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Rapid automated spectrophotometric competitive complexation studies of drugs with cyclodextrins using the flow injection gradient technique: Tricyclic antidepressant drugs with α-cyclodextrin

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dc.contributor.author Georgiou, ME en
dc.contributor.author Georgiou, CA en
dc.contributor.author Koupparis, MA en
dc.date.accessioned 2014-06-06T06:43:58Z
dc.date.available 2014-06-06T06:43:58Z
dc.date.issued 1999 en
dc.identifier.issn 00032654 en
dc.identifier.uri http://dx.doi.org/10.1039/a808426b en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/1595
dc.subject.other acid en
dc.subject.other alpha cyclodextrin en
dc.subject.other amitriptyline en
dc.subject.other cyclodextrin en
dc.subject.other doxepin en
dc.subject.other imipramine en
dc.subject.other maprotiline en
dc.subject.other methyl orange en
dc.subject.other nitrophenol en
dc.subject.other nortriptyline en
dc.subject.other protriptyline en
dc.subject.other tricyclic antidepressant agent en
dc.subject.other accuracy en
dc.subject.other article en
dc.subject.other calibration en
dc.subject.other complex formation en
dc.subject.other controlled study en
dc.subject.other flow injection analysis en
dc.subject.other spectrophotometry en
dc.subject.other stoichiometry en
dc.title Rapid automated spectrophotometric competitive complexation studies of drugs with cyclodextrins using the flow injection gradient technique: Tricyclic antidepressant drugs with α-cyclodextrin en
heal.type journalArticle en
heal.identifier.primary 10.1039/a808426b en
heal.publicationDate 1999 en
heal.abstract An automated gradient flow injection (FI) spectrophotometric technique for competitive complexation studies of tricyclic antidepressant drugs with α-cyclodextrin (α-CD) using Methyl Orange (MO) as a probe is described. Formation constants for the complexes were determined utilising the total information contained in transient FI signals at 510 nm, the λ(max) of the MO probe. The study was carried out rapidly in three steps: (a) calibration of the FI concentration gradient by injection of p-nitrophenol in a buffered carrier stream, (b) determination of the probe-α-CD complex formation constant by injecting α-CD into the probe carrier stream and (c) determination of the drug-α-CD complex formation constant by injecting α-CD into the probe-drug carrier stream. In this way the preparation and measurement of a great number of mixed drug-probe-α-CD solutions was automated, resulting in the fast and precise determination of complexation constants of ligands (drugs), that are optically transparent, with α-CD. Methyl Orange was found to be an excellent probe for α-CD in acidic solutions (pH 1.0) with a complexation constant of (5.3 ± 0.1) x 102 mol-1 l. Complex formation constants determined at 26.5 ± 0.5°C and pH 1.0 (HCl) utilising transient α-CD concentrations in the range (1-1000) x 10-4 mol l-1, were (1.2 ± 0.1) x 102 mol-1 l for protriptyline, (0.7 ± 0.1) x 102 mol-1 l for nortriptyline, (2.4 ± 0.1) x 102 mol-1 l for maprotiline, (1.4 ± 0.1) x 102 mol-1 l for doxepin, (1.13 ± 0.07) x 102 mol-1 l for amitriptyline and (1.3 ± 0.2) x 102 mol-1 l for imipramine. A 1:1 stoichiometry was found in all cases. The within- and between-run precisions ranged from 1.2 to 6.4% and from 4.2 to 15.4% (RSD), respectively. The determined complex formation constants were in good agreement with those in the literature. Using the proposed FI gradient technique, the tedious manual preparation of a great number of mixed solutions with variable α-CD to drug ratios and the subsequent spectrophotometric measurements are replaced by a single FI measurement lasting 80 s. en
heal.journalName Analyst en
dc.identifier.issue 3 en
dc.identifier.volume 124 en
dc.identifier.doi 10.1039/a808426b en
dc.identifier.spage 391 en
dc.identifier.epage 396 en


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