Nicola Hughes,
1 Antony Harvey,
2 Witold Winnik,
3
Jean-Jacques Dunyach,
2 Maan Amad,
2 Maurizio Splendore,
2 and Gary Paul
3
1Biovail Contract Research,Toronto,Ontario,Canada;
2Thermo Finnigan,San Jose,CA,USA;
3Thermo Finnigan,Somerset, NJ,USA
Systemic Plasma Analysis
The data presented here was acquired on a Thermo Finnigan TSQ Quantum
mass spectrometer
Overview
Quantitation of low plasma concentrations of the pharmaceutical cabergoline
is performed to demonstrate the sensitivity and selectivity of the TSQ Quantum
mass spectrometer. Samples with analyte concentrations ranging five orders
of magnitude are analyzed to demonstrate precision and accuracy over a linear
dynamic range suitable for pharmacokinetic applications. Analysis of 50
fg of cabergoline on column in minimally treated plasma samples is performed
to demonstrate the sensitivity, ruggedness, and practicality of the bioanalytical
method in a complex matrix.
Introduction
Pharmaceuticals with potent activity achieve their
desired therapeutic effects when administered at low
doses. Consequently, their systemic plasma levels are
extremely low and require highly sensitive techniques
for detection. Cabergoline, a synthetic ergoline
derivative with a powerful dopaminergic activity,
is usually administered in 0.25 mg, biweekly doses,
yielding plasma concentrations in the pg/mL level.
[1,2]
A variety of analytical methods have been employed
to quantify low levels of cabergoline in plasma; these
include high performance liquid chromatography
(HPLC), radioimmunassay (RIA), and liquid chromatogra
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