Concepts for increasing gentamicin release from handmade bone cement beads. 2009

Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
Department of Biomedical Engineering, University Medical Center Groningen and the University of Groningen, the Netherlands.

OBJECTIVE Commercial gentamicin-loaded bone cement beads (Septopal) constitute an effective delivery system for local antibiotic therapy. These beads are not available in all parts of the world, and are too expensive for frequent use in others. Thus, orthopedic surgeons worldwide make antibiotic-loaded beads themselves. However, these beads are usually not as effective as the commercial beads because of inadequate release kinetics. Our purpose was to develop a simple, cheap, and effective formulation to prepare gentamicin-loaded beads with release properties and antibacterial efficacy similar to the commercially ones. METHODS Acrylic beads were prepared with variable monomer content: 100% (500 microL/g polymer), 75%, and 50% to increase gentamicin release through creation of a less dense polymer matrix. Using the optimal monomer content, different gel-forming polymeric fillers were added to enhance the permeation of fluids into the beads. Polyvinylpyrrolidone (PVP) 17 was selected as a suitable filler; its concentration was varied and the antibiotic release and antibacterial efficacy of these beads were compared with the corresponding properties of the commercial ones. RESULTS Gentamicin release rate and the extent of release from beads prepared with 50% monomer increased when the PVP17 content was increased. Beads with 15 w/w% PVP17 released 87% of their antibiotic content. This is substantially more than the gentamicin release from Septopal beads (59%). Acrylic beads with 15 w/w% PVP17 reduced bacterial growth by up to 93%, which is similar to the antibacterial properties of the commercial ones. CONCLUSIONS A simple, cheap, and effective formulation and preparation process has been described for hand-made gentamicin-releasing acrylic beads, with better release kinetics and with antibacterial efficacy similar to that of the commercial ones.

UI MeSH Term Description Entries
D008422 Materials Testing The testing of materials and devices, especially those used for PROSTHESES AND IMPLANTS; SUTURES; TISSUE ADHESIVES; etc., for hardness, strength, durability, safety, efficacy, and biocompatibility. Biocompatibility Testing,Biocompatible Materials Testing,Hemocompatibility Testing,Testing, Biocompatible Materials,Testing, Hemocompatible Materials,Hemocompatibility Testings,Hemocompatible Materials Testing,Materials Testing, Biocompatible,Materials Testing, Hemocompatible,Testing, Biocompatibility,Testing, Hemocompatibility,Testing, Materials,Testings, Biocompatibility
D008768 Methylmethacrylates The methyl esters of methacrylic acid that polymerize easily and are used as tissue cements, dental materials, and absorbent for biological substances.
D010019 Osteomyelitis INFLAMMATION of the bone as a result of infection. It may be caused by a variety of infectious agents, especially pyogenic (PUS - producing) BACTERIA. Osteomyelitides
D001843 Bone Cements Adhesives used to fix prosthetic devices to bones and to cement bone to bone in difficult fractures. Synthetic resins are commonly used as cements. A mixture of monocalcium phosphate, monohydrate, alpha-tricalcium phosphate, and calcium carbonate with a sodium phosphate solution is also a useful bone paste. Bone Cement,Bone Glues,Bone Pastes,Bone Glue,Bone Paste,Cement, Bone,Cements, Bone,Glue, Bone,Glues, Bone,Paste, Bone,Pastes, Bone
D004337 Drug Carriers Forms to which substances are incorporated to improve the delivery and the effectiveness of drugs. Drug carriers are used in drug-delivery systems such as the controlled-release technology to prolong in vivo drug actions, decrease drug metabolism, and reduce drug toxicity. Carriers are also used in designs to increase the effectiveness of drug delivery to the target sites of pharmacological actions. Liposomes, albumin microspheres, soluble synthetic polymers, DNA complexes, protein-drug conjugates, and carrier erythrocytes among others have been employed as biodegradable drug carriers. Drug Carrier
D004339 Drug Compounding The preparation, mixing, and assembly of a drug. (From Remington, The Science and Practice of Pharmacy, 19th ed, p1814). Drug Formulation,Drug Preparation,Drug Microencapsulation,Pharmaceutical Formulation,Compounding, Drug,Formulation, Drug,Formulation, Pharmaceutical,Microencapsulation, Drug,Preparation, Drug
D004343 Drug Implants Small containers or pellets of a solid drug implanted in the body to achieve sustained release of the drug. Drug Implant,Drug Pellet,Pellets, Drug,Drug Pellets,Implant, Drug,Implants, Drug,Pellet, Drug
D005839 Gentamicins A complex of closely related aminoglycosides obtained from MICROMONOSPORA purpurea and related species. They are broad-spectrum antibiotics, but may cause ear and kidney damage. They act to inhibit PROTEIN BIOSYNTHESIS. Gentamicin Sulfate (USP),Gentamycin,G-Myticin,Garamycin,Gentacycol,Gentamicin,Gentamicin Sulfate,Gentamycins,Gentavet,Genticin,G Myticin,GMyticin,Sulfate, Gentamicin
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D016459 Prosthesis-Related Infections Infections resulting from the implantation of prosthetic devices. The infections may be acquired from intraoperative contamination (early) or hematogenously acquired from other sites (late). Prosthesis Related Infection,Prosthesis-Related Infection,Infections, Prosthesis-Related,Infection, Prosthesis Related,Prosthesis Related Infections,Related Infection, Prosthesis,Related Infections, Prosthesis

Related Publications

Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
October 1989, Clinical pharmacokinetics,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
October 1986, Acta orthopaedica Scandinavica,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
December 1988, The Journal of bone and joint surgery. American volume,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
June 1986, Clinical orthopaedics and related research,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
October 1972, Der Chirurg; Zeitschrift fur alle Gebiete der operativen Medizen,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
January 1977, Revue de chirurgie orthopedique et reparatrice de l'appareil moteur,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
October 1990, Clinical pharmacokinetics,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
December 1989, Acta orthopaedica Scandinavica,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
September 1985, Journal of biomedical materials research,
Hermawan N Rasyid, and Henny C van der Mei, and Henderik W Frijlink, and Soegijardjo Soegijoko, and Jim R van Horn, and Henk J Busscher, and Daniëlle Neut
July 1998, The Journal of bone and joint surgery. British volume,
Copied contents to your clipboard!