Rapid Improvements for LC–MS-MS Analysis Using the New Phree? Phospholipid Removal Plates

September 1, 2012

The Application Notebook

The Application Notebook, The Application Notebook-09-01-2012, Volume 0, Issue 0

When performing LC–MS-MS analysis, phospholipids are perhaps one of the most troublesome components of bioanalytical samples. The presence of phospholipids not only reduces the column lifetime and sensitivity but can also cause a phenomenon known as ion suppression.

When performing LC–MS-MS analysis, phospholipids are perhaps one of the most troublesome components of bioanalytical samples. The presence of phospholipids not only reduces the column lifetime and sensitivity but can also cause a phenomenon known as ion suppression.

This work compares the presence of phospholipids in plasma samples after two different sample preparation techniques, protein precipitation and simultaneous protein precipitation and phospholipid removal using a new product, Phree.

Table I: Sample preparation protocols

Experimental Conditions

Plasma samples from the same lot were prepared (Table I) and were injected on a Kinetex® 2.6 µm C18 core–shell column coupled with an API 3000 MS (AB SCIEX) (Figure 1). A total phospholipid profile was monitored using m/z 184–184.

Figure 1: Total phospholipid profile.

Results and Discussion

When monitoring the total phospholipid profile, the protein precipitated plasma showed a large amount of phospholipids. In comparison, the plasma sample that was prepared using Phree showed virtually no phospholipids (Figure 1).

We also studied analyte response by comparing diclofenac spiked plasma samples. After sample preparation, 20 µL samples were injected on a Kinetex® 2.6 µm C18 core–shell column. The diclofenac signal in the protein precipitated samples was immediately lower than the signal in the Phree extracted samples. The signal in the protein precipitated sample rapidly decreases. The Phree extracted sample shows a steadier signal and is able to withstand > 250 injections (Figure 2). The higher signal strength of the Phree extracted sample is due to the reduction of phospholipid induced ion suppression. The significant reduction in phospholipid build up on the column and MS source also resulted in an increase in column lifetime and a decrease in the amount of MS maintenance required.

Figure 2: Column sensitivity after 250 injections.

Conclusion

By preparing samples with Phree, analysts can remove proteins and phospholipids in four short steps resulting in immediate improvements to their chromatography work.

For more information about Phree, visit www.phenomenex.com/Phree

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