1997
DOI: 10.1016/s0731-7085(96)02033-x
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Physicochemical properties of enrofloxacin

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Cited by 90 publications
(69 citation statements)
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“…Above this pH, ENF is negatively charged and shows hydrophilic properties. Nearly all quinolones show hydrophobic properties that depend on structure and pH (Lizondo et al 1997). ENF has encapsulated negative charge in MLVs suspension (pH∼7.5), and the addition of DCP (negatively charged) into liposome formulation increased this negativity and decreased the encapsulation capacity to 57.9% as seen in Table 1.…”
Section: Characterization Of Enf Liposomesmentioning
confidence: 99%
See 1 more Smart Citation
“…Above this pH, ENF is negatively charged and shows hydrophilic properties. Nearly all quinolones show hydrophobic properties that depend on structure and pH (Lizondo et al 1997). ENF has encapsulated negative charge in MLVs suspension (pH∼7.5), and the addition of DCP (negatively charged) into liposome formulation increased this negativity and decreased the encapsulation capacity to 57.9% as seen in Table 1.…”
Section: Characterization Of Enf Liposomesmentioning
confidence: 99%
“…Therefore ENF does not concentrate effectively in the cell pathogens and this problem affects the therapeutic efficiency of free ENF. It has been pointed out that encapsulations of fluoroquinolones in liposomes could improve their effectiveness in cells (Montero et al 1994;Puglisi et al 1995;Cabanes et al 1995;Lizondo et al 1997;Baş et al 2000). However, there is limited information on liposomal form of ENF (Cabanes et al 1995;Baş et al 2000Baş et al , 2002Sezer et al 2002Sezer et al , 2004.…”
mentioning
confidence: 99%
“…The octanol-aqueous buffer pH 7.0 partition coefficient for enrofloxacin is 3.48. Therefore, this drug is considered highly lipophilic (18). According to Seedher (19), enrofloxacin water solubility is 146 mg/mL, and it is listed as poorly soluble based on pharmacopeial criteria.…”
Section: Solubility Determination and Sink Conditionsmentioning
confidence: 99%
“…Depending on the pH, it can exist in four forms: cationic (C), neutral non-ionized (N), zwitterionic (Z) and anionic (A) (Fig. 1) [28,29]. In strong acidic conditions, only the 7-piperazinyl group is positively charged, while in strongly basic medium, only the 3-carboxylic group is negatively charged.…”
Section: Effect Of Phmentioning
confidence: 99%