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Development of an apolipoprotein E mimetic peptide-lipid conjugate for efficient brain delivery of liposomes
by
Kato, Naoya
, Matsumoto, Makoto
, Arima, Hidetoshi
, Yamada, Sakura
, Suzuki, Rino
, Iida, Yoshiki
, Fumoto, Shintaro
, Mukai, Hidefumi
, Kawakami, Shigeru
in
Animals
/ Apolipoprotein E mimetic peptide
/ Apolipoproteins
/ Apolipoproteins - pharmacology
/ Apolipoproteins E
/ blood-brain barrier
/ Brain
/ brain-targeting
/ Drug Delivery Systems
/ Endothelial Cells
/ Humans
/ Lipids
/ Lipids - pharmacology
/ liposomes
/ Liposomes - pharmacology
/ Mice
/ Peptides
/ Peptides - pharmacology
/ Permeability
/ Polyethylene glycol
/ Polyethylene Glycols - pharmacology
/ tissue clearing
2023
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Development of an apolipoprotein E mimetic peptide-lipid conjugate for efficient brain delivery of liposomes
by
Kato, Naoya
, Matsumoto, Makoto
, Arima, Hidetoshi
, Yamada, Sakura
, Suzuki, Rino
, Iida, Yoshiki
, Fumoto, Shintaro
, Mukai, Hidefumi
, Kawakami, Shigeru
in
Animals
/ Apolipoprotein E mimetic peptide
/ Apolipoproteins
/ Apolipoproteins - pharmacology
/ Apolipoproteins E
/ blood-brain barrier
/ Brain
/ brain-targeting
/ Drug Delivery Systems
/ Endothelial Cells
/ Humans
/ Lipids
/ Lipids - pharmacology
/ liposomes
/ Liposomes - pharmacology
/ Mice
/ Peptides
/ Peptides - pharmacology
/ Permeability
/ Polyethylene glycol
/ Polyethylene Glycols - pharmacology
/ tissue clearing
2023
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Development of an apolipoprotein E mimetic peptide-lipid conjugate for efficient brain delivery of liposomes
by
Kato, Naoya
, Matsumoto, Makoto
, Arima, Hidetoshi
, Yamada, Sakura
, Suzuki, Rino
, Iida, Yoshiki
, Fumoto, Shintaro
, Mukai, Hidefumi
, Kawakami, Shigeru
in
Animals
/ Apolipoprotein E mimetic peptide
/ Apolipoproteins
/ Apolipoproteins - pharmacology
/ Apolipoproteins E
/ blood-brain barrier
/ Brain
/ brain-targeting
/ Drug Delivery Systems
/ Endothelial Cells
/ Humans
/ Lipids
/ Lipids - pharmacology
/ liposomes
/ Liposomes - pharmacology
/ Mice
/ Peptides
/ Peptides - pharmacology
/ Permeability
/ Polyethylene glycol
/ Polyethylene Glycols - pharmacology
/ tissue clearing
2023
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Development of an apolipoprotein E mimetic peptide-lipid conjugate for efficient brain delivery of liposomes
Journal Article
Development of an apolipoprotein E mimetic peptide-lipid conjugate for efficient brain delivery of liposomes
2023
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Overview
Liposomes are versatile carriers that can encapsulate various drugs; however, for delivery to the brain, they must be modified with a targeting ligand or other modifications to provide blood-brain barrier (BBB) permeability, while avoiding rapid clearance by reticuloendothelial systems through polyethylene glycol (PEG) modification. BBB-penetrating peptides act as brain-targeting ligands. In this study, to achieve efficient brain delivery of liposomes, we screened the functionality of eight BBB-penetrating peptides reported previously, based on high-throughput quantitative evaluation methods with in vitro BBB permeability evaluation system using Transwell, in situ brain perfusion system, and others. For apolipoprotein E mimetic tandem dimer peptide (ApoEdp), which showed the best brain-targeting and BBB permeability in the comparative evaluation of eight peptides, its lipid conjugate with serine-glycine (SG)
5
spacer (ApoEdp-SG-lipid) was newly synthesized and ApoEdp-modified PEGylated liposomes were prepared. ApoEdp-modified PEGylated liposomes were effectively associated with human brain capillary endothelial cells via the ApoEdp sequence and permeated the membrane in an in vitro BBB model. Moreover, ApoEdp-modified PEGylated liposomes accumulated in the brain 3.9-fold higher than PEGylated liposomes in mice. In addition, the ability of ApoEdp-modified PEGylated liposomes to localize beyond the BBB into the brain parenchyma in mice was demonstrated via three-dimensional imaging with tissue clearing. These results suggest that ApoEdp-SG-lipid modification is an effective approach for endowing PEGylated liposomes with the brain-targeting ability and BBB permeability.
Publisher
Taylor & Francis,Taylor & Francis Ltd,Taylor & Francis Group
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