A method for detecting related substances of afatinib maleate by high performance liquid chromatography
A technology of high performance liquid chromatography and alfa maleate, which is applied in the field of high performance liquid chromatography to detect afatinib maleate related substances, and can solve the problem that the product quality cannot be effectively controlled, and the process impurity degradation cannot be completely separated. problem, to achieve the effect of good accuracy, high sensitivity and strong specificity
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Embodiment 1
[0043] Example 1: System suitability testing
[0044] Instrument: Shimadzu LC-20A high performance liquid chromatograph and its workstation VWD (or PDA) detector;
[0045] Chromatographic column: Waters XBridge C184.6×250mm, 3.5μm;
[0046] Mobile phase A: 0.002mol / L dipotassium hydrogen phosphate buffer (use 2mol / L sodium hydroxide to adjust the pH to 10.0);
[0047] Mobile phase B: acetonitrile;
[0048] Detection wavelength: 254nm;
[0049] Flow rate: 0.5mL / min;
[0050] Injection volume: 10μL;
[0051] Column temperature: 40°C;
[0052] Gradient elution table: see Table 1;
[0053] Diluent: Methanol;
[0054] Take an appropriate amount of afatinib maleate (approximately equivalent to 25mg of afatinib), put it in a 50ml measuring bottle, measure the appropriate amount of impurity I, SM1, CL-SM1, M, D stock solution, dissolve and dilute with methanol Made to contain maleic acid, afatinib, impurities I, SM1, CL-SM1, M, and D at concentrations of 0.24mg / ml, 0.5mg / ml, 5...
Embodiment 2
[0057] Example 2: Detection of afatinib and its impurity mixed solution
[0058] Instrument: Shimadzu LC-20A high performance liquid chromatograph and its workstation VWD (or PDA) detector
[0059] Chromatographic column: Waters XBridge C184.6×250mm, 3.5μm;
[0060] Mobile phase A: 0.002mol / L dipotassium hydrogen phosphate buffer (use 2mol / L sodium hydroxide to adjust the pH to 10.0);
[0061] Mobile phase B: acetonitrile;
[0062] Detection wavelength: 254nm;
[0063] Flow rate: 0.5mL / min;
[0064] Injection volume: 10μL;
[0065] Column temperature: 40°C;
[0066] Gradient elution table: see Table 1;
[0067] Diluent: Methanol;
[0068] Measure the appropriate amount of afatinib maleate, impurity A, B, E, F, G, H, J, L, M, SM1, CL-SM1, and I stock solutions, dissolve and dilute with methanol to make A mixed solution of about 2.5ug / ml of Fatinib, about 5ug / ml of impurity I, and about 0.75ug / ml of other impurity monomers is used as a mixed solution of Afatinib and its ...
Embodiment 3
[0078] Embodiment 3: detection of afatinib bulk drug
[0079] Instrument: Shimadzu LC-20A high performance liquid chromatograph and its workstation VWD (or PDA) detector;
[0080] Chromatographic column: Waters XBridge C184.6×250mm, 3.5μm;
[0081] Mobile phase A: 0.002mol / L dipotassium hydrogen phosphate buffer (use 2mol / L sodium hydroxide to adjust the pH to 10.0);
[0082] Mobile phase B: acetonitrile;
[0083] Detection wavelength: 254nm;
[0084] Flow rate: 0.5mL / min;
[0085] Injection volume: 10μL;
[0086] Column temperature: 40°C;
[0087] Gradient elution table: see Table 1;
[0088] Diluent: Methanol;
[0089] Take afatinib maleate, add diluent to make a solution containing about 0.5 mg / mL of afatinib.
[0090] Get the maleic acid afatinib solution, measure according to the chromatographic conditions of this embodiment, record the chromatogram, the results are shown in Figure 4 .
[0091] Figure 4 The chromatographic peak whose retention time is 47.635m...
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