In vitro screening of nanomedicines through the blood brain barrier: A critical review

被引:44
作者
Aparicio-Blanco, Juan [1 ]
Martin-Sabroso, Cristina [1 ]
Torres-Suarez, Ana-Isabel [1 ,2 ]
机构
[1] Univ Complutense, Fac Pharm, Dept Pharmaceut Technol, E-28040 Madrid, Spain
[2] Univ Complutense, Univ Inst Ind Pharm, E-28040 Madrid, Spain
关键词
Central nervous system; Brain targeting; Nanomedicine; Parallel artificial membrane permeability assay; Cell culture; In vitro blood-brain barrier model; MICROVASCULAR ENDOTHELIAL-CELLS; DRUG-DELIVERY SYSTEM; MEMBRANE-PERMEABILITY ASSAY; SOLID LIPID NANOPARTICLES; ADVANCE TRANSLATIONAL RESEARCH; JUNCTION PROTEIN EXPRESSION; IRON-OXIDE NANOPARTICLES; CENTRAL-NERVOUS-SYSTEM; VESICLE-BASED BARRIER; P-GLYCOPROTEIN;
D O I
10.1016/j.biomaterials.2016.06.051
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
The blood-brain barrier accounts for the high attrition rate of the treatments of most brain disorders, which therefore remain one of the greatest health-care challenges of the twenty first century. Against this background of hindrance to brain delivery, nanomedicine takes advantage of the assembly at the nanoscale of available biomaterials to provide a delivery platform with potential to raising brain levels of either imaging or therapeutic agents. Nevertheless, to prevent later failure due to ineffective drug levels at the target site, researchers have been endeavoring to develop a battery of in vitro screening procedures that can predict earlier in the drug discovery process the ability of these cutting-edge drug delivery platforms to cross the blood-brain barrier for biomedical purposes. This review provides an in-depth analysis of the currently available in vitro blood-brain barrier models (both cell-based and non-cell-based) with the focus on their suitability for understanding the biological brain distribution of forthcoming nanomedicines. The relationship between experimental factors and underlying physiological assumptions that would ultimately lead to a more predictive capacity of their in vivo performance, and those methods already assayed for the evaluation of the brain distribution of nanomedicines are comprehensively discussed. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:229 / 255
页数:27
相关论文
共 385 条
[1]
Abbott NJ, 2012, METHODS MOL BIOL, V814, P415, DOI 10.1007/978-1-61779-452-0_28
[2]
Structure and function of the blood-brain barrier [J].
Abbott, N. Joan ;
Patabendige, Adjanie A. K. ;
Dolman, Diana E. M. ;
Yusof, Siti R. ;
Begley, David J. .
NEUROBIOLOGY OF DISEASE, 2010, 37 (01) :13-25
[3]
Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[4]
ABBOTT NJ, 1992, J CELL SCI, V103, P23
[5]
Abbruscato TJ, 1999, J PHARMACOL EXP THER, V289, P668
[6]
Anandamide-loaded nanoparticles: Preparation and characterization [J].
Aberturas, M. R. ;
Hernan, D. ;
Gil, M. E. ;
Ligresti, L. A. ;
De Petrocellis, L. ;
Torres, A. I. ;
Di Marzo, V. ;
Molpeceres, J. .
JOURNAL OF MICROENCAPSULATION, 2011, 28 (03) :200-210
[7]
Permeability of PEGylated Immunoarsonoliposomes Through In Vitro Blood Brain Barrier-Medulloblastoma Co-culture Models for Brain Tumor Therapy [J].
Al-Shehri, Abdulghani ;
Favretto, Marco E. ;
Ioannou, Panayiotis V. ;
Romero, Ignacio A. ;
Couraud, Pierre-Olivier ;
Weksler, Babette Barbash ;
Parker, Terry L. ;
Kallinteri, Paraskevi .
PHARMACEUTICAL RESEARCH, 2015, 32 (03) :1072-1083
[8]
Penetrating the Blood-Brain Barrier: Promise of Novel Nanoplatforms and Delivery Vehicles [J].
Ali, Iqbal Unnisa ;
Chen, Xiaoyuan .
ACS NANO, 2015, 9 (10) :9470-9474
[9]
Anand P., 2015, SCIREP, V5, P10
[10]
Glioblastoma Multiforme and Lipid Nanocapsules: A Review [J].
Aparicio-Blanco, Juan ;
Torres-Suarez, Ana-Isabel .
JOURNAL OF BIOMEDICAL NANOTECHNOLOGY, 2015, 11 (08) :1283-1311