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Novel lipoamino acid- and liposaccharide-based system for peptide delivery: Application for oral administration of tumor-selective somatostatin analogues
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1999 (English)In: Journal of Medicinal Chemistry, ISSN 0022-2623, E-ISSN 1520-4804, Vol. 42, no 19, 4010-1013 p.Article in journal (Refereed) Published
Abstract [en]

Lipoamino acid and liposaccharide conjugates of somatostatin analogue TT-232 were synthesized to modify the physicochemical properties of the parent peptide. The relative position, the number, and the nature of the lipid and/or saccharide moieties were varied. Experiments in vitro clearly showed that many compounds modified at the N- and/or C-terminus with lipid or sugar moieties retained the biological activity of the parent compound. An interesting construct was synthesized containing lipid and sugar units at opposite ends of the somatostatin analogue, so that the entire molecule could be considered as an amphipathic surfactant.

Place, publisher, year, edition, pages
1999. Vol. 42, no 19, 4010-1013 p.
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Natural Sciences
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URN: urn:nbn:se:uu:diva-50458DOI: 10.1021/jm9910167PubMedID: 10508449OAI: oai:DiVA.org:uu-50458DiVA: diva2:78366
Available from: 2008-10-17 Created: 2008-10-17 Last updated: 2017-12-05Bibliographically approved

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Lazorova, Luis

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