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Title: Compositions for prevention and treatment of
symptoms associated with ethyl alcohol consumption
United States Patent: 6,967,031
Issued: November 22, 2005
Inventors: Oslick; Brian Douglas (1803 Shepherd Ct. Suite
107, Waukesha, WI 53186); Barclay; Donald (1235 W. Barry Unit B, Chicago, IL
60657)
Appl. No.: 005261
Filed: December 7, 2004
Abstract
Described is a composition for the prevention and treatment of symptoms
associated with ethyl alcohol consumption. The composition comprises
silymarin, salicin, at least one B vitamin, magnesium, molybdenum and
manganese. Treatment of symptoms associated with the consumption of ethyl
alcohol involves ingesting the described composition prior to, during, or
after the consumption of the alcohol.
Description of the Invention
FIELD OF THE INVENTION
The invention relates to compositions and methods for prevention or
treatment of negative effects of consuming ethyl alcohol in the form of
alcoholic beverages. The composition can be used in the form of a
nutritional supplement and the treatment may be administered prior to,
during, or after the consumption of ethyl alcohol.
BACKGROUND OF THE INVENTION
The consumption of ethyl alcohol may be followed by a syndrome known as
hangover. Symptoms of a hangover include headache, dehydration, nausea,
nerve and muscle pain, lethargy, congestion, chills, tremor, diarrhea and
fever. These symptoms may be particularly severe, especially after heavy
consumption of alcoholic drinks. While not life-threatening, these symptoms
are unpleasant and may interfere with job performance or home life.
Additionally, the condition of alcohol induced hangover may cause a person
to suffer a social stigma associated with the condition.
Ethyl alcohol, or ethanol, is typically consumed by ingesting a liquid
containing ethyl alcohol is typically produced by yeast in a fermentation
process which converts sugars to alcohol and is then consumed, as is, in the
case of beer or wine, for example. The fermented alcohol may be distilled to
form spirits and then consumed, as is, in the case of vodka, for example.
Additional sweeteners, water and other ingredients may be added. Once
consumed; the ethyl alcohol in the beverage is absorbed by the stomach or
small intestine and transferred to the liver through blood vessels.
Metabolism of the alcohol takes place in a two-step enzymatic reaction.
First, the alcohol is oxidized to acetaldehyde by alcohol dehydrogenases.
Second, the acetaldehyde is oxidized to acetic acid by acetaldehyde
dehydrogenases. The acetic acid is transported to the muscles and adipose
tissue where it will be further broken down into carbon dioxide and water.
The rate at which alcohol is metabolized depends upon the level of presence
and activity of these enzymes. The rate at which alcohol is metabolized and
eliminated from the body varies greatly among individuals.
The negative effects of consumption of ethanol are due mainly to the toxic
effects of acetaldehyde. Acetaldehyde provokes disturbances in bodily
processes by, for example, forming adducts with hemoglobin and proteins of
plasma of the brain and other organs; and inhibiting the transfer of
reducing agents along the mitochondrial respiratory chain. Acetaldehyde also
accumulates in the cerebellum causing headache by contracting cerebral blood
vessels thereby decreasing blood flow resulting in pain.
The symptoms of hangover have been treated with painkillers, such as aspirin
or non-steroid anti-inflammatory drugs ("NSAIDs") or antacids. However,
painkillers may cause additional stomach upset and do not, alone, treat
other symptoms of hangover. Acetaminophen, which is neither aspirin nor an
NSAID, has been used to treat headaches and pains associated with hangover,
but acetaminophen in combination with ethanol can result in extensive liver
damage. The diuretic effect of alcohol results in dehydration and is
generally treated with the consumption of large amounts of water after
drinking ethanol. The consumption of water after drinking alcohol, however,
does not alleviate the problems associated with the build up of acetaldehyde
in the liver.
Other means for treating hangover symptoms include "hair-of-the-dog" type
treatments involving additional ethyl alcohol consumption for its analgesic
properties. Such remedies ultimately prolong the effects of overindulgence,
are dangerous and may lead to alcohol addiction.
Herbal remedies have been used to alleviate or prevent symptoms of hangover.
Examples of herbal remedies include teas made from the extracts of leaves,
stems or roots of alder or mountain ash. This tea is rich in tannin that is
said to provide protection to the stomach mucosa. Extracts of fruits of
other plants may be added to the teas for their Vitamin C, amino acids and
beta-carotene content. The beta-carotene is effective at clearing up cough
and phlegm.
