HPLC method for the separation and determination of pasniazid and its related impurities
A technology of pasniazid and related substances, which is applied in the field of analytical chemistry, can solve problems such as control, and achieve the effects of ensuring quality control, improving efficiency, and precise quality control
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Embodiment 1
[0067] Chromatographic conditions:
[0068] Chromatographic column: Shimadzu VP ODS 250×4.6mm, 5.0μm
[0069] Column flow rate: 1.0ml / min
[0070] Detection wavelength: UV 280nm
[0071] Column temperature: 30°C
[0072] Injection volume: 20μl
[0073] Solvent: buffer salt (disodium hydrogen phosphate 8.7g, sodium dihydrogen phosphate 3.4g, add water to dissolve and dilute to 1000ml)-methanol=90:10
[0074] Mobile phase: A: Phosphate buffer (8.7g disodium hydrogen phosphate, 3.4g sodium dihydrogen phosphate, 2.0g tetrabutylammonium hydrogen sulfate, add water to dissolve, and dilute to 1000ml)
[0075] B: Methanol
[0076] Gradient elution:
[0077]
[0078]
[0079] 1. Solution preparation
[0080] System suitability solution: take the appropriate amount of pasniazid reference substance, impurity A, impurity B, impurity C, impurity D, and impurity E, dissolve in methanol and dilute with a solvent to make about 1 mg of pasniazid and impurity per 1 ml 2ug mixed so...
Embodiment 2
[0087] Embodiment 2 comparative example
[0088] The national drug standard [WS-10001-(HD-0322)-2002] contains the quality standard of this product, and the relevant substances are not controlled;
[0089] According to the Chinese Pharmacopoeia 2015 edition persinazid related substance items only m-aminophenol (impurity B) is controlled, using isocratic elution, the mobile phase is: phosphate buffer (disodium hydrogen phosphate 8.7g, sodium dihydrogen phosphate 3.4g, add appropriate amount of water to dissolve, 10% tetrabutylammonium hydroxide solution 23ml, and dilute to 1000ml)-methanol=90:10. As a result, it was found that the main peak of impurity B and isoniazid could not be effectively separated under the conditions of this chromatographic system; the main peak of impurity D (a possible degradation impurity) coincided with the main peak of p-aminosalicylic acid and could not be effectively detected; the peak of impurity E appeared under isocratic elution conditions The ...
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