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. - 1985. - 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 |