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Therapeutically optimized rates of drug release can be achieved by varying the drug-to-lipid ratio in liposomal vincristine formulations. 2006 (English)In: Biochim Biophys Acta, ISSN 0006-3002, Vol. 1758, no 1, p. 55-64Article in journal (Refereed) Published

Place, publisher, year, edition, pages

2006. Vol. 1758, no 1, p. 55-64

Keywords [en]

Adenocarcinoma/drug therapy/metabolism, Animals, Chemistry; Pharmaceutical, Cryoelectron Microscopy, Female, Half-Life, Humans, Ionophores/chemistry, Kinetics, Lipids/*chemistry/pharmacokinetics, Liposomes/*chemistry/metabolism, Mice, Mice; Inbred ICR, Research Support; Non-U.S. Gov't, Time Factors, Vincristine/*chemistry/pharmacokinetics/pharmacology

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URN: urn:nbn:se:uu:diva-81681PubMedID: 16487476OAI: oai:DiVA.org:uu-81681DiVA, id: diva2:109596

Available from: 2006-08-30 Created: 2006-08-30 Last updated: 2011-01-11

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PubMedhttp://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Retrieve&list_uids=16487476&dopt=Citation

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Edwards, KatarinaKarlsson, Göran

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Edwards, KatarinaKarlsson, Göran

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Physical ChemistryDepartment of Physical and Analytical Chemistry

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