Anneliese M Rittau1, Andrew J McLachlan. 1. Faculty of Pharmacy, University of Sydney and Centre for Education and Research on Ageing, Concord Repatriation General Hospital, Sydney, NSW, Australia.
Abstract
OBJECTIVE: The aim of this study was to develop, validate and apply a high performance liquid chromatography (HPLC) assay for analysis of paracetamol, paracetamol glucuronide and paracetamol sulfate in plasma (venous and capillary) and saliva to study paracetamol pharmacokinetics in healthy volunteers. METHODS: Samples were prepared using protein precipitation and analysed using reverse phase HPLC with UV detection. This assay was applied to venous and capillary plasma and saliva samples from 20 healthy volunteers after paracetamol 1g four times daily for three days. KEY FINDINGS: The HPLC assay for paracetamol and its metabolites was found to be sensitive and selective in plasma and saliva samples over the range 0.05-50 mg/l with an inter- and intraday precision and accuracy within 11.2% and 11.1%, respectively. Mean recoveries for all analytes were > 88%. A study of paracetamol pharmacokinetics in healthy volunteers found close agreement between the sampling matrices for paracetamol and metabolites (metabolites were not detected in saliva). The value for area under the concentration-time curve over the 6h dosing interval of venous plasma (45.3±12.9mg/l.h) was significantly higher than that observed for capillary plasma (33.8±12.9mg/l.h) or saliva (35.1±9.4mg/l.h; P>0.01). CONCLUSIONS: Capillary blood and saliva collection were found to be reliable sampling matrices for the evaluation of paracetamol pharmacokinetics, although paracetamol metabolites were not detected in saliva.
OBJECTIVE: The aim of this study was to develop, validate and apply a high performance liquid chromatography (HPLC) assay for analysis of paracetamol, paracetamol glucuronide and paracetamol sulfate in plasma (venous and capillary) and saliva to study paracetamol pharmacokinetics in healthy volunteers. METHODS: Samples were prepared using protein precipitation and analysed using reverse phase HPLC with UV detection. This assay was applied to venous and capillary plasma and saliva samples from 20 healthy volunteers after paracetamol 1g four times daily for three days. KEY FINDINGS: The HPLC assay for paracetamol and its metabolites was found to be sensitive and selective in plasma and saliva samples over the range 0.05-50 mg/l with an inter- and intraday precision and accuracy within 11.2% and 11.1%, respectively. Mean recoveries for all analytes were > 88%. A study of paracetamol pharmacokinetics in healthy volunteers found close agreement between the sampling matrices for paracetamol and metabolites (metabolites were not detected in saliva). The value for area under the concentration-time curve over the 6h dosing interval of venous plasma (45.3±12.9mg/l.h) was significantly higher than that observed for capillary plasma (33.8±12.9mg/l.h) or saliva (35.1±9.4mg/l.h; P>0.01). CONCLUSIONS: Capillary blood and saliva collection were found to be reliable sampling matrices for the evaluation of paracetamol pharmacokinetics, although paracetamol metabolites were not detected in saliva.
Authors: Niklas Wester; Bjørn F Mikladal; Ilkka Varjos; Antti Peltonen; Eija Kalso; Tuomas Lilius; Tomi Laurila; Jari Koskinen Journal: Anal Chem Date: 2020-09-11 Impact factor: 6.986
Authors: Lucia Mainero Rocca; Nunziata L'Episcopo; Andrea Gordiani; Matteo Vitali; Alessandro Staderini Journal: Int J Environ Res Public Health Date: 2021-03-16 Impact factor: 3.390