Determination of the immunostimulatory drug—glucosoaminyl‐muramyl‐dipeptide—in human plasma using HPLC–MS/MS and its application to a pharmacokinetic study

• Published in: Biomedical chromatography Vol. 34; no. 12; pp. e4948 - n/a
• Main Authors: Moskaleva, Natalia E., Markin, Pavel A., Kuznetsov, Roman M., Andronova, Tatiana M., Appolonova, Svetlana A.
• Format: Journal Article
• Language: English
• Published: England 01-12-2020
• Subjects: Acetylmuramyl-Alanyl-Isoglutamine - administration & dosage; Acetylmuramyl-Alanyl-Isoglutamine - blood; Acetylmuramyl-Alanyl-Isoglutamine - chemistry; Acetylmuramyl-Alanyl-Isoglutamine - pharmacokinetics; Administration, Oral; Adolescent; Adult; Chromatography, High Pressure Liquid - methods; glucosoaminyl‐muramyl‐dipeptide (N‐acetylglucosoaminyl‐N‐acetylmuramyl‐l‐alanyl‐d‐isoglutamine); GMDP; Humans; immunostimulatory drugs; LC–MS/MS, muramyl peptides; Limit of Detection; Linear Models; Male; Middle Aged; pharmacokinetics; Reproducibility of Results; Tandem Mass Spectrometry - methods; Young Adult; pharmacokinetics; immunostimulatory drugs; GMDP; glucosoaminyl-muramyl-dipeptide (N-acetylglucosoaminyl-N-acetylmuramyl-l-alanyl-d-isoglutamine); LC-MS/MS, muramyl peptides
• ISSN: 0269-3879; 1099-0801
• DOI: 10.1002/bmc.4948

GMDP (glucosoaminyl‐muramyl‐dipeptide), a synthetic analog of the peptidoglycan fragment of the bacterial cell wall, is an active component of the immunomodulatory drug Licopid. But the pharmacokinetic parameters of GMDP in humans after oral administration have not been investigated yet. The present study aimed at developing and validating a sensitive LC–MS/MS method for the analysis of GMDP in human plasma. The sample was prepared by solid‐phase extraction using Strata‐X 33 μm polymeric reversed‐phase 60 mg/3 mL cartridges Phenomenex (Torrance, CA, USA). The analytes were separated using an Acquity UPLC BEN C18 column, 1.7 μm 2.1 × 50 mm Waters (Milford, USA). GMDP and internal standard growth hormone releasing peptide‐2 (pralmorelin) were ionized in positive electrospray ionization mode and detected in multiple reaction monitoring mode. The developed method was validated within a linear range of 50–3000 pg/mL for GMDP. Accuracy for all analytes, given as the deviation between the nominal and measured concentration and assay variability , ranged from 1.61 to 3.02% and from 0.89 to 1.79%, respectively, for both within‐ and between‐run variabilities. The developed and validated HPLC–MS/MS method was successfully used to obtain the plasma pharmacokinetic profiles of GMDP distribution in human plasma.