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  4. PH-Responsive Nanophotosensitizer for an Enhanced Photodynamic Therapy of Colorectal Cancer Overexpressing EGFR
 
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PH-Responsive Nanophotosensitizer for an Enhanced Photodynamic Therapy of Colorectal Cancer Overexpressing EGFR

Journal
Molecular Pharmaceutics
Journal Volume
15
Journal Issue
4
Pages
1432-1444
Date Issued
2018
Author(s)
Chu W.-Y.
Tsai M.-H.
Peng C.-L.
Shih Y.-H.
Luo T.-Y.
Yang S.-J.
MING-JIUM SHIEH  
DOI
10.1021/acs.molpharmaceut.7b00925
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85044717281&doi=10.1021%2facs.molpharmaceut.7b00925&partnerID=40&md5=fecfc8cdc564efee4dc3328579fd8b0d
https://scholars.lib.ntu.edu.tw/handle/123456789/465715
Abstract
Photodynamic therapy (PDT) has been shown to kill cancer cells and improve survival and quality of life in cancer patients, and numerous new approaches have been considered for maximizing the efficacy of PDT. In this study, a new multifunctional nanophotosensitizer Ce6/GE11- (pH) micelle was developed to target epidermal growth factor receptor (EGFR) overexpressing colorectal cancer (CRC) cells. This nanophotosensitizer was synthesized using a micelle comprising pH-responsive copolymers (PEGMA-PDPA), biodegradable copolymers (mPEG-PCL), and maleimide-modified biodegradable copolymers (Mal-PEG-PCL) to entrap the potential hydrophobic photosensitizer chlorin e6 (Ce6) and to present EGFR-targeting peptides (GE11) on its surface. In the presence of Ce6/GE11- (pH) micelles, Ce6 uptake by EGFR-overexpressing CRC cells significantly increased due to GE11 specificity. Moreover, Ce6 was released from Ce6/GE11- (pH) micelles in tumor environments, leading to improved elimination of cancer cells in PDT. These results indicate enhanced efficacy of PDT using Ce6/GE11- (pH) micelle, which is a powerful nanophotosensitizer with high potential for application to future PDT for CRC. ? 2018 American Chemical Society.
Subjects
Ce6; epidermal growth factor receptor; micelle; Photodynamic therapy
SDGs

[SDGs]SDG3

Other Subjects
copolymer; epidermal growth factor receptor; maleimide; photosensitizing agent; singlet oxygen; epidermal growth factor receptor; nanoparticle; peptide; photosensitizing agent; polymer; absorption spectroscopy; animal experiment; animal model; animal tissue; Article; cell proliferation; cell viability; chemical structure; colorectal cancer; controlled study; critical micelle concentration; cytotoxicity; drug synthesis; electron spin resonance; ex vivo study; female; fluorescence spectroscopy; immunohistochemistry; in vitro study; in vivo study; incubation time; miscibility; molecular weight; mouse; MTT assay; nonhuman; pH; photocytotoxicity; photodynamic therapy; priority journal; proton nuclear magnetic resonance; proton transport; surface property; transmission electron microscopy; tumor microenvironment; tumor volume; animal; chemistry; colorectal tumor; HCT 116 cell line; human; metabolism; micelle; pH; tumor cell line; Animals; Cell Line, Tumor; Colorectal Neoplasms; ErbB Receptors; HCT116 Cells; Humans; Hydrogen-Ion Concentration; Mice; Micelles; Nanoparticles; Peptides; Photosensitizing Agents; Polymers
Publisher
American Chemical Society
Type
journal article

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