| Literature DB >> 26846161 |
Xi Zhu1,2, Jun Wu2, Wei Shan1, Wei Tao2, Lili Zhao2, Jong-Min Lim2,3, Mathew D'Ortenzio2, Rohit Karnik3, Yuan Huang4, Jinjun Shi5, Omid C Farokhzad6,7.
Abstract
Effective delivery of therapeutic proteins is a formidable challenge. Herein, using a unique polymer family with a wide-ranging set of cationic and hydrophobic features, we developed a novel nanoparticle (NP) platform capable of installing protein ligands on the particle surface and simultaneously carrying therapeutic proteins inside by a self-assembly procedure. The loaded therapeutic proteins (e.g., insulin) within the NPs exhibited sustained and tunable release, while the surface-coated protein ligands (e.g., transferrin) were demonstrated to alter the NP cellular behaviors. In vivo results revealed that the transferrin-coated NPs can effectively be transported across the intestinal epithelium for oral insulin delivery, leading to a notable hypoglycemic response.Entities:
Keywords: drug delivery; insulin; nanoparticles; polymers; transcytosis
Mesh:
Substances:
Year: 2016 PMID: 26846161 PMCID: PMC4835185 DOI: 10.1002/anie.201509183
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336