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作 者:张春红[1] 余志贤[1] 张晓颖[1] 石大伟[1]
机构地区:[1]温州医学院附属第一医院,浙江温州325000
出 处:《中国药业》2008年第15期64-65,共2页China Pharmaceuticals
摘 要:目的建立测定尿液样本中表阿霉素的反相高效液相色谱法。方法尿液标本用氯仿-甲醇-异丙醇(5:2:3,V/V/V)重复萃取,萃取液用空气吹干,流动相溶解后用于分析。采用C18柱(150mm×4.6mm,5μm),乙腈-水(35:65,V/V)为流动相,柱温为35.0℃,流速为1.0mL/min,进样量20μL,检测波长为233nm。结果尿液样本中表阿霉素的质量浓度在16~48μg/mL范围内与峰面积呈良好的线性关系,r=0.9977,平均回收率为92.47%。结论该方法比较准确,出峰迅速,专属性强。Objective To develop the assay method for detecting uric epirubiein concentration by RP- HPLC in order to meet the need of uric epirubiein concentration monitoring and pharmaeokineties. Methods Urine sample was extracted twice with chloroform:methanol: isopropyl alcohol (5 : 2 : 3, V/ V/ V). The C18 analytieal column was used. The measurement wavelength was 233 nm. The mixture of water and aeetonitile (35:65, V/ V) was as the mobile phase at the flow rate of 1.0 mL/min. Results The calibration eurve was linear within the eoneentration range of 16-52 μg/mL. The average reeovery was 92. 47%. Conclusion The method is suitable for the pharmaeokinetie monitor and determination of epirubiein.
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