WO2015008101A1 - Composition of a drink for enhanced reduction of blood alcohol level - Google Patents

Composition of a drink for enhanced reduction of blood alcohol level Download PDF

Info

Publication number
WO2015008101A1
WO2015008101A1 PCT/IB2013/001535 IB2013001535W WO2015008101A1 WO 2015008101 A1 WO2015008101 A1 WO 2015008101A1 IB 2013001535 W IB2013001535 W IB 2013001535W WO 2015008101 A1 WO2015008101 A1 WO 2015008101A1
Authority
WO
WIPO (PCT)
Prior art keywords
drink
blood alcohol
alcohol
composition
vitamin
Prior art date
Application number
PCT/IB2013/001535
Other languages
French (fr)
Inventor
Rolf A. SCHAUMLÖFFEL
Original Assignee
Schaumlöffel Rolf A
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Schaumlöffel Rolf A filed Critical Schaumlöffel Rolf A
Priority to PCT/IB2013/001535 priority Critical patent/WO2015008101A1/en
Publication of WO2015008101A1 publication Critical patent/WO2015008101A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • AHUMAN NECESSITIES
    • A23FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23LFOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L2/00Non-alcoholic beverages; Dry compositions or concentrates therefor; Their preparation
    • A23L2/52Adding ingredients
    • A23L2/60Sweeteners

Definitions

  • Composition of a Drink for Enhanced Reduction of Blood Alcohol Level .
  • the invention relates to a combination of ingredients for a fitness drink and more exactly to a combination of enzymes which enhance the liver metabolism of alcohol, added by fructose and caffeine and similar agents to accelerate so- matic reaction.
  • ADH alcohol dehydrogenases
  • US 7.544356 B2 proposes Lactobacillus brevis HY 7401 , Lactobellis fermentum CS332, Lactobacillus acidophilus CSG, Bifidobacterium Longum HY 8001 , Alder treee extract, selfheal extract, a milk thistle extract, bean-rice bran fermentation extract, turnip, -tomato, pinapple and broccoli extract, whereas the extract from artichoke, well-known for its curative effect on the human liver, and main ingredient in allegedly alcohol reducing drink "security" (http://securityfeelbetter.com), was not indicated in patent literature. DESCRIPTION OF THE INVENTION
  • ADHs develop their catalytic effect particularly in a balanced aquae- ous solution.
  • Direct exposition to gastric acid may be the reason, why alcohol- reducing medicaments for oral application had only poor effect.
  • the idea therefore is to combine it with a drink, where ADHs can fulfil their catalytic effect due to the predetermined aqueous mix.
  • the other inventive step is the combination of these enzymes with fructose, as known from prior art.
  • fructose is not only stimulating the liver metabolism.
  • its complementary effect is used to sweeten the bitter enzymes and added fruit acids and to stabilize the ADH component.
  • arginines and asparagines may be added to enhance the metabolism, particularly the discharge of ammonia residues, as well as fumaric acids, which are known for reducing hangover effects by stimulating the citric acid cycle.
  • Phenylalanine naturally found in the breast milk of mammals. It is reputed for its analgesic and antidepressant effects. It is a direct precursor to the neuromodulator phenylethylamine, a commonly used dietary supplement.
  • L-arginine may be added, which also helps rid the body of ammonia (a waste product) and stimulates the release of insulin.
  • L-arginine is used to enhance the delivery of nitric oxide (a compound that relaxes the blood vessels) and therefore may reduce headaches.
  • Further embodiments may enclose caffeines, e.g. Guarana to further enhance physical activity, mineral nutriments and adapted flavors to make a recovering drink.
  • the composition therefore may contain in each 200 mililiter drink a composition of: Fructoses 40.000 - 8000 mg
  • Lower curve is with and upper curve without consummation of 250 ml of the here disclosed mixture at 21 :30 h.

Abstract

Composition of a Drink for Enhanced Reduction of Blood Alcohol Level. A fitness drink for enhancing reduction of blood alcohol comprising ADH (Alcohol dehydrogenases) is sweetened with high dosis of fructose and recharged with malic acid, fumaric acid, arginine, phenylalanine, asparagine, ascorbic acid, vitamin Bl, vitamin B6 and caffeine.

Description

Composition of a Drink for Enhanced Reduction of Blood Alcohol Level .
FIELD OF THE INVENTION
The invention relates to a combination of ingredients for a fitness drink and more exactly to a combination of enzymes which enhance the liver metabolism of alcohol, added by fructose and caffeine and similar agents to accelerate so- matic reaction.
BACKGROUND OF THE INVENTION
The use of alcohol may ease communication with reducing tensions and psychi- cal inhibitions and therefore is frequently consumed on parties, reunions and in discotheques.
But not only a hangover in cases of over-consumption may be the consequence, the strongly reduced ability to safely drive a car jeopardizes even social drinkers to an inacceptable extent.
However, even strong intent to keep from too much drinking might be foiled by social effects, as the need to accept invitations, etc.
Thus, there may be a need of quite quickly to reduce blood alcohol , particularly if there is only a short period of rest or sleep before re-entering into commuting and returning to business.
It is well known, that there are amino acids, as phenylalanine and asparagine that enhance the liver metabolism and that it is alcohol dehydrogenases (ADH) in the liver and stomach, which breaks down alcohol directly. The amount of ADH represented in the human body is recognized responsible for interpersonal and interracial differences of toxic reactions to alcohol . However, these enzymes are only effectively deployed in a watery dilution, and ADH may be instable at particular conditions. Furthermore, almost all of these enzymes taste extremely bitter and therefore are not used in drinks sofar.
There are other substances known to enhance reduction of blood alcohol , like maltodextrine, which recondition the anterior cingular cortex to stimulate physical activity and therewith may help to reduce effects of alcohol . But this as well is quite untasty.
Therefore it is the task of the here disclosed invention to create a drink, that helps to quickly reduce the blood alcohol level in terms of a dietary supplement, but has acceptable taste. PRIOR ART
There are quite a few propositions known to reduce blood alcohol while drinking, as in WO2002055093 A2 . with swallowing limestone and activated chara- coal , active dry yeast (WO 20003006642 A 1) or edible crystal zeolite (WO 12987000049 A 1) -where people could wonder, what for then to drink alcohol .
But most propositions refer to reducing the alcohol level after drinking, wether by injections with enzyme alcohol oxidase (US 54.450.153 A) or Potassium sorbate) and later indicated standard ingredients in EP 2223817, or again by swallowing dry yeast (EP 1412490 Al) or charcoal (EP0264430 Al) or food preparations with potassium bitartrate and sodium bicarbonate (EP 2172115 Al), or compositions with animal glandular extract, again yeast and bacterial extracts and divers plant extracts (WO 2005123099 A2).
However, since the side effects of alcohol, particularly hangover, are closely related to corporal dehydration, application of active agents are preferably administered in drinks. So almost all of the following formulations contain water and fructose, which is known for enhancing liver metabolism and is commonly used as sweetening agent, furthermore vitamins, particularly of the B6 and B 12 group and Vitamin C:
US 6.514.544 B2 and WO 20000030477 Al are simply adding taurine to that, as others use cafeine to enhance metabolism, whereas EP 0205634 B l additionally proposes quinine, sodium chloride and tripoassium citrate, and EP 0631778 A l relies on L-aspartate or L-asparagine, the effects of which on blood alcohol are quite antithetically discussed in the scientific community.
A few other rather exotic ingredients, the evaluation of which is not possible here, is besides saccarides (which are less expensive, but poorly active in liver metabolism compared to fructose) and sodium ion a plus Yacon Syrop, another sugar substitute (EP 2323693 B l), Kudzu and Nopal (sofar only known as Mexican vegetable, a cactus specimen) and white willow bark extract, named beside N-acetyl cysteine in WO 20120558589 Al . US 7.544356 B2 proposes Lactobacillus brevis HY 7401 , Lactobellis fermentum CS332, Lactobacillus acidophilus CSG, Bifidobacterium Longum HY 8001 , Alder treee extract, selfheal extract, a milk thistle extract, bean-rice bran fermentation extract, turnip, -tomato, pinapple and broccoli extract, whereas the extract from artichoke, well-known for its curative effect on the human liver, and main ingredient in allegedly alcohol reducing drink "security" (http://securityfeelbetter.com), was not indicated in patent literature. DESCRIPTION OF THE INVENTION
One idea therefore was stimulated by the drop in prices for ADHs, which formerly had to be extracted from horse livers and -due to low yield- were quite expensive.
Since their demand rose sharply for catalysts to the synthesis of fuels from bio- mass, biotechnological methods have been developed, particularly their extraction from modified yeast, that might allow their application in consumer products.
However, ADHs develop their catalytic effect particularly in a balanced aquae- ous solution. Direct exposition to gastric acid may be the reason, why alcohol- reducing medicaments for oral application had only poor effect.
The idea therefore is to combine it with a drink, where ADHs can fulfil their catalytic effect due to the predetermined aqueous mix.
The other inventive step is the combination of these enzymes with fructose, as known from prior art. In an accordingly high dosage fructose is not only stimulating the liver metabolism. Here its complementary effect is used to sweeten the bitter enzymes and added fruit acids and to stabilize the ADH component.
In another developmental step arginines and asparagines may be added to enhance the metabolism, particularly the discharge of ammonia residues, as well as fumaric acids, which are known for reducing hangover effects by stimulating the citric acid cycle.
Other enhancing effects are known from Phenylalanine, naturally found in the breast milk of mammals. It is reputed for its analgesic and antidepressant effects. It is a direct precursor to the neuromodulator phenylethylamine, a commonly used dietary supplement.
Moreover ascorbic acid, well proven for reducing side-effects of alcohol, that provoke hangover, and L-arginine may be added, which also helps rid the body of ammonia (a waste product) and stimulates the release of insulin. In addition, L-arginine is used to enhance the delivery of nitric oxide (a compound that relaxes the blood vessels) and therefore may reduce headaches. Further embodiments may enclose caffeines, e.g. Guarana to further enhance physical activity, mineral nutriments and adapted flavors to make a recovering drink.
The composition therefore may contain in each 200 mililiter drink a composition of: Fructoses 40.000 - 8000 mg
Phenylalanine 600 - 800 mg
Asparagine/Paraxine 500 - 700 mg
Fumaric Acid 300 - 500 mg
ADH 5 - 10 mg
Malic acid 250 - 400 mg
Arginine 700 - 1.000 mg
Its to be stated, that these agents and their dosage are meeting EU-regulation 2002/46/EG and the German LFGB for dietary supplements, whereas in USA the FDA would allow higher dosages and even claims for therapeutic application.
DESCRIPTION OF THE DRAWING
Figl demonstrates the physical effects of the here disclosed drink on a human body:
It shows the averaged relative blood alcohol level in per mil of 15 male test persons, quite equally mixed from 19 up to 70 years, the night after consummation of each one bottle (3/4 liters) of red wine between 20:30 and 21 :30, measured consecutively each 1/2 hour after 22:00 h.
Lower curve is with and upper curve without consummation of 250 ml of the here disclosed mixture at 21 :30 h.

Claims

WHAT IS CLAIMED IS:
1. A Fitness drink for quickly reducing blood alcohol , comprising the follow components in 200 ml carbonized water at the given dosage range of:
Fructoses 40.000 - 8000 mg
ADH 5 - 10 mg
2. A Fitness drink according to claim 1 , further containing:
Malic acid 250 - 400 mg
Arginine 700 - 1.000 mg
Phenylalanine 600 - 800 mg
A sparagi ne/Paraxi ne 500 - 700 mg
Fumaric acid 300 - 500 mg
Ascorbic acid 200 - 400 mg
Vitamin B l 2 - 4 mg
Vitamin B6 1 - 3 mg
Caffeine 40 - 70 mg
Fructal flavoring ad lib.
PCT/IB2013/001535 2013-07-15 2013-07-15 Composition of a drink for enhanced reduction of blood alcohol level WO2015008101A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/IB2013/001535 WO2015008101A1 (en) 2013-07-15 2013-07-15 Composition of a drink for enhanced reduction of blood alcohol level

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/IB2013/001535 WO2015008101A1 (en) 2013-07-15 2013-07-15 Composition of a drink for enhanced reduction of blood alcohol level

Publications (1)

Publication Number Publication Date
WO2015008101A1 true WO2015008101A1 (en) 2015-01-22

Family

ID=49034115

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2013/001535 WO2015008101A1 (en) 2013-07-15 2013-07-15 Composition of a drink for enhanced reduction of blood alcohol level

Country Status (1)

Country Link
WO (1) WO2015008101A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016036254A1 (en) * 2014-09-03 2016-03-10 Kystvågen Slip & Mek As Crawler configured for submarine use

Citations (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4450153A (en) 1982-09-30 1984-05-22 Phillips Petroleum Company Alcohol removal from blood with alcohol oxidase
WO1987000049A1 (en) 1985-07-02 1987-01-15 Gatehouse Technical Ventures Limited Adsorbent composition
EP0205634B1 (en) 1985-06-24 1988-03-02 Manfred Bannes Beverage containing fructose, vitamin c, quinine and/or derivatives thereof
EP0264430A1 (en) 1986-04-14 1988-04-27 MARGOLIN, Ely Composition and method for reducing blood alcohol content
EP0631778A1 (en) 1993-06-28 1995-01-04 Miwon Co., Ltd. Use of L-aspartate or L-asparagine to prevent alcohol toxicity
WO2000030477A1 (en) 1998-11-19 2000-06-02 Norbert Fuchs Beverage for increasing the body's capacity to break down alcohol
CN1279111A (en) * 1999-06-23 2001-01-10 詹莉 Nutritive bioenzyme liquor for sobering up and its preparing process
WO2002055093A2 (en) 2001-01-12 2002-07-18 Innovation Ventures, Llc Activated charcoal based composition and method for reducing hangover symptoms associated with the consumption of alcohol containing beverages
WO2003006642A1 (en) 2000-02-25 2003-01-23 Owades Joseph L Mediating the effects of alcohol consumption by orally administering active dry yeast
EP1412490A1 (en) 2001-07-11 2004-04-28 Joseph L. Owades Mediating the effects of alcohol consumption by orally administering active dry yeast
WO2005123099A2 (en) 2004-06-08 2005-12-29 Enzymedix, Inc. Methods and compositions for accelerating alcohol metabolism
US7544356B2 (en) 2005-04-19 2009-06-09 Korea Yakult Co., Ltd. Composition for the improvement of liver function, the reduction of serum ethanol level and antioxidant activity enhancement
KR20090091653A (en) * 2008-02-25 2009-08-28 주식회사 기영약품 Composition for relieving and preventing hangover
EP2172115A1 (en) 2008-10-03 2010-04-07 Ivan Biffi Composition for use in the reduction of blood alcohol content
EP2223817A2 (en) 2009-02-27 2010-09-01 Magna Car Top Systems GmbH Locking device for a cabriolet roof
WO2012058589A1 (en) 2010-10-28 2012-05-03 Jonathan Burg Compositions and methods to reduce hangover and reduce blood alcohol levels after alcohol consumption
WO2012091251A1 (en) * 2010-12-27 2012-07-05 순천대학교 산학협력단 Drink composition for hangover relief, containing cucumber vinegar
EP2323692B1 (en) 2008-09-04 2013-04-24 Early Bird Drinks B.V. Hangover relief by compositions comprising oral rehydration solution

Patent Citations (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4450153A (en) 1982-09-30 1984-05-22 Phillips Petroleum Company Alcohol removal from blood with alcohol oxidase
EP0205634B1 (en) 1985-06-24 1988-03-02 Manfred Bannes Beverage containing fructose, vitamin c, quinine and/or derivatives thereof
WO1987000049A1 (en) 1985-07-02 1987-01-15 Gatehouse Technical Ventures Limited Adsorbent composition
EP0264430A1 (en) 1986-04-14 1988-04-27 MARGOLIN, Ely Composition and method for reducing blood alcohol content
EP0631778A1 (en) 1993-06-28 1995-01-04 Miwon Co., Ltd. Use of L-aspartate or L-asparagine to prevent alcohol toxicity
WO2000030477A1 (en) 1998-11-19 2000-06-02 Norbert Fuchs Beverage for increasing the body's capacity to break down alcohol
US6514544B2 (en) 1998-11-19 2003-02-04 Jhs-Privatstiftung Beverage for increasing the body's capacity to break down alcohol and method thereof
CN1279111A (en) * 1999-06-23 2001-01-10 詹莉 Nutritive bioenzyme liquor for sobering up and its preparing process
WO2003006642A1 (en) 2000-02-25 2003-01-23 Owades Joseph L Mediating the effects of alcohol consumption by orally administering active dry yeast
WO2002055093A2 (en) 2001-01-12 2002-07-18 Innovation Ventures, Llc Activated charcoal based composition and method for reducing hangover symptoms associated with the consumption of alcohol containing beverages
EP1412490A1 (en) 2001-07-11 2004-04-28 Joseph L. Owades Mediating the effects of alcohol consumption by orally administering active dry yeast
WO2005123099A2 (en) 2004-06-08 2005-12-29 Enzymedix, Inc. Methods and compositions for accelerating alcohol metabolism
US7544356B2 (en) 2005-04-19 2009-06-09 Korea Yakult Co., Ltd. Composition for the improvement of liver function, the reduction of serum ethanol level and antioxidant activity enhancement
KR20090091653A (en) * 2008-02-25 2009-08-28 주식회사 기영약품 Composition for relieving and preventing hangover
EP2323692B1 (en) 2008-09-04 2013-04-24 Early Bird Drinks B.V. Hangover relief by compositions comprising oral rehydration solution
EP2172115A1 (en) 2008-10-03 2010-04-07 Ivan Biffi Composition for use in the reduction of blood alcohol content
EP2223817A2 (en) 2009-02-27 2010-09-01 Magna Car Top Systems GmbH Locking device for a cabriolet roof
WO2012058589A1 (en) 2010-10-28 2012-05-03 Jonathan Burg Compositions and methods to reduce hangover and reduce blood alcohol levels after alcohol consumption
WO2012091251A1 (en) * 2010-12-27 2012-07-05 순천대학교 산학협력단 Drink composition for hangover relief, containing cucumber vinegar

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
DATABASE EPODOC [online] EUROPEAN PATENT OFFICE, THE HAGUE, NL; 5 July 2012 (2012-07-05), "Drink composition for hangover relief, containing cucumber vinegar", XP002713345, Database accession no. KR-2011007213-W *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016036254A1 (en) * 2014-09-03 2016-03-10 Kystvågen Slip & Mek As Crawler configured for submarine use
GB2544024A (en) * 2014-09-03 2017-05-03 Kystvágen Slip & Mek As Crawler configured for submarine use
GB2544024B (en) * 2014-09-03 2020-04-08 Kystvagen Slip & Mek As Crawler configured for submarine use

Similar Documents

Publication Publication Date Title
CN102218096B (en) Composition for relieving the effects of alcohol and preventing hangover and disintoxicating drink having the composition
CN101889679B (en) Composition with disintoxicating and liver-protecting effects and application thereof in food and health-care food
CN101460159B (en) Fatigue-reducing agent
CN105942533B (en) A kind of functional beverage and functional beverage effervescent tablet
CA2434388C (en) Activated charcoal based composition and method for reducing hangover symptoms associated with the consumption of alcohol containing beverages
US10945979B1 (en) Amino acid compositions to promote endothelial health
US20190314298A1 (en) Compositions for preventing and relieving hangover & liver damage which occur due to alcohol consumption
RU2757379C2 (en) Composition for the treatment of veisalgia
JP4119629B2 (en) Antihypertensive agent
JP2008120754A (en) Antifatigue agent
CN101861959A (en) Pearl nutritional vinegar oral liquid
WO2015008101A1 (en) Composition of a drink for enhanced reduction of blood alcohol level
JP2008088101A (en) Antifatigue agent
JP2007008866A (en) Hypotensive agent composition
KR20130119424A (en) Ingredients derived from sphaeranthus indicus
ES2618930T5 (en) Composition comprising diamine oxidase for the prevention of hangover symptoms
US20160038405A1 (en) Effervescent multi-vitamin/mineral additive for coffee and tea
CN105708966A (en) Wintercherry effervescent tablets with blood glucose reduction function and preparation method of wintercherry effervescent tablets
JP5946240B2 (en) Method for enhancing physiological action of caffeine
US20230270711A1 (en) Improved Anti-Hangover Composition, Its Preparation and Uses
KR20130065117A (en) Composition comprising water extracts from tremella foliacea fr. for treating or preventing obesity
US7390513B2 (en) Food supplement formulation
US20190320688A1 (en) Compositions for preventing and relieving hangover & liver damage which occur due to alcohol consumption
JP2006328079A (en) Composition stimulating specific metalloenzyme
Berbari et al. Secondary hypertension: infrequently considered aspects—illicit/recreational substances, herbal remedies, and drug-associated hypertension

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 13752921

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 13752921

Country of ref document: EP

Kind code of ref document: A1