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Dose response22 |
Ecotoxicty1 |
Exposure and release2 |
Metadata only3 |
Phys-chem characterisation29 |
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Analytical Methods8 |
Barrier integrity1 |
Cell Viability11 |
Computational models metadata1 |
Crystalline phase1 |
Density3 |
Dustiness1 |
Genetic toxicity in vitro4 |
Immunotoxicity1 |
Material composition1 |
Omics metadata2 |
Oxidative Stress5 |
Particle size distribution (Granulometry)6 |
Short-term toxicity to aquatic inverterbrates2 |
Specific surface area2 |
Surface chemistry1 |
Use and exposure information2 |
Water solubility3 |
Zeta potential2 |
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| Template Wizard link | Template | Project/Provider | Type | Category | Status | |
|---|---|---|---|---|---|---|
| ALAMARBLUE | Alamar Blue The Alamar Blue (AB) assay is a high throughput, cell metabolism-based method largely applied in toxicology and nanotoxicology to investigate cell viability (cytotoxicity), cell proliferation and cellular metabolic activity in response to chemicals and nanomaterials. | RISKGONE/NILU | doseresponse | Cell Viability | published | |
| BARRIERCROSSING | Barrier crossing | NANOINFORMATIX/ | doseresponse | Barrier integrity | published | |
| BIOIMPEDANCE | Bio impedance - human cells Label-free Cell monitoring by Electrical Impedance (bioimpedance). This method can assess cell viability, proliferation, cell-cell and cell-substrate interaction of adherent cells growing onto a microelectrode array. | RISKGONE/University of Bergen (UiB) | doseresponse | Cell Viability | published | |
| BIOIMPEDANCE_ECOTOX | Bio impedance - ecotoxicity Label-free Cell monitoring by Electrical Impedance (bioimpedance). This method can assess cell viability, proliferation, cell-cell and cell-substrate interaction of adherent cells growing onto a microelectrode array. | RISKGONE/University of Bergen (UiB) | doseresponse | Cell Viability | published | |
| CARBONYLATION | Determining Protein Carbonylation | GRACIOUS/BfR | doseresponse | Cell Viability | published | |
| CBMN | Acute 2D/3D cytokinesis-blocked micronucleus (CBMN) assay The micronucleus assay is considered the gold standard for detecting chromosomal damage in vitro. The assay is designed so that cells exposed to a genotoxic test agent result in chromosomal breakage forming small spherical nuclei (micronuclei) being detected as fixed DNA damage. | NANOINFORMATIX/FIOH | doseresponse | Genetic toxicity in vitro | published | |
| CFE | Colony Forming Efficiency The colony forming efficiency assay (CFE) (also called clonogenic or plating efficiency assay) measures the ability of cells to survive and form colonies, which is an ultimate index of cytotoxicity. | RISKGONE/NILU | doseresponse | Cell Viability | published | |
| COMET | COMET The comet assay, also called SCGE (Single Cell Gel Electrophoresis), is a rapid and informative method to detect DNA damage at single cell level used on many different cell types. The assay detects single and double strand DNA breaks as a consequence of a direct damage or as intermediate of DNA repair processes and it is successfully applied both in in vivo and in vitro genotoxicity testing. | RISKGONE/NILU | doseresponse | Genetic toxicity in vitro | published | |
| COMPOSITION | Define material composition (CC BY 4.0) Detailed information of material component (chemistry, role, identifiers). https://doi.org/10.5281/zenodo.7751340 | HARMLESS/IDEA | pchem | Material composition | published | |
| COMPOSITION_ICPMS | Elemental composition by ICP-MS (CC BY-SA 4.0) http://dx.doi.org/10.2760/142959 | GRACIOUS/JRC | pchem | Analytical Methods | published |
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