ASTM E1589-2005(2010) Standard Test Method for Evaluation of First Aid Antiseptic Drug Products《急救抗菌药制品评定的标准试验方法》.pdf

《ASTM E1589-2005(2010) Standard Test Method for Evaluation of First Aid Antiseptic Drug Products《急救抗菌药制品评定的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM E1589-2005(2010) Standard Test Method for Evaluation of First Aid Antiseptic Drug Products《急救抗菌药制品评定的标准试验方法》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E1589 05 (Reapproved 2010)Standard Test Method forEvaluation of First Aid Antiseptic Drug Products1This standard is issued under the fixed designation E1589; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revision, the year of

2、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 The tests described in this test method are designed toevaluate antimicrobial agents in formulations intended for usea

3、s first aid antiseptic products for their ability to reduce orsuppress the growth, or both, of the skin microflora.1.2 A knowledge of microbiological techniques is requiredfor these procedures.1.3 Performance of this procedure requires the knowledgeof regulations pertaining to the protection of huma

4、n subjects.(See CFR Parts 50 and 56.)1.4 The values stated in SI units are to be regarded asstandard. No other units of measurement are included in thisstandard.1.5 This standard does not purport to address all of thesafety concerns, if any, associated with its use. It is theresponsibility of the us

5、er of this standard to establish appro-priate safety and health practices and determine the applica-bility of regulatory limitations prior to use.2. Referenced Documents2.1 ASTM Standards:2D1193 Specification for Reagent WaterE1054 Test Methods for Evaluation of Inactivators of An-timicrobial Agents

6、2.2 Federal Standards:3CFR Parts 50 and 563. Terminology3.1 active ingredient, na substance performing a functiondefined by this method.3.2 neutralization, na process which results in quenchingor inactivating inactivation of the antimicrobial activity of aformulation. This may be achieved with dilut

7、ion of theformulation, or with the use of chemical agents, called neu-tralizers.3.3 neutralizer, na procedure or chemical agent used toinactivate, neutralize, or quench the microbiocidal properties ofan antimicrobial agent.3.4 resident microorganisms , nmicroorganisms that liveand multiply on skin,

8、forming a permanent population.3.5 sampling fluid, na recovery fluid that may or may notcontain a neutralizer to inactivate the active ingredients in testand internal reference formulations.3.6 test formulation , na formulation containing an activeingredient(s).3.7 transient microorganisms, nmicroor

9、ganisms that con-taminate but do not normally permanently colonize the skin.4. Summary of Test Methods4.1 These test methods describe standard in vivo techniquesto determine the following:4.1.1 Effect of the Test Formulation to Reduce an ArtificiallyEnhanced Skin Microbial FloraThe forearms of subje

10、cts areoccluded for 48 h prior to application of the test formulation toincrease the microbial population on the skin of the volarforearm surface. At treatment the occlusion material is re-moved and the skin is allowed to dry, the test formulation isthen applied to selected sites. At a pre-determine

11、d time(s)following application, the sites are microbiologically sampledand the samples plated for total aerobic bacteria count. Thecounts obtained from the treated sites are compared to countsobtained from untreated occluded sites.4.1.2 Effect of the Test Formulation to Suppress the Growthof Normal

12、Skin Flora When Applied As a DressingThedressings are applied to the forearm for 24 h. The density of theresident microorganisms that develop under the dressings arecompared to the population that develops on a similar untreatedoccluded site. Following 24 h of occlusion, the sites aremicrobiological

13、ly sampled and the samples plated for totalaerobic bacteria count.1This test method is under the jurisdiction of ASTM Committee E35 onPesticides and Alternative Control Agents and is the direct responsibility ofSubcommittee E35.15 on Antimicrobial Agents.Current edition approved April 1, 2010. Publi

14、shed May 2010. Originallyapproved in 1994. Last previous edition approved in 2005 as E1589 05. DOI:10.1520/E1589-05R10.2For 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

15、to the standards Document Summary page onthe ASTM website.3Available from U.S. Government Printing Office, Superintendent of Docu-ments, Washington DC, 20402.1Copyright ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959, United States.4.2 The principal of the te

16、st is that the microflora of forearmskin is sparse. The impermeable dressing will increase surfacemoisture by preventing diffusional water loss and thus expandtransient resident skin microorganisms population. A signifi-cant antimicrobial effect by the test agent will be reflected bysignificantly lo

17、wer population recovered from the nontreatedsite.5. Significance and Use5.1 The procedures in this test method should be used for invivo evaluation the antimicrobial activity of drug productsapplied topically to the skin that are intended to help preventinfection in minor cuts, scrapes and burns.5.1

