US20020110600A1 - Composition for treating symptoms of influenza - Google Patents
Composition for treating symptoms of influenza Download PDFInfo
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- US20020110600A1 US20020110600A1 US09/783,027 US78302701A US2002110600A1 US 20020110600 A1 US20020110600 A1 US 20020110600A1 US 78302701 A US78302701 A US 78302701A US 2002110600 A1 US2002110600 A1 US 2002110600A1
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- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 208000024891 symptom Diseases 0.000 title claims abstract description 17
- 206010022000 influenza Diseases 0.000 title claims abstract description 10
- RFWGABANNQMHMZ-UHFFFAOYSA-N 8-acetoxy-7-acetyl-6,7,7a,8-tetrahydro-5H-benzo[g][1,3]dioxolo[4',5':4,5]benzo[1,2,3-de]quinoline Natural products CC=C1C(CC(=O)OCCC=2C=C(O)C(O)=CC=2)C(C(=O)OC)=COC1OC1OC(CO)C(O)C(O)C1O RFWGABANNQMHMZ-UHFFFAOYSA-N 0.000 claims abstract description 14
- HKVGJQVJNQRJPO-UHFFFAOYSA-N Demethyloleuropein Natural products O1C=C(C(O)=O)C(CC(=O)OCCC=2C=C(O)C(O)=CC=2)C(=CC)C1OC1OC(CO)C(O)C(O)C1O HKVGJQVJNQRJPO-UHFFFAOYSA-N 0.000 claims abstract description 14
- RFWGABANNQMHMZ-HYYSZPHDSA-N Oleuropein Chemical compound O([C@@H]1OC=C([C@H](C1=CC)CC(=O)OCCC=1C=C(O)C(O)=CC=1)C(=O)OC)[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O RFWGABANNQMHMZ-HYYSZPHDSA-N 0.000 claims abstract description 14
- RFWGABANNQMHMZ-CARRXEGNSA-N oleuropein Natural products COC(=O)C1=CO[C@@H](O[C@H]2O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]2O)C(=CC)[C@H]1CC(=O)OCCc3ccc(O)c(O)c3 RFWGABANNQMHMZ-CARRXEGNSA-N 0.000 claims abstract description 14
- 235000011576 oleuropein Nutrition 0.000 claims abstract description 14
- 239000000843 powder Substances 0.000 claims abstract description 14
- 235000013500 Melia azadirachta Nutrition 0.000 claims abstract description 11
- 229940114496 olive leaf extract Drugs 0.000 claims abstract description 11
- 240000005343 Azadirachta indica Species 0.000 claims abstract description 10
- 230000001632 homeopathic effect Effects 0.000 claims abstract description 10
- 241000227129 Aconitum Species 0.000 claims abstract description 7
- 241001106067 Atropa Species 0.000 claims abstract description 7
- 244000133098 Echinacea angustifolia Species 0.000 claims abstract description 7
- 241001473306 Eupatorium perfoliatum Species 0.000 claims abstract description 7
- 235000014134 echinacea Nutrition 0.000 claims abstract description 7
- WBJZTOZJJYAKHQ-UHFFFAOYSA-K iron(3+) phosphate Chemical compound [Fe+3].[O-]P([O-])([O-])=O WBJZTOZJJYAKHQ-UHFFFAOYSA-K 0.000 claims abstract description 7
- 241001136643 Gelsemium sempervirens Species 0.000 claims abstract description 6
- 239000000284 extract Substances 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 7
- 238000000605 extraction Methods 0.000 claims description 3
- 238000004108 freeze drying Methods 0.000 claims description 3
- 238000001035 drying Methods 0.000 claims description 2
- 240000007817 Olea europaea Species 0.000 description 10
- 241000700605 Viruses Species 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 4
- 235000002725 Olea europaea Nutrition 0.000 description 4
- 230000000840 anti-viral effect Effects 0.000 description 4
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 235000001014 amino acid Nutrition 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- LXHSHPBNTMXMPF-RKLWNDDOSA-L calcium 2-[(2S,3S,4S)-3-formyl-5-methoxycarbonyl-2-methyl-3,4-dihydro-2H-pyran-4-yl]acetate Chemical compound [Ca++].COC(=O)C1=CO[C@@H](C)[C@@H](C=O)[C@@H]1CC([O-])=O.COC(=O)C1=CO[C@@H](C)[C@@H](C=O)[C@@H]1CC([O-])=O LXHSHPBNTMXMPF-RKLWNDDOSA-L 0.000 description 3
- 238000000338 in vitro Methods 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- FIKLMMHLPVXWJN-WRWORJQWSA-N Elenolic acid Chemical compound COC(=O)C1=CO[C@@H](O)C(=CC)[C@@H]1CC(O)=O FIKLMMHLPVXWJN-WRWORJQWSA-N 0.000 description 2
- 101000867232 Escherichia coli Heat-stable enterotoxin II Proteins 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 2
