Development and validation of a simple and sensitive LC-MS/MS method for quantification of ampicillin and sulbactam in human plasma and its application to a clinical pharmacokinetic study

被引:0
|
作者
Nalbant, Demet [1 ]
Reeder, Joshua A. [1 ]
Li, Peizhi [2 ]
O'Sullivan, Cormac T. [3 ]
Rogers, William K. [4 ]
An, Guohua [1 ]
机构
[1] Univ Iowa, Coll Pharm, Div Pharmaceut & Translat Therapeut, 115 S Grand Ave, Iowa City, IA 52242 USA
[2] Univ Iowa, Coll Pharm, Iowa City, IA 52242 USA
[3] Univ Iowa Hosp & Clin, Coll Nursing, Iowa City, IA 52242 USA
[4] Univ Minnesota, Dept Anesthesia, Med Sch, M Hlth Fairview, Minneapolis, MN 55455 USA
关键词
LC/MS/MS; Ampicillin-sulbactam; Clinical pharmacokinetics study; Assay development and validation; Human plasma antibiotic redosing; PERFORMANCE LIQUID-CHROMATOGRAPHY;
D O I
10.1016/j.jpha.2021.113899
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Ampicillin-sulbactam is a broad-spectrum combination antibiotic used for a variety of clinical applications, including as a prophylactic agent to reduce the risk of surgical site infection. The pharmacokinetics of ampicillin-sulbactam after redosing during prolonged surgeries remains incompletely understood. In anticipation of further studying the intra-operative pharmacokinetics of this drug, we have developed a novel liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the quantification of ampicillin and sulbactam. The plasma samples were prepared using a simple protein precipitation method. Gradient chromatographic elution was used to separate analytes, and MS/MS analysis was performed in negative ionization mode for both analytes via multiple reaction monitoring (MRM). All validation parameters were evaluated under a good laboratory practice (GLP) environment. For both ampicillin and sulbactam, the lower limit of quantitation (LLOQ) was established as 0.25 tig/mL. The calibration curve ranged from 0.25 to 200 mu g/mL for ampicillin and 0.25-100 mu g/mL for sulbactam. Inter- and intra-day precisions for both analytes were <= 11.5 % for quality controls and <= 17.4 % for LLOQ; accuracies ranged from -11.5 to 12.5% for 3 quality control levels and-18.1-18.7% for LLOQ. In addition to sensitivity, accuracy and precision, 13 other parameters were also validated for both analytes, and the results met the acceptance criteria. Our method was successfully applied to quantify ampicillin and sulbactam concentrations in patients undergoing surgery. (C) 2021 Elsevier B.V. All rights reserved.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Development and validation of an LC-MS/MS method for the determination of tigecycline in human plasma and cerebrospinal fluid and its application to a pharmacokinetic study
    Mei, Shenghui
    Luo, Xuying
    Li, Xingang
    Li, Qian
    Huo, Jiping
    Yang, Li
    Zhu, Leting
    Feng, Weixing
    Zhou, Jianxin
    Shi, Guangzhi
    Zhao, Zhigang
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2016, 30 (12) : 1992 - 2002
  • [42] Development and validation of an LC-MS/MS method for quantification of favipiravir in human plasma
    Challenger, Elizabeth
    Penchala, Sujan Dilly
    Hale, Colin
    Fitzgerald, Richard
    Walker, Lauren
    Reynolds, Helen
    Chiong, Justin
    Fletcher, Tom
    Khoo, Saye
    Else, Laura
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2023, 233
  • [43] A simple and sensitive LC-MS/MS method for the determination of polyphyllin VII in rat plasma and its application to pharmacokinetic study
    Wang, Hao
    Han, Han
    Xu, Ying
    Yang, Yishun
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2023, 37 (05)
  • [44] Development and validation of a rapid and sensitive LC-MS/MS method for the determination of polyphyllin II in rat plasma and its application in a pharmacokinetic study
    Yang, Qiaoling
    Li, Hongjing
    Gui, Mingzhu
    Li, Zhiling
    Sun, Huajun
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2020, 34 (03)
  • [45] LC-MS/MS METHOD FOR THE QUANTIFICATION OF DICLOFENAC FROM HUMAN PLASMA AND ITS APPLICATION TO PHARMACOKINETIC STUDIES
    Muntean, Dana
    Vlase, Laurian
    Cuciureanu, Rodica
    Cuciureanu, Magdalena
    [J]. REVUE ROUMAINE DE CHIMIE, 2011, 56 (01) : 19 - +
  • [46] Development and validation of a highly sensitive LC-MS/MS method for the determination of dexamethasone in nude mice plasma and its application to a pharmacokinetic study
    Yuan, Yin
    Zhou, Xuan
    Li, Jian
    Ye, Suofu
    Ji, Xiwei
    Li, Liang
    Zhou, Tianyan
    Lu, Wei
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2015, 29 (04) : 578 - 583
  • [47] Simple and sensitive LC-MS/MS method for simultaneous determination of crizotinib and its major oxidative metabolite in human plasma: Application to a clinical pharmacokinetic study
    Qi, Xiaoyan
    Zhao, Lin
    Zhao, Qiuping
    Xu, Qiaoxia
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2018, 155 : 210 - 215
  • [48] Development and Validation of LC-MS/MS Assay for the Quantification of Progesterone in Rat Plasma and its Application to Pharmacokinetic Studies
    Sasaki, M.
    Ochiai, H.
    Takahashi, K.
    Suzuki, R.
    Minato, K.
    Fujikata, A.
    [J]. DRUG RESEARCH, 2015, 65 (09) : 484 - 489
  • [49] Quantification of endostar in rat plasma by LC-MS/MS and its application in a pharmacokinetic study
    Li, Ying Chun
    Liang, Yan
    Tang, Zhi Yuan
    Xiao, Ya Nan
    Hao, Hai Ping
    Wang, Guang Ji
    [J]. JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2012, 70 : 505 - 511
  • [50] Development and validation of a sensitive LC-MS/MS method with electrospray ionization for quantitation of doxofylline in human serum: application to a clinical pharmacokinetic study
    Sreenivas, Nimmagadda
    Narasu, M. Lakshmi
    Shankar, B. Prabha
    Mullangi, Ramesh
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2008, 22 (06) : 654 - 661