Dextran-protamine coated nanostructured lipid carriers as mucuspenetrating nanoparticles for lipophilic drugs

被引:75
作者
Beloqui, Ana [1 ]
Angeles Solinis, Maria [1 ]
des Rieux, Anne [2 ]
Preat, Veronique [2 ]
Rodriguez-Gascon, Alicia [1 ]
机构
[1] Univ Basque Country UPV EHU, Fac Pharm, Ctr Invest Lascaray Ikergunea, Pharmacokinet Nanotechnol & Gene Therapy Grp Phar, Vitoria 01006, Spain
[2] Catholic Univ Louvain, Louvain Drug Res Inst Pharmaceut & Drug Delivery, B-1200 Brussels, Belgium
关键词
NLCs; Mucus; HT29-MTX; Caco-2; Saquinavir; Permeability; IN-VITRO; POLYMERIC NANOPARTICLES; CELL-LINES; DELIVERY; TRANSPORT; MUCUS; NANOCAPSULES; SAQUINAVIR; MECHANISM; PLATFORM;
D O I
10.1016/j.ijpharm.2014.04.027
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The main objectives of the present study were (i) to evaluate the effect of the mucus layer on saquinavir-loaded nanostructured lipid carriers (SQV-NLCs) uptake and (ii) to evaluate the mucopenetrating properties of dextran-protamine (Dex-Prot) coating on NLCs as per SQV permeability enhancement. Three different NLC formulations differing on particle size and surfactant content were obtained and coated with Dex-Prot complexes. SQV permeability was then evaluated across Caco-2 cell monolayers (enterocyte-like model) and Caco-2/HT29-MTX cell monolayers (mucus model). In the Caco-2 monolayers, Dex-Prot-NLCs increased up to 9-fold SQV permeability in comparison to uncoated nanoparticles. In the Caco-2/HT29-MTX monolayers, Dex-Prot-NLCs presenting a surface charge close to neutrality significantly increased SQV permeability. Hence, Dex-Prot complex coating is a promising strategy to ensure successful nanoparticle mucus-penetration, and thus, an efficient nanoparticle oral delivery. To our knowledge, this is the first time that Dex-Prot coating has been described as a nanoparticle muco-penetration enhancer across the intestinal mucus barrier. (C) 2014 Elsevier B. V. All rights reserved.
引用
收藏
页码:105 / 111
页数:7
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