Effect of binary and ternary polyvinylpyrrolidone and/or hydroxypropyl-β-cyclodextrin complexes on the photochemical and photosensitizing properties of Naproxen

[EN]The effect of the polyvinylpyrrolidone and/or hydroxypropyl-b-cyclodextrin on the photolability of aqueous solutions of the antiinflammatory drug Naproxen was studied. Kinetic studies revealed that the presence of all of these additives reduced drug photodegradation. In all cases, the presence o...

Full description

Bibliographic Details
Authors: Valero Juan, Margarita; Esteban, Brígida
Format: Article
Status:Published version
Publication date:2004
Country:España
Institution:Universidad de Salamanca (USAL)
Repository:GREDOS. Repositorio Institucional de la Universidad de Salamanca
OAI Identifier:oai:dnet:gredos______::c4c7d3459b132ce67757573104b9dd16
Online Access:http://hdl.handle.net/10366/171081
Access Level:Open access
Keyword:Naproxen photodegradation
Hydroxypropyl-b-cyclodextrin
Polyvinyl pyrrolidone
Binary complex
Ternary complex
Photosensitizing effects
Naproxen
Ternary Complex Factors
Photosensitizing Agents
fármacos fotosensibilizantes
naproxeno
factores complejos ternarios
Description
Summary:[EN]The effect of the polyvinylpyrrolidone and/or hydroxypropyl-b-cyclodextrin on the photolability of aqueous solutions of the antiinflammatory drug Naproxen was studied. Kinetic studies revealed that the presence of all of these additives reduced drug photodegradation. In all cases, the presence of the different additives elicited a change in the photomixture composition, being the alcoholic derivative the major photoproduct formed. Nevertheless, the change in the efficiency of the process and the amount of the photoproducts formed in the different systems were not related with the biodamage produced by the drug. In this sense, the presence of free Naproxen clearly sensitized the photoperoxidation of linoleic acid. The photosensitizing effect decreased as the PVP concentration increased. Different protection provides the binary (Naproxen:HP-b-CD) and ternary (Naproxen:HP-b- CD:PVP) complexes. The binary complex formation had not effect on the prevention of photooxidation of linoleic acid sensitized by the drug, whereas the ternary complex formation supresses the drug effect. The different behaviour observed with b-CD and HPb- CD and the structural differences of both cyclodextrins seem to indicate that in the case of the HP-b-CD the linoleic binds with the CD and takes contact with the drug. These results confirm that in these systems the prevention of biodamage would be due to a decrease in the contact between the short-lived species generated during Naproxen photodegradation and biological structures, rather than due to the nature or amount of the photoproducts. In addition, the ability of the complex to interact with the biological structure depends on the structure of both interacting species.