Premium
Amphiphilic Polymethacrylate‐ and Polystyrene‐Based Chemical Delivery Systems for Damascones
Author(s) -
Berthier Damien,
Trachsel Alain,
Fehr Charles,
Ouali Lahoussine,
Herrmann Andreas
Publication year - 2005
Publication title -
helvetica chimica acta
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.74
H-Index - 82
eISSN - 1522-2675
pISSN - 0018-019X
DOI - 10.1002/hlca.200590249
Subject(s) - chemistry , polystyrene , polymer , polymer chemistry , amphiphile , monomer , methacrylic acid , radical polymerization , copolymer , aqueous solution , solvent , poly(methacrylic acid) , carboxylic acid , polymerization , organic chemistry
Amphiphilic polystyrene‐ and polymethacrylate‐based β ‐acyloxy ketones were investigated as potential delivery systems for the controlled release of damascones by retro ‐1,4‐addition in applications of functional perfumery. A series of random copolymers being composed of the hydrophobic damascone‐release unit and a second hydrophilic monomer were obtained by radical polymerization in organic solution by using 2,2′‐azobis[2‐methylpropanenitrile] (AIBN) as the radical source ( Schemes 2 and 3 ). A first evaluation of the polymer conjugates in acidic or alkaline buffered aqueous solution, and in the presence of a surfactant, showed that polymethacrylates and polystyrenes having a carboxylic acid function as hydrophilic group are particularly interesting for the targeted applications ( Table 2 ). The release of δ ‐damascone ( 1 ) from polymers with poly(methacrylic acid) and poly(vinylbenzoic acid) comonomers in different stoichiometric ratios was thus followed over several days at pH 4, 7, and 9 by comparison of fluorescence probing, solvent extraction, and particle‐size measurements ( Tables 3 and 4 ). In acidic media, the polymers were found to be stable, and almost no δ ‐damascone ( 1 ) was released. In neutral or alkaline solution, where the carboxylic acid functions are deprotonated, the concentration of 1 increased over time. In the case of the polymethacrylates, the fluorescence probing experiments showed an increasing hydrophilicity of the polymer backbone with increasing fragrance release, whereas in the case of the polystyrene support, the hydrophilicity of the environment remained constant. These results suggest that the nature of the polymer backbone may have a stronger influence on the fragrance release than the ratio of hydrophilic and hydrophobic monomers in the polymer chain.