Engineering of multifunctional temperature-sensitive liposomes for synergistic photothermal, photodynamic, and chemotherapeutic effects
Temperature-sensitive liposomes containing anti-cancer agent tanespimycin and photosensitizer IR 820 (LP-AI). [Display omitted] Heterogeneity of cancer cells and drug resistance require multiple therapeutic approaches for comprehensive treatment. In this study, temperature-sensitive liposomes contai...
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Veröffentlicht in: | International journal of pharmaceutics 2017-08, Vol.528 (1-2), p.692-704 |
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container_title | International journal of pharmaceutics |
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creator | Tran, Tuan Hiep Nguyen, Hanh Thuy Le, Nam Van Tran, Thi Thu Phuong Lee, Jong Seong Ku, Sae Kwang Choi, Han-Gon Yong, Chul Soon Kim, Jong Oh |
description | Temperature-sensitive liposomes containing anti-cancer agent tanespimycin and photosensitizer IR 820 (LP-AI).
[Display omitted]
Heterogeneity of cancer cells and drug resistance require multiple therapeutic approaches for comprehensive treatment. In this study, temperature-sensitive liposomes containing anti-cancer agent tanespimycin (17-AAG) and photosensitizer IR 820 were developed for combination of phototherapy and chemotherapy. The temperature-sensitive liposomes composed of DPPC, cholesterol, DSPE-PEG, 17-AAG, and IR 820 (LP-AI) at weight ratio of 35/15/3/2/2 were formulated as a thin film using extrusion and evaluated for particle size, morphology and drug release profile. Furthermore, the anticancer effect of combined therapy was examined in vitro and in vivo in SCC-7 and MCF-7 cell lines. As a result, LP-AI was prepared at particle size of 166.7±1.3nm, PDI of 0.153±0.012, and ζ-potential of −32.6±0.8mV. After NIR irradiation (660 and 808nm laser), LP-AI could generate heat and ROS and enhance drug release from nanoparticles which were useful to kill the cancer cells. These were confirmed by in vitro cytotoxicity as well as in vivo effective ablation of tumors. In conclusion, fast drug release and enhanced treatment efficacy of LP-AI indicate the potential of integrating photo- and chemotherapy for synergistic anti-cancer effects. |
doi_str_mv | 10.1016/j.ijpharm.2017.06.069 |
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[Display omitted]
Heterogeneity of cancer cells and drug resistance require multiple therapeutic approaches for comprehensive treatment. In this study, temperature-sensitive liposomes containing anti-cancer agent tanespimycin (17-AAG) and photosensitizer IR 820 were developed for combination of phototherapy and chemotherapy. The temperature-sensitive liposomes composed of DPPC, cholesterol, DSPE-PEG, 17-AAG, and IR 820 (LP-AI) at weight ratio of 35/15/3/2/2 were formulated as a thin film using extrusion and evaluated for particle size, morphology and drug release profile. Furthermore, the anticancer effect of combined therapy was examined in vitro and in vivo in SCC-7 and MCF-7 cell lines. As a result, LP-AI was prepared at particle size of 166.7±1.3nm, PDI of 0.153±0.012, and ζ-potential of −32.6±0.8mV. After NIR irradiation (660 and 808nm laser), LP-AI could generate heat and ROS and enhance drug release from nanoparticles which were useful to kill the cancer cells. These were confirmed by in vitro cytotoxicity as well as in vivo effective ablation of tumors. In conclusion, fast drug release and enhanced treatment efficacy of LP-AI indicate the potential of integrating photo- and chemotherapy for synergistic anti-cancer effects.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2017.06.069</identifier><identifier>PMID: 28642202</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Antineoplastic Agents - pharmacology ; Benzoquinones - pharmacology ; Cell Line, Tumor ; Chemotherapy ; Humans ; IR 820 ; Lactams, Macrocyclic - pharmacology ; Liposomes - chemistry ; Photochemotherapy ; Phototherapy ; Tanespimycin ; Temperature ; Temperature-sensitive liposome</subject><ispartof>International journal of pharmaceutics, 2017-08, Vol.528 (1-2), p.692-704</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-7a1db53a93fd66acf3898c7845538fb746528b49d561538836c0224dfca2fcb43</citedby><cites>FETCH-LOGICAL-c365t-7a1db53a93fd66acf3898c7845538fb746528b49d561538836c0224dfca2fcb43</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijpharm.2017.06.069$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28642202$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tran, Tuan Hiep</creatorcontrib><creatorcontrib>Nguyen, Hanh Thuy</creatorcontrib><creatorcontrib>Le, Nam Van</creatorcontrib><creatorcontrib>Tran, Thi Thu Phuong</creatorcontrib><creatorcontrib>Lee, Jong Seong</creatorcontrib><creatorcontrib>Ku, Sae Kwang</creatorcontrib><creatorcontrib>Choi, Han-Gon</creatorcontrib><creatorcontrib>Yong, Chul Soon</creatorcontrib><creatorcontrib>Kim, Jong Oh</creatorcontrib><title>Engineering of multifunctional temperature-sensitive liposomes for synergistic photothermal, photodynamic, and chemotherapeutic effects</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>Temperature-sensitive liposomes containing anti-cancer agent tanespimycin and photosensitizer IR 820 (LP-AI).
