| Literature DB >> 24990548 |
Jun Wu1, Nazila Kamaly, Jinjun Shi, Lili Zhao, Zeyu Xiao, Geoffrey Hollett, Rohit John, Shaunak Ray, Xiaoyang Xu, Xueqing Zhang, Philip W Kantoff, Omid C Farokhzad.
Abstract
One limitation of current biodegradable polymeric nanoparticles is their inability to effectively encapsulate and sustainably release proteins while maintaining protein bioactivity. Here we report the engineering of PLGA-polycation nanoparticles with a core-shell structure that act as a robust vector for the encapsulation and delivery of proteins and peptides. The optimized nanoparticles can load high amounts of proteins (>20 % of nanoparticles by weight) in aqueous solution without organic solvents through electrostatic interactions by simple mixing, thereby forming nanospheres in seconds with diameters <200 nm. The relationship between nanosphere size, surface charge, PLGA-polycation composition, and protein loading is also investigated. The stable nanosphere complexes contain multiple PLGA-polycation nanoparticles, surrounded by large amounts of protein. This study highlights a novel strategy for the delivery of proteins and other relevant molecules.Entities:
Keywords: nanoparticles; polycations; polymers; protein delivery; structure-function relationships
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Year: 2014 PMID: 24990548 PMCID: PMC4143165 DOI: 10.1002/anie.201404766
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336