SYNTHESIS OF TETRACYCLINE IMPRINTED POLYMERS WITH METHACRYLIC ACID AS FUNCTIONAL MONOMER IN METHANOL-CHLOROFORM MIXTURE USING BULK AND PRECIPITATION POLYMERIZATION METHOD

Shendi Suryana, Kharisma Devy Shabrina, Dang Soni

Abstract


The content of tetracycline residues in poultry meat products can cause antibiotic resistance in humans who consume these products, so it is necessary to develop sensitive analytical techniques to determine the levels of tetracycline residues to assess the safety of these products for consumption. The molecular imprinting technique is a method to produce sorbents with molecular recognition capability of target compounds that can be used to increase the selectivity of solid phase extraction to extract tetracycline residues for further analysis. This study aimed to obtain a sorbent synthesized by molecular imprinting technique to analyze tetracycline in poultry meat products. The stages of the research began with the study of the interaction of functional monomers with template molecules, determining the association constants of functional monomers with template molecules, synthesis of imprinted polymer molecules using bulk and precipitation methods, evaluating the ability and adsorption capacity of the synthesized polymers, assess the selectivity of polymers for analog structures and physical characteristics with FTIR. The research showed that methacrylic acid was the best functional monomer with a binding energy value of -27.3776 kcal/mol. The higher adsorption capacity was achieved by Molecularly Imprinted Polymer (MIP) that was synthesized by precipitation method (MIP2) than the other MIP synthesized by bulk polymerization (MIP1) with a value of 0.8748 mg/g and 0.4077 mg/g, respectively. The analogous compounds' imprinting factor values for each MIP were 1.197 and 1.1272. The polymer synthesized by molecular imprinting technique is selective for extracting and analyzing tetracycline from poultry meat matrix.


Keywords


adsorption capacity, molecular imprinting, tetracycline

Full Text:

DOWNLOAD (PDF)

References


Etikaningrum E, Iwantoro S. Study of antibiotics residue on poultry produscts in Indonesia. J Ilmu Produksi dan Teknol Has Peternak. 2017;5(1):29–33.

Nofita N, Rinawati R, Qudus HI. Validasi metode matrix solid phase dispersion (mspd) spektrofotometri uv untuk analisis residu tetrasiklin dalam daging ayam pedaging. J Kesehat. 2016;7(1):136.

Boes E, Kantasubrata J, Karossi A. Penggunaan ekstraksi fasa padat untuk analisis tetrasiklin dalam contoh udang. J Kim Terap Indones. 1993;3(2):74–8.

Fernanda MAHF, Chrisnandari RD. Kajian residu tetrasiklin HCl dalam daging dan hati ayam broiler pada beberapa peternakan di Kabupaten Lamongan menggunakan metode spektrofotometri ultraviolet. J Pharm Sci. 2021;6(1):47–52.

Hasanah AN, Kartasasmita RE, Ibrahim S. Sintesis sorbent ekstraksi fase padat dengan teknik molecular imprinting dengan monomer akrilamid untuk ekstraksi glibenklamid dari serum darah. J Farm Indones. 2015;7(4):233–41.

Kulsum INS, Suryana S, Soni D. Review: moleculary imprinted polymer solid phase extraction (mip-spe) untuk pengujian glibenklamid dalam cairan biologis. J Sains dan Kesehat. 2022;4(2):205–13.

Jupri R, Fauziah S, Taba P. Sintesis dan karakterisasi molecularly imprinted polymers menggunakan metil metakrilat dan etilen glikol dimetakrilat sebagai adsorben di-(2-etilheksil) ftalat. Indones J Pure Appl Chem. 2022;5(3):85–95.

Abdurrahman F, Tahir I, Pradipta MF. Pemodelan dan simulasi untuk rancangan polimer tercetak molekul brazilein dengan asam metakrilat sebagai monomer fungsional. J Math Nat Sci. 2018;25(3):224–32.

Nurhamidah N, Marinda P, Koryanti E. Pembuatan molecularly imprinted polymer (mip) melamin menggunakan metode cooling-heating. In: Prosiding Seminar Nasional Fisika (E-Journal) SNF2017. Jakarta: Fakultas MIPA, Universitas Negeri Jakarta; 2017. p. 45–50.

Soni D, Hasanah AN, Mutakin. Pemilihan monomer fungsional pada molecularly imprinted polymer ( MIP ) diazepam dengan teknik komputasi. J Ilm Farm Bahari. 2018;9(2):1–15.

Hammam MA, Abdel-Halim M, Madbouly A, Wagdy HA, El Nashar RM. Computational design of molecularly imprinted polymer for solid phase extraction of moxifloxacin hydrochloride from Avalox® tablets and spiked human urine samples. Microchem J. 2019;148:51–6.

Yang K, Wang GN, Liu HZ, Liu J, Wang JP. Preparation of dual-template molecularly imprinted polymer coated stir bar based on computational simulation for detection of fluoroquinolones in meat. J Chromatogr B Anal Technol Biomed Life Sci. 2017;1046:65–72.

Gilormini P, Verdu J. On the role of hydrogen bonding on water absorption in polymers. Polymer (Guildf). 2018;142:164–9.

Suryana S, Mutakin M, Rosandi Y, Hasanah AN. Rational design of salmeterol xinafoate imprinted polymer through computational method: functional monomer and crosslinker selection. Polym Adv Technol. 2022;33(1):221–34.

Zhang Y, Qu X, Wang FF, Wu G, Li J, Hong H, et al. Effect of the solvent on improving the recognition properties of surface molecularly imprinted polymers for precise separation of erythromycin. RSC Adv. 2015;5(102):83619–27.

Hasanah AN, Suherman M, Susanti I, Pitaloka I, Mustarichie R. Performance evaluation of atenolol molecular imprinted polymer using two different polymerization and two different porogen. Rasayan J Chem. 2019;12(3):1269–78.

Hasanah AN, Suryana S, Mutakin, Rahayu D. Evaluation performance of molecularly imprinted polymer prepared by two different polymerization method for atenolol recognition in human plasma. Asian J Chem. 2017;29(11):2429–33.

Pardeshi S, Singh SK. Precipitation polymerization: a versatile tool for preparing molecularly imprinted polymer beads for chromatography applications. RSC Adv. 2016;6(28):23525–36.

Adauto A, Khan S, Augusto da Silva M, Gomes Neto JA, Picasso G, Sotomayor M del PT. Synthesis, characterization and application of a novel ion hybrid imprinted polymer to adsorb Cd(II) in different samples. Environ Res. 2020;187:109669.

Fauziah S, Taba P, Amran B, Budi P, Hariani N. Synthesis, characterization, and optimization of sitosterol imprinted polymers using tfmaa as functional monomer. Int J Appl Chem. 2015;11(4):487–95.




DOI: http://dx.doi.org/10.52434/jifb.v15i1.2790

Refbacks

  • There are currently no refbacks.


Creative Commons License
This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International License.

Visitor :

Web Analytics