Ferrocene-Modified Phospholipid : An Innovative Precursor for Redox-Triggered Drug Delivery Vesicles Selective to Cancer Cells

Controlled payload release is one of the key elements in the creation of a reliable drug delivery system. We report the discovery of a drug delivery vessel able to transport chemotherapeutic agents to target cancer cells and selectively trigger their release using the electrochemical activity of a f...

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Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1999. - 32(2016), 17 vom: 03. Mai, Seite 4169-78
1. Verfasser: Noyhouzer, Tomer (VerfasserIn)
Weitere Verfasser: L'Homme, Chloé, Beaulieu, Isabelle, Mazurkiewicz, Stephanie, Kuss, Sabine, Kraatz, Heinz-Bernhard, Canesi, Sylvain, Mauzeroll, Janine
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2016
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article Research Support, Non-U.S. Gov't Drug Carriers Ferrous Compounds Metallocenes Phospholipids Doxorubicin 80168379AG ferrocene U96PKG90JQ
Beschreibung
Zusammenfassung:Controlled payload release is one of the key elements in the creation of a reliable drug delivery system. We report the discovery of a drug delivery vessel able to transport chemotherapeutic agents to target cancer cells and selectively trigger their release using the electrochemical activity of a ferrocene-modified phospholipid. Supported by in vitro assays, the competitive advantages of this discovery are (i) the simple one step scalability of the synthetic process, (ii) the stable encapsulation of toxic drugs (doxorubicin) during transport, and (iii) the selective redox triggering of the liposomes to harness their cytotoxic payload at the cancer site. Specifically, the redox-modified giant unilamellar vesicle and liposomes were characterized using advanced methods such as scanning electrochemical microscopy (SECM), transmission electron microscopy (TEM), dynamic light scattering (DLS), and fluorescent imaging
Beschreibung:Date Completed 29.05.2018
Date Revised 31.03.2022
published: Print-Electronic
Citation Status MEDLINE
ISSN:1520-5827
DOI:10.1021/acs.langmuir.6b00511