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Review
. 2018 Nov 16;44(Suppl 2):131.
doi: 10.1186/s13052-018-0563-0.

Possible strategies to cross the blood-brain barrier

Affiliations
Review

Possible strategies to cross the blood-brain barrier

Cinzia M Bellettato et al. Ital J Pediatr. .

Abstract

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.

Keywords: Blood–brain barrier; Central nervous system; Drug delivery; Mucopolysaccharidoses.

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Competing interests

The authors declare that they have no competing interests.

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Figures

Fig. 1
Fig. 1
Angioarchitecture of the blood–brain barrier and techniques for brain drug delivery

References

    1. Lampe C, Bellettato CM, Karabul N, Scarpa M. Mucopolysaccharidoses and other lysosomal storage diseases. Rheum Dis Clin N Am. 2013;39(2):431–455. doi: 10.1016/j.rdc.2013.03.004. - DOI - PubMed
    1. Rousselle C, Clair P, Lefauconnier JM, Kaczorek M, Scherrmann JM, Temsamani J. New advances in the transport of doxorubicin through the blood–brain barrier by a peptide vector-mediated strategy. Mol Pharmacol. 2000;57(4):679–686. doi: 10.1124/mol.57.4.679. - DOI - PubMed
    1. Tosi G, Bortot B, Ruozi B, Dolcetta D, Vandelli MA, Forni F, et al. Potential use of polymeric nanoparticles for drug delivery across the blood–brain barrier. Curr Med Chem. 2013;20(17):2212–2225. doi: 10.2174/0929867311320170006. - DOI - PubMed
    1. Sanchez-Covarrubias L, Slosky LM, Thompson BJ, Davis TP, Ronaldson PT. Transporters at CNS barrier sites: obstacles or opportunities for drug delivery? Curr Pharm Des. 2014;20(10):1422–1449. doi: 10.2174/13816128113199990463. - DOI - PMC - PubMed
    1. Begley DJ, Pontikis CC, Scarpa M. Lysosomal storage diseases and the blood–brain barrier. Curr Pharm Des. 2008;14(16):1566–1580. doi: 10.2174/138161208784705504. - DOI - PubMed

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