Cambridge Polymer Group researcher Gavin Braithwaite will be presenting his work on hydrogels used in medical devices at the upcoming Polymers and Plastics in Medical Devices conference held in San Francisco, CA from June 26-28th, 2013. Dr. Braithwaite's work discusses injectable hydrogels for nucleus pulposus and tissue augmentation, as well as cartilage replacement technologies.
Link to conference information
Hexafluoroisopropanol (HFIP), also known as hexafluoro-2-propanol, is a fluorinated alcohol commonly used in processing of polyethylene terephthalate, polyacrylonitriles, some polyketones, and polyamides. It is a fairly toxic material, causing several eye damage and respiratory problems. Consequently, manufacturers who use HFIP need to measure how much residual HFIP remains in their processed goods, particularly if the goods are being used for biomedical purposes.
HFIP can be quantified with solvent extraction followed by gas chromatography-mass spectroscopy. This method can be used to detect HFIP concentrations down to approximately 100 ppb. The technique requires a reliable extraction methodology, and a GC-MS protocol that will provide separation of HFIP from any other co-eluting species that may be extracted from the test sample.
Contact Cambridge Polymer Group for more information.
On September 25-26, 2013, an international symposium on polyetherether ketone (PEEK) will be held at Drexel University. PEEK is finding increasing use in the biomedical community, particularly in the area of permanent implants. Spinal implants have been composed of PEEK for several years, finding use as stabilization rods, spacers, and articulating surfaces.
Characterization of PEEK has received increasing attention as a consequence. This material has unusual crystallization behavior, and the method of analysis can lead to different results. In a paper written by researchers from Cambridge Polymer Group, Brigham and Women's Hospital, and Stryker "Macromolecular and Morphological Characterization of Medical Grade PEEK", we describe 4 methods to measure crystallinity in PEEK (X-ray, DSC, density, and FTIR), and compare the results of multiple grades of PEEK.
Details on the conference
Fatigue crack propagation (FCP) analysis is a method to monitor the resistance of a material to crack inception and propagation under cyclical loading. ASTM E647 describes the methodology for measuring crack propagation in materials. An example of the typical data obtained in FCP analysis is shown above for GUR 1020 UHMWPE subjected to ionizing radiation measured at Cambridge Polymer Group. There are two principle regimes in a crack propagation plot: (1) crack inception, where the minimum load range required to start a crack to grow is determined; (2) Paris regime, where steady crack growth occurs. The x-axis shows DK, which is derived from linear elastic mechanics and is dependent on the cyclical load range (Pmax-Pmin) and the crack length (a). The expression for DK will depend on the shape of the test specimen, which is often a compact tensile geometry. The y-axis shows the crack growth as a function of number of fatigue cycles. The main reportable items for FCP analysis are the DKincep, or the load conditions for crack growth to reach 1e-6 mm/cycle, and the slope and intercept of the curve in the Paris regime (m and C, respectively). With highly crosslinked UHMWPE, the DKincep tends to decrease, and the material sometimes shows a higher sensitivity to DK in the Paris regime.
Contact Cambridge Polymer Group for more information on E647 testing.
Link to Application Note on fatigue crack testing
A link to a video showing a time lapse of a growing fatigue crack in UHMWPE can be found here.
Ultra high molecular weight polyethylene (UHMWPE) is the most commonly used bearing surface in hip and knee arthroplasties. Due to its high molecular weight, UHMWPE cannot be injection molded or extruded with a screw extruder. Compression molding or ram extrusion are the two consolidation processes used for UHMWPE, whereby the combination of temperature and pressure sinter the flakes of UHMWPE together. These processes do not result in co-mingling of the UHMWPE powder, however, so that the original flakes can be readily seen in a cryo-fractured surface (see above). Regulators are interested in verify that consolidation defects, or voids, do not exist in the consolidated UHMWPE. These defects can result in crack formation and failure of the device if the defects are in sufficient quantity and size. SEM analysis of cryo-fractured surfaces is a commonly used technique to look for consolidation defects, along with optical microscopy of microtomed films of the material. Regulatory submissions usually require these analyses, comparing a new formulation of UHMWPE with a cleared and marketed formulation.
The increasing prevalence of Vitamin E, a naturally-occuring antioxidant, in medical grade plastics has resulted in a need for analysis methods that can track the effect of processing on this compound. Vitamin E is effective as an antioxidant due to the hydroxyl group sitting on the aromatic ring at one end of the molecule. This hydroxyl group can readily lose a hydrogen and capture a free radical, a culprit in oxidation reactions. The free radical is thereafter stabilized by the Vitamin E molecule.
When processing medical grade plastics, the plastics are exposed to high heats and pressures during molding. Additionally, cleaning agents and ionizing radiation are often used to clean and sterilize the finished components. All these steps can potentially modify some of the Vitamin E molecules.
As a result, medical device manufacturers are usually required to identify and quantify these modified molecules to ensure both that they are safe for in vivo use, and that the material remains adequately oxidatively stabilized. Researchers at Cambridge Polymer Group have developed a series of assays to analyze potential transformation products of Vitamin E, using a combination of chromatography and spectroscopy. Additionally, we have a series of analyses to test the oxidation resistance of stabilized plastics. All these methods have been successfully used for regulatory submissions.
The ASTM Committee on Medical Devices (F04) met last week in Atlanta, GA. Cambridge Polymer Group staff attended several of the task groups, and reported back the following activities.
Medical Device Cleanliness
Several draft standards are in development, including guidance on cleanline validation, synthetic test soils to verify cleaning efficacy, guidance on how to design for cleaning, and methods of establishing allowable cleanliness levels. The first 3 items will be submitted for a sub-committee ballot in January, and more input is required for the last item. Additionally, a new wear particle isolation method was introduced to ASTM F561 a few years ago, and was ballotted last year. Discussions were held on negative ballots received. The votes on these negatives will occur in January.
Polyether ether Ketone
Discussions of ASTM F2026 suggested that specifications for different grades of PEEK based on molecular weight be introduced into this standard. The three manufacturers of medical grade PEEK (Solvay, Invibio, and Evonik) were invited to submit their data for evaluation.
UHMWPE
It was suggested to remove a few test methods from ASTM F648, including net ash on consolidated resin and Charpy Impact. The committee is considering these items. A round robin study on small punch testing (ASTM F2183) is being developed to establish a precision and bias statement for this method. Lastly, a micro-tensile dogbone standard is being developed for UHMWPE to allow characterization of explanted acetabular cups.
Bone Cement
A new benzoyl peroxide assay was introduced by CPG scientists as a replacement for the existing test method in ASTM F451. The committee is arranging to prepare several formulations of bone cement with varying benzoyl peroxide concentrations to evaluate the new method.