Re-Examining the Impact of Minimal Scans in Liquid Chromatography-Mass Spectrometry Analysis

被引:11
作者
Cai, Jingwei [1 ]
Yan, Zhengyin [1 ]
机构
[1] Genentech Inc, Dept Drug Metab & Pharmacokinet, San Francisco, CA 94080 USA
关键词
TRIPLE QUADRUPOLE; LC-MS; METABOLISM; PHARMACODYNAMICS; PERFORMANCE; RALOXIFENE; MIDAZOLAM; ALGORITHM; HRMS;
D O I
10.1021/jasms.1c00073
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Liquid chromatography-mass spectrometry (LC-MS) is one of the most widely used analytical tools. High analysis volumes and sample complexity often demand more informative LC-MS acquisition schemes to improve efficiency and throughput without compromising data quality, and such a demand has been always hindered by the prerequisite that a minimum of 13-20 MS scans (data points) across an analyte peak are required for accurate quantitation. The current study systematically re-evaluated and compared the impact of different scan numbers on quantitation analysis using both triple quadrupoles mass spectrometry (TQMS) and high-resolution mass spectrometry (HRMS). Contrary to the 13-20 minimal scan prerequisite, the data obtained from a group of eight commercial drugs in the absence and presence of biological matrices suggest that 6 scans per analyte peak are sufficient to achieve highly comparable quantitation results compared to that obtained using 10 and 20 scans, respectively. The fewer minimal scan prerequisite is presumably attributed to an improved LC system and advanced column technology, better MS detector, and more intelligent peak detection and integration algorithms leading to a more symmetric peak shape and smaller peak standard deviation. As a result, more informative acquisition schemes can be broadly set up for higher throughput and more data-rich LC-MS/MS analysis as demonstrated in a hepatocyte clearance assay in which fewer MS scans executed on HRMS led to broader metabolite coverage without compromising data quality in hepatic clearance assessment. The demonstrated acquisition scheme would substantially increase the throughput, robustness, and richness of the nonregulatory analysis, which can be broadly applied in diverse fields including pharmaceutical, environmental, forensic, toxicological, and biotechnological.
引用
收藏
页码:2110 / 2122
页数:13
相关论文
共 51 条
[1]  
Allen Darren R, 2019, Clin Biochem Rev, V40, P135, DOI 10.33176/AACB-19-00023
[2]   Challenges and achievements of LC-MS in environmental analysis:: 25 years on [J].
Barcelo, Damia ;
Petrovic, Mira .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 2007, 26 (01) :2-11
[3]   Teaching Undergraduates LC-MS/MS Theory and Operation via Multiple Reaction Monitoring (MRM) Method Development [J].
Betts, Thomas A. ;
Palkendo, Julie A. .
JOURNAL OF CHEMICAL EDUCATION, 2018, 95 (06) :1035-1039
[4]   Hepatic metabolism of diclofenac:: Role of human CYP in the minor oxidative pathways [J].
Bort, R ;
Macé, K ;
Boobis, A ;
Gómez-Lechón, MJ ;
Pfeifer, A ;
Castell, J .
BIOCHEMICAL PHARMACOLOGY, 1999, 58 (05) :787-796
[5]  
Campbell JL, 2012, BIOANALYSIS, V4, P487, DOI [10.4155/bio.12.14, 10.4155/BIO.12.14]
[6]   Overcoming Matrix Effects in Liquid Chromatography-Mass Spectrometry [J].
Cappiello, Achille ;
Famiglini, Giorgio ;
Palma, Pierangela ;
Pierini, Elisabetta ;
Termopoli, Veronica ;
Trufelli, Helga .
ANALYTICAL CHEMISTRY, 2008, 80 (23) :9343-9348
[7]   The emerging interface of mass spectrometry with materials [J].
Chakraborty, Papri ;
Pradeep, Thalappil .
NPG ASIA MATERIALS, 2019, 11 (1)
[8]   Advances in mass spectrometry-based clinical biomarker discovery [J].
Crutchfield, Christopher A. ;
Thomas, Stefani N. ;
Sokoll, Lori J. ;
Chan, Daniel W. .
CLINICAL PROTEOMICS, 2016, 13
[9]   Mass spectrometry in drug metabolism and pharmacokinetics: Current trends and future perspectives [J].
Cuyckens, Filip .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2019, 33 :90-95
[10]   Quantitative monitoring of tamoxifen in human plasma extended to 40 metabolites using liquid-chromatography high-resolution mass spectrometry: new investigation capabilities for clinical pharmacology [J].
Dahmane, Elyes ;
Boccard, Julien ;
Csajka, Chantal ;
Rudaz, Serge ;
Decosterd, Laurent ;
Genin, Eric ;
Duretz, Benedicte ;
Bromirski, Maciej ;
Zaman, Khalil ;
Testa, Bernard ;
Rochat, Bertrand .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2014, 406 (11) :2627-2640