Ginkgo biloba extract and taurine are components of another composition that
has been used to alleviate hangover symptoms. The taurine is taken for liver
protection and the Ginkgo biloba for its antioxidant effects against
ethanol-derived oxidation and also facilitates circulation in the brain.
Several methods of preventing alcohol absorption or allaying drunkenness are
known. Abstinence, charcoal ingestion and charcoal ingestion in combination
with Vitamin B-6 and Ephedra are examples. By abstaining from the
consumption of alcoholic beverages a person avoids absorption of any ethanol
and subsequent build up of acetaldehyde in the liver. However, the abstainer
also will not enjoy the intoxicating effects of alcohol consumption.
Charcoal ingestion is intended to absorb the alcohol in the stomach or small
intestines resulting in a lower blood alcohol level. Charcoal ingestion
therefore will decrease the socially desired effects associated with the
consumption of ethanol. The Ephedra in the combination of Ephedra, charcoal
and Vitamin B-6, acts as a vasoconstrictor of blood vessels, a stimulant,
and a bronchiodialator. Galenic compositions have also been used to decrease
the amount of blood alcohol. Another method of allaying drunkenness has been
to ingest a combination of succinic acid, an L-glutamate compound, a fumaric
acid compound, ascorbic acid, an energizer and a sugar. This method is also
intended to dampen the intoxicating effects of alcohol consumption as well
as treat the negative symptoms.
There is a need for compositions and preventative treatments for ethanol
induced hangover symptoms that are effective at treating the various
symptoms of hangover without aggravating the symptoms further. Further,
there is a need for the compositions and treatments for hangover symptoms to
allow the user to enjoy the desired social effects of ethanol consumption
while treating the cause of the negative effects of alcohol consumption.
The invention provides a composition and method for preventing or treating
ethanol induced hangover symptoms while avoiding the worsening of symptoms.
These compositions and methods also allow for the enjoyment of the desired
social effects of ethanol while preventing or treating the negative effects
of ethanol consumption.
BRIEF SUMMARY OF THE INVENTION
One embodiment of the invention is a composition comprising silymarin,
salicin, at least one B vitamin, magnesium, molybdenum and manganese. In one
form of the composition, the at least one B vitamin is a combination of
folic acid, Vitamin B12 and Vitamin B6.
In one embodiment, the silymarin is soluble and in another embodiment the
silymarin is a methylglucamine salt of silymarin.
Another embodiment is a beverage comprising the composition of silymarin,
salicin, at least one B vitamin, magnesium, molybdenum, manganese and a
sweetener. In other embodiment, the beverage comprises the composition of
silymarin, salicin, at least one B vitamin, magnesium, molybdenum, manganese
and natural or artificial flavors.
In yet a further embodiment of the invention, a method is provided for
decreasing the negative effects of ethyl alcohol consumption comprising the
step of administering to a person an amount of the composition sufficient to
decrease the effects of acetaldehyde build up.
Further, alternate embodiments include practicing the method prior to,
simultaneously with or subsequent to the ingestion of ethyl alcohol.
DETAILED DESCRIPTION OF THE INVENTION
The composition of the present invention comprises essentially silimarin,
salicin, B vitamins, magnesium, molybdenum and manganese. The composition
may be administered before, during or after the consumption of ethanol to
prevent or treat the negative effects of ethanol consumption while allowing
the consumer of ethanol to enjoy the pleasant social effects of the alcohol.
The terms "ethyl alcohol" and "ethanol" as used herein refer to any ethyl
alcohol containing, or alcoholic, beverage including beer, wine, spirits and
the like.
Silymarin is a compound contained in a plant named Milk thistle (Silybum
marianum) and is commonly known as St. Mary's thistle and Our Lady's
thistle. Silymarin consists of various forms of hepatoprotectant
flavonolignins. Silymarins protect the liver against a variety of toxins.
The active components in silymarin include silybin, silychristin and
silydianin. Silymarin repair mechanisms include increased synthesis of
cellular proteins, increased rate of hepatocellular repair and anti-oxidant
activity. Silymarin contributes to the regenerative activity of the liver by
stimulating RNA polymerase and increasing synthesis of ribosomes.
