Title : Using a stable isotope-labeled internal standard for liquid chromatography-tandem mass spectrometry quantitation of meloxicam in human plasma.

Pub. Date : 2021 Dec

PMID : 34405424






2 Functional Relationships(s)
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1 After a single-dose oral administration of 7.5 mg meloxicam, the main pharmacokinetic parameters were as follows: Cmax , 814.79 +- 201.37 ng mL-1 ; Tmax , 4.54 +- 1.42 h; AUC0-t , 24,572.04 +- 5766.93 ng h mL-1 ; AUC0- , 25,810.89 +- 6796.60 ng h mL-1 and t1/2 , 21.11 +- 5.35 h. Meloxicam L1 cell adhesion molecule Mus musculus
2 After a single-dose oral administration of 7.5 mg meloxicam, the main pharmacokinetic parameters were as follows: Cmax , 814.79 +- 201.37 ng mL-1 ; Tmax , 4.54 +- 1.42 h; AUC0-t , 24,572.04 +- 5766.93 ng h mL-1 ; AUC0- , 25,810.89 +- 6796.60 ng h mL-1 and t1/2 , 21.11 +- 5.35 h. Meloxicam L1 cell adhesion molecule Mus musculus