Re: Double Blind Bind
From: Nancy Berntsen (email_address_at_end-of-post.com)
Date: 06/14/04
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Date: Mon, 14 Jun 2004 03:29:40 GMT
-- Email: berntsen AT oikourgos.com <William@Occam.com> wrote in message news:0qtlc0ppr60tqt22p94sfre8p89pik1s8p@4ax.com... > Have you read the articles that I posted recently? I skimmed at least this a couple days ago; then read this one more thoroughly tonight. > > Here's some of the text from J. Wound Care. (2004) 13:154-155. Note > the use of ASAP. I am not familiar with ASAP. I used Futurebiotics (stated as 5ppm) for the first 2-4 weeks and then switched to homemade. > Three samples of colloidal silver were tested: > . One sample which is available commercially on > the internet > . Two samples which were prepared in our laboratory > using standard chemical methods, whereby a > silver nitrate solution was reduced with either > tannic acid or sodium citrate. I am not familiar with the above methods for making colloidal silver. It sounds like a "reduced" silver nitrate was used, yet it was called colloidal silver. This method is completely foreign to me. I would be very surprised if anyone who makes their own CS uses a method like this. > > The reduction with tannic acid was carried out > using the procedure described by James.14 To 500ml > of doubly distilled water, 20ml of 0.1M silver nitrate > solution and 5ml of 0.1% tannic acid solution were > added. The mixture was heated to 70-80°C, and > 10ml of 1% sodium carbonate solution was added > to portions that were continually stirred, yielding a > clear, tea-coloured, colloidal silver solution. > The third sample was prepared according to the > method described by Bell and Myrick.15 500ml of > 3.83 x 10-3 M silver nitrate solution in doubly distilled > water was heated to boiling point, and 3ml of > 0.442M sodium citrate was added to it drop by drop > over one hour, during which time the solution was > stirred vigorously, producing a cloudy, greyish colloidal > solution. This was then boiled for one hour, > cooled and its volume made up to 500ml with distilled > water. My CS was clear and pale yellow or colorless depending on the batch and the method (low vac dc 30 volts or high vac). I don't have any idea if what they are calling colloidal silver is actually colloidal silver. I don't understand why they made it in a way so different to how the commercial and homemade CS are made. My very first tested batch was 3 ppm; a subsequent batch was 7 ppm as I recall. I increased process time to approximate 10 ppm with the dc low vac unit. I followed manufacturer's directions to approximate 15-30 ppm solution using my commercial hi vac AC unit. > We can only speculate about the positive laboratory > results presented on the internet. These might > be related to impurities of the solutions and the > presence of silver ions and oxidising agents resulting > from the ionisation of the water by an electric > current. Silver ions from silver salts such as silver > nitrate and from preparations such as silver sulphadiazine > that slowly release them have a strong bactericidal > activity.1-4 This is in contrast to the absence > of antimicrobial effects in metallic colloidal silver. > Silver,8 who performs fundamental research on > the genetics of silver resistance of silver-binding > bacteria, warned that 'the wide and uncontrolled > use of silver products may result in more bacteria > developing resistance, analogous to the worldwide > emergence of antibiotic and other biocide-resistant > bacteria'. It is quite apparent that at least two of the three specimens they tested were not made in the manner most commonly implemented by most individuals I know of who make CS. So I can not assume that the results apply to my CS, especially since mine did help me get well. So this study, though interesting, does not shed any more light on just how my kind of CS works. They only speculate that it could be "impurities," silver ions and/or oxidants. I wonder if they will go on and research these speculations... Nancy
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