MINERAL FORMULAS * CELL TRANSPORT THEORY
USES & BIOLOGICAL MECHANISMS
MINERAL TRANSPORTER DEFINITIONS
Minerals bound to Orotic Acid (B13). These penetrate the entire
cellular membrand and delivers the active mineral to the INTRACELLULAR
structures (Mitrochondria, Organelles)
This mineral form is bound to the amino acid arginine.
It is able to penetrate the cell and deliver the mineral specifically
to the plasma and inner layer of the outter cell membrane.
This mineral form is bound to the amino acid arginine. It is
able to deliver the mineral to the outter layer of the Inner
(2-amino-ethyl-phosphate): is a lipid delivery system.
It delivers the mineral to the outter layer of the cell membrane,
creating a sealing effect..a cellular patch. It is also known
as the membrane integrity factor since it binds and acts as a
sealant...preventing the entry of viruses and toxins into the
Dr.Neiper was a German physician
and physicist. He was an acting consultant to Memorial Sloan Kettering
in the 1970's where he met and worked with Ralph Moss, Ph.D. who
was also there doing work on Laetrile (Ralph wrote the forward
to Hans' book below). Dr.Neiper was from Hannover, Germany where
he had his clinic the Paraclesus Klinik (now owned by another
physician) after Hans death in 1999.
Hans was involved with the founder
of the NCI, Dr.Burke, and also Dr.Sugiura doing the ground breaking
work on the Laetrile discovery. Later on, Sloan-ettering's leaders
publically disavowed it and denied the positive results of their
years of research (read the excellent book by Ralph Moss on this
subject called "The Cancer Industry".
- Hans went on to discover an
entire group of compounds which seem to have even more beneficial
effects on cancer than laetrile did...working with German chemist
Dr.Franz Kohler Sr. (Kohler Chemicals) to make a molecule by
which the L-glucose portion of Laetrile is replaced by urea.
Together they produced what they called ureyl-, nicotynl-, and
para-aminobenzoic mandelonitriles, which Hans used successfully
in his German clinic and which many other clinics in Germany
have used for many years in the treatment of cancer.
contributions to healthcare have been astonishing. In cancer,
he pioneered an entire class of gene-repair and gene-extinguishing
substances. These include such things as squalene (from shark
liver oil),carnivorous plant extracts such as carnivora (venus
fly trap), didrovaltrate which is an herbal extract from the
Himalayan valerian plant; Acetaldehyde; benzaldehyde; DHEA; iridodial
from ants,oncostatins and tumosteron...
His work with MS is legendary
with the use of his mineral transport formulas (2-AEP) to not
only stop the progression but to reverse the damage!
There are many many things Dr.Neiper
accomplished (more than we can cover here) which are written in his book "The
Curious Man--the life and times of Hans Neiper, M.D.", available
from Avery Publishing ISBN 0-89529-864-3
- Dr. Nieper's first publication
(translation from German into English in 1985) is "Revolution
in Technology, Medicine & Society". Conversion of Gravity
Field Energy(Tachyeon). He was the patent inventor of the Hydrogen
Fuel Cell among others--licensed to the German government. Facinating
book on energy, magnestism, medicine, etc. Very very technical
for those who are not physicists, but well worth the read. Out
of print. ISBN 3-925188-07-X An excellent website to learn more
on these topics is
BREIF OVERVIEW W/
WHAT ARE THE ADVANTAGES OF MINERAL
Mineral transporters have a much higher absorption rate (70-90%).
Free minerals stay bound up and are for the most part unavailable
to the cell membranes for use...they're too unspecific. These
are Tissue Specific minerals.
