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450   Potential Impacts of Nanomaterials

        to a chemical suggests the chemical has antimicrobial activity. Growth
        inhibition tests use plating methods or spectrophotometric methods to
        determine the amount of growth in a culture. Some environmental con-
        taminants can be mutagenic and cause changes in the genetic code of
        receptor organisms. These include carcinogens that affect somatic cells,
        such as benzene, and teratogens that affect germ cells, such as
        thalidomide.
          To examine a compound’s potential mutagenicity, several assays deter-
        mine the compound’s ability to damage microbial DNA. Most of the tests,
        such as the Ames test and Mutatox test, look at the frequency of muta-
        tions caused by the chemical that restore some previously damaged func-
        tion to the microbe. Table 12.2 summarizes some of the more popular
        mutagenicity tests available, along with other common microbial assays
        that are used to assess the general toxicity of a compound. However,
        only a few of these assays have been applied to nanomaterials [24].
          Developmental toxicity tests for eukaryotic, multicellular organisms
        are also commonly used to identify xenobiotics that may alter ecosys-
        tems. These tests analyze impacts on the embryonic development of
        higher order organisms. Full life cycle chronic toxicity tests that expose
        all life stages of an organism to a toxicant can be quite long and costly.
        Short-term acute developmental toxicity tests, however, can be used to
        predict chronic effects with far less time and cost, allowing for broader
        evaluation of factors that influence toxicity. Furthermore, due to the
        higher sensitivity of organisms in their embryonic stage than during




        TABLE 12.2  Selected Bacterial Toxicity Assays
        Test type     Test name   Test principle            Reference
        Enzyme        MetPAD &    Colorimetric assay for    25
                       MetPLATE     -galactosidase activity
                      MitoScan    Monitor electron transfer    26
                                   inhibition by NADH
                                   production or consumption in
                                   submitochondrial particles
        Growth        Pseudomonas  Monitor turbidity of cell   27
         inhibition    putida      culture
        Bioluminescent  Microtox  Monitor luminescence of   www.azurenv.com
                                   Vibrio fischeri
        Mutagen       Ames        Look for reversion of     28, 29
                                   mutations in Salmonella
                                   typhimurium restoring ability
                                   to produce histidine
                      Mutatox     Look for V. fischeri with  www.azurenv.com
                                   increased luminescence
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