Establishment of a sensitive UPLC-MS/MS method to quantify safinamide in rat plasma

A fast, simple, and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was established for the quantification of safinamide in rat plasma. Plasma samples were treated with acetonitrile for protein precipitation, and diazepam was used as an internal standar...

Full description

Saved in:
Bibliographic Details
Main Authors: Ying Wang (Author), Guan-An Zhao (Author), Xia Li (Author), En Zhang (Author), Wei Tan (Author), Jia-qi Chen (Author)
Format: Book
Published: Frontiers Media S.A., 2023-08-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_c86efbd00fae4ebd9a0dc56ca1f07af3
042 |a dc 
100 1 0 |a Ying Wang  |e author 
700 1 0 |a Guan-An Zhao  |e author 
700 1 0 |a Xia Li  |e author 
700 1 0 |a En Zhang  |e author 
700 1 0 |a Wei Tan  |e author 
700 1 0 |a Jia-qi Chen  |e author 
245 0 0 |a Establishment of a sensitive UPLC-MS/MS method to quantify safinamide in rat plasma 
260 |b Frontiers Media S.A.,   |c 2023-08-01T00:00:00Z. 
500 |a 1663-9812 
500 |a 10.3389/fphar.2023.1211383 
520 |a A fast, simple, and sensitive ultra performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) method was established for the quantification of safinamide in rat plasma. Plasma samples were treated with acetonitrile for protein precipitation, and diazepam was used as an internal standard (IS). The analytes were separated on an Acquity UPLC C18 (2.1 mm × 50 mm, 1.7 μm) chromatographic column with gradient elution using a mobile phase (0.1% formic acid-acetonitrile). Then, the eluates were detected by electrospray ionization (ESI) in positive ion mode. The analytes were quantified by multiple reaction monitoring (MRM) using the transition m/z 303.3→215.0 of safinamide and m/z 285.0→154.0 of IS. Safinamide had good linearity in the concentration range of 1.0-2000 ng/mL, and the lower limit of quantitation (LLOQ) was 1.0 ng/mL. The intra- and inter-day precision and accuracy of safinamide were less than 7.63%, while the average recovery rate was 92.98%-100.29%. The method was validated to be stable and had low noise, short chromatographic run time, wide linear range, small sample volumes, low sample injection volumes, and high sensitivity. Therefore, it can be used in pharmacokinetics and preclinical and clinical studies. 
546 |a EN 
690 |a UPLC-MS/MS 
690 |a rat 
690 |a safinamide 
690 |a plasma 
690 |a pharmacokinetics 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Frontiers in Pharmacology, Vol 14 (2023) 
787 0 |n https://www.frontiersin.org/articles/10.3389/fphar.2023.1211383/full 
787 0 |n https://doaj.org/toc/1663-9812 
856 4 1 |u https://doaj.org/article/c86efbd00fae4ebd9a0dc56ca1f07af3  |z Connect to this object online.