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Solubility of antibiotics in different solvents. 1. Hydrochloride forms of tetracycline, moxifloxacin, and ciprofloxacin

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dc.contributor.author Varanda, F en
dc.contributor.author Pratas De Melo, MJ en
dc.contributor.author Caco, AI en
dc.contributor.author Dohrn, R en
dc.contributor.author Makrydaki, FA en
dc.contributor.author Voutsas, E en
dc.contributor.author Tassios, D en
dc.contributor.author Marrucho, IM en
dc.date.accessioned 2014-03-01T01:25:10Z
dc.date.available 2014-03-01T01:25:10Z
dc.date.issued 2006 en
dc.identifier.issn 0888-5885 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/17575
dc.subject.classification Engineering, Chemical en
dc.subject.other Computer simulation en
dc.subject.other Mathematical models en
dc.subject.other Phase equilibria en
dc.subject.other Solubility en
dc.subject.other Solvents en
dc.subject.other Temperature distribution en
dc.subject.other Thermal effects en
dc.subject.other Ciprofloxacin en
dc.subject.other Moxifloxacin en
dc.subject.other Tetracycline en
dc.subject.other Antibiotics en
dc.subject.other Antibiotics en
dc.subject.other Computer simulation en
dc.subject.other Mathematical models en
dc.subject.other Phase equilibria en
dc.subject.other Solubility en
dc.subject.other Solvents en
dc.subject.other Temperature distribution en
dc.subject.other Thermal effects en
dc.title Solubility of antibiotics in different solvents. 1. Hydrochloride forms of tetracycline, moxifloxacin, and ciprofloxacin en
heal.type journalArticle en
heal.identifier.primary 10.1021/ie060055v en
heal.identifier.secondary http://dx.doi.org/10.1021/ie060055v en
heal.language English en
heal.publicationDate 2006 en
heal.abstract The solubilities of tetracycline hydrochloride, moxifloxacin hydrochloride, and ciprofloxacin hydrochloride were measured in several solvents, such as water, ethanol, 2-propanol, and acetone, in the temperature range of 293.15-323.15 K for ciprofloxacin.HCl and moxifloxacin.HCl and 288.15-310.15 K for tetracycline. All the antibiotics have the same solubility order; that is, they are more soluble in water than in ethanol, and more soluble in ethanol than in 2-propanol and acetone. The solubility in water is ∼3 orders of magnitude higher than that in acetone. The modeling of the experimental solid-liquid equilibria (SLE) data, using the NRTL and UNIQUAC models, proves that these models can correlate the solubility of studied antibiotics satisfactorily in the temperature range for which experimental data are available, with the UNIQUAC model generally being slightly superior to the NRTL model, when only two adjustable parameters are used for each binary system. © 2006 American Chemical Society. en
heal.publisher AMER CHEMICAL SOC en
heal.journalName Industrial and Engineering Chemistry Research en
dc.identifier.doi 10.1021/ie060055v en
dc.identifier.isi ISI:000239932100031 en
dc.identifier.volume 45 en
dc.identifier.issue 18 en
dc.identifier.spage 6368 en
dc.identifier.epage 6374 en


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