PMID- 15348951 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20050307 LR - 20191026 IS - 0957-4530 (Print) IS - 0957-4530 (Linking) VI - 9 IP - 12 DP - 1998 Dec TI - In vitro response of osteoblasts to hydroxyapatite-reinforced polyethylene composites. PG - 845-8 AB - A primary human cell culture model was used to investigate a range of hydroxyapaptite (HA)-reinforced high-density polyethylene (HDPE) composites (HAPEX). These materials are being developed as potential bone-substitute materials. When designing and optimizing a second-generation biomaterial, it is important to achieve a balance between mechanical and biological properties without compromising either. Biochemical and histological parameters have been used to compare the biological response of 20% and 40% volume HA in HDPE. Cellular DNA and incorporation of tritiated thymidine was measured to assess cell proliferation. Alkaline phosphatase (ALP) production was used as a marker of osteoblast phenotype expression. In this preliminary study, osteoblasts cultured on the 20% HAPEX showed a greater increase in the rate of proliferation and osteoblast expression as indicated by an increase in ALP activity compared to the 40% HAPEX over the time period studied. Osteoblast-like cells showed a flattened morphology on both composites and in some cases a greater covering was observed on the 20% HAPEX. These results indicate that the composites may not be identical in terms of bioactivity and that further research on surface topography and physico-chemical properties is required to assess fully the biological response of these composites. CI - Copyright 1998 Kluwer Academic Publishers FAU - Di Silvio, L AU - Di Silvio L AD - IRC in Biomedical Materials, Institute of Orthopaedics (UCL), Brockley Hill, Stanmore, Middlesex HA7 4LP, UK. ldisilvio@ucl.ac.uk FAU - Dalby, M AU - Dalby M FAU - Bonfield, W AU - Bonfield W LA - eng PT - Journal Article PL - United States TA - J Mater Sci Mater Med JT - Journal of materials science. Materials in medicine JID - 9013087 EDAT- 2004/09/07 05:00 MHDA- 2004/09/07 05:01 CRDT- 2004/09/07 05:00 PHST- 2004/09/07 05:00 [pubmed] PHST- 2004/09/07 05:01 [medline] PHST- 2004/09/07 05:00 [entrez] AID - 230476 [pii] AID - 10.1023/a:1008900312950 [doi] PST - ppublish SO - J Mater Sci Mater Med. 1998 Dec;9(12):845-8. doi: 10.1023/a:1008900312950.