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- Posts: 7
- Joined: Wed Aug 24, 2011 11:50 pm
What I am anticipating happening from time to time is that I will inject my system suit, then my samples in duplicate, and they will fail. This would need either more of the insecticide intermediate in the batch (if samples fail low), or more of the batch made, minus the intermediate (if samples fail high) and add this mixture to the batch. What I want to aviod is injecting another system suit, which will take an hour or so if I can simply pause the sequence and wait for the adjusted batch sample to inject.
On a side note, would there be any GLP/GMP problem with this? I worked in a pharma lab before, and the LCs would have a problem finding the next vial in a sequence, but the system could simply be resumed from where it left off if the mobile phase ran continuously, so I am assuming the same would work for GC. (Let me know if this is not the case).
Additional side note: I am just finishing writing this method (first time ive done this from scratch), and my system suit will include two test injections to equilibrate, a diluent blank, and a CCV injection. The samples will be injected in duplicate, and bracketed with another CCV. There is no extraction or filter process, so I am not including a surrogate or internal standard, and the samples will be quantitated using a 5 point initial calibration curve. This sound good enough?
Thanks
Sam