4.8 Article

Sub-50 nm Nanoparticles with Biomimetic Surfaces to Sequentially Overcome the Mucosal Diffusion Barrier and the Epithelial Absorption Barrier

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 26, Issue 16, Pages 2728-2738

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.201505000

Keywords

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Funding

  1. National Natural Science Foundation of China [81173010]
  2. National Major Scientific and Technological Special Project for Significant New Drugs Development during the Twelfth Five-year Plan Period [2015ZX09501007-003]
  3. Technology Development Grant of Pudong New Area [PKF2014-C01]
  4. Guangdong Innovative Research Team Program [2009010057]

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Although nanoparticles (NPs) have been used for many drug delivery applications, oral absorption of NPs has remained a big challenge. NPs for oral delivery of biotherapeutics have to penetrate both the diffusion barrier of the mucus and the absorption barrier of the epithelium. This creates an obstacle for developing an effective NP platform for oral delivery because overcoming these two barriers requires different or even contradictory surface properties. Inspired by the features of some viruses, this study reports the development of a unique sub-50 nm polymeric NP platform that possesses a large amount of targeting ligands anchored on the surface while being moderately concealed under a muco-inert shield. NP library screening demonstrates a strong correlation between the relative lengths of the surface components and NP behavior on mucosal tissue. When a balance is obtained regarding optimal shielding of ligands, the NPs exhibit both excellent mucus permeation and transepithelial transport, and are efficiently absorbed into systemic circulation. Insulin-loaded NPs as a model oral therapy for diabetes generates a hypoglycemic response on diabetic animals following oral administration. This study demonstrates the great potency of a NP platform that exhibits an affinity balance between mucus and epithelium in facilitating the oral delivery of biotherapeutics.

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