1、Designation:F160800(Reapproved 2009)Standard Test Method forMicrobial Ranking of Porous Packaging Materials(ExposureChamber Method)1This standard is issued under the fixed designation F1608;the number immediately following the designation indicates the year oforiginal adoption or,in the case of revi
2、sion,the year of last revision.A number in parentheses indicates the year of last reapproval.Asuperscript epsilon()indicates an editorial change since the last revision or reapproval.1.Scope1.1 This test method is used to determine the passage ofairborne bacteria through porous materials intended fo
3、r use inpackaging sterile medical devices.This test method is designedto test materials under conditions that result in the detectablepassage of bacterial spores through the test material.1.1.1 A round-robin study was conducted with eleven labo-ratories participating.Each laboratory tested duplicate
4、 samplesof six commercially available porous materials to determinethe LRV.Materials tested under the standard conditions de-scribed in this test method returned average values that rangefrom LRV 1.7 to 4.3.1.1.2 Results of this round-robin study indicate that cautionshould be used when comparing te
5、st data and rankingmaterials,especially when a small number of sample replicatesare used.In addition,further collaborative work(such asdescribed in Practice E691)should be conducted before thistest method would be condsidered adequate for purposes ofsetting performance standards.1.2 This test method
6、 requires manipulation of microorgan-isms and should be performed only by trained personnel.TheU.S.Department of Health and Human Services publicationBiosafety in Microbiological and Biomedical Laboratories(CDC/NIH-HHS Publication No.84-8395)should be con-sulted for guidance.1.3 The values stated in
7、 SI units are to be regarded asstandard.No other units of measurement are included in thisstandard.1.4 This standard does not purport to address all of thesafety concerns,if any,associated with its use.It is theresponsibility of the user of this standard to establish appro-priate safety and health p
8、ractices and determine the applica-bility of regulatory limitations prior to use.2.Referenced Documents2.1 ASTM Standards:2E177 Practice for Use of the Terms Precision and Bias inASTM Test MethodsE691 Practice for Conducting an Interlaboratory Study toDetermine the Precision of a Test Method3.Termin
9、ology3.1 Definitions:3.1.1 porous packaging material,na material used inmedical packaging which is intended to provide an environ-mental and biological barrier,while allowing sufficient air flowto be used in gaseous sterilization methods(for example,EO,steam,gas plasma).4.Summary of Test Method4.1 S
10、amples of porous materials are subjected to an aerosolof Bacillus subtilis var.niger spores within an exposurechamber.Spores which pass through the porous sample arecollected on membrane filters and enumerated.The logarithmreduction value(LRV)is calculated by comparing the loga-rithm of the number o
11、f spores passing through the porousmaterial with the logarithm of the microbial challenge.4.2 Standard Set of Conditions This test method specifiesa standard set of conditions for conducting the exposurechamber test method.Astandard set of conditions is required toenable evaluation of materials betw
12、een laboratories.The con-ditions stated in this test method were chosen for severalreasons.First,it is difficult to maintain an aerosol of sporesover long periods of time.(Also,if the spore challenge time islong,the cost of the test increases).Second,to determine thedifferences between materials,it
13、is necessary to test thematerials under conditions which allow passage of bacterialspores.If a material does not allow any passage of spores,allthat can be stated is that it has better resistance to penetrationthan the severity of the challenge conditions.Third,it isnecessary to have a large spore c
14、hallenge level to be able to1This test method is under the jurisdiction ofASTM Committee F02 on FlexibleBarrier Packaging and is the direct responsibility of Subcommittee F02.15 onChemical/Safety Properties.Current edition approved Oct.1,2009.Published November 2009.Originallyapproved in 1995.Last p
15、revious edition approved in 2004 as F1608 00(2004).DOI:10.1520/F1608-00R09.2For referenced ASTM standards,visit the ASTM website,www.astm.org,orcontact ASTM Customer Service at serviceastm.org.For Annual Book of ASTMStandards volume information,refer to the standards Document Summary page onthe ASTM
16、 website.Copyright ASTM International,100 Barr Harbor Drive,PO Box C700,West Conshohocken,PA 19428-2959.United States1 detect the passage of spores through the entire range ofcommercially available porous packaging materials.The stan-dard conditions stated in this test method are based upon thesefactors.(Additional information may be found in the Refer-ences section).However,since many factors influence thedetermination of an appropriate porous material(outlined in5.1.1 5.1.4),each user may modi
