| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 600870 | Colloids and Surfaces B: Biointerfaces | 2012 | 9 Pages |
Cylindrical copolypeptide brushes PLLF-g-(PLF-b-PLG) with poly(l-lysine-co-l-phenylalanine) (PLLF) as the backbone and poly(l-phenylalanine)-b-poly(l-glutamic acid) (PLF-b-PLG) as the side chains have been synthesized and evaluated as drug delivery carriers. The synthesized copolypeptide brushes were characterized by 1H NMR, gel permeation chromatography (GPC), and transmission electron microscopy (TEM). In aqueous solution, the copolypeptide brushes adopt cylindrical morphologies and resemble unimolecular polymeric micelles with a hydrophobic poly(l-phenylalanine) core and a hydrophilic poly(l-glutamate) shell. An encapsulation study demonstrated that these water soluble, biodegradable copolypeptide brushes encapsulate hydrophobic compounds and cationic hydrophilic guest molecules simultaneously. Furthermore, the encapsulated cationic model compounds exhibit a pH-responsive releasing property.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► We design and synthesize amphiphilic cylindrical copolypeptide brushes. ► Copolypeptide brushes resemble unimolecular micelles. ► Copolypeptide brushes encapsulate hydrophobic and cationic guest molecules simultaneously. ► Structure of these polymer brushes is easily extended and modulated.
