Hydroxyapatite formed on/in agarose gel induces activation of blood coagulation and platelets aggregation

J Biomed Mater Res B Appl Biomater. 2007 May;81(2):456-61. doi: 10.1002/jbm.b.30684.

Abstract

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.

MeSH terms

  • Adenosine Diphosphate / pharmacology
  • Adsorption
  • Blood Coagulation / drug effects*
  • Bone Substitutes / chemistry
  • Bone Substitutes / isolation & purification*
  • Bone Substitutes / pharmacology*
  • Durapatite / chemistry
  • Durapatite / isolation & purification*
  • Durapatite / pharmacology*
  • Gels
  • Hemostasis / drug effects
  • Humans
  • In Vitro Techniques
  • Materials Testing
  • Microscopy, Electron, Scanning
  • Partial Thromboplastin Time
  • Platelet Aggregation / drug effects*
  • Powders
  • Prothrombin Time
  • Sepharose
  • Surface Properties
  • Vitronectin / pharmacokinetics
  • X-Ray Diffraction

Substances

  • Bone Substitutes
  • Gels
  • Powders
  • Vitronectin
  • Adenosine Diphosphate
  • Sepharose
  • Durapatite