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5929 Baker Road, Suite 430 · Minnetonka, MN 55345 · P: 952.933.1152 · F: 952.933.1186 · E: [email protected] 1 Medical Device Corrosion Testing The human body and its immune and inflammatory mechanisms can create an aggressive environment for metallic implants resulting in implant rejection and failure (Gilbert, Corrosion, 2017;73(12):1478-1495). In vitro testing of small implants is typically performed per ASTM F2129-17b to mitigate these risks. While this testing helps determine implant susceptibility to corrosion, it does not take into account the effects of cells, proteins, and other biological effects that implants will experience in vivo. Despite its limitations, ASTM F2129-17b has undergone several revisions since its original publication in 2001 to better assist medical device manufacturers in assessing their small implants’ resistance to putting and crevice corrosion. The standard provides a test method for conducting cyclic (forward and reverse) potentiodynamic polarization measurements on whole devices in their final form and finish. In the sections below, we describe the test methods, apparatus, results and acceptance criteria used in vitro corrosion testing of small implants. Test Apparatus A typical multiport electrochemical test cell is shown on the right. It has inflow/outflow ports for the nitrogen gas and heated water circulation, ports for the reference, graphite counter and working/sample electrodes, and an inner chamber for the saline bath. Additional components include: potentiostat, computer, pH meter, nitrogen tank, water pump, conductive epoxy with UV lamp and mask for curing, and stainless steel wire for sample attachment. Reagents such as phosphate buffered saline are used for the bath, and isopropyl alcohol and type II reagent grade water for sample rinsing. Optical and electron scanning microscopes are used for pre- and post-test inspections. Test Method Table 1 provides a brief terminology summary; for further details consult the ASTM F2129-17b standard.

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Page 1: Medical Device Corrosion Testing

5929BakerRoad,Suite430·Minnetonka,MN55345·P:952.933.1152·F:952.933.1186·E:[email protected]

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MedicalDeviceCorrosionTestingThehumanbodyanditsimmuneandinflammatorymechanismscancreateanaggressiveenvironmentformetallicimplantsresultinginimplantrejectionandfailure(Gilbert,Corrosion,2017;73(12):1478-1495).InvitrotestingofsmallimplantsistypicallyperformedperASTMF2129-17btomitigatetheserisks.Whilethistestinghelpsdetermineimplantsusceptibilitytocorrosion,itdoesnottakeintoaccounttheeffectsofcells,proteins,andotherbiologicaleffectsthatimplantswillexperienceinvivo.Despiteitslimitations,ASTMF2129-17bhasundergoneseveralrevisionssinceitsoriginalpublicationin2001tobetterassistmedicaldevicemanufacturersinassessingtheirsmallimplants’resistancetoputtingandcrevicecorrosion.Thestandardprovidesatestmethodforconductingcyclic(forwardandreverse)potentiodynamicpolarizationmeasurementsonwholedevicesintheirfinalformandfinish.Inthesectionsbelow,wedescribethetestmethods,apparatus,resultsandacceptancecriteriausedinvitrocorrosiontestingofsmallimplants. TestApparatus Atypicalmultiportelectrochemicaltestcellisshownontheright.Ithasinflow/outflowportsforthenitrogengasandheatedwatercirculation,portsforthereference,graphitecounterandworking/sampleelectrodes,andaninnerchamberforthesalinebath.Additionalcomponentsinclude:potentiostat,computer,pHmeter,nitrogentank,waterpump,conductiveepoxywithUVlampandmaskforcuring,andstainlesssteelwireforsampleattachment.Reagentssuchasphosphatebufferedsalineareusedforthebath,andisopropylalcoholandtypeIIreagentgradewaterforsamplerinsing.Opticalandelectronscanningmicroscopesareusedforpre-andpost-testinspections. TestMethod Table1providesabriefterminologysummary;forfurtherdetailsconsulttheASTMF2129-17bstandard.

Page 2: Medical Device Corrosion Testing

5929BakerRoad,Suite430·Minnetonka,MN55345·P:952.933.1152·F:952.933.1186·E:[email protected]

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Table1:TerminologyEb Breakdownpotential Potentialatwhichpittingorcrevicecorrosionwillinitiateand

propagate.Er Restpotential Potentialintheopencircuitbeforecyclictestbegins.Ef Finalpotential Presetpotentialwherethetestisstopped.Ei Initialpotential Initialpotentialforthecyclictest;sameasEr.Ep Protectionpotential Potentialatwhichthereversescancrossestheforwardscanlower

thanEb.Ifasurfaceisalreadypitted,furtherpittingcanbeginunderEbbutaboveEp.

