Salmon calcitonin (sCT) is characterized by a poor oral availability. A new copolymer, β-poly(N-2-hydroxyethyl)-graft-{N-2-ethylene[2-poly(methacrylic acid sodium salt)isobutyrate]}-d,l-aspartamide (PHEA-IB-p(MANa+)), was designed for the oral administration of sCT through the formation of supramolecular aggregates (SAs) based on electrostatic interactions. Several sCT/PHEA-IB-p(MANa+) weight ratios were characterized by turbidimetry, DLS, zeta potential, and microscopy analysis. After the incubation of sCT/PHEA-IB-p(MANa+) complex with digestive enzymes, 10% (w/w) of loaded sCT was released in the native form. In vitro investigation was carried out to determine the copolymer effect on the permeability of sCT in Caco-2 cell monolayers. sCT pharmacokinetic profile and the pharmacodynamic effect on calcium plasma level were determined following an oral administration of the lead sCT/PHEA-IB-p(MANa+) SA (1/5 ratio) in rats. The SA yielded a marked prolongation of the sCT lowering calcium ...

Licciardi, M., Pasut, G., Amato, G., Scialabba, C., Mero, A., Montopoli, M., et al. (2013). PHEA-graft-polymethacrylate supramolecular aggregates for protein oral delivery. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 84(1), 21-28 [10.1016/j.ejpb.2012.12.011].

PHEA-graft-polymethacrylate supramolecular aggregates for protein oral delivery

LICCIARDI, Mariano;AMATO, Giovanni;SCIALABBA, Cinzia;CAVALLARO, Gennara;GIAMMONA, Gaetano
2013-01-01

Abstract

Salmon calcitonin (sCT) is characterized by a poor oral availability. A new copolymer, β-poly(N-2-hydroxyethyl)-graft-{N-2-ethylene[2-poly(methacrylic acid sodium salt)isobutyrate]}-d,l-aspartamide (PHEA-IB-p(MANa+)), was designed for the oral administration of sCT through the formation of supramolecular aggregates (SAs) based on electrostatic interactions. Several sCT/PHEA-IB-p(MANa+) weight ratios were characterized by turbidimetry, DLS, zeta potential, and microscopy analysis. After the incubation of sCT/PHEA-IB-p(MANa+) complex with digestive enzymes, 10% (w/w) of loaded sCT was released in the native form. In vitro investigation was carried out to determine the copolymer effect on the permeability of sCT in Caco-2 cell monolayers. sCT pharmacokinetic profile and the pharmacodynamic effect on calcium plasma level were determined following an oral administration of the lead sCT/PHEA-IB-p(MANa+) SA (1/5 ratio) in rats. The SA yielded a marked prolongation of the sCT lowering calcium ...
2013
Licciardi, M., Pasut, G., Amato, G., Scialabba, C., Mero, A., Montopoli, M., et al. (2013). PHEA-graft-polymethacrylate supramolecular aggregates for protein oral delivery. EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 84(1), 21-28 [10.1016/j.ejpb.2012.12.011].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/78193
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