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Status: Bibliographieeintrag

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Verfasst von:Funk, Dorothee [VerfasserIn]   i
 Schrenk, Hans-Hermann [VerfasserIn]   i
 Frei, Eva [VerfasserIn]   i
Titel:Development of a novel polyethylene glycol-corticosteroid-conjugate with an acid-cleavable linker
Verf.angabe:Dorothee Funk, Hans-Hermann Schrenk & Eva Frei
Jahr:2011
Umfang:12 S.
Fussnoten:Gesehen am 01.06.2023 ; Online veröffentlicht: 02 Aug 2010
Titel Quelle:Enthalten in: Journal of drug targeting
Ort Quelle:Abingdon : Taylor & Francis Group, 1993
Jahr Quelle:2011
Band/Heft Quelle:19(2011), 6, Seite 434-445
ISSN Quelle:1029-2330
Abstract:Background: Corticosteroids like dexamethasone are often used in the treatment of inflammatory diseases. Despite efficacy, their use is limited by severe side-effects. Targeted drug-delivery to the site of inflammation would be advantageous for the patients. Macromolecules can be used for this approach, because they accumulate at sites of inflammation due to the enhanced permeability and retention effect.Purpose: Our aim was to develop a polymer-corticosteroid-conjugate for the treatment of inflammatory diseases. The authors covalently linked a derivative of dexamethasone to the macromolecule polyethylene glycol (PEG), using an acid-cleavable linker to achieve lysosomal drug-release.Methods: The corticosteroid-PEG-conjugate was synthesized and characterized by nuclear magnetic resonance spectroscopy (NMR) and mass spectrometry. Cleavage experiments were performed to study the nature of products after incubation at acidic pH, and the efficacy of the conjugate was tested in two model cell lines.Results: Acid hydrolysis of the novel corticosteroid-PEG-conjugate resulted in two new derivatives of dexamethasone. The conjugate was effective in both model cell lines showing lysosomal release and efficacy of the cleavage products.Discussion and conclusion: The authors new corticosteroid-PEG-conjugate shows glucocorticoid activity and should be developed further to treat inflammatory diseases with reduced side-effects while retaining drug efficacy.
DOI:doi:10.3109/1061186X.2010.504271
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.3109/1061186X.2010.504271
 DOI: https://doi.org/10.3109/1061186X.2010.504271
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:dexamethasone
 drug targeting
 inflammatory disease
 lysosome
 Polyethylene glycol
K10plus-PPN:1847135501
Verknüpfungen:→ Zeitschrift

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