate and 3.8g sodium n-pentanesulfonate monohydrate to 1L water, adjust the pH value to 3.5 with phosphoric acid;
[0055] The second mobile phase: the volume ratio of methanol and acetonitrile is 50:50;
[0056] In the gradient elution, the total volume of the mobile phase is 100%, and the conditions of the gradient elution are set according to time as shown in Table 1:
[0057] Table 1
[0058] time (min) The first mobile phase (%) Second mobile phase (%) 0-10 50 50 10-30 50-30 50-70 ...
Embodiment 2
[0065] The solution in the preparation example 1 is analyzed with high performance liquid chromatography, and the record chromatogram, the chromatographic condition of described high performance liquid chromatography is as follows:
[0066] Chromatographic column: 150mm×4.6μm 5μm C18, column temperature 35℃
[0067] Wavelength: 230nm
[0068] Injection volume: 10μL
[0069] Flow rate: 1.0mL / min
[0070] The first mobile phase: add 2.0g potassium dihydrogen phosphate and 3.8g sodium n-pentanesulfonate monohydrate to 1L water, adjust the pH value to 3.0 with phosphoric acid;
[0071] The second mobile phase: the volume ratio of methanol and acetonitrile is 50:50;
[0072] In the gradient elution, the total volume of the mobile phase is taken as 100%, and the conditions of the gradient elution are set as shown in Table 3 by time.
[0073] table 3
[0074] time (min) The first mobile phase (%) Second mobile phase (%) 0-10 50 50 10-30 50-30 50-70 ...
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