Development and application of a liquid chromatography coupled to mass spectrometry method for the simultaneous determination of 23 antineoplastic drugs at trace levels.
Antineoplastic Agents
/ analysis
Busulfan
Carboplatin
Chromatography, Liquid
Cyclophosphamide
/ analysis
Cytarabine
Dacarbazine
Daunorubicin
Docetaxel
Doxorubicin
/ analysis
Epirubicin
Etoposide
Fluorouracil
Ganciclovir
Humans
Idarubicin
Ifosfamide
Irinotecan
Methanol
Methotrexate
Oxaliplatin
Paclitaxel
/ analysis
Pemetrexed
Tandem Mass Spectrometry
/ methods
Topotecan
Vinblastine
Vincristine
Water
Antineoplastic drug
Mass spectrometry
Reversed phase liquid chromatography
Surface analyses
Trace analysis
Journal
Journal of pharmaceutical and biomedical analysis
ISSN: 1873-264X
Titre abrégé: J Pharm Biomed Anal
Pays: England
ID NLM: 8309336
Informations de publication
Date de publication:
30 Nov 2022
30 Nov 2022
Historique:
received:
18
07
2022
revised:
05
09
2022
accepted:
06
09
2022
pubmed:
13
9
2022
medline:
14
10
2022
entrez:
12
9
2022
Statut:
ppublish
Résumé
The goal of this study was to develop a method for the simultaneous quantification of 23 commonly used antineoplastic drugs in a hospital pharmacy, using ultra-high pressure liquid chromatography separation coupled to tandem mass spectrometry detection (UHPLC-MS/MS). The following drugs were investigated: 5-fluorouracil, cytarabine, ganciclovir, gemcitabine, dacarbazine, methotrexate, pemetrexed, busulfan, topotecan, rentitrexed, ifosfamide, cyclophosphamide, etoposide, irinotecan, doxorubicin/epirubicin, vincristine, docetaxel, paclitaxel, daunorubicin, idarubicin, vinblastine, oxaliplatin and carboplatin. The chromatographic separation was performed on a phenyl-hexyl column (2.1 ×100 mm, 1.7 µm) with a gradient elution of methanol and water containing 10 mM ammonium formate adjusted to pH 4.9. All compounds were analyzed in less than 13 min and detected with a triple quadrupole mass spectrometer operating in MRM mode. Limits of detection (LODs) and limits of quantification (LOQs) were comprised between 0.01 and 5 ng.mL
Identifiants
pubmed: 36095884
pii: S0731-7085(22)00455-1
doi: 10.1016/j.jpba.2022.115034
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
Cytarabine
04079A1RDZ
Pemetrexed
04Q9AIZ7NO
Oxaliplatin
04ZR38536J
Water
059QF0KO0R
Docetaxel
15H5577CQD
Epirubicin
3Z8479ZZ5X
Vincristine
5J49Q6B70F
Vinblastine
5V9KLZ54CY
Etoposide
6PLQ3CP4P3
Irinotecan
7673326042
Dacarbazine
7GR28W0FJI
Topotecan
7M7YKX2N15
Doxorubicin
80168379AG
Cyclophosphamide
8N3DW7272P
Carboplatin
BG3F62OND5
Busulfan
G1LN9045DK
Paclitaxel
P88XT4IS4D
Ganciclovir
P9G3CKZ4P5
Fluorouracil
U3P01618RT
Ifosfamide
UM20QQM95Y
Methanol
Y4S76JWI15
Methotrexate
YL5FZ2Y5U1
Idarubicin
ZRP63D75JW
Daunorubicin
ZS7284E0ZP
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
115034Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.