vettori nanoparticellari lipidici contenenti riluzolo e composizioni farmaceutiche che li contengono (Brevetto)

Type
Label
  • vettori nanoparticellari lipidici contenenti riluzolo e composizioni farmaceutiche che li contengono (Brevetto) (literal)
Anno
  • 2006-01-01T00:00:00+01:00 (literal)
Alternative label
  • M.L.Bondì, G.Giammona, E.F. Craparo, F. Drago (2006)
    vettori nanoparticellari lipidici contenenti riluzolo e composizioni farmaceutiche che li contengono
    (literal)
Titolo
  • vettori nanoparticellari lipidici contenenti riluzolo e composizioni farmaceutiche che li contengono (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • M.L.Bondì, G.Giammona, E.F. Craparo, F. Drago (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#proprieta
  • CNR-UNIPA-UNICT (literal)
Http://www.cnr.it/ontology/cnr/brevetti.owl#tipoDiBrevetto
  • Internazionale (literal)
Numero brevetto
  • MI2006A001274;PCT/EP2007/005654; (literal)
Anno di deposito
  • 2006 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • ISMN-CNR (literal)
Titolo
  • vettori nanoparticellari lipidici contenenti riluzolo e composizioni farmaceutiche che li contengono (literal)
Abstract
  • The nanoparticles systems prepared from our group of search, thanks to their biocompatibility, biodegradability and ability to entrap hydrophilic and lipophilic drugs, are proposed for controlled release and targeting of riluzole to the brain. These systems represent an alternative carrier system to the traditional colloidal carriers, such emulsions, liposomes. These systems combine advantages of the traditional systems but avoid some of their major disadvantages. The advantages include: possibility to produce a controlled release and a targeting of the drug, long-term stability of the drug, loading capacity, drug incorporation and drug release, possibility to load lipophilic and hydrophilic drugs, absence of biotoxicity of the carrier for employed lipids. They are produced in absence organic solvents. These systems are suitable to entrap peptides and oligo-nucleotides. For their small dimensions they can be used for the several ways of administration, comprised that intravenous. (literal)
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