Synthesis of ciprofloxacin imprinted polymer by using precipitation polymerization technique

Authors

  • Vuong Bui Nhat Thao
  • Dong Thi Anh Ngoc
  • Do Minh Huy
  • Thach Ut Dong

Abstract

Ciprofloxacin imprinted polymers have garnered significant attention due to the high demand for application in the monitoring of antibiotics. This study focuses on the synthesis and selective adsorption properties of ciprofloxacin imprinted polymers. The polymers were synthesized via precipitation polymerization technique. Optimal condition was achieved using acetonitrile:water (8:2, v/v) and a molar ratio of ciprofloxacin:acid methacrylic:ethylene glycol dimethacrylate of 1:6:30. Physicochemical characterization utilizing FT-IR, TGA-DSC, SEM, and N2 adsorption isotherm confirmed the desired properties of the polymer. Adsorption properties (kinetic, pH, and isotherm) indicated selective adsorption of ciprofloxacin onto the imprinted polymer with an imprinting factor of 1.34 and adsorption capacity up to 11.6 mg g-1. These findings underscore the potential of the ciprofloxacin imprinted polymer as a stationary phase for solid-phase extraction columns.

Downloads

Download data is not yet available.

References

E. Turiel, A. Martin-Esteban, J.L. Tadeo, J Chromatogr A 1172 (2007) 97. https://doi.org/10.1016/j.chroma.2007.10.003

G.N. Wang, K. Yang, H.Z. Liu, M.X. Feng, J.P. Wang, Anal Methods 8 (2016) 5511. https://doi.org/10.1039/c6ay00810k

R. Mirzajani, F. Kardani, J Pharm Biomed Anal 122 (2016) 98. https://doi.org/10.1016/j.jpba.2016.01.046

H.S. Andersson, J.G. Karlsson, S.A. Piletsky, A.-C. Koch-Schmidt, K. Mosbach, I.A. Nicholls, J Chromatogr A 848 (1999) 39. https://doi.org/10.1016/S0021-9673(99)00483-5

A. Speltini, A. Scalabrini, F. Maraschi, M. Sturini, A. Profumo, Anal Chim Acta 974 (2017) 1. https://doi.org/10.1016/j.aca.2017.04.042

L. Chen, X. Wang, W. Lu, X. Wu, J. Li, Chem Soc Rev 45 (2016) 2137. https://doi.org/10.1039/c6cs00061d

F. Tan, D. Sun, J. Gao, Q. Zhao, X. Wang, F. Teng, X. Quan, J. Chen, J Hazard Mater 244-245 (2013) 750. https://doi.org/10.1016/j.jhazmat.2012.11.003

A. Sarafraz-Yazdi, N. Razavi, TrAC, Trends Anal Chem 73 (2015) 81. https://doi.org/10.1016/j.trac.2015.05.004

L. Chen, B. Li, Food Chem 141 (2013) 23. https://doi.org/10.1016/j.foodchem.2013.02.085

C. Schirmer, H. Meisel, J Chromatogr A 1132 (2006) 325. https://doi.org/10.1016/j.chroma.2006.09.032

T. Wang, J. Tong, M. Sun, L. Chen, J Sep Sci 34 (2011) 1886. https://doi.org/10.1002/jssc.201100046

C. Schirmer, H. Meisel, Anal Bioanal Chem 392 (2008) 223. https://doi.org/10.1007/s00216-008-2269-4

M.L. Mena, L. Agui, P. Martinez-Ruiz, P. Yanez-Sedeno, A.J. Reviejo, J.M. Pingarron, Anal Bioanal Chem 376 (2003) 18. https://doi.org/10.1007/s00216-003-1846-9

A. Prieto, S. Schrader, C. Bauer, M. Moder, Anal Chim Acta 685 (2011) 146. https://doi.org/10.1016/j.aca.2010.11.038

U.D. Thach, H.H. Nguyen Thi, T.D. Pham, H.D. Mai, T.T. Nhu-Trang, Polymers 13 (2021). https://doi.org/10.3390/polym13162788

H.T. Nguyen, N.T. Vuong Bui, W.G. Kanhounnon, K.L. Vu Huynh, T.V. Nguyen, H.M. Nguyen, M.H. Do, M. Badawi, U.D. Thach, RSC Adv 11 (2021) 34281. https://doi.org/10.1039/d1ra05505d

B. Tegegne, L. Chimuka, B.S. Chandravanshi, F. Zewge, Sep Sci Technol 56 (2020) 2217. https://doi.org/10.1080/01496395.2020.1819323

Downloads

Published

30-03-2024