Biomimetic piezoelectric quartz sensor for caffeine based on a molecularly imprinted polymer

被引:54
作者
Ebarvia, BS
Binag, CA
Sevilla, F [1 ]
机构
[1] Univ Santo Tomas, Natl Ctr Sci Res, Manila, Philippines
[2] Ind Technol Dev Inst, Dept Sci & Technol, Manila, Philippines
[3] Univ Santo Tomas, Manila PHilippines Res Ctr Nat Sci, Grad Sch, Manila, Philippines
关键词
molecularly imprinted polymer; piezoelectric quartz crystal; caffeine; surface characterization; chemical sensor; methacrylic acid;
D O I
10.1007/s00216-003-2433-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A piezoelectric quartz sensor coated with molecularly imprinted polymer (MIP) for caffeine was developed. The MIP was prepared by co-polymerizing methacrylic acid (MAA) and ethylene glycol dimethacrylate (EDMA) in the presence of azobis(isobutyronitrile) as initiator, caffeine as template molecule, and chloroform as solvent. The MIP suspension in polyvinyl chloride/tetrahydrofuran (6:2:1 w/w/v) solution was spin coated onto the surface of the electrode of a 10 MHz AT-cut quartz crystal. The sensor exhibited a linear relationship between the frequency shift and caffeine concentration in the range of 1x10(-7) mg mL(-1) up to 1x10(-3) mg mL(-1) [correlation coefficient (r)=0.9935] in a stopped flow measurement mode. It has a sensitivity of about 24 Hz/ln(concentration, mg mL(-1)). A steady-state response was achieved in less than 10 min. The performance characteristic of the sensor shows a promising and inexpensive alternative method of detecting caffeine. Surface studies were carried out for the reagent phase of the sensor using SEM, AFM, and XPS analysis in order to elucidate the imprinting of the caffeine molecule. The SEM micrograph, AFM image, and XPS spectra confirmed the removal of caffeine by Soxhlet extraction in the imprinting process and the rebinding of caffeine to the MIP sensing layer during measurement.
引用
收藏
页码:1331 / 1337
页数:7
相关论文
共 39 条
[1]   Separation of individual antiviral nucleotide prodrugs from synthetic mixtures using cross-reactivity of a molecularly imprinted stationary phase [J].
Allender, CJ ;
Brain, KR ;
Ballatore, C ;
Cahard, D ;
Siddiqui, A ;
McGuigan, C .
ANALYTICA CHIMICA ACTA, 2001, 435 (01) :107-113
[2]   A solid binding matrix/molecularly imprinted polymer-based sensor system for the determination of clenbuterol in bovine liver using differential-pulse voltammetry [J].
Andrea, P ;
Miroslav, S ;
Silvia, S ;
Stanislav, M .
SENSORS AND ACTUATORS B-CHEMICAL, 2001, 76 (1-3) :286-294
[3]   Molecular imprinting of cyclodextrin in water for the recognition of nanometer-scaled guests [J].
Asanuma, H ;
Akiyama, T ;
Kajiya, K ;
Hishiya, T ;
Komiyama, M .
ANALYTICA CHIMICA ACTA, 2001, 435 (01) :25-33
[4]   Chromatographic characterization of a molecular imprinted polymer binding cortisol [J].
Baggiani, C ;
Giraudi, G ;
Trotta, F ;
Giovannoli, C ;
Vanni, A .
TALANTA, 2000, 51 (01) :71-75
[5]  
Dela Cruz EO, 1999, ANAL LETT, V32, P841
[6]   Molecularly imprinted sensor layers for the detection of polycyclic aromatic hydrocarbons in water [J].
Dickert, FL ;
Tortschanoff, M ;
Bulst, WE ;
Fischerauer, G .
ANALYTICAL CHEMISTRY, 1999, 71 (20) :4559-4563
[7]   Molecular imprinting in chemical sensing - Detection of aromatic and halogenated hydrocarbons as well as polar solvent vapors [J].
Dickert, FL ;
Forth, P ;
Lieberzeit, P ;
Tortschanoff, M .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1998, 360 (7-8) :759-762
[8]   Molecular imprints as artificial antibodies - a new generation of chemical sensors [J].
Dickert, FL ;
Lieberzeit, P ;
Tortschanoff, M .
SENSORS AND ACTUATORS B-CHEMICAL, 2000, 65 (1-3) :186-189
[9]   Selective piezoelectric odor sensors using molecularly imprinted polymers [J].
Ji, HS ;
McNiven, S ;
Ikebukuro, K ;
Karube, I .
ANALYTICA CHIMICA ACTA, 1999, 390 (1-3) :93-100
[10]   Probing the molecular basis for ligand-selective recognition in molecularly imprinted polymers selective for the local anaesthetic bupivacaine [J].
Karlsson, JG ;
Andersson, LI ;
Nicholls, IA .
ANALYTICA CHIMICA ACTA, 2001, 435 (01) :57-64