Mineral Transporters are absorbed in an Intact State (general
free minerals aren't)
Mineral Transporters are attracted to and bio-utilized by
specific tissues of the body, making therapeutic use more specific
and effective. They act as "homing pigeons" for certain
tissues. In today's terms, these are called "Targeted"
minerals because they're delivered to specific tissues at specific
HOW ARE THESE DIFFERENT FROM OTHER
They provide selective organ uptake / nutrition
They provide an opportunity for sub-cellular nutrition
They are analogous to "Special Delivery" v.s. "Bulk"
WHAT ARE THE ADVANTAGES OF MINERAL
Minerals are transported "in tact" into the cells
without the concern of hydrochloric acid to break them down
The transport molecule is then incorporated into biochemical
processes, releasing the mineral at specific sites in the cell
membrane and inside the cell itself at specific targets
Absorption is only one facet of bioutilization
Suplements that transport ionized minerals into the blood
stream are less available at a cell level than mineral transporters,
which are able to penetrate te cell membrane nd enter the cell.
Ionized minerals may or may not enter the cell and be available
for use intracellularly.
BIOLOGICAL UTILIZATION OF MINERALS
Involves not only absorption, but also transport and delivery
to the tissues where they're needed
Mineral transporters solve these issues since they have high
absorption nd are absorbed in tact
Mineral transporters have the ability to cross the cellular
membrane and the cell membrane barrier, delivering the cells
in a form the cells recognize and can utilize immediately
Mineral transporters are efficiently taken up by specific
Orotates are taken up by tissues that embryonically from
mesenchyme: bone, cartilage, liver, blood vessels, heart and
the blood brain barrier
Aspartates are taken up by muscles, heart, liver, breast
and endocrine tissues
WHY USE MINERAL TRANSPORTERS WHEN
THEY'RE MORE EXPENSIVE?
Because pharmacological doses of nutrients can create imbalances
in other nutrients (pharmacological doses are those that are
higher than physiological norms).
Instead, mineral transporters deliver minerals in physiological
doses to tissues and cells, reducin the potentil of creating
tissue damage and antagonism with other nutrients.
Because of the poor utilization of other forms of minerals
and the higher dosing required, these transporter mineral forms
from Neiper are actually LESS expensive overall than other forms
or delivery systems.
WHY ARE NEIPER MINERAL TRANSPORTERS
SUPERIOR TO OTHER MINERAL TRANSPORTERS?
Dr.Neiper found that mineral transporters work better, when
each granule is enterically coated by a micro-vortex process,
which ensures intact passage of the compound through the acidic
environment of the stomach. Other products who don't utilize
this patented process end up providing "free" minerals
and amino acids, which aren't targeted (tissue specific).
Micro-vortex coating of mineral transporters is when individual
granules are enterically coated with a soluable compound which
resists the stomach acid and yet is readily dissolved in the
alkaline environment of the small intestine.
Micro-vortex enteric coating delivers the mineral transporter
into the small intestine in tact where it is moved into the blood
stream in tact, where the transporters enter the cells and the
minerals are released at specific cell sites.
NEIPER MINERALS FUNCTION, BIOLOGICAL
ROLE AND THEIR USES
Can Alter membrane composition, transport
Allow entry of nutrients, but not toxic
Maintain and renew the capacitance
function of the cell mebrane allowing for production of the cell's
natural electromagnetic field
Seals the cell from toxic effects
- 2-AEP Mineral Transporter (2-aminoethylphosphate)
AEP is an effective substance in repairing
the membranes of cells since it is a NATURAL CONSTITUTENT of
the cell membrane
If you have a hole in your brick wall,
you fix it with bricks, not wood (other mineral forms the body
can't use). Non-natural compounds are toxic.
It is a membrane integrity factor
It is a lipid mineral complex, making
it a mineral transporter
AEP binds to and acts as a sealant
to the outer surface of the cell membrane, which Dr.Neiper believed
reduces the entry of viruses and toxins into the cells. It is
a cellular patch, verified by electronmicrograph studies.
Controls membrane composition
Controls membrane permeability
Controls membrane transport
Controls membrane charge (capacitance)
Corrects structural cellular abnormalities
and returns the cell to a normal state of function
Assists the cell in maintaining its
capacitance function, allowing for roper production of cellular
- BIOLOGICAL ROLE & FUNCTION OF
Myelin (a capacitator, not an insulator,
Science magazine, 1984)
Membranes of the pulmonary alveoli
Endothelial lining of microvessels
Especially retinal arteries
- 2-AEP has a unique role in preserving
membrane function in:
- USEFUL FOR:
- Pulmonary Fibrosis
- Systemic Lupus (SLE)
- Thyroiditis (Hashimotos, etc.)
