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Liposomal encapsulation of topotecan enhances anticancer efficacy in murine and human xenograft models
Topotecan was encapsulated in sphingomyelin/cholesterol liposomes using an ionophore-generated proton gradient. After i.v. injection, liposomal topotecan was eliminated from the plasma much more slowly than free drug, resulting in a 400-fold increase in plasma area under the curve. Further, high-per...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 2000-07, Vol.60 (13), p.3389-3393 |
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creator | TARDI, P CHOICE, E MASIN, D REDELMEIER, T BALLY, M MADDEN, T. D |
description | Topotecan was encapsulated in sphingomyelin/cholesterol liposomes using an ionophore-generated proton gradient. After i.v. injection, liposomal topotecan was eliminated from the plasma much more slowly than free drug, resulting in a 400-fold increase in plasma area under the curve. Further, high-performance liquid chromatography analysis of plasma samples demonstrated that topotecan was protected from hydrolysis within the liposomal carrier with >80% of the drug remaining as the active, lactone species up to 24 h. The improved pharmacokinetics observed with liposomal topotecan correlated with increased efficacy in both murine and human tumor models. In the L1210 ascitic tumor model, optimal doses of liposomal topotecan resulted in a 60-day survival rate of 60-80%, whereas in a L1210 liver metastasis model, 100% long-term survival (>60 days) was achieved. In contrast, long-term survivors were rarely seen after treatment with free topotecan. Further, in a human breast carcinoma model (MDA 435/LCC6), liposomal topotecan provided greatly improved increase in life span relative to the free drug. These results suggest that liposomal encapsulation can significantly enhance the therapeutic activity of topotecan. |
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D</creator><creatorcontrib>TARDI, P ; CHOICE, E ; MASIN, D ; REDELMEIER, T ; BALLY, M ; MADDEN, T. D</creatorcontrib><description>Topotecan was encapsulated in sphingomyelin/cholesterol liposomes using an ionophore-generated proton gradient. After i.v. injection, liposomal topotecan was eliminated from the plasma much more slowly than free drug, resulting in a 400-fold increase in plasma area under the curve. Further, high-performance liquid chromatography analysis of plasma samples demonstrated that topotecan was protected from hydrolysis within the liposomal carrier with >80% of the drug remaining as the active, lactone species up to 24 h. The improved pharmacokinetics observed with liposomal topotecan correlated with increased efficacy in both murine and human tumor models. In the L1210 ascitic tumor model, optimal doses of liposomal topotecan resulted in a 60-day survival rate of 60-80%, whereas in a L1210 liver metastasis model, 100% long-term survival (>60 days) was achieved. In contrast, long-term survivors were rarely seen after treatment with free topotecan. Further, in a human breast carcinoma model (MDA 435/LCC6), liposomal topotecan provided greatly improved increase in life span relative to the free drug. These results suggest that liposomal encapsulation can significantly enhance the therapeutic activity of topotecan.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 10910044</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Animals ; Antineoplastic agents ; Antineoplastic Agents - administration & dosage ; Antineoplastic Agents - pharmacokinetics ; Antineoplastic Agents - therapeutic use ; Biological and medical sciences ; Breast Neoplasms - drug therapy ; Chemotherapy ; Drug Carriers ; Female ; Humans ; Leukemia L1210 - drug therapy ; Leukemia L1210 - pathology ; Liposomes ; Liver Neoplasms - drug therapy ; Liver Neoplasms - secondary ; Medical sciences ; Mice ; Mice, Inbred BALB C ; Mice, Inbred Strains ; Mice, SCID ; Pharmacology. Drug treatments ; Survival Rate ; Topotecan - administration & dosage ; Topotecan - pharmacokinetics ; Topotecan - therapeutic use ; Transplantation, Heterologous</subject><ispartof>Cancer research (Chicago, Ill.), 2000-07, Vol.60 (13), p.3389-3393</ispartof><rights>2000 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1454173$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10910044$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>TARDI, P</creatorcontrib><creatorcontrib>CHOICE, E</creatorcontrib><creatorcontrib>MASIN, D</creatorcontrib><creatorcontrib>REDELMEIER, T</creatorcontrib><creatorcontrib>BALLY, M</creatorcontrib><creatorcontrib>MADDEN, T. D</creatorcontrib><title>Liposomal encapsulation of topotecan enhances anticancer efficacy in murine and human xenograft models</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Topotecan was encapsulated in sphingomyelin/cholesterol liposomes using an ionophore-generated proton gradient. After i.v. injection, liposomal topotecan was eliminated from the plasma much more slowly than free drug, resulting in a 400-fold increase in plasma area under the curve. Further, high-performance liquid chromatography analysis of plasma samples demonstrated that topotecan was protected from hydrolysis within the liposomal carrier with >80% of the drug remaining as the active, lactone species up to 24 h. The improved pharmacokinetics observed with liposomal topotecan correlated with increased efficacy in both murine and human tumor models. In the L1210 ascitic tumor model, optimal doses of liposomal topotecan resulted in a 60-day survival rate of 60-80%, whereas in a L1210 liver metastasis model, 100% long-term survival (>60 days) was achieved. In contrast, long-term survivors were rarely seen after treatment with free topotecan. Further, in a human breast carcinoma model (MDA 435/LCC6), liposomal topotecan provided greatly improved increase in life span relative to the free drug. These results suggest that liposomal encapsulation can significantly enhance the therapeutic activity of topotecan.