18、.1 This test method is applicable for testing liquids,ointments, powders, films, or dressing containing or impreg-nated with an antimicrobial for their effect to reduce anenhanced skin microflora or their effects to suppress the growthof the skin flora, or both.6. Apparatus6.1 Colony CounterAny of s

19、everal types may be used, forexample, Quebec colony counter.6.2 IncubatorAny incubator capable of maintaining atemperature of 35 6 2C.6.3 SterilizerAny suitable steam sterilizer capable ofproducing the conditions or sterilization.6.4 Timer (Stop-Clock)One that can be read for hours andminutes.7. Rea

20、gents and Materials7.1 Bacteriological Pipette5.0 and 2.2 mL or 1.1 mLcapacity.NOTE 1Presterilized/disposable bacteriological pipettes are availablefrom most laboratory supply houses.7.2 Water Dilution BottlesAny sterilizable container hav-ing a 150 to 200 mL capacity and tight closure.7.3 Scrubbing

21、 CupsSterile cylinders, (Recommendedheight approximately 2.5 cm, inside diameter 23 cm.7.4 Rubber PolicemanCan be fashioned in the laboratoryor purchased from most laboratory supply houses.7.5 Test FormulationWith directions for use.7.6 Occlusive Plastic WrapUsed to occlude skin sites.7.7 Sampling S

22、olutionDissolve 0.4 g KH2PO4, 10.1 gNa2HPO4and 1.0 g octylphenoxypolyethoxyethanol (see Note2) in 1 L of distilled water or higher purity water that meets orexceeds, Specification D1193, Type III or better. Include in thisformulation a neutralizer specific for the antimicrobial in thetest formulatio

23、n (see Test Methods E1054) if appropriate.Adjust to pH 7.8 6 0.1. Dispense appropriate volumes andsterilize .NOTE 2Also known as Triton X-100.7.8 Dilution FluidButterfields phosphate buffered water4adjusted to pH 7.2, and containing an antimicrobial activatorspecific for the test formulation. (See P

24、ractices E1054.)7.9 Plating MediumSoybean-casein digest agar medium5or commercial equivalent.7.10 Personal Hygiene Kitcontents may include variousnon-antimicrobial formulations such as shampoo, hand soap,non-aerosol deodorant, and gloves at the discretion of theinvestigator.7.11 Adhesive Tapesurgica

25、l or other appropriate adhesivetape.8. Procedure8.1 Reduction of Microbial Flora by Products That Are NotApplied Under Dressings.8.1.1 Number of SubjectsSample size calculations shouldbe done to determine the number of subjects necessary to findstatistically significant differences (reductions) from

26、 baseline.The number of subjects required depends on the statisticalconfidence required for the expected results, the variabilityencountered in the data collection (for example, variability inreductions from baseline), and the expected efficacy of the testproduct (for example, its expected reduction

27、 from baseline).The minimum number of subjects (n) required for each testformulation can be estimated from the following equation:n.S2SZa/21Zb!2D2 D(1)S2= estimate of variance (of reductions from baselinebased on in-house data pool)(Za/2= cumulative probability of the standard normaldistribution, =

28、1.96 for a=0.05,Zb= power of the test = 0.842 for b = 0.80,D = expected efficacy (expected reduction from base-line).NOTE 3Experience has shown that a range from 1218 subjectsprovides acceptable data.8.1.2 Subject Inclusion Criteria:8.1.2.1 Individuals between the ages of 18 and 65 yearsbeing prefer

29、ably both male and female,8.1.2.2 Hands and forearms free of dermatoses, lesions,open wounds hangnails, or other skin disorders, and8.1.2.3 Are in general good health as evidenced by historyand limited medical examination.8.1.3 Subject Exclusion Criteria:8.1.3.1 Exposure to antimicrobial agents, med

30、icated soaps,medicated shampoos or medicated lotions during the two weekwashout period or test period,8.1.3.2 Exposure of hands or forearms to strong detergents,solvents or other irritants during the two week pre-wash periodor test period,8.1.3.3 Currently receiving a typical or systemic antibiotic,

31、and8.1.3.4 Not willing to fulfill the requirements of the proto-col.8.1.4 Subject InstructionsSubjects are to refrain fromusing any product containing an antimicrobial agent for at least4Downes, F.P. and K. Ito, Compendium of Methods for the MicrobiologicalExamination of Foods,American Public Health

32、Association, Washington, DC, 2001,p. 637 and p. 643.5U.S. Pharmacopeia 2567, United States Pharmacopeial Convention, Inc.,Rockville, MD,200234, see Chapter entitled 9Microbial Limits Test.9E1589 05 (2010)2two weeks prior to the test. Kits containing non-medicated barsoap, shampoo, and roll-on or sti

33、ck antiperspirant for useduring this time are provided. Subjects are instructed not to usemedicated creams, ointments, or take antibiotics. Bathing inbiocide treated pools, hot tubs, and spas is not permitted.Subjects are instructed not to shower in the 48 h periodproceeding the sampling period; how

34、ever, a sponge bathexcluding the test areas is permitted.8.1.5 Test Site OcclusionFollowing a two-week wash-outperiod, the forearms of each of the human subjects areoccluded with occlusive plastic wrap patches. The occlusiveplastic wrap is cut to fashion a patch that will cover the volaraspect of th

35、e forearm, approximately 8 to 10 cm by 18 to 20cm. A patch is placed in the mid-volar surface of each arm andanchored with adhesive tape.8.1.6 Treatment ProcedureA test formulation treatmentand two control sites, no treatment and vehicle control (for-mula without the active), are located on the vola

36、r aspect ofeach forearm, each site measures 3.5 cm by 3.5 cm. Theassignment of the treatment and two controls to the three siteson each forearm is made according to a predetermined ran-domization scheme. Approximately 48 h following occlusion,individual sites are exposed to air prior to treatment, u

37、ntilvisibly dry. The test formulation and vehicle control sites aretreated with the appropriate material according to the productlabel instructions. The treated test formulation sites and vehiclecontrol sites are to be sampled after a 30 min exposure period.(Other appropriate time intervals may be u

38、sed.) The untreatedcontrol sites are sampled without treatment at the samepost-treatment time interval.8.1.7 Bacterial Sampling (Cup Scrubbing Method):8.1.7.1 Delineate the area to be sampled by a sterile sam-pling cylinder. Firmly hold it against the skin during samplingto ensure that the washing f

39、luid does not leak from thesampling site.8.1.7.2 Three mL of sterile sampling fluid is pipeted into thecup, and the entire area is scrubbed with moderate pressure forone minute using a sterile rubber 9policeman.98.1.7.3 The sampling fluid is removed with a sterile pipetteand retained.8.1.7.4 The scr

40、ubbing procedure is repeated and the fluidsfrom the two washes are pooled.8.1.7.5 Dilution fluid is Butterfields phosphate buffer thatcontains a neutralizer for the antimicrobial agent.8.1.7.6 Plating medium: Soybean casein digest agar usingstandard pour or spread plate procedure may be used.8.1.7.7

41、 Promptly after the collection of the washing fluid,aliquots are plated 100through 10-4for all samples.8.1.7.8 All plating is in duplicate, and plates are incubatedaerobically at 35C 6 2C for 48 6 4 h before counting.8.1.8 Analysis of DataTransform counts from each testsite on each arm to log10and u

42、se the log10counts for statisticalevaluation. Evaluate differences between treatments and per-form an overall analysis to test the null hypothesis of nodifference among treatments. Test treatment differences forstatistical significance at the 95 % confidence level, usingappropriate parametric or non

43、-parametric procedures, or both.8.2 Suppression of Growth Under a Dressing:8.2.1 Number of SubjectsSame as 8.1.1.NOTE 4Experience has shown that at least 10 subjects providesacceptable data.8.2.2 Eligibility of Test SubjectsSame as 8.1.2 and 8.1.3.8.2.3 Subject InstructionsSame as 8.1.4.8.2.4 Treatm

44、ent Procedure:8.2.4.1 Application SitesA test product treatment and twocontrol sites, no treatment and vehicle control (formula withoutthe active), are located on the volar aspect of each forearm.Following a two-week washout period, application of the testproduct and controls to the arms are made ac

45、cording to apredetermined randomization.8.2.4.2 Application of Liquid, Ointment and PowdersOnemLor1gofthetest material is spread over each 25 cm2site.The product treated site, vehicle control site, and the untreatedcontrol site are immediately covered with a 25 cm2ofocclusive wrap. Each site is occl

46、usively sealed with occlusivewrap and tape. A strip of adhesive tape is placed between eachsite to prevent translocation of the test agents and the micro-organisms from one site to another.8.2.4.3 Application of Impregnated DressingsApplydressings according to label directions.8.2.4.4 Each site is q

47、uantitatively sampled after 24 h ofocclusion using the procedure described in 8.1.6.8.2.5 Analysis of DataSame as 8.1.8.9. Neutralizer Validation9.1 When neutralizers are added to culture media or dilutingfluids, or both, validate the effectiveness of the systemsaccording Test Method E1054.10. Preci

48、sion and Bias10.1 A precision and bias statement cannot be made for thistest method at this time.11. Keywords11.1 antiseptic; bacteria; bandages; cup scrub; dressing; firstaid; efficacy; first aid; impregnated dressing; occlusion; skinmicrofloraE1589 05 (2010)3ASTM International takes no position re

49、specting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility.This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn. Your comments are invited either for revision of this standard or