High-Sensitivity and High-Throughput Quantification of Everolimus in Human Whole Blood Using Ultrahigh-Performance Liquid Chromatography Coupled With Tandem Mass Spectrometry

被引:2
|
作者
Miyagi, Chika [1 ]
Tanaka, Ryota [1 ]
Hirata, Kenshiro [2 ]
Watanabe, Takuma [1 ]
Tatsuta, Ryosuke [1 ]
Miyamura, Shigeyuki [2 ]
Itoh, Hiroki [1 ]
机构
[1] Oita Univ Hosp, Dept Clin Pharm, 1-1 Idaigaoka, Yufu, Oita 8795593, Japan
[2] Sojo Univ, Fac Pharmaceut Sci, Dept Clin Pharmaceut, Kumamoto, Japan
基金
日本学术振兴会;
关键词
everolimus; therapeutic drug monitoring; ultrahigh-performance liquid chromatography coupled with tandem mass spectrometry; latex agglutination turbidimetric; solid-phase extraction; LC-MS/MS; POLARIZATION IMMUNOASSAY; IMMUNOSUPPRESSIVE DRUGS; HPLC-UV; TACROLIMUS; SIROLIMUS; CYCLOSPORINE; PHARMACOKINETICS; THERAPY;
D O I
10.1097/FTD.0000000000000985
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Rigorous dose adjustment by therapeutic drug monitoring (TDM) is recommended when everolimus (EVR) is administered for immunosuppression. In this study, the authors developed a highly sensitive ultrahigh-performance liquid chromatography coupled with the tandem mass spectrometry (UHPLC-MS/MS) method for measuring EVR concentrations in whole blood using a high-throughput solid-phase extraction method for sample pretreatment. Furthermore, the blood EVR concentrations in routine TDM samples from patients who underwent renal transplantation measured using the established UHPLC-MS/MS method were compared with those measured using the latex agglutination turbidimetric immunoassay (LTIA). Methods: Blood samples were pretreated by solid-phase extraction using a 96-well HLB mu Elution plate. The clinical application of the newly developed method was evaluated using 87 blood samples from 19 patients who underwent kidney transplant. Results: The calibration curve showed good linearity over a wide range of 0.1-50 ng/mL, with relative error <= 15% obtained from the back calculation of calibrators, and <= 20% for the lower limit of quantification. Within-batch and batch-to-batch accuracies and precisions fulfilled the acceptance criteria of the US Food and Drug Administration guidelines for bioanalytical method validation. The extraction recovery rates were good (>= 65.2%), and almost no matrix effects were found in any of the quality control samples. Blood EVR concentrations measured by UHPLC-MS/MS were positively correlated with those measured by LTIA. A Bland-Altman plot indicated that the UHPLC-MS/MS method yielded better measurements than the LTIA method, regardless of the concentration. Conclusions: Therefore, the authors succeeded in developing a novel high-sensitivity and high-throughput method for measuring blood EVR concentration by UHPLC-MS/MS using a mu Elution plate for sample pretreatment.
引用
收藏
页码:633 / 640
页数:8
相关论文
共 50 条
  • [1] Everolimus quantification in peripheral blood mononuclear cells using ultra high performance liquid chromatography tandem mass spectrometry
    Roullet-Renoleau, Francois
    Lemaitre, Florian
    Antignac, Marie
    Zahr, Noel
    Farinotti, Robert
    Fernandez, Christine
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2012, 66 : 278 - 281
  • [2] Analytical Performance of a New Liquid Chromatography/Tandem Mass Spectrometric Method for Determination of Everolimus Concentrations in Whole Blood
    McMillin, Gwendolyn A.
    Johnson-Davis, Kamisha
    Dasgupta, Amitava
    THERAPEUTIC DRUG MONITORING, 2012, 34 (02) : 222 - 226
  • [3] High-throughput plasma docetaxel quantification by liquid chromatography-tandem mass spectrometry
    Corona, Giuseppe
    Elia, Caterina
    Casetta, Bruno
    Frustaci, Sergio
    Toffoli, Giuseppe
    CLINICA CHIMICA ACTA, 2011, 412 (3-4) : 358 - 364
  • [4] High-sensitivity simultaneous quantification of tacrolimus and 13-O-demethyl tacrolimus in human whole blood using ultra-performance liquid chromatography coupled to tandem mass spectrometry
    Ono, Hiroyuki
    Suzuki, Yosuke
    Kaneko, Tetsuya
    Tanaka, Ryota
    Sato, Fuminori
    Sato, Yuhki
    Mimata, Hiromitsu
    Itoh, Hiroki
    BIOMEDICAL CHROMATOGRAPHY, 2019, 33 (09)
  • [5] Simultaneous profiling and quantification of 25 eicosanoids in human serum by ultrahigh-performance liquid chromatography coupled to tandem mass spectrometry
    Lu, Yuanyuan
    Mai, Zhitong
    Zhou, Hongxia
    Guan, Wenda
    Wu, Shiguan
    Zou, Heyan
    Shen, Maoting
    Zhan, Yangqing
    Ye, Feng
    Qiu, Minshan
    Shen, Lihan
    Zhao, Beibei
    Yang, Zifeng
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2022, 414 (29-30) : 8233 - 8244
  • [6] Simultaneous quantification of tacrolimus and sirolimus, in human blood, by high-performance liquid chromatography - Tandem mass spectrometry
    Taylor, PJ
    Salm, P
    Lynch, SV
    Pillans, PI
    THERAPEUTIC DRUG MONITORING, 2000, 22 (05) : 608 - 612
  • [7] High-throughput liquid chromatography-tandem mass spectrometric analysis of sirolimus in whole blood
    Wallemacq, PE
    Vanbinst, R
    Asta, S
    Cooper, DP
    CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2003, 41 (07) : 921 - 925
  • [8] Development and Validation of a High-Throughput Ultrahigh-Performance Liquid Chromatography-Mass Spectrometry Approach for Screening of Oxylipins and Their Precursors
    Wolfer, Arnaud M.
    Gaudin, Mathieu
    Taylor-Robinson, Simon D.
    Holmes, Elaine
    Nicholson, Jeremy K.
    ANALYTICAL CHEMISTRY, 2015, 87 (23) : 11721 - 11731
  • [9] High-throughput determination of atrasentan in human plasma by high-performance liquid chromatography coupled with electrospray ionization tandem mass spectrometry
    Wang, PG
    Wei, J
    Chang, M
    El-Shourbagy, T
    BIOMEDICAL CHROMATOGRAPHY, 2005, 19 (09) : 663 - 670
  • [10] Sensitive, wide-range and high-throughput quantification of cyclosporine in whole blood using ultra-performance liquid chromatography coupled to tandem mass spectrometry and comparison with an antibody-conjugated magnetic immunoassay
    Watanabe, Takuma
    Tanaka, Ryota
    Ono, Hiroyuki
    Suzuki, Yosuke
    Tatsuta, Ryosuke
    Itoh, Hiroki
    BIOMEDICAL CHROMATOGRAPHY, 2021, 35 (08)