Evaluation of a Resorcinarene-Based Sorbent as a Solid-Phase Extraction Material for the Enrichment of L-Carnitine from Aqueous Solutions

Abstract

We present five new sorbents for the evaluation of the pre-concentration of L-carnitine. The sorbents were obtained from copolymerization between butylmethacrylate (BuMA) and ethylene dimethacrylate (EDMA), which were physically modified on their surface by each one of the five synthetized resorcinarenes of variable chain length studied, with long-chain resorcinarenes exhibiting better fixation on the copolymer. The characterization of the synthesized resorcinarenes was done using FTIR-ATR, 1H NMR, 13C NMR, and mass spectrometry, while characterization of the sorbents was done using FTIR-ATR and scanning electron micrography (SEM). The molecular interaction between L-carnitine and the synthesized resorcinarenes was studied in DMSO via 1H-NMR spectroscopy and, in the gas phase, via electrospray ionization-mass spectrometry (ESI-MS). The results showed that the short-chain resorcinarenes underwent a stable interaction with the neurotransmitter. Once the sorption of resorcinarenes on the copolymer was accomplished, the best parameters for the evaluation of the L-carnitine preconcentration were established. The solution tests were carried out through LC/MS analysis, obtaining better results for L-carnitine absorption with the short-chain resorcinarenes such as tetra(ethyl)calix[4]resorcinarene and tetra(propyl)calix[4]resorcinarene.