Abstract |
Infection with human cytomegalovirus (HCMV) can cause serious complications in bone-marrow and solid-organ transplant recipients, and current therapies are not optimal. We evaluated 2 orally active ether lipid ester analogues of cidofovir (CDV)--hexadecyloxypropyl-CDV ( HDP-CDV) and octadecyloxyethyl-CVD (ODE-CDV)--in severe combined immunodeficient mice in which either human fetal retinal tissue or human fetal thymus and liver tissue had been implanted and was later infected with HCMV. Our results indicate that orally administered treatment with either HDP-CDV or ODE-CDV is 4-8-fold more active, on a molar basis, than is intraperitoneally administered CDV. These data suggest that HDP-CDV and ODE-CDV should be further evaluated as potential antiviral agents for treatment of HCMV infection.
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Authors | Deborah J Bidanset, James R Beadle, W Brad Wan, Karl Y Hostetler, Earl R Kern |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 190
Issue 3
Pg. 499-503
(Aug 01 2004)
ISSN: 0022-1899 [Print] United States |
PMID | 15243923
(Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antiviral Agents
- Esters
- Lipids
- Organophosphonates
- Organophosphorus Compounds
- Prodrugs
- Ether
- Cytosine
- Cidofovir
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Topics |
- Administration, Oral
- Animals
- Antiviral Agents
(administration & dosage, chemistry, therapeutic use)
- Cidofovir
- Cytomegalovirus
(drug effects)
- Cytomegalovirus Infections
(drug therapy, virology)
- Cytosine
(administration & dosage, analogs & derivatives, chemistry, therapeutic use)
- Disease Models, Animal
- Esters
(chemistry)
- Ether
(chemistry)
- Humans
- Lipids
(chemistry)
- Male
- Mice
- Mice, SCID
- Organophosphonates
- Organophosphorus Compounds
(administration & dosage, chemistry, therapeutic use)
- Prodrugs
(administration & dosage, therapeutic use)
- Treatment Outcome
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