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Imprinted Polymers in Drug Delivery

Another requirement for MIPs to be used for this piuy)ose, is that they should not only be resilient against the biological reactions they will be prone to in the body, they should also have proper structual characteristics, as well as drug release kinetics. Table [Pg.276]

1 provides an overview of the research in the area in recent years [214-242]. [Pg.276]

Drug Name Mip Ingredients and Synthesis Apphcation in Drug Dehvery Reference [Pg.277]

Omeprazole The optimized imprinted polymer was prepared in chloroform as a porogen. 4-vinylpyridine and ethylene glycol dimethacrylate were selected as a functional monomer and a crosslinker, respectively. (Because of the instability of OMP under polymerization conditions and the inability of the molecule to form effective interactions with monomers, pantoprazole (PANTO) was used as a dummy template for the imprinting process.) For OMP controlled release [223] [Pg.278]


Puoci, F. Cirillo, G. Curcio, M. Parisi, O.I. lemma, F. Picci, N. (2011). Molecularly Imprinted Polymers in Drug Delivery state of art and future perspectives. Expert Opinion on Drug Delivery, DOI 10.1517/17425247.2011.609166. [Pg.211]

F. Puoci, G. Cirillo, M. Curcio, O.I. Parisi, F. lemma and N. Pied, Molecularly imprinted polymers in drug delivery State of art and future perspectives. Expert Opinion on Drug... [Pg.308]


See other pages where Imprinted Polymers in Drug Delivery is mentioned: [Pg.276]   


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