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The outlook for aseptically processed low acid beverages in pet bottles

After many years the flood gates are about ready to be opened: Aseptically processed low-acid beverages in PET bottles produced in the U.S. will finally be a reality. Look out America! Anyone who has followed the saga of aseptically processed low-acid beverages in PET bottles knows that this is a story that would be challenging to describe in a just a 750-word column. Consider this the abridged version.

There are 3 criteria for a low-acid packaged product to be considered aseptic. A) The product must be commercially sterilized before it is filled into the container. B) The environment in which the product is filled must be commercially sterilized, basically like a sterile operating room. C) The container must be commercially sterilized before the products are filled. Criteria A and B are relatively easy to achieve...the real challenge is C.

Low acid products have been packaged aseptically for many years in the US in metal cans. Examples would be cheese sauce in #10 cans and low acid diet drinks like Slim Fast in 12 ounce cans. Prior to filling the product into the containers, the cans are flushed with superheated steam for sufficient time in order to sufficiently kill organisms of public health significance (e.g., C. botulinum and B. cereus). Metal cans, of course, can tolerate superheated steam quite well. But a conventional PET bottle cannot. As heat cannot be used to commercialize the PET bottles, some other technique must be used in order to ensure they are commercially sterilized.

Though a variety of techniques—including such things as irradiation—have been experimented with, the major viable option today is chemical sterilants. Paracetic acid is a chemical sterilant that has been used for sterilizing PET bottles for many years throughout Europe and other parts of the world. For example, Nestlé has aseptically packaged its Nesquik line of flavored milk products in PET bottles for several years in France and other parts of Europe using paracetic acid. To make a long story short, in the U.S. the Food and Drug Administration was concerned that paracetic acid might not be able to sufficiently eliminate B. cereus if it was present. The FDA was so concerned about plant contamination that it wouldn’t even allow B. cereus to be introduced into beverage plants to test that it could be sufficiently eliminated. What finally seemingly convinced the FDA was the commercial development of non-toxigenic surrogates that simulate
B. cereus. In fact we can thank two companies for successfully commercializing these nontoxigenic surrogates for this application: Ecolab and FMC. In addition to the FDA, the federal EPA allowed the use of the non-toxigenic sterilants in the U.S. for these applications.

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