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. 2026 Jan 10;18(1):91. doi: 10.3390/pharmaceutics18010091
TDM Therapeutic drug monitoring
UPLC-qTOF-MS/MS Ultraperformance Liquid Chromatography-quadrupole-Time-of-Flight-Mass Spectrometry
LC Liquid chromatography
MRM Multiple Reaction Monitoring
IS Internal standard
EMA European Medicine Agency
MRSA Methicillin-resistant staphylococcus aureus
CE Collision energy
DP Declustering potential
QC Quality control
LOQ Limit of quantification
LQC Low-quality control
MQC Medium-quality control
HQC High-quality control
CONC Concentration
AVG Average
S/N Signal-to-noise ratio
CV Coefficient of variation
ER Extraction recovery
ME Matrix effect
CI Continuous infusion