21
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Responsive Polymer Brushes

      Journal of Macromolecular Science, Part C: Polymer Reviews
      Informa UK Limited

      Read this article at

      ScienceOpenPublisher
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Related collections

          Most cited references96

          • Record: found
          • Abstract: found
          • Article: not found

          Polymer vesicles.

          Vesicles are microscopic sacs that enclose a volume with a molecularly thin membrane. The membranes are generally self-directed assemblies of amphiphilic molecules with a dual hydrophilic-hydrophobic character. Biological amphiphiles form vesicles central to cell function and are principally lipids of molecular weight less than 1 kilodalton. Block copolymers that mimic lipid amphiphilicity can also self-assemble into vesicles in dilute solution, but polymer molecular weights can be orders of magnitude greater than those of lipids. Structural features of vesicles, as well as properties including stability, fluidity, and intermembrane dynamics, are greatly influenced by characteristics of the polymers. Future applications of polymer vesicles will rely on exploiting unique property-performance relations, but results to date already underscore the fact that biologically derived vesicles are but a small subset of what is physically and chemically possible.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Polymersomes: tough vesicles made from diblock copolymers.

            Vesicles were made from amphiphilic diblock copolymers and characterized by micromanipulation. The average molecular weight of the specific polymer studied, polyethyleneoxide-polyethylethylene (EO40-EE37), is several times greater than that of typical phospholipids in natural membranes. Both the membrane bending and area expansion moduli of electroformed polymersomes (polymer-based liposomes) fell within the range of lipid membrane measurements, but the giant polymersomes proved to be almost an order of magnitude tougher and sustained far greater areal strain before rupture. The polymersome membrane was also at least 10 times less permeable to water than common phospholipid bilayers. The results suggest a new class of synthetic thin-shelled capsules based on block copolymer chemistry.
              Bookmark
              • Record: found
              • Abstract: not found
              • Article: not found

              Conformations of Polymers Attached to an Interface

                Bookmark

                Author and article information

                Journal
                Journal of Macromolecular Science, Part C: Polymer Reviews
                Journal of Macromolecular Science, Part C: Polymer Reviews
                Informa UK Limited
                1532-1797
                1520-5746
                December 2006
                December 2006
                : 46
                : 4
                : 397-420
                Article
                10.1080/15583720600945402
                f2358a73-1515-46f6-ae0f-edc0c6d9ab07
                © 2006
                History

                Comments

                Comment on this article