- Nephritis, Cystitis
(Minerals proprietarily bound to aspartic acid) Delivers mineral
to the inner layer of the outter cell membrane.
- GENERAL TISSUE ACTIONS: Bone, Muscle, Glands, Mycocardium, Liver,
- CALCIUM l-dl-ASPARTATE:
- Recalcification of bone as in Osteoporosis,
Osteomyletis, post-radiation necrosis, cancer metastisis, etc.
- Fibrocystic Breast Pain
- POTASSIUM - MAGNESIUM ASPARTATE:
- Tissue Action: Heart, Arteries, Liver
- Reduces risk of cardiac necrosis, coronary
thrombosis, arteriosclerosis, and sudden cardiac arrest.
- Promotes detoxification of the liver
by removing ammonia which can cause liver failure.
- Reduces tension in the lungs, benefiting
- ZINC ASPARTATE: combined with magnesium
orotate, it is beneficial for non-Hodgkins lymphoma, viral infections
and other immune related issues
- Effective combination for arresting
replication of viruses.
- Inhibits the activity of thymadine
kinase, involved in the etiology of lymphomas & helps maintain
elevated C3c blood levels to prevent tumor reoccurances
- Activates the thymus gland the the
formation of T-lymphocytes, a key component of the immune system.
- Seems to increase production of Insulin
from Islets of Langerhans cells in the pancreas, a valuable tool
(Minerals proprietarily bound to the amino acid L-Arginine )
Delivers mineral to the inner layer of the outter cell membrane
- TISSUE ACTION:
- Calcium Arginate:
- Lowers Blood Sugars/ Used in Diabetes
- Seems to be beneficial for inner-ear
- Magnesium Arginate & Zinc Arginates:
- Helps lower blood sugar
- Helps transport fats into the mitochrondria
for use as fuel, of great benefit for hearts which use fatty
acids for primary fuel
- Beneficial for the Immune System which
can't function without bioavailable zinc
bound to Orotic Acid, vitamin B13)
CALCIUM OROTATE: Calcium salts bound
to orotic acid
- Premier Re-calcification for cancer
metastasis to bone, bone post-radiation necrosis (destruction),
osteoporosis, osteomylitis. Even better for pain when combined
with 2-AEP Calcium.
- Anti-inflammatory: arthritis, phlebitis,
retinitis, arteriosclerosis, psoriasis, etc.
LITHIUM OROTATE: Lithium salts bound
to orotic acid. Does not have the toxic side effects of pharmaceutical
lithium salts of acetate, carbonate, citrate. Cannot be measured
- Depression, Mood Swings, Anti-edema
- Migraines & Headeaches
- Pain Syndromes
MAGNESIUM OROTATE: Magnesium Salts bound
to orotic acid.
- 200-600 mg./day dramatically reduces
- Prevents Hardening of the Arteries
& restores arterial cells better than Cal.Aspartate
- Prevents Kidney Failure from chronic
hypertension and diabetes
- Combines with Zinc Aspartate, inhibits
POTASSIUM OROTATE: Potassium salts bound
to orotic acid.
- Maintains intracellular potassium
- Replaces lost intracellular potassium
faster than any other method, combined with lithium orotate...
- Protects heart tissue destruction (heart
uses more potassium in regulation of heart beat than any other
- IMPORTANT NOTE: PRODUCTS FOUND IN THE HEALTHFOOD
STORES WHICH MIGHT HAVE "ASPARTATE",
- "ARGINATE" OR "OROTATE"
IN THEIR NAMES ARE NOT THE SAME FORMULAS OR STABILIZED
OR MIXED THE SAME WAY...THESE HAVE A SPECIAL STABILIZATION PROCESS
THEY'RE SUBJECTED TO WHICH DR.NEIPER DEVELOPED TO INSURE THEIR
DELIVERY TO THEIR CELLULAR DESTINATION TO INSURE DEPENDABLE CLINICAL
- SUPPLEMENTS & NUTRACEUTICS
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