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·临床药学·

        同位素稀释-超高效液相色谱-串联质谱法测定人血浆中氟康唑

        的浓度        Δ


              *
        杨浩天 ,吴 茵,宋浩静,邱志宏,董占军(河北省人民医院药学部,石家庄 050051)
                                             #
        中图分类号 R927.2;R978.5        文献标志码 A           文章编号     1001-0408(2019)02-0235-05
        DOI  10.6039/j.issn.1001-0408.2019.02.19

        摘  要   目的:建立测定人血浆中氟康唑浓度的方法。方法:血浆样品经乙腈沉淀蛋白后,以同位素氟康唑-d4为内标,采用超高
        效液相色谱-串联质谱法测定。色谱柱为ACQUITY UPLC BEH C18,流动相为0.1%甲酸溶液-乙腈(梯度洗脱),流速为0.3 mL/min,
        柱温为40 ℃,进样量为3 μL;采用电喷雾离子源,以多反应监测模式进行正离子扫描,用于定量分析的离子对分别为m/z 307.1→
        220.0(氟康唑)和m/z 311.1→223.0(内标)。结果:氟康唑血药浓度检测的线性范围为10~5 000 ng/mL(r=0.998 1),定量下限为
        10 ng/mL;日内、日间RSD均低于8%,准确度为95.8%~106.7%;提取回收率为97.3%~107.3%(RSD<5.0%,n=6),基质效应、
        稀释效应及残留效应均不影响待测物的定量分析。结论:该方法简便、快速、专属性强、准确度高,可用于氟康唑治疗药物监测及
        药动学研究。
        关键词 氟康唑;同位素内标;超高效液相色谱-串联质谱法;血药浓度;治疗药物监测

        Determination of Fluconazole in Human Plasma by UPLC-MS/MS with Isotopes Dilution
        YANG Haotian,WU Yin,SONG Haojing,QIU Zhihong,DONG Zhanjun(Dept. of Pharmacy,Hebei General
        Hospital,Shijiazhuang 050051,China)

        ABSTRACT   OBJECTIVE:To establish a method for determination of fluconazole concentration in human plasma. METHODS:
        UPLC-MS/MS method was adopted to determine plasma after precipitated with acetonitrile. Using isotope fluconazole-d4 as internal
        standard,the determination was performed on ACQUITY UPLC BEH C18 column with mobile phase consisted of 0.1% formic
        acid-acetonitrile(gradient elution)at the flow rate of 0.3 mL/min. The column temperature was 40 ℃,and the sample size was 3 μL.
        ESI was used for positive ion scanning by multiple reaction monitoring mode. The ion pairs for quantitative analysis were m/z
        307.1→220.0(fluconazole)and m/z 311.1→223.0(internal standard). RESULTS:The linear range of fluconazole was 10-5 000 ng/mL
       (r=0.998 1). The limits of quantitation was 10 ng/mL. RSDs of intra-day and inter-day were less than 8% ;accuracy ranged
        95.8% -106.7% . The extraction recovery ranged 97.3% -107.3% (RSD<5.0% ,n=6),and matrix effect,dilution effect and
        residual effect didn’t influence quantitative analysis of the substance to be measured. CONCLUSIONS:The method is simple,
        rapid,specific and accurate,which can be used for therapeutic drug monitoring and pharmacokinetic study of fluconazole.
        KEYWORDS    Fluconazole;Isotope internal standard;UPLC-MS/MS;Plasma concentration;Therapeutic drug monitoring



        

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           *药师,硕士。研究方向:药物质量控制、药动学。电话:0311-
        85988640。E-mail:yanghaotian0917@163.com                         (收稿日期:2018-02-24   修回日期:2018-11-08)
           # 通信作者:主任药师,硕士。研究方向:临床药学、临床药理                                                        (编辑:余庆华)
        学。电话:0311-85988945。E-mail:651405530@qq.com


        中国药房    2019年第30卷第2期                                               China Pharmacy 2019 Vol. 30 No. 2  ·235  ·
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