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Details
1.1 This test method measures the aerosol filtration performance of porous packaging materials by creating a defined aerosol of 1.0 µm particles and assessing the filtration efficiency of the material using either single or dual particle counters.
1.2 This test method is applicable to porous materials used to package terminally sterilized medical devices.
1.3 The intent of this test apparatus is to determine the flow rate through a material at which maximum penetration occurs.
1.4 The values stated in SI units are to be regarded as the standard. The values given in parentheses are for information only.
1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.
1.6 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.
Significance and Use:
6.1 This test method has been developed as a result of research performed by Air Dispersion Limited (Manchester, UK) and funded by the Barrier Test Consortium Limited. The results of this research have been published in a peer-reviewed journal.4 This research demonstrated that testing the barrier performance of porous packaging materials using microorganisms correlates with measuring the filtration efficiency of the materials.
6.2 This test method does not require the use of microbiological method, in addition, the test method can be conducted in a rapid and timely manner.
6.3 When measuring the filtration efficiency of porous packaging materials a typical filtration efficiency curve is determined (see Fig. 1). Since the arc of these curves is dependent upon the characteristics of each individual material, the appropriate way to make comparison among materials is using the parameter that measures maximum penetration through the material.
FIG. 1 A Typical Curve Showing Penetration as a Function of Flow Rate
Note 1: The point of maximum penetration is indicated by the upward pointing triangle.
6.4 The particle filtration method is a quantitative procedure for determining the microbial barrier properties of materials using a challenge of 1.0 µm particles over range of pressure differentials from near zero to approximately 30 cm water column (WC) (2942 Pa). This test method is based upon the research of Tallentire and Sinclair4 and uses physical test methodology to allow for a rapid determination of microbial barrier performance.
Additional Info
| Author | American Society for Testing and Materials (ASTM International) |
|---|---|
| Committee | F02.15 - Committee F02 on Primary Barrier Packaging |
| Published by | ASTM |
| Document type | Standard |
| Theme | ,Packaging materials and accessories |
| ICS | 55.040 : Packaging materials and accessories
|
| Number of pages | 15 |
| Replace | ASTM F2638-18 + Redline |
| Set | ASTM Volume 15.10 - Multi-User - Single-Site Online |
| Keyword | F2638 |
