Influence of nanoporous poly(ether imide) particle extracts on human aortic endothelial cells (HAECs)
Influence of nanoporous poly(ether imide) particle extracts on human aortic endothelial cells (HAECs)
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Date
2016-01-01
Authors
Kumar, Reddi K.
Basu, Sayantani
Lemke, Horst Dieter
Jankowski, Joachim
Kratz, Karl
Lendlein, Andreas
Tetali, Sarada D.
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Abstract
Accumulated uremic toxins like indoxyl sulphate, hippuric acid and p-cresyl sulphates in renal failure patients stimulate proinflammatory effects, and consequently kidney and cardiovascular diseases. Low clearance rate of these uremic toxins from the blood of uremic patients by conventional techniques like hemodialysis is due to their strong covalent albumin binding (greater than 95) and hydrophobic nature, which led to alternatives like usage of hydrophobic adsorber's in removing these toxins from the plasma of kidney patients. Polymers like polyethylene, polyurethane, polymethylmethacrylate, cellophane and polytetrafluoroethylene were already in use as substitutes for metal devices as dialysis membranes. Among new synthetic polymers, one such ideal adsorber material are highly porous microparticles of poly(ether imide) (PEI) with diameters in the range from 50-180μm and a porosity around 88±2 prepared by a spraying and coagulation process. It is essential to make sure that these synthetic polymers should not evoke any inflammatory or apoptotic response during dialysis. Therefore in our study we evaluated in vitro effect of PEI microparticle extracts in human aortic endothelial cells (HEACs) concerning toxicity, inflammation and apoptosis. No cell toxicity was observed when HAECs were treated with PEI extracts and inflammatory/apoptotic markers were not upregulated in presence of PEI extracts. Our results ensure biocompatibility of PEI particles and further hemocompatibility of particles will be tested.
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Keywords
apoptosis,
biomaterial,
inflammation,
medical devices,
Poly(ether imide) (PEI),
Tumor necrosis factor-alpha (TNF-α)
Citation
Clinical Hemorheology and Microcirculation. v.64(4)