- 208000002193 Pain Diseases 0.000 description 2
- 206010037660 Pyrexia Diseases 0.000 description 2
- 241001354013 Salmonella enterica subsp. enterica serovar Enteritidis Species 0.000 description 2
- 229960001948 caffeine Drugs 0.000 description 2
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 239000012141 concentrate Substances 0.000 description 2
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 2
- 229960002179 ephedrine Drugs 0.000 description 2
- 229930182478 glucoside Natural products 0.000 description 2
- 150000008131 glucosides Chemical class 0.000 description 2
- 238000001727 in vivo Methods 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 208000015181 infectious disease Diseases 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 230000003253 viricidal effect Effects 0.000 description 2
- 102000004506 Blood Proteins Human genes 0.000 description 1
- 108010017384 Blood Proteins Proteins 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 102000004190 Enzymes Human genes 0.000 description 1
- 108090000790 Enzymes Proteins 0.000 description 1
- 241001113926 Gelsemium Species 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- HNDVDQJCIGZPNO-YFKPBYRVSA-N L-histidine Chemical compound OC(=O)[C@@H](N)CC1=CN=CN1 HNDVDQJCIGZPNO-YFKPBYRVSA-N 0.000 description 1
- KDXKERNSBIXSRK-YFKPBYRVSA-N L-lysine Chemical compound NCCCC[C@H](N)C(O)=O KDXKERNSBIXSRK-YFKPBYRVSA-N 0.000 description 1
- 102000007330 LDL Lipoproteins Human genes 0.000 description 1
- 108010007622 LDL Lipoproteins Proteins 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 244000237986 Melia azadirachta Species 0.000 description 1
- 241000207836 Olea <angiosperm> Species 0.000 description 1
- 206010044565 Tremor Diseases 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 239000012675 alcoholic extract Substances 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- 229940082880 azadirachta indica flower extract Drugs 0.000 description 1
- 238000002512 chemotherapy Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 241000411851 herbal medicine Species 0.000 description 1
- HNDVDQJCIGZPNO-UHFFFAOYSA-N histidine Natural products OC(=O)C(N)CC1=CN=CN1 HNDVDQJCIGZPNO-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000002018 neem oil Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000036407 pain Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 230000003389 potentiating effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 208000010110 spontaneous platelet aggregation Diseases 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000021 stimulant Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/28—Asteraceae or Compositae (Aster or Sunflower family), e.g. chamomile, feverfew, yarrow or echinacea
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/56—Loganiaceae (Logania family), e.g. trumpetflower or pinkroot
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/58—Meliaceae (Chinaberry or Mahogany family), e.g. Azadirachta (neem)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/63—Oleaceae (Olive family), e.g. jasmine, lilac or ash tree
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/71—Ranunculaceae (Buttercup family), e.g. larkspur, hepatica, hydrastis, columbine or goldenseal
- A61K36/714—Aconitum (monkshood)
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/185—Magnoliopsida (dicotyledons)
- A61K36/81—Solanaceae (Potato family), e.g. tobacco, nightshade, tomato, belladonna, capsicum or jimsonweed
Definitions
- the invention relates to the field of natural compositions, particularly herbal compositions, for treating symptoms of influenza.
- Oleuropein is a bitter glucoside found in olives and the roots, leaves and bark of the olive tree, Olea europaea .
- Medicinal use of this extract dates back to the early 1800s when it was used in liquid form as a treatment for malarial infections.
- Oleuropein undergoes mild acid hydrolysis to form elenolic acid, this process being similar to an enzyme based hydrolysis of the compound which takes place in the human body.
