Preparation and evaluation of heparin-immobilized poly (lactic acid) (PLA) membrane for hemodialysis

被引:161
作者
Gao, Ailin [1 ]
Liu, Fu [1 ]
Xue, Lixin [1 ]
机构
[1] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Poly (lactic acid) membrane; Hemodialysis; Heparinization; Bio-based material; SURFACE MODIFICATION; POLY(L-LACTIC ACID); BLOOD COMPATIBILITY; PERMEABILITY; POLYDOPAMINE; PERFORMANCE; FIBER; FILM;
D O I
10.1016/j.memsci.2013.10.016
中图分类号
TQ [化学工业];
学科分类号
081705 [工业催化];
摘要
Bio-based poly (lactic acid) membrane with asymmetric porous structure was developed for hemodialysis via phase inversion for the first time. Heparin was immobilized to PLA membrane surface through the strong adhesion ability of dopamine, as confirmed by attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS) respectively. The morphologies variations of PLA membranes induced by dopamine coating and heparin immobilization were analyzed by scanning electron microscope (SEM) and atomic force microscopy (AFM). Hydrophilicity and permeability of PLA membranes before and after modification were characterized. Particularly, platelet adsorption, plasma recalcification time and hemolysis ratio were executed to evaluate the blood compatibility of PLA membranes decorated by heparin. The in vitro results demonstrated that surface heparinization improved the hemocompatibility of PLA membrane, suppressed the adhesion of platelet, extended plasma recalcilication time, and also decreased hemolysis ratio. The dialysis simulation experiments including urea and lysozyme clearance as well as bovine serum albumin (BSA) rejection were implemented to determine the dialysis performances. The results showed that 79% of urea and 18% of lysozyme were cleaned and over 90% of BSA was retained. This study disclosed a window of opportunity to produce novel hemodialysis membranes using bio-based materials. (C) 2013 Elsevier B.V. All rights reserved
引用
收藏
页码:390 / 399
页数:10
相关论文
共 35 条
[1]
LATE DEGRADATION TISSUE-RESPONSE TO POLY(L-LACTIDE) BONE PLATES AND SCREWS [J].
BERGSMA, JE ;
DEBRUIJN, WC ;
ROZEMA, FR ;
BOS, RRM ;
BOERING, G .
BIOMATERIALS, 1995, 16 (01) :25-31
[2]
Development of poly(L-lactic acid) hollow fiber membranes for artificial vasculature in tissue engineering scaffolds [J].
Bettahalli, N. M. S. ;
Steg, H. ;
Wessling, M. ;
Stamatialis, D. .
JOURNAL OF MEMBRANE SCIENCE, 2011, 371 (1-2) :117-126
[3]
MECHANISM OF THE ANTICOAGULANT ACTION OF HEPARIN [J].
BJORK, I ;
LINDAHL, U .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1982, 48 (03) :161-182
[4]
Surface modification of electrospun PLLA nanofibers by plasma treatment and cationized gelatin immobilization for cartilage tissue engineering [J].
Chen, Jyh-Ping ;
Su, Chien-Hao .
ACTA BIOMATERIALIA, 2011, 7 (01) :234-243
[5]
The hydrodynamic permeability and surface property of polyethersulfone ultrafiltration membranes with mussel-inspired polydopamine coatings [J].
Cheng, Chong ;
Li, Shuang ;
Zhao, Weifeng ;
Wei, Qiang ;
Nie, Shengqiang ;
Sun, Shudong ;
Zhao, Changsheng .
JOURNAL OF MEMBRANE SCIENCE, 2012, 417 :228-236
[6]
Poly(lactic-co-glycolic acid) hollow fibre membranes for use as a tissue engineering scaffold [J].
Ellis, Marianne J. ;
Chaudhuri, Julian B. .
BIOTECHNOLOGY AND BIOENGINEERING, 2007, 96 (01) :177-187
[7]
Poly(lactic acid) fiber: An overview [J].
Gupta, Bhuvanesh ;
Revagade, Nilesh ;
Hilborn, Jons .
PROGRESS IN POLYMER SCIENCE, 2007, 32 (04) :455-482
[8]
Hydrophilic, semipermeable membranes fabricated with poly(ethylene oxide)-polysulfone block copolymer [J].
Hancock, LF ;
Fagan, SM ;
Ziolo, MS .
BIOMATERIALS, 2000, 21 (07) :725-733
[9]
Preparation and performance of protein-adsorption-resistant asymmetric porous membrane composed of polysulfone/phospholipid polymer blend [J].
Hasegawa, T ;
Iwasaki, Y ;
Ishihara, K .
BIOMATERIALS, 2001, 22 (03) :243-251
[10]
The blood and vascular cell compatibility of heparin-modified ePTFE vascular grafts [J].
Hoshi, Ryan A. ;
Van Lith, Robert ;
Jen, Michele C. ;
Allen, Josephine B. ;
Lapidos, Karen A. ;
Ameer, Guillermo .
BIOMATERIALS, 2013, 34 (01) :30-41