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Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR-conjugate in skin cancer in CD1 mice
Summary Background Indocyanine green (ICG) is a promising photosensitive agent for photodynamic therapy (PDT) of tumors. Encapsulating ICG dye in polymeric nanoparticles based on PEBBLE technology forming (ICG-PEBBLE) could improve the aqueous stability of the entrapped ICG molecules. The study obje...
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Published in: | Photodiagnosis and photodynamic therapy 2013-12, Vol.10 (4), p.446-459 |
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description | Summary Background Indocyanine green (ICG) is a promising photosensitive agent for photodynamic therapy (PDT) of tumors. Encapsulating ICG dye in polymeric nanoparticles based on PEBBLE technology forming (ICG-PEBBLE) could improve the aqueous stability of the entrapped ICG molecules. The study objective is to investigate the PDT effect of free ICG-PEBBLE and its Anti-EGFR conjugate. Methods Skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12- O -tetradecanoyl-phorbol-13-acetate (TPA) followed by a PDT protocol for four weeks. Results PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR decreased skin tumor sizes. Our findings revealed that the inflammatory mediators tumor necrosis factor (TNF-α), nitric oxide (NO), cycloxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), the angiogenic mediator vascular endothelial growth factor (VEGF), and proliferating cell nuclear antigen (PCNA) were decreased, while apoptosis, caspase-3 and histone acetylation were induced in tumor bearing groups after PDT using both of ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR. Conclusion The present study indicated the effectiveness of PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR as an inhibitor modality for tumor size, apoptosis, angiogenesis and tumor inflammation. The conjugating of ICG-PEBBLE to anti-EGFR was found to be more effective in inhibiting VEGF and in increasing caspase-3 compared to free ICG-PEBBLE, but there were no other preferential PDT efficacy. |
doi_str_mv | 10.1016/j.pdpdt.2013.03.013 |
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Encapsulating ICG dye in polymeric nanoparticles based on PEBBLE technology forming (ICG-PEBBLE) could improve the aqueous stability of the entrapped ICG molecules. The study objective is to investigate the PDT effect of free ICG-PEBBLE and its Anti-EGFR conjugate. Methods Skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12- O -tetradecanoyl-phorbol-13-acetate (TPA) followed by a PDT protocol for four weeks. Results PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR decreased skin tumor sizes. Our findings revealed that the inflammatory mediators tumor necrosis factor (TNF-α), nitric oxide (NO), cycloxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), the angiogenic mediator vascular endothelial growth factor (VEGF), and proliferating cell nuclear antigen (PCNA) were decreased, while apoptosis, caspase-3 and histone acetylation were induced in tumor bearing groups after PDT using both of ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR. Conclusion The present study indicated the effectiveness of PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR as an inhibitor modality for tumor size, apoptosis, angiogenesis and tumor inflammation. The conjugating of ICG-PEBBLE to anti-EGFR was found to be more effective in inhibiting VEGF and in increasing caspase-3 compared to free ICG-PEBBLE, but there were no other preferential PDT efficacy.</description><identifier>ISSN: 1572-1000</identifier><identifier>EISSN: 1873-1597</identifier><identifier>DOI: 10.1016/j.pdpdt.2013.03.013</identifier><identifier>PMID: 24284098</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>5-LOX ; Animals ; Antibodies, Monoclonal - therapeutic use ; Apoptosis ; Caspase-3 ; COX-2 ; Female ; Hematology, Oncology and Palliative Medicine ; Indocyanine green ; Indocyanine Green - administration & dosage ; Internal Medicine ; Mice ; Nanocapsules - chemistry ; Nanocapsules - therapeutic use ; Nanocapsules - ultrastructure ; Nitric oxide ; PCNA ; PEBBLE ; Photochemotherapy - methods ; Photodynamic therapy ; Photosensitizing Agents - therapeutic use ; Polymeric nanoparticles ; Polymers - chemistry ; Receptor, Epidermal Growth Factor - antagonists & inhibitors ; Receptor, Epidermal Growth Factor - metabolism ; Siloxanes - chemistry ; Skin cancer ; Skin Neoplasms - drug therapy ; Skin Neoplasms - metabolism ; Skin Neoplasms - pathology ; TNF-α ; Treatment Outcome ; VEGF</subject><ispartof>Photodiagnosis and photodynamic therapy, 2013-12, Vol.10 (4), p.446-459</ispartof><rights>Elsevier B.V.</rights><rights>2013 Elsevier B.V.