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- Posts: 292
- Joined: Wed Jan 19, 2005 2:20 pm
I''ve been given a task of analysing lecithin samples by HPLC.
I was given this paper as a starting point: http://www.springerlink.com/content/x68h782u17148p38/
Essentially it is normal phase with a quite old (and obscure column - porasil) - I'm aiming to just subsitute this column with a modern equivalent - Luna bare Silica (2) - will this perform ok do people think? Will I still need water in the mobile phase as per the method in the journal?
I'm not concerened about separating out the individual lecithin components by rather just assessing for "total lecithin" content in some API samples. Not sure what levles will be present, but lets say as an estimate I need to get to be able to see 1% w/w - so need a relatively low LoQ.
I'm also goint to try and keep it simple with respect to dteectors - i.e. UV down at 210 nm - so we can easily transfer it for routine analysis by chemists.