This application note demonstrates to evaluate the source robustness by injecting samples of verapamil spiked into human plasma.
The robustness and reproducibility for samples on biological matrices has been evaluated by analyzing verapamil in protein-precipitated plasma
The Quattro Premier Tandem Quadrupole Mass Spectrometer has a newly developed ZSpray interface designed to meet the demands of high throughput analyses from biological matrices in the pharmaceutical industry. In this environment robustness and sensitivity are the driving forces for successful bioanalysis.
The following study has been developed to evaluate the source robustness by injecting samples of verapamil spiked into human plasma. The spiked plasma was protein-precipitated and the supernatant injected directly into the source. The study ran over a 24-hour period in positive ion electrospray ionization mode (ESI+ve).
The newly designed ZSpray source for the Waters Micromass Quattro Premier incorporates the best features of the Quattro micro API but with a smaller ion block that reduces the volume of the source chamber. The new features are highlighted in Figure 1 and are explained in Tech Note 720000826EN.
A quality control (QC) solution of verapamil in human plasma was prepared at a concentration of 10 pg/mL. The QC's were then protein-precipitated by adding acetonitrile (1:1), the resultant mixture was centrifuged (ca 3000 rpm, 10 mins) and the supernatant taken for analysis by LC-MS/MS, 200 repeat injections were performed.
LC system: |
Waters 2695 |
Column: |
Waters Atlantis, C18 3.5 μm, 2.1 x 100 mm |
Flow rate: |
0.2 mL/min |
Gradient: |
Isocratic at 55% water: 45% acetonitrile 0.1% Formic acid |
Mass spectrometer: |
Waters Micromass Quattro Premier |
Ion mode: |
ESI +ve |
Capillary voltage: |
3.2 V |
Cone voltage: |
40 V |
Collision energy: |
27 eV |
Detection mode: |
MRM (455.40 > 165.10) |
Dwell: |
0.5 seconds |
Collision gas: |
Argon (3.6 x 10-3 mbar) |
The MRM chromatograms for the verapamil analysis were integrated automatically using Waters proprietary ApexTrack peak integration algorithm and the resulting peak areas were plotted against injection number to show the reproducibility of response over the analysis period. A relative standard deviation of 3.0% was observed across all 200 analyses (see Figure 2).
The plot of peak area against concentration showed good linearity over the range 0.5–5000 pg/μL. The calibration line was plotted using a linear fit with 1/x weighting and gave a correlation coefficient of 0.9978, with all calibration points resulting in <8% deviation (see Figure 3)
The new Waters Micromass Quattro Premier Tandem Quadrupole Mass Spectrometer has been developed for quantitative LC-MS/MS. The robustness and reproducibility for samples on biological matrices has been evaluated by analyzing verapamil in protein-precipitated plasma.
The results also show that the Quattro Premier sensitivity was maintained with a relative standard deviation of 3.0% during 200 injections. This demonstrates the robustness of the modified ZSpray source for analyses from complex matrices. The calibration line resulted in a linear plot over 4 orders of magnitude (0.5 to 5000 pg/μL) with a correlation coefficient of 0.9978.
720000824, March 2004