variation in response of the analyte and internal standard [Bioanalytics]

posted by haydonat – Turkey, 2011-01-15 16:16 (5640 d 08:14 ago) – Posting: # 6420
Views: 5,627

Dear Helmut,

Thanks for replying me :-)

I don't have any problem about getting the extracts into solution, I use diethylether:n-hexane (7:3) mixture during extraction, after evaporation step of my procedure; reconstitution was done mobile phase before but result were not satisfying so water+25mM ammonia+ACN (50:50), pH: 9.9 mixture is begin to use.

Also; validation was completed and this problem is occured in study so, I cannot change any of my conditions/solutions/pH.

By the way; I think this problem leads to ionization problem. What can you think about changing desolvation temperature and desolvation gas flow? And if I change desolvation temperature and/or desolvation gas flow, do I have to perform whole validation once more?


Edit: Full quote removed. Please delete anything from the text of the original poster which is not necessary in understanding your answer; see also this post! [Helmut]

Complete thread:

UA Flag
Activity
 Admin contact
23,655 posts in 4,993 threads, 1,571 registered users;
143 visitors (0 registered, 143 guests [including 22 identified bots]).
Forum time: 01:30 CEST (Europe/Vienna)

The great tragedy of Science – the slaying
of a beautiful hypothesis by an ugly fact.    Thomas Henry Huxley

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5