| Literature DB >> 30165574 |
Iwona Cicha1, Cédric Chauvierre2, Isabelle Texier3, Claudia Cabella4, Josbert M Metselaar5, János Szebeni6, László Dézsi6, Christoph Alexiou1, François Rouzet2,7, Gert Storm8,9, Erik Stroes10, Donald Bruce11, Neil MacRitchie12, Pasquale Maffia12,13,14, Didier Letourneur2.
Abstract
Cardiovascular diseases (CVD) account for nearly half of all deaths in Europe and almost 30% of global deaths. Despite the improved clinical management, cardiovascular mortality is predicted to rise in the next decades due to the increasing impact of aging, obesity, and diabetes. The goal of emerging cardiovascular nanomedicine is to reduce the burden of CVD using nanoscale medical products and devices. However, the development of novel multicomponent nano-sized products poses multiple technical, ethical, and regulatory challenges, which often obstruct their road to successful approval and use in clinical practice. This review discusses the rational design of nanoparticles, including safety considerations and regulatory issues, and highlights the steps needed to achieve efficient clinical translation of promising nanomedicinal products for cardiovascular applications.Entities:
Mesh:
Year: 2018 PMID: 30165574 PMCID: PMC6198738 DOI: 10.1093/cvr/cvy219
Source DB: PubMed Journal: Cardiovasc Res ISSN: 0008-6363 Impact factor: 10.787