Visitors Now: | |
Total Visits: | |
Total Stories: |
ANALYSIS AND CONCLUSION: One control animal died immediately after dosing and one control animal was noted with convulsions immediately after dosing. The animal noted with convulsions later recovered and was noted as normal throughout the remainder of the study. Since not more than 2 control animals died or were observed with clinical signs of toxicity, and since no lost weight in excess of lo%, the test was considered valid. The injection of sterile water that was not isotonic was likely the cause of the reactions observed in the control animals. None of the test article solution treated animals were observed with clinical signs consistent with toxicity at any of the observation periods and body weight changes were within acceptable parameters over the course of the study. These findings indicate that the requirements of the IS0 Acute Systemic Injection Test have been met by Nelson Laboratories, Inc., NutraSilver (Beneficial Solutions, LLC.).
RESULTS: None of the test animals on study were observed with abnormal clinical signs indicative of toxicity during the 72 hour test period. Body weight loss was within acceptable parameters over the course of the study for the test animals.
July 10, 2009
FINAL REPORT #090312-201
AN EVALUATION WITH STATISTICAL ANALYSIS OF ONE TEST PRODUCT AT THREE CONCENTRATIONS FOR ITS ANTIMICROBIAL PROPERTIES WHEN CHALLENGED WITH
STAPHYLCOCCUS AUREUS MRSA USING AN IN-VITRO TIME-KILL METHOD
Prepared for:
BENEFICIAL SOLUTIONS, LLC (SPONSOR)
1648 Lone Oak Trail
Reno, Nevada 89523
Prepared by:
BIOSCIENCE LABORATORIES, INC. (TESTING FACILITY)
300 N. Willson Avenue
Bozeman, Montana 59715
(406) 587-5735
An In-Vitro Time-Kill evaluation of one test product tested at three concentrations and one control product was performed versus a challenge suspension of Staphylococcus aureus MRSA (Clinical Isolate; NARSA Strain NRS384 [USA300]; BSLI #120607MRSa7). The test product was evaluated at concentrations of 99% (v/v), 10% (v/v), and 0.1% (v/v). The control product was evaluated at a 99% (v/v) concentration. All testing was performed in duplicate, and all agar-plating was performed in duplicate. The percent and log10 reductions from the initial population of the challenge species were determined following 60-second and 90-second exposures to each test product concentration and to the control product.
The Test Product, NutraSilver, at 99% (v/v) concentration produced a greater than 6.0 log10 reduction in Staphylococcus aureus MRSA (Clinical Isolate; NARSA Strain NRS384 [USA300]; BSLI #120607MRSa7) following 60-second exposures, reducing the organism by 1,339,999,000 CFU/mL (from 1.340 x 109 CFU/mL to less than 1.00 x 103 CFU/mL, the detection limit of this test).
The Test Product at 10% (v/v) and 0.1% (v/v) concentrations produced no reductions in Staphylococcus aureus MRSA (Clinical Isolate; NARSA Strain NRS384 [USA300]; BSLI #120607MRSa7) following 60-second or 90-second exposures.
TABLE I
Test Product: NutraSilver at a 99% (v/v) concentration vs.
Staphylococcus aureus MRSA (Clinical Isolate; NARSA Strain NRS384 [USA300]; BSLI #120607MRSa7)
Initial Population (CFU/mL) |
Replicate |
Exposure Time |
Post-Exposure Population (CFU/mL) |
Log10 Reduction |
Percent Reduction |
1.340 x 109 |
1 |
60 sec. |
< 1.00 x 103 |
6.1271 |
99.9999% |
2 |
60 sec. |
< 1.00 x 103 |
6.1271 |
99.9999% |
|
1 |
90 sec. |
< 1.00 x 103 |
6.1271 |
99.9999% |
|
2 |
90 sec. |
< 1.00 x 103 |
6.1271 |
99.9999% |
"The critical effect in humans ingesting silver is argyria, a medically benign but permanent bluish-gray discoloration of the skin. Argyria results from the deposition of silver in the dermis and also from silver-induced production of melanin. Although silver has been shown to be uniformly deposited in exposed and unexposed areas, the increased pigmentation becomes more pronounced in areas exposed to sunlight due to photo-activated reduction of the metal. Although the deposition of silver is permanent, it is not associated with any adverse health effects. No pathological changes or inflammatory reactions have been shown to result from silver deposition."
Toxicity is important to know before you begin to take any Dietary Supplement or medicine. It is wonderfully assuring to know from these and many other tests that NutraSilver® has ZERO toxicity and cannot harm you in any way.
Usually, when these types of tests are conducted, the mice are expected to diminish there activity, yet the opposite happened: they actually thrived on NutraSilver and even gained weight which is very unusual for toxicity testing. None of the mice was harmed in any way by NutraSilver®.
Some practitioners claim that colloidal silver can build up and damage the liver and kidneys. This is blatantly false as there is no known evidence to support this rumor.
NOTHING, NOT ONE THING IN THE REPORT YOU POSTED CERTIFIES 3,600 PPM!
Thanks liar boy!
Liar boy?
Your vocabulary has improved dramatically, we are so proud of you!!!!!!
Yet I’m not the one who LIED! am I?? NO!
Where is the report you said you would share?? you remember that don’t you, it’s allegedly from the fda certified lab that PROVES your colloidal silver contains 3,600 ppm .
Where is that?? I’m still waiting!!
and you knew INSTANTLY who I was referring to you!!! who needs a vocabulary when I got my point across without even mentioning your name!!
YET ANOTHER advertisement from this goon. Seriously are Google and Facebook pay-per-click too expensive to you? More claims with no proof. Never expecting anyone to actually test your claims. See, that’s the thing with you unscientific snake oil salesmen. You don’t understand investigation. You couldn’t possibly grasp the most basic fundamentals of reality so instead, you spew out this garbage to turn a profit on the backs desperate, dying, and worried well. YOU DISGUST ME.