Xango-Mangosteen



Test Results for the New Silver Solution



Here are just a few of the many test Results for the New Silver Solution

American Silver’s Antibacterial Product (The NEW Silver Solution -14ppm) Testing Results Summary. The following results suggest that The NEW Silver Solution is a broad spectrum antimicrobial agent – it is able to effectively stop the growth of, and in fact kill, a variety of bacteria.

Tuberculosis type B (tuberculosis is the number one human-killing bacteria world wide)

Staphylococcus aureus (Pneumonia, eye infections, skin infections (boils, impetigo, cellulitis, and post-operative wound infections), toxic shock syndrome, meningitis, food poisoning, osteomyelitis, and many others) inhibited @ 2.5 ppm[c][12] and killed @ 5 ppm. 1/22/99 BYU Report.

Shigella boydii (Bacillary dysentery–characterized by severe cramping abdominal pain and bloody diarrhea) inhibited @ 1.25 ppm and killed @ 2.5 ppm. 1/22/99 BYU Report.

Salmonella arizona (Food poisoning, etc.) inhibited @ 2.5 ppm and killed @ 5 ppm. 1/28/99 BYU Report.

Salmonella typhimurium (Food poisoning and enteric fever) inhibited and killed @ 2.5 ppm. 6/7/99 BYU Report.

E. coli (Food poisoning, urinary tract infections, traveler’s diarrhea, diarrhea in infants, respiratory tract infections, and wound infections) inhibited and killed @ 2.5 ppm. 1/22/99 BYU Report.

Haemophilus influenzae (Otitis media (ear infection), pneumonia, meningitis, throat and sinus infections (including epiglottitis in children and sinusitis), and suppurative arthritis in children) inhibited and killed @ 1.25 ppm. 1/22/99 BYU Report.

Enterobacter aerogenes ( wound infections, urinary tract infections, bacteremia, and meningitis) inhibited and killed @ 2.5 ppm. 6/7/99 BYU Report.

Enterobacter cloacae ( causes illnesses similar to the E. aerogenes) inhibited and killed @ 5 ppm. 6/7/99 BYU Report.

Klebsiella pneumoniae (lower respiratory tract infections, nosocomial infections (infections spread in hospitals), urinary tract and wound infections, and bacteremia) inhibited and killed @ 2.5 ppm. 1/28/99 BYU Report.

Klebsiella oxytoca, (Similar to those infections caused by K. pneumoniae) inhibited and killed @ 2.5 ppm. 6/7/99 BYU Report.

Pseudomonas aeruginosa (severe burn and wound infections, keratitis, pneumonia, meningitis, nosocomial infections, urinary tract infections, etc.) inhibited @ 2.5 ppm and killed @ 5 ppm. 1/22/99 BYU Report.

Streptococcus pneumoniae (pneumonia, meningitis, sinusitis, otitis media (ear infection) inhibited @ 2.5 ppm and killed @ 5 ppm. 4/21/99 BYU Report.

Streptococcus pyogenes (skin infections, upper respiratory infections (i.e. strep throat) impetigo, hospital-acquired infections, scarlet fever, etc.) inhibited and killed @ 1.25 ppm. 1/22/99 BYU Report.

Streptococcus faecalis (Urinary tract infections, endocarditis, wound infections, etc.) inhibited @ 2.5 ppm and killed @ 5 ppm. 1/22/99 BYU Report.

Streptococcus mutans (A major cause dental plaque and tooth decay etc.) inhibited and killed @ 5 ppm. 2/3/99 BYU Report.

Streptococcus gordonii (Tooth decay, also implicated in infective endocarditis-an infection of the heart valves) inhibited and killed @ 5 ppm. BYU Report 2/12/99 .
David A. Revelli
Microbiologist
Brigham Young University

Dr. Ron W. Leavitt , Ph.D.
Professor of Microbiology/Molecular Biology
Brigham Young University
 

THE NEW SILVER SOLUTION vs. OTHER COLLOIDAL SILVERS

Microbiology Department
Brigham Young University

June 18, 1999

From: David Revelli
Brigham Young University

We have tested and compared the activity of The Silver Solution against three commerical colloidal silver solutions using the Minimum Inhibitory Concentration test (MIC) and the Minimum Bacteriocidal Concentration (MBC) test. The data obtained suggests that The Silver Solution is at least two to three times more effective depending on the bacteria tested than the commerical colloidal silver products tested.

