Tailored surface silica nanoparticles for blood-brain barrier penetration: Preparation and in vivo investigation

被引:23
作者
Tamba, B. I. [1 ,2 ,3 ]
Streinu, V. [1 ]
Foltea, G. [1 ]
Neagu, A. N. [4 ]
Dodi, G. [1 ,5 ]
Zlei, M. [6 ]
Tijani, A. [7 ,8 ]
Stefanescu, C. [1 ]
机构
[1] Grigore T Popa Univ Med & Pharm, Iasi 700115, Romania
[2] Oxygen Handel Gmbh, D-68219 Mannheim, Germany
[3] A&B Pharm Corp, Roman 611075, Romania
[4] Alexandru Ioan Cuza Univ, Iasi 700506, Romania
[5] SCIENT Res Ctr Instrumental Anal, Bucharest 077167, Romania
[6] Reg Oncol Inst, Iasi 700483, Romania
[7] Inst Pasteur, NanoSERVE, F-59019 Lille, France
[8] FHNW, Sch Life Sci, CH-4132 Muttenz, Switzerland
关键词
Blood-brain barrier; Silica nanoparticles; Glucose; PEG; In vivo; Brain uptake; DRUG-DELIVERY; PLGA NANOPARTICLES; VITRO; PERMEABILITY; TRANSPORT; SYSTEMS; PROBES; CELL; PEG;
D O I
10.1016/j.arabjc.2018.03.019
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Surface modified fluorescent silica nanoparticle derivatives (Ru@SNPs), namely, glucose (Glu) and glucose-poly (ethylene glycol) methyl ether amine (Glu-PEG) coated SNPs were designed and tested for their ability to penetrate the blood-brain barrier (BBB) in mice brain. The new obtained nanoparticles were characterized by field emission scanning electron microscope (FE-SEM), dynamic light scattering (DLS) and Fourier transform infrared (FTIR-ATR) analysis. The BBB penetration and distribution of tailored SNPs in mice brain were examined using confocal laser scanning microscopy (CLSM), flow cytometer (FACS) and transmission electron microscopy (TEM). The promising results obtained by in vivo experiments, point out that silica nanoparticle derivatives are an efficient permeable delivery vehicle that are able to cross the BBB and reach the brain tissues via specific and non-specific mechanisms. These findings will enrich the knowledge to rationally engineer multifunctional nanoparticles, and bring new insights into BBB permeability. (C) 2018 The Authors. Production and hosting by Elsevier B.V. on behalf of King Saud University.
引用
收藏
页码:981 / 990
页数:10
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