4.7 Article

Fabricating hemocompatible bi-continuous PEGylated PVDF membranes via vapor-induced phase inversion

Journal

JOURNAL OF MEMBRANE SCIENCE
Volume 470, Issue -, Pages 18-29

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.memsci.2014.07.014

Keywords

PEGylated PVDF membrane; VIPS process; Formation mechanisms; Antibiofouling; Hemocompatibility

Funding

  1. National Science Council Taiwan (NSC) [103-2221-E-033-074]
  2. NSC-ANR Blanc International ll Program (Taiwan-France Project: Super-NAM) [ANR-12-IS08-0002, NSC 102-2923-E-033-001-MY3]

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Lack of knowledge on their hemocompatibility limit the use of PVDF membranes in biomedical applications. Herein, we investigated the in situ modification of PVDF membranes by a PEGylatecl copolymer (PS60-b-PEGMA(108)) using vapor-induced phase separation (VIPS) process. Efforts were first oriented toward the characterization of the effect of copolymer on membrane formation, membranes physical properties and membranes surface chemistry. Then, biolouling was investigated before moving onto the hemocompatibility of membranes. Membranes structure tended to evolve from nodular to bicontinuous with PS60-b-PEGMA(108) content, evidencing a change of dominating phenomena during phase inversion (crystallization-gelling vs non-crystallization gelling), associated to a change of prevailing crystalline polymorph (beta-polymorph vs. alpha-polymorph). Furthermore, the hydration of membranes was importantly enhanced, affecting nano-biofouling: bovine serum albumin, lysozyme and fibrinogen adsorption were drastically reduced, despite rough surfaces, highlighting the efficiency of the copolymer. Bacterial attachment tests revealed that macro-biofouling was inhibited as well Results of erythrocytes, leukocytes, and thrombocytes adhesion indicated that membranes prepared from a casting solution containing 5 wt% copolymer are highly hemocompatible, result supported by low hemolysis ratio (1%) and delay of plasma clotting time. Overall, this study unveils that in situ modification coupled to the VIPS method can readily lead to hemocompatible PVDF membranes. (C) 2014 Elsevier B.V. All rights reserved,

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