Development and application of a thin-film molecularly imprinted polymer for the measurement of mycophenolic acid in human plasma

被引:2
作者
Langille, Evan [1 ]
Bottaro, Christina S. [1 ]
机构
[1] Mem Univ Newfoundland, Dept Chem, St John, NF, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
human plasma assays; molecularly imprinted polymer; mycophenolic acid; tandem mass spectrometry; therapeutic drug monitoring; thin-film microextraction; PERFORMANCE LIQUID-CHROMATOGRAPHY; TANDEM MASS-SPECTROMETRY; DRUG; TRANSPLANTATION; QUANTIFICATION; PHARMACOKINETICS; EXTRACTION; RECIPIENTS; MOFETIL; SAMPLES;
D O I
10.1002/jcla.24864
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
BackgroundMycophenolic acid (MPA) is used to suppress the immune response following organ transplantation; however, complex pharmacokinetic behavior and a large interpersonal variability necessitate therapeutic drug monitoring. To overcome the limitations of current sample preparation techniques, we present a novel thin-film molecularly imprinted polymer (TF-MIP) extraction device as part of a simple, sensitive, and fast method for analysis of MPA from human plasma. MethodsMycophenolic acid is extracted from plasma using a tailor-made TF-MIP that is subsequently desorbed into an organic solvent system compatible with mass spectrometry. The MIP yielded higher recovery of MPA relative to a corresponding non-imprinted polymer. The method allows for the determination of MPA in 45 min including analysis time and can be scaled for high throughput to process as many as 96 samples per hour. ResultsThe method gave an LOD of 0.3 ng mL(-1) and was linear from 5 to 250 ng mL(-1). Patient plasma samples (35 mu L) were diluted using charcoal-stripped pooled plasma to a final extraction volume of 700 mu L; when MPA in patient plasma is high, this ratio can easily be adjusted to ensure samples are within the method linear range. Intra- and inter-day variability were 13.8% and 4.3% (at 15 ng mL(-1)) and 13.5% and 11.0% (at 85 ng mL(-1)), respectively (n = 3); inter-device variability was 9.6% (n = 10). ConclusionsLow inter-device variability makes these devices suitable for single use in a clinical setting, and the fast and robust method is suitable for therapeutic drug monitoring, where throughput and time-to-result are critical.
引用
收藏
页数:9
相关论文
共 35 条
  • [11] Egli SN, 2015, ANAL METHODS-UK, V7, P2028, DOI [10.1039/c4ay02849j, 10.1039/C4AY02849J]
  • [12] Molecular Imprinting Techniques Used for the Preparation of Biosensors
    Erturk, Gizem
    Mattiasson, Bo
    [J]. SENSORS, 2017, 17 (02)
  • [13] Microextraction techniques in therapeutic drug monitoring
    Farhadi, Khalil
    Hatami, Mehdi
    Matin, Amir Abbas
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2012, 26 (08) : 972 - 989
  • [14] Safety considerations with mycophenolate sodium
    Filler, Guido
    Buffo, Ilan
    [J]. EXPERT OPINION ON DRUG SAFETY, 2007, 6 (04) : 445 - 449
  • [15] Do we need to worry about mycophenolate overdose?
    Filler, Guido
    Ferrand, Amaryllis
    [J]. EXPERT OPINION ON DRUG SAFETY, 2014, 13 (05) : 521 - 524
  • [16] MYCOPHENOLATE MOFETIL FOR TRANSPLANTATION - NEW DRUG, OLD PROBLEMS
    GRAY, DWR
    [J]. LANCET, 1995, 346 (8972): : 390 - 390
  • [17] The pharmacokinetic-pharmacodynamic relationship for mycophenolate mofetil in renal transplantation
    Hale, MD
    Nicholls, AJ
    Bullingham, RES
    Hené, R
    Hoitsma, A
    Squifflet, JP
    Weimar, W
    Vanrenterghem, Y
    Van de Woude, FJ
    Verpooten, GA
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 1998, 64 (06) : 672 - 683
  • [18] Molecularly imprinted polymer thin-film as a micro-extraction adsorbent for selective determination of trace concentrations of polycyclic aromatic sulfur heterocycles in seawater
    Hijazi, Hassan Y.
    Bottaro, Christina S.
    [J]. JOURNAL OF CHROMATOGRAPHY A, 2020, 1617
  • [19] Therapeutic monitoring of mycophenolate mofetil
    Jeong, Hyunyoung
    Kaplan, Bruce
    [J]. CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2007, 2 (01): : 184 - 191
  • [20] Population Pharmacokinetics of Mycophenolic Acid: An Update
    Kiang, Tony K. L.
    Ensom, Mary H. H.
    [J]. CLINICAL PHARMACOKINETICS, 2018, 57 (05) : 547 - 558