Abstract
Despite the availability of more recent antimicrobial agents, the treatment of bone diseases like osteomyelitis, caused by microbial infection remains an important orthopaedic problem. The characteristics of bone make chronic osteomyelitis refractory. Hard walls surround the soft tissues of bone and inflammation of the contained tissues causes circulatory disturbances which can readily lead to necrosis of various parts of the bone. These anatomical features provide an environment suited for the localization and colonization by bacteria1. Then, the surgical removal of necrotic tissues and the antibiotic administration are the primary methods of treatment of chronic osteomyelitis2. Necrotic bone provides an appropriate surface for the development of a biofilm3 and the causative bacteria produce large amount of extracellular fibrous glycocalyx materials4. Therefore, the antibiotic concentration must be many times higher than the MIC (Minimum Inhibitory Concentration) to eradicate bacteria encased in this biofilm5. This may be one reason why the disease is uneasy to treat even though the penetration of some antibiotics into infected bone is higher than into normal bone6.
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References
D.S. Kahn and K.P.H. Pritzker, The pathophysiology of bone infection, Clin. Orthop 96:12–19 (1973).
F.A. Waldvogel, G. Medoff and M.N. Swartz, Osteomyelitis: a review of clinical features, therapeutic considerations and unusual aspects, N. Engl. J. Med 282:198–322 (1970).
T.J. Marrie and J.W. Costerton, Mode of growth of bacterial pathogens in chronic polymicrobial human osteomyelitis, J Clin. Microbiol 22:924–933 (1985).
K.J. Mayberry-Carson, B. Tober-Meyer, J.K. Smith, D.W. Jr Lambe and J.W. Costerton, Bacterial adherence and glycocalyx formation in osteomyelitis experimentally induced with Staphylococcus aureus, Infect. Immun 43:825–833 (1984).
J.C. Nickel, I. Ruseska, J.B. Wright and J.W. Costerton, Tobramycin resistance of Pseudomonas aeruginosa cells growing as a biofilm on urinary catheter material, Antimicrob. Agents Chemother 27:619–624(1985).
B.B. Hall and R.H. Fitzgerald, The pharmacokinetics of penicillin in osteomyelitis canine bone, J. Bone Joint Surg 65A: 526–532 (1983).
Ch. Jr Organ, The utilization of massive doses of antimicrobial agents with isolation perfusion in the treatment of chronic osteomyelitis, Clin. Orthop 76:185–192 (1971).
H.N. Oguachuba, Use of instillation-suction technique in treatment of chronic osteomyelitis, Acta Orthop. Scand 54:452458 (1983).
C.R. Perry, J.K. Ritterbusch, S.H. Rice, K. Davenport and R.E. Burdge, Antibiotics delivered by an implantable drug pump. A new application for treating osteomyelitis, Am. J. Med 30 Suppl. 6B:222–227(1986).
K. Klemm, Die behandlung chronischer knocken infektionen mit gentamycin PMMA-kelten and-Kugelen. In: Gentamycin PMMA Kette, Gentamycin PMMA Kugelin Symposium, H. Contzen, Ed., VLE Verlag, Munchen pp. 20–25 (1977).
W.R. Murray, Use of antibiotic-containing bone cement, Clin. Orthop 190:89–95 (1984).
T.N. Gerhart, R.D. Roux, G. Horowitz, R.L. Miller, P. Hanff and W.C. Hayes, Antibiotic release from an experimental biodegradable bone cement, J. Orthop. Res 6:585–592 (1988).
Y. Ikada, S.H. Hyon, K. Jamshidi, S. Higashi, T. Yamamuro, Y. Katutani and T. Kitsugi, Release of antibiotic from composites of hydroxyapatite and poly(lactic acid), J. Controlled Rel 2:179–186 (1985).
S.S. Sampath, K. Garvin and D.H. Robinson, Preparation and characterization of biodegradable poly (L-lactic acid) gentamicin delivery systems, Int. J. Pharm 78:165–174 (1992).
G. Wei, Y. Kotoura, M. Oka, T. Yamamuro, R. Wada, S.H. Hyon and Y. Ikada, A bioabsorbable delivery system for antibiotic treatment of osteomyelitis-The use of lactic acid oligomer as carrier, J. Bone Joint Surg 73B:246–251 (1991).
P. Ylinen, Filling of bone defects with porous hydroxyapatite reinforced with polylactide or polyglycolide fibres, J. Materials Sci. M. M 5:522–528 (1994).
H. Oghushi, V.M. Goldberg and A.I. Caplan, Repair of bone defects with marrow cells and porous ceramic-Experiments in rats, Acta Orthop. Scand 60:334–339 (1989).
Y. Yamazaki, S. Oida, Y. Akimoto and S. Shioda, Response of the mouse femoral muscle to an implant of a composite of bone morphogenetic protein and plaster of Paris, Clin. Orthop 234:240–249 (1988).