Ev Vertexpotential Presetpotentialwherethescanreverses.It Thresholdcurrent

densityPresetcurrentdensityatwhichthescandirectionisreversed.Typically,thescanisreversedwhenacurrentdensitytwodecadeshigherthanthecurrentdensityatthebreakdownpotential,Eb,isreached.

Briefly,theimplantisheldinsalineat37±1°CwithstartingpHat7.4±0.2inthesetupshownontheright.Apotentialisintroducedbetweentheimplantandareferenceelectrodeandrampeduptoabovephysiologicalpotentials.Abreakdownwilltypicallywillresultinarapidincreasecurrentdensity,asevidencedontheoutputplotofpotentialvs.logcurrentdensity.Thetotalsurfaceareaofthesampleexposedtothesolutionneedstobecalculatedsothatthecurrentdensitygeneratedbythesamplecanbedetermined.Samplesarepreparedfortestingandthoroughlyinspected.Conductiveepoxyisusedastheinterfacetothesample(specimenholdersvarydependingonthedevicetype),connectedtoapotentiostatthroughawire,andresistanceischeckedtoensuregoodconnection.Thetestcellisfilledwithsaline(minimumof500mL,typically1L),heatedtothetargettemperature,andnitrogengasflowat150mL/minisinitiated.Nitrogengasflowisusedtodeaeratethesolutionandlowerdissolvedoxygenconcentrationtodecreasethepotentialatwhichoxidationandreductioncurrentsareequal. Temperature,pH,andnitrogengasflowtime(30minminimum)arerecorded,thenthedeviceisrinsedandinsertedinthetestcellwiththewire.Salineisaddedintothereferenceelectrodeholder,andtheelectrodeisinsertedat5mmorlessfromthesample,butnotincontactwiththesample.Thenitrogenpurgeiscontinuedthroughoutthetest.Theopencircuittestisinitiated,andErisrecordedafter1hour.Then,thecyclicpolarizationtestisinitiatedata1mV/sscanratebysettingEiandEftoEr.Thecyclicpolarizationiscloselymonitored;ifacurrentdensityincreaselargerthantwodecadesoccurs,voltageisreversed. Whenthetestiscompleted,thefinaltemperature,pH,Er,Eb,Ef,andEparerecorded.Thesampleisremovedfromthetestandrinsed,thewireisclipped~1inchabovethesample,andthesampleisstoredforfurtherpost-testinspection.Whilethestandarddoesnotindicatehowmanysamplesshouldbetested,wetypicallysee3-8samplespersurfacefinish.

Page 3: Medical Device Corrosion Testing

5929BakerRoad,Suite430·Minnetonka,MN55345·P:952.933.1152·F:952.933.1186·E:[email protected]

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TestResults Testconditionsarerecordedforeachsample:nitrogenflowtime,initialtemperature,initialpH,finaltemperatureandfinalpH.Sampletestresultsaretypicallyprovidedintabularandgraphicalformats.Pre-andpost-testobservationsandinspectionresultsarealsoprovided. Thegraphaboveshowsresultsfromacorrosiontestof8samplesofanitinoldeviceplottedaspotential(mV)vs.logcurrent(A).Resultsshowconsistencybetweenthe8samples;thepurpledatasetwiththeincreaseincurrentdensityisanexampleofabreakdownpotential.AcceptanceCriteria ASTMF2129-17bdoesnotdefineacceptancecriteriabutidentifiesEbasthecriticaldatapointabovewhichpitsnucleateandgrow.Therefore,thehighertheEbis,themoreresistantthemetalistopittingcorrosion.ItisalsorecommendedthatEbvaluesarecomparedtothoseofpredicatedevicesthathavedemonstratedgoodcorrosionresistanceinvivoasreference.Devicemanufacturersdefinetheacceptancecriteriafortheirimplants.Inourexperience,acceptableEbvaluesaremostcommonlysetabove300mV,andtheyareoftensetatmuchhigherthresholdvalues. ConsultationWeoftenperformcorrosiontestingonmedicaldevicestocharacterizetheircorrosionpotential.Ifyouwouldlikeassistancewithyourdevice’scorrosionand/orfatiguetesting,pleasefilloutourtestquestionnaireorcallusat952-933-1152todiscusshowwecanhelp. ElementMaterialsTechnologyoffersthebroadestscopeofmedicaldevicetesting,soifyouarelookingforservicessuchaspackagetesting,microbiologicaltesting,acceleratedshelflifetestingorEMC/EMItesting,contactustoconnectwiththerightlab.