Mar 30, 2010
This method of making your own LIPOSOMAL
ENCAPSULATED VITAMIN C enables individuals to have the effectiveness of
Intravenous Vitamin C for a price that that equates to pennies on a dollar.
Avoids that experience of diarrhea when one takes Vit C in pill form.
Recently I had a toothache, about 4-5/10 pain, took Lip. Vit C, pain was
gone next day.
re-posted from Brooks Bradley, process inventor
Dear List Members, I have been somewhat remiss in not supplying additional
information which might make prosecuting an acceptable generation
process....somewhat easier. To that end, I offer a few elaborating comments.
First, using some form of blender to enhance/accelerate the process is
perfectly acceptable....and effective. However, one must understand the
limitations of using this modality. To wit: Because the entire encapsulation
process is, essentially, a refined homogenization process the researcher is
bound within the limits of the chosen process....itself. e.g. Using a
blender in the early stages of the ultrasonic type protocol, places a limit
(especially particle size) on the resultant compounds. As a general rule,
the smallest liposomes achievable...are going to be larger than 150 nm in
size—-even after extensive agitating. Therefore, if smaller particles are
desired.....some procedure must be invoked to achieve this. Ultrasonic
energy is an excellent way to achieve this. Ultrasonic energy applied to
solutions having, previously, been mixed using mechanical blenders (of the
household type) will improve the encapsulation process greatly (sometimes as
much as an order of magnitude) through the immediate size reduction of the
encapsulated particle size. Additionally, both power levels and exposure
time experienced from the US energy......have a pronounced effect on the end
product. e.g. simply by extending the time exposed to the US energy will
yield a product with a majority of particles of a markedly reduced physical
size (sometimes by more than one-half). Also, by increasing the power
spectral density [energy delivered to the target], considerable size and
complexity reduction may be achieved. (Sometimes from larger,
multiple-layered liposomes, down to single-layered liposomes of much smaller
size).This one characteristic, alone, should justify the selection of the
larger US unit over the smaller one....as the larger US power level output
is much higher. The way to capitalize on this advantage is to limit the
depth of the parent solution in the larger US unit, to 3/4″ to 1″. Because
the distance from the US energy! source and the mass of the target material
DOES, in fact, have a powerful effect on the delivered energy. Direct visual
observation alone, will confirm the powerful increase in cavitations (energy
field) of the liquid medium. This type innovation will yield effects that in
some cases....challenge the results of laboratory-grade, high pressure (over
3000 psi) impact plate systems.....costing $10,000 and up. What most
commercial producers (and labs) do, is they RECIRCULATE their candidate
solutions.....in order to achieve smaller—-and more isolated—-end products.
By extending your exposure time, using shallow solutions, DIYs can...in many
cases, actually challenge, to some degree, the levels accomplished by
these very high dollar commercial machines.....using their own DIY homemade systems. Someone asked the question...does pre-agitation via blending devices damage or compromise the candidate solutions. The short answer is NO. Almost any type of agitation aids in the homogenization process. I have some descriptive information relative to the use of blending devices, which may prove of use to the list membership, but I must go at this time. Sincerely, Brooks Bradley.
There is granular sunflower lecithin (google it ) also available for those not wanting to use soy lecithin.
from google "sunflower lecithin" ONLY AVAILABLE IN LIQUID FORM