In vivo inflammatory response to polymethylmethacrylate particulate debris: Effect of size, morphology, and surface area

Particulate debris, including that from polymethylmethacrylate (PMMA) cement, is observed commonly in the membrane surrounding loose joint prostheses. Such debris is assumed to cause an inflammatory response and contributes to osteolysis and failure of the implant. A subcutaneous rat air‐pouch model was used to assess quantitatively the in vivo effects of the size, morphology, and surface area of PMMA particles on the acute inflammatory response. PMMA particles were divided into three groups. In Group A, mechanical grinding of cured bone cement produced irregularly shaped particles; Group B included spherical particles of PMMA powder (Simplex P); and Group C consisted of commercially prepared spherical latex particles. All three groups had two size distributions: < 20 μm and 50–350 μm. For a given mass or dose, the small, irregularly shaped mechanically produced particles in Group A elicited a significantly greater inflammatory reaction than the large particles in Group A, as expressed by the release of tumor necrosis factor (TNF), neutral metalloprotease (NMP), and prostaglandin E2 (PGE2) and the white blood cell (WBC) count within a 24‐hour period. Similar findings were seen in Group B. Particles in Group C were used to compare the effect of absolute numbers of large and small particles and surface area. Large (10–126 μm) spherical PMMA particles at a dose of 1.7 × 106 particles/ml caused a significantly higher inflammatory response, as measured by WBC count and production of NMP and PGE2, than small (1–10 μm) spheres at a dose of 4 × 106 particles/ml. However, the production of TNF in the rats was significantly increased with small particles (p < 0.05) at a concentration 4‐fold less than that with the large particles (4 × 105 compared with 1.7 × 106 particles/ml). This finding may reflect a different cellular mechanism for the TNF component of the inflammatory response than is measured by WBC counts or by levels of PGE2 and NMP. As the calculated surface area of the PMMA particles increased, a threshold level was reached, at which point the inflammatory response increased dramatically. The size of particles has a role in the prolongation and intensity of the release of specific cytokines. The total surface area of the particles appeared to be an important factor in determining the inflammatory response, as measured by WBC count, PGE2, TNF, and NMP.

[1]  L. P. Yasenchak,et al.  Tissue response to implanted polymers: the significance of sample shape. , 1976, Journal of biomedical materials research.

[2]  W H Harris,et al.  The synovial-like membrane at the bone-cement interface in loose total hip replacements and its proposed role in bone lysis. , 1983, The Journal of bone and joint surgery. American volume.

[3]  H R Schumacher,et al.  Prolonged inflammatory reactions induced by artificial ceramics in the rat air pouch model. , 1988, The Journal of rheumatology.

[4]  F. Dewhirst,et al.  Synergistic interactions between interleukin 1, tumor necrosis factor, and lymphotoxin in bone resorption. , 1987, Journal of immunology.

[5]  J. Vilček,et al.  Tumor necrosis factor and interleukin 1: cytokines with multiple overlapping biological activities. , 1987, Laboratory investigation; a journal of technical methods and pathology.

[6]  N. Ziats,et al.  In vitro and in vivo interactions of cells with biomaterials. , 1988, Biomaterials.

[7]  A. Mantovani,et al.  Tumor necrosis factor is chemotactic for monocytes and polymorphonuclear leukocytes. , 1987, Journal of immunology.

[8]  B. K. Vaughn,et al.  Aseptic loosening in total hip arthroplasty secondary to osteolysis induced by wear debris from titanium-alloy modular femoral heads. , 1989, The Journal of bone and joint surgery. American volume.

[9]  P. Bullough,et al.  Pathologic studies of total joint replacement. , 1988, The Orthopedic clinics of North America.

[10]  P. D. Wilson,et al.  Metallic wear in failed titanium-alloy total hip replacements. A histological and quantitative analysis. , 1988, The Journal of bone and joint surgery. American volume.

[11]  J. H. Herman,et al.  Polymethylmethacrylate-induced release of bone-resorbing factors. , 1989, The Journal of bone and joint surgery. American volume.

[12]  T J Chambers,et al.  The pathobiology of the osteoclast. , 1985, Journal of clinical pathology.

[13]  D. A. Willoughby,et al.  The formation of a structure with the features of synovial lining by subcutaneous injection of air: An in vivo tissue culture system , 1981, The Journal of pathology.

[14]  J. Hageman,et al.  Assaying proteinases with azocoll. , 1984, Analytical biochemistry.

[15]  B. Aggarwal,et al.  Human lymphotoxin. Production by a lymphoblastoid cell line, purification, and initial characterization. , 1984, The Journal of biological chemistry.

[16]  J. Charnley The reaction of bone to self-curing acrylic cement. A long-term histological study in man. , 1970, The Journal of bone and joint surgery. British volume.

[17]  N. Eftekhar,et al.  Incidence and mechanism of failure of cemented acetabular component in total hip arthroplasty. , 1988, The Orthopedic clinics of North America.