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机构地区:[1]河北医科大学第二医院药学部,石家庄050000 [2]浙江海正药业股份有限公司药理中心,浙江台州318000
出 处:《中国药房》2016年第18期2570-2572,共3页China Pharmacy
摘 要:目的:建立测定盐酸左西替利嗪咀嚼片中有关物质的方法。方法:采用反相高效液相色谱法。色谱柱为Venusil XBP-CN,流动相为乙腈-0.05 mol/L磷酸二氢钠溶液(以磷酸调节pH至3.0)(60∶40,V/V),检测波长为230 nm,流速为1.0 ml/min,柱温为25℃,进样量为20μl。结果:盐酸左西替利嗪与有关物质分离度良好;盐酸左西替利嗪检测质量浓度线性范围为1.2~2.8μg/ml(r=0.9999);定量限和检测限分别为1.4、0.3 ng/ml;精密度、稳定性、重复性试验的RSD<1%;加样回收率为96.3%~105.0%,RSD=1.7%(n=9);样品中有关物质含量≤0.17%。结论:该方法操作简单,灵敏度高,重复性好,结果准确、可靠,可用于盐酸左西替利嗪原料药及其制剂的有关物质测定。OBJECTIVE:To establish a method for the determination of related substances in Levo-cetirizine hydrochloride chewable tablet. METHODS:RP-HPLC was performed on the column of Venusil XBP-CN with mobile phase of acetonitrile-0.05 mol/L Sodium dihydrogen phosphate solution(pH value adjusted to 3.0 by phosphoric acid)(60∶40,V/V)at a flow rate of 1.0 ml/min, the detection wavelength was 230 nm,column temperature was 25 ℃,and volume injection was 20 μl. RESULTS:Levo-cetirizine hydrochloride chewable tablet showed good separation with related substances;the linear range of levo-cetirizine hydrochloride was 1.2-2.8 μg/ml(r=0.999 9);the quantification limit and detection limit was 1.4 ng/ml and 0.3 ng/ml,respectively;RSDs of preci-sion,stability and reproducibility tests were lower than 1%;recovery was 96.3%-105.0%(RSD=1.7%,n=9);the contents of re-lated substances were no more than 0.17%. CONCLUSIONS:The method is simple,sensitive,reproducible,accurate and reli-able,and can be used for the determination of related substances in Levo-cetirizine hydrochloride chewable tablet.
关 键 词:盐酸左西替利嗪咀嚼片 有关物质 反相高效液相色谱法
分 类 号:R917[医药卫生—药物分析学]
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