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桂利嗪原料中有害残留溶剂三氯甲烷和苯的检测

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目的:建立用于测定桂利嗪原料药中有机溶剂三氯甲烷和苯残留量的方法.方法:采用色谱柱为DB-624(60 m×0.32 mm × 1.80 μm)毛细管色谱柱;检测器为FID;进样口温度为250℃;升温程序:起始温度为55℃,维持时间10 min,以20 ℃·min-1的速率升温至220 ℃,维持5 min;检测器温度为280 ℃;载气流速为3.0 mL·min-1;分流比为5∶1;顶空进样,平衡温度为90 ℃,平衡时间为20 min.结果:三氯甲烷在1.50~18.04μg·mL-1和苯在0.050~0.603 μg·mL-1范围内,线性关系良好(r>0.99 9)平均回收率分别为97.5%(RSD=2.0%)和97.7%(RSD=3.1%).结论:本方法灵敏度高、准确度好、重现性好,可用于桂利嗪原料药中三氯甲烷和苯残留量测定.
Determination of Harmful Residual Solvent Trichloromethane and Benzene in Cinnarizine Material
Objective:To establish GC method for determination of residual organic solvent Trichloromethane and Benzene in cinnariz-ine API.Methods:GC was used with DB-624(60 m × 0.32 mm × 1.80 μm)Capillary column.The detector was FID,Inlet temperature was 250 ℃.Temperature programming:the initial column temperature was 55 ℃,kept for 10 min,and then rised to 220 ℃ with a rate of 20 ℃·min-1 and kept for 5 min.The detector temperature was 280 ℃.The flow rate was 3.0 mL·min-1;split ratio was 5∶1.Headspace sampling was used with an temperature of equilibrium at 90 ℃ and an equilibrium time 20 min.Results:The linear equations of trichloromethane(1.50-18.04 μg·mL-1)and benzene(0.050-0.603μg·mL-1)were in good linear range(r>0.999).The average recovery of trichloromethane and benzene were 97.5%(RSD=2.0%)and 97.7%(RSD=3.1%).Conclusion:The method is sensitive and accurate with good reproducibility,which can be used to determine the contents of trichloromethane and benzene in cinnariz-ine API.

Cinnarizine APIResidual solventTrichloromethaneBenzeneGas chromatography

王鹏、刘贞、郭艳芳、钟振华

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江西省药品检验检测研究院,国家药品监督管理局中成药质量评价重点实验室,江西省药品与医疗器械质量工程技术研究中心,江西南昌 330029

桂利嗪原料药 残留溶剂 三氯甲烷 气相色谱

2024

中国药物评价
国家食品药品监督管理局信息中心

中国药物评价

影响因子:1.09
ISSN:2095-3593
年,卷(期):2024.41(2)
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