Neutrophil targeted nano-drug delivery system for chronic obstructive lung diseases

被引:57
作者
Vij, Neeraj [1 ,3 ]
Min, Taehong [2 ,5 ]
Bodas, Manish [1 ,3 ]
Gorde, Aakruti [1 ,6 ]
Roy, Indrajit [4 ,7 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pediat Resp Sci, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Dept Biomed Engn, Baltimore, MD 21205 USA
[3] Cent Michigan Univ, Coll Med, Mt Pleasant, MI 48859 USA
[4] SUNY Buffalo, Dept Chem, Buffalo, NY USA
[5] Genentech Inc, 1 DNA Way, San Francisco, CA USA
[6] Novartis Inst Biomed Res, Boston, MA USA
[7] Univ Delhi, Dept Chem, New Delhi, India
关键词
Nanoparticle; Drug delivery; Cystic fibrosis; COPD; Emphysema; Neutrophils; NF kappa B; Lungs; NF-KAPPA-B; POLYMERIC NANOPARTICLES; PLGA NANOPARTICLES; CREMOPHOR-FREE; GENEXOL-PM; COPD; CHALLENGES; MICELLES; PATHOPHYSIOLOGY; FORMULATION;
D O I
10.1016/j.nano.2016.06.008
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The success of drug delivery to target airway cell(s) remains a significant challenge due to the limited ability of nanoparticle (NP) systems to circumvent protective airway-defense mechanisms. The size, density, surface and physical-chemical properties of nanoparticles are the key features that determine their ability to navigate across the airway-barrier. We evaluated here the efficacy of a PEGylated immuno-conjugated PLGA-nanoparticle (PINP) to overcome this challenge and selectively deliver drug to specific inflammatory cells (neutrophils). We first characterized the size, shape, surface-properties and neutrophil targeting using dynamic laser scattering, transmission electronmicroscopy and flow cytometry. Next, we assessed the efficacy of neutrophil-targeted PINPs in transporting through the airway followed by specific binding and release of drug to neutrophils. Finally, our results demonstrate the efficacy of PINP mediated non-steroidal anti-inflammatory drug-(ibuprofen) delivery to neutrophils in murine models of obstructive lung diseases, based on its ability to control neutrophilic-inflammation and resulting lung disease. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:2415 / 2427
页数:13
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