Source:http://linkedlifedata.com/resource/pubmed/id/11287818
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
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| pubmed:dateCreated |
2001-4-5
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| pubmed:abstractText |
Etoposide exerts its antineoplastic effect by forming a ternary complex with topo-isomerase II and DNA, leading to DNA breaks and cell death. However, it causes myelosuppression and its lipophilicity poses a major limitation during administration. Liposomes have been reported to increase the efficacy and reduce the toxicity of antineoplastic agents. Recent evidence suggests that cationic liposomes bind efficiently to tumours. The present study was thus designed to encapsulate etoposide in cationic liposomes and to evaluate its antitumour efficacy and systemic toxicity in comparison with a conventional parenteral formulation. Etoposide encapsulated in liposomes was synthesised by thin film hydration followed by an extrusion method. Fibrosarcoma was induced in mice by subcutaneous administration of 20-methylcholanthrene. Chemotherapy was started when the tumour reached 200 mm(3) in volume. Liposomal etoposide (10 mg/m(2)/day for 5 days) significantly delayed tumour growth as compared to non-liposomal etoposide. The median time of death was calculated to be 19.5, 26.25 and 56 days in vehicle-treated controls, non-liposomal-etoposide- and liposomal-etoposide-treated groups, respectively. A transient reduction in body weight was seen in both the liposomal- and non-liposomal-etoposide-treated groups. The maximum tolerated dose was however significantly higher in the group treated with liposomal etoposide, which also exhibited a lesser degree of myelosuppression than the animals treated with non-liposomal etoposide. The present findings suggest that cationic liposomes could be considered as potential for delivery of etoposide to tumours.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical | |
| pubmed:status |
MEDLINE
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| pubmed:issn |
0031-7012
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| pubmed:author | |
| pubmed:copyrightInfo |
Copyright 2001 S. Karger AG, Basel
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| pubmed:issnType |
Print
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| pubmed:volume |
62
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
163-71
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| pubmed:dateRevised |
2003-11-14
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| pubmed:meshHeading |
pubmed-meshheading:11287818-Animals,
pubmed-meshheading:11287818-Antineoplastic Agents, Phytogenic,
pubmed-meshheading:11287818-Blood Platelets,
pubmed-meshheading:11287818-Body Weight,
pubmed-meshheading:11287818-Capsules,
pubmed-meshheading:11287818-Etoposide,
pubmed-meshheading:11287818-Fibrosarcoma,
pubmed-meshheading:11287818-Leukocytes,
pubmed-meshheading:11287818-Liposomes,
pubmed-meshheading:11287818-Male,
pubmed-meshheading:11287818-Mice,
pubmed-meshheading:11287818-Random Allocation
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| pubmed:year |
2001
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| pubmed:articleTitle |
Encapsulation in cationic liposomes enhances antitumour efficacy and reduces the toxicity of etoposide, a topo-isomerase II inhibitor.
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| pubmed:affiliation |
Department of Pharmacology, All India Institute of Medical Sciences, New Delhi, India. ss307@hermes.cam.ac.uk
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| pubmed:publicationType |
Journal Article
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