Drug targeting systems for antiviral agents: options and limitations
- 15 June 1992
- journal article
- review article
- Published by Elsevier in Antiviral Research
- Vol. 18 (3-4) , 215-258
- https://doi.org/10.1016/0166-3542(92)90058-d
Abstract
No abstract availableKeywords
This publication has 127 references indexed in Scilit:
- Formaldehyde treated albumin contains monomeric and polymeric forms that are differently cleared by endothelial and kupffer cells of the liver: Evidence for scavenger receptor heterogeneityBiochemical and Biophysical Research Communications, 1991
- A novel cationic liposome reagent for efficient transfection of mammalian cellsBiochemical and Biophysical Research Communications, 1991
- The Lipophilic Muramyl Peptide MTP-PE Is a Potent Inhibitor of HIV Replication in MacrophagesAIDS Research and Human Retroviruses, 1990
- Lipid conjugates of antiretroviral agents. II. Disodium palmityl phosphonoformate: Anti-HIV activity, physical properties, and interaction with plasma proteinsBiochemical and Biophysical Research Communications, 1990
- Lipid conjugates of antiretroviral agents. I. Azidothymidine-monophosphate-diglyceride: Anti-HIV activity, physical properties, and interaction with plasma proteinsBiochemical and Biophysical Research Communications, 1990
- Drug targeting: Anti-HSV-1 activity of mannosylated polymer-bound 9-(2-phosphonylmethoxyethyl)adenineBiochemical and Biophysical Research Communications, 1990
- Relations between the intracellular pathways of the receptors for transferrin, asialoglycoprotein, and mannose 6-phosphate in human hepatoma cells.The Journal of cell biology, 1989
- Preparation of EGF labeled liposomes and their uptake by hepatocytesBiochemical and Biophysical Research Communications, 1989
- Phospholipid-nucleoside conjugates. 5. The interaction of selected 1-β-D-arabinofuranosylcytosine-5′-diphosphate-L-1,2-diacylglycerols with serum lipoproteinsBiochemical and Biophysical Research Communications, 1983
- Cis-aconityl spacer between daunomycin and macromolecular carriers: A model of pH-sensitive linkage releasing drug from a lysosomotropic conjugateBiochemical and Biophysical Research Communications, 1981