Combination Therapy of Surgical Tumor Resection with Implantation of a Hydrogel Containing Camptothecin-Loaded Poly(lactic-co-glycolic acid) Microspheres in a C6 Rat Glioma Model
We have developed a drug-loaded poly(lactic-co-glycolic acid) (PLGA) microsphere-containing thermoreversible gelation polymer (TGP) (drug/PLGA/TGP) formulation as a novel device for implantation after surgical glioma resection. TGP is a thermosensitive polymer that is a gel at body temperature and a...
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Veröffentlicht in: | Biological & pharmaceutical bulletin 2012/04/01, Vol.35(4), pp.545-550 |
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creator | Ozeki, Tetsuya Kaneko, Daiki Hashizawa, Kosuke Imai, Yoshihiro Tagami, Tatsuaki Okada, Hiroaki |
description | We have developed a drug-loaded poly(lactic-co-glycolic acid) (PLGA) microsphere-containing thermoreversible gelation polymer (TGP) (drug/PLGA/TGP) formulation as a novel device for implantation after surgical glioma resection. TGP is a thermosensitive polymer that is a gel at body temperature and a sol at room temperature. When a drug/PLGA/TGP formulation is injected into a target site, PLGA microspheres in TGP gel localize at the injection site and do not diffuse across the entire brain tissue, and thus, sustained drug release from the PLGA microspheres at the target site is expected. Using in vivo imaging, we confirmed that the implantation of indocyanine green (ICG)/PLGA/TGP formulation exhibited a stronger localization of ICG at the injection site 28 d after injection compared with that of ICG/PLGA formulation. The therapeutic effect (mean survival) was evaluated in a C6 rat glioma model. Surgical tumor resection alone showed almost no effect on survival (controls, 18 d; surgical resection; 18.5 d). Survival was prolonged after the treatment with a camptothecin (CPT; 10 µg)/PLGA/TGP formulation (24 d). The combination treatment of surgical tumor resection and CPT/PLGA/TGP showed almost the same therapeutic effect (24 d) compared with CPT/PLGA/TGP alone, while the combination treatment produced long term survivors (>60 d). Therefore, the CPT/PLGA/TGP formulation can be an effective candidate for localized and sustained long-term glioma therapy. |
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TGP is a thermosensitive polymer that is a gel at body temperature and a sol at room temperature. When a drug/PLGA/TGP formulation is injected into a target site, PLGA microspheres in TGP gel localize at the injection site and do not diffuse across the entire brain tissue, and thus, sustained drug release from the PLGA microspheres at the target site is expected. Using in vivo imaging, we confirmed that the implantation of indocyanine green (ICG)/PLGA/TGP formulation exhibited a stronger localization of ICG at the injection site 28 d after injection compared with that of ICG/PLGA formulation. The therapeutic effect (mean survival) was evaluated in a C6 rat glioma model. Surgical tumor resection alone showed almost no effect on survival (controls, 18 d; surgical resection; 18.5 d). Survival was prolonged after the treatment with a camptothecin (CPT; 10 µg)/PLGA/TGP formulation (24 d). The combination treatment of surgical tumor resection and CPT/PLGA/TGP showed almost the same therapeutic effect (24 d) compared with CPT/PLGA/TGP alone, while the combination treatment produced long term survivors (>60 d). Therefore, the CPT/PLGA/TGP formulation can be an effective candidate for localized and sustained long-term glioma therapy.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.35.545</identifier><identifier>PMID: 22466559</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject><![CDATA[Animals ; Antineoplastic Agents, Phytogenic - administration & dosage ; Brain Neoplasms - drug therapy ; Brain Neoplasms - surgery ; Camptothecin - administration & dosage ; Cell Line, Tumor ; Combined Modality Therapy ; Drug Carriers - administration & dosage ; Drug Implants ; Glioma - drug therapy ; Glioma - surgery ; glioma therapy ; Hydrogels - administration & dosage ; Lactic Acid - administration & dosage ; Male ; Microspheres ; poly(lactic-co-glycolic acid) microsphere ; Polyglycolic Acid - administration & dosage ; Polylactic Acid-Polyglycolic Acid Copolymer ; Rats ; Rats, Sprague-Dawley ; surgical tumor resection ; sustained release ; thermoreversible gelation polymer]]></subject><ispartof>Biological and Pharmaceutical Bulletin, 2012/04/01, Vol.35(4), pp.545-550</ispartof><rights>2012 