Silybins are only partially soluble in aqueous environments such as the
body. Aqueous solutions of the compositions described herein are preferred
for their increased bioavailability of silybins. The solubility of silybins
is increased by forming salts of the compound or by chelation forming salt
like compounds. Salts of silymarin extract have greater aqueous solubility
and therefore greater bioavailability. One such salt of silymarin is an
esterified hemisuccinate salt of silymarin. In particular, methylglucamine
salt of silymarin is preferred for increased aqueous solubility and
bioavailability. Chelation between methylglucamine and silymarin forms a
salt. The methylglucamine salt of silymarin is available from Infinity
Industries, Inc. (Ronkonkoma, N.Y.), as are all ingredients of the
compositions described herein.
The bioavailability of silymarin may also be increased by preparing a fluid
mixture of Milk thistle dry extract in polyethylene glycol as described in
EP 1 021 198 B 1.
Concentrations or methylglucamine salt of silymarin in the range of from
about 1.3 to about 27 percent by weight are used in the composition to
alleviate hangover symptoms. A preferred concentration is about 3.6% by
weight.
Salicin is a compound contained in a plant known as Willow Bark or White
Willow Bark. The extract of Willow Bark contains salicinium which reduces
headache pain. The pain-relieving effects of salicin are similar to those of
aspirin without side effects such as stomach upset. Salicin is converted to
aspirin in vivo and provides a delayed pain relieving affect after the
ingestion of the compositions disclosed herein. Therefore, stomach upset is
delayed or may not be perceived due to the pain relieving effects of the
alcohol ingested. Salicin's inhibitory effect on prostaglandin synthesis in
nerve cells is the mechanism by which salicin relieves pain. White willow
bark extract or pure salicin in the concentration range of from about 1.5 to
about 21 percent by weight are used in the compositions described herein to
provide relief from hangover symptoms. A concentration of about 4.5% is
preferred.
B vitamins combat the depressive effects of ethanol consumption,
particularly vitamins B12 and folic acid. Vitamin B6, in addition to
combating depression, also assists in the transmission of chemicals in the
nervous system. B vitamins are lost during the consumption of ethanol due to
the diuretic effects of such consumption. It is preferred to use vitamins
B6, B12 and folic acid in combination as these vitamins in combination
increase levels of tetrahydropterin, a coenzyme necessary for the production
of serotonin (and thus melatonin), dopamine, epinephrine and norepinephrine.
A concentration of vitamin B6 in the range of from about 0.12 to about 2.05
percent by weight is used in the composition and a concentration of about
0.36% by weight is preferred. Concentrations of folic acid of from about
0.05 to about 0.8 percent by weight are used and a concentration of about
0.14% by weight is preferred. Concentrations of vitamin B12 of from about
0.06 to about 1.03 are used and a preferred concentration is about 0.18% by
weight.
Magnesium is a component of red blood cells and plays role in controlling
blood pressure. Maintaining control of blood pressure is a factor in
controlling the severity of a headache. Magnesium may be included in the
compositions disclosed herein the forms of magnesium citrate in
concentrations of from about 55% to about 97.45% by weight and preferably
about 90% by weight.
Molybdenum acts as a co-factor of aldehyde dehydrogenase in the oxidation
process that results in the conversion of alcohol to acetic acid.
Specifically, molybdenum assists the enzyme aldehyde oxidase or aldehyde
dehydrogenase in acetaldehyde to acetic acid. Molybdenum also alleviates the
allergenic effects of aldehydes or ketones in persons sensitive to these
compounds. Molybdenum may be added to the compositions disclosed herein in
the form of chelated molybdenum in concentrations that from about 0.03% to
about 1.03% by weight and preferably about 0.18% by weight.
Manganese directly oxidizes acetaldehyde to acetic acid and therefore
quickens the alleviation of negative symptoms caused by acetaldehyde build
up after the consumption of ethanol. Aldehyde dehydrogenase enzyme may use
manganese as a cofactor instead of molybdenum. Preferred manganese compounds
exhibit the lowest oxidation state (+2). The Manganese may be added to the
compositions disclosed herein in the form of manganese sulfate in
concentrations that range from about 0.3% to about 5% by weight and
preferably about 0.9% by weight.
The formulations described herein may be administered by any appropriate
means. The preferred means of administration is by oral route. The
formulation may be ingested in pill, tablet, capsule or liquid form. The
liquid form is preferred for its higher bioavailibity of silymarin.
Effective amounts of the compositions may be administered before or after
the consumption of an alcoholic beverage, preferably before the consumption
of alcohol so that the active components are available when acetaldehyde
levels begin to build. The compositions may be administered during the
consumption of alcohol alone or in combination with a specific ethanol as a
drink mixer.
