| Literature DB >> 25698504 |
Hugo Peluffo1, Ugutz Unzueta2, María Luciana Negro-Demontel1, Zhikun Xu2, Esther Váquez2, Neus Ferrer-Miralles2, Antonio Villaverde2.
Abstract
The increasing incidence of diseases affecting the central nervous system (CNS) demands the urgent development of efficient drugs. While many of these medicines are already available, the Blood Brain Barrier and to a lesser extent, the Blood Spinal Cord Barrier pose physical and biological limitations to their diffusion to reach target tissues. Therefore, efforts are needed not only to address drug development but specially to design suitable vehicles for delivery into the CNS through systemic administration. In the context of the functional and structural versatility of proteins, recent advances in their biological fabrication and a better comprehension of the physiology of the CNS offer a plethora of opportunities for the construction and tailoring of plain nanoconjugates and of more complex nanosized vehicles able to cross these barriers. We revise here how the engineering of functional proteins offers drug delivery tools for specific CNS diseases and more transversally, how proteins can be engineered into smart nanoparticles or 'artificial viruses' to afford therapeutic requirements through alternative administration routes.Entities:
Keywords: Artificial viruses; BBB; Drug delivery; Gene therapy; Nanoparticles; Protein engineering; Recombinant proteins
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Year: 2015 PMID: 25698504 DOI: 10.1016/j.biotechadv.2015.02.004
Source DB: PubMed Journal: Biotechnol Adv ISSN: 0734-9750 Impact factor: 14.227