Liquid chromatography tandem mass spectrometry in the clinical laboratory

被引:66
作者
Adaway, Joanne E. [1 ,2 ]
Keevil, Brian G. [1 ,2 ]
Owen, Laura J. [1 ,2 ]
机构
[1] Univ S Manchester Hosp, Dept Biochem, Manchester M23 9LT, Lancs, England
[2] Univ Manchester, Manchester Acad Hlth Sci Ctr, Manchester, Lancs, England
关键词
Liquid chromatography; tandem mass spectrometry; applications; future developments; SOLID-PHASE EXTRACTION; LC-MS/MS METHOD; PLASMA-RENIN ACTIVITY; URINARY FREE CORTISOL; DRIED BLOOD SPOT; CONGENITAL ADRENAL-HYPERPLASIA; DEUTERATED INTERNAL STANDARDS; II NEOEPITOPE PEPTIDE; FREE THYROID-HORMONES; ISOTOPE-DILUTION;
D O I
10.1177/0004563214557678
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
Clinical laboratory medicine has seen the introduction and evolution of liquid chromatography tandem mass spectrometry in routine clinical laboratories over the last 10-15 years. There still exists a wide diversity of assays from very esoteric and highly specialist manual assays to more simplified kit-based assays. The technology is not static as manufacturers are continually making improvements. Mass spectrometry is now commonly used in several areas of diagnostics including therapeutic drug monitoring, toxicology, endocrinology, paediatrics and microbiology. Some of the most high throughput analyses or common analytes include vitamin D, immunosuppressant monitoring, androgen measurement and newborn screening. It also offers flexibility for the measurement of analytes in a variety of different matrices which would prove difficult with immunoassays. Unlike immunoassays or high-pressure liquid chromatography assays using ultraviolet or fluorescence detection, mass spectrometry offers better specificity and reduced interferences if attention is paid to potential isobaric compounds. Furthermore, multiplexing, which enables multiple analytes to be measured with the same volume of serum is advantageous, and the requirement for large sample volumes is decreasing as instrument sensitivity increases. There are many emerging applications in the literature. Using mass spectrometry to identify novel isoforms or modified peptides is possible as is quantification of proteins and peptides, with or without protein digests. Future developments by the manufacturers may also include mechanisms to improve the throughput of samples and strategies to decrease the level of skill required by the operators.
引用
收藏
页码:18 / 38
页数:21
相关论文
共 263 条
  • [1] Determination of thyroid hormones and their metabolites in tissue using SPE UPLC-tandem MS
    Ackermans, M. T.
    Kettelarij-Haas, Y.
    Boelen, A.
    Endert, E.
    [J]. BIOMEDICAL CHROMATOGRAPHY, 2012, 26 (04) : 485 - 490
  • [2] Home fingerprick sampling for immunosuppressant drug monitoring in pediatric renal transplant patients - Commentary
    Acott, PD
    [J]. NATURE CLINICAL PRACTICE NEPHROLOGY, 2006, 2 (06): : 304 - 305
  • [3] Therapeutic drug monitoring and LC-MS/MS
    Adaway, Joanne E.
    Keevil, Brian G.
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2012, 883 : 33 - 49
  • [4] Multicomponent LC-MS/MS screening method for detection of new psychoactive drugs, legal highs, in urine-Experience from the Swedish population
    Al-Saffar, Yasir
    Stephanson, Niclas Nikolai
    Beck, Olof
    [J]. JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 930 : 112 - 120
  • [5] Comparison of Direct Colony Method versus Extraction Method for Identification of Gram-Positive Cocci by Use of Bruker Biotyper Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry
    Alatoom, Adnan A.
    Cunningham, Scott A.
    Ihde, Sherry M.
    Mandrekar, Jayawant
    Patel, Robin
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (08) : 2868 - 2873
  • [6] Standardization of LC-MS for Therapeutic Drug Monitoring of Tacrolimus
    Annesley, Thomas M.
    McKeown, Denise A.
    Holt, David W.
    Mussell, Christopher
    Champarnaud, Elodie
    Harter, Leonie
    Calton, Lisa J.
    Mason, Donald S.
    [J]. CLINICAL CHEMISTRY, 2013, 59 (11) : 1630 - 1637
  • [7] Simple extraction protocol for analysis of immunosuppressant drugs in whole blood
    Annesley, TM
    Clayton, L
    [J]. CLINICAL CHEMISTRY, 2004, 50 (10) : 1845 - 1848
  • [8] Ion suppression in mass spectrometry
    Annesley, TM
    [J]. CLINICAL CHEMISTRY, 2003, 49 (07) : 1041 - 1044
  • [9] [Anonymous], 2001, Guidance for industry, bioanalytical method validation
  • [10] [Anonymous], 2012, BMC CLIN PHARM