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Enhanced immunocompatibility of ligand-targeted liposomes by attenuating natural IgM absorption.


ABSTRACT: Targeting ligands are anticipated to facilitate the precise delivery of therapeutic agents to diseased tissues; however, they may also severely affect the interaction of nanocarriers with plasma proteins. Here, we study the immunocompatibility of brain-targeted liposomes, which inversely correlates with absorbed natural IgM. Modification of long, stable positively charged peptide ligands on liposomes is inclined to absorb natural IgM, leading to rapid clearance and enhanced immunogenicity. Small peptidomimetic D8 developed by computer-aided peptide design exhibits improved immunocompatibility by attenuating natural IgM absorption. The present study highlights the effects of peptide ligands on the formed protein corona and in vivo fate of liposomes. Stable positively charged peptide ligands

SUBMITTER: Guan J 

PROVIDER: S-EPMC6065320 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

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