کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1204918 | 965173 | 2010 | 8 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Retention of structurally diverse drugs in human serum albumin chromatography and its potential to simulate plasma protein binding Retention of structurally diverse drugs in human serum albumin chromatography and its potential to simulate plasma protein binding](/preview/png/1204918.png)
The retention behavior of 39 structurally diverse neutral, basic and acidic drugs was investigated on an HSA stationary phase using PBS buffer (pH 7.0) and acetonitrile or 2-propanol as organic modifiers. Extrapolated or directly measured log kw values as well as isocratic retention factors were correlated with plasma protein binding data taken from the literature. Retention factors determined in the presence of 10% acetonitrile led to high quality 1:1 correlation with apparent log KHSA values. The derived reference equation was successfully validated using a secondary set of 24 drugs. Further analysis of HSA retention into more fundamental properties revealed the involvement of anionic species in solute-stationary phase interactions, expressed by the negatively charged fraction, besides the partitioning mechanism which was reflected by lipophilicity. Protonation of basic drugs, although less important, may also influence retention, leading to reduced partitioning into the HSA surface as a net effect, while it seems to have no effect on HSA binding. The above results were further confirmed by linear solvation energy relationships (LSER).
Journal: Journal of Chromatography A - Volume 1217, Issue 37, 10 September 2010, Pages 5761–5768