Enhanced efficacy of liposome-encapsulated ribavirin against Rift Valley fever virus infection in mice
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Published in | Antimicrobial Agents and Chemotherapy Vol. 27; no. 6; pp. 903 - 907 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Washington, DC
American Society for Microbiology
01.06.1985
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AbstractList | Administration of liposome-encapsulated ribavirin to mice led to ribavirin concentrations in the liver, the primary site of Rift Valley fever virus proliferation, that were fivefold greater than those attained with the same doses of free ribavirin. Liposomal ribavirin given at a dose of either 25 or 50 mg of drug per kg of body weight protected mice against a rapidly lethal high-titer challenge with Rift Valley fever virus, whereas similar doses of free drug or empty liposomes had no detectable benefit. Hence, tissue targeting of ribavirin with liposomes substantially increased the therapeutic index by increasing the efficacy of the treatment. By using liposomes as drug carriers, a nontoxic, low-dose regimen of ribavirin had a therapeutic effect that was comparable to that achieved with higher but potentially more toxic doses of free ribavirin. Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology. For an alternate route to AAC .asm.org, visit: AAC Administration of liposome-encapsulated ribavirin to mice led to ribavirin concentrations in the liver, the primary site of Rift Valley fever virus proliferation, that were fivefold greater than those attained with the same doses of free ribavirin. Liposomal ribavirin given at a dose of either 225 or 50 mg of drug per kg of body weight protected mice against a rapidly lethal high-titer challenge with Rift Valley fever virus, whereas similar doses of free drug or empty liposomes had no detectable benefit. Hence, tissue targeting of ribavirin with liposomes substantially increased the therapeutic indix by increasing the efficacy of the treatment. By using liposomes as drug carriers, a nontoxic, low-dose regimen of ribavirin had a therapeutic effect that was comparable to that achieved with higher but potentially more toxic doses of free ribavirin. |
Author | C R Alving P G Canonico M Kende W L Rill G M Swartz Jr |
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Keywords | Therapeutic efficiency Encapsulation Transportation system Liver Rodentia Liposome Rift valley fever virus Infection Virus Vertebrata Chemotherapy Mammalia Bunyaviridae Mouse Animal Viral disease Antiviral Phlebovirus |
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SubjectTerms | Animals Antibiotics. Antiinfectious agents. Antiparasitic agents Antiviral agents Biological and medical sciences Female Injections, Intravenous Liposomes Liposomes - administration & dosage Medical sciences Mice Pharmacology. Drug treatments Research Article Ribavirin Ribavirin - administration & dosage Ribavirin - metabolism Ribavirin - therapeutic use Ribonucleosides Ribonucleosides - therapeutic use Rift Valley Fever Rift Valley Fever - drug therapy Rift Valley fever virus Time Factors Tissue Distribution |
Title | Enhanced efficacy of liposome-encapsulated ribavirin against Rift Valley fever virus infection in mice |
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