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Design Principles for Peptide‐Amphiphile‐Induced Liposomal Receptor‐Targeting with Intracellular Thermosensitivity
Author(s) -
Shroff Kamlesh,
Liu Dalong,
Aravalli Rajagopal N.,
Forster Colleen L.,
Pengo Thomas,
Sanders Mark A.,
Ebbini Emad S.,
Kokkoli Efrosini
Publication year - 2016
Publication title -
chemnanomat
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.947
H-Index - 32
ISSN - 2199-692X
DOI - 10.1002/cnma.201500138
Subject(s) - liposome , calcein , peptide , endocytosis , amphiphile , in vivo , receptor , internalization , chemistry , intracellular , in vitro , biophysics , biochemistry , biology , membrane , microbiology and biotechnology , organic chemistry , copolymer , polymer
Thermosensitive stealth liposomes were created by mixing lipids and PEGylated lipids with single‐tail peptide‐amphiphiles. We demonstrated for the first time that the peptide‐amphiphiles provided receptor‐specific binding and cell internalization while inducing the thermosensitive properties of the liposomes. The formulations were stable at 37 °C in the presence of serum, with faster release of their encapsulated load at 41 °C compared to stealth liposomes without the peptide‐amphiphiles or commercially available thermosensitive stealth liposomes. The thermosensitive properties of our formulation were also examined in vivo. Preliminary work showed increased release of the encapsulated calcein after heating the liver of a mouse with a dual‐mode ultrasound array system for 20 s to 41–43 °C, 4 h after receiving tail vein injections of the liposomes, compared to a mouse that received the liposomal injections but no heating. The receptor‐targeting ability of the peptide‐functionalized liposomes was examined in vitro with MDA‐MB‐231 breast cancer cells. Our liposomes outperformed the other formulations as they showed specific binding, receptor‐mediated endocytosis, and increased intracellular temperature‐triggered release of encapsulated calcein.