Kikuko Fukumoto

Modification of polysulfone with phospholipid polymer for improvement of the blood compatibility. Part 2. Protein adsorption and platelet adhesion.

Protein adsorption and platelet adhesion from human plasma on polysulfone (PSf) membranes modified with 2-methacryloyloxyethyl phosphorylcholine (MPC) polymer were studied. The modification was carried out by blending of the MPC polymer in the PSf. The amount of protein adsorbed on the PSf/MPC polymer blend membrane was significantly decreased with an increase in the composition of the blended MPC polymer. The distribution of the specific proteins adsorbed on the membrane surface was also determined by a gold-colloid immunoassay. Albumin, gamma-globulin and fibrinogen were observed on every membrane surface after contact with plasma. However, in the case of the blended membrane, the density of the adsorbed proteins decreased compared with that of original PSf membrane. That is, the MPC polymer blended in the membrane could function as a protein-adsorption-resistant additive. The number of platelets adhered on the PSf membrane was reduced, and change in the morphology of adherent platelets was also suppressed by the modification with the MPC polymer. Therefore, the PSf/MPC polymer blend membrane had improved blood compatibility compared with the PSf membrane.

Modification of polysulfone with phospholipid polymer for improvement of the blood compatibility. Part 1. Surface characterization

To improve the surface blood compatibility of polysulfone (PSf) membranes, we prepared novel polymeric additives which have suitable blood compatibility. They were polymers with a phosphorylcholine group, a 2-methacryloyloxyethyl phosphorylcholine (MPC) unit. The MPC polymer could be blended with polysulfone by a solvent evaporation method during membrane processing, and a transparent membrane could be obtained. The mechanical properties of the blend membrane were similar to that of the original PSf membrane. Surface analysis of the blend membrane by X-ray photoelectron spectroscopy and dynamic contact angle measurement revealed that the MPC unit in the polymeric additive was concentrated on the surface of the membrane. The blend membrane significantly reduced plasma protein adsorption compared with that of the PSf membrane.

Improvement of blood compatibility on cellulose dialysis membrane I. Grafting of 2-methacryloyloxyethyl phosphorylcholine on to a cellulose membrane surface

A methacrylate with a phospholipid polar group, 2-methacryloyloxyethyl phosphorylcholine (MPC), was grafted on cellulose membrane for haemodialysis in an aqueous medium using cerium ion (Ce4+) as an initiator. The effects of the concentrations of MPC and Ce4+, and degassing of feed solution on the grafting of MPC on the surface and the membrane properties such as permeability and mechanical strength were examined. The grafted MPC composition depended on the concentrations of both the monomer and initiator in the feed solution. When the grafted MPC distribution was controlled by the monomer concentration, the permeability of the membrane decreased with an increase in grafted MPC distribution. On the other hand, the permeability was not changed from the original membranes value when the MPC distribution was regulated by Ce4+ concentration. The tensile strength of the membrane did not change during the grafting of MPC and this indicated that the grafting had taken place in the amorphous region of the cellulose. These results suggested that this method is a promising way to improve the blood compatibility of a cellulose membrane without having an adverse effect on the haemodialysis membrane.

Improvement of blood compatibility on cellulose dialysis membrane: 2. Blood compatibility of phospholipid polymer grafted cellulose membrane

The blood compatibility of a cellulose haemodialysis membrane whose surface was grafted with a methacrylate having a phospholipid polar group, 2-methacryloyloxyethyl phosphorylcholine, was evaluated with attention to platelet adhesion to the membrane surface and complement activation induced by the membrane. When the original cellulose membrane came in contact with platelet-rich plasma for 30 min, numerous platelets adhered to the surface and aggregated. On the other hand, the membrane grafted with 2-methacryloyloxyethyl phosphorylcholine effectively suppressed platelet adhesion and activation. This effect became more pronounced with increasing surface distribution. Especially, the 2-methacryloyloxyethyl phosphorylcholine grafted membranes, whose distribution exceeded 0.27, completely inhibited platelet adhesion, even when the contact time was 180 min. Moreover, the complement activation was also reduced with increased 2-methacryloyloxyethyl phosphorylcholine distribution on the surface of the membrane.

HYDROGEN-BONDING-DRIVEN SPONTANEOUS GELATION OF WATER-SOLUBLE PHOSPHOLIPID POLYMERS IN AQUEOUS MEDIUM

It has been found that mixing of two kinds of water-soluble phospholipids polymers, such as poly(2-methacryloyloxyethyl phosphorylcholine-co-methacrylic acid) (PMA) and poly(2-methacryloyloxyethyl phosphorylcholine-co-n-butyl methacrylate) (PMB), spontaneously forms a hydrogel in aqueous medium at room temperature without any chemical treatment. However, the mechanism of spontaneous gelation has not been clarified yet. The purpose of this study is to investigate the gelation mechanism of the hydrogel. Moreover, effects of ions on gelation and dissolution behavior were observed. We investigated the mechanism of the hydrogel formation by spectroscopic techniques and a rheological method with attention to the interactions between polymer chains. Both Raman spectroscopic analysis and FT-IR analysis revealed that carboxyl groups in methacrylic acid (MA) formed dimer when two polymer solutions were mixed, and the results of the rheological study showed dissociation of carboxyl groups caused dissolution of the hydrogel. Thus, the gelation occurred due to the formation of dimers by hydrogen bonding which acts as a physical cross-linking of polymer chains. The hydrogel dissolved in a large amount of aqueous medium. We also observed the addition of inorganic salts during the preparation of the hydrogel affected the gelation and dissolution behaviors by a rheological and a weight measuring method, respectively. The gelation period became longer in the presence of NaCl and CaCl2 compared with that in the absence of these salts. NaCl and CaCl2 disturbed the formation of hydrogen bonding between carboxyl groups by stabilization of carboxylate anion of the MA units. On the other hand, addition of FeCl3 made the gelation period shorter and stabilized the hydrogel in the aqueous medium. This is because FeCl3 can suppress dissociation of the carboxyl groups by acidic condition of FeCl3 aqueous solution and cross-link the carboxylate anions in the PMA effectively.