The compositions may be self-administered and the amount required to be
taken is dependent upon several factors regarding the person ingesting the
ethanol. The amount, type and strength of the alcoholic beverage the person
intends to consume, knowledge of ethanol tolerance of the person and the
need for alertness and/or focus for activities that will follow consumption
of such beverages are factors considered when determining dose.
Subjective tests were conducted by asking individuals who used the
compositions described herein before during and after the consumption of
alcoholic beverages how they felt after consuming several alcoholic drinks.
The following compositions offered noticeable relief to the negative effects
to alcohol consumption:
 | 20-150 mg of silymarin methylglucamine (1.23-35.81 wt %); |
 | 10-75 mg salicin (0.59-21.17 wt %); |
 | 2-6 mg of Vitamin B6 (0.11-2.05 wt %); |
 | 0.8-2.4 mg folic acid (0.03-0.83 wt %); |
 | 1-3 mg Vitamin B12 (0.05-1.03 wt %); |
 | 250-1500 mg of magnesium citrate (49.56-97.45 wt %); |
 | 0.5-3 mg of chelated molybdenum (0.03-1.03 wt %); and |
 | 5-15 mg of manganese sulfate (0.29-5.01 wt %)
Preferred ranges of the individual components of the composition are: |
 | 20-60 mg of silymarin methylglucamine (1.23-10.09 wt %); |
 | 25-75 mg salicin (1.55-21.17 wt %); |
 | 2-6 mg of Vitamin B6 (0.11-2.05 wt %); |
 | 0.8-2.4 mg folic acid (0.05-0.83 wt %); |
 | 1-3 mg Vitamin B12 (0.06-1.03 wt %); |
 | 500-1500 mg of magnesium citrate 75.26-97.45 wt %); |
 | 1-3 mg of chelated molybdenum (0.06-1.03 wt %); and |
 | 5-15 mg of manganese sulfate (0.29-5.01 wt %) |
All references, including publications, patent applications, and patents,
cited herein are hereby incorporated by reference to the same extent as if
each reference were individually and specifically indicated to be
incorporated by reference and were set forth in its entirety herein.
The use of the terms "a" and "an" and "the" and similar referents in the
context of describing the invention (especially in the context of the
following claims) are to be construed to cover both the singular and the
plural, unless otherwise indicated herein or clearly contradicted by
context. Recitation of ranges of values herein are merely intended to serve
as a shorthand method of referring individually to each separate value
falling within the range, unless otherwise indicated herein, and each
separate value is incorporated into the specification as if it were
individually recited herein. All methods described herein can be performed
in any suitable order unless otherwise indicated herein or otherwise clearly
contradicted by context. The use of any and all examples, or exemplary
language (e.g., "such as") provided herein, is intended merely to better
illuminate the invention and does not pose a limitation on the scope of the
invention unless otherwise claimed. No language in the specification should
be construed as indicating any non-claimed element as essential to the
practice of the invention.
While some potential advantages and objects have been expressly identified
herein, it should be understood that some embodiments of the invention may
not provide all, or any, of the expressly identified advantages and objects.
Preferred embodiments of this invention are described herein, including the
best mode known to the inventors for carrying out the invention. Of course,
variations of those preferred embodiments will become apparent to those of
ordinary skill in the art upon reading the foregoing description. The
inventors expect skilled artisans to employ such variations as appropriate,
and the inventors intend for the invention to be practiced otherwise than as
specifically described herein. Accordingly, this invention includes all
modifications and equivalents of the subject matter recited in the claims
appended hereto as permitted by applicable law. Moreover, any combination of
the above-described elements in all possible variations thereof is
encompassed by the invention unless otherwise indicated herein or otherwise
clearly contradicted by context.
The following examples further illustrate the invention but, of course,
should not be construed as in any way limiting its scope.
Example 1 includes the following formulation (values are in wt %):
| silymarin methylglucamine |
9.94 |
| salicin |
16.75 |
| Thiamine HCL |
1.23 |
| Riboflavin |
1.68 |
| Niacinamide |
1.68 |
| pantothenic acid |
0.84 |
| Vitamin B6 |
0.17 |
| folic acid |
0.03 |
| Vitamin B12 |
0.05 |
| Chelated molybdenum |
0.03 |
| magnesium citrate |
67.15 |
| manganese sulfate |
0.45 |
Claim 1 of 8 Claims
1. A method for decreasing the negative effects of ethyl alcohol
consumption, the method comprising the step of administering to a person
an amount of a composition comprising:
a silymarin;
salicin;
at least one B vitamin;
magnesium;
molybdenum; and
manganese.
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