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Molecular imprinting - A way to prepare effective mimics of natural antibodies and enzymes
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Wulff G. Molecular imprinting - a way to prepare effective mimics of natural antibodies and enzymes. Stud. Surf. Sci. Catal. 141:2002;35-44.
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Wulff, G.1
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Molecular imprinting of synthetic network polymers: The de-novo synthesis of macromolecular binding and catalytic sites
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Shea K.J. Molecular imprinting of synthetic network polymers: the de-novo synthesis of macromolecular binding and catalytic sites. Trends Polym. Sci. 2:1994;166.
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Molecularly imprinted polymers for bioanalysis: Chromatography, binding assays and biomimetic sensors
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Ansell R.J., Kriz D., Mosbach K. Molecularly imprinted polymers for bioanalysis: chromatography, binding assays and biomimetic sensors. Curr. Opin. Biotechnol. 7:1996;89-94.
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Ansell, R.J.1
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0030922975
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Evaluation of binding and origins of specificity of 9-ethyladenine imprinted polymers
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Spivak D., Gilmore M.A., Shea K.J. Evaluation of binding and origins of specificity of 9-ethyladenine imprinted polymers. J. Am. Chem. Soc. 119:1997;4388-4393.
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Spivak, D.1
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Enzyme-like catalysis by molecularly imprinted polymers
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Wulff G. Enzyme-like catalysis by molecularly imprinted polymers. Chem. Rev. 102:2002;1-27.
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The application of molecular imprinting technology to solid phase extraction
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Lanza F., Sellergren B. The application of molecular imprinting technology to solid phase extraction. Chromatographia. 53:2001;599-611.
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Lanza, F.1
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0034807787
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Molecularly imprinted polymers: New tailor-made materials for selective solid-phase extraction
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Masque N., Marce R.M., Borrull F. Molecularly imprinted polymers: new tailor-made materials for selective solid-phase extraction. Trends Anal. Chem. 20:2001;477-486.
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Masque, N.1
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Molecularly imprinted polymers and their use in biomimetic sensors
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Haupt K., Mosbach K. Molecularly imprinted polymers and their use in biomimetic sensors. Chem. Rev. 100:2000;2495-2504.
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Haupt, K.1
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Kriz D., Ramstrom O., Mosbach K. Molecular imprinting - new possibilities for sensor technology. Anal. Chem. 69:1997;A345-A349.
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Kriz, D.1
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Design and properties of polymers as materials for fine chemistry
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Guyot A., Bartholin M. Design and properties of polymers as materials for fine chemistry. Prog. Polym. Sci. 8:1982;277-331.
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0033556047
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Combinatorial molecular imprinting: An approach to synthetic polymer receptors
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A proof-of-concept paper and the first example of a semi-automated combinatorial approach for synthesizing and analyzing a library of small-scale MIPs to determine the optimal MIP formulations for two triazine herbicides, ametryn and atrazine.
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Takeuchi T., Fukuma D., Matsui J. Combinatorial molecular imprinting: an approach to synthetic polymer receptors. Anal. Chem. 71:1999;285-290 A proof-of-concept paper and the first example of a semi-automated combinatorial approach for synthesizing and analyzing a library of small-scale MIPs to determine the optimal MIP formulations for two triazine herbicides, ametryn and atrazine.
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Takeuchi, T.1
Fukuma, D.2
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Combinatorial molecular imprinting for formation of atrazine decomposing polymers
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Takeuchi T., Fukuma D., Matsui J., Mukawa T. Combinatorial molecular imprinting for formation of atrazine decomposing polymers. Chem. Lett. 1:2001;530-531.
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Takeuchi, T.1
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Matsui, J.3
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0035097017
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Molecularly imprinted polymer library on a microtiter plate. High-throughput synthesis and assessment of cinchona alkaloid-imprinted polymers
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Takeuchi T., Seko A., Matsui J., Mukawa T. Molecularly imprinted polymer library on a microtiter plate. High-throughput synthesis and assessment of cinchona alkaloid-imprinted polymers. Instrum. Sci. Technol. 29:2001;1-9.
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Takeuchi, T.1
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0033152024
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Method for synthesis and screening of large groups of molecularly imprinted polymers
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••], a semi-automated approach was used to synthesize and analyze a library of 'mini-MIPs' to determine an optimal MIP formulation for a triazine herbicide, terbutylazine.
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••], a semi-automated approach was used to synthesize and analyze a library of 'mini-MIPs' to determine an optimal MIP formulation for a triazine herbicide, terbutylazine.
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Anal. Chem.
