PubMed Health⌕ Search

PubMed · 9239463

Friction in hip prostheses.

Abstract

Although the reduction of frictional torques was the driving force behind the design of the Charnley prosthesis, later concerns about wear and subsequent loosening of this and other hip replacements have dominated debate within the bioengineering community. To stimulate discussion on the role of friction in loosening, a review of the frictional characteristics of different prostheses was undertaken. The use of simple laboratory screening-type machines in the frictional assessment of different material combinations is discussed together with experiments performed on single axis simulators using both conventional and experimental prostheses. In particular, recent developments in the use of soft layer components are highlighted. Further, the possible link between excessively high frictional torques and loosening is discussed in the light of current results obtained from explanted prostheses.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

R M Hall, A Unsworth. 1997. Friction in hip prostheses.. https://doi.org/10.1016/s0142-9612(97)00034-3

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related citations

Combinatorial discovery of alloy electrocatalysts for amperometric glucose sensors.

Combinatorial methods were used to search for active alloy electrocatalysts for use in enzyme-free amperometric glucose sensors. Electrode arrays (715-member) containing combinations of Pt, Pb, Au, Pd, and Rh were prepared and screened by converting anodic current to visible fluorescence. The most active compositions contained both Pt and Pb. Bulk quantities of catalysts with compositions corresponding to those identified in the screening experiments were prepared and characterized. The best alloy electrocatalysts catalyzed glucose oxidation at substantially more negative potentials than pure platinum in enzyme-free voltammetric measurements. They were also insensitive to potential interfering agents (ascorbic and uric acids, and 4-acetamidophenol), which are oxidized at slightly more positive potentials. Rotating disk electrode (RDE) experiments were carried out to study the catalytic mechanism. The improvement in catalytic performance was attributed to the inhibition of adsorption of oxidation products, which poison Pt electrodes.

Alloys↗

Costimulatory molecule expression following exposure to orthopaedic implants wear debris.

Patients with long-term orthopedic implants may develop inflammatory reactions due to the accumulation of biomaterial particles both around the implant and in distant organs. The exact impact of these particles on the normal immune cell function still remain relatively unclear. Activation of T-cells following exposure to biomaterial particles is driven by macrophages and requires synergistic signals primed by both antigen presentation and costimulation. The pattern of costimulatory molecule expression (CD80,CD86) was primarily examined using immunohistochemistry on tissue specimens of bone/implant interface membranes taken from sites of bone erosion. Additionally, costimulatory molecule expression was also assessed in the monocytic leukemia cell line U937 following exposure to clinically relevant titanium aluminum vanadium (TiAlV) and stainless steel particles (FeCrNi) cultured in vitro. This study demonstrates the induction and prominent expression of CD86 on almost all macrophage subsets at the bone/implant interface, including fused forms and large multinucleated giant cells (MNGC). In vitro analysis also indicated phagocytosis of metal particles by differentiated U937 caused significant induction of both CD80 and CD86 (p < 0.01), although the expression of CD86 dominated following prolonged exposure. The data presented highlights that CD86 is the predominant costimulatory molecule ligating to the complementary CD28 molecule at the inflammatory lesion of the interface. We propose that the intracellular presence of indigestible implant material, in addition to elevated costimulatory molecule expression, may promote T-cell inflammatory reactions at sites close to and distant from the orthopedic implant.

Alloys↗