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Porous silicon-cyclodextrin based polymer composites for drug delivery applications

Year: 2014

Journal: CARBOHYDRATE POLYMERS, Vol. 110, p 238-252, 20150722

Authors: Hernandez-Montelongo, J.; Naveas, N.; Degoutin, S.; Tabary, N.; Chai, F.; Spampinato, V.; Ceccone, G.; Rossi, F.; Torres-Costa, V.; Manso-Silvan, M.; Martel, B.

Organizations: Univ Autonoma Madrid, Dept Fis Aplicada, E-28049 Madrid, Spain; Univ Lille 1, Unite Mat & Transformat UMET, F-59655 Villeneuve Dascq, France; Univ Lille 2, Fac Med, INSERM U1008, Grp Rech Biomat, F-59045 Lille, France; European Commiss, Joint Res Ctr, Inst Hlth & Consumer Protect, I-21020 Ispra, Va, Italy

One of the main applications of porous silicon (PSi) in biomedicine is drug release, either as a single material or as a part of a composite. PSi composites are attractive candidates for drug delivery systems because they can display new chemical and physical characteristics, which are not exhibited by the individual constituents alone. Since cyclodextrin-based polymers have been proven efficient materials for drug delivery, in this work beta-cyclodextrin-citric acid in-situ polymerization was used to functionalize two kinds of PSi (nanoporous and macroporous). The synthesized composites were characterized by microscopy techniques (SEM and AFM), physicochemical methods (ATR-FTIR, XPS, water contact angle, TGA and TBO titration) and a preliminary biological assay was performed. Both systems were tested as drug delivery platforms with two different model drugs, namely, ciprofloxacin (an antibiotic) and prednisolone (an anti-inflammatory), in two different media: pure water and PBS solution. Results show that both kinds of PSi/beta-cyclodextrin-citric acid polymer composites, nano- and macro-, provide enhanced release control for drug delivery applications than non-functionalized PSi samples. (C) 2014 Elsevier Ltd. All rights reserved.