WO1987006135A1 - Composition and method for reducing blood alcohol content - Google Patents

Composition and method for reducing blood alcohol content Download PDF

Info

Publication number
WO1987006135A1
WO1987006135A1 PCT/US1987/000813 US8700813W WO8706135A1 WO 1987006135 A1 WO1987006135 A1 WO 1987006135A1 US 8700813 W US8700813 W US 8700813W WO 8706135 A1 WO8706135 A1 WO 8706135A1
Authority
WO
WIPO (PCT)
Prior art keywords
activated charcoal
alcohol
composition
blood
diminution
Prior art date
Application number
PCT/US1987/000813
Other languages
French (fr)
Inventor
Ely Margolin
Original Assignee
Ely Margolin
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 Ely Margolin filed Critical Ely Margolin
Publication of WO1987006135A1 publication Critical patent/WO1987006135A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K33/00Medicinal preparations containing inorganic active ingredients
    • A61K33/44Elemental carbon, e.g. charcoal, carbon black

Definitions

  • This invention is concerned with a method and compositions for reducing the concentration of ethanol in the blood of persons who have been drinking. It has been found that the oral administration of activated charcoal in sufficient amounts to a person who has been drinking has a marked effect in reducing the alcohol blood level.
  • activated charcoal is an effective absorbent.
  • "Activated Charcoal” is defined in J.E. Schmidt, "Attorney's Dictionary of Medicine and Word Finder," VoL. 1, Matthew Bonder, New York, N.Y. 1981 as "Powdered charcoal treated in a special way, to increase its power of absorption. It is used as an antidote in treating cases of poisoning; it is also useful, in combination with other ingredients, in the treatment of excessive acidity of the stomach, diarrhea etc. Also called 'medicinal charcoal'.”
  • an effective method for reducing the concentration of gastrointestinal alcohol and of alcohol in the blood is by the ingestion of a sufficient amount of pharmaceutical grade activated charcoal so as to result in the adsorption of significant quantities of alcohol.
  • the charcoal may be administered in tablet or capsule form or as a slurry, although it is expected that the use of tablets or capsules will make the treatment more generally available in locations where the consumption of alcohol takes place.
  • the tablets may be coated so as to make them easier to swallow than uncoated tablets. Flavoring may be added to make the charcoal more palatable.
  • Binders may be used to prevent the disintegration of the tablets in the esophagus. The addition of coatings, binders or flavoring must be done so as to avoid any substantial reduction in the adsorptive capacity of the activated charcoal. DETAILED DESCRIPTIONS OF THE PRITERRED EMBODIMEN ⁇ S
  • the charcoal to be used for the purpose of this invention must be of pharmaceutical grade, meaning originating from animal or vegetable sources and having a high enough surface area so as not to require the ingestion of substantially excessive quantities of charcoal.
  • Kurt M. Dubowski reported a study of 922 men involved in traffic offenses in which the rate of diminution of alcohol blood content was found to vary from 0.006 to 0.04 percent per hour. The generally accepted average rate of diminution of our blood alcohol content is 0.015% per hour. See Erwin, R.E.
  • the ingestion of a sufficient amount of activated charcoal to just cause the rate of blood alcohol diminution to be greater than the rate of blood alcohol diminution in the absence of activated charcoal ingestion is at the outer limits of efficacy.
  • a preferred increase in the rate of diminution is at least 0.005% per hour greater than the normal or ingestion free rate of the person ingesting the activated charcoal. Expressed alternately on the average, a minimal does of activated charcoal will result in a rate of blood alcohol diminution of at least 0.02% per hour.
  • Flavors may be used to make the charcoal more palatable, but it is important to avoid adding potential adsorbates which will reduce the surface area and effectiveness of the activated charcoal.
  • the instrument which was used to arrive at the blood alcohol content was a breath measuring device called the "Breath Alcohol Test Instrument SX3A” manufactured by Sirchie Finger Print Labs of Raleigh, N.C. The instrument was calibrated by the manufacturer prior to the conduct of the majority of the tests. Periodically the Sirchie instrument was checked against the "Blood Level Monitor CXG 212" distributed by the Hannamax Corp., Chicago, IL. The alcohol concentrations given represent an average of three readings taken within several minutes of each other.
  • EXAMPLE 1 A 90.7 kg male, ingested about 177 ml of 100 proof vodka within five minutes of time zero. At sixty minutes, the subject swallowed a capsule containing about 260 mg. of Activated Charcoal U.S.P. which had an average particle size of 0.1 micron as measured by a Coulter counter. The results are shown in Table I, Column 1. Between 60 and 80 minutes, the rate of diminution of blood alcohol content was about 0.056% per hour falling to an average of about 0.04% per hour thereafter.
  • EXAMPLE 2 A 97.5 kg male, ingested 118 ml of 100 proof vodka three hours after his last meal in two trials, A and B.
  • the greatest rate of diminution of blood alcohol content for 2A is about 0.161% per hour and the average slope thereafter is about 0.0662 per hour.

