ASTM_D_7102_-_17_2022.pdf

Designation:D710217(Reapproved 2022)Standard Guide forDetermination of Endotoxin on Sterile Medical Gloves1This standard is issued under the fixed designation D7102;the number immediately following the designation indicates the year oforiginal adoption or,in the case of revision,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.INTRODUCTIONThis guide is established and designed to determine the qualitative or quantitative presence ofbacterial endotoxin on sterile medical gloves.Bacterial endotoxins are found in the outer membraneof Gram negative bacteria and may contaminate gloves during the manufacturing process.Conse-quences of endotoxin introduced into a patient during invasive procedures are dose dependent and mayinclude inflammation,fever,nausea,pain,clot formation,hypoglycemia and reduced profusion of theheart,kidney,and liver as well as endotoxic shock.Endotoxins are not inactivated by routine methodsutilized in the routine sterilization of medical gloves including irradiation(gamma or E-beam),ethylene oxide,or steam.1.Scope1.1 This guide covers a selection of methodologies for thedetermination of bacterial endotoxin on gloves when such adetermination is appropriate.1.2 As bacteria may continue to grow on non-sterile gloves,reportable endotoxin levels are only appropriate for gloveslabeled as sterile.Because most environments containendotoxin,once a box of gloves is opened and the gloves aremanipulated,endotoxin levels will increase making it inappro-priate to report endotoxin levels on boxed gloves(ex.exami-nation gloves).This is true even if the box had undergonesterilization prior to distribution.1.3 This guide may also be appropriate for internal qualitycontrol or alert purposes at different stages of manufacturing orduring process change evaluations.1.4 This guide is not applicable to the determination ofpyrogens other than bacterial endotoxins.1.5 The sample preparation method described must be usedregardless of the test method selected.This method does notdescribelaboratorytestmethodvalidation,analystqualification,or reagent confirmation.Product-specific valida-tion is addressed.1.6 The safe and proper use of medical gloves is beyond thescope of this guide.1.7 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,health,and environmental practices and deter-mine the applicability of regulatory limitations prior to use.1.8 This international standard was developed in accor-dance with internationally recognized principles on standard-ization established in the Decision on Principles for theDevelopment of International Standards,Guides and Recom-mendations issued by the World Trade Organization TechnicalBarriers to Trade(TBT)Committee.2.Referenced Documents2.1 EN Standard:2EN 455-3:2015 Medical Gloves for Single UsePart 3:Requirements and Testing for Biological Evaluation2.2 ANSI Standard:2ANSI/AAMI ST 72:2011 Bacterial EndotoxinsTestMethodologies,Routine Monitoring and Alternatives toBatch Testing3.Terminology3.1 Definitions:3.1.1 bacterial endotoxin test(BET)a method for deter-mining the qualitative or quantitative presence of endotoxin inan aqueous test sample utilizing Limulus amebocyte lysate(LAL)reagent and measuring the resulting proportional reac-tion.1This guide is under the jurisdiction of ASTM Committee D11 on Rubber andRubber-like Materials and is the direct responsibility of Subcommittee D11.40 onConsumer Rubber Products.Current edition approved June 1,2022.Published July 2022.Originally approvedin 2004.Last previous edition approved in 2017 as D7102 17.DOI:10.1520/D7102-17R22.2Available from American National Standards Institute(ANSI),25 W.43rd St.,4th Floor,New York,NY 10036.Copyright ASTM International,100 Barr Harbor Drive,PO Box C700,West Conshohocken,PA 19428-2959.United StatesThis international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for theDevelopment of International Standards,Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade(TBT)Committee.13.1.2 batchdefined quantity of intermediate or finishedproduct produced in a defined cycle of manufacture that is saidto be of uniform quality.3.1.3 chromogenic(colorimetric)techniqueBET method-ology that quantifies or detects endotoxin on the basis of ameasured color-producing reaction proportional to the interac-tion of LAL and endotoxin.3.1.4 control standard endotoxin(CSE)purified endotoxinproduct supplied at a known potency and utilized as a standardcontrol in endotoxin testing.3.1.5 devicewith regard to medical gloves,a device isdefined as a pair of gloves when they are packaged in pairs anda single glove when packaged singly.3.1.6 endo