Supramolecular analytical chemistry: Spectrofluorimetric determination of 6-hydroxymelatonin with hydroxypropyl-β-cyclodextrin

The effect of the addition of native (α, β and γ) and derivative (methyl-β and hydroxypropyl-β) cyclodextrins (CD) on the fluorescence of 6-hydroxymelatonin (6HM) in water solutions was studied. The fluorescence of the substrate in the presence of hydroxypropyl-β-CD (HPCD) showed the maximum enhance...

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Bibliographic Details
Authors: Bracamonte, Angel Guillermo, Miñambres, Guadalupe Gloria, Veglia, Alicia Viviana
Format: article
Status:Published version
Publication Date:2011
Country:Argentina
Institution:Consejo Nacional de Investigaciones Científicas y Técnicas
Repository:CONICET Digital (CONICET)
Language:English
OAI Identifier:oai:ri.conicet.gov.ar:11336/61852
Online Access:http://hdl.handle.net/11336/61852
Access Level:Open access
Keyword:6-HYDROXYMELATONIN
CYCLODEXTRIN
DETERMINATION
SPECTROFLUORIMETRY
SUPRAMOLECULAR INTERACTION
https://purl.org/becyt/ford/1.4
https://purl.org/becyt/ford/1
Description
Summary:The effect of the addition of native (α, β and γ) and derivative (methyl-β and hydroxypropyl-β) cyclodextrins (CD) on the fluorescence of 6-hydroxymelatonin (6HM) in water solutions was studied. The fluorescence of the substrate in the presence of hydroxypropyl-β-CD (HPCD) showed the maximum enhancement and the association constant (KA, mol-1 L) was determined (60±2) and interpreted. The fluorescence quantum yield ratio between the complex and free substrate (φ6HMCD/φ6HM) = 6.0±0.2 provides analytical advantages. On the basis of this supramolecular interaction, an alternative and sensitive spectrofluorimetric method for the determination of 6HM was developed with a detection limit of 0.71 ng mL-1. The validation of the method was performed in urine samples with very good recoveries 95-109 %.