The compatibility of materials with industrial technologies of sterilization
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Sophie ROUIF
Manager Research & Development in IONISOS
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Among these techniques, ionizing radiations and ethylene oxide are used at the industrial scale and allow the processing of products without manipulation to either product or pallet configuration, and in high volumes. With these technologies, the products are treated in carton boxes or in pallets.
The principles of radiation and ethylene oxide induce the chemical modification of biological molecules and thus alter the microbial metabolism, resulting in the destruction of organisms (bacteria, yeast fungi ...). These chemical modifications are, at first, not necessarily specific to biological molecules, and secondary reactions on the materials of medical devices are not excluded. The metals do not present any problem of compatibility with the sterilization technologies.
Plastics may be exposed to secondary or side effects, and they also are largely used in medical applications. The knowledge of major trends and information from plastics suppliers allows the choice of suitable materials from the beginning of a new project / product.

Chamber of ethylene oxide treatment
In the structure of polymers, the most sensitive chemical bonds are affected first. This is mainly polymers with halogen atoms (fluorine, chlorine), such as polyvinyl chloride (PVC) or polytetrafluoroethylene (PTFE), and polymers presenting quaternary carbon atoms (substituted by four different groups), as butyl rubber or polypropylene (PP).
Radiolysis reactions and degradation are highly favored by the presence of oxygen, less temperature, and very little in the dose rate.
But the dose is the main factor of influence. The dose is the amount of energy received per kilogram of material, its unit is the kiloGray (1 kGy = 1 kJ / kg). Most polymers are resistant to sterilization doses of about 25 kGy to 75 kGy, however they deteriorate beyond. This is the case of PP, PVC and cellulose. PTFE degrades at low dose, POM from 25 kGy and butyl rubber at a slightly higher dose, depending on the grade.
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RESISTANT
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To consider with attention
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DEGRADATION
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Polyolefine
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PS, PE
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PP, PVC
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Technical thermoplastics
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EVA, EVOH,
ABS, ABS/PC
PA 6, PA 66
PET, PBT
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PMMA
PC
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POM
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High performance thermoplastics
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UHMWPE,
PA46, PA11, PA12
PPA, PAA
PPS, PPO
PSU, PPSU
PI, PAI, PEI
PEEK
LCP
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PVDF, CTFE
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PTFE
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Thermoplastic elastomers (TPE)
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SBS, SEBS
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PP/EPDM
PEBA
TPU
COPE (ether – ester copolymer)
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Elastomers
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NR, NBR, HNBR, SBR
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Butyl rubber, chlorobutyl rubber,
Neoprene,
EPDM, EPR
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High performance elastomers
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Fluoroelastomers,
Fluorosilicones
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Silicones,
AEM/ACM
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This technique uses a sterilizing gas, which is also characterized by a high diffusivity and permeability, associated with conditions favoring these two factors: the products are brought into contact with the ETO under controlled conditions of temperature, humidity, pressure and time of exposure. It is often used when materials are sensitive to radiation and steam.
Sterilization is due to the alkylation reaction occurring at the ends of the chains of enzymes and DNA and RNA molecules. The functions -OH,-COOH,-SH and-NH react with the radical - CH2 - CH2 - OH of the ETO, altering the microbial metabolism.
The chemical structures of plastics (except cellulosic polymers) are not rich in functions that can react by alkylation with the ETO. Such functions can be found at the ends of polymer chains, but these are often blocked by initiators or by polymerization additives. In such conditions, the biological molecules are the most sensitive to ETO. Therefore, secondary reactionswith plastics are quite limited. Particular attention should be paid to the polystyrene (PS) and its derivative SAN (styrene-acrylonitrile). In both cases, according to the grade, a loss of mechanical properties of 30 % can be observed. This does not limit the use of the product, it will depend on the intended use of the components made of these materials. Physical conditions (temperature, pressure and humidity) of the process influence more the choice of the materials, including plastics. The steps of preparation (conditioning) and of contact with the ETO are conducted at a temperature generally between 40°C and 50°C in conditions of relative humidity of 50 % to 60 % for 6 to 8 hours. Particular attention, through a validation test, must paid to plastics whose service temperature ranges up to 70 ° C - 80 ° C, as for example polyolefins, and hydrophilic coatings, which can swell.
The ability of the material to adsorb the ETO and to allow its migration through it is the most important parameter to ensure the sterility of the whole product. This can be checked in existing tables and by trials to validate the conditions of treatment.
It should be noted that a few materials commonly used in the medical sector, including PP, PS, PMMA, PC and the butyl rubber, should be paid special attention. The main risks are yellowing in the case of radiation and a slight degradation of PS in the case of ETO. We suggest to make sure from your suppliers of the compatibility of the medical grades they offer with the techniques of sterilization, and then to perform some validation trials.


