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Imprinted polymer modified electrodes

Suedee, R., Intakong, W. and Dickert, E.L. (2006) Molecularly imprinted polymer-modified electrode for on-line conductometric monitoring of haloacetic acids in chlorinated water. Anal Chim Acta, 569 (1-2), 66-75. [Pg.249]

Yeh, W.-M., and K.-C. Ho. 2005. Amperometric morphine sensing using a molecularly imprinted polymer-modified electrode. Anal Chim Acta 542 76. [Pg.1534]

Kang, J. Zhang, H. Wang, Z. Wu, G. Lu, X. (2009). A novel amperometric sensor for salicylic acid based on molecularly imprinted polymer-modified electrodes. Polymer - Plastics Technology and Engineering, 48,639-645. [Pg.207]

Blanco-Lopez, M. C., Lobo-Castandn, M. J., Miranda-Ordieres, A. J. and Tunon-Blanco, P. (2003) Voltammetric sensor for vaniUylmandelic acid based on molec-ularly imprinted polymer-modified electrodes . Biosensors and Bioelectronics, 18,353-362. [Pg.395]

Cervini, P. and E.T.G. Cavalheiro, Strategies for Preparation of Molecularly Imprinted Polymers Modified Electrodes and Their Application in Electroanalysis A Review. Anal. Lett, 2012. 45 p. 297-313. [Pg.191]

N. Kirsch, K.C. Honeychurch, J.P. Hart and M.J. Whitcombe, Voltammetric determination of urinary 1-hydroxypyrene using molecularly imprinted polymer-modified screen-printed carbon electrodes, Electroanalysis, 17 (2005) 571-578. [Pg.554]

Shoji, R., T. Takeuchi, and I. Kubo (2003). Atrazine sensor based on molecularly imprinted polymer-modified gold electrode. Anal. Chem., 75(18) 4882-4886. [Pg.271]

Sadeghi, S., Motaharian, A., and Moghaddam, A. Z. (2012). Electroanalytical determination of sulfasalazine in pharmaceutical and biological samples using molecularly imprinted polymer modified carbon paste electrode. Sens. Actuators B. 168, 336-344. [Pg.610]

Prasad, B, Madhuri, R., Tiwari, M. P., and Sharma, P. S. (2010). Layer-by-layer assembled molecularly imprinted polymer modified silver electrode for enantioselective detection of d- and 1-thyroxine, Anal. Chim. Acta. 681,16-26. [Pg.613]

Patel, A.K. Sharma, P.S. Prasad, B.B. Development of a creatinine sensor based on a molecularly imprinted polymer-modified sol-gel film on graphite electrode. Electroanalysis 2008, 20 (19), 2102 2112. [Pg.528]

Del Moral, P. Diez, M.T. Resines, J.A. Bravo, I.G. An n, M.J. Simultaneous measurements of creatinine and purine derivatives in ruminant s urine using ion-pair HPLC. J. Liq. Chromatogr. Rel. Technol. 2003, 26 (17), 2961 2968. Patel, A.K. Sharma, P.S. Prasad, B.B. Development of a creatinine sensor based on a molecularly imprinted polymer-modified sol-gel film on graphite electrode. Electroanalysis 2008, 20 (19), 2102-2112. [Pg.529]

Chen, Z., Tang, C., Zeng, Y, Liu, H., Yin, Z., and Li, L. (2014) Determination of bisphenol A using an electrochemical sensor based on a molecularly imprinted polymer-modified mul-tiwalled carbon nanotube paste electrode. Anal. Lett, 47, 996-1014. [Pg.419]

Table 12, Some examples of application of intrinsically conducting polymer modified electrodes for the development of molecularly imprinted polymers... Table 12, Some examples of application of intrinsically conducting polymer modified electrodes for the development of molecularly imprinted polymers...
Prasad, B.B. Srivastava, S. Tiwari, K. Sharma, P.S. (2009). Development of uracil and 5-fluorouracil sensors based on molecularly imprinted polymer-modified hanging mercury drop electrode. Sensors and Materials, 21, 291-306. [Pg.211]

H.T. Wang, H.M. Zhao, X. Quan and S. Chen, Electrochemical determination of tetracy-chne using molecularly imprinted polymer modified carbon nanotube-gold nanoparticles electrode. Electroanalysis, 23 (8) 1863-1869, 2011. [Pg.322]

B.B. Prasad, S. Srivastava, K. Tiwari and PS. Sharma, Ascorbic acid sensor based on molecularly imprinted polymer-modified hanging mercury drop electrode. Mat. Scl Eng. C-Bio. S., 29 (4) 1082-1087,2009. [Pg.324]

Electrochemical sensors using surfaces modified with imprinted polymers are finding increasing use in analytical chemistry [46]. Electrode surfaces can be modified in a similar way to the crystal surface of a QCM. The application of imprinted polymer particles as an ink to the surface of an electrode is a convenient way of preparing an imprinted surface and can provide a cheap and relatively simple route to prepare a sensing device. Imprinted electrode surfaces have also been prepared... [Pg.263]

Prasad, B.B. Madhuri, R. Tiwari, M.P. Sharma, P.S. (2010c). Electrochemical sensor for folic acid based on a hyperbranched molecularly imprinted polymer-immobilized sol-gel-modified pencil graphite electrode. Sensors and Actuators, B Chemical, 146, 321-330. [Pg.211]

Blanco-Lopez, M. C., S. Gutierrez-Fernandez, M. J. Lobo-Castanon, A. J. Miranda-Ordieres, and P. Tunon-Blanco, 2004. Electrochemical sensing with electrodes modified with molecularly imprinted polymer films. Anal Bioanal Chem 378 1922-28. [Pg.301]

MIP-based tramadol sensing devices include the highly selective MWCNTs carbon paste electrode modified with molecularly imprinted polymers with differential pulse voltammetric detection. The device had a linear response range of 10 to 10" M [350]. The other report was on an MIP-electrochemical sensor prepared by coating SiO, Fe O, as the core and the supporting material, with an MIP based on ethyleneglycol dimethacrylate as the crosslinker and functional monomers. The MIP-modified particles prepared this way were eventually incorporated into the modified carbon paste electrode, which was used for cyclicvoltammetry of the analyte within a linear range of 0.01-20 pmolL-i [366]. [Pg.296]

An (-)-Ephedrine voltammetric sensor prepared through the immobilization of an MIP imprinted polymer for ephedrine in the range of 0.5-3 mM [426], and the MIP-coated gold electrode modified by chitosan-platinum nanoparticles (CS-PtNPs) and graphene-gold nanoparticles (GR-AuNPs) nanocomposites for the determination of erythromycin are other examples of the application of MIPs for the analysis of pharmaceutical species. The latter report used erythromycin as template and 2-mercapto-nicotinic acid functional monomers and yielded a linear response in the range of 7.0 x 10 -9.0 X 10 M and a detection limit of 2.3 x 10 M [378]. [Pg.298]


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