A sensitive assay for the determination of E7090, a novel selective inhibitor of fibroblast growth factor receptors, and its metabolite in human plasma by UPLC-MS/MS with at-column dilution

被引:1
|
作者
Mano, Yuji [1 ,2 ]
Nitanai, Ikumi [3 ]
Hotta, Koichiro [1 ]
机构
[1] Eisai & Co Ltd, Global Drug Metab & Pharmacokinet, Tokodai 5-1-3, Tsukuba, Ibaraki 3002635, Japan
[2] Univ Tsukuba, Fac Med, Grad Sch Comprehens Human Sci, Lab Genom based Drug Discovery, Tennodai 1-1-1, Tsukuba, Ibaraki 3058575, Japan
[3] Sunplanet Co Ltd, Tsukuba R&D Supporting Div, DMPK & Bioanal Unit, Tokodai 5-1-3, Tsukuba, Ibaraki 3002635, Japan
关键词
E7090; LC-MS; Validation; Human; Metabolite; At-column dilution;
D O I
10.1016/j.jpba.2023.115866
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
E7090, a novel fibroblast growth factor receptors inhibitor, is currently under clinical development for the treatment of patients with solid tumors. The previous assay was insufficient in detection sensitivity for E7090 and high exposure of a dealkylated metabolite, M2, was noted in a clinical trial at low doses. Thus, a sensitive assay for the simultaneous determination of E7090 and M2 in human plasma has been developed using ultraperformance liquid chromatography with tandem mass spectrometer (UPLC-MS/MS). E7090 and M2 were extracted from 0.1 mL of plasma by protein precipitation and chromatographed on a reverse phase column utilizing at-column dilution which enables larger volume sample injection to the UPLC-MS/MS. E7090 and M2 were quantifiable from 0.025 ng/mL, which was 40-fold higher sensitivity than the previous assay. Accuracy as relative error and precision as relative standard deviation were within +/- 15% and 15%, respectively, ensuring the reproducibility of the assay. The developed assay method was applied to a clinical trial of E7090, and plasma concentrations of E7090 and M2 were quantifiable up to 144 h postdose. These results indicated that the developed more sensitive assay was reproducible and was successfully applied to a clinical trial of E7090.
引用
收藏
页数:9
相关论文
共 45 条
  • [31] UPLC-MS/MS assay for the simultaneous quantification of carvedilol and its active metabolite 4-hydroxyphenyl carvedilol in human plasma to support a bioequivalence study in healthy volunteers
    Patel, Daxesh P.
    Sharma, Primal
    Sanyal, Mallika
    Singhal, Puran
    Shrivastav, Pranav S.
    BIOMEDICAL CHROMATOGRAPHY, 2013, 27 (08) : 974 - 986
  • [32] Determination of sunitinib and its active metabolite, N-desethyl sunitinib in mouse plasma and tissues by UPLC-MS/MS: assay development and application to pharmacokinetic and tissue distribution studies
    Chen, Xiao
    Wang, Zhong
    Liu, Mengping
    Liao, Min
    Wang, Xinfeng
    Du, Huajuan
    Chen, Jiefeng
    Yao, Meicun
    Li, Qing
    BIOMEDICAL CHROMATOGRAPHY, 2015, 29 (05) : 679 - 688
  • [33] Development and validation of a UPLC-MS/MS method for simultaneous determination of vicagrel and its major metabolites in rat or human plasma: An optimized novel strategy for the stabilization of vicagrel
    Tai, Ting
    Zhou, Huan
    Zhu, Ting
    Jia, Yu-Meng
    Ji, Jin-Zi
    Li, Yi-Fei
    Mi, Qiong-Yu
    Xie, Hong-Guang
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2020, 179
  • [34] DETERMINATION OF TOTAL AND UNBOUND LEVELS OF A POTENT INHIBITOR OF FIBROBLAST GROWTH FACTOR RECEPTOR, INFIGRATINIB, IN HUMAN PLASMA, CEREBROSPINAL FLUID AND BRAIN TUMOR BY A VALIDATED LC-MS/MS ASSAY
    Margaryan, Tigran
    Sanai, Nader
    Tovmasyan, Artak
    NEURO-ONCOLOGY, 2021, 23 : 76 - 77
  • [35] Simultaneous quantitative determination of seven novel tyrosine kinase inhibitors in plasma by a validated UPLC-MS/MS method and its application to human microsomal metabolic stability study
    Ezzeldin, Essam
    Iqbal, Muzaffar
    Herqash, Rasheed N.
    ElNahhas, Toqa
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2020, 1136 (1136):
  • [36] A Rapid and Sensitive LC-MS/MS Assay for the Determination of Saxagliptin and its Active Metabolite 5-hydroxy Saxagliptin in Human Plasma and its Application to a Pharmacokinetic Study
    Batta, N.
    Pilli, N. R.
    Derangula, V. R.
    Vurimindi, H. B.
    Damaramadugu, R.
    Yejella, R. P.
    DRUG RESEARCH, 2015, 65 (03) : 133 - 140
  • [37] Simultaneous determination and pharmacokinetics study of valsartan, sacubitril and its major metabolite in human plasma, urine and peritoneal dialysis fluid in patients with end-stage renal disease by UPLC-MS/MS
    Jin, Ying
    He, Yi
    Di, Xiangjie
    Fu, Lisha
    Qi, Xiaohui
    Liu, Runhan
    Zheng, Li
    Wang, Yongsheng
    Zhong, Hui
    Wang, Zhenlei
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2022, 1208
  • [38] Development of an LC-MS/MS method for quantifying ASK120067, a novel mutant-selective inhibitor of the epidermal growth factor receptor (EGFR) as well as its main metabolite in human plasma and its application in a pharmacokinetic study
    Cui, Xinge
    Wang, Shaoyuan
    Gao, Huitao
    Li, Baolan
    Shi, Yuankai
    Guo, Haifang
    Song, Tingting
    Zheng, Xin
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2021, 1162
  • [39] Method development and validation of the simultaneous determination of a novel topoisomerase 1 inhibitor, the prodrug, and the active metabolite in human plasma using column-switching LC-MS/MS, and its application in a clinical trial
    Kamei, Tomonori
    Uchimura, Takahide
    Nishimiya, Kazuhiro
    Kawanishi, Takehiko
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2011, 879 (30): : 3415 - 3422
  • [40] Sensitive, selective and rapid determination of bupropion and its major active metabolite, hydroxybupropion, in human plasma by LC-MS/MS: application to a bioequivalence study in healthy Indian subjects
    Parekh, Jignesh M.
    Sutariya, Dipen K.
    Vaghela, Rajendrasinh N.
    Sanyal, Mallika
    Yadav, Manish
    Shrivastav, Pranav S.
    BIOMEDICAL CHROMATOGRAPHY, 2012, 26 (03) : 314 - 326