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ASTM_F_719_-_81_2012.pdf

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1、Designation:F71981(Reapproved 2012)Standard Practice forTesting Biomaterials in Rabbits for Primary Skin Irritation1This standard is issued under the fixed designation F719;the number immediately following the designation indicates the year of originaladoption or,in the case of revision,the year of

2、last revision.Anumber in parentheses indicates the year of last reapproval.Asuperscriptepsilon()indicates an editorial change since the last revision or reapproval.1.Scope1.1 This practice covers a procedure by which the irritancyof a biomaterial may be assessed through contact with abradedand intac

3、t skin of rabbits.1.2 The results of this practice depend upon the effective-ness with which contact between the skin and the test materialis established and maintained.Because of the operator tech-nique included in performing this test,it is important that thetest be performed by personnel with app

4、ropriate training.1.3 The values stated in 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

5、establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2.Referenced Documents2.1 ASTM Standards:2F619 Practice for Extraction of Medical Plastics3.Summary of Practice3.1 Exposure of skin to the test material is accomplished bymeans

6、of a patch test technique employing two intact and twoabraded sites on the back of each of six albino rabbits.The skinis clipped free of hair one day prior to testing.The testsubstance is applied using 0.5 mL for liquids,0.5 g for solidsor semisolids,and a 2.5 by 2.5-cm square patch for films.Aftera

7、pplication,each test site is covered with a 2.5 by 2.5-cm gauzeflat,and the entire trunk is occluded with a polyethylene sleeve.After 24 h,the sleeve,flat,and test material are removed,andtest sites are evaluated for erythema and edema.4.Significance and Use4.1 Materials that are to be in contact wi

8、th the skin shouldnot cause irritation to the skin.Since it is probably thesubstances leached from a material that cause the irritation,thispractice provides for direct material-skin contact testing or forskin exposure to the liquid extract of the test material.Therationale for this rabbit test is t

9、hat it is a comparatively quickand inexpensive method which,through use over the years,hasbecome a generally accepted method.5.Materials and Manufacture5.1 Young New Zealand Albino Rabbits,5.2 Gauze Flats,2.5 by 2.5-cm,5.3 Polyethylene Sleeves,extra clear,and5.4 Adhesive Tape,12-in.6.Test Specimen6.

10、1 The test specimen may be one of three forms:6.1.1 Test 0.5 mL of liquids or saline extract liquids ob-tained in accordance with Practice F619.6.1.2 Test 0.5 g of solids or semisolids.6.1.3 Test films 2.5 by 2.5 cm.NOTE1A vehicle control for liquids is required because of thepotential for false pos

11、itives due to skin temperature changes whenhandling rabbits.Positive controls may be used to validate the test method.The use of 5%procaine HCl as a positive control is suggested.36.2 The pH of the solutions should be measured andreported,if appropriate.7.Procedure7.1 Preparation of Test Animals:7.1

12、.1 Twenty-four hours before the test,clip the hair fromthe backs of the animals so as to expose two test areas on eachside of the spine,which are 10 cm apart.7.1.2 To obtain more effective contact between the skin andthe test substance,it may be necessary to use a non-irritatingdepilatory agent.This

13、 test method may be used to ensure thatthe depilatory agent is non-irritating.1This practice is under the jurisdiction ofASTM Committee F04 on Medical andSurgical Materials and Devices and is the direct responsibility of SubcommitteeF04.16 on Biocompatibility Test Methods.Current edition approved Oc

14、t.1,2012.Published October 2012.Originallyapproved in 1981.Last previous edition approved in 2007 as F719 81(2007)1.DOI:10.1520/F0719-81R12.2For referenced ASTM standards,visit the ASTM website,www.astm.org,orcontact ASTM Customer Service at serviceastm.org.For Annual Book of ASTMStandards volume in

15、formation,refer to the standards Document Summary page onthe ASTM website.3H.H.Draize,Appraisal of the Safety of Chemicals in Foods,Drugs,andCosmetics,1965,p.46.Copyright ASTM International,100 Barr Harbor Drive,PO Box C700,West Conshohocken,PA 19428-2959.United States1 7.1.3 Test sites may be desig

16、nated as two on each side of thespine.Alternatively,the area may be divided into quadrantswith test and control substances applied to each quadrant.7.2 Test Procedure:7.2.1 Wipe the exposed area of the back with alcohol.7.2.2 Using a sterile blade,abrade two of the four sites bymoving the blade at right angles to the cutting surface in ascraping motion to create a denuded area of skin.Alternatively,make four epidermal incisions(which penetrate the stratumcorneum but not the dermis),with two perp

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