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Articles

Hemocompatibility of pseudozwitterionic polymer brushes with a systematic well-defined charge-bias control

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Pages 1558-1572 | Received 31 Mar 2014, Accepted 03 May 2014, Published online: 04 Jun 2014
 

Abstract

In this study, a pseudozwitterionic surface bearing positively and negatively mixed charged moieties was developed as a potential hemocompatible material for biomedical applications. In this work, hemocompatility of pseudozwitterionic surface prepared from copolymerization of negatively charged 3-sulfopropyl methacrylate (SA) and positively charged [2-(methacryloyloxy)ethyl] trimethylammonium (TMA) was delineated. Mixed charge distribution in the prepared poly(TMA-co-SA)-grafted surface can be controlled by regulating TMA and SA monomer ratios via surface-initiated atom transfer radical polymerization. The effects of grafting composition and charge bias variations on blood compatibility of poly(TMA-co-SA)-grafted surface were reported. The protein adsorption on different poly(TMA-co-SA)-grafted surfaces from human plasma protein (fibrinogen, HSA, and γ-globulin) solutions was evaluated using an enzyme-linked immunosorbent assay. Blood platelet adhesion and time measurements on plasma clotting were conducted to determine the platelet activation on the grafted surface. It was found that the protein resistance and anti-blood cell adhesion of prepared surface can be precisely controlled by controlling the charge balance of TMA/SA compositions. In addition, different charge bias variations on the poly(TMA-co-SA)-grafted surface would induce electrostatic interactions between plasma proteins and prepared surfaces which lead to adsorptions of interfacial protein and blood cells, plasma clotting, and blood cell hemolysis. Results from this study suggest that the hemocompatility of mixed charged poly(TMA-co-SA)-grafted surface depends on the charge bias level. This provides a great potential for designing biomaterial with unique surface chemical structure which could be used in contact with human blood.

Acknowledgments

The authors would like to acknowledge the Center-of-Excellence (COE) Program on Membrane Technology from the Ministry of Education (MOE), R.O·C., the project of Outstanding Professor Research Program in the Chung Yuan Christian University, Taiwan (CYCU-00RD-RA002-11,757), and the Ministry of Science and Technology (100-2628-E-033-001-MY3 and 102-2221-E-033-009-MY3) for their financial support. Deanship of Scientific Research, College of Science Research Center, King Saud University, and Kingdom of Saudi Arabia are also acknowledged. Yung Chang thanks the King Saud University, Riyadh, Kingdom of Saudi Arabia, for the Visiting Professorship.

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