- a salt of elenolic acid, calcium elenolate was reported to have in vitro antiviral activity in an article by Renis, “In Vitro Antiviral Activity of Calcium Elenolate,” Antimicrobial Agents and Chemotherapy 10 1969, pages 167-172. In this article, calcium elenolate was reported to have activity against a wide variety of viruses, with the greatest activity under alkaline conditions (pH 7.5).
- U.S. Pat. No. 5,714,150 discloses a method for extracting oleuropein from olive leaves in a form which retains medicinal activity in vivo, with multiple extractions taking place with a hydroethanolic solvent, followed by distillation under vacuum to produce and concentrate, and then drying. The steps take place at about 20 to 88° C.
- the invention is directed to a composition for relief of symptoms of colds and influenza, comprising, by weight, about 80-88% olive leaf extract powder containing oleuropein, about 5-10% neem leaf powder and about 4-8% of a homeopathic blend for symptom relief, and which preferably comprises one or more components from the group aconitum napelius, belladonna, eupatorium perfoliatum, gelsemium sermpervirens, Echinacea angustifolia and ferrum phosphoricum.
- the invention also relates to a method of substantially eliminating or ameliorating the symptoms of viral and microbial illness of human patients comprising administering to a human patient in need of thereof an effective amount of a composition such as set forth above.
- the major ingredient of the composition of the invention is an olive leaf extract powder, the olive leaf preferably extracted according to the disclosure of U.S. Pat. No. 5,714,150, which is incorporated herein by reference.
- olive leaves are treated with an alcohol and water solution to produce an alcoholic extract, the alcohol and water solution is drained from the olive leaves, the olive leaves are treated with fresh alcohol and water solution at least two more times, the hydroethanolic extracts produced are then combined and distilled under vacuum at a temperature of about 20° to 88° C. to produce a concentrated extract having a solids content of about 30 to 40%.
- the concentrated extract can then be spray dried or oven dried under vacuum to produce a dry powder extract comprising approximately 30-40% by weight oleuropein.
- these process steps must be conducted at a temperature no greater than about 88° C., since destruction of the effective glucoside is thought to occur at higher temperatures. It is thought that by conducting a plurality of low temperature hydroethanolic extractions followed by a low temperature distillation, the resultant oleuropein contains a high proportion of R-oleuropein as compared with L-oleuropein, the d-oleuropein not binding to amino acids or serum proteins in the human body, and therefore remaining active in vivo.
- the olive leaf concentrate can also be dried by freeze drying. Applicants believe that a more potent extract can be obtained by freeze drying.
- the composition of the invention will contain about 80-88% by weight olive leaf extract powder, preferably about 84-86% by weight.
- composition of the invention will also contain about 5-10% by weight neem leaf extract.
- the neem tree also known as Azadiracha indica , has for many centuries been a source of herbal medicines on the Indian subcontinent.
- a number of uses for neem extracts are known, including the use of neem oil as an insect repellant (U.S. Pat. No. 5,885,600) and the use of neem extract for healing the skin (U.S. Pat. No. 6,126,950).
- composition of the invention contains about 5-10% by weight of a hydroethanolic extract of neem leaf, dried to a powder form.
- This material is available commercially from, for example, Rym Exports of Worli, Mumbai, India.
- the composition of the invention also contains up to about 8% by weight of a homeopathic blend useful in reducing symptoms of colds and fevers.
- a preferred blend contains aconitum napelius , belladonna, eupatorium perfoliatum, gelsemium sempervirens, Echinacea angostifolia and ferrum phosphoricum.
- Aconitum napelius, belladonna and ferrum phosphoricum are used for treatment of fever
- eupatorium perfoliatum and gelsemium sempervirens are used to relieve symptoms of aches and pains, headaches and trembling
- Echinacea angustifolia is used for treatment of infections.
- This blend is typically added in an amount of about 6-8% by weight.
- Other blends including some of the above materials, or other material for the same general purposes may also be used in effective amounts.
- compositions of the invention will typically contain pharmaceutically acceptable excipients of the type well known in the art necessary for proper tableting of the composition. Such excipients may make up about 10-20% by weight of the final tablet.
