Biological Consulting Services
of North Florida, Inc.
Luis Gomez
President
P.O. Box 221074
Hollywood FL
33022
(954) 922-5976
Dear Mr. Gomez,
Greetings.
We
conducted the microbiological challenge experiments on the BioActive™ disinfectant liquid sample that you delivered to our Laboratory. As per our conversation, testing
was conducted to satisfy US EPA request of analysis according to AOAC Method 961.02 (AOAC Official methods of Analysis; 2005).
The BioActive™ disinfectant liquid that you provided exhibited excellent antibacterial and antifungal efficacy by passing the above-mentioned
test using various microorganisms. In the following pages, you will find a summary
of the methodology used and the results of our analysis.
Should
you have any further concerns please do not hesitate to contact me.
Best
Regards,
George
Lukasik, Ph.D.
Laboratory
Director
AOAC Official Method 961.02
Germicidal Spray Products as Disinfectants (2005)
The following
tests were conducted for Mr Luis Gomez from ENVIRO-TECH MANUFACTURING, INC. The Disinfectant Solutions were delivered to the
laboratory for analysis on the day challenge. The solutions were labeled Bio
Active™ and were produced according to ENVIRO-TECH by a proprietary technology (Aqua Master™) under the following
U.S.A. PATENTS: 4,959,155, 5,126,046,
5,013,450, 6,712.050, and U.S.A. provisional
patent:, 60,948,022
Staphylococcus aureus
(ATCC 6538), E. coli O157:H7 (ATCC 43895) Pseudomonas aeruginosa (ATCC 15442), Listeria monocytogenes (ATCC
4428), Salmonella choleraesuis (ATCC 10708), Tricophyton mentagrophytes (ATCC 9533) and Stachybotrys
chartarum (ATCC 9182) stock cultures were obtained from American Type
Culture Collection and were maintained as per the described methodology and in AOAC 961.02 and the referenced related AOAC
protocols. For Challenge experiments, cultures were grown at the temperature
and incubation times specified in the specified method. E. coli O157:H7 and Listeria monocytogenes were grown as per
method 991.47. Fungal spores of Tricophyton mentagrophytes and Stachybotrys
chartarum were grown and harvested as outlined in Method 955.17. All
media used for microbial growth were manufactured by Beckton Dickinson (Sparks, MD) and were purchased from ThermoFisher Scientific (Waltham, MA). All media used was new and was purchased specifically for the project. Positive and negative controls were performed as outlined in the Method.
On August 06, 2007, Mr.
Luis Gomez Delivered nine 1-gallon bottles labeled “Bio Active™”. On the same day, one bottle of each of the above was opened for each bacterial species challenge study. The liquid was placed into handheld spray bottles (Fisher Scientific). Cultures of the following bacteria were grown as specified in Method 961.02: Staphylococcus aureus, E. coli O157:H7, Pseudomonas aeruginosa, Listeria monocytogenes, and Salmonella choleraesuis. Ten-microliters of the bacterial suspension was placed and spread onto sterile 25x25
mm glass slides (Fisher Scientific, PA). Ten slides for each bacterial species were used for challenge; additionally, one
un-inoculated slide was used as a negative control and one inoculated slide was used as a positive growth control. The inoculum was allowed to dry at 37°C for 40 minutes.
The slides were the sprayed for 10 seconds with the provided solutions; the glass slides were completely covered with solution.
The slides were allowed to incubate at room temperature for 10 minutes. After
drying, the slides were removed, excess liquid was shaken off, and they were placed into 20 ml of appropriate growth media
and allowed to incubate as per method requirements. The tubes were examined
for microbial growth at 48 and 72 hour intervals. Sub cultures were also removed
and examined for growth as described in the method. Tubes demonstrating no growth
following the incubation period were inoculated with 10-100 cfu of the respective
microorganisms and were observed for growth after 24 hours; this was done to ensure the absence of residual antimicrobial
residual effect.
On August 27, 2007, Mr.
Luis Gomez Delivered one additional 1-gallon bottle labeled “Bio Active™”. On the same day, the bottle was opened and the liquid was placed into handheld spray
bottles (ThermoFisher Scientific). Spores of Tricophyton mentagrophytes and
Stachybotrys chartarum were harvested earlier that morning as described in AOAC method 955.17. The above mentioned challenge was repeated using the spore inoculate as per AOAC 961.02
All data is summarized in the following Tables..
Table 1. Inactivation of
bacterial and fungal species by Bioactive™ Spray disinfectant provided by Enviro-Tech Engineering. Test Conducted as per AOAC Official Method 961.02; Germicidal Spray Products as Disinfectants (2005)
Microorganism |
Number of Inoculated Glass Slides Sprayed with BioActive™ |
Number of Tubes Demonstrating Growth |
Positive Control (un-sprayed slide) |
Negative Control (un-inoculated slide) |
Staphylococcus
aureus |
10 |
None |
Growth |
No-Growth |
E.
coli O157:H7 |
10 |
None |
Growth |
No-Growth |
Pseudomonas
aeruginosa |
10 |
None |
Growth |
No-Growth |
Listeria
monocytogenes |
10 |
None |
Growth |
No-Growth |
Salmonella
choleraesuis |
10 |
None |
Growth |
No-Growth |
Tricophyton
mentagrophytes |
10 |
None |
Growth |
No-Growth |
Stachybotrys
chartarum |
10 |
None |
Growth |
No-Growth |