Amphiphilic vinyl polymers effectively prolong liposome circulation time in vivo
- 1 October 1994
- journal article
- research article
- Published by Elsevier in Biochimica et Biophysica Acta (BBA) - Biomembranes
- Vol. 1195 (1), 181-184
- https://doi.org/10.1016/0005-2736(94)90025-6
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Why do Polyethylene Glycol-Coated Liposomes Circulate So Long?: Molecular Mechanism of Liposome Steric Protection with Polyethylene Glycol: Role of Polymer Chain FlexibilityJournal of Liposome Research, 1994
- Sterically stabilized liposomesBiochimica et Biophysica Acta (BBA) - Reviews on Biomembranes, 1992
- Repulsive interactions and mechanical stability of polymer-grafted lipid membranesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1992
- Targeted accumulation of polyethylene glycol‐coated immunoliposomes in infarcted rabbit myocardiumThe FASEB Journal, 1992
- The role of surface charge and hydrophilic groups on liposome clearance in vivoBiochimica et Biophysica Acta (BBA) - Biomembranes, 1992
- Sterically stabilized liposomes: a hypothesis on the molecular origin of the extended circulation timesBiochimica et Biophysica Acta (BBA) - Biomembranes, 1991
- Pharmacokinetics of stealth versus conventional liposomes: effect of doseBiochimica et Biophysica Acta (BBA) - Biomembranes, 1991
- Amphipathic polyethyleneglycols effectively prolong the circulation time of liposomesFEBS Letters, 1990
- Immunochemical studies of conjugates of isomaltosyl oligosaccharides to lipid. I. Antigenicity of the glycolipids and the production of specific antibodies in rabbits.The Journal of Experimental Medicine, 1981