Title of Invention	AN EDIBLE THERAPEUTIC HERBAL COMPOSITION FOR TREATING HYPERGLYCEMIA
Abstract	The present invention provides a process of Therapeutic/ Edible composition for treating hyperglycemia, comprising herbs Prunus amygdalus of concentration of about 30% w/w, Ocimum sanctum of concentration of about 20% w/w, Azadirachta indica of concentration of about 20% w/w, Aegle marelose of concentration of about 15% w/w and Vitus vinefera of concentration of about 15% w/w.

Full Text

AN EDIBLE THERAPEUTIC HERBAL COMPOSITION FOR TREATING HYPERGLYCEMIA Field of Invention The present invention relates to an edible therapeutic herbal composition for treating hyperglycemia agent for lowering the blood glucose levels in mammals, especially humans, suffering from diabetic mellitus. Background of the Invention Diabetes mellitus is an insidious medical condition for which there is no permanent cure. Across the globe many humans are suffering with this disease and with its implications such as heart attacks, strokes, loss of eyesight, difficulty in wound healing, more susceptible to disorders of aging and such conditions worsening to death. The onset of diabetes can occur in early age of life although many people are getting in much later par! of life. The medical condition of diabetes characterized by the inability of the pancreas gland to secrete "insulin". Insulin is produced in the body by the beta cells of pancreas gland and helps in the metabolism of glucose to produce the energy required by the humans. In the diabetic patients the pancreas gland deteriorates and the beta cells arc loo small and insufficiently numerous to produce a proