Arimura Shin-ichiro, Kawahara Ko-ichi, Biswas Kamal Krishna, Abeyama Kazuhiro, Tabata Masashi, Shimoda Toru, Ogomi Daisuke, Matsusaki Michiya, Kato Shinya, Ito Takashi, Sugihara Kazumasa, Akashi Mitsuru, Hashiguchi Teruto, Maruyama Ikuro
Developmental Therapeutics Course, Oral and Maxillofacial Rehabilitation, Department of Maxillofacial Diagnostic and Surgical Science, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
J Biomed Mater Res B Appl Biomater. 2007 May;81(2):456-61. doi: 10.1002/jbm.b.30684.
We reported earlier that hydroxyapatite (HA) formed on/in agarose gels (HA/agarose) produced by alternate soaking process is a bone-filling material possessing osteoconductive and hemostatic effects. This process could allow us to make bone-like apatite that was formed on/in organic polymer hydrogel matrices. Here, we investigated the mechanism of hemostasis induced by HA/agarose and found that HA/agarose, but not agarose or HA powder, significantly shortened activated partial thromboplastin time (APTT). While HA/agarose did not show significant platelet aggregation, it markedly enhanced adenosine diphosphate (ADP)-induced platelet aggregation. Moreover, Western blot analysis revealed selective adsorption of vitronectin onto HA/agarose. We also observed marked differences between HA powder and HA/agarose in their XRD patterns. The crystallinity of HA powder was much higher compared to that of HA/agarose. Furthermore, 50-100 nm of tube-form aggregations was observed in HA powder on the other hand 100-200 nm of particles was observed in HA/agarose by SEM observation. Thus 100-200 nm of low crystallized particles on the surface structure of HA/agarose may play an important role in hemostasis. Our results demonstrated a crucial role of HA/agarose in the mechanism of hemostasis and suggested a potential role for HA/agarose as a bone-grafting material.