In Vitro and in Vivo Studies on the Transport of PEGylated Silica Nanoparticles across the Blood-Brain Barrier

被引:119
作者
Liu, Dan [1 ]
Lin, Bingqian [1 ]
Shao, Wei [1 ]
Zhu, Zhi [1 ]
Ji, Tianhai [1 ]
Yang, Chaoyong [1 ]
机构
[1] Xiamen Univ, Affiliated Chenggong Hosp,Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces,Dept Chem, Key Lab Chem Biol Fujian Prov,MOE Key Lab Spectro, Xiamen 361005, Peoples R China
关键词
PEGylated silica nanoparticles; blood-brain barrier; different size; transportation; ENDOTHELIAL-CELLS; DELIVERY; PROTEIN; BIODISTRIBUTION; NANOTECHNOLOGY; NANOCARRIERS; PERMEABILITY; TRANSCYTOSIS; MODEL;
D O I
10.1021/am405219u
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Transport of PEGylated silica nanoparticles (PSiNPs) with diameters of 100, 50, and 25 nm across the blood-brain barrier (BBB) was evaluated using an in vitro BBB model based on mouse cerebral endothelial cells (bEnd.3) cultured on transwell inserts within a chamber. In vivo animal experiments were further performed by noninvasive in vivo imaging and ex vivo optical imaging after injection via carotid artery. Confocal fluorescence studies were carried out to evaluate the uptake of PSiNPs by brain endothelial cells. The results showed that PSiNPs can traverse the BBB in vitro and in vivo. The transport efficiency of PSiNPs across BBB was found to be size-dependent, with increased particle size resulting in decreased efficiency. This work points to the potential application of small sized silica nanoparticles in brain imaging or drug delivery.
引用
收藏
页码:2131 / 2136
页数:6
相关论文
共 49 条
[1]   Oncotic pressures opposing filtration across non-fenestrated rat microvessels [J].
Adamson, RH ;
Lenz, JE ;
Zhang, X ;
Adamson, GN ;
Weinbaum, S ;
Curry, FE .
JOURNAL OF PHYSIOLOGY-LONDON, 2004, 557 (03) :889-907
[2]   The blood-brain barrier: an overview - Structure, regulation, and clinical implications [J].
Ballabh, P ;
Braun, A ;
Nedergaard, M .
NEUROBIOLOGY OF DISEASE, 2004, 16 (01) :1-13
[3]   Organically Modified Silica Nanoparticles Are Biocompatible and Can Be Targeted to Neurons In Vivo [J].
Barandeh, Farda ;
Phuong-Lan Nguyen ;
Kumar, Rajiv ;
Iacobucci, Gary J. ;
Kuznicki, Michelle L. ;
Kosterman, Andrew ;
Bergey, Earl J. ;
Prasad, Paras N. ;
Gunawardena, Shermali .
PLOS ONE, 2012, 7 (01)
[4]   Solid lipid nanoparticles for targeted brain drug delivery [J].
Blasi, Paolo ;
Glovagnoli, Stefano ;
Schoubben, Aurelie ;
Ricci, Maurizio ;
Rossi, Carlo .
ADVANCED DRUG DELIVERY REVIEWS, 2007, 59 (06) :454-477
[5]   Poly(ethylene glycol)-coated hexadecylcyanoacrylate nanospheres display a combined effect for brain tumor targeting [J].
Brigger, I ;
Morizet, J ;
Aubert, G ;
Chacun, H ;
Terrier-Lacombe, MJ ;
Couvreur, P ;
Vassal, G .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2002, 303 (03) :928-936
[7]   Tight junction protein expression and barrier properties of immortalized mouse brain microvessel endothelial cells [J].
Brown, Rachel C. ;
Morris, Andrew P. ;
O'Neil, Roger G. .
BRAIN RESEARCH, 2007, 1130 (01) :17-30
[8]   Gastrointestinal uptake of biodegradable microparticles: Effect of particle size [J].
Desai, MP ;
Labhasetwar, V ;
Amidon, GL ;
Levy, RJ .
PHARMACEUTICAL RESEARCH, 1996, 13 (12) :1838-1845
[9]   Receptor-mediated transcytosis of lactoferrin through the blood-brain barrier [J].
Fillebeen, C ;
Descamps, L ;
Dehouck, MP ;
Fenart, L ;
Benaïssa, M ;
Spik, G ;
Cecchelli, R ;
Pierce, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (11) :7011-7017
[10]   Primary cultures of brain microvessel endothelial cells: a valid and flexible model to study drug transport through the blood-brain barrier in vitro [J].
Franke, H ;
Galla, HJ ;
Beuckmann, CT .
BRAIN RESEARCH PROTOCOLS, 2000, 5 (03) :248-256