首页> 外文期刊>American Journal of Chemistry >Development and Validation of Headspace Method for Determination of Residual Solvents in Diphenoxylate Hydrochloride Bulk Drug
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Development and Validation of Headspace Method for Determination of Residual Solvents in Diphenoxylate Hydrochloride Bulk Drug

机译:顶空法测定盐酸苯乙氧基化物原料药中残留溶剂的方法开发与验证

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Organic volatile impurities by Headspace GC method was developed and validated for Diphenoxylate hydrochloride bulk drug for its seven residual solvents. Analysis was performed on Perkin Elmer HS 40 system with auto injector. Carrier gas Helium was used with constant flow rate of 2.5mL/min as carrier gas and the separation of residual solvents were achieved on DB-5 column. The thermostat temperature was 125 °C for 20 minute for each vial and after the equilibration the vials were pressurized and injected on GC column. FID detector was used for detection. The parameter for which the method was validated included specificity, limit of detection and quantification, linearity, precision, accuracy and robustness. The method was successfully used to quantify the levels of specified limit for residual solvents in Diphenoxylate hydrochloride bulk drug.
机译:通过顶空气相色谱法开发了有机挥发性杂质,并验证了盐酸苯乙氧基化物散装药物中七种残留溶剂的有效性。在具有自动进样器的Perkin Elmer HS 40系统上进行分析。使用载气氦气以2.5 mL / min的恒定流速作为载气,并在DB-5色谱柱上实现了残留溶剂的分离。每个小瓶的恒温器温度为125°C 20分钟,平衡后将小瓶加压并注入GC柱中。 FID检测器用于检测。验证该方法的参数包括特异性,检测和定量限,线性,精度,准确性和鲁棒性。该方法已成功用于定量盐酸苯乙氧基化物散装药物中残留溶剂的指定限量水平。

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