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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/41828
Title: Polymer-lipid-PEG hybrid nanoparticles as photosensitizer carrier for photodynamic therapy
Authors: Sasivimon Pramual
Kriengsak Lirdprapamongkol
Jisnuson Svasti
Magnus Bergkvist
Valérie Jouan-Hureaux
Philippe Arnoux
Céline Frochot
Muriel Barberi-Heyob
Nuttawee Niamsiri
Mahidol University
Chulabhorn Research Institute
University at Albany State University of New York
CRAN Centre de Recherche en Automatique de Nancy
Université de Lorraine
Keywords: Biochemistry, Genetics and Molecular Biology;Health Professions
Issue Date: 1-Aug-2017
Citation: Journal of Photochemistry and Photobiology B: Biology. Vol.173, (2017), 12-22
Abstract: © 2017 Elsevier B.V. Polymer-lipid-PEG hybrid nanoparticles were investigated as carriers for the photosensitizer (PS), 5,10,15,20-Tetrakis(4-hydroxy-phenyl)-21H,23H-porphine (pTHPP) for use in photodynamic therapy (PDT). A self-assembled nanoprecipitation technique was used for preparing two types of core polymers poly(D,L-lactide-co-glycolide) (PLGA) and poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) with lipid-PEG as stabilizer. The resulting nanoparticles had an average particle size of 88.5 ± 3.4 nm for PLGA and 215.0 ± 6.3 nm for PHBV. Both nanoparticles exhibited a core-shell structure under TEM with high zeta potential and loading efficiency. X-ray powder diffraction analysis showed that the encapsulated pTHPP molecules in polymeric nanoparticles no longer had peaks of free pTHPP in the crystalline state. The pTHPP molecules encapsulated inside the polymeric core demonstrated improved photophysical properties in terms of singlet oxygen generation and cellular uptake rate in a FTC-133 human thyroid carcinoma cell line, compared to non-encapsulated pTHPP. The pTHPP-loaded polymer-lipid-PEG nanoparticles showed better in vitro phototoxicity compared to free pTHPP, in both time- and concentration-dependent manners. Overall, this study provides detailed analysis of the photophysical properties of pTHPP molecules when entrapped within either PLGA or PHBV nanoparticle cores, and demonstrates the effectiveness of these systems for delivery of photosensitizers. The two polymeric systems may have different potential benefits, when used with cancer cells. For instance, the pTHPP-loaded PLGA system requires only a short time to show a PDT effect and may be suitable for topical PDT, while the delayed photo-induced cytotoxic effect of the pTHPP-loaded PHBV system may be more suitable for cancer solid tumors. Hence, both pTHPP-encapsulated polymer-lipid-PEG nanoparticles can be considered promising delivery systems for PDT cancer treatment.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019839532&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/41828
ISSN: 18732682
10111344
Appears in Collections:Scopus 2016-2017

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