One-pot synthesis of highly hemocompatible polyurethane/polyethersulfone composite membranes

被引:7
|
作者
Wang, Chen [1 ]
Wang, Qian [1 ]
Li, Shuangsi [1 ]
Zhang, Man [1 ]
Zhao, Weifeng [1 ]
Sun, Shudong [1 ]
Zhao, Changsheng [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat Engn, Chengdu 610065, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
POLYETHERSULFONE ULTRAFILTRATION MEMBRANE; NANOFILTRATION MEMBRANE; ANTIFOULING PROPERTIES; SURFACE MODIFICATION; CELL-ADHESION; HIGH-FLUX; OXIDE; ANTICOAGULANT; PERFORMANCE; FABRICATION;
D O I
10.1007/s00289-017-1922-5
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this study, polyethersulfone (PES) membranes were modified by in situ cross-linking polymerization of polyurethane with functional groups of -COOH and -SO3H using PEG as the chain extender in one pot, followed with a phase inversion technique. The composite membranes were characterized by FTIR, water contact angle, and scanning electron microscope. Comparing with pristine PES membrane, the modified membranes showed decreased water contact angles and changed cross-sectional morphology. The modified membranes also showed decreased protein adsorption and suppressed platelet adhesion, as well as improved antifouling property. In addition, the composite membranes had prolonged activated partial thromboplastin times due to the functional groups and improved hydrophilicity. The results of contact activation and complement activation also indicated that the modified membranes had good blood compatibility. Furthermore, the cytocompatibility was significantly improved. The highly hemocompatible PES composite membranes fabricated by the in situ cross-linking polymerization of polyurethane may have great potential to be used in the field of blood purification.
引用
收藏
页码:3797 / 3818
页数:22
相关论文
共 50 条
  • [21] An organocatalyzed highly regioselective one-pot approach to the synthesis of tetrahydrobenzofuranones
    Chawla, Ruchi
    Singh, Atul K.
    Yadav, Lal Dhar S.
    TETRAHEDRON LETTERS, 2012, 53 (26) : 3382 - 3384
  • [22] One-pot synthesis of highly fluorescent polycyclic benzimidazole derivatives
    Manna, Susanta Kumar
    Mondal, Suresh Kumar
    Ahmed, Atiur
    Mandal, Arabinda
    Jana, Atanu
    Ikbal, Mohammed
    Samanta, Shubhankar
    Ray, Jayanta K.
    RSC ADVANCES, 2014, 4 (05): : 2474 - 2481
  • [23] An Efficient Organocatalysis: A One-Pot Highly Enantioselective Synthesis of -Aminophosphonates
    Thorat, Prashant B.
    Goswami, Santosh V.
    Magar, Rupali L.
    Patil, Bhagwan R.
    Bhusare, Sudhakar R.
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2013, 2013 (24) : 5509 - 5516
  • [24] One-pot synthesis of highly functionalised 1-tosylpyrazolidines
    Mohebat, Razieh
    Naseri, Samira
    Hassanabadi, Alireza
    JOURNAL OF CHEMICAL RESEARCH, 2014, (03) : 175 - 177
  • [25] One-Pot Synthesis of Highly Dispersible Fluorescent Nanodiamonds for Bioconjugation
    Terada, Daiki
    Sotoma, Shingo
    Harada, Yoshie
    Igarashi, Ryuji
    Shirakawa, Masahiro
    BIOCONJUGATE CHEMISTRY, 2018, 29 (08) : 2786 - 2792
  • [26] One-pot synthesis of new highly substituted allylic phosphorodiamidates
    Bahri, Leila
    Barhoumi-Slimi, T.
    Mallek, R.
    Sanhoury, M. A. K.
    Crousse, B.
    Ben Dhia, M. T.
    JOURNAL OF FLUORINE CHEMISTRY, 2016, 189 : 96 - 101
  • [27] One-Pot, Highly Stereoselective Synthesis of Dithioacetal-α,α-Diglycosides
    Davila, Maria F. Cespedes
    Schneider, Jeremy P.
    Godard, Amelie
    Hazelard, Damien
    Compain, Philippe
    MOLECULES, 2018, 23 (04):
  • [28] Stereoselective one-pot synthesis of highly differently substituted thiochromans
    Seifert, Andrea
    Mahrwald, Rainer
    TETRAHEDRON LETTERS, 2009, 50 (47) : 6466 - 6468
  • [29] One-pot synthesis of responsive polymers with highly branched structures
    Gao, Haifeng
    Shi, Yi
    Cao, Xiaosong
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253
  • [30] Cellulose–silica composite aerogels from “one-pot” synthesis
    Arnaud Demilecamps
    Gudrun Reichenauer
    Arnaud Rigacci
    Tatiana Budtova
    Cellulose, 2014, 21 : 2625 - 2636