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HPLC-RID法测定吸附无细胞百白破联合疫苗中甘油的残留量 被引量:2

Determination of residual glycerol in adsorbed acellular DTP combined vaccine by HPLC-RID
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摘要 目的:建立高效液相色谱-示差折光(HPLC-RID)法测定吸附无细胞百白破联合疫苗中甘油残留量的方法,为其检测提供参考。方法:采用NH;色谱柱(250 mm×4.6 mm,5μm),以乙腈-水(85∶15)为流动相,柱温30℃,RID检测器温度35℃,流速1.0 mL·min^(-1)。结果:甘油在43.5~2 173.0μg·mL^(-1)浓度范围内呈良好的线性关系(R^(2)=1.000),平均回收率为99.98%,RSD为0.65%(n=9)。结论:该方法简便、准确,专属性强,可用于甘油残留量的测定,使产品质量更加有效地得到控制。 Objective:To establish an HPLC-RID method for the determination of residual glycerol in adsorbed a-cellular DTP combined vaccine and to provide reference for the quality control.Methods:The test was performedin NH;column under the isocratic elution of acetonitrile-water(85∶15).The column temperature was 30℃,the RID detector temperature was 35℃and the flow rate was 1.0 mL·min^(-1).Results:The linear range of glycerolfell into 43.5-2173.0μg·mL^(-1)(R^(2)=1.000),and the average recovery was 99.98%with RSD as 0.65%(n=9).Conclusion:The method was convenient,accurate and specific.It can be used for the determination of glycerol residue in this vaccine,and helpful for the quality control of the product.
作者 张雅军 杨英超 马霄 肖新月 吴先富 ZHANG Yajun;YANG Yingchao;MA Xiao;XIAO Xinyue;WU Xianfu(National Institutes for Food and Drug Control,Beijing 102629,China)
出处 《中国药品标准》 CAS 2022年第1期5-8,共4页 Drug Standards of China
关键词 高效液相色谱-示差折光法 吸附无细胞百白破联合疫苗 甘油残留 HPLC-RID diphtheria tetanus and acellular pertussis combined vaccine adsorbed glycerol residue
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