| Literature DB >> 25805413 |
Ugutz Unzueta1, María Virtudes Céspedes2, Esther Vázquez1, Neus Ferrer-Miralles1, Ramón Mangues3, Antonio Villaverde4.
Abstract
High resistance and recurrence rates, together with elevated drug clearance, compel the use of maximum-tolerated drug doses in cancer therapy, resulting in high-grade toxicities and limited clinical applicability. Promoting active drug accumulation in tumor tissues would minimize such issues and improve therapeutic outcomes. A new class of therapeutic drugs suitable for the task has emerged based on the concept of virus-mimetic nanocarriers, or 'artificial viruses'. Among the spectrum of materials under exploration in nanocarrier research, proteins offer unparalleled structural and functional versatility for designing virus-like molecular vehicles. By exhibiting 'smart' functions and biomimetic traits, protein-based nanocarriers will be a step ahead of the conventional drug-protein conjugates already in the clinic in ensuring efficient delivery of passenger antitumor drugs.Entities:
Keywords: biomaterials; biomimetics; drug delivery; protein engineering; protein nanoparticles; targeted therapy
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Year: 2015 PMID: 25805413 DOI: 10.1016/j.tibtech.2015.02.007
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536