Possible strategies to cross the blood-brain barrier

被引:186
作者
Bellettato, Cinzia M. [1 ,2 ]
Scarpa, Maurizio [1 ,2 ,3 ,4 ]
机构
[1] Brains Brain Fdn, Padua, Italy
[2] MetabERN, European Reference Network Hereditary Metab Dis, Wiesbaden, Germany
[3] Helios Dr Horst Schmidt Kliniken, Ctr Rare Dis, Dept Child & Adolescent Med, Ludwig Erhard Str 100, D-65199 Wiesbaden, Germany
[4] Univ Padua, Dept Woman & Child Hlth, Padua, Italy
关键词
Mucopolysaccharidoses; Blood-brain barrier; Central nervous system; Drug delivery; CENTRAL-NERVOUS-SYSTEM; LYSOSOMAL STORAGE DISEASES; ENZYME-REPLACEMENT THERAPY; MUCOPOLYSACCHARIDOSIS TYPE-I; GENE-THERAPY; DRUG-DELIVERY; NANOPARTICLES; CELL; MANIFESTATIONS; MODEL;
D O I
10.1186/s13052-018-0563-0
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
The mucopolysaccharidoses (MPS) are a heterogeneous group of in-born metabolic conditions caused by genetic defects that result in the absence or severe deficiency of one of the lysosomal hydrolases responsible for the degradation of glycosaminoglycans (GAGs). Such enzyme deficiency causes accumulation of GAGs that begins in infancy and progressively worsens, often affecting several organs including the central nervous system (CNS) inducing mental retardation, progressive neurodegeneration, and premature death. Over the last years, enormous progress has been made in the treatment of many MPS types, and available treatments are efficacious for many of them. Nevertheless, treatment of MPS with CNS involvement is limited mostly because of delivery impediments related to the presence of the blood-brain barrier (BBB). This chapter presents an overview of the BBB and of the different strategies that have been developed to overcome the problem of drug transport at the BBB, assuring efficient delivery of therapeutic agents to the brain.
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页数:7
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