Improved HPLC Quantification of 6-Mercaptopurine Metabolites in Red Blood Cells: Monitoring Data and Literature Analysis.
Adult
Azathioprine
/ metabolism
Child
Chromatography, High Pressure Liquid
/ methods
Dithiothreitol
Erythrocytes
/ metabolism
Humans
Immunosuppressive Agents
/ therapeutic use
Inflammatory Bowel Diseases
/ metabolism
Mercaptopurine
/ therapeutic use
Nucleotides
/ metabolism
Thioguanine
/ therapeutic use
6-mercaptopurine
6-thiopurines
acute leukemia
chronic inflammatory bowel disease
monitoring
pharmacogenetics
thiopurines
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
06 Oct 2022
06 Oct 2022
Historique:
received:
25
08
2022
revised:
23
09
2022
accepted:
27
09
2022
entrez:
14
10
2022
pubmed:
15
10
2022
medline:
18
10
2022
Statut:
epublish
Résumé
Thiopurine drugs azathioprine (AZA) and 6-mercaptopurine (6-MP) are used extensively in pediatric and adult patients with inflammatory and neoplastic diseases. They are metabolized to 6-thioguanine nucleotides (6-TGN) or to 6-methyl-mercaptopurine nucleotides (6-MMPN). The balance between 6-TGN and 6-MMPN is highly variable and monitoring is recommended, but its benefit in outcome gives rise to conflicting results, potentially increased by differences in quantifying 6-MP metabolism. Our aim was to report (1) the HPLC-UV procedure used in our laboratory to quantify red blood cells (RBCs) with 6-TGN and 6-MMPN (as its derivate: 6-MMP(d)) in patients treated with thiopurines and (2) additional tests, sometimes confirmatory, to improve method standardization. The comparison of two methods to count RBCs shows that metabolite concentrations were slightly lower in the washed and resuspended RBCs than in whole blood. Perchloric acid (0.7 M), dithiothreitol (DTT, final 0.013 M sample concentration) and 60 min hydrolysis were selected for acid hydrolysis. (3) Monitoring data from 83 patients receiving AZA or 6-MP showed that at steady state, only 53/183 (29%) had 6-TGN and 6-MMPN in the recommended therapeutic range. Our method is discussed in light of the technical conditions and sample stability data from 17 publications identified since the first analytical report in 1987. Monitoring data demonstrate, if required, that inter-patient variability in 6-TGN and 6-MMPN concentrations is high in samples from treated patients.
Identifiants
pubmed: 36233187
pii: ijms231911885
doi: 10.3390/ijms231911885
pmc: PMC9570176
pii:
doi:
Substances chimiques
Immunosuppressive Agents
0
Nucleotides
0
Mercaptopurine
E7WED276I5
Thioguanine
FTK8U1GZNX
Azathioprine
MRK240IY2L
Dithiothreitol
T8ID5YZU6Y
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
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