</rights><rights>Copyright © 2013 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c414t-2c8d08656cd263e12d2b942b8efc7f178abca3ff1656693008628cdf60da74c13</citedby><cites>FETCH-LOGICAL-c414t-2c8d08656cd263e12d2b942b8efc7f178abca3ff1656693008628cdf60da74c13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24284098$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gamal-Eldeen, Amira M., M.Sc</creatorcontrib><creatorcontrib>El-Daly, Sherien M</creatorcontrib><creatorcontrib>Borai, Ibrahim H</creatorcontrib><creatorcontrib>Wafay, Hanaa A</creatorcontrib><creatorcontrib>Abdel-Ghaffar, Abdel-Rahman B</creatorcontrib><title>Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR-conjugate in skin cancer in CD1 mice</title><title>Photodiagnosis and photodynamic therapy</title><addtitle>Photodiagnosis Photodyn Ther</addtitle><description>Summary Background Indocyanine green (ICG) is a promising photosensitive agent for photodynamic therapy (PDT) of tumors. Encapsulating ICG dye in polymeric nanoparticles based on PEBBLE technology forming (ICG-PEBBLE) could improve the aqueous stability of the entrapped ICG molecules. The study objective is to investigate the PDT effect of free ICG-PEBBLE and its Anti-EGFR conjugate. Methods Skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12- O -tetradecanoyl-phorbol-13-acetate (TPA) followed by a PDT protocol for four weeks. Results PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR decreased skin tumor sizes. Our findings revealed that the inflammatory mediators tumor necrosis factor (TNF-α), nitric oxide (NO), cycloxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), the angiogenic mediator vascular endothelial growth factor (VEGF), and proliferating cell nuclear antigen (PCNA) were decreased, while apoptosis, caspase-3 and histone acetylation were induced in tumor bearing groups after PDT using both of ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR. Conclusion The present study indicated the effectiveness of PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR as an inhibitor modality for tumor size, apoptosis, angiogenesis and tumor inflammation. The conjugating of ICG-PEBBLE to anti-EGFR was found to be more effective in inhibiting VEGF and in increasing caspase-3 compared to free ICG-PEBBLE, but there were no other preferential PDT efficacy.</description><subject>5-LOX</subject><subject>Animals</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Apoptosis</subject><subject>Caspase-3</subject><subject>COX-2</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Indocyanine green</subject><subject>Indocyanine Green - administration & dosage</subject><subject>Internal Medicine</subject><subject>Mice</subject><subject>Nanocapsules - chemistry</subject><subject>Nanocapsules - therapeutic use</subject><subject>Nanocapsules - ultrastructure</subject><subject>Nitric oxide</subject><subject>PCNA</subject><subject>PEBBLE</subject><subject>Photochemotherapy - methods</subject><subject>Photodynamic therapy</subject><subject>Photosensitizing Agents - therapeutic use</subject><subject>Polymeric nanoparticles</subject><subject>Polymers - chemistry</subject><subject>Receptor, Epidermal Growth Factor - antagonists & inhibitors</subject><subject>Receptor, Epidermal Growth Factor - metabolism</subject><subject>Siloxanes - chemistry</subject><subject>Skin cancer</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - metabolism</subject><subject>Skin Neoplasms - pathology</subject><subject>TNF-α</subject><subject>Treatment Outcome</subject><subject>VEGF</subject><issn>1572-1000</issn><issn>1873-1597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFUstu1TAQjRCIPuALkFCWbHLx6-axAAld-kCqRFVgbfna49ZpYgfbQcpv9Is74RYWbJBG9rF8zox9ZoriDSUbSmj9vt9MZjJ5wwjlG4JB-bPimLYNr-i2a54j3jasooSQo-IkpZ4QLjoiXhZHTLBWkK49Lh6u70IOZvFqdLrMdxDVBHNGDNaCzmWwpfMm6EV556G8jQC-BJ-RN4HBu3IKwzJCRIlXPkwqonqAVCpv1oQuIsquOrs4v6l08P18qzKswnSPi1ZeQ1yPu8-0xEfAq-KFVUOC10_7afHj_Oz77rK6-nrxZffpqtKCilwx3RrS1ttaG1ZzoMywfSfYvgWrG0ubVu214tZSpNQdJ8hlrTa2JkY1QlN-Wrw75J1i-DlDynJ0ScMwKA9hTpKKmjW1qMVK5QeqjiGlCFZO0Y0qLpISuTZD9vJ3M-TaDEkwKEfV26cC834E81fzx30kfDgQAL_5y0GUSTtAP4yL6L00wf2nwMd_9Hpw3mk13MMCqQ9z9OigpDIxSeS3dR7WcaDoBhHdlj8Cz1-yxg</recordid><startdate>20131201</startdate><enddate>20131201</enddate><creator>Gamal-Eldeen, Amira M., M.Sc</creator><creator>El-Daly, Sherien M</creator><creator>Borai, Ibrahim H</creator><creator>Wafay, Hanaa A</creator><creator>Abdel-Ghaffar, Abdel-Rahman B</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20131201</creationdate><title>Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR-conjugate in skin cancer in CD1 mice</title><author>Gamal-Eldeen, Amira M., M.Sc ; El-Daly, Sherien M ; Borai, Ibrahim H ; Wafay, Hanaa A ; Abdel-Ghaffar, Abdel-Rahman B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c414t-2c8d08656cd263e12d2b942b8efc7f178abca3ff1656693008628cdf60da74c13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>5-LOX</topic><topic>Animals</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Apoptosis</topic><topic>Caspase-3</topic><topic>COX-2</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Indocyanine green</topic><topic>Indocyanine Green - administration & dosage</topic><topic>Internal Medicine</topic><topic>Mice</topic><topic>Nanocapsules - chemistry</topic><topic>Nanocapsules - therapeutic use</topic><topic>Nanocapsules - ultrastructure</topic><topic>Nitric oxide</topic><topic>PCNA</topic><topic>PEBBLE</topic><topic>Photochemotherapy - methods</topic><topic>Photodynamic therapy</topic><topic>Photosensitizing Agents - therapeutic use</topic><topic>Polymeric nanoparticles</topic><topic>Polymers - chemistry</topic><topic>Receptor, Epidermal Growth Factor - antagonists & inhibitors</topic><topic>Receptor, Epidermal Growth Factor - metabolism</topic><topic>Siloxanes - chemistry</topic><topic>Skin cancer</topic><topic>Skin Neoplasms - drug therapy</topic><topic>Skin Neoplasms - metabolism</topic><topic>Skin Neoplasms - pathology</topic><topic>TNF-α</topic><topic>Treatment Outcome</topic><topic>VEGF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gamal-Eldeen, Amira M., M.Sc</creatorcontrib><creatorcontrib>El-Daly, Sherien M</creatorcontrib><creatorcontrib>Borai, Ibrahim H</creatorcontrib><creatorcontrib>Wafay, Hanaa A</creatorcontrib><creatorcontrib>Abdel-Ghaffar, Abdel-Rahman B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Photodiagnosis and photodynamic therapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gamal-Eldeen, Amira M., M.Sc</au><au>El-Daly, Sherien M</au><au>Borai, Ibrahim H</au><au>Wafay, Hanaa A</au><au>Abdel-Ghaffar, Abdel-Rahman B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR-conjugate in skin cancer in CD1 mice</atitle><jtitle>Photodiagnosis and photodynamic therapy</jtitle><addtitle>Photodiagnosis Photodyn Ther</addtitle><date>2013-12-01</date><risdate>2013</risdate><volume>10</volume><issue>4</issue><spage>446</spage><epage>459</epage><pages>446-459</pages><issn>1572-1000</issn><eissn>1873-1597</eissn><abstract>Summary Background Indocyanine green (ICG) is a promising photosensitive agent for photodynamic therapy (PDT) of tumors. Encapsulating ICG dye in polymeric nanoparticles based on PEBBLE technology forming (ICG-PEBBLE) could improve the aqueous stability of the entrapped ICG molecules. The study objective is to investigate the PDT effect of free ICG-PEBBLE and its Anti-EGFR conjugate. Methods Skin squamous cell carcinoma was induced in CD1 mice by dimethylbenzanthracene (DMBA) and 12- O -tetradecanoyl-phorbol-13-acetate (TPA) followed by a PDT protocol for four weeks. Results PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR decreased skin tumor sizes. Our findings revealed that the inflammatory mediators tumor necrosis factor (TNF-α), nitric oxide (NO), cycloxygenase-2 (COX-2) and 5-lipoxygenase (5-LOX), the angiogenic mediator vascular endothelial growth factor (VEGF), and proliferating cell nuclear antigen (PCNA) were decreased, while apoptosis, caspase-3 and histone acetylation were induced in tumor bearing groups after PDT using both of ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR. Conclusion The present study indicated the effectiveness of PDT using ICG-PEBBLE or ICG-PEBBLE-Anti-EGFR as an inhibitor modality for tumor size, apoptosis, angiogenesis and tumor inflammation. The conjugating of ICG-PEBBLE to anti-EGFR was found to be more effective in inhibiting VEGF and in increasing caspase-3 compared to free ICG-PEBBLE, but there were no other preferential PDT efficacy.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24284098</pmid><doi>10.1016/j.pdpdt.2013.03.013</doi><tpages>14</tpages></addata></record> |
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subjects | 5-LOX Animals Antibodies, Monoclonal - therapeutic use Apoptosis Caspase-3 COX-2 Female Hematology, Oncology and Palliative Medicine Indocyanine green Indocyanine Green - administration & dosage Internal Medicine Mice Nanocapsules - chemistry Nanocapsules - therapeutic use Nanocapsules - ultrastructure Nitric oxide PCNA PEBBLE Photochemotherapy - methods Photodynamic therapy Photosensitizing Agents - therapeutic use Polymeric nanoparticles Polymers - chemistry Receptor, Epidermal Growth Factor - antagonists & inhibitors Receptor, Epidermal Growth Factor - metabolism Siloxanes - chemistry Skin cancer Skin Neoplasms - drug therapy Skin Neoplasms - metabolism Skin Neoplasms - pathology TNF-α Treatment Outcome VEGF |
title | Photodynamic therapeutic effect of indocyanine green entrapped in polymeric nanoparticles and their anti-EGFR-conjugate in skin cancer in CD1 mice |
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