Guest guest Posted June 3, 2008 Report Share Posted June 3, 2008 Hello everyone, I’m making my first batch of ‘soup’ – can anyone advise or correct in case I am doing something wrong ? Here’s my methodology :- 2 kgs fresh washed stem/leaf, cut into 2.5 cm pieces. Cover with 10 litres of water, boiling 3.5 hours. Let stand for 2 hours to ensure extraction was complete as after boiling, the raw material still seemed quite tough. This stage is not in recipe, any comments? Strain & remove exhausted plant material. Concentrating by boiling to 1.010 SG (in progress) Then will cool and filter using lab grade paper. I plan adding alcohol for preservation using 95% alcohol. I plan to add 1 part 95% alcohol to 3 parts extract at 1.010 S.G. I do not plan to add syrup or other sweetener at this point. Does this meet the approval of experienced soup makers ? Any guidelines for dosing for this strength of extract ? Does anyone know the approximate ratio of fresh NO leaf/stem to the finished extract and dosing for the same ? This is the usual method I use for standardising strength of extracts and subsequent dosing – equivalent raw material factor. I’m also processing graviola for trials on patients with a doctor friend. I’m wondering if graviola might be a good and compatable synergist to combine with NOE. Marc uses sutherlandia with NOE in a similar way. Any info on preparing a N.O. power format for capsules? In the case of N.O. I cannot disperse the extract onto dried powder of the same plant material due to toxicity – that’s where the graviola may come in. Does anyone have info on the FDA guidelines for the ‘compassionate use’ clause for using ‘experimental’ products (such as NOE) as a last resort treatment? Does anyone have any input on producing a bioavailable selenium product for cancer use ? A colloidal or ionic form maybe? Maybe Tony can comment here. I’m making CS now and will be looking into the Gaia Research formulation that includes colloidal copper & zinc with silver. Another one for Tony ! The problem in Indonesia is that people are poor and cannot afford imported supplements etc., making our own effective and cheap products is the way I want to go. I refuse to cater for people on the basis of money, products must be available to all ! Keep up the good work. For a better world ! Phillip on Java Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 3, 2008 Report Share Posted June 3, 2008 It is after midnight here and so I will only be able to address a few items before my brain shuts down for the night. First of all, you may be able to alter the process - but my instructions clearly say to follow them exactly. And my instructions call for just enough liquid to cover the top of your plants in the pot and then reducing the original liquid down to 30% over the course of the two boilings and then mixing 50% (half and half) with vodka or apple cider vinegar. I would highly suggest you follow the instructions before starting gto improvise. If you do otherwise, you need to figure out a way to figure dosage based on the original instructions. Secondly, even if you are using filter paper I would still filter twice. Filtering is the key to avoiding common side effects. I will have to address the rest of your message tomorrow. Perhaps Marc will notice your question and guide you by way of specific gravity measurements. oleander soup , Phillip Johnson <ilonapj wrote: > > > Hello everyone, > > I'm making my first batch of `soup' – can anyone > advise or correct in case I am doing something wrong > ? > > Here's my methodology :- > > 2 kgs fresh washed stem/leaf, cut into 2.5 cm pieces. > Cover with 10 litres of water, boiling 3.5 hours. > Let stand for 2 hours to ensure extraction was > complete as after boiling, the raw material still > seemed quite tough. This stage is not in recipe, any > comments? > > Strain & remove exhausted plant material. > Concentrating by boiling to 1.010 SG (in progress) > Then will cool and filter using lab grade paper. > > I plan adding alcohol for preservation using 95% > alcohol. > I plan to add 1 part 95% alcohol to 3 parts extract at > 1.010 S.G. > > I do not plan to add syrup or other sweetener at this > point. > > Does this meet the approval of experienced soup makers > ? > > Any guidelines for dosing for this strength of extract > ? > > Does anyone know the approximate ratio of fresh NO > leaf/stem to the finished extract and dosing for the > same ? This is the usual method I use for > standardising strength of extracts and subsequent > dosing – equivalent raw material factor. > > I'm also processing graviola for trials on patients > with a doctor friend. I'm wondering if graviola might > be a good and compatable synergist to combine with > NOE. Marc uses sutherlandia with NOE in a similar way. > > > Any info on preparing a N.O. power format for > capsules? In the case of N.O. I cannot disperse the > extract onto dried powder of the same plant material > due to toxicity – that's where the graviola may come > in. > > Does anyone have info on the FDA guidelines for the > `compassionate use' clause for using `experimental' > products (such as NOE) as a last resort treatment? > > Does anyone have any input on producing a bioavailable > selenium product for cancer use ? A colloidal or > ionic form maybe? Maybe Tony can comment here. > > I'm making CS now and will be looking into the Gaia > Research formulation that includes colloidal copper & > zinc with silver. Another one for Tony ! > > The problem in Indonesia is that people are poor and > cannot afford imported supplements etc., making our > own effective and cheap products is the way I want to > go. I refuse to cater for people on the basis of > money, products must be available to all ! > > Keep up the good work. > > For a better world ! > > Phillip on Java > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 6, 2008 Report Share Posted June 6, 2008 Thanks Tony & Marc for info – I will filter many times as per your directions to ensure best quality. Status Report:- I broke my hydrometer while boiling the soup down (clumsy). Rather than waste the batch, I decided to made a concentrate for use in a cream to test for skin cancers, liver spots etc. From 2kgs leaf/stem + 10 kgs water (which was enough to cover the material, as per the standard recipe) the yield was 270 grams of a thick brown extract. I will buy some accurate scales for SG testing for an oral NO product. I am not online at home - so forgive me if my answers are a little late. Marc, you say the powder is difficult to make for capsules etc. NO seems to be tolerant to heat, so drying the soup concentrate onto a powder base (graviola in my case maybe) should be a viable and not too difficult option. I am lucky as in Indonesia almost anything is easily available in small quantites, solvents, chemicals, capsules, you name it. Any comment on possible combination I could use for the NO as a base or synergist? What are your thoughts on graviola as a possibility? BTW - I make graviola capsules containing leaf powder that has been impregnated with a 50% ethanol extract of graviola. This means I can make a 1 gram ‘leaf equivalent’ dosage in one OO capsule. Evaporation is done under partial vacuum. Anyone have any info on the compassion clause by FDA for the use of expermimentals? Many thanks, Phillip on Java Quote Link to comment Share on other sites More sharing options...
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