When this test applies
ISO 10993-1:2025 makes chemical characterisation to ISO 10993-18 the starting point of a biological evaluation for prolonged and long-term contact devices, and the preferred route to the systemic, genotoxicity and carcinogenicity endpoints wherever good extractables data can replace an animal study. Non-volatiles are the fraction GC/MS cannot see — polymer additives, oligomers, surfactants and degradation products — and IPA is the mid-polarity solvent, bridging the aqueous and non-polar conditions.
When to run it
With the other organic screens, on finished, sterilised material, once the material and process are locked. It is normally ordered as part of a three-solvent set with the SVOC and VOC screens so the extractables profile is complete across polarity and volatility.
What the result tells you
A list of non-volatile compounds identified in the isopropyl alcohol (IPA) migrate, each semi-quantified against a justified analytical evaluation threshold (AET). Compounds above the AET are reported for toxicological evaluation; a compound above the AET is assessed, not automatically a failure. Identification confidence is reported, because high-resolution MS identifies many non-volatiles tentatively rather than against a library.
What it does not tell you
Nothing about volatiles or semi-volatiles, which need GC-based methods, and nothing about what the other solvents would extract. Chemical characterisation has no independent pass or fail: the data mean nothing until a toxicologist reads them against exposure under ISO 10993-17, and the screen cannot see compounds the solvent did not extract or the technique cannot detect.
Method
Testing per ISO 10993-18:2020/Amd 1:2022. The sample is extracted in isopropyl alcohol (IPA), followed by a concentration step, and the extract is analysed by HPLC coupled to quadrupole time-of-flight mass spectrometry; compounds are identified from accurate mass and fragmentation and semi-quantified against an internal standard. Extraction ratio follows ISO 10993-12: 6 cm²/mL for material under 0.5 mm thick, 3 cm²/mL at 0.5 mm or thicker, or 0.1 to 0.2 g/mL where surface area is indeterminate.
Where it runs
Testing is performed to Groenakker protocols at an ISO/IEC 17025 accredited laboratory in Groenakker’s network, and the report is issued under Groenakker’s ISO 13485:2016 certified quality system, in Groenakker’s report template or in your document template on request at no extra cost.
Usually ordered alongside
The other screens that make up a complete extractables profile — VOC, SVOC, NVOC and heavy metals across the three solvents — then the toxicological risk assessment (GRK-2001) that turns the compound list into a conclusion. The ChemTox packages bundle all of this for one price.