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Lanza, F.1
Sellergren, B.2
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16
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0035901845
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Development of a semiautomated procedure for the synthesis and evaluation of molecularly imprinted polymers applied to the search for functional monomers for phenytoin and nifedipine
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Lanza F., Hall A.J., Sellergren B., Bereczki A., Horvai G., Bayoudh S., Cormack P.A.G., Sherrington D.C. Development of a semiautomated procedure for the synthesis and evaluation of molecularly imprinted polymers applied to the search for functional monomers for phenytoin and nifedipine. Anal. Chim. Acta. 435:2001;91-106.
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Anal. Chim. Acta
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Lanza, F.1
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Bereczki, A.4
Horvai, G.5
Bayoudh, S.6
Cormack, P.A.G.7
Sherrington, D.C.8
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17
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0034663439
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Selective trace enrichment of chlorotriazine pesticides from natural waters and sediment samples using terbuthylazine molecularly imprinted polymers
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Ferrer I., Lanza F., Tolokan A., Horvath V., Sellergren B., Horvai G., Barcelo D. Selective trace enrichment of chlorotriazine pesticides from natural waters and sediment samples using terbuthylazine molecularly imprinted polymers. Anal. Chem. 72:2000;3934-3941.
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Ferrer, I.1
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Horvai, G.6
Barcelo, D.7
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18
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Selective solid phase extraction of a drug lead compound using molecularly imprinted polymers prepared by the target analogue approach
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Dirion B., Lanza F., Sellergren B., Chassaing C., Venn R., Berggren C. Selective solid phase extraction of a drug lead compound using molecularly imprinted polymers prepared by the target analogue approach. Chromatographia. 56:2002;237-241.
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Chromatographia
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Dirion, B.1
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19
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0034801534
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Target analogue imprinted polymers with affinity for folic acid and related compounds
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Quaglia M., Chenon K., Hall A.J., De Lorenzi E., Sellergren B. Target analogue imprinted polymers with affinity for folic acid and related compounds. J. Am. Chem. Soc. 123:2001;2146-2154.
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Quaglia, M.1
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Molecularly imprinted polymer for metsulfuron-methyl and its binding characteristics for sulfonylurea herbicides
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Zhu Q.Z., Haupt K., Knopp D., Niessner R. Molecularly imprinted polymer for metsulfuron-methyl and its binding characteristics for sulfonylurea herbicides. Anal. Chim. Acta. 468:2002;217-227.
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21
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0034771717
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'Bite-and-Switch' approach using computationally designed molecularly imprinted polymers for sensing of creatinine
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One of the first examples of the computational approach to 'rationally design' an imprinted polymer. A virtual library of functional and crosslinking monomers was designed and screened against the template, creatinine, using a molecular modeling software. This screening gave an optimized MIP composition. When this MIP was synthesized in the laboratory, it demonstrated superior selectivity in comparison to a MIP prepared using a more traditional functional monomer, MAA.
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Subrahmanyam S., Piletsky S.A., Piletska E.V., Chen B.N., Karim K., Turner A.P.F. 'Bite-and-Switch' approach using computationally designed molecularly imprinted polymers for sensing of creatinine. Biosens. Bioelectron. 16:2001;631-637 One of the first examples of the computational approach to 'rationally design' an imprinted polymer. A virtual library of functional and crosslinking monomers was designed and screened against the template, creatinine, using a molecular modeling software. This screening gave an optimized MIP composition. When this MIP was synthesized in the laboratory, it demonstrated superior selectivity in comparison to a MIP prepared using a more traditional functional monomer, MAA.
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(2001)
Biosens. Bioelectron.
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Subrahmanyam, S.1
Piletsky, S.A.2
Piletska, E.V.3
Chen, B.N.4
Karim, K.5
Turner, A.P.F.6
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22
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0034749511
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Recognition of ephedrine enantiomers by molecularly imprinted polymers designed using a computational approach
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Piletsky S.A., Karim K., Piletska E.V., Day C.J., Freebairn K.W., Legge C., Turner A.P.F. Recognition of ephedrine enantiomers by molecularly imprinted polymers designed using a computational approach. Analyst. 126:2001;1826-1830.
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Analyst
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Piletsky, S.A.1
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Day, C.J.4
Freebairn, K.W.5
Legge, C.6
Turner, A.P.F.7
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23
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0037086245
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Rational design of a polymer specific for microcystin-LR using a computational approach
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Using a computational approach, a highly selective MIP was 'rationally designed' for the cyanobacterial toxin microcystin-LR. A virtual library of functional and crosslinking monomers was designed and screened against the template using molecular modeling software. The optimal MIP formulation, synthesized in the laboratory, had an affinity and sensitivity comparable with those of polyclonal antibodies and superior chemical and thermal stabilities compared with those of biological antibodies.