J.A. Setterstrom, T.R. Tice and E. Jacob, Chemotherapeutic treatment of bacterial infections with an antibiotic encapsulated within a biodegradable polymer matrix, Patent WO 91/13595 (1991).
K. Yamamura, H. Iwata and T. Yotsuyanagi, Synthesis of antibiotic loaded hydroxyapatite beads and in vitro drug release testing, J. Biomed. Mater. Res 26:1053–1064 (1992).
X. Zhang, U.P. Wyss, D. Pichora, M.F.A. Goosen, Biodegradable controlled antibiotic release devices for osteomyelitis. Optimization of release properties, J. Pharm. Pharmacol 46:718–724 (1994).
H. Dreesman, Ueber Knochenplombierung, Beitr. Klin. Chir 9:804–810 (1892).
V. Dacquet, A. Varlet, R.N. Tandogan, M.M. Tahon, L. Fournier, F. Jehl, H. Monteil and G. Bascoulergue, Antibiotic-impregnated plaster of Paris beads. Trials with teicoplanin, Clin. Orthop 282:241–249 (1992).
D. Mackey, A. Varlet and D. Debeaumont, Antibiotic loaded plaster of Paris pellets: an in vitro study of a possible method of local antibiotic therapy in bone infection, Clin. Orthop 167:263–268 (1982).
B. Mousset, M.-A. Benoit, C. Delloye, R. Bouillet and J. Gillard, Biodegradable implants for potential use in bone infection: in vitro study of antibiotic-loaded calcium sulfate, Int. Orthop 19:157–161 (1995).
B. Mousset, M.-A. Benoit, R. Bouillet and J. Gillard, Le plâtre de Paris: un vecteur d’antibiotiques pour le traitement des infections osseuses, Acta Orthop. Belg 59:239–248 (1993).
L.F. Peltier, The use of plaster of Paris to fill defects in bone, Clin. Orthop 21:1–31 (1961).
A. Petrova, Gipsfüllung von knochenhöhlen bei osteomyelitis, Zentralorg. Ges. Chir 43:885 (1928).
R. Bouillet, B. Bouillet, N. Kadima and J. Gillard, Traitement de l’ostéomyélite chronique en milieu africain par implants de plâtre imprégné d’antibiotiques, Acta Orthop. Belg 55:1–11 (1989).
J. Evrard, Expérience clinique des linguettes de plâtre chargées d’antibiotique dans le traitement des ostéites chroniques, Orthop. Traumatol 3:59–64 (1993).
I. Sulo, Granules de plâtre à la gentalline dans le traitement de l’infection osseuse, Rev. Chir. Orthop 79:299–305 (1993).
A. Varlet and P. Dauchy, Billes de plâtre de Paris aux antibiotiques dans le traitement de l’infection osseuse. Nouvelles associations plâtre-antibiotiques, Rev. Chir. Orthop 69:239–244 (1983).
D.K. Kuechle, G.C. Landon, D.M. Musher and P.C. Noble, Elution of vancomycin, daptomycin, and/ amikacin from acrylic bone cement, Clin. Orthop 264:302–308 (1991).
M.-A. Benoit, B. Mousset, R. Bouillet and J. Gillard, Antibiotic-loaded biodegradable pellets for bone infection. Long term treatment, Proceed. J. Bone Joint Surg, in press.
D.E. Cutright and E.E. Hunsuck, Tissue reaction to the biodegradable polylactic acid suture, Oral Surg 31:134–139(1971).
R.K. Kulkarni, K.C. Pani, C. Neuman and F. Leonard, Polylactic acid for surgical implants, Arch. Surg 93:839–843 (1966).
J. Mauduit, N. Bukh and M. Vert, Gentamycin / poly(lactic acid) blends aimed at sustained release local antibiotic therapy administered per-operatively. III-The case of gentamycin sulfate in films prepared from high and low molecular weight poly(DL-lactic acids), J. Controlled Rel 25:43–49 (1993).
M. Vert, P. Christel, P. Chabot and J. Leray, Bioresorbable plastic materials for bone surgery. In: Macromolecular Biomaterials, G.W. Hashings and P. Ducheyne, Eds, CRC Press, Boca Raton, pp. 119–142(1984).
D.C. Grove, A.W. Randall, Assay methods of antibiotics, Medical Encyclopedia Inc. New-York (1955).
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Benoit, MA., Mousset, B., Bouillet, R., Delloye, C., Gillard, J. (1998). Vancomycin-Loaded Calcium Sulfate for the Treatment of Osteomyelitis — Controlled Release by a Poly(Lactide-Co-Glycolide) Polymer. In: Hıncal, A.A., Kaş, H.S. (eds) Biomedical Science and Technology. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-5349-6_21
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DOI: https://doi.org/10.1007/978-1-4615-5349-6_21
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