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plasma protein binding

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

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I want to quantify the amount of unmetabolised drug after injecting into mice - unfortunately it would seem that most of the drug is binding to plasma proteins, therefore when I filter the sample the drug is lost along with the protein

is there a way to "unbind" my drug, e.g. changing pH? I'm going to try this but thought I should post on here first to see if anyone has any experience of this issue.

thanks in advance.

Is the mechanism of binding known – e.g. hydrogen bonding, charge (ion) attraction, hydrophobic interactions etc. ?
Is the drug ionizable at all and if so do you know the pKa?

Best Regards
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Dancho Dikov
2 posts Page 1 of 1

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