Thornton Cleveleys, England (PRWEB) September 12, 2006
Invibio®, a leading provider of biomaterial solutions to the medical device market, today announced the launch of ENDOLIGN™ composite, a new biocompatible carbon fibre-reinforced thermoplastic material for use in implantable load bearing medical device applications requiring blood, bone or tissue contact of more than 30 days. The ENDOLIGN composite and process offer the first non-metallic biomaterial available for medical implants providing the high strength of metals combined with the extensive biocompatibility and imaging compatibility of polymers.
Biocompatibility testing of ENDOLIGN composite confirms that it exceeds the requirements of ISO 10993 standards for long-term implantable medical devices. ENDOLIGN is manufactured to ISO 9001 quality standards by combining high levels of continuous carbon fibres with a PEEK-OPTIMA® polymer matrix in the form of a pre-impregnated tape. This tape can then be moulded into rods or other forms. The continuous carbon fibres significantly enhance the mechanical properties of the material, increasing its flexural strength when tested in moulded unidirectional rod form, from approximately 150MPa for PEEK-OPTIMA polymer to more than 1000MPa and its stiffness from 3.5GPa to 150GPa.
The mechanical properties of processed ENDOLIGN composite products may be comparable to those of traditionally used metallic materials, such as cobalt chromium alloys, titanium alloys and stainless steel, with the added benefit that ENDOLIGN material offers superior imaging compatibility. Because it is radiolucent, ENDOLIGN enables clear visualization through imaging techniques such as X-ray and Computer Tomography (CT) and being non-metallic, the material is compatible with MRI. Traditional metallic implant materials can generate imaging artefacts and scatter, preventing a comprehensive inspection of the surrounding tissue and bone.
In cases where X-ray visibility is an advantage, ENDOLIGN can be tailored by adding a radiopaque component in different concentrations to vary the level of X-ray contrast.
ENDOLIGN composite can also be repeatedly sterilised using conventional methods including steam, gamma radiation and ethylene oxide processes without adversely affecting its mechanical properties or biocompatibility. Few polymers can be sterilised by all of these methods because of changes that occur within the materials, often leading to embrittlement or hydrolytic degradation.
Invibio’s ENDOLIGN composite is currently provided as a pre-preg tape for conventional high performance thermoplastic composite processing by compression moulding, autoclave moulding, filament winding or pultrusion, or as custom-made pre-formed unidirectionally reinforced rods. Parts can also be fabricated using the novel method of composite flow moulding (CFM) by icotec (http://www.icotec.ch) for which there are CE marked and FDA cleared devices. ENDOLIGN based medical devices also have the potential to be machined from rod stock, plate or other semi-finished product.
ENDOLIGN composite is currently used in the development of load bearing applications including spinal fixation devices like translaminar fixation pins, spinal fusion cages and in traumatology devices such as bone fracture plates, screws and intermedullary nails.
Invibio® is a global leader providing high performance biomaterials, advanced technical research and consultative solutions to medical device manufacturers across a wide range of markets. The company provides medical device manufacturers with implantable-grade PEEK-OPTIMA® and ENDOLIGN™ polymers and medical-grade PEEK-CLASSIX™ polymer for the development of long- and short-term implantable medical devices.
For more information, please contact Invibio at: 866 468 4246 (U.S.), +44 (0) 1253 866812 (U.K.), +852 2366 4448 (Asia Pacific) or online at http://www.invibio.com.
For more Invibio information, press only:
Tracy Conger, HSR Business to Business, (513) 346-5557.
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