[Display omitted]
Heterogeneity of cancer cells and drug resistance require multiple therapeutic approaches for comprehensive treatment. In this study, temperature-sensitive liposomes containing anti-cancer agent tanespimycin (17-AAG) and photosensitizer IR 820 were developed for combination of phototherapy and chemotherapy. The temperature-sensitive liposomes composed of DPPC, cholesterol, DSPE-PEG, 17-AAG, and IR 820 (LP-AI) at weight ratio of 35/15/3/2/2 were formulated as a thin film using extrusion and evaluated for particle size, morphology and drug release profile. Furthermore, the anticancer effect of combined therapy was examined in vitro and in vivo in SCC-7 and MCF-7 cell lines. As a result, LP-AI was prepared at particle size of 166.7±1.3nm, PDI of 0.153±0.012, and ζ-potential of −32.6±0.8mV. After NIR irradiation (660 and 808nm laser), LP-AI could generate heat and ROS and enhance drug release from nanoparticles which were useful to kill the cancer cells. These were confirmed by in vitro cytotoxicity as well as in vivo effective ablation of tumors. In conclusion, fast drug release and enhanced treatment efficacy of LP-AI indicate the potential of integrating photo- and chemotherapy for synergistic anti-cancer effects.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Benzoquinones - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>Chemotherapy</subject><subject>Humans</subject><subject>IR 820</subject><subject>Lactams, Macrocyclic - pharmacology</subject><subject>Liposomes - chemistry</subject><subject>Photochemotherapy</subject><subject>Phototherapy</subject><subject>Tanespimycin</subject><subject>Temperature</subject><subject>Temperature-sensitive liposome</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU2LFDEQDaK44-pPUHL0sD3mo5NOn0SW1RUWvOg5pNOVmQydpE3SC_ML9m_b44xeFwqKqnqvHlUPofeUbCmh8tNh6w_z3uSwZYR2WyLX6F-gDVUdb3jbyZdoQ3inGkE7foXelHIghEhG-Wt0xZRsGSNsg57u4s5HgOzjDieHwzJV75Zoq0_RTLhCmCGbumRoCsTiq38EPPk5lRSgYJcyLscIeedL9RbP-1RT3UMOZro5V-MxmuDtDTZxxHYP4e_czLCcCOAc2FreolfOTAXeXfI1-vX17uftffPw49v32y8PjeVS1KYzdBwENz13o5TGOq56ZTvVCsGVG7pWCqaGth-FpGtHcWkJY-3orGHODi2_Rh_Pe-ecfi9Qqg6-WJgmEyEtRdOect4LqugKFWeozamUDE7P2QeTj5oSffJAH_TFA33yQBO5Rr_yPlwkliHA-J_17-kr4PMZAOuhjx6yLtZDtDD6vP5Cj8k_I_EH9KOfSQ</recordid><startdate>20170807</startdate><enddate>20170807</enddate><creator>Tran, Tuan Hiep</creator><creator>Nguyen, Hanh Thuy</creator><creator>Le, Nam Van</creator><creator>Tran, Thi Thu Phuong</creator><creator>Lee, Jong Seong</creator><creator>Ku, Sae Kwang</creator><creator>Choi, Han-Gon</creator><creator>Yong, Chul Soon</creator><creator>Kim, Jong Oh</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>20170807</creationdate><title>Engineering of multifunctional temperature-sensitive liposomes for synergistic photothermal, photodynamic, and chemotherapeutic effects</title><author>Tran, Tuan Hiep ; Nguyen, Hanh Thuy ; Le, Nam Van ; Tran, Thi Thu Phuong ; Lee, Jong Seong ; Ku, Sae Kwang ; Choi, Han-Gon ; Yong, Chul Soon ; Kim, Jong Oh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-7a1db53a93fd66acf3898c7845538fb746528b49d561538836c0224dfca2fcb43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Benzoquinones - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>Chemotherapy</topic><topic>Humans</topic><topic>IR 820</topic><topic>Lactams, Macrocyclic - pharmacology</topic><topic>Liposomes - chemistry</topic><topic>Photochemotherapy</topic><topic>Phototherapy</topic><topic>Tanespimycin</topic><topic>Temperature</topic><topic>Temperature-sensitive liposome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tran, Tuan Hiep</creatorcontrib><creatorcontrib>Nguyen, Hanh Thuy</creatorcontrib><creatorcontrib>Le, Nam Van</creatorcontrib><creatorcontrib>Tran, Thi Thu Phuong</creatorcontrib><creatorcontrib>Lee, Jong Seong</creatorcontrib><creatorcontrib>Ku, Sae Kwang</creatorcontrib><creatorcontrib>Choi, Han-Gon</creatorcontrib><creatorcontrib>Yong, Chul Soon</creatorcontrib><creatorcontrib>Kim, Jong Oh</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>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tran, Tuan Hiep</au><au>Nguyen, Hanh Thuy</au><au>Le, Nam Van</au><au>Tran, Thi Thu Phuong</au><au>Lee, Jong Seong</au><au>Ku, Sae Kwang</au><au>Choi, Han-Gon</au><au>Yong, Chul Soon</au><au>Kim, Jong Oh</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineering of multifunctional temperature-sensitive liposomes for synergistic photothermal, photodynamic, and chemotherapeutic effects</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2017-08-07</date><risdate>2017</risdate><volume>528</volume><issue>1-2</issue><spage>692</spage><epage>704</epage><pages>692-704</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><abstract>Temperature-sensitive liposomes containing anti-cancer agent tanespimycin and photosensitizer IR 820 (LP-AI).
[Display omitted]
Heterogeneity of cancer cells and drug resistance require multiple therapeutic approaches for comprehensive treatment. In this study, temperature-sensitive liposomes containing anti-cancer agent tanespimycin (17-AAG) and photosensitizer IR 820 were developed for combination of phototherapy and chemotherapy. The temperature-sensitive liposomes composed of DPPC, cholesterol, DSPE-PEG, 17-AAG, and IR 820 (LP-AI) at weight ratio of 35/15/3/2/2 were formulated as a thin film using extrusion and evaluated for particle size, morphology and drug release profile. Furthermore, the anticancer effect of combined therapy was examined in vitro and in vivo in SCC-7 and MCF-7 cell lines. As a result, LP-AI was prepared at particle size of 166.7±1.3nm, PDI of 0.153±0.012, and ζ-potential of −32.6±0.8mV. After NIR irradiation (660 and 808nm laser), LP-AI could generate heat and ROS and enhance drug release from nanoparticles which were useful to kill the cancer cells. These were confirmed by in vitro cytotoxicity as well as in vivo effective ablation of tumors. In conclusion, fast drug release and enhanced treatment efficacy of LP-AI indicate the potential of integrating photo- and chemotherapy for synergistic anti-cancer effects.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>28642202</pmid><doi>10.1016/j.ijpharm.2017.06.069</doi><tpages>13</tpages></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Benzoquinones - pharmacology Cell Line, Tumor Chemotherapy Humans IR 820 Lactams, Macrocyclic - pharmacology Liposomes - chemistry Photochemotherapy Phototherapy Tanespimycin Temperature Temperature-sensitive liposome |
title | Engineering of multifunctional temperature-sensitive liposomes for synergistic photothermal, photodynamic, and chemotherapeutic effects |
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