The paper deals with the development of an antinucleating strategy to prevent the crystallization of Artemisinin (ART), a potent natural antimalarial agent, through its encapsulation into core-shell nanofibers, constituted by a core of ART blended with a hyperbranched poly(butylene adipate) (HB), covered with a shell of poly(vinyl pyrrolidone) (PVP). The highly branched polymer acted as an effective antinucleating agent. Scanning and transmission electron microscopy analyses evidenced the regular and homogenous morphology of the core-shell electrospun nanofibers. Attenuated total reflectance spectroscopy, differential scanning calorimetry and X-ray diffraction analysis were utilized to assess the activity and the physical state of ART into the nanofibers. It was demonstrated that ART was successfully encapsulated in electrospun nanofibers and could efficiently retain its amorphous state.

A hyperbranched polyester as antinucleating agent for Artemisinin in electrospun nanofibers

I Bonadies;C Carfagna
2014

Abstract

The paper deals with the development of an antinucleating strategy to prevent the crystallization of Artemisinin (ART), a potent natural antimalarial agent, through its encapsulation into core-shell nanofibers, constituted by a core of ART blended with a hyperbranched poly(butylene adipate) (HB), covered with a shell of poly(vinyl pyrrolidone) (PVP). The highly branched polymer acted as an effective antinucleating agent. Scanning and transmission electron microscopy analyses evidenced the regular and homogenous morphology of the core-shell electrospun nanofibers. Attenuated total reflectance spectroscopy, differential scanning calorimetry and X-ray diffraction analysis were utilized to assess the activity and the physical state of ART into the nanofibers. It was demonstrated that ART was successfully encapsulated in electrospun nanofibers and could efficiently retain its amorphous state.
2014
Istituto per i Polimeri, Compositi e Biomateriali - IPCB
Artemisinin
Core-shell nanofibers
Crystallinity inhibition
Drug delivery system
Electrospinning
Hyperbranched polymer
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/279201
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