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反相高效液相色谱法测定隐球菌性脑膜炎患者脑脊液中两性霉素B的含量
引用本文:高文慧,刘世霆,晏媛,吕田明,方敏,陈志良.反相高效液相色谱法测定隐球菌性脑膜炎患者脑脊液中两性霉素B的含量[J].药物分析杂志,2012(1):44-46.
作者姓名:高文慧  刘世霆  晏媛  吕田明  方敏  陈志良
作者单位:南方医科大学附属南方医院药学部;广州医学院附属肿瘤医院药剂科;南方医科大学附属南方医院神经内科
基金项目:广东省科技计划项目(项目编号:2007B031511011)
摘    要:目的:建立反相高效液相色谱法测定人脑脊液中两性霉素B,并用于隐球菌性脑膜炎患者脑脊液样品的测定。方法:采用Agilent C18(5μm,4.6 mm×250 mm)色谱柱,流动相为0.005 mol.L-1乙二胺四乙酸二钠-甲醇(21∶79),流速1.0 mL.min-1,检测波长380 nm,室温下进样20μL。结果:由于患者脑脊液中药物的含量测定范围较大,故采用2个浓度线性范围:1.25~30μg.mL-1(r=0.9999),高、中、低3种浓度的平均回收率为94.9%,日内RSD≤1.38%,日间RSD≤2.67%;0.11~5μg.mL-1(r=0.9999),高、中、低3种浓度的平均回收率为93.1%,日内RSD≤1.73%,日间RSD≤4.09%。结论:本法灵敏度高,重现性好,专属性强,可用于椎管内持续给予两性霉素B的临床药代动力学研究及脑脊液中该药物浓度的临床检测。

关 键 词:两性霉素B  生物样品分析  脑脊液  高效液相色谱法  药代动力学  临床药物监测

RP-HPLC determination of amphotericin B in cerebrospinal fluid of patients with cryptococcal meningitis
GAO Wen-hui,LIU Shi-ting,YAN Yuan,L Tian-ming,FANG Min,CHEN Zhi-liang.RP-HPLC determination of amphotericin B in cerebrospinal fluid of patients with cryptococcal meningitis[J].Chinese Journal of Pharmaceutical Analysis,2012(1):44-46.
Authors:GAO Wen-hui  LIU Shi-ting  YAN Yuan  L Tian-ming  FANG Min  CHEN Zhi-liang
Affiliation:1(1.Department of Pharmacy,Nanfang Hospital,Nanfang Medical University,Guangzhou 510515,China;2.Department of Pharmacy,Cancer Hospital,Guangzhou Medical University,Guangzhou 510095,China;3.Department of Neurology,Nanfang Hospital,Nanfang Medical University,Guangzhou 510515,China)
Abstract:Objective: To establish an RP-HPLC method for the determination of amphotericin B in human cerebrospinal fluid(CSF) and apply the method to determination of CSF samples of patients with cryptococcal meningitis.Methods: The chromatographic separation was performed on Agilent C18(5 μm,4.6 mm × 250 mm) column.0.005 mol.L-1 EDTA-2Na-methanol(21∶ 79,v / v) was taken as the mobile phase with the flow rate at 1.0 mL.min-1,and the detection wavelength was set at 380 nm.The sample injection volume was 20 μL under room temperature.Results: Because of a wide measurement range of the drug content in patients’CSF,double linear concentration ranges were used: one was 1.25-30 μg.mL-1;Its average recovery rate for the 3(high,middle and low) concentrations was 94.9%,and the intra-day RSD and the inter-day RSD were separately less than 1.38% and 2.67%.The other was 0.11-5 μg.mL-1;Its average recovery rate for the 3(high,middle and low) concentrations was 93.1%,and the intra-day RSD and the inter-day RSD were separately less than 1.73% and 4.09%.Conclusions: The method is sensitive,reproducible and specific,which can be used for clinical pharmacokinetic study of continuous infusion of amphotericin B into the spinal canal and the clinical monitoring of the concentration of amphotericin B in CSF.
Keywords:amphotericin B  biological sample analysis  human cerebrospinal fluid  HPLC  pharmacokinetics  therapeutic drug monitoring
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