David A. Revelli
Microbiologist
Brigham Young University


 

THE NEW SILVER SOLUTION vs. ANTHRAX
IIT RESEARCH INSTITUTE                                                 Re: IITRI Project 1708 SN1

December 18, 2001

William D. Moeller
American Biotech Labs
70 West Canyon Crest Road, Suite D
Alpine, UT 84004

Dear Mr. Moeller:

The study, IITRI 1708 SN1, investigating the sporicidal properties of 22 ppm NEW Silver Solution PLUS against anthrax is complete. The protocol and results are as follows:

Bacillus anthracis ANR-1 was grown on sporulation media, harvested into deionized water, heat-shocked, and stored as a spore suspension. The final concentration of this spore suspension was approximately 1 x 109 spores/ml.

A total of 33 conical tubes were filled with 4.95 ml 22 ppm NEW Silver Solution PLUS and inoculated with 50µl of B. anthracis spore suspension, for a final concentration of approximately 1 x 107 spores/ml. Three of the tubes were harvested immediately by dispensing 1 ml into 9 ml TSB, serially diluting in saline, and plating on TSA. Fifteen of the tubes were incubated at room temperature, while the remaining 15 were incubated at 37ºC. At time points 30 min, 1 hour, 2 hours, 4 hours and 6 hours three tubes from each incubation temperature were harvested as above. An additional Time 0 control of 50µl spore suspension in 4.95 ml sterile water was also used. The plates were incubated at 37ºC for 48 hours, and colonies were counted. The results in Table 1.

TABLE 1

Time
Temperature
Average CFU/ml
Log
Log Reduction
0 hour control
room temp
1.01E+07
7.01
 
0 hour
room temp
7.15E+06
6.65
0.15
30 min
room temp
8.88E+06
6.95
0.06
 
37 degrees
1.03E+07
7.01
-0.01
1 hour
room temp
8.33E+06
6.92
0.08
 
37 degrees
6.90E+06
6.84
0.17
2 hours
room temp
1.01E+07
7.00
0.00
 
37 degrees
8.97E+06
6.95
0.05
4 hours
room temp
3.23E+06
6.51
0.50
 
37 degrees
2.01E+06
6.30
0.70
6 hours
room temp
3.56E+06
6.55
0.45
 
37 degrees
8.37E+05
5.92
1.08

Minimal reduction in spore numbers was seen compared to the Time 0 control. After 4 hours, a reduction of approximately half a log (93%) was seen at both incubation temperatures, while at 6 hours a reduction of approximately 1 log (99%) was seen only at 37ºC.

Environmental controls were negative for growth, and no contamination was observed on the plates.

Sincerely,

Bruce A. Gingras, Ph.D.
Study Director
Research Microbiologist
Life Sciences Operation
Margaret A. Juergensmeyer, Ph.D.
Study Supervisor
Research Microbiologist
Life Sciences Operation
Robert Sherwood, Ph.D.
Division Manager
Life Sciences Operation
 

WATER TREATMENT TESTS

FROM: Bill Dodds                        TO: Gerard Yates

RE: NEW Silver Solution water tests

Procedure: I collected 500 ml of raw (Provo River water) sample and inoculated the sample with 2 loops (3mm) of Klebsiella oxtyoca. Using the membrane filter technique for total coliform, five 100 ml of aliquots of the sample were filtered.

Number 1 was spiked with a .10 mg/l concentration of silver solution. Number 2 was spiked with a .20 mg/l concentration of silver solution. Numbers 3 and 4 were each spiked with a .50 mg/l concentration of silver solution. A positive control of 100 ml was used without silver addition.

A 1.5 minute contact time was allowed on sample 1 before filtering. A 2 minute contact time was used on sample 2. A 10 minute contact time was used for samples 3 and 4.

The filters were incubated at 35° C for 24 hours.

RESULTS: The positive control = 705 cfu/100 ml. Samples 1 thru 4 contained 0 cfu/100 ml. William J. Dodds
Lab Director

TO: American Silver
FROM: Gerard Yates

CONCLUSION: The NEW Silver Solution effectively killed all colony forming units (bacteria) in a spiked raw river water sample containing a 0.10 ppm concentration of NEW Silver Solution in 1.5 minutes of contact.

Note: The NEW Silver Solution was not removed from the water sample prior to filtration. Therefore The NEW Silver Solution residual on the membrane filter may have inhibited growth during incubation.

Gerard Yates
Director