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c529t-b200aa21291a06ecdc1bc0d271be25daeab191ca046351bb060a06db4e3900193</citedby><cites>FETCH-LOGICAL-c529t-b200aa21291a06ecdc1bc0d271be25daeab191ca046351bb060a06db4e3900193</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22466559$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ozeki, Tetsuya</creatorcontrib><creatorcontrib>Kaneko, Daiki</creatorcontrib><creatorcontrib>Hashizawa, Kosuke</creatorcontrib><creatorcontrib>Imai, Yoshihiro</creatorcontrib><creatorcontrib>Tagami, Tatsuaki</creatorcontrib><creatorcontrib>Okada, Hiroaki</creatorcontrib><title>Combination Therapy of Surgical Tumor Resection with Implantation of a Hydrogel Containing Camptothecin-Loaded Poly(lactic-co-glycolic acid) Microspheres in a C6 Rat Glioma Model</title><title>Biological & pharmaceutical bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>We have developed a drug-loaded poly(lactic-co-glycolic acid) (PLGA) microsphere-containing thermoreversible gelation polymer (TGP) (drug/PLGA/TGP) formulation as a novel device for implantation after surgical glioma resection. TGP is a thermosensitive polymer that is a gel at body temperature and a sol at room temperature. When a drug/PLGA/TGP formulation is injected into a target site, PLGA microspheres in TGP gel localize at the injection site and do not diffuse across the entire brain tissue, and thus, sustained drug release from the PLGA microspheres at the target site is expected. Using in vivo imaging, we confirmed that the implantation of indocyanine green (ICG)/PLGA/TGP formulation exhibited a stronger localization of ICG at the injection site 28 d after injection compared with that of ICG/PLGA formulation. The therapeutic effect (mean survival) was evaluated in a C6 rat glioma model. Surgical tumor resection alone showed almost no effect on survival (controls, 18 d; surgical resection; 18.5 d). Survival was prolonged after the treatment with a camptothecin (CPT; 10 µg)/PLGA/TGP formulation (24 d). The combination treatment of surgical tumor resection and CPT/PLGA/TGP showed almost the same therapeutic effect (24 d) compared with CPT/PLGA/TGP alone, while the combination treatment produced long term survivors (>60 d). Therefore, the CPT/PLGA/TGP formulation can be an effective candidate for localized and sustained long-term glioma therapy.</description><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - administration & dosage</subject><subject>Brain Neoplasms - drug therapy</subject><subject>Brain Neoplasms - surgery</subject><subject>Camptothecin - administration & dosage</subject><subject>Cell Line, Tumor</subject><subject>Combined Modality Therapy</subject><subject>Drug Carriers - administration & dosage</subject><subject>Drug Implants</subject><subject>Glioma - drug therapy</subject><subject>Glioma - surgery</subject><subject>glioma therapy</subject><subject>Hydrogels - administration & dosage</subject><subject>Lactic Acid - administration & dosage</subject><subject>Male</subject><subject>Microspheres</subject><subject>poly(lactic-co-glycolic acid) microsphere</subject><subject>Polyglycolic Acid - administration & dosage</subject><subject>Polylactic Acid-Polyglycolic Acid Copolymer</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>surgical tumor resection</subject><subject>sustained release</subject><subject>thermoreversible gelation polymer</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp90U9v0zAYBvAIgVgZXPgAyBIHBlKK_8RpfEIogm1SJ9Ao5-i187Z15cSZnQjla_EJ8ejWAwcutmT__Mj2k2WvGV0yXlQf9aCXQi5lIZ9kCyaKVS45k0-zBVWsyksmq7PsRYwHSumKcvE8O-O8KEsp1SL7XftO2x5G63uy2WOAYSZ-S35MYWcNOLKZOh_ILUY0f80vO-7JdTc46MfjqaSBXM1t8Dt0pPZp3fa235EaumH04x6N7fO1hxZb8t27-cJByjK58fnOzcY7awgY274nN9YEH4d0DYzE9im3LsktjOTSWd8BufEtupfZsy24iK8e5vPs59cvm_oqX3-7vK4_r3MjuRpzzSkF4IwrBrRE0xqmDW35imnksgUEzRQzQItSSKY1LWlyrS5QKEqZEufZu2PuEPzdhHFsOhsNuvRy9FNsVCkqIVhRJXnxX8mEUoqKdK1E3_5DD34KfXpHw4pCiYoLzpL6cFT33xEDbpsh2A7C3DDa3HfepM4bIZvUecJvHiIn3WF7oo8lJ_DpCA5xhB2eAITUgsPHrOI4pMjTjtlDaLAXfwDUz798</recordid><startdate>20120401</startdate><enddate>20120401</enddate><creator>Ozeki, Tetsuya</creator><creator>Kaneko, Daiki</creator><creator>Hashizawa, Kosuke</creator><creator>Imai, Yoshihiro</creator><creator>Tagami, Tatsuaki</creator><creator>Okada, Hiroaki</creator><general>The Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7QO</scope><scope>7X8</scope></search><sort><creationdate>20120401</creationdate><title>Combination Therapy of Surgical Tumor Resection with Implantation of a Hydrogel Containing Camptothecin-Loaded Poly(lactic-co-glycolic acid) Microspheres in a C6 Rat Glioma Model</title><author>Ozeki, Tetsuya ; Kaneko, Daiki ; Hashizawa, Kosuke ; Imai, Yoshihiro ; Tagami, Tatsuaki ; Okada, Hiroaki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c529t-b200aa21291a06ecdc1bc0d271be25daeab191ca046351bb060a06db4e3900193</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - administration & dosage</topic><topic>Brain Neoplasms - drug therapy</topic><topic>Brain Neoplasms - surgery</topic><topic>Camptothecin - administration & dosage</topic><topic>Cell Line, Tumor</topic><topic>Combined Modality Therapy</topic><topic>Drug Carriers - administration & dosage</topic><topic>Drug Implants</topic><topic>Glioma - drug therapy</topic><topic>Glioma - surgery</topic><topic>glioma therapy</topic><topic>Hydrogels - administration & dosage</topic><topic>Lactic Acid - administration & dosage</topic><topic>Male</topic><topic>Microspheres</topic><topic>poly(lactic-co-glycolic acid) microsphere</topic><topic>Polyglycolic Acid - administration & dosage</topic><topic>Polylactic Acid-Polyglycolic Acid Copolymer</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>surgical tumor resection</topic><topic>sustained release</topic><topic>thermoreversible gelation polymer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ozeki, Tetsuya</creatorcontrib><creatorcontrib>Kaneko, Daiki</creatorcontrib><creatorcontrib>Hashizawa, Kosuke</creatorcontrib><creatorcontrib>Imai, Yoshihiro</creatorcontrib><creatorcontrib>Tagami, Tatsuaki</creatorcontrib><creatorcontrib>Okada, Hiroaki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological & pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ozeki, Tetsuya</au><au>Kaneko, Daiki</au><au>Hashizawa, Kosuke</au><au>Imai, Yoshihiro</au><au>Tagami, Tatsuaki</au><au>Okada, Hiroaki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combination Therapy of Surgical Tumor Resection with Implantation of a Hydrogel Containing Camptothecin-Loaded Poly(lactic-co-glycolic acid) Microspheres in a C6 Rat Glioma Model</atitle><jtitle>Biological & pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2012-04-01</date><risdate>2012</risdate><volume>35</volume><issue>4</issue><spage>545</spage><epage>550</epage><pages>545-550</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>We have developed a drug-loaded poly(lactic-co-glycolic acid) (PLGA) microsphere-containing thermoreversible gelation polymer (TGP) (drug/PLGA/TGP) formulation as a novel device for implantation after surgical glioma resection. TGP is a thermosensitive polymer that is a gel at body temperature and a sol at room temperature. When a drug/PLGA/TGP formulation is injected into a target site, PLGA microspheres in TGP gel localize at the injection site and do not diffuse across the entire brain tissue, and thus, sustained drug release from the PLGA microspheres at the target site is expected. Using in vivo imaging, we confirmed that the implantation of indocyanine green (ICG)/PLGA/TGP formulation exhibited a stronger localization of ICG at the injection site 28 d after injection compared with that of ICG/PLGA formulation. The therapeutic effect (mean survival) was evaluated in a C6 rat glioma model. Surgical tumor resection alone showed almost no effect on survival (controls, 18 d; surgical resection; 18.5 d). Survival was prolonged after the treatment with a camptothecin (CPT; 10 µg)/PLGA/TGP formulation (24 d). The combination treatment of surgical tumor resection and CPT/PLGA/TGP showed almost the same therapeutic effect (24 d) compared with CPT/PLGA/TGP alone, while the combination treatment produced long term survivors (>60 d). Therefore, the CPT/PLGA/TGP formulation can be an effective candidate for localized and sustained long-term glioma therapy.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>22466559</pmid><doi>10.1248/bpb.35.545</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antineoplastic Agents, Phytogenic - administration & dosage Brain Neoplasms - drug therapy Brain Neoplasms - surgery Camptothecin - administration & dosage Cell Line, Tumor Combined Modality Therapy Drug Carriers - administration & dosage Drug Implants Glioma - drug therapy Glioma - surgery glioma therapy Hydrogels - administration & dosage Lactic Acid - administration & dosage Male Microspheres poly(lactic-co-glycolic acid) microsphere Polyglycolic Acid - administration & dosage Polylactic Acid-Polyglycolic Acid Copolymer Rats Rats, Sprague-Dawley surgical tumor resection sustained release thermoreversible gelation polymer |
title | Combination Therapy of Surgical Tumor Resection with Implantation of a Hydrogel Containing Camptothecin-Loaded Poly(lactic-co-glycolic acid) Microspheres in a C6 Rat Glioma Model |
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