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Blood-brain barrier models and their relevance for a successful development of CNS drug delivery systems: A review
被引:192
|作者:
Bicker, Joana
[1
,2
]
Alves, Gilberto
[2
,3
]
Fortuna, Ana
[1
,2
]
Falcao, Amilcar
[1
,2
]
机构:
[1] Univ Coimbra, Pharmacol Lab, Coimbra, Portugal
[2] Univ Coimbra, CNC Ctr Neurosci & Cell Biol, Coimbra, Portugal
[3] Univ Beira Interior, CICS UBI Hlth Sci Res Ctr, P-6200506 Covilha, Portugal
关键词:
Brain uptake;
Cell culture;
CNS drugs;
Drug discovery and development;
In vitro;
In vivo;
Neurovascular unit;
PAMPA;
Permeability screening;
Targeted drug delivery;
IN-VITRO MODEL;
MICROVASCULAR ENDOTHELIAL-CELLS;
POSITRON-EMISSION-TOMOGRAPHY;
MEMBRANE-PERMEABILITY ASSAY;
JUNCTION PROTEIN EXPRESSION;
PEG-PLA NANOPARTICLES;
P-GLYCOPROTEIN;
COCULTURE MODEL;
CELLULAR UPTAKE;
FUNCTIONAL-CHARACTERIZATION;
D O I:
10.1016/j.ejpb.2014.03.012
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
During the research and development of new drugs directed at the central nervous system, there is a considerable attrition rate caused by their hampered access to the brain by the blood-brain barrier. Throughout the years, several in vitro models have been developed in an attempt to mimic critical functionalities of the blood-brain barrier and reliably predict the permeability of drug candidates. However, the current challenge lies in developing a model that retains fundamental blood-brain barrier characteristics and simultaneously remains compatible with the high throughput demands of pharmaceutical industries. This review firstly describes the roles of all elements of the neurovascular unit and their influence on drug brain penetration. In vitro models, including non-cell based and cell-based models, and in vivo models are herein presented, with a particular emphasis on their methodological aspects. Lastly, their contribution to the improvement of brain drug delivery strategies and drug transport across the blood-brain barrier is also discussed. (C) 2014 Elsevier B.V. All rights reserved.
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页码:409 / 432
页数:24
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