Poly(2-oxazolines) in biological and biomedical application contexts

被引:424
|
作者
Adams, Nico [2 ]
Schubert, Ulrich S. [1 ,3 ,4 ]
机构
[1] Eindhoven Univ Technol, Lab Macromol Chem & Nanosci, NL-5600 MB Eindhoven, Netherlands
[2] Univ Cambridge, Univ Chem Lab, Unilever Ctr Mol Sci Informat, Cambridge CB1 9SB, England
[3] Dutch Polymer Inst, NL-5612 AB Eindhoven, Netherlands
[4] Univ Jena, Lab Organ & Macromol Chem, D-07743 Jena, Germany
关键词
polyoxazoline; biomaterials; self-assembly; drug delivery; gene delivery; stimuli-responsive polymers;
D O I
10.1016/j.addr.2007.08.018
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Polyoxazolines of various architectures and chemical functionalities can be prepared in a living and therefore controlled manner via cationic ring-opening polymerisation. They have found widespread applications, ranging from coatings to pigment dispersants. Furthermore, several polyoxazolines are water-soluble or amphiphilic and relatively non-toxic, which makes them interesting as biomaterials. This paper reviews the development of polyoxazoline-based polymers in biological and biomedical application contexts since the beginning of the millennium. This includes nanoscalar systems such as membranes and nanoparticles, drug and gene delivery applications, as well as stimuli-responsive systems. (c) 2007 Published by Elsevier B.V.
引用
收藏
页码:1504 / 1520
页数:17
相关论文
共 50 条
  • [31] Poly(2-oxazolines) triblock copolymers with mutually immiscible hydrophilic, hydrophobic and fluorophilic blocks
    Kaberov, Leonid
    Verbraeken, Bart
    Filippov, Sergey
    Hruby, Martin
    Riabtseva, Anna
    Kovacik, Lubomir
    Stepanek, Petr
    Hoogenboom, Richard
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 252
  • [32] BLOCK AND GRAFT-COPOLYMERS OF 2-OXAZOLINES
    KOBAYASHI, S
    SAEGUSA, T
    MAKROMOLEKULARE CHEMIE-MACROMOLECULAR CHEMISTRY AND PHYSICS, 1985, : 11 - 24
  • [33] ASYMMETRIC-SYNTHESIS OF GLYCIDIC 2-OXAZOLINES
    LIDDELL, R
    WHITELEY, C
    JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1983, (24) : 1535 - 1537
  • [34] THERMAL POLYMERIZATION OF 2-(MERCAPTOALKYL)-2-OXAZOLINES
    GUNATILLAKE, PA
    ODIAN, G
    TOMALIA, DA
    MACROMOLECULES, 1987, 20 (10) : 2356 - 2362
  • [35] Hypervalent iodine oxidation of indolic 2-oxazolines
    Braun, NA
    Bray, JD
    Ciufolini, MA
    TETRAHEDRON LETTERS, 1999, 40 (27) : 4985 - 4988
  • [36] Rearrangement of 3-Hydroxyazetidines into 2-Oxazolines
    Ruggeri, Michele
    Dombrowski, Amanda W.
    Djuric, Stevan W.
    Baxendale, Ian R.
    JOURNAL OF ORGANIC CHEMISTRY, 2020, 85 (11): : 7276 - 7286
  • [37] Comparison of the π-electron delocalization in 2-oxazolines and esters
    Luef, Klaus
    Fimberger, Martin
    Fischer, Roland
    Stelzer, Franz
    Kallay, Mihaly
    Wiesbrock, Frank
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2016, 251
  • [38] MACROMOLECULAR ENGINEERING ON THE BASIS OF THE POLYMERIZATION OF 2-OXAZOLINES
    SAEGUSA, T
    CHUJO, Y
    MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1991, 51 : 1 - 10
  • [39] BLOCK AND GRAFT-COPOLYMERS OF 2-OXAZOLINES
    ROLF
    SCHULZ, C
    DWORAK, A
    MACROMOLECULAR SYMPOSIA, 1994, 85 : 203 - 210
  • [40] 2-OXAZOLINES - POLYMERIZATION CHEMISTRY AND POLYMER PROPERTIES
    SAEGUSA, T
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1988, 195 : 11 - POLY