VCAM-1 directed target-sensitive liposomes carrying CCR2 antagonists bind to activated endothelium and reduce adhesion and transmigration of monocytes

作者:Calin Manuela*; Stan Daniela; Schlesinger Martin; Simion Viorel; Deleanu Mariana; Constantinescu Cristina Ana; Gan Ana Maria; Pirvulescu Monica Madalina; Butoi Elena; Manduteanu Ileana; Bota Marian; Enachescu Marius; Borsig Lubor; Bendas Gerd; Simionescu Maya
来源:European Journal of Pharmaceutics and Biopharmaceutics, 2015, 89: 18-29.
DOI:10.1016/j.ejpb.2014.11.016

摘要

Chemokines are critically involved in the development of chronic inflammatory-associated diseases such as atherosclerosis. We hypothesized that targeted delivery of compounds to the surface of activated endothelial cells (EC) interferes with chemokine/receptor interaction and thereby efficiently blocks inflammation. We developed PEGylated target-sensitive liposomes (TSL) encapsulating a CCR2 antagonist (Teijin compound 1) coupled with a specific peptide recognized by endothelial VCAM-1 (Vp-TSL-Tj). TSL were characterized for size (by dynamic light scattering), the amount of peptide coupled at the liposomal surface and Teijin release (by HPLC). We report that Vp-TSL-Tj binds specifically to activated EC in vitro and in situ, release the entrapped Teijin and prevent the transmigration of monocytes through activated EC. This is the first evidence that nanocarriers which transport and release chemokine inhibitors at specific pathological sites can reduce chemokine-dependent inflammatory processes.

  • 出版日期2015-1