Poly(ether imide) (PEI) is being explored as potential biomaterial for cardiovascular applications.Different studies showed that human umbilical venous endothelial cells (HUVEC) are able to adhere and proliferate on PEI membranes (R q = 13.20 ± 1.58 nm). A recently published study revealed evidence for much lower platelet adhesion on very smooth PEI-films (R q = 2.37 ± 1.40 nm). Therefore, we explored whether primary human venous endothelial cells (HUVEC) are able to adhere and proliferate on such very smooth PEI-films compared to tissue-cultured polystyrene (TCP) as reference material.Cytotoxicity testing revealed that PEI had a slight cytotoxic effect on HUVEC accompanied by a marginal reduced integrity of the plasma membrane and a significant lower mitochondrial activity.However long-term seeding experiments up to eleven days exhibited that HUVEC were able to proliferate on the PEI-films till confluence (TCP 96,190 ± 18,289 cells/cm²; PEI 91,590 ± 19,583 cells/cm²). Further studies are planned to monitor the influence of shear force on the endothelial cell monolayer in a dynamic test system to determine its stability in view of shear resistant endothelialization of PEI for cardiovascular devices.
-draft version paper -
Viability and function of primary human endothelial cells on smooth poly(ether imide) filmsDipl.-Biochem. Christian Schulz Seite 2 von 21 16.08.2012
Validation of remaining solvent by headspace GCSteam sterilized PEI-film (1 g, ~150 cm²) was incubated in a sealed sample flask with 9 ml Millipore water under shaking at 37 °C for 96 hours. The supernatant atmosphere was analyzed by gas chromatography (GC) using headspace GC (HP 7694 Headspace-Sampler, HP 5890 Series II GC, DB-624, 75m column).-draft version paper -
Viability and function of primary human endothelial cells on smooth poly(ether imide) filmsDipl.-Biochem. Christian Schulz Seite 4 von 21 16.08.2012
Surface characterization by contact angle and atomic force measurements (AFM)Surface contact angle measurements (DSA 100, Krüss, captive bubble, water -air) were carried out at three different areas of each sample (n = 3) analyzing the advancing (Ѳ adv. ) and receding (Ѳ rec. ) contact angle with subsequent calculating of the hysteresis.Surface topography of the PEI-films was characterized by using atomic force microscopy (AFM, NanoScope, MultiMode V, Bruker Nano GmbH, tapping mode). Prior the samples were pre-wetted in phosphate buffered saline without calcium and magnesium ions (PBS -/-) at pH 7.4. The scanning area for each scan was 50 µm square size. Surface mean roughness (R a ) and mean square roughness (R q ) were determined by analyzing three samples on three different areas.
Endotoxin loadThe endotoxin load of the PEI-film (n = 4) was determined by using the Limulus amebocyte lysate (LAL) test (QCL 1000™, Lonza, Cologne, Germany).
Cell culture
L929-fibroblastsL929-fibroblasts (NCTC clone 929) from the connective tissue of mice were purchased from ATCC (LGC Standards GmbH, Wesel, Germany) and cultured under static cell culture co...