Dear Imh, thank you for your reply.
Nitrogen generators provide a very low quality of nitrogen compared to what comes out of a cylinder. It's not suitable as a collision gas. Nitrogen generator gas should only be used as a drying gas/nebulising gas in the ion source, and nothing much else.
In the instrument we have there is one inlet called "Curtain gas", and from this inlet nitrogen is fed into ESI source as a curtain and into CID chamber as well. Our service engineer advised us to buy such N2 generator as this one: model NM40Z, Peak Scientific, and in specifications of this generator it is written: "The NM40Z is a specifically configured Nitrogen Generator designed to operate multiple Applied Biosystems/ MDS SCIEX LC/MS/MS instruments, producing the required flow rates, purities and pressures for curtain, source and exhaust gas with one generator." So as far as I understand it should be suitable... However, the purity of nitrogen is not indicated... I should think about it more.
If you have varying peak areas in MS, there are many possible reasons, many of which may be nothing to do with your instrument, but have more to do with the sample. For instance the ion source may be becoming dirty with time, or there may be components of your mixture that coelute with the analyte of interest and change its ionisation efficiency.
The problem is that we have varying peak areas not only for our samples, but also for our calibration points which are injected from the same vials.
The angle of calibration curve changes in time. It can move up and then down and then again up... And if we inject the same standard sample in ACN from the same vial for few hours, the signal drifts as well... Our column is rather new and it shouldn't be a problem such as washing of any impurities from column.
You can keep the instrument cleaner by doing some sample clean-up before injecting, and by diverting sample to waste (if you have an appropriate valve) for the first minute or two of a run, and for the end of gradient runs where you are washing the "dirt" off the column. If you have a coeluting cosuppressor, unfortunately there may be little you can do, except use a proper internal standard to compensate.
But of course you are right to try to exclude instrument problems.
Good luck!
Yes, we didn't try diverting sample to waste yet, and we should do it. As for the internal sample - we have performed some experiments, and normalization to IS peak area didn't help to eliminate the problem of signal instability completely (however, it helps to some extent).
Thank you again for your help.
Elena