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Chianella I., Lotierzo M., Piletsky S.A., Tothill I.E., Chen B.N., Karim K., Turner A.P.F. Rational design of a polymer specific for microcystin-LR using a computational approach. Anal. Chem. 74:2002;1288-1293 Using a computational approach, a highly selective MIP was 'rationally designed' for the cyanobacterial toxin microcystin-LR. A virtual library of functional and crosslinking monomers was designed and screened against the template using molecular modeling software. The optimal MIP formulation, synthesized in the laboratory, had an affinity and sensitivity comparable with those of polyclonal antibodies and superior chemical and thermal stabilities compared with those of biological antibodies.
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(2002)
Anal. Chem.
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Chianella, I.1
Lotierzo, M.2
Piletsky, S.A.3
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Chen, B.N.5
Karim, K.6
Turner, A.P.F.7
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24
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0037864006
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Synthesis and screening of a molecularly imprinted polymer library targeted for penicillin G
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A highly selective MIP for penicillin G was synthesized using a MIP formulation that was discovered by evaluating a library of large-scale MIPs. The optimized penicillin G-imprinted polymer was found to have some cross-reactivity with structurally similar antibiotics in radioligand binding assays. This work demonstrated the potential of MIPs as a crude preliminary screen for the rapid selection of ligands from a library of structurally related compounds.
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Cederfur J., Pei Y., Meng Z., Kempe M. Synthesis and screening of a molecularly imprinted polymer library targeted for penicillin G. J. Comb. Chem. 5:2003;67-72 A highly selective MIP for penicillin G was synthesized using a MIP formulation that was discovered by evaluating a library of large-scale MIPs. The optimized penicillin G-imprinted polymer was found to have some cross-reactivity with structurally similar antibiotics in radioligand binding assays. This work demonstrated the potential of MIPs as a crude preliminary screen for the rapid selection of ligands from a library of structurally related compounds.
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J. Comb. Chem.
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Cederfur, J.1
Pei, Y.2
Meng, Z.3
Kempe, M.4
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25
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0034716343
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Discrimination between enantiomers of structurally related molecules: Separation of benzodiazepines by molecularly imprinted polymers
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A receptors were synthesized by imprinting benzodiazepines. The stereochemistry and the amide nitrogen of the imprinted benzodiazepine were found to be the major determinants of molecular recognition at the MIP receptor site.
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A receptors were synthesized by imprinting benzodiazepines. The stereochemistry and the amide nitrogen of the imprinted benzodiazepine were found to be the major determinants of molecular recognition at the MIP receptor site.
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(2000)
J. Am. Chem. Soc.
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Hart, B.R.1
Rush, D.J.2
Shea, K.J.3
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26
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0000329874
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Screening of a combinatorial steroid library using molecularly imprinted polymers
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Ramstrom O., Ye L., Krook M., Mosbach K. Screening of a combinatorial steroid library using molecularly imprinted polymers. Anal. Commun. 35:1998;9-11.
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(1998)
Anal. Commun.
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Ramstrom, O.1
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Mosbach, K.4
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27
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0034961766
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Towards the development of molecularly imprinted artificial receptors for the screening of estrogenic chemicals
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Ye L., Yu Y.H., Mosbach K. Towards the development of molecularly imprinted artificial receptors for the screening of estrogenic chemicals. Analyst. 126:2001;760-765.
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(2001)
Analyst
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Ye, L.1
Yu, Y.H.2
Mosbach, K.3
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28
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0034604814
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Affinity screening by packed capillary high-performance liquid chromatography using molecular imprinted sorbents I. Demonstration of feasibility
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Vallano P.T., Remcho V.T. Affinity screening by packed capillary high-performance liquid chromatography using molecular imprinted sorbents I. Demonstration of feasibility. J. Chromatogr. A. 888:2000;23-34.
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(2000)
J. Chromatogr. A
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Vallano, P.T.1
Remcho, V.T.2
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29
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0035854380
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Affinity screening by packed capillary high performance liquid chromatography using molecular imprinted sorbents II. Covalent imprinted polymers
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Khasawneh M.A., Vallano P.T., Remcho V.T. Affinity screening by packed capillary high performance liquid chromatography using molecular imprinted sorbents II. Covalent imprinted polymers. J. Chromatogr. A. 922:2001;87-97.
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(2001)
J. Chromatogr. A
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Khasawneh, M.A.1
Vallano, P.T.2
Remcho, V.T.3
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