Biomimetic proteolipid vesicles for targeting inflamed tissues

• Published in: Nature materials Vol. 15; no. 9; pp. 1037 - 1046
• Main Authors: Molinaro, R., Corbo, C., Martinez, J. O., Taraballi, F., Evangelopoulos, M., Minardi, S., Yazdi, I. K., Zhao, P., De Rosa, E., Sherman, M. B., De Vita, A., Toledano Furman, N. E., Wang, X., Parodi, A., Tasciotti, E.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.09.2016; Nature Publishing Group
• Subjects: 639/925/352/152; 692/308/575; Biomaterials; Biomimetics; Carriers; Condensed Matter Physics; Dexamethasone; Drug delivery systems; Formulations; Leukocytes; Lipids; Materials Science; Mathematical models; Nanoparticles; Nanotechnology; Optical and Electronic Materials; Physicochemical properties; Proteins; Strategy; Vesicles; Walls
• ISSN: 1476-1122; 1476-4660
• DOI: 10.1038/nmat4644

A multitude of micro- and nanoparticles have been developed to improve the delivery of systemically administered pharmaceuticals, which are subject to a number of biological barriers that limit their optimal biodistribution. Bioinspired drug-delivery carriers formulated by bottom-up or top-down strategies have emerged as an alternative approach to evade the mononuclear phagocytic system and facilitate transport across the endothelial vessel wall. Here, we describe a method that leverages the advantages of bottom-up and top-down strategies to incorporate proteins derived from the leukocyte plasma membrane into lipid nanoparticles. The resulting proteolipid vesicles—which we refer to as leukosomes—retained the versatility and physicochemical properties typical of liposomal formulations, preferentially targeted inflamed vasculature, enabled the selective and effective delivery of dexamethasone to inflamed tissues, and reduced phlogosis in a localized model of inflammation. Lipid nanoparticles incorporating proteins from the leukocyte plasma membrane retain the properties of liposomal formulations and enable delivery of drugs to inflamed tissues.