Abstract
Due to excellent mechanical properties and good corrosion resistance, titanium–aluminium–vanadium (Ti‐6Al‐4V) and titanium–aluminium–niobium (Ti‐6Al‐7Nb) are extensively used for orthopedic surgery. Concern has been voiced concerning the implications of the constituent vanadium in Ti‐6Al‐4V on the surrounding environment. Particularly in osteosynthesis where the alloys stand in direct contact to skeletal muscle, undesirable biologic reactions may have severe consequences. In a comparative study, we assessed in vivo nutritive perfusion and leukocytic response of striated muscle to the metals Ti‐6Al‐4V, Ti‐6Al‐7Nb, and commercially pure titanium (cpTi), thereby drawing conclusions on their short‐term inflammatory potential. In 28 hamsters, utilizing the dorsal skinfold chamber preparation and intravital microscopy, we quantified primary and secondary leukocyte–endothelial cell interaction, leukocyte extravasation, microvascular diameter change, and capillary perfusion in collecting and postcapillary venules of skeletal muscle. A manifest discrepancy between the metals concerning impact on local microvascular parameters was not found. All metals induced an only transient and moderate inflammatory response. Only a slight increase in leukocyte recruitment and a more sluggish recuperation of inflammatory parameters in animals treated with Ti‐6Al‐4V compared to the other two metals suggested a minor, overall not significant discrepancy in biocompatibility. Gross toxicity of bulk Ti‐6Al‐4V on surrounding tissue could not be found. Conclusively, the commonly used biomaterials Ti‐6Al‐4V, Ti‐6Al‐7Nb, and cpTi induce an only transient inflammatory answer of the skeletal muscle microvascular system. Our results indicate that on the microvascular level the tested bulk Ti‐alloys and cpTi do not cause adverse biologic reactions in striated muscle. © 2006 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 24:531–540, 2006