Measurement of albuterol in guinea pig serum by high performance liquid chromatography with fluorescence detection

Citation
Jr. Loss et al., Measurement of albuterol in guinea pig serum by high performance liquid chromatography with fluorescence detection, BIOMED CHRO, 14(1), 2000, pp. 1-5
Citations number
13
Categorie Soggetti
Chemistry & Analysis
Journal title
BIOMEDICAL CHROMATOGRAPHY
ISSN journal
02693879 → ACNP
Volume
14
Issue
1
Year of publication
2000
Pages
1 - 5
Database
ISI
SICI code
0269-3879(200002)14:1<1:MOAIGP>2.0.ZU;2-9
Abstract
A sensitive, simple and reproducible high performance liquid chromatographi c method for detecting and quantifying albuterol in guinea pig serum is des cribed. A structurally related compound, bamethan, was used as an internal standard. The method employs ion-pair extraction with di(2-ethylhexyl)phosp hate followed by chromatography on a Zorbax SE C18 reversed-phase column. F luorescence detection was used to identify the compounds of interest. The c alibration curve was Linear between 1 and 50 ng/ mt albuterol hemisulfate s alt (0.83 and 41.50 ng/mL albuterol base), and the Limit of detection for a 1 mt sample was 1 ng/mL albuterol hemisulfate salt (0.83 ng/mL albuterol b ase). Serum levels of albuterol were quantified from guinea pigs that had r eceived the drug by continuous subcutaneous infusion at a dose of 0.2 mg/kg /day for 1, 5 or 10 days, or 10 days followed by a 24 h washout period. Cop yright (C) 2000 John Wiley & Sons, Ltd.