Product Development, Testing and Consulting
of Personal Care Products
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Dear Mr. Tvedten:
On
With aseptic technique we cut approximately 1 gram from each sample and added these to a sterile tube containing TAT Broth Base for cultivation of microorganisms from highly viscous or gelatinous materials.
From the above tube we extracted, with a sterile pipette, 2 mls and placed 1 ml into each of two sterile petri dishes. In one of the petri dishes we added (TSA) Tryptic Soy Agar (Soybean-Casein Digest Agar) Base for a general purpose medium. In the second plate we added (SA) Sabouraud Dextrose Agar Base for the cultivation of fungi and aciduric microorganisms.
Plates tested with Tryptic Soy Agar were incubated for 72 hours at 37°C (+/- 2°C). Plates tested with Sabouraud Dextrose Agar were incubated for 5 days at 25°C (+/- 2°C).
Tests were conducted two times under the same procedures (Results 1 & 2, 1A & 2A respectively). The results and conclusions are attached for your review.
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Test Results
Test # Description TSA Count SA Count
1 Original Positive 140cfu/gm Positive TNTC
2 Treated Positive 30cfu/gm Negative <10cfu/gm
1A Original Positive 110cfu/gm Positive TNTC
2A Treated Positive 10cfu/gm Negative <10cfu/gm
Description
Positive = Micro contamination present
Negative = No micro contamination is present
TNTC = Too Numerous To Count
Conclusions
After the tests were performed, our conclusions indicate that samples described as “treated” were less susceptible to bacteria/fungi growth.
Samples labeled “original” had bacteria present.
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Bacteria and mold were retarded even though the twice patented biopesticide (Safe Solutions Enzyme Cleaner with Peppermint) was dry and simply laid on the petri dishes - the control of bacteria and mold results would have been even better if the enzyme cleaner was used as a spray or as a cleaner.
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