TY - JOUR
T1 - Core-shell microspheres by dispersion polymerization as promising delivery systems for proteins
AU - Sparnacci, Katia
AU - Laus, Michele
AU - Tondelli, Luisa
AU - Bernardi, Cinzia
AU - Magnani, Laura
AU - Corticelli, Franco
AU - Marchisio, Marco
AU - Ensoli, Barbara
AU - Castaldello, Arianna
AU - Caputo, Antonella
N1 - Funding Information:
This work was supported by the Italian Program on HIV/AIDS Research and by the Italian Concerted Action for the development of an HIV/AIDS Vaccine (ICAV), grants 40D.48 and 45D/1.02. We are grateful to Marco Ballestri (CNR) for his expert technical assistance.
PY - 2005/12
Y1 - 2005/12
N2 - Functional poly(methyl methacrylate) core-shell microspheres were prepared by dispersion polymerization. An appropriate selection of experimental parameters and in particular of the initiator and stabilizer amount and of the medium solvency power allowed a monodisperse sample as large as 600 nm to be prepared. To this purpose, low initiator concentration, high steric stabilizer amount and a low solvency power medium were employed. The microspheres present a core-shell structure in which the outer shell is constituted by the steric stabilizer which affords carboxylic groups able to interact with basic proteins, such as trypsin, whose adsorption is essentially driven by the carboxylic group density in the microsphere shell. Finally, fluorescent microspheres were prepared for biodistribution studies and shown to be readily taken up by the cells both in vitro and in vivo. These results suggest that these microspheres are promising delivery systems for the development of novel protein-based vaccines.
AB - Functional poly(methyl methacrylate) core-shell microspheres were prepared by dispersion polymerization. An appropriate selection of experimental parameters and in particular of the initiator and stabilizer amount and of the medium solvency power allowed a monodisperse sample as large as 600 nm to be prepared. To this purpose, low initiator concentration, high steric stabilizer amount and a low solvency power medium were employed. The microspheres present a core-shell structure in which the outer shell is constituted by the steric stabilizer which affords carboxylic groups able to interact with basic proteins, such as trypsin, whose adsorption is essentially driven by the carboxylic group density in the microsphere shell. Finally, fluorescent microspheres were prepared for biodistribution studies and shown to be readily taken up by the cells both in vitro and in vivo. These results suggest that these microspheres are promising delivery systems for the development of novel protein-based vaccines.
KW - Core-shell microspheres
KW - Delivery
KW - Dispersion polymerization
KW - Protein
KW - Vaccine
UR - https://www.scopus.com/pages/publications/33644875789
U2 - 10.1163/156856205774576673
DO - 10.1163/156856205774576673
M3 - Article
SN - 0920-5063
VL - 16
SP - 1557
EP - 1574
JO - Journal of Biomaterials Science, Polymer Edition
JF - Journal of Biomaterials Science, Polymer Edition
IS - 12
ER -