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Nanohybrids for controlled antibiotic release in topical applications

TitoloNanohybrids for controlled antibiotic release in topical applications
Tipo di pubblicazioneArticolo su Rivista peer-reviewed
Anno di Pubblicazione2007
AutoriTammaro, Loredana, Costantino U., Bolognese A., Sammartino G., Marenzi G., Calignano A., Tetè S., Mastrangelo F., Califano L., and Vittoria V.
RivistaInternational Journal of Antimicrobial Agents
Volume29
Paginazione417-423
ISSN09248579
Parole chiaveAdministration, Aluminum, aluminum magnesium hydroxide, anion, Anti-Bacterial Agents, article, Chloramphenicol, Chloramphenicol hemisuccinate, controlled release formulation, Delayed-Action Preparations, Drug Carriers, drug delivery system, film, fractionation, Ion exchange, Mechanics, Nanostructures, nanotechnology, nitrate, polycaprolactone, priority journal, thermodynamics, thermogravimetry, Topical, X ray diffraction, X-Ray Diffraction
Abstract

New polymeric composite materials containing a nanohybrid to be used for the controlled release of an antibiotic molecule, chloramphenicol succinate, have been formulated, prepared and characterised. The nanohybrid consists of a layered double hydroxide of Mg-Al hydrotalcite-type, in which the nitrate anions present in the host galleries were replaced with chloramphenicol succinate anions (CFS-) by a simple ion-exchange reaction. Different amounts of the hybrid material were incorporated in polycaprolactone and processed as films of 0.15 mm thickness. The composite materials were analysed by X-ray diffractometry and thermogravimetry and their mechanical properties were determined. They showed properties even better than those of the pristine polymer. The release process of the antibiotic molecules was found to be very interesting and promising for tuneable drug delivery. It consists of two stages: an initial stage of a very rapid burst, in which a small fraction of drug is released; and a second stage that is much slower, extending for a longer and longer time. This behaviour is profoundly different and much slower than that of a sample in which the antibiotic molecule is directly incorporated into the polymeric matrix. The parameters influencing drug release have been individuated and discussed. © 2007 Elsevier B.V. and the International Society of Chemotherapy.

Note

cited By 54

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-33847405671&doi=10.1016%2fj.ijantimicag.2006.11.019&partnerID=40&md5=828935e6e8eabbdf7e62dff36aaa35a0
DOI10.1016/j.ijantimicag.2006.11.019
Citation KeyTammaro2007417