- a typical tablet or capsule according to the invention will contain about 500 mg olive leaf extract powder, 50 mg neem leaf extract powder and 40 mg of the homeopathic blend, all weights ⁇ 10%.
- the adult dosage of this composition is 2 tablets or capsules, 4 times a day, at the first sign of a cold or flu, taken with a large quantity of water. While symptoms may disappear rapidly, the treatment should be continued for at least three days for best effect.
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- Health & Medical Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Engineering & Computer Science (AREA)
- Mycology (AREA)
- Microbiology (AREA)
- Medical Informatics (AREA)
- Botany (AREA)
- Biotechnology (AREA)
- Alternative & Traditional Medicine (AREA)
- Medicines Containing Plant Substances (AREA)
Abstract
Description
- The invention relates to the field of natural compositions, particularly herbal compositions, for treating symptoms of influenza.
- Colds and influenza are major causes of illness and loss of productivity both within the United States, and throughout the world at large. Approximately 10-15% of adult colds are thought to be caused by viruses which are also responsible for other serious illnesses, including influenza.
- An effective treatment for a wide variety of illnesses caused by viruses and bacteria has long been sought, both in terms of antiviral and antimicrobial action, and in terms of symptom relief. Some traditional Chinese medicine herbal formulas have been found somewhat effective in this regard, as is disclosed, for example, in U.S. Pat. Nos. 5,834,000, 5,989,556 and 6,083,291. Some of the traditional compositions have contained stimulants such as caffeine and ephedrine, which have proved to be undesirable.
- One material which has been found to have antiviral properties is oleuropein. Oleuropein is a bitter glucoside found in olives and the roots, leaves and bark of the olive tree, Olea europaea. Medicinal use of this extract dates back to the early 1800s when it was used in liquid form as a treatment for malarial infections. Oleuropein undergoes mild acid hydrolysis to form elenolic acid, this process being similar to an enzyme based hydrolysis of the compound which takes place in the human body. A salt of elenolic acid, calcium elenolate, was reported to have in vitro antiviral activity in an article by Renis, “In Vitro Antiviral Activity of Calcium Elenolate,” Antimicrobial Agents and Chemotherapy 10 1969, pages 167-172. In this article, calcium elenolate was reported to have activity against a wide variety of viruses, with the greatest activity under alkaline conditions (pH 7.5).
- However, when incubation was carried out with amino acids prior to incubation with virus, losses in virucidal activity were detected, especially in the presence of glycine, lysine, cysteine and histidine, and to a lesser extent with other amino acids. More recently, oleuropein has been found to be effective, in-vitro, against Salmonella enteritidis (“Inhibition of Salmonella enteritidis by oleuropein in broth and in a model foodsystem,” Lett Appl Microbiol 20(2):120-4, February 1995), and enterotoxin B (“The effect of the olive phenolic compound, oleuropein, on growth and enterotoxin B production,” J. Appl. Bacteriology 74(3):253-9, March 1993). In addition, oleuropein has been found to protect low density lipoprotein from oxidation (Life Sci 55(24):1965-71, 1994) and to inhibit platelet aggregation (Thromb Res 78(2):151-60, Apr. 15, 1995). U.S. Pat. No. 5,714,150 discloses a method for extracting oleuropein from olive leaves in a form which retains medicinal activity in vivo, with multiple extractions taking place with a hydroethanolic solvent, followed by distillation under vacuum to produce and concentrate, and then drying. The steps take place at about 20 to 88° C.
- It is therefore an object of the invention to provide a pharmacologically effective composition which is effective against a broad spectrum of viruses and bacteria.
- It is another object of the invention to provide a composition which is completely plant based in nature and does not contain caffeine, ephedrine, or similar undesirable components.
- It is a further object of the invention to provide a composition which alleviates symptoms of colds and influenza.
- To achieve these and other objects, the invention is directed to a composition for relief of symptoms of colds and influenza, comprising, by weight, about 80-88% olive leaf extract powder containing oleuropein, about 5-10% neem leaf powder and about 4-8% of a homeopathic blend for symptom relief, and which preferably comprises one or more components from the group aconitum napelius, belladonna, eupatorium perfoliatum, gelsemium sermpervirens, Echinacea angustifolia and ferrum phosphoricum.
