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Sonochemical degradation of antibiotics from representative classes-Considerations on structural effects, initial transformation products, antimicrobial activity and matrix

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Google Scholar Scholar | Altres documents de l'autor: Serna-Galvis, Efraim A.; Montoya-Rodríguez, Diana; Isaza-Pineda, Laura; Ibáñez Martínez, María; Hernández Hernández, Félix; Moncayo-Lasso, Alejandro; Torres Palma, R.Microsoft Academico
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comunitat-uji-handle:10234/9

comunitat-uji-handle2:10234/7013

comunitat-uji-handle3:10234/8638

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Metadades

Títol
Sonochemical degradation of antibiotics from representative classes-Considerations on structural effects, initial transformation products, antimicrobial activity and matrix
Autor (s)
Serna-Galvis, Efraim A.OrcidScopusMendeley;
Montoya-Rodríguez, Diana;
Isaza-Pineda, Laura;
 Ibáñez Martínez, María;
Hernández Hernández, Félix;
Moncayo-Lasso, AlejandroOrcid;
Torres Palma, R.
Data de publicació
2019
URI
http://hdl.handle.net/10234/182149
Versió de l'editor
https://www.sciencedirect.com/science/article/pii/S1350417718309064
DOI
https://doi.org/10.1016/j.ultsonch.2018.09.012
ISSN
1350-4177; 1873-2828
Editor
Elsevier
Resum
In this work, the sonochemical treatment (at 354 kHz and 88 W L-120 ) of six relevant antibiotics belonging to fluoroquinolones (ciprofloxacin and norfloxacin), penicillins (oxacillin and cloxacillin) and cephalosporins ... [+]
In this work, the sonochemical treatment (at 354 kHz and 88 W L-120 ) of six relevant antibiotics belonging to fluoroquinolones (ciprofloxacin and norfloxacin), penicillins (oxacillin and cloxacillin) and cephalosporins (cephalexin and cephadroxyl) classes was evaluated. Firstly, the ability of the process to eliminate them was tested, showing that sonodegradation of these antibiotics is strongly chemical structure25 dependent. Thus, correlations among initial degradation rate of pollutants (Rd), solubility in water (Sw), water-octanol partition coefficient (Log P) and topological polar surface area (TPSA) were tested. Rd exhibited a good correlation with Log P (i.e., the hydrophobicity degree of antibiotics). The considered penicillins had the fastest elimination and from the constitutional analysis using Lemke method was clear that the functional groups arrangement on these antibiotics made them highly hydrophobics. The penicillins were degraded closer at cavitation bubble than the fluoroquinolones or cephalosporins. The investigation of degradation products showed that sonogenerated hydroxyl radical primary attacked the β-lactam ring of cloxacillin and cephalexin, whereas on norfloxacin induced a decarboxylation. On the other hand, the evolution of antimicrobial activity was also followed. It was evidenced the process capacity to remove antimicrobial activity from treated solutions, which was associated to the transformations of functional groups on antibiotics with important role for interaction with bacteria. Additionally, degradation of antibiotics having the highest (the most hydrophobic, i.e., cloxacillin) and lowest (the most hydrophilic, i.e., cephadroxyl) Rd, was performed in synthetic matrices (hospital wastewater and seawater). Ultrasound degraded both antibiotics; for cloxacillin in such waters higher eliminations than in distilled water were observed (probably due to a salting-out effect exerted by matrix components). Meanwhile, for cephadroxyl a moderate inhibition of degradation in hospital wastewater and seawater respect to distilled water was found, this was related to competition by hydroxyl radical of the other substances in the matrices. These results show the quite selectivity of high frequency ultrasound to eliminate antibiotics form different classes even in complex matrices. [-]
Paraules clau / Matèries
antibiotic structure differences | advanced oxidation process | matrix effects | water treatment | pollutants degradation | ultrasound
Proyecto de investigación
The authors gratefully acknowledge COLCIENCIAS through the projects "Remoción de antibióticos y bacterias resistentes en aguas residuales hospitalarias empleando tecnologías avanzadas de oxidación (No. 111577757323)” and “Aproximación a la Remoción Eficiente de Drogas Ilícitas y Farmacéuticas Presentes en Aguas Residuales Mediante Métodos Avanzados de Oxidación (No. 123371552034)”, as well as Universidad de Antioquia UdeA through “Programa de Sostenibilidad”, for funding the research. E.A. Serna-Galvis also thanks COLCIENCIAS by his doctoral scholarship (Convocatoria 647 de 2014). The Oscar Pozo helping in the elucidation of transformation products is much appreciated. Authors from UJI acknowledge the support from Generalitat Valenciana, Spain (research group of excellence Prometeo II 2014/023)
Cita bibliogràfica
SERNA-GALVIS, Efraím A., et al. Sonochemical degradation of antibiotics from representative classes-Considerations on structural effects, initial transformation products, antimicrobial activity and matrix. Ultrasonics sonochemistry, 2019, vol. 50, p.157-165
Tipus de document
info:eu-repo/semantics/article
Drets d'accés
info:eu-repo/semantics/openAccess
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HispanaEuropeanaRePEc: Research Papers in EconomicsTesis Doctorals en XarxaGoogle ScholarRecolectaOpenDOARRevistes Catalanes d'Accés ObertOpenAIREMaterials Docents en Xarxa

Ministerio Aquest projecte ha rebut una ajuda de la Direcció General del Llibre, Arxius i Biblioteques del Ministeri de Cultura.
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Metadades subjectes a :Public Domain | Informació i consultes:biblioteca@uji.es | Centre de seguretat i privacitat | Nota legal
Universitat Jaume I - Av. de Vicent Sos Baynat, s/n 12071 Castelló de la Plana, Espanya - Tel.: +34 964 72 87 61 Fax: +34 964 72 87 78