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ASTM F 1439 : 2003 : R2018

Current

Current

The latest, up-to-date edition.

Standard Guide for Performance of Lifetime Bioassay for the Tumorigenic Potential of Implant Materials

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

01-04-2018

€56.53
Excluding VAT

Committee
F 04
DocumentType
Guide
Pages
6
PublisherName
American Society for Testing and Materials
Status
Current
Supersedes

1.1This guide is intended to assist the biomaterials testing laboratory in the conduct and evaluation of tumorigenicity tests to evaluate the potential for new materials to evoke a neoplastic response. The procedure is generally reserved only for those materials which have not previously been used for human implantation for a significant period of time.

1.2Assessment of tumorigenicity is one of several procedures employed in determining the biological response to a material as recommended in Practice F748. It is assumed that the investigator has already determined that this type of testing is necessary for a particular material before consulting this guide. The recommendations of Practice F748 should be considered before a study is commenced.

1.3Whenever possible, it is recommended that a battery of genotoxicity procedures be initiated and proposed as an alternative to an in-vivo tumorigenicity bioassay. Genotoxicity assays may also be considered as initial screening procedures due to the sensitivity of the assays, the significant reduction in time to gain valuable data, and the desire to reduce the use of animals for testing. Genotoxicity assays that may be considered are outlined in Guides E1262, E1263, E1280, and E2186, and Practices E1397 and E1398. Additionally, other genotoxicity testing which might be considered (but which do not yet have ASTM test methods) include Salmonella/Mammalian-Microsomal Plate Incorporation Mutagenicity Assay, In Vivo Cytogenetics Bone Marrow Chromosomal Damage Assay, BALB/3T3 Morphological Transformation of Mouse Embryo Cells, and the Mouse Micronucleus Assay. The investigator is advised to consider carefully the appropriateness of a particular method for his application after a review of the published literature.

1.4This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.

1.5This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

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ASTM F 748 : 2016 Standard Practice for Selecting Generic Biological Test Methods for Materials and Devices
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ASTM E 1398 : 1991 : R1998 Standard Practice for the in vivo Rat Hepatocyte DNA Repair Assay
ASTM E 1262 : 1988 : R1996 Standard Guide for Performance of the Chinese Hamster Ovary Cell/Hypoxanthine Guanine Phosphoribosyl Transferase Gene Mutation Assay
ASTM E 1263 : 1997 Standard Guide for Conduct of Micronucleus Assays in Mammalian Bone Marrow Erythrocytes
ASTM E 1262 : 1988 : R2018 Standard Guide for Performance of Chinese Hamster Ovary Cell/Hypoxanthine Guanine Phosphoribosyl Transferase Gene Mutation Assay
ASTM E 2186 : 2002 : REV A : R2023 Standard Guide for Determining DNA Single-Strand Damage in Eukaryotic Cells Using the Comet Assay
ASTM E 1397 : 1991 : R1998 Standard Practice for the in vitro Rat Hepatocyte DNA Repair Assay
ASTM E 1280 : 1997 Standard Guide for Performing the Mouse Lymphoma Assay for Mammalian Cell Mutagenicity
ASTM E 2186 : 2002 : REV A : R2016 Standard Guide for Determining DNA Single-Strand Damage in Eukaryotic Cells Using the Comet Assay
ASTM E 2186 : 2002 Standard Guide for Determining DNA Single-Strand Damage in Eukaryotic Cells Using the Comet Assay

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