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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
1981-10-14
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pubmed:abstractText |
The potential prolongation of survival of actinomycin D entrapped in liposomes was examined in Balb C/Cr mice inoculated intrarenally with renal cell adenocarcinoma. There were five groups of animals: group A, a control group, received phosphate-buffered saline 0.3 cm3 i.p.; group B received free actinomycin D 300 micrograms/kg i.p.; group C received liposomes containing actinomycin D 300 micrograms/kg i.p.; group D received a mixture of free actinomycin D 300 micrograms/kg and empty liposomes i.p.; group E received empty liposomes i.p. The best median survival was of group D (free drug) - 54 days followed by group C (liposome entrapped actinomycin D) 45.2 days and group E (a mixture of free and entrapped actinomycin D) - 42 days. In vitro studies utilizing cell lines obtained from the tumor showed no statistical difference in ID50 or in cytotoxicity between the cells treated with free actinomycin D and those treated with liposomes containing drug.
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pubmed:grant | |
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 |
0030-2414
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
38
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
|
pubmed:pagination |
311-4
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:7266972-Adenocarcinoma,
pubmed-meshheading:7266972-Animals,
pubmed-meshheading:7266972-Cells, Cultured,
pubmed-meshheading:7266972-Dactinomycin,
pubmed-meshheading:7266972-Graft Survival,
pubmed-meshheading:7266972-Kidney Neoplasms,
pubmed-meshheading:7266972-Liposomes,
pubmed-meshheading:7266972-Mice,
pubmed-meshheading:7266972-Mice, Inbred BALB C,
pubmed-meshheading:7266972-Neoplasm Transplantation,
pubmed-meshheading:7266972-Neoplasms, Experimental,
pubmed-meshheading:7266972-Transplantation, Homologous
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pubmed:year |
1981
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pubmed:articleTitle |
Failure of actinomycin D entrapped in liposomes to prolong survival in renal cell adenocarcinoma-bearing mice.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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