“…As FQs often contain one or more ionizable functional groups, such as carboxylic and amine, they can exist in various ionization states under environmental pH conditions. As a result, the photodegradation of zwitterionic FQs may exhibit strong dependence on their ionization state due to the varying ability of neutral and charged species to activate molecular oxygen by 3 FQ* de-excitation in self-sensitized photolysis, as well as their different reactivity under the attack of electrophilic reagents (i.e., reactive oxygen species, ROSs). − The ionization of antibiotics has been well observed to result in the apparent pH dependence of their photodegradation rate constants. − For instance, the zwitterionic species of gemifloxacin, balofloxacin, lomefloxacin, norfloxacin, and ofloxacin were found to photodegrade faster than the cationic and anionic ones. , In contrast, the cationic ciprofloxacin species was reported to have the highest photodegradation rate among all chemical forms . The quantum yields for photodegradation of lomefloxacin, norfloxacin, and ofloxacin decreased in the order of zwitterionic > anionic > cationic, and their pathways of photodegradation were found to depend strongly on the ionization state, with more significant defluorination occurring when lomefloxacin and norfloxacin existed in zwitterionic forms …”