Comparative LC-MS/MS and HPLC-UV Analyses of Meropenem and Piperacillin in Critically III Patients

被引:6
|
作者
Paal, Michael [1 ]
Heilmann, Marcus [2 ]
Koch, Simone [2 ]
Bertsch, Thomas [2 ]
Steinmann, Joerg [3 ]
Hoehl, Rainer [3 ]
Liebchen, Uwe [4 ]
Schuster, Carina [1 ]
Kleine, Frederick M. [1 ]
Vogeser, Michael [1 ]
机构
[1] Univ Hosp, Inst Lab Med, LMU Munich, Munich, Germany
[2] Paracelsus Med Univ, Gen Hosp Nuremberg, Inst Clin Chem Lab Med & Transfus Med, Nurnberg, Germany
[3] Paracelsus Med Univ, Gen Hosp Nuremberg, Inst Med Microbiol Hyg & Clin Infectiol, Nurnberg, Germany
[4] Univ Hosp, Dept Anesthesiol, LMU Munich, Munich, Germany
关键词
therapeutic drug monitoring (TDM); antibiotics; intensive care units (ICU); pharmacokinetic and pharmacodynamic (PK/PK); isotope dilution liquid chromatography tandem mass spectrometry (ID-LC-MS/MS); high performance liquid chromatography with ultra-violet detector (HPLC-UV); BETA-LACTAM ANTIBIOTICS; HUMAN SERUM; ILL PATIENTS; CARE; QUANTIFICATION; INFECTION; CEFEPIME; MODELS;
D O I
10.7754/Clin.Lab.2019.190210
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: Therapeutic drug monitoring (TDM) of beta-lactam antibiotics has become a valuable tool to guide dosing in critically ill patients. The main goal of the study was to compare two routinely used techniques for beta-lactam TDM in intensive care unit (ICU) patient samples, namely isotope dilution liquid chromatography tandem mass spectrometry (ID-LC-MS/MS) and high-performance liquid chromatography combined with ultra-violet detection (HPLC-UV). Methods: A set of 80 sera/plasma samples from ICU patients receiving therapeutic meropenem or piperacillin dosage was investigated. Sample duplicates and quality assessment samples were assayed in parallel with an in-house LC-MS/MS and a commercially available IVD HPLC-UV kit. A pharmacokinetic and pharmacodynamic (PK/PD) target with >= 22.5 mg/L for piperacillin and >= 8.0 mg/L for meropenem was used for medical assessment of trough sample (n = 40) antibiotic concentrations. Results: There was no difference between serum and Li-heparin plasmas. Concentration deviations were found for 4% of meropenem and 17% of piperacillin samples. Eliminating the influence of the systemic bias of approximately 10% for piperacillin, measurement discrepancies >= 25% between LC-MS/MS and HPLC-UV analyses were only observed for approximate to 4 - 6% of all samples. In the same way, identical PK/PD target attainment rates of 50 - 60% could be obtained. Conclusions: After correction of the analytical bias for piperacillin measurements, both methods showed comparable results, also with respect to clinical decision limits. HPLC-UV analysis is an adequate TDM methodology for testing of beta-lactam antibiotics in centers where no special knowledge in LC-MS/MS based TDM is present. However, potential matrix effects, interferences, and calibration issues for both methods must be taken into account.
引用
收藏
页码:1675 / 1680
页数:6
相关论文
共 50 条
  • [41] Determination of osthol and its metabolites in a phase I reaction system and the Caco-2 cell model by HPLC-UV and LC-MS/MS
    Yuan, Zhenting
    Xu, Haiyan
    Wang, Ke
    Zhao, Zhonghua
    Hu, Ming
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2009, 49 (05) : 1226 - 1232
  • [42] Configuring HPLC systems for LC-MS
    Wehr, T
    LC GC NORTH AMERICA, 2000, 18 (04) : 406 - +
  • [43] Investigation on the photochemical stability of lercanidipine and its determination in tablets by HPLC-UV and LC-ESI-MS/MS
    Fiori, J
    Gotti, R
    Bertucci, C
    Cavrini, V
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2006, 41 (01) : 176 - 181
  • [44] A concise review of HPLC, LC-MS and LC-MS/MS methods for determination of azithromycin in various biological matrices
    Sharma, Kuldeep
    Mullangi, Ramesh
    BIOMEDICAL CHROMATOGRAPHY, 2013, 27 (10) : 1243 - 1258
  • [45] Assessment of an LC-MS method for plasma quantification of the new immunosuppressant FK778 through comparison with HPLC-UV
    Molinaro, M
    Carazzone, C
    Barbano, D
    Abbiati, F
    Bartoli, A
    Alessiani, M
    Regazzi, M
    THERAPEUTIC DRUG MONITORING, 2005, 27 (02) : 235 - 236
  • [46] LC-MS analyses of microcystins in fish tissues overestimate toxin levels—critical comparison with LC-MS/MS
    J. Kohoutek
    O. Adamovský
    M. Oravec
    Z. Šimek
    M. Palíková
    R. Kopp
    L. Bláha
    Analytical and Bioanalytical Chemistry, 2010, 398 : 1231 - 1237
  • [47] Evaluation of tamoxifen and metabolites by LC-MS/MS and HPLC methods
    Heath, D. D.
    Flatt, S. W.
    Wu, A. H. B.
    Pruitt, M. A.
    Rock, C. L.
    BRITISH JOURNAL OF BIOMEDICAL SCIENCE, 2014, 71 (01) : 33 - 39
  • [48] Determinations of residual furazolidone and its metabolite, 3-amino-2-oxazolidinone (AOZ), in fish feeds by HPLC-UV and LC-MS/MS, respectively
    Hu, Xiao-Zhong
    Xu, Ying
    Yediler, Ayfer
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (04) : 1144 - 1149
  • [49] Assessment of an LC-MS method for plasma quantification of the new immunosuppressant FK778 through comparison with HPLC-UV
    Molinaro, M
    Carazzone, C
    Barbano, D
    Abbiati, F
    Alessiani, M
    Regazzi, M
    TRANSPLANTATION PROCEEDINGS, 2005, 37 (06) : 2722 - 2727
  • [50] Analysis of flavonoids in fruits, vegetables and beverages by HPLC-UV and LC-MS and estimation of the total daily flavonoid intake in Denmark
    Leth, T
    Justesen, U
    COST 916 - POLYPHENOLS IN FOOD: BIOACTIVE PLANT CELL WALL COMPONENTS IN NUTRITION AND HEALTH, 1998, : 39 - 40