Pregled bibliografske jedinice broj: 612851
Photolytic degradation of norfloxacin, enrofloxacin and ciprofloxacin in various aqueous media
Photolytic degradation of norfloxacin, enrofloxacin and ciprofloxacin in various aqueous media // Chemosphere, 91 (2013), 11; 1635-1642 doi:10.1016/j.chemosphere.2012.12.072 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 612851 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Photolytic degradation of norfloxacin,
enrofloxacin and ciprofloxacin in various
aqueous media
Autori
Babić, Sandra ; Periša, Martina ; Škorić, Irena
Izvornik
Chemosphere (0045-6535) 91
(2013), 11;
1635-1642
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
pharmaceuticals ; fluoroquinolones ; photodegradation pathways ; wastewater ; surface water
Sažetak
The photolytic degradation of norfloxacin, enrofloxacin and ciprofloxacin, fluoroquinolone antibacterials widely used in human and veterinary medicine, was investigated under simulated solar irradiation in different water matrices (river water and synthetic wastewater similar by composition to wastewater of pharmaceutical industry). The results showed that investigated fluoroquinolones degrade very quickly and photodegradation followed pseudo first order kinetics. The slowest photodegradation rate was observed in river water for all three fluoroquinolones. In the case of pharmaceutical mixture irradiation, no significant differences in rate constants were observed compared to single- component experiments. The structures of photodegradation products were determined and photodegradation pathways were suggested. Two main processes occured primary from enrofloxacin depending on pH values: (I) cyclopropane ring cleavage at pH 4 and (II) oxidative photodegradation at pH 8. The structures of the photoproducts E-1 to E-6 are unknown and have not been reported for this fluoroquinolone. For ciprofloxacin two main processes were also identified depending on experimental conditions. Under acidic conditions (pH 4), reactions involved rather the quinolone ring (cleavage of the cyclopropane ring and fluorine solvolysis), while at pH 8 the side- chain reactions took place. The photodegradation pathway of norfloxacin somewhat differed from the previous two. There was no significant dependence on reaction conditions and there were no two different pathways. Determination and identification of photodegradation products were performed by liquid chromatography-mass spectrometry (LC-MS/MS). The obtained results are of importance for assessing the environmental fate of fluoroquinolonesin aqueous media.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
MZOS-125-0982933-2926 - Heteropolicikli, strukturne osnove za bioaktivne spojeve. Sinteza i fotokemija (Škorić, Irena, MZOS ) ( CroRIS)
MZOS-125-1253008-1350 - Razvoj naprednih analitičkih metoda za određivanje farmaceutika u okolišu (Babić, Sandra, MZOS ) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- CA Search (Chemical Abstracts)