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Agents - administration & dosage</subject><subject>Antineoplastic Agents - pharmacokinetics</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Chemotherapy</subject><subject>Drug Carriers</subject><subject>Female</subject><subject>Humans</subject><subject>Leukemia L1210 - drug therapy</subject><subject>Leukemia L1210 - pathology</subject><subject>Liposomes</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - secondary</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Inbred Strains</subject><subject>Mice, SCID</subject><subject>Pharmacology. Drug treatments</subject><subject>Survival Rate</subject><subject>Topotecan - administration & dosage</subject><subject>Topotecan - pharmacokinetics</subject><subject>Topotecan - therapeutic use</subject><subject>Transplantation, Heterologous</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LxDAQhoMo7rr6FyQH8VZINknTHmXxCwpe9FymycSNtEltWnD_vRFXPM07PM8MzJyQNVeiKrSU6pSsGWNVoaTershFSh-5VZypc7LirOaMSbkmrvFjTHGAnmIwMKalh9nHQKOjcxzjjAZCRnsIBhOFMHvzEyeKzuVoDtQHOiyTD5ippftlyANfGOL7BG6mQ7TYp0ty5qBPeHWsG_L2cP-6eyqal8fn3V1T7LeazYWoO1vpDoVSzrnaga0Fx5JVspS6EnVVmRI110xYlrngpUVgJTJrbScliA25_d07TvFzwTS3g08G-x4CxiW1mm9FzTnP4vVRXLoBbTtOfoDp0P59Jgs3RwGSgd5N-Wqf_j2pJNdCfAMjEG7w</recordid><startdate>20000701</startdate><enddate>20000701</enddate><creator>TARDI, P</creator><creator>CHOICE, E</creator><creator>MASIN, D</creator><creator>REDELMEIER, T</creator><creator>BALLY, M</creator><creator>MADDEN, T. D</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20000701</creationdate><title>Liposomal encapsulation of topotecan enhances anticancer efficacy in murine and human xenograft models</title><author>TARDI, P ; CHOICE, E ; MASIN, D ; REDELMEIER, T ; BALLY, M ; MADDEN, T. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h270t-39bd87be355fff9fad931e608464783988c6e71703d0ff9316dea06e0dddb44a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Agents - administration & dosage</topic><topic>Antineoplastic Agents - pharmacokinetics</topic><topic>Antineoplastic Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Chemotherapy</topic><topic>Drug Carriers</topic><topic>Female</topic><topic>Humans</topic><topic>Leukemia L1210 - drug therapy</topic><topic>Leukemia L1210 - pathology</topic><topic>Liposomes</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - secondary</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Inbred Strains</topic><topic>Mice, SCID</topic><topic>Pharmacology. Drug treatments</topic><topic>Survival Rate</topic><topic>Topotecan - administration & dosage</topic><topic>Topotecan - pharmacokinetics</topic><topic>Topotecan - therapeutic use</topic><topic>Transplantation, Heterologous</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>TARDI, P</creatorcontrib><creatorcontrib>CHOICE, E</creatorcontrib><creatorcontrib>MASIN, D</creatorcontrib><creatorcontrib>REDELMEIER, T</creatorcontrib><creatorcontrib>BALLY, M</creatorcontrib><creatorcontrib>MADDEN, T. 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D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Liposomal encapsulation of topotecan enhances anticancer efficacy in murine and human xenograft models</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2000-07-01</date><risdate>2000</risdate><volume>60</volume><issue>13</issue><spage>3389</spage><epage>3393</epage><pages>3389-3393</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Topotecan was encapsulated in sphingomyelin/cholesterol liposomes using an ionophore-generated proton gradient. After i.v. injection, liposomal topotecan was eliminated from the plasma much more slowly than free drug, resulting in a 400-fold increase in plasma area under the curve. Further, high-performance liquid chromatography analysis of plasma samples demonstrated that topotecan was protected from hydrolysis within the liposomal carrier with >80% of the drug remaining as the active, lactone species up to 24 h. The improved pharmacokinetics observed with liposomal topotecan correlated with increased efficacy in both murine and human tumor models. In the L1210 ascitic tumor model, optimal doses of liposomal topotecan resulted in a 60-day survival rate of 60-80%, whereas in a L1210 liver metastasis model, 100% long-term survival (>60 days) was achieved. In contrast, long-term survivors were rarely seen after treatment with free topotecan. Further, in a human breast carcinoma model (MDA 435/LCC6), liposomal topotecan provided greatly improved increase in life span relative to the free drug. These results suggest that liposomal encapsulation can significantly enhance the therapeutic activity of topotecan.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>10910044</pmid><tpages>5</tpages></addata></record> |
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subjects | Animals Antineoplastic agents Antineoplastic Agents - administration & dosage Antineoplastic Agents - pharmacokinetics Antineoplastic Agents - therapeutic use Biological and medical sciences Breast Neoplasms - drug therapy Chemotherapy Drug Carriers Female Humans Leukemia L1210 - drug therapy Leukemia L1210 - pathology Liposomes Liver Neoplasms - drug therapy Liver Neoplasms - secondary Medical sciences Mice Mice, Inbred BALB C Mice, Inbred Strains Mice, SCID Pharmacology. Drug treatments Survival Rate Topotecan - administration & dosage Topotecan - pharmacokinetics Topotecan - therapeutic use Transplantation, Heterologous |
title | Liposomal encapsulation of topotecan enhances anticancer efficacy in murine and human xenograft models |
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