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Platelet adhesion on the gradient surfaces grafted with phospholipid polymer
Y Iwasaki1, K Ishihara, N Nakabayashi
1Institute for Medical and Dental Engineering, Tokyo Medical and Dental University, Japan.
Journal of Biomaterials Science. Polymer Edition
|September 2, 1998
Summary
Omega-methacryloyloxyalkyl phosphorylcholine (MAPC) polymers create a biomembrane-like surface, enhancing blood compatibility by attracting phospholipids. This study optimized MAPC polymer grafting on polyethylene for improved blood-contacting materials.
Area of Science:
- Biomaterials Science
- Polymer Chemistry
- Surface Chemistry
Background:
- Blood-compatible materials are crucial for medical devices.
- Existing materials often trigger adverse biological responses.
- Omega-methacryloyloxyalkyl phosphorylcholine (MAPC) polymers show promise due to their phospholipid affinity.
Purpose of the Study:
- To synthesize and evaluate MAPC polymers for blood compatibility.
- To investigate the effect of MAPC chemical structure on blood compatibility.
- To create a gradient poly(MAPC)-grafted polyethylene surface to study these effects.
Main Methods:
- Synthesis of MAPC polymers.
- Corona discharge treatment to graft poly(MAPC) onto polyethylene (PE).
- X-ray photoelectron spectroscopy (XPS) for surface composition (P/C ratio).
- Contact angle measurements for surface hydrophilicity.
- Platelet adhesion tests.
Main Results:
- Gradient poly(MAPC) grafting on PE was achieved, confirmed by increasing P/C ratio and decreasing water contact angle with corona irradiation energy.
- Surface density of MAPC units increased and plateaued, indicating complete surface coverage.
- Longer methylene chains in MAPC enhanced phospholipid exposure and surface hydrophobicity.
- Platelet adhesion significantly reduced on surfaces with constant P/C ratio.
Conclusions:
- MAPC polymers exhibit excellent blood compatibility due to biomembrane-like surface formation via phospholipid adsorption.
- Surface modification of PE with MAPC, controlled by corona discharge, effectively improves blood compatibility.
- The chemical structure, specifically methylene chain length, influences surface properties and blood interaction.