-
- Posts: 49
- Joined: Wed Feb 08, 2006 2:58 pm
We must analise a corticosteroid ointment by HPLC-UV. Chromatographic separation is fantastic, but we have suffering a lot on improving the corticosteroid exctration from the ointment. During extration we have utilized the pair iso-Octane and aqueous phosphate buffer / MeOH solution. In true, the mixture aqueous phosphate buffer and MeOH is our mobile phase. All % recovery results were very bad: 97; 93; 89; 96; 95!
So, please, could you share with us your experience?
See, our Ointment Solubilities:
- Water: very low
- Phosphate buffer/MeOH: low
- MeOH: low
- DMF: low
- iso-Octane: moderate
- Hexane: moderate
- DMSO: moderate
See, our recent sample test preparation process
- Add the sample (1g) to a becker containing hot mobile phase: ointment melts in few minutes
- Transfer the mixture to a separator containing ico-Octane
- Extraction recovering the mobile phase
- Clean twice the ico-Octane
Any experience will be welcomed, considere that we are "in a jungle with a good rifle but with one unique bullet, and the fierce wolf comes toward us very angry".
Thank you so much,
Carlos de Souza Teixeira
teixeiracs@yahoo.com
