Cn. Kraft et al., Impact of a nickel-reduced stainless steel implant on striated muscle microcirculation: A comparative in vivo study, J BIOMED MR, 57(3), 2001, pp. 404-412
The impairment of skeletal muscle microcirculation by a biomaterial may hav
e profound consequences. With moderately good physical and corrosion charac
teristics, implant-quality stainless steel is particularly popular in ortho
pedic surgery. However, due to the presence of a considerable amount of nic
kel in the alloy, concern has been voiced in respect to local tissue respon
ses. More recently a stainless steel alloy with a significant reduction of
nickel has become commercially available. We, therefore, studied bi vivo nu
tritive perfusion and leukocytic response of striated muscle to this nickel
-reduced alloy, and compared these results with those of the materials conv
entional stainless steel and titanium. Using the hamster dorsal skinfold ch
amber preparation and intravital microscopy, we could demonstrate that redu
ction of the nickel quantity in a stainless steel implant has a positive ef
fect on local microvascular parameters. Although the implantation of a conv
entional stainless steel sample led to a distinct and persistent activation
of leukocytes combined with disruption of the microvascular endothelial in
tegrity, marked leukocyte extravasation, and considerable venular dilation,
animals with a nickel-reduced stainless steel implant showed only a modera
te increase of these parameters, with a clear tendency of recuperation. Tit
anium implants merely caused a transient increase of leukocyte-endothelial
cell interaction within the first 120 min, and no significant change in mac
romolecular leakage, leukocyte extravasation, or venular diameter. Pending
biomechanical and corrosion testing, nickel-reduced stainless steel may be
a viable alternative to conventional implant-quality stainless steel for bi
omedical applications. Concerning tolerance by the local vascular system, t
itanium currently remains unsurpassed, (C) 2001 John Wiley & Sons, Inc.