The innovative application of a novel bone adhesive for facial fracture osteosynthesis-in vitro and in vivo results.

This study evaluates a novel adhesive fixation technique to affix cortical bone fragments to osteosynthesis plates using common PMMA cement. This technique utilizes a new amphiphilic bone bonding agent adhering with both hydrophilic bone and hydrophobic PMMA cement. After in vitro biomechanical testing of the bonding strength with explanted bovine and rabbit calvarian bone samples, osteosynthesis plates with screw holes of 1.3 and 1.5 mm were placed on the cranial bone of New Zealand white rabbits and the bond strength of these plates was determined through tension tests. In vitro bond strengths of 19.8-26.5 MPa were obtained. Control samples, prepared without a bone bonding agent, exhibited bone bonding strengths <0.2 MPa. In vivo respective bond strengths at the cranium of the white rabbits were 2.5-4.1 MPa 2 weeks post surgery and 1.9-2.5 MPa 12 weeks after implantation. This new innovative fixation method can be envisioned for cases in which conventional fixation techniques of screws and plates are insufficient or not possible due to the bone or trauma conditions. The observed bonding strengths support implementing this technique in nonload bearing regions, such as the central midface or frontal sinus, facilitating immobilization until bone reunion is complete.

In vitro study of adhesive polymethylmethacrylate bone cement bonding to cortical bone in maxillofacial surgery.

PURPOSE: In the treatment of midface fractures, the fragments are immobilized using screws and plates for osteosynthesis until reunion has occurred. This method involves drilling holes for the insertion of the screws, which can be associated with additional fracturing of the corresponding bone owing to the complex architecture and thin layers of facial bone. To alleviate this problem, new adhesive techniques for fixing the plates for osteosynthesis have been investigated, mitigating the detrimental effects of screw hole drilling. In the present experimental study, the strength of this adhesive bond and its resistance to hydrolysis were investigated. MATERIALS AND METHODS: To determine the adhesive bonding strength, a tension test was implemented. Osteosynthesis plates with screw holes 1.3 mm in diameter were fixed to cortical bone samples of bovine femur using ultraviolet (UV) light-curing polymethylmethacrylate bone cement. To facilitate bonding, the surface of the bone was conditioned with an amphiphilic bonding agent before cementing. UV light curing was implemented using either a conventional UV unit, such as is used in dentistry, or with a specialized UV unit with a limited emission spectrum but high luminosity. Reference control samples were prepared without application of the bone bonding agent. After this procedure, the samples were stored for 1 to 7 days at 37°C submerged in 0.9% saline solution before being subjected to the tension test. RESULTS: Without the bone bonding agent, the bonding strength was 0.2 MPa. The primary average bonding strength at day 0 was 8.5 MPa when cured with the conventional UV unit and 14 MPa for the samples cured with the specialized UV unit. An almost constant average bond strength of 8 and 16 MPa was noted for all samples stored up to 7 days after curing with the conventional and specialized UV unit, respectively. CONCLUSION: With the development of a new bone bonding agent, a method is now available to promote the bonding between the hydrophilic bone surface and the hydrophobic polymethylmethacrylate bone cement by creating an interlayer that is beneficial for adhesion. In the present in vitro study, the strength of this bond and its resistance to hydrolysis were investigated. This new method could have clinical bearing in cases in which conventional fixation with screws and plates is limited, such as can occur in comminuted fractures. The observed average bonding strengths of 8 to 16 MPa support the implementation of this technique in nonload-bearing regions such as the midface, facilitating immobilization until the bone reunion is complete.

A new adhesive technique for internal fixation in midfacial surgery.

BACKGROUND: The current surgical therapy of midfacial fractures involves internal fixation in which bone fragments are fixed in their anatomical positions with osteosynthesis plates and corresponding screws until bone healing is complete. This often causes new fractures to fragile bones while drilling pilot holes or trying to insert screws. The adhesive fixation of osteosynthesis plates using PMMA bone cement could offer a viable alternative for fixing the plates without screws. In order to achieve the adhesive bonding of bone cement to cortical bone in the viscerocranium, an amphiphilic bone bonding agent was created, analogous to the dentin bonding agents currently on the market. METHODS: The adhesive bonding strengths were measured using tension tests. For this, metal plates with 2.0 mm diameter screw holes were cemented with PMMA bone cement to cortical bovine bone samples from the femur diaphysis. The bone was conditioned with an amphiphilic bone bonding agent prior to cementing. The samples were stored for 1 to 42 days at 37 degrees C, either moist or completely submerged in an isotonic NaCl-solution, and then subjected to the tension tests. RESULTS: Without the bone bonding agent, the bonding strength was close to zero (0.2 MPa). Primary stability with bone bonding agent is considered to be at ca. 8 MPa. Moist storage over 42 days resulted in decreased adhesion forces of ca. 6 MPa. Wet storage resulted in relatively constant bonding strengths of ca. 8 MPa. CONCLUSION: A new amphiphilic bone bonding agent was developed, which builds an optimizied interlayer between the hydrophilic bone surface and the hydrophobic PMMA bone cement and thus leads to adhesive bonding between them. Our in vitro investigations demonstrated the adhesive bonding of PMMA bone cement to cortical bone, which was also stable against hydrolysis. The newly developed adhesive fixing technique could be applied clinically when the fixation of osteosynthesis plates with screws is impossible. With the detected adhesion forces of ca. 6 to 8 MPa, it is assumed that the adhesive fixation system is able to secure bone fragments from the non-load bearing midfacial regions in their orthotopic positions until fracture consolidation is complete.