ASTM E2149 PDF

ASTM E Antimicrobial Standard Test Method for Determining the Antimicrobial Activity of Immobilized Antimicrobial Agents Under Dynamic Contact. ASTM E Standard Test Method for Determining the Antimicrobial Activity of Immobilized Antimicrobial Agents Under Dynamic Contact Conditions. ASTM E Standard Test Method for Determining the Antimicrobial Activity of Immobilized Antimicrobial Agents under Dynamic Contact Conditions. The test.

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Active view current version of standard. Test Package Request Form. Accept Decline Privacy policy. Summary of Test Method: The test determines the antimicrobial activity zstm a treated specimen by shaking samples of surface-bound materials in a concentrated bacterial suspension for a one hour contact time. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

Organisms typically used in this method: No other units of measurement are included in this standard. Historical Version asgm – view previous versions of standard.

ASTM E2149 Antimicrobial Activity

It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use. Work Item s – proposed revisions of this standard.

Facebook Linkedin Instagram Twitter Google. This website stores cookies on your computer. Surface antimicrobial activity is determined by comparing results from the test sample to controls run simultaneously.

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This dynamic shake flask test was developed for routine quality control and screening tests in order to overcome difficulties in using classical antimicrobial test methods to evaluate substrate-bound antimicrobials. This standard does not purport to address all of the safety concerns, if any, associated with its use. The test quantitatively evaluates the atm of a sample treated with a non-leaching antimicrobial agent by shaking in an organism suspension.

Record and report presence of solution activity.

For example, water soluble antimicrobials will be prone to removal from the test surface using the method described in Section 13 but insoluble compounds will not. This test method standardizes both the growth conditions of the challenge species and substrate contact times to reduce the variability associated with growth phase of the microorganism.

This dynamic shake flask test was developed for routine quality control and screening tests in order to overcome difficulties in using classical antimicrobial test methods to evaluate substrate-bound antimicrobials. Immobilized antimicrobial agents, such as surface bonded materials, are not free to diffuse into their environment under normal conditions of ee2149.

This dynamic shake flash test was developed for routine quality control and screening test.

If an antimicrobial agent that is shown to be removed from the surface by Section 13 is utilized in this test methodology, controls must be included such that appropriate neutralization steps are including during recovery and enumeration. These cookies collect information about how you interact with our website and allow us to remember aztm.

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ASTM E – Microbe Investigations (MIS)

A single cookie will be used in your browser to remember your preference not to be asrm. To find out more about the cookies we use, see our Privacy Policy. The number of viable organisms from the suspension is determined and the percent reduction is calculated by comparing retrievals from appropriate controls.

This test method ensures good contact between the bacteria and the treated fiber, fabric, or other substrate, by constant agitation of the test specimen aatm a challenge suspension during the test period. The presence of a leaching antimicrobial is determined post-test.

This test ensures good contact between bacteria and the treated fibre by constant agitation of the test specimen in a bacterial suspension during the test period 1hour.

Microbial concentrations in the treated and untreated samples are usually determined at 0, 1 or 24 hours contact time.

It has been developed for routine quality control and screening tests and is used to evaluate substrate bound antimicrobials. This test method is designed to evaluate the resistance of specimens treated with a non-leaching antimicrobial agent to the growth of microbes under dynamic contact conditions. One-hour contact time in a buffer solution allows for metabolic stasis in the population.