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Ligand-based targeted delivery of a peptide modified nanocarrier to endothelial cells in adipose tissue

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Please use this identifier to cite or link to this item:http://hdl.handle.net/2115/44240

Title: Ligand-based targeted delivery of a peptide modified nanocarrier to endothelial cells in adipose tissue
Authors: Hossen, Md. Nazir Browse this author
Kajimoto, Kazuaki Browse this author
Akita, Hidetaka Browse this author
Hyodo, Mamoru Browse this author
Ishitsuka, Taichi Browse this author
Harashima, Hideyoshi Browse this author
Keywords: Adipose tissue
Ligand targeting
Peptide modified nanocarrier
Endocytosis
Intracellular uptake
Issue Date: 15-Oct-2010
Publisher: Elsevier B.V.
Journal Title: Journal of Controlled Release
Volume: 147
Issue: 2
Start Page: 261
End Page: 268
Publisher DOI: 10.1016/j.jconrel.2010.07.100
PMID: 20647023
Abstract: Ligand-based targeted delivery is an emerging platform in nanomedicine. We report herein on a peptide modified nanocarrier for a ligand-based targeted delivery system. The liposomal surface of the carrier was first modified with a linear peptide, followed by an adipose tissue-specific circular peptide (KGGRAKD) via a polyethylene glycol (PEG) spacer. To evaluate the specificity of the carrier, we purified primary cells from the endothelium of adipose tissue. The liposomes bound only to isolated primary cultured endothelial cells derived from inguinal adipose tissue (pcEC-IWAT) and not to other endothelial cell lines, such as MBEC-4 and MFLM-4. Cellular uptake was confirmed both qualitatively and quantitatively by confocal laser scanning microscopy (CLSM) and flow cytometry. The mechanism for the intracellular uptake of tPep-PEG-LPs into pcEC-IWAT, as evidenced by three independent experiments, involves saturation of receptor binding sites by excess free peptide, the blocking of receptors by an anti-prohibitin antibody and low temperature (4℃) experiments, resulting in the inhibition of up-take of tPep-PEG-LPs into pcEC-IWAT, suggesting that receptor mediated endocytosis largely contributed to the observed cellular uptake. A co-localization study using double labeled modified liposomes (lipid membrane: NBD-DOPE and aqueous phase: rhodamine) indicated that a predominant part of tPep-PEG-LPs was found without co-localization with lysosomes and retained their intactness. The selective delivery of tPep-PEG-LPs to endothelial cells in adipose tissue represents a potential approach for the design of diverse nanocarrier-based targeted delivery systems for targeting the vasculature in adipose tissue.
Type: article (author version)
URI: http://hdl.handle.net/2115/44240
Appears in Collections:薬学研究院 (Faculty of Pharmaceutical Sciences) > 雑誌発表論文等 (Peer-reviewed Journal Articles, etc)

Submitter: 梶本 和昭

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