@article {GE2025465830,
	title = {Green synthesis of magnetic aromatic polyamide composites via mechanochemical ball milling with a deep eutectic system for the magnetic solid-phase extraction of antibiotics from water},
	journal = {Journal of Chromatography A},
	volume = {1747},
	year = {2025},
	pages = {465830},
	abstract = {<p>Magnetic aromatic polyamide (MAPA) composites were synthesized using a green mechanochemical ball milling process and used for magnetic solid-phase extraction (MSPE) and detection of trace level fluoroquinolone antibiotics (FQs) from water samples. The formation of MAPAs was facilitated by deep eutectic systems (DESys) created from magnetic beads and organic monomers during ball milling. A comprehensive study was conducted to investigate the kinetics, thermodynamics, and mechanisms of MAPA adsorption of ciprofloxacin hydrochloride (CIP) and ofloxacin (OFL) from water. The maximum adsorption capacities for CIP and OFL were found to be 151.5 mg/g and 164.1 mg/g, respectively. Additionally, the recyclability and selective adsorption capabilities of MAPAs were evaluated. MAPAs were subsequently used for MSPE of CIP and OFL in water samples. Both UV\&ndash;Vis spectrometry and HPLC methods can be used for analysis, the MSPE-HPLC method showed superior linearity for CIP (0.06\&ndash;1500 μg/L) and OFL (1\&ndash;1200 μg/L), with R\&sup2; values of 0.9995 and 0.9999, and limit of detection (LOD) as low as 0.006 μg/L and 0.02 μg/L, respectively. Both analytical methods are highly effective and practical for use with real water samples. MAPA used for MSPE offer a promising green approach for detecting antibiotic contamination in aquatic ecosystems.</p>},
	keywords = {antibiotics, Deep eutectic solvent, Deep eutectic system, Magnetic aromatic polyamide composites, Magnetic solid phase extraction, Mechanochemical method},
	issn = {0021-9673},
	doi = {https://doi.org/10.1016/j.chroma.2025.465830},
	url = {https://www.sciencedirect.com/science/article/pii/S0021967325001785},
	author = {Wuxia Ge and Yumei Chen and Xinru Ding and Wentao Bi and David D. Y. Chen}
}
@article {2493,
	title = {Total Synthesis and Stereochemical Assignment of Micrococcin P1},
	journal = {Angewandte Chemie-International Edition},
	volume = {48},
	number = {23},
	year = {2009},
	note = {ISI Document Delivery No.: 452GHTimes Cited: 11Cited Reference Count: 41Lefranc, David Ciufolini, Marco A.},
	pages = {4198-4201},
	type = {Article},
	keywords = {ACID, antibiotics, CHEMISTRY, DOMAIN, FRAGMENT A-C, GE2270-A, HETEROCYCLES, MICROCOCCIN P1, P-1, PROTEIN-SYNTHESIS, THIOPEPTIDE ANTIBIOTICS, thiopeptides, THIOSTREPTON},
	isbn = {1433-7851},
	url = {<Go to ISI>://000266527800024},
	author = {Lefranc, D. and Ciufolini,Marco A.}
}
@article {3357,
	title = {CHARACTERIZATION OF AN OLIGONUCLEOTIDE-BINDING FLUORESCENT LIGAND FOR APPLICATION IN AFFINITY PURIFICATION OF DSDNA},
	journal = {Biotechnology and Bioengineering},
	volume = {48},
	number = {1},
	year = {1995},
	note = {ISI Document Delivery No.: RU627Times Cited: 1Cited Reference Count: 39},
	month = {Oct},
	pages = {25-35},
	type = {Article},
	abstract = {The fluorescent probe PO-PRO-3 was investigated as a potential ligand for the affinity immobilization and purification of genomic or plasmid DNA fragments. Affinities and mechanisms for PO-PRO-3 binding to superhelical and linearized pUC 18 plasmid DNA were examined through measurement of binding isotherms, continuous-variation analysis, and DNA titrations. In addition, the effects of DNA conformation, protein and RNA contaminants, solvent polarity, and ionic strength are examined with the aim of optimizing binding and elution conditions and of assigning limits to the range of applicability of the affinity purification. (C) 1995 John Wiley \& Sons, Inc.},
	keywords = {ANTHRACYCLINE, antibiotics, BIO-POLYMERS, DNA AMPLIFICATION, DNA PURIFICATION, DNA-BINDING FLUOROPHORE, DYES, FLUORESCENT LIGAND, POLYMERASE CHAIN-REACTION, SENSITIVITY},
	isbn = {0006-3592},
	url = {<Go to ISI>://A1995RU62700004},
	author = {Haynes, C. A. and Sherwood, C. S. and Turner, R. F. B.}
}