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Preparation (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A method for reducing blood alcohol content in a person by the administration of an effective amount of activated charcoal.

Description

COMPOSITION AND METHOD FOR REDUCING BLOOD ALCOHOL CONTENT
BACKGROUND OF THE INVENTION
This invention is concerned with a method and compositions for reducing the concentration of ethanol in the blood of persons who have been drinking. It has been found that the oral administration of activated charcoal in sufficient amounts to a person who has been drinking has a marked effect in reducing the alcohol blood level.
The use of various compounds to combat the toxic effects of alcohol is demonstrated in a number of patents. For example, B. Tabokoff in U.S. Pat. No. 4,528,295 proposes the use of methionine to reduce the blood acetaldehyde level (acetaldehyde being a harmful metabolite of alcohol ingestion) by ingestion of methionine prior to imbibation of alcohol. F.N. Marshall in U.S. Pat. No. 3,860,719 claims that 2- [(3,4-dichlorophenoxy) methy] -2- imidazoline or a pharmaceutically acceptable salt thereof is effective in combating ethanol intoxication in mammals when administered internally. Many other compounds have been claimed effective for this purpose.
It has been known that activated charcoal is an effective absorbent. "Activated Charcoal" is defined in J.E. Schmidt, "Attorney's Dictionary of Medicine and Word Finder," VoL. 1, Matthew Bonder, New York, N.Y. 1981 as "Powdered charcoal treated in a special way, to increase its power of absorption. It is used as an antidote in treating cases of poisoning; it is also useful, in combination with other ingredients, in the treatment of excessive acidity of the stomach, diarrhea etc. Also called 'medicinal charcoal'."
Its use in medical applications is exemplified in several U.S. Patents. R. Adler in U.S. Pat. No. 1,589,081 treats a vegetable charcoal so as to remove objectionable impurities and binds the charcoal particles with a soluble binder so as to cause the product to readily disintegrate in the alimentary canal for treating "...foul breath and other unpleasant symptoms and conditions, especially of the stomach." T.J. Van der Weel, U.S. Pat No. 2,787,579 coats charcoal tablets with carboxyalkycelluloses so as to facilitate swallowing of the tablets. J. H. Geils, in U.S. Pat. No. 4,122,169. uses a combination of activated charcoal and sorbitol, a sweetener which has a laxative action, to remove undesirable, noxious substances from the gastrointestinal (G.I.) tract of humans by absorption and quick transport through the G.I. tract. However, no in vivo studies of the use of activated charcoal to counteract the effects of alcohol consumption appear to have been reported either for animals or humans. A.H. Anderson has studied the use of activated charcoal as an adsorbent for poisons extensively and reported on the results of a comparative in vitro study which included alcohol in 2 Acta pharmacol 69-78 (1946). The study placed alcohol next to the least adsorbed of the compounds studied and Anderson says, "As far as alcohol is concerned, its adsorption cannot be said to be slight. Still considering the adsorbability of alcohol in relation to the doses of this substance usually ingested before the question of charcoal therapy becomes topical, this treatment must be looked upon beforehand as useless in alcohol intoxication." op cit., pp. 75-76. Although there have been subsequent studies on the use of activated charcoal as an antidote for poisons in vitro and in vivo, e.g. W.J. Decker et al., 13 Toxicology and Applied Pharmacology 454-460 (1968), and A.L. Picchioni, 17 Pediatric Clinics of North America (3), 535-542 (1970) for example, no studies appear to have been reported on the use of activated charcoal as a method for reducing the concentration of alcohol in the G.I. tract, in vitro or in vivo. It is clearly desirable to have a means of simply, safely and quickly reducing the alcohol concentration in the G. I. tract and in the blood of a person who has consumed sufficient alcohol to become intoxicated.
We have found, unexpectedly, that oral administration of activated charcoal reduces the blood alcohol concentration of a drinking person significantly."
SUMMARY OF THE INVENTION
According to the present invention, an effective method for reducing the concentration of gastrointestinal alcohol and of alcohol in the blood is by the ingestion of a sufficient amount of pharmaceutical grade activated charcoal so as to result in the adsorption of significant quantities of alcohol. The charcoal may be administered in tablet or capsule form or as a slurry, although it is expected that the use of tablets or capsules will make the treatment more generally available in locations where the consumption of alcohol takes place. The tablets may be coated so as to make them easier to swallow than uncoated tablets. Flavoring may be added to make the charcoal more palatable. Binders may be used to prevent the disintegration of the tablets in the esophagus. The addition of coatings, binders or flavoring must be done so as to avoid any substantial reduction in the adsorptive capacity of the activated charcoal. DETAILED DESCRIPTIONS OF THE PRITERRED EMBODIMENΓS
The charcoal to be used for the purpose of this invention must be of pharmaceutical grade, meaning originating from animal or vegetable sources and having a high enough surface area so as not to require the ingestion of substantially excessive quantities of charcoal. In a paper presented to the National Conference on Alcohol and Traffic Safety in 1961 and published in Alcohol and Safety Traffic by the U.S. Department of Health, Education and Welfare (Public Health Service Publication #1043), Kurt M. Dubowski reported a study of 922 men involved in traffic offenses in which the rate of diminution of alcohol blood content was found to vary from 0.006 to 0.04 percent per hour. The generally accepted average rate of diminution of our blood alcohol content is 0.015% per hour. See Erwin, R.E. , Defense of Drunk Driving Cases, 3rd Ed., Matthew Bender, New York, N.Y. , p 15-7. The ingestion of a sufficient amount of activated charcoal to just cause the rate of blood alcohol diminution to be greater than the rate of blood alcohol diminution in the absence of activated charcoal ingestion is at the outer limits of efficacy. A preferred increase in the rate of diminution is at least 0.005% per hour greater than the normal or ingestion free rate of the person ingesting the activated charcoal. Expressed alternately on the average, a minimal does of activated charcoal will result in a rate of blood alcohol diminution of at least 0.02% per hour. The ingestion of activated charcoal resulting in a rate of blood alcohol diminution of greater than about 0.04% per hour is preferred because this value appears to exceed the highest unaided rate of diminution. Increasing doses of activated charcoal will both increase the rate of diminution of blood alcohol content and extend the period of effectiveness. Any form of activated charcoal which can be tolerated by the individual may be used but tablets or capsules are especially convenient although aqueous slurries may also be used. Treatment may be prior to, simultaneous or following alcohol ingestion.
Flavors may be used to make the charcoal more palatable, but it is important to avoid adding potential adsorbates which will reduce the surface area and effectiveness of the activated charcoal. In the following examples, the instrument which was used to arrive at the blood alcohol content was a breath measuring device called the "Breath Alcohol Test Instrument SX3A" manufactured by Sirchie Finger Print Labs of Raleigh, N.C. The instrument was calibrated by the manufacturer prior to the conduct of the majority of the tests. Periodically the Sirchie instrument was checked against the "Blood Level Monitor CXG 212" distributed by the Hannamax Corp., Chicago, IL. The alcohol concentrations given represent an average of three readings taken within several minutes of each other.
EXAMPLE 1 A 90.7 kg male, ingested about 177 ml of 100 proof vodka within five minutes of time zero. At sixty minutes, the subject swallowed a capsule containing about 260 mg. of Activated Charcoal U.S.P. which had an average particle size of 0.1 micron as measured by a Coulter counter. The results are shown in Table I, Column 1. Between 60 and 80 minutes, the rate of diminution of blood alcohol content was about 0.056% per hour falling to an average of about 0.04% per hour thereafter. EXAMPLE 2 A 97.5 kg male, ingested 118 ml of 100 proof vodka three hours after his last meal in two trials, A and B. Forty minutes into each trial, the subject swallowed two capsules containing about 260 mg each of Activated Charcoal U.S.P. having an average particle diameter of about 0.1 micron as measured by Coulter counter. The results are shown in Table I, columns 2A and 2B.
The greatest rate of diminution of blood alcohol content for 2A is about 0.161% per hour and the average slope thereafter is about 0.0662 per hour.
For 2B, the greatest rate of blood alcohol diminution is about 0.0842 per hour and the average thereafter is about 0.064% per hour.
EXAMPUE 3
A 77 kg male, drank 177 ml of 100 proof vodka on an "empty" stomach approximately at time zero. At forty minutes, the subject swallowed four capsules containing about 260 mg each of Activated Charcoal U.S.P. having an average particle diameter of about 0.1 micron as measured by Coulter counter. The results are shown in Table I, column 3. The resulting average rate of blood alcohol diminution is about 0.157% per hour.
EXAMPLE 4
A 95.3 kg male, drank 177 ml of 100 proof vodka on an empty stomach approximately at time zero. At forty minutes, the subject swallowed four capsules containing about 260 mg each of Activated Charcoal U.S.P. having an average particle diameter of about 0.1 micron as measured by Coulter counter. The results are shown in Table I, column 4. The resulting average rate of blood alcohol diminution is about 0.155% per hour. EXAMPLE 5 An 86.2 kg male, drank 177 ml of 100 proof vodka approximately at time zero. The subject did not swallow any activated charcoal. The alcohol content results are shown in Table I, column 5. In this example the alcohol content appears to plateau before dropping and reaches an average slope of about 0.039% per hour.
Figure imgf000009_0001

