6533b7d4fe1ef96bd1263476
RESEARCH PRODUCT
Amphiphilic poly(hydroxyethylaspartamide) derivative-based micelles as drug delivery systems for ferulic acid
Ognibene Maria ChiaraBondì Maria LuisaGiammona GaetanoEmanuela Fabiola CraparoTeresi GirolamoCavallaro Gennarasubject
Coumaric AcidsAction PotentialsPharmaceutical ScienceBuffersCoumaric acidMicelleFerulic acidMicechemistry.chemical_compoundDrug Delivery SystemsPhagocytosisamphiphilic copolymers micelles ferulic acidPolymer chemistryAmphiphileZeta potentialCopolymerAnimalsHumansTechnology PharmaceuticalOrganic chemistryMicellespolymeric micellesFluorescent DyesAmphiphilic copolymersalphabeta-poly(N-2-hydroxyethyl)-DL-aspartamidePlant ExtractsRhodaminesMacrophagesHydrogen-Ion ConcentrationchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliveryPEGylationCaco-2 CellsK562 CellsPeptidesRhodamine B baseferulic aciddescription
Self-assembling micelles, potentially useful as drug delivery systems for ferulic acid (FA), were obtained in aqueous media from amphiphilic alpha,beta-poly(N-2-hydroxyethyl)-dl-aspartamide (PHEA) copolymers bearing at the polyamino acidic backbone both poly(ethyleneglycol) (2000 or 5000 Da) and hexadecylamine (C(16)) moieties, at a concentration of 7 x 10(- 3) and 4 x 10(- 3) g/l, respectively, with nanometre size and negative zeta potential. These micelles were able to entrap FA and to release it in a prolonged way in phosphate buffer solution at pH 7.4 and human plasma. These systems were also stable in storage conditions and have no cytotoxic effects on Caco-2, 16 HBE, HuDe and K562 cell lines. Moreover, PHEA-PEG(2000)-C(16) and PHEA-PEG(5000)-C(16) micelles were able to escape from phagocytosis by murine macrophages as a function of the surface PEGylation.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2008-11-19 | Journal of Drug Targeting |