Synthesis and properties of molecular imprints of darifenacin: The potential of molecular imprinting for bioanalysis

被引:56
作者
Venn, RF [1 ]
Goody, RJ [1 ]
机构
[1] Pfizer Ltd, Cent Res, Dept Drug Metab, Sandwich CT13 9NJ, Kent, England
关键词
column liquid chromatography; solid-phase extraction; molecular imprinting; bioanalysis;
D O I
10.1007/BF02490734
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A molecularly imprinted polymer has been developed which subsequently demonstrated an ability to selectively retain darifenacin (UK-88,525-S) from aqueous acetonitrile when used as a stationary phase in HPLC columns and as a packing in solid-phase extraction cartridges. The imprinted polymer is applicable to a wide range of analytical methods including extraction from plasma, purification of radiolabelled UK-88,525, chiral separations and separation of metabolites and structural analogues. The polymer is able to extract darifenacin directly from a protein-precipitated human plasma/acetonitrile (1:1 v/v) mixture with 100 % recovery. The imprinted polymer can also effect a repurification of C-14-labelled darifenacin. The drawbacks of molecular imprints for ultra-trace bioanalysis (in the sub-nanogram/mL range) are discussed. These centre on the difficulty of removing all the template from the polymer and the consequent effects of template bleed on assay precision and accuracy when used as solid-phase extraction cartridges. Possible solutions to this problem are considered.
引用
收藏
页码:407 / 414
页数:8
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