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Engineering multi-stage nanovectors for controlled degradation and tunable release kinetics
Authors:Jonathan O Martinez  Ciro Chiappini  Arturas Ziemys  Ari M Faust  Milos Kojic  Xuewu Liu  Mauro Ferrari  Ennio Tasciotti
Institution:1. Department of Nanomedicine, The Methodist Hospital Research Institute, 6670 Bertner Ave., Houston, TX 77030, USA;2. Graduate School of Biomedical Sciences, University of Texas Health Science Center, 6767 Bertner Ave., Houston, TX 77030, USA;3. Department of Biomedical Engineering, University of Texas at Austin, 107 W. Dean Keeton, Austin, TX 78712, USA
Abstract: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.
Keywords:Degradation  Drug delivery  Nanoparticle  Porosity  Porous silicon  Nanovector
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