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Biosan Laboratories
Presents
Standardized Antibacterial
Material Testing Methods
Introduction
Microorganisms cause disease after reaching
out to a potential host. They move around the
environment in various but typically passive
ways such as aerosols, and direct contact
between two animated objects, and fomites.
1
2
Certain microbes can retain their pathogenic potential whilst
outside their host for a longer period of time. According to
studies, they can survive from days to a few weeks on inanimate
surfaces like metals and plastics which are usually considered
hygienic surfaces.
Testing the Efficacy of Antimicrobial Materials (AMM)
3
Standardised test methods are required and considered
inevitable in the development of a unique antimicrobial
material. In order to define a material as antimicrobial,
efficacy should be evaluated under reproducible
conditions that mimic later in-use environments.
Antimicrobial testing is mandatory here.
4
The method needs to enable them who have special
interest in AMM to establish a confidence in their
material, offering some positive data that bolsters
further exploration for testing the material either
under conditions more precise to the intended point
of use or even in practice.
6
A renowned microbial testing laboratory
performs the relevant standardized test method
to validate the reproducibility of an antimicrobial
material and achieve results that are all within
the natural error range for such a test. The
validity of data resulting from individual test
methods should be acknowledged. On the other
hand a growing need exists for accurate and
reproducible methods, as many different AMM
fall short when being tested by independent
reviewers.
Standardized Tests for AMMs in Vitro
High surface area to volume ratio tests
Agar zone of inhibition tests
Suspension tests
Adhesion tests
5
Biofilm tests
High surface area to volume ratio tests
Such methods focus on maximizing the
contact between the surface and the
microorganism, so the cells and the surface
are essentially always touching and
interacting. This is usually done by placing
the bacteria between the test sample and
another sterilized non-antimicrobial material
such as glass or plastic.
8
Agar zone of inhibition tests
9
Methods that utilize zones of inhibition, for which
there are two existing standardized methods
provide only an indicator of whether any
antimicrobial effect might be present under
permanently wet conditions. The first, ISO
20645:2004 is based on a disk diffusion method,
where the AMM is placed on top of an inoculated
nutrient agar plate, incubated at the required
temperature for a set time depending on the
requirements for the bacteria being tested
Suspension tests
10
Suspension methods focus on inoculating and
incubating bacteria in a liquid medium containing
the antimicrobial surface, and then determining
the remaining viable CFUs by taking an aliquot of
this liquid and performing a dilution plate count
using it. This allows assessment of materials that
exhibit antimicrobial-release properties.
Adhesion tests
11
These tests focus on quantifying the number of
bacteria that can adhere to an antimicrobial
material. There are two approaches to this form
of testing. The first requires that the test surface
is inoculated with the bacteria and incubated for
1 to 4 h.
Biofilm tests
12
A biofilm is an assemblage of microorganisms that are
associated with a surface and often become encased in
a matrix of polysaccharide material. They are one of the
most common forms that microorganisms take on
Earth and can cause significant problems when they
form in certain artificial environments.
Conclusion
13
Both clinical and non-clinical settings are prone to
growth of microorganisms. Various methods are used
to control microorganisms on surfaces in those
settings. In clinical environments, methods to
chemically disinfect surfaces are often used, but may
be performed inadequately, (through poor adherence
to cleaning protocols), allowing pathogens to be
spread more rapidly throughout wards, following
recontamination of disinfected surfaces via contact
with fomites.
ThankYou
Biosan Laboratories, Inc.
1950 Tobsal Court,
Warren, MI 48091-1351
USA
www.biosan.com
Email: info@biosan.com

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Standardized Antibacterial Material Testing Methods

  • 2. Introduction Microorganisms cause disease after reaching out to a potential host. They move around the environment in various but typically passive ways such as aerosols, and direct contact between two animated objects, and fomites. 1
  • 3. 2 Certain microbes can retain their pathogenic potential whilst outside their host for a longer period of time. According to studies, they can survive from days to a few weeks on inanimate surfaces like metals and plastics which are usually considered hygienic surfaces.
  • 4. Testing the Efficacy of Antimicrobial Materials (AMM) 3 Standardised test methods are required and considered inevitable in the development of a unique antimicrobial material. In order to define a material as antimicrobial, efficacy should be evaluated under reproducible conditions that mimic later in-use environments. Antimicrobial testing is mandatory here.
  • 5. 4 The method needs to enable them who have special interest in AMM to establish a confidence in their material, offering some positive data that bolsters further exploration for testing the material either under conditions more precise to the intended point of use or even in practice.
  • 6. 6 A renowned microbial testing laboratory performs the relevant standardized test method to validate the reproducibility of an antimicrobial material and achieve results that are all within the natural error range for such a test. The validity of data resulting from individual test methods should be acknowledged. On the other hand a growing need exists for accurate and reproducible methods, as many different AMM fall short when being tested by independent reviewers.
  • 7. Standardized Tests for AMMs in Vitro High surface area to volume ratio tests Agar zone of inhibition tests Suspension tests Adhesion tests 5 Biofilm tests
  • 8. High surface area to volume ratio tests Such methods focus on maximizing the contact between the surface and the microorganism, so the cells and the surface are essentially always touching and interacting. This is usually done by placing the bacteria between the test sample and another sterilized non-antimicrobial material such as glass or plastic. 8
  • 9. Agar zone of inhibition tests 9 Methods that utilize zones of inhibition, for which there are two existing standardized methods provide only an indicator of whether any antimicrobial effect might be present under permanently wet conditions. The first, ISO 20645:2004 is based on a disk diffusion method, where the AMM is placed on top of an inoculated nutrient agar plate, incubated at the required temperature for a set time depending on the requirements for the bacteria being tested
  • 10. Suspension tests 10 Suspension methods focus on inoculating and incubating bacteria in a liquid medium containing the antimicrobial surface, and then determining the remaining viable CFUs by taking an aliquot of this liquid and performing a dilution plate count using it. This allows assessment of materials that exhibit antimicrobial-release properties.
  • 11. Adhesion tests 11 These tests focus on quantifying the number of bacteria that can adhere to an antimicrobial material. There are two approaches to this form of testing. The first requires that the test surface is inoculated with the bacteria and incubated for 1 to 4 h.
  • 12. Biofilm tests 12 A biofilm is an assemblage of microorganisms that are associated with a surface and often become encased in a matrix of polysaccharide material. They are one of the most common forms that microorganisms take on Earth and can cause significant problems when they form in certain artificial environments.
  • 13. Conclusion 13 Both clinical and non-clinical settings are prone to growth of microorganisms. Various methods are used to control microorganisms on surfaces in those settings. In clinical environments, methods to chemically disinfect surfaces are often used, but may be performed inadequately, (through poor adherence to cleaning protocols), allowing pathogens to be spread more rapidly throughout wards, following recontamination of disinfected surfaces via contact with fomites.
  • 14. ThankYou Biosan Laboratories, Inc. 1950 Tobsal Court, Warren, MI 48091-1351 USA www.biosan.com Email: info@biosan.com