4.8 Article

Engineering multi-stage nanovectors for controlled degradation and tunable release kinetics

Journal

BIOMATERIALS
Volume 34, Issue 33, Pages 8469-8477

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.biomaterials.2013.07.049

Keywords

Degradation; Drug delivery; Nanoparticle; Porosity; Porous silicon; Nanovector

Funding

  1. Alliance for Nanohealth (DOD TATRC grants) [W81XWH-09-2-0139, W81XWH-10-2-0125]
  2. Defense Advanced Research Projects Agency [W911NF-09-1-0044]
  3. NIH [1F31CA154119]

Ask authors/readers for more resources

Nanovectors hold substantial promise in abating the off-target effects of therapeutics by providing a means to selectively accumulate payloads at the target lesion, resulting in an increase in the therapeutic index. A sophisticated understanding of the factors that govern the degradation and release dynamics of these nanovectors is imperative to achieve these ambitious goals. In this work, we elucidate the relationship that exists between variations in pore size and the impact on the degradation, loading, and release of multistage nanovectors. Larger pored vectors displayed faster degradation and higher loading of nanoparticles, while exhibiting the slowest release rate. The degradation of these particles was characterized to occur in a multi-step progression where they initially decreased in size leaving the porous core isolated, while the pores gradually increased in size. Empirical loading and release studies of nanoparticles along with diffusion modeling revealed that this prolonged release was modulated by the penetration within the porous core of the vectors regulated by their pore size. (C) 2013 Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available