the protein adsorption assay, and onto a glass substrate for the cell and platelet adhesion assay. The samples were subsequently heated to 100 C under vacuum for 1 h. It was confirmed by XPS (O/C atomic ratio) that the surface structure of the present sample (heated at 100 C for 1 h) was almost the same as that of the equilibrated sample [8], which was heated at 140 C for 12±24 h.Surface Analysis: The surfaces of the samples were observed using an SEM (XL30, FEI Japan Ltd., Japan), a profile measurement microscope (VF-7500, Keyence Co., Japan), and an XPS (Quantum 2000, Ulvac-Phi Inc., Japan). In the XPS measurements, monochromated Al Ka X-rays were used as the source, and the photoelectron take-off angle was set at 45.Protein Adsorption Assay: The samples were immersed in 2 mL of a phosphate-buffered saline (PBS), supplemented with fibrinogen (40 lg mL ±1 , Sigma-Aldrich, USA) or albumin (460 lg mL ±1 , SigmaAldrich., USA) at 37 C for 2 h. After removal from the saline solution, the samples were gently rinsed with PBS three times, and then dried. The N/C atomic ratio on the sample surface was determined from XPS measurements.Cell Adhesion Assay: The samples were placed in a 24-well PS plate. The L929 cells (Riken Bioresource Center, Japan) were suspended in Dulbecco's modified eagle medium supplemented with 5 % horse serum at a concentration of 1.2 10 5 cells mL
±1. 2 mL of the cell suspensions were added to the samples in each well, and the cells were cultured at 37 C in a 5 % CO 2 atmosphere for 20 h. After cell culturing, the samples were gently rinsed with PBS three times. Cells adhering to the sample surface were detached from the samples using an ethylenediaminetetraacetic acid (EDTA)-trypsin solution, and then stained with trypan blue. The number of stained cells was counted using a hemocytometer.Platelet Adhesion Assay: Blood was collected in a heparin-containing polypropylene tube from a 22-year-old man with his consent. The blood, containing 2 U mL ±1 of heparin, was centrifuged twice at 160 g to obtain platelet-rich plasma. This was then centrifuged at 1300 g for 10 min to separate the platelets from the plasma. The platelets were labeled with 5-or 6-(N-succinimidyloxycarbonyl)-3¢,6¢-O,O¢-diacetylfluorescein at 37 C for 30 min, and then centrifuged at 1300 g for 10 min. The labeled platelets were then suspended in the supernatant fluid separated centrifugally from the platelet-rich plasma at a near physiological concentration of 1.0 10 5 platelets mL ±1 . The samples, PMMA (negative control), and HUVEC (positive control) were subjected to a shear flow of the platelet suspension at a rate of 50 s ±1 using a cone and plate-type viscometer [9] equipped with a microscope and a silicon-intensified target camera. The number of platelets adhering to the sample was counted at 5, 10, and 15 min after imposing the shear flow.