2009
DOI: 10.1016/j.chemosphere.2009.03.022
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Photo-degradation of the antimicrobial ciprofloxacin at high pH: Identification and biodegradability assessment of the primary by-products

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Cited by 188 publications
(75 citation statements)
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“…Thus, the total toxicity of remaining ciprofloxacin and formed photo-products had been reduced, i.e. the toxicity of the photo-products was probably no higher than that of ciprofloxacin itself (Vasconcelos et al, 2009). Ge et al (2010) studied the aquatic photochemistry of fluoroquinolones and the toxicity of the oxidation products as well as luminescence inhibition to Vibrio fischeri.…”
Section: Ecotoxicitymentioning
confidence: 99%
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“…Thus, the total toxicity of remaining ciprofloxacin and formed photo-products had been reduced, i.e. the toxicity of the photo-products was probably no higher than that of ciprofloxacin itself (Vasconcelos et al, 2009). Ge et al (2010) studied the aquatic photochemistry of fluoroquinolones and the toxicity of the oxidation products as well as luminescence inhibition to Vibrio fischeri.…”
Section: Ecotoxicitymentioning
confidence: 99%
“…Vasconcelos et al (2009) studied the photodegradation of ciprofloxacin, identifying the primary by-products, and assessed their biodegradability and toxicity. The photo-products were obtained by irradiation with a medium-pressure mercury arc lamp.…”
Section: Ecotoxicitymentioning
confidence: 99%
“…The continuously decrease of toxicity during CWAO was possibly caused by the consumption of the catalysts used, the substantial decomposition of ENR and generation of less toxic products. However, some studies showed an increase trends of toxicity after ozonation or photodegradation of several types of antibiotics (Vasconcelos et al, 2009;Ge et al, 2010;Homem and Santos, 2011). This encourages further optimization of CWAO as treatment technique for wastewater loaded with quinolones.…”
Section: Biodegradability and Toxicity Of Reaction Mixture By Cwaomentioning
confidence: 99%
“…generated compound 11 (Guinea et al, 2010). The antimicrobial activity of fluoroquinolones was believed to derive from the quinolone moiety (Vasconcelos et al, 2009). As described in Scheme 1, most existing intermediates still exhibited an intact quinolone core with carboxylic acid group, fluoride and intact piperazine ring on position 7.…”
Section: Proposed Primary Degradation Products and Reaction Pathwaysmentioning
confidence: 99%
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