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Auteur Margherita Sessa
Documents disponibles écrits par cet auteur
Affiner la rechercheSupercritical phase Inversion to form drug-loaded poly(vinylidene fluoride-co-hexafluoropropylene) membranes / Stefano Cardea in Industrial & engineering chemistry research, Vol. 49 N° 6 (Mars 2010)
[article]
in Industrial & engineering chemistry research > Vol. 49 N° 6 (Mars 2010) . - pp. 2783–2789
Titre : Supercritical phase Inversion to form drug-loaded poly(vinylidene fluoride-co-hexafluoropropylene) membranes Type de document : texte imprimé Auteurs : Stefano Cardea, Auteur ; Margherita Sessa, Auteur ; Ernesto Reverchon, Auteur Année de publication : 2010 Article en page(s) : pp. 2783–2789 Note générale : Inustrial Chemistry Langues : Anglais (eng) Mots-clés : Drug; Poly; vinylidene; fluoride; co-hexafluoropropylene; Membranes Résumé : Membranes loaded with an active principle are one of the alternatives proposed to obtain controlled release pharmaceutical formulations. Until now, several methods have been proposed for the fabrication of membranes as drug delivery devices, such as phase inversion, gas foaming/particulate leaching, and solvent evaporation. Supercritical CO2 (SC-CO2) phase inversion offers an alternative process to obtain solvent-free membranes with short processing times, avoiding the collapse of the structure. We prepared poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF−HFP) loaded membranes by SC-CO2 phase inversion, performing experiments at pressures ranging between 150 and 250 bar and at temperatures ranging between 35 and 55 °C. We selected as the base case the PVDF−HFP−acetone solution at 15% w/w polymer and modified the drug (amoxicillin) concentration from 20 to 50% w/w with respect to PVDF−HFP. Different membranes morphologies, ranging from nanometric gel-like networks (mean pores diameter of about 150 nm) to micrometric cellular structures (mean cells diameter ranging between 5 and 12 μm), and different drug distributions were obtained, depending on the process conditions. Drug-controlled release experiments were also performed to study the kinetics and duration of the release process. Note de contenu : Bibiogr. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie901616n [article] Supercritical phase Inversion to form drug-loaded poly(vinylidene fluoride-co-hexafluoropropylene) membranes [texte imprimé] / Stefano Cardea, Auteur ; Margherita Sessa, Auteur ; Ernesto Reverchon, Auteur . - 2010 . - pp. 2783–2789.
Inustrial Chemistry
Langues : Anglais (eng)
in Industrial & engineering chemistry research > Vol. 49 N° 6 (Mars 2010) . - pp. 2783–2789
Mots-clés : Drug; Poly; vinylidene; fluoride; co-hexafluoropropylene; Membranes Résumé : Membranes loaded with an active principle are one of the alternatives proposed to obtain controlled release pharmaceutical formulations. Until now, several methods have been proposed for the fabrication of membranes as drug delivery devices, such as phase inversion, gas foaming/particulate leaching, and solvent evaporation. Supercritical CO2 (SC-CO2) phase inversion offers an alternative process to obtain solvent-free membranes with short processing times, avoiding the collapse of the structure. We prepared poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF−HFP) loaded membranes by SC-CO2 phase inversion, performing experiments at pressures ranging between 150 and 250 bar and at temperatures ranging between 35 and 55 °C. We selected as the base case the PVDF−HFP−acetone solution at 15% w/w polymer and modified the drug (amoxicillin) concentration from 20 to 50% w/w with respect to PVDF−HFP. Different membranes morphologies, ranging from nanometric gel-like networks (mean pores diameter of about 150 nm) to micrometric cellular structures (mean cells diameter ranging between 5 and 12 μm), and different drug distributions were obtained, depending on the process conditions. Drug-controlled release experiments were also performed to study the kinetics and duration of the release process. Note de contenu : Bibiogr. ISSN : 0888-5885 En ligne : http://pubs.acs.org/doi/abs/10.1021/ie901616n