- The invention also relates to a method of substantially eliminating or ameliorating the symptoms of viral and microbial illness of human patients comprising administering to a human patient in need of thereof an effective amount of a composition such as set forth above.
- The major ingredient of the composition of the invention is an olive leaf extract powder, the olive leaf preferably extracted according to the disclosure of U.S. Pat. No. 5,714,150, which is incorporated herein by reference. In that process, olive leaves are treated with an alcohol and water solution to produce an alcoholic extract, the alcohol and water solution is drained from the olive leaves, the olive leaves are treated with fresh alcohol and water solution at least two more times, the hydroethanolic extracts produced are then combined and distilled under vacuum at a temperature of about 20° to 88° C. to produce a concentrated extract having a solids content of about 30 to 40%. The concentrated extract can then be spray dried or oven dried under vacuum to produce a dry powder extract comprising approximately 30-40% by weight oleuropein.
- Importantly, these process steps must be conducted at a temperature no greater than about 88° C., since destruction of the effective glucoside is thought to occur at higher temperatures. It is thought that by conducting a plurality of low temperature hydroethanolic extractions followed by a low temperature distillation, the resultant oleuropein contains a high proportion of R-oleuropein as compared with L-oleuropein, the d-oleuropein not binding to amino acids or serum proteins in the human body, and therefore remaining active in vivo.
- In keeping with the low temperature processing requirements, the olive leaf concentrate can also be dried by freeze drying. Applicants believe that a more potent extract can be obtained by freeze drying. The composition of the invention will contain about 80-88% by weight olive leaf extract powder, preferably about 84-86% by weight.
- The composition of the invention will also contain about 5-10% by weight neem leaf extract. The neem tree, also known as Azadiracha indica, has for many centuries been a source of herbal medicines on the Indian subcontinent. A number of uses for neem extracts are known, including the use of neem oil as an insect repellant (U.S. Pat. No. 5,885,600) and the use of neem extract for healing the skin (U.S. Pat. No. 6,126,950).
- The composition of the invention contains about 5-10% by weight of a hydroethanolic extract of neem leaf, dried to a powder form. This material is available commercially from, for example, Rym Exports of Worli, Mumbai, India.
- Preferably, the composition of the invention also contains up to about 8% by weight of a homeopathic blend useful in reducing symptoms of colds and fevers. A preferred blend contains aconitum napelius, belladonna, eupatorium perfoliatum, gelsemium sempervirens, Echinacea angostifolia and ferrum phosphoricum. Aconitum napelius, belladonna and ferrum phosphoricum are used for treatment of fever, eupatorium perfoliatum and gelsemium sempervirens are used to relieve symptoms of aches and pains, headaches and trembling, and Echinacea angustifolia is used for treatment of infections. This blend is typically added in an amount of about 6-8% by weight. Other blends including some of the above materials, or other material for the same general purposes may also be used in effective amounts.
- In addition to the above ingredients, the compositions of the invention will typically contain pharmaceutically acceptable excipients of the type well known in the art necessary for proper tableting of the composition. Such excipients may make up about 10-20% by weight of the final tablet.
- A typical tablet or capsule according to the invention will contain about 500 mg olive leaf extract powder, 50 mg neem leaf extract powder and 40 mg of the homeopathic blend, all weights ±10%. The adult dosage of this composition is 2 tablets or capsules, 4 times a day, at the first sign of a cold or flu, taken with a large quantity of water. While symptoms may disappear rapidly, the treatment should be continued for at least three days for best effect.
- While not wishing to be held to any particular theory, Applicants recognize that various olive extracts have been known to be effective against viruses for many years, and the neem leaf which has been long used in Asia for symptom relief, is thought to provide additional bacteriacidal and virucidal properties.
Claims (9)
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| Application Number | Priority Date | Filing Date | Title |
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| US09/783,027 US6455070B1 (en) | 2001-02-15 | 2001-02-15 | Composition for treating symptoms of influenza |
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| US09/783,027 US6455070B1 (en) | 2001-02-15 | 2001-02-15 | Composition for treating symptoms of influenza |
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| WO2010130869A1 (en) * | 2009-05-14 | 2010-11-18 | Sanidad Y Residencias 21, S. A. | Use of olive leaf extracts in a pharmaceutical composition for inducing angiogenesis and vasculogenesis |
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