Pregled bibliografske jedinice broj: 888183
Nitrofurantoin hydrolytic degradation in the environment
Nitrofurantoin hydrolytic degradation in the environment // Chemosphere, 186 (2017), 660-668 doi:10.1016/j.chemosphere.2017.08.011 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 888183 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Nitrofurantoin hydrolytic degradation in the environment
Autori
Biošić, Martina ; Škorić, Irena ; Beganović, Jasmina ; Babić, Sandra
Izvornik
Chemosphere (0045-6535) 186
(2017);
660-668
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
antibiotics ; nitrofurans ; hydrolysis ; kinetics ; degradation pathways ; environmental fate
Sažetak
Occurrence of pharmaceuticals, especially antibiotics in the environment increased attention to their environmental fate. Hydrolysis is one of two abiotic processes by which compounds are degraded in the environment. According to authors knowledge this is the first study investigating hydrolytic degradation of nitrofurantoin at pH-values normally found in the environment based on the OECD 111 procedure. Nitrofurantoin hydrolytic degradation appeared to be much slower at acidic (pH 4) solution compared to neutral (pH 7) and alkaline (pH 9) solutions at all three investigated temperatures (20 °C, 40 °C and 60 °C). In all cases nitrofurantoin hydrolysis followed the first- order kinetics with half-lives ranged from 0.5 days at pH 9 and 60 °C to 3.9 years at pH 4 and 20 °C. Temperature dependence of the hydrolysis rate constant was quantified by Arrhenius equation ; obtained Ea values were as follows: 100.7 kJ mol-1 at pH 4, 111.2 kJ mol-1 at pH 7 and 102.3 kJ mol-1 at pH 9. Increase in hydrolysis rate constants for each 10 C increase in temperature were 3.4, 3.9 and 3.5 at pH 4, pH 7 and pH 9, respectively. The structures of hydrolytic degradation products were determined and degradation pathways were suggested. Three main processes occurred depending on pH-values: protonation of the nitrofurantoin followed by cleavage of the N-N single bond, heterocyclic non-aromatic ring cleavage, and reduction of the non-aromatic heterocyclic ring.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
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)