Amphiphilic Polypeptoids Rupture Vesicle Bilayers To Form Peptoid-Lipid Fragments Effective in Enhancing Hydrophobic Drug Delivery
Peptoids are highly biocompatible pseudopeptidic polyglycines with designable substituents on the nitrogen atoms. The therapeutic and drug-carrying potential of these materials requires a fundamental understanding of their interactions with lipid bilayers. In this work, we use amphiphilic polypeptoi...
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Bibliographische Detailangaben
Veröffentlicht in: | Langmuir : the ACS journal of surfaces and colloids. - 1992. - 35(2019), 47 vom: 26. Nov., Seite 15335-15343
|
1. Verfasser: |
Zhang, Yueheng
(VerfasserIn) |
Weitere Verfasser: |
Heidari, Zahra,
Su, Yang,
Yu, Tianyi,
Xuan, Sunting,
Omarova, Marzhana,
Aydin, Yucel,
Dash, Srikanta,
Zhang, Donghui,
John, Vijay |
Format: | Online-Aufsatz
|
Sprache: | English |
Veröffentlicht: |
2019
|
Zugriff auf das übergeordnete Werk: | Langmuir : the ACS journal of surfaces and colloids
|
Schlagworte: | Journal Article
Research Support, U.S. Gov't, Non-P.H.S.
Antineoplastic Agents
Drug Carriers
Lipid Bilayers
Liposomes
Peptoids
Phosphatidylcholines
Protein Kinase Inhibitors
Surface-Active Agents
mehr...
Sorafenib
9ZOQ3TZI87 |