Preliminary in vivo study of apatite and laminin‐apatite composite layers on polymeric percutaneous implants
Source abstract
Abstract
Abstract A polymeric material coated with a hydroxyapatite (HA) layer would be useful as a flexible percutaneous device with good biocompatibility and resistance to bacterial infection. We have recently developed a simple, safe, and mild coating process to form an HA layer on the surfaces of polymeric materials. In this study, our coating process was applied to an ethylene‐vinyl alcohol copolymer film. The resulting HA‐coated film was percutaneously implanted in the scalp of a rat to examine the stability and biocompatibility of the HA layer. From the results of histological analysis, the HA layer remained undissolved on the film surface under the skin tissue even 3 days after implantation. Owing to the good biocompatibility of HA, the HA‐coated film suppressed a host's foreign‐body response and integrated with the surrounding skin tissue for as long as 14 days, in a similar fashion to a conventional percutaneous device composed of ceramic HA. Immobilization of a cell adhesion protein, laminin, into the HA layer was found to improve the adhesion strength between the film and the surrounding skin tissue without compromising good biocompatibility of HA. Our coating process to form HA and laminin‐HA composite layers would be useful in fabricating polymeric percutaneous devices with a reduced risk of bacterial infection, although further in vivo studies are required. © 2011 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 2011.
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Research context
OpenAlex topics: Polymer Surface Interaction Studies · Surgical Sutures and Adhesives · Dental materials and restorations
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (32)
Show source-provided references
1. 10.1002/jbm.82018040310.1002/jbm.820180403 ↗
2. 10.4065/81.9.115910.4065/81.9.1159 ↗
3. 10.1093/jac/dkl23410.1093/jac/dkl234 ↗
4. 10.1097/00005373-200106000-0000610.1097/00005373-200106000-00006 ↗
5. 10.1016/j.biomaterials.2006.01.02910.1016/j.biomaterials.2006.01.029 ↗
6. 10.1007/BF0201760710.1007/BF02017607 ↗
7. Aoki H · 1991 · 193
8. 10.1097/00002480-199407000-0012610.1097/00002480-199407000-00126 ↗
9. 10.1002/jbm.b.1000210.1002/jbm.b.10002 ↗
10. 10.1007/s10856-007-3051-410.1007/s10856-007-3051-4 ↗
11. 10.1002/jbm.a.3139110.1002/jbm.a.31391 ↗
12. 10.1016/j.biomaterials.2009.01.00410.1016/j.biomaterials.2009.01.004 ↗
13. Tissue cellular and subcellular events at bone‐ceramic hydroxyapatite interface
14. LeGeros RZ · 1993 · 158
15. 10.1016/j.biomaterials.2004.07.04810.1016/j.biomaterials.2004.07.048 ↗
16. 10.1002/jbm.a.3039710.1002/jbm.a.30397 ↗
17. 10.1007/s10856-007-3024-710.1007/s10856-007-3024-7 ↗
18. 10.1002/jbm.b.3102510.1002/jbm.b.31025 ↗
19. Ultra‐structural study of the laminin‐apatite composite layer formed on ethylene‐vinyl alcohol copolymer by a biomimetic process
20. 10.1002/jbm.a.3020510.1002/jbm.a.30205 ↗
21. 10.1016/j.biomaterials.2005.06.00110.1016/j.biomaterials.2005.06.001 ↗
22. Preparation of laminin‐apatite‐polymer composites using metastable calcium phosphate solutions
23. 10.1088/1748-6041/5/6/06500810.1088/1748-6041/5/6/065008 ↗
24. 10.1038/sj.gt.330304110.1038/sj.gt.3303041 ↗
25. Fibronectin‐DNA‐apatite composite layer for highly efficient and area‐specific gene transfer10.1002/jbm.a.32449 ↗
26. 10.1002/jgm.142510.1002/jgm.1425 ↗
27. 10.1016/S0021-9258(19)83607-410.1016/S0021-9258(19)83607-4 ↗
28. 10.1146/annurev.cb.03.110187.00042110.1146/annurev.cb.03.110187.000421 ↗
29. 10.1016/0945-053X(94)90192-910.1016/0945-053X(94)90192-9 ↗
30. 10.1016/j.msec.2009.01.01210.1016/j.msec.2009.01.012 ↗
31. 10.1002/adma.20040015210.1002/adma.200400152 ↗
32. Elliot JC · 1994 · 310