Claims

What is claimed is:
1. A method for reducing the concentration of alcohol in the blood resulting from its ingestion by administering to the ingesting person an effective amount of activated charcoal.
2. The method in accordance with Claim 1 wherein the effective administered amount of activated charcoal is at least enough to increase the rate of blood alcohol diminution by about 0.005 percent per hour more than the rate of blood alcohol diminution in the absence of the administration of activated charcoal.
3. Tne method in accordance with Claim 1 wherein an effective administered amount of activated charcoal is at least enough to result in an average rate of blood alcohol diminution of greater than about 0.04 percent per hour.
4. A composition for reducing the concentration of alcohol in the blood resulting from its ingestion which comprises activated charcoal.
5. The composition of Claim 4 wherein the activated charcoal has an average particle diameter of about 0.1 micron or less.
6. The composition of Claim 4 wherein the activated charcoal is contained in a capsule.
7. The composition of Claim 4 wherein the activated charcoal is in the form of a tablet.
8. The composition of Claim 4 wherein the activated charcoal is in the form of an aqueous slurry.
PCT/US1987/000813 1986-04-14 1987-04-08 Composition and method for reducing blood alcohol content WO1987006135A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US85280486A 1986-04-14 1986-04-14
US852,804 1986-04-14

Publications (1)

Publication Number Publication Date
WO1987006135A1 true WO1987006135A1 (en) 1987-10-22

Family

ID=25314262

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1987/000813 WO1987006135A1 (en) 1986-04-14 1987-04-08 Composition and method for reducing blood alcohol content

Country Status (3)

Country Link
EP (1) EP0264430A1 (en)
AU (1) AU7308087A (en)
WO (1) WO1987006135A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015008101A1 (en) 2013-07-15 2015-01-22 Schaumlöffel Rolf A Composition of a drink for enhanced reduction of blood alcohol level
EP3357541B1 (en) 2017-02-06 2021-03-31 Italfarmacia S.r.l. Methylsulfonylmethane composition for reducing blood alcohol content

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1589081A (en) * 1919-12-05 1926-06-15 Adler Rudolf Adsorptive charcoal for medicinal purposes
US3917821A (en) * 1973-10-23 1975-11-04 Milton Manes Palatable activated carbon
US4594249A (en) * 1985-06-14 1986-06-10 21St Century Marketing, Inc. Method of altering intoxicating effects of alcohol

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1589081A (en) * 1919-12-05 1926-06-15 Adler Rudolf Adsorptive charcoal for medicinal purposes
US3917821A (en) * 1973-10-23 1975-11-04 Milton Manes Palatable activated carbon
US4594249A (en) * 1985-06-14 1986-06-10 21St Century Marketing, Inc. Method of altering intoxicating effects of alcohol

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Acta Pharmaocol., Vol. 2 issued 1946, (ANDERSEN), "Experimental Studies on the Pharmaclogy of Activated Charcoal", see pages 69-78. *

Also Published As

Publication number Publication date
EP0264430A1 (en) 1988-04-27
AU7308087A (en) 1987-11-09

Similar Documents

Publication Publication Date Title
US4193985A (en) Multiple-units drug dose
CA2587924C (en) Oral compositions for absorption of phosphorus compounds
EP2222314B1 (en) Uses and means for otaining bronchorelaxation
JPS627169B2 (en)
EP2048948A2 (en) Liquid compositions of calcium acetate
EP0125634B1 (en) Use of a secretolytically active substance for the manufacture of a remedy against snoring and for combating snore phenomenon
US20100272814A1 (en) Method and means for producing bronchorelaxation
RU2384339C2 (en) Application of simethicon for patients predisposed to constipation
WO1995017889A1 (en) Therapeutic composition for hyperparathyroidism of patient subjected to artificial dialysis
EP1539156B1 (en) Liquid dosage forms of acid labile drugs
JPH0729916B2 (en) Pharmaceutical composition having analgesic properties
US5397573A (en) Laxative compositions
US6576665B2 (en) Encapsulated calcium acetate caplet and a method for inhibiting gastrointestinal phosphorous absorption
WO2016120787A1 (en) Oral n-acetylcysteine in the treatment of upper respiratory tract infections and symptoms
US4608258A (en) Medicament for treatment of diarrhea
WO1987006135A1 (en) Composition and method for reducing blood alcohol content
US6165482A (en) Gastrointestinal drug composition
JPH0142927B2 (en)
US20120045526A1 (en) Pharmaceutical compound which includes clinoptilolite
WO1994005273A1 (en) Gastrointestinal compositions containing dimethylsulfone and dimethylsulfoxide
JP3751987B2 (en) Hangover prevention or improvement agent
KR100208969B1 (en) Anti-ulcers drug containing extract from chap-rice
CN101406496A (en) Prescription for treating prostatitis and other reproductive system diseases of male
CH694687A5 (en) Drugs to treat viral infections from Vernonia Oligocephalus.
KR840001449B1 (en) A novel poroces and carbonaceous product

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AT AU BG CH DE DK FI GB HU JP KP KR NL NO RO SE SU

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): AT BE CH DE FR GB IT NL SE

REG Reference to national code

Ref country code: DE

Ref legal event code: 8642