Incorporation and Controlled Release of Silyl Ether Prodrugs from PRINT Nanoparticles
作者:Matthew C. Parrott、Mathew Finniss、J. Chris Luft、Ashish Pandya、Anuradha Gullapalli、Mary E. Napier、Joseph M. DeSimone
DOI:10.1021/ja301710z
日期:2012.5.9
Asymmetric bifunctional silylether (ABS) prodrugs of chemotherapeutics were synthesized and incorporated within 200 nm × 200 nm particles. ABS prodrugs of gemcitabine were selected as model compounds because of the difficulty to encapsulate a water-soluble drug within a hydrogel. The resulting drug delivery systems were degraded under acidic conditions and were found to release only the parent or active
ASYMMETRIC BIFUNCTIONAL SILYL MONOMERS AND PARTICLES THEREOF AS PRODRUGS AND DELIVERY VEHICLES FOR PHARMACEUTICAL, CHEMICAL AND BIOLOGICAL AGENTS
申请人:The University of North Carolina at Chapel Hill
公开号:US20170021030A1
公开(公告)日:2017-01-26
Asymmetric bifunctional silyl (ABS) monomers comprising covalently linked pharmaceutical, chemical and biological agents are described. These agents can also be covalently bound via the silyl group to delivery vehicles for delivering the agents to desired targets or areas. Also described are delivery vehicles which contain ABS monomers comprising covalently linked agents and to vehicles that are covalently linked to the ABS monomers. The silyl modifications described herein can modify properties of the agents and vehicles, thereby providing desired solubility, stability, hydrophobicity and targeting.