ASTM E1883-2002 Standard Test Method for Assessment of an Antibacterial Handwash Product by Multiple Basin Wash Technique《用多盆洗涤技术评定抗菌手洗物的标准试验方法》.pdf

《ASTM E1883-2002 Standard Test Method for Assessment of an Antibacterial Handwash Product by Multiple Basin Wash Technique《用多盆洗涤技术评定抗菌手洗物的标准试验方法》.pdf》由会员分享，可在线阅读，更多相关《ASTM E1883-2002 Standard Test Method for Assessment of an Antibacterial Handwash Product by Multiple Basin Wash Technique《用多盆洗涤技术评定抗菌手洗物的标准试验方法》.pdf（4页珍藏版）》请在麦多课文档分享上搜索。

1、Designation: E 1883 02Standard Test Method forAssessment of an Antibacterial Handwash Product byMultiple Basin Wash Technique1This standard is issued under the fixed designation E 1883; the number immediately following the designation indicates the year oforiginal adoption or, in the case of revisio

2、n, the year of last revision. A number in parentheses indicates the year of last reapproval. Asuperscript epsilon (e) indicates an editorial change since the last revision or reapproval.1. Scope1.1 This test method covers determining the effectiveness ofan antibacterial handwash for reducing the lev

3、el of aerobicbacterial flora on the hands, following an extended period ofuse.1.2 A knowledge of microbiological techniques is requiredfor these procedures.1.3 In this test method metric units are used for all applica-tions, except for distance. In this case, inches are used andmetric units follow i

4、n parentheses.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 practices and determine the applica-bility of regulatory limitations prior to use.1

5、.5 Performance of this procedure requires the knowledgeof regulations pertaining to the protection of human subjects.(Title 21 CFR, Part 50)2. Referenced Documents2.1 ASTM Standards:2D 1193 Specification for Reagent WaterE 1054 Practices for Evaluating Inactivators of Antimicro-bial Agents Used in D

6、isinfectant, Sanitizer, Antiseptic, orPreserved Products2.2 Other Standard:Title 21 Code of Federal Regulations (CFR), Part 50 Pro-tection of Human Subjects: Informed Consent Verificationand, 1.0 mLand 0.1 mL aliquots of a 1:10 dilution of the basin contents insoybean-casein digest agar.10.4 Dilutio

7、nsSample dilutions are prepared in 9.0 mLblanks of Butterfields phosphate buffer.10.5 IncubationAll plates are incubated for 48 6 4 hrs at30 6 2C. After incubation, the colonies on the plates that arecountable are enumerated with the aid of a colony counter. Thetotal bacteria count per liter from th

8、e basin contents iscalculated.11. Neutralizer for the Test Formulation11.1 When neutralizers are added to culture media ordilution fluids, or both, validate the effectiveness of the systemsaccording to Practice E 1054.12. Analysis of Data12.1 Calculation of Bacterial Reduction:E188302312.1.1 Bacteri

9、al counts per litre from the first and or fifthbasin or each sampling day are determined and converted tolog10in order to minimize the effect of variability in countsobtained from different subjects. Data from the two baselinecounts obtained from the first and or fifth basin samples areaveraged for

10、each individual. Geometric means of the data arecalculated.12.1.2 The following percent reductions may be calculated:Percent Reduction Basin 1 Bacterial Population 51Geometric Mean of First2Basin Counts Test Day!Geometric Mean of the 2 Baseline First Basin Counts3 100(2)Percent Reduction Basin 5 Bac

11、terial Population 51Geometric Mean of Fifth2Basin Counts Test Day!Geometric Mean of the 2 Baseline Fifth Basin Counts3 100(3)12.1.3 Estimate the standard deviation for each percentreduction value calculated above; using the assumption of a lognormal distribution, construct 95 % confidence interval f

12、or thepercent reduction value (S). Perform Students independentt-tests to determine if there is a statistically significant bacterialreduction of the transient and or resident bacterial populationson test formulation washed hands when compared to blandcleansing formulation (see 6.6) after twelve day

13、s of testformulation use.13. Precision and Bias13.1 A precision and bias statement cannot be made for thistest method at this time.14. Keywords14.1 antimicrobial; Cade; efficacy; handwashASTM International takes no position respecting the validity of any patent rights asserted in connection with any

14、 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

15、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 for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at

16、 a meeting of theresponsible technical committee, which you may attend. If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.This standard is copyrighted by ASTM International, 100 Barr Harbor D

17、rive, PO Box C700, West Conshohocken, PA 19428-2959,United States. Individual reprints (single or multiple copies) of this standard may be obtained by contacting ASTM at the aboveaddress or at 610-832-9585 (phone), 610-832-9555 (fax), or serviceastm.org (e-mail); or through the ASTM website(www.astm.org).E1883024