Sustained release chemotherapeutic microspheres provide superior efficacy over systemic therapy and local bolus infusions
The present studies evaluated the ability of injectable, biodegradable microspheres releasing carboplatin, doxorubicin, or 5-fluorouracil to suppress the growth of solid tumors implanted subcutaneously or intramuscularly. Seven to 10 days after implantation of MATB-III cells, rats received systemic...
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Veröffentlicht in: | Pharmaceutical research 2002-07, Vol.19 (7), p.1052-1060 |
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creator | EMERICH, Dwaine F SNODGRASS, Pamela LAFRENIERE, Denise DEAN, Reginald L SALZBERG, Heather MARSH, Joanne PERDOMO, Brigido ARASTU, Mahin WINN, Shelley R BARTUS, Raymond T |
description | The present studies evaluated the ability of injectable, biodegradable microspheres releasing carboplatin, doxorubicin, or 5-fluorouracil to suppress the growth of solid tumors implanted subcutaneously or intramuscularly.
Seven to 10 days after implantation of MATB-III cells, rats received systemic chemotherapy, intratumoral bolus chemotherapy, or injections of chemotherapeutic microspheres into the tumor center or multiple sites along the outer perimeter of the tumor.
A single treatment with carboplatin, doxorubicin, or 5-fluorouracil microspheres along the perimeter of the tumors produced a significant, dose-related suppression in tumor growth, relative to injections directly into the tumor center. Moreover, five temporally-spaced microsphere treatments along the tumor perimeter (with either doxorubicin or 5-fluorouracil microspheres) completely eradicated 100% of the subcutaneous tumors and 40-53% of the intramuscular tumors. Polypharmacy, accomplished by blending doxorubicin- and 5-fluorouracil-loaded microspheres and injecting them into the tumors was even more efficacious than sustained delivery of either drug alone. Comparable doses of systemic chemotherapy or intratumoral bolus chemotherapy were ineffective.
Injectable microspheres might be ideal for local, sustained delivery of chemotherapeutic agents to solid tumors. However, attention must be paid to the placement of the microspheres, for injections around the tumor perimeter may be required for efficacy. |
doi_str_mv | 10.1023/A:1016434926649 |
format | Article |
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Seven to 10 days after implantation of MATB-III cells, rats received systemic chemotherapy, intratumoral bolus chemotherapy, or injections of chemotherapeutic microspheres into the tumor center or multiple sites along the outer perimeter of the tumor.
A single treatment with carboplatin, doxorubicin, or 5-fluorouracil microspheres along the perimeter of the tumors produced a significant, dose-related suppression in tumor growth, relative to injections directly into the tumor center. Moreover, five temporally-spaced microsphere treatments along the tumor perimeter (with either doxorubicin or 5-fluorouracil microspheres) completely eradicated 100% of the subcutaneous tumors and 40-53% of the intramuscular tumors. Polypharmacy, accomplished by blending doxorubicin- and 5-fluorouracil-loaded microspheres and injecting them into the tumors was even more efficacious than sustained delivery of either drug alone. Comparable doses of systemic chemotherapy or intratumoral bolus chemotherapy were ineffective.
Injectable microspheres might be ideal for local, sustained delivery of chemotherapeutic agents to solid tumors. However, attention must be paid to the placement of the microspheres, for injections around the tumor perimeter may be required for efficacy.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1023/A:1016434926649</identifier><identifier>PMID: 12180539</identifier><identifier>CODEN: PHREEB</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Animals ; Antineoplastic agents ; Antineoplastic Agents - administration & dosage ; Biological and medical sciences ; Chemotherapy ; Delayed-Action Preparations - administration & dosage ; Dose-Response Relationship, Drug ; General pharmacology ; Infusions, Parenteral ; Injections, Intralesional ; Injections, Intramuscular ; Injections, Subcutaneous ; Male ; Medical sciences ; Microspheres ; Neoplasm Transplantation - methods ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Rats ; Rats, Inbred F344 ; Tumor Cells, Cultured - transplantation ; Xenograft Model Antitumor Assays - methods</subject><ispartof>Pharmaceutical research, 2002-07, Vol.19 (7), p.1052-1060</ispartof><rights>2002 INIST-CNRS</rights><rights>Copyright Kluwer Academic Publishers Jul 2002</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-8b4eb56084e106535dabaf3c27710cd1d327f0be65e1a9819da90828f693bf963</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13849628$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12180539$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>EMERICH, Dwaine F</creatorcontrib><creatorcontrib>SNODGRASS, Pamela</creatorcontrib><creatorcontrib>LAFRENIERE, Denise</creatorcontrib><creatorcontrib>DEAN, Reginald L</creatorcontrib><creatorcontrib>SALZBERG, Heather</creatorcontrib><creatorcontrib>MARSH, Joanne</creatorcontrib><creatorcontrib>PERDOMO, Brigido</creatorcontrib><creatorcontrib>ARASTU, Mahin</creatorcontrib><creatorcontrib>WINN, Shelley R</creatorcontrib><creatorcontrib>BARTUS, Raymond T</creatorcontrib><title>Sustained release chemotherapeutic microspheres provide superior efficacy over systemic therapy and local bolus infusions</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><description>The present studies evaluated the ability of injectable, biodegradable microspheres releasing carboplatin, doxorubicin, or 5-fluorouracil to suppress the growth of solid tumors implanted subcutaneously or intramuscularly.
Seven to 10 days after implantation of MATB-III cells, rats received systemic chemotherapy, intratumoral bolus chemotherapy, or injections of chemotherapeutic microspheres into the tumor center or multiple sites along the outer perimeter of the tumor.
A single treatment with carboplatin, doxorubicin, or 5-fluorouracil microspheres along the perimeter of the tumors produced a significant, dose-related suppression in tumor growth, relative to injections directly into the tumor center. Moreover, five temporally-spaced microsphere treatments along the tumor perimeter (with either doxorubicin or 5-fluorouracil microspheres) completely eradicated 100% of the subcutaneous tumors and 40-53% of the intramuscular tumors. Polypharmacy, accomplished by blending doxorubicin- and 5-fluorouracil-loaded microspheres and injecting them into the tumors was even more efficacious than sustained delivery of either drug alone. Comparable doses of systemic chemotherapy or intratumoral bolus chemotherapy were ineffective.
Injectable microspheres might be ideal for local, sustained delivery of chemotherapeutic agents to solid tumors. However, attention must be paid to the placement of the microspheres, for injections around the tumor perimeter may be required for efficacy.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Chemotherapy</subject><subject>Delayed-Action Preparations - administration & dosage</subject><subject>Dose-Response Relationship, Drug</subject><subject>General pharmacology</subject><subject>Infusions, Parenteral</subject><subject>Injections, Intralesional</subject><subject>Injections, Intramuscular</subject><subject>Injections, Subcutaneous</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Microspheres</subject><subject>Neoplasm Transplantation - methods</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. 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Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Rats</topic><topic>Rats, Inbred F344</topic><topic>Tumor Cells, Cultured - transplantation</topic><topic>Xenograft Model Antitumor Assays - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>EMERICH, Dwaine F</creatorcontrib><creatorcontrib>SNODGRASS, Pamela</creatorcontrib><creatorcontrib>LAFRENIERE, Denise</creatorcontrib><creatorcontrib>DEAN, Reginald L</creatorcontrib><creatorcontrib>SALZBERG, Heather</creatorcontrib><creatorcontrib>MARSH, Joanne</creatorcontrib><creatorcontrib>PERDOMO, Brigido</creatorcontrib><creatorcontrib>ARASTU, Mahin</creatorcontrib><creatorcontrib>WINN, Shelley R</creatorcontrib><creatorcontrib>BARTUS, Raymond T</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</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 China</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>EMERICH, Dwaine F</au><au>SNODGRASS, Pamela</au><au>LAFRENIERE, Denise</au><au>DEAN, Reginald L</au><au>SALZBERG, Heather</au><au>MARSH, Joanne</au><au>PERDOMO, Brigido</au><au>ARASTU, Mahin</au><au>WINN, Shelley R</au><au>BARTUS, Raymond T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sustained release chemotherapeutic microspheres provide superior efficacy over systemic therapy and local bolus infusions</atitle><jtitle>Pharmaceutical research</jtitle><addtitle>Pharm Res</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>19</volume><issue>7</issue><spage>1052</spage><epage>1060</epage><pages>1052-1060</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><coden>PHREEB</coden><abstract>The present studies evaluated the ability of injectable, biodegradable microspheres releasing carboplatin, doxorubicin, or 5-fluorouracil to suppress the growth of solid tumors implanted subcutaneously or intramuscularly.
Seven to 10 days after implantation of MATB-III cells, rats received systemic chemotherapy, intratumoral bolus chemotherapy, or injections of chemotherapeutic microspheres into the tumor center or multiple sites along the outer perimeter of the tumor.
A single treatment with carboplatin, doxorubicin, or 5-fluorouracil microspheres along the perimeter of the tumors produced a significant, dose-related suppression in tumor growth, relative to injections directly into the tumor center. Moreover, five temporally-spaced microsphere treatments along the tumor perimeter (with either doxorubicin or 5-fluorouracil microspheres) completely eradicated 100% of the subcutaneous tumors and 40-53% of the intramuscular tumors. Polypharmacy, accomplished by blending doxorubicin- and 5-fluorouracil-loaded microspheres and injecting them into the tumors was even more efficacious than sustained delivery of either drug alone. Comparable doses of systemic chemotherapy or intratumoral bolus chemotherapy were ineffective.
Injectable microspheres might be ideal for local, sustained delivery of chemotherapeutic agents to solid tumors. However, attention must be paid to the placement of the microspheres, for injections around the tumor perimeter may be required for efficacy.</abstract><cop>New York, NY</cop><pub>Springer</pub><pmid>12180539</pmid><doi>10.1023/A:1016434926649</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Antineoplastic agents Antineoplastic Agents - administration & dosage Biological and medical sciences Chemotherapy Delayed-Action Preparations - administration & dosage Dose-Response Relationship, Drug General pharmacology Infusions, Parenteral Injections, Intralesional Injections, Intramuscular Injections, Subcutaneous Male Medical sciences Microspheres Neoplasm Transplantation - methods Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Rats Rats, Inbred F344 Tumor Cells, Cultured - transplantation Xenograft Model Antitumor Assays - methods |
title | Sustained release chemotherapeutic microspheres provide superior efficacy over systemic therapy and local bolus infusions |
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