
Liposomal Nutrient Delivery – Is it just a Gimmick?
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The Nutrition Academy (Changing Habits' education sector) gathers students from all over the world and from all walks of life. The most consistent quality possessed by the students and graduates is their thirst for knowledge about health and nutrition and their incessant inquisitive minds.
Recently one of the students asked the following question:
"I'm seeing many naturopaths and nutritionists promoting liposomal supplements. Cyndi quickly touched on liposomal supplements in one of the modules but I was wondering if she could expand on that and explain how they work and if/when they are good (or not) to use?"
Thus allowing me to delve into a concept I really thought was just a gimmick when it came to marketing supplements!
I’m a food girl. The only supplements I will consider on a daily basis are those that are grown in the ground, such as Changing Habits Peak Performance, Supreme Green Blend, Camu Camu, Probiotics, Health Essentials, Turmeric, Colloidal Minerals and nutrient-dense food, salts and spices that Changing Habits sources and sells. I am confident in taking my own food-based supplements on a daily basis; in fact, this includes two daily non-negotiables being Peak Performance and Colloidal Minerals, and always using my organic spices, foods and salt in my cooking.
In a health emergency or in a time of chronic disease where my body requires it, I may consider a higher dose of a single nutrient for a period of time, but not for a prolonged period of time.
So let me break down the complex structure of liposomal supplements so that you can make an educated decision about whether you want to take them daily or in an emergency or chronic condition.
There are 2 components that make up the liposomal supplement, the Liposome and the Nutrient.
What is a Liposome?
Today’s liposomes are essentially nanotechnology of a phospholipid bilayer that has been modified into a sphere. The sphere has an empty space in the middle that, when manipulated, can be filled with therapeutic substances. This method of delivery is being used as a vector for the administration of drugs, cancer treatments, vaccines, genes and nutrients. Simply, a Liposome is a tiny bubble made from the same materials as a cell membrane that can carry nutrients or drugs into the body's system. It is this manipulation and addition of more additives to this artificial cell bubble that can be advantageous or create havoc within the body.
The History of Liposomes
In 1965 Alec Bangham (1921-2010) haematologist had an interest in cell membranes (phospholipid layers) which furthered his interest in phospholipid molecules dispersed in water and found that they could organize themselves into a double layer resembling membranes, then under the electron microscope, it was revealed that these dispersions took the form of cell-sized closed vesicles (spaces), like a tiny avocado without the seed and the void being ready to be filled with a substance (drug, vaccine, gene and nutrient). He saw this as a vehicle for delivering drugs and other materials into the cell through the cell membrane. He named these vesicles ‘multilamellar smectic mesophases’ or for short bangosomes which were later termed liposomes. (1)
Not all Liposomal Technology is Equal
There were problems with the first generation of liposomes including;
- The enclosed substance leaking out of the liposome membrane before it reached its target, this was fixed by adding cholesterol and sphinogomyelin to the lipid bilayer which switched it from a fluid phase to a solid phase, reducing leakage.
- The liver and spleen's production of phagocytes destroying the liposome reduced the distribution capabilities and increased toxicity of the drug being delivered, the addition of the cholesterol and sphinogomyelin increased the circulation of the liposomes which reduced the chances of being destroyed by the body’s immune system. To increase the ‘stealthiness’ of the liposome, polyethylene glycol (PEG) was grafted onto the membrane of the liposome. This is called PEGylated. PEGylates remain in the system without damage from phagocytes and can be almost dosage independent. This was sometimes termed a stealth liposome. But as you will read further on this too has created problems.
- Not all drugs were able to be delivered passively, therefore the addition to the manipulated liposome of receptor-mediated endocytosis (ligand targeted) allowed for specific targeted administration of the drug delivery. (10)
- Triggering the release of the contents of the liposome was difficult. Heat, pH, light or an intrinsic (made by the body) enzyme may be remote, therefore targeting the signal. For example, heat to a tumor for the delivery of a drugpor designing liposomes to release their contents at a certain pH proved to also be helpful in delivery. (2)(8)
- https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(10)60950-6/fulltext
- https://liposomes.weebly.com/history1.html
- https://patents.google.com/patent/US2680749A/en
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598536/
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4664963/ (graphic)
- https://www.youtube.com/watch?v=r61aEKpccBA
- https://www.youtube.com/watch?v=ypkXVwo_ZwU
- https://www.naturalmedicinejournal.com/blog/secret-effective-liposomal-delivery
- https://www.health.nsw.gov.au/environment/factsheets/Pages/ethlyene-oxide.aspx
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