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Liposomal IR-780 as a Highly Stable Nanotheranostic Agent for Improved Photothermal/Photodynamic Therapy of Brain Tumors by Convection-Enhanced Delivery
As a hydrophobic photosensitizer, IR-780 suffers from poor water solubility and low photostability under near infrared (NIR) light, which severely limits its use during successive NIR laser-assisted photothermal/photodynamic therapy (PTT/PDT). To solve this problem, we fabricate cationic IR-780-load...
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Published in: | Cancers 2021-07, Vol.13 (15), p.3690 |
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description | As a hydrophobic photosensitizer, IR-780 suffers from poor water solubility and low photostability under near infrared (NIR) light, which severely limits its use during successive NIR laser-assisted photothermal/photodynamic therapy (PTT/PDT). To solve this problem, we fabricate cationic IR-780-loaded liposomes (ILs) by entrapping IR-780 within the lipid bilayer of liposomes. We demonstrate enhanced photostability of IR-780 in ILs with well-preserved photothermal response after three repeated NIR laser exposures, in contrast to the rapid decomposition of free IR-780. The cationic nature of ILs promotes fast endocytosis of liposomal IR-780 by U87MG human glioblastoma cells within 30 min. For PTT/PDT in vitro, ILs treatment plus NIR laser irradiation leads to overexpression of heat shock protein 70 and generation of intracellular reactive oxygen species by U87MG cells, resulting in enhanced cytotoxicity and higher cell apoptosis rate. Using intracranial glioma xenograft in nude mice and administration of ILs by convection enhanced delivery (CED) to overcome blood-brain barrier, liposomal IR-780 could be specifically delivered to the brain tumor, as demonstrated from fluorescence imaging. By providing a highly stable liposomal IR-780, ILs significantly improved anti-cancer efficacy in glioma treatment, as revealed from various diagnostic imaging tools and histological examination. Overall, CED of ILs plus successive laser-assisted PTT/PDT may be an alternative approach for treating brain tumor, which can retard glioma growth and prolong animal survival times from orthotopic brain tumor models. |
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To solve this problem, we fabricate cationic IR-780-loaded liposomes (ILs) by entrapping IR-780 within the lipid bilayer of liposomes. We demonstrate enhanced photostability of IR-780 in ILs with well-preserved photothermal response after three repeated NIR laser exposures, in contrast to the rapid decomposition of free IR-780. The cationic nature of ILs promotes fast endocytosis of liposomal IR-780 by U87MG human glioblastoma cells within 30 min. For PTT/PDT in vitro, ILs treatment plus NIR laser irradiation leads to overexpression of heat shock protein 70 and generation of intracellular reactive oxygen species by U87MG cells, resulting in enhanced cytotoxicity and higher cell apoptosis rate. Using intracranial glioma xenograft in nude mice and administration of ILs by convection enhanced delivery (CED) to overcome blood-brain barrier, liposomal IR-780 could be specifically delivered to the brain tumor, as demonstrated from fluorescence imaging. By providing a highly stable liposomal IR-780, ILs significantly improved anti-cancer efficacy in glioma treatment, as revealed from various diagnostic imaging tools and histological examination. Overall, CED of ILs plus successive laser-assisted PTT/PDT may be an alternative approach for treating brain tumor, which can retard glioma growth and prolong animal survival times from orthotopic brain tumor models.</description><identifier>ISSN: 2072-6694</identifier><identifier>EISSN: 2072-6694</identifier><identifier>DOI: 10.3390/cancers13153690</identifier><identifier>PMID: 34359590</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Apoptosis ; Blood-brain barrier ; Brain cancer ; Brain tumors ; Cancer therapies ; Convection ; Cytotoxicity ; Efficiency ; Endocytosis ; Flow velocity ; Glioblastoma ; Glioblastoma cells ; Glioma ; Heat ; Heat shock proteins ; Hsp70 protein ; Hydrophobicity ; Intracellular ; Laboratory animals ; Lasers ; Light ; Lipid bilayers ; Lipids ; Liposomes ; Nanomaterials ; Neuroimaging ; Photodynamic therapy ; Reactive oxygen species ; Tumors ; Xenografts</subject><ispartof>Cancers, 2021-07, Vol.13 (15), p.3690</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). 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To solve this problem, we fabricate cationic IR-780-loaded liposomes (ILs) by entrapping IR-780 within the lipid bilayer of liposomes. We demonstrate enhanced photostability of IR-780 in ILs with well-preserved photothermal response after three repeated NIR laser exposures, in contrast to the rapid decomposition of free IR-780. The cationic nature of ILs promotes fast endocytosis of liposomal IR-780 by U87MG human glioblastoma cells within 30 min. For PTT/PDT in vitro, ILs treatment plus NIR laser irradiation leads to overexpression of heat shock protein 70 and generation of intracellular reactive oxygen species by U87MG cells, resulting in enhanced cytotoxicity and higher cell apoptosis rate. Using intracranial glioma xenograft in nude mice and administration of ILs by convection enhanced delivery (CED) to overcome blood-brain barrier, liposomal IR-780 could be specifically delivered to the brain tumor, as demonstrated from fluorescence imaging. By providing a highly stable liposomal IR-780, ILs significantly improved anti-cancer efficacy in glioma treatment, as revealed from various diagnostic imaging tools and histological examination. Overall, CED of ILs plus successive laser-assisted PTT/PDT may be an alternative approach for treating brain tumor, which can retard glioma growth and prolong animal survival times from orthotopic brain tumor models.</description><subject>Apoptosis</subject><subject>Blood-brain barrier</subject><subject>Brain cancer</subject><subject>Brain tumors</subject><subject>Cancer therapies</subject><subject>Convection</subject><subject>Cytotoxicity</subject><subject>Efficiency</subject><subject>Endocytosis</subject><subject>Flow velocity</subject><subject>Glioblastoma</subject><subject>Glioblastoma cells</subject><subject>Glioma</subject><subject>Heat</subject><subject>Heat shock proteins</subject><subject>Hsp70 protein</subject><subject>Hydrophobicity</subject><subject>Intracellular</subject><subject>Laboratory animals</subject><subject>Lasers</subject><subject>Light</subject><subject>Lipid bilayers</subject><subject>Lipids</subject><subject>Liposomes</subject><subject>Nanomaterials</subject><subject>Neuroimaging</subject><subject>Photodynamic therapy</subject><subject>Reactive oxygen species</subject><subject>Tumors</subject><subject>Xenografts</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkcFu1DAQhi0EolXpmaslLlzC2rEd2xekspR2pRUgWM6W49gbV4kd7GSlvAmP26StEHQuM6P55tf8GgDeYvSBEIk2RgdjU8YEM1JJ9AKcl4iXRVVJ-vKf-gxc5nyHliAE84q_BmeEEiaZROfgz94PMcded3D3o-ACQZ2hhrf-2HYz_DnqurPwqw5xbG1aUh69gVdHG0boYoK7fkjxZBv4vY3jA7MobR6aZg66X-DDujjMMDr4KWkf4GHqY8qwnuE2hpM1o4-huA7t6qaBn23nTzbNb8Arp7tsL5_yBfj15fqwvS32325226t9YYgUY2EFxw0SsjG4wo2ra4y0M05bwSixTW0IYdyJRppSUCSppthUjmJecy1qTsgF-PioO0x1bxuzOEu6U0PyvU6zitqr_yfBt-oYT0oQylC1Crx_Ekjx92TzqHqfje06HWycsioZk5QQztCCvnuG3sUphcXeSgleypKXC7V5pEyKOSfr_h6DkVofr549ntwDZS2jxQ</recordid><startdate>20210722</startdate><enddate>20210722</enddate><creator>Lu, Yu-Jen</creator><creator>S., Anilkumar T.</creator><creator>Chuang, Chi-Cheng</creator><creator>Chen, Jyh-Ping</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6527-4801</orcidid><orcidid>https://orcid.org/0000-0003-1898-7264</orcidid><orcidid>https://orcid.org/0000-0001-9670-7550</orcidid></search><sort><creationdate>20210722</creationdate><title>Liposomal IR-780 as a Highly Stable Nanotheranostic Agent for Improved Photothermal/Photodynamic Therapy of Brain Tumors by Convection-Enhanced Delivery</title><author>Lu, Yu-Jen ; S., Anilkumar T. ; Chuang, Chi-Cheng ; Chen, Jyh-Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c398t-e871d089dc161dfbb10afcfae8543edbc3357f8d9c284094a41c6f417b7a8b733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Apoptosis</topic><topic>Blood-brain barrier</topic><topic>Brain cancer</topic><topic>Brain tumors</topic><topic>Cancer therapies</topic><topic>Convection</topic><topic>Cytotoxicity</topic><topic>Efficiency</topic><topic>Endocytosis</topic><topic>Flow velocity</topic><topic>Glioblastoma</topic><topic>Glioblastoma cells</topic><topic>Glioma</topic><topic>Heat</topic><topic>Heat shock proteins</topic><topic>Hsp70 protein</topic><topic>Hydrophobicity</topic><topic>Intracellular</topic><topic>Laboratory animals</topic><topic>Lasers</topic><topic>Light</topic><topic>Lipid bilayers</topic><topic>Lipids</topic><topic>Liposomes</topic><topic>Nanomaterials</topic><topic>Neuroimaging</topic><topic>Photodynamic therapy</topic><topic>Reactive oxygen species</topic><topic>Tumors</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lu, Yu-Jen</creatorcontrib><creatorcontrib>S., Anilkumar T.</creatorcontrib><creatorcontrib>Chuang, Chi-Cheng</creatorcontrib><creatorcontrib>Chen, Jyh-Ping</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lu, Yu-Jen</au><au>S., Anilkumar T.</au><au>Chuang, Chi-Cheng</au><au>Chen, Jyh-Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liposomal IR-780 as a Highly Stable Nanotheranostic Agent for Improved Photothermal/Photodynamic Therapy of Brain Tumors by Convection-Enhanced Delivery</atitle><jtitle>Cancers</jtitle><date>2021-07-22</date><risdate>2021</risdate><volume>13</volume><issue>15</issue><spage>3690</spage><pages>3690-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>As a hydrophobic photosensitizer, IR-780 suffers from poor water solubility and low photostability under near infrared (NIR) light, which severely limits its use during successive NIR laser-assisted photothermal/photodynamic therapy (PTT/PDT). To solve this problem, we fabricate cationic IR-780-loaded liposomes (ILs) by entrapping IR-780 within the lipid bilayer of liposomes. We demonstrate enhanced photostability of IR-780 in ILs with well-preserved photothermal response after three repeated NIR laser exposures, in contrast to the rapid decomposition of free IR-780. The cationic nature of ILs promotes fast endocytosis of liposomal IR-780 by U87MG human glioblastoma cells within 30 min. For PTT/PDT in vitro, ILs treatment plus NIR laser irradiation leads to overexpression of heat shock protein 70 and generation of intracellular reactive oxygen species by U87MG cells, resulting in enhanced cytotoxicity and higher cell apoptosis rate. Using intracranial glioma xenograft in nude mice and administration of ILs by convection enhanced delivery (CED) to overcome blood-brain barrier, liposomal IR-780 could be specifically delivered to the brain tumor, as demonstrated from fluorescence imaging. By providing a highly stable liposomal IR-780, ILs significantly improved anti-cancer efficacy in glioma treatment, as revealed from various diagnostic imaging tools and histological examination. Overall, CED of ILs plus successive laser-assisted PTT/PDT may be an alternative approach for treating brain tumor, which can retard glioma growth and prolong animal survival times from orthotopic brain tumor models.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34359590</pmid><doi>10.3390/cancers13153690</doi><orcidid>https://orcid.org/0000-0001-6527-4801</orcidid><orcidid>https://orcid.org/0000-0003-1898-7264</orcidid><orcidid>https://orcid.org/0000-0001-9670-7550</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Blood-brain barrier Brain cancer Brain tumors Cancer therapies Convection Cytotoxicity Efficiency Endocytosis Flow velocity Glioblastoma Glioblastoma cells Glioma Heat Heat shock proteins Hsp70 protein Hydrophobicity Intracellular Laboratory animals Lasers Light Lipid bilayers Lipids Liposomes Nanomaterials Neuroimaging Photodynamic therapy Reactive oxygen species Tumors Xenografts |
title | Liposomal IR-780 as a Highly Stable Nanotheranostic Agent for Improved Photothermal/Photodynamic Therapy of Brain Tumors by Convection-Enhanced Delivery |
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