In-tube molecularly imprinted polymer solid-phase microextraction for the selective determination of propranolol

被引:213
作者
Mullett, WM [1 ]
Martin, P [1 ]
Pawliszyn, J [1 ]
机构
[1] Univ Waterloo, Dept Chem, Waterloo, ON N2L 3G1, Canada
关键词
D O I
10.1021/ac0100502
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A molecularly imprinted polymer (MIP) material was synthesized for use as an in-tube solid-phase microextraction (SPME) adsorbent. The inherent selectivity and chemical and physical robustness of the MIP material was demonstrated as an effective stationary-phase material for in-tube SPME. An automated and on-line MIP SPME extraction method nas developed for propranolol determination in biological fluids. This simplified the sample preparation process and the chromatographic separation of several P-blocker compounds. The method developed for propranolol showed improved selectivity in comparison to alternative in-tube stationary-phase materials, overcoming the limitations of existing SPME coating materials. Preconcentration of the sample by the MIP adsorbent increased the sensitivity, yielding a limit of detection of 0.32 mug/mL by UV detection. Excellent method reproducibility (RSD < 5.0%) and column reusability(> 500 injections) were observed over a fairly wide linear dynamic range (0.5-100 mug/mL) in serum samples. To our knowledge, this is the first report on the automated application of a MIP material for in-tube SPME. The method was inexpensive, simple to set up, and simplified the choice of SPME adsorbent for in-tube extraction. The approach can potentially be extended to other MIPs for the determination of a wide range of chemically significant analytes.
引用
收藏
页码:2383 / 2389
页数:7
相关论文
共 33 条
[1]   Molecular imprinting for drug bioanalysis - A review on the application of imprinted polymers to solid-phase extraction and binding assay [J].
Andersson, LI .
JOURNAL OF CHROMATOGRAPHY B, 2000, 739 (01) :163-173
[2]   Application of molecular imprinting to the development of aqueous buffer and organic solvent based radioligand binding assays for (S)-propranolol [J].
Andersson, LI .
ANALYTICAL CHEMISTRY, 1996, 68 (01) :111-117
[3]  
EISERT R, 1998, J ANAL CHEM+, V69, P3140
[4]   Tailor-made materials for tailor-made applications: application of molecular imprints in chemical analysis [J].
Ensing, K ;
de Boer, T .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1999, 18 (03) :138-145
[5]   Development of new SPME fibers by sol-gel technology for SPME-HPLC determination of organometals [J].
Gbatu, TP ;
Sutton, KL ;
Caruso, JA .
ANALYTICA CHIMICA ACTA, 1999, 402 (1-2) :67-79
[6]   Theory of analyte extraction by selected porous polymer SPME fibres [J].
Górecki, T ;
Yu, XM ;
Pawliszyn, J .
ANALYST, 1999, 124 (05) :643-649
[7]  
HAGINAKA J, IN PRESS ANAL CHEM
[8]   Automated in tube solid-phase microextraction coupled with liquid chromatography/electrospray ionization mass spectrometry for the determination of β-blockers and metabolites in urine and serum samples [J].
Kataoka', H ;
Narimatsu, S ;
Lord, HL ;
Pawliszyn, J .
ANALYTICAL CHEMISTRY, 1999, 71 (19) :4237-4244
[9]   Determination of carphedon in human urine by solid-phase microextraction using capillary gas chromatography with nitrogen-phosphorus detection [J].
Kim, S ;
Park, JH ;
Myung, SW ;
Lho, DS .
ANALYST, 1999, 124 (11) :1559-1562
[10]   Solid-phase microextraction/capillary gas chromatography for the profiling of confiscated ecstacy and amphetamine [J].
Kongshaug, KE ;
Pedersen-Bjergaard, S ;
Rasmussen, KE ;
Krogh, M .
CHROMATOGRAPHIA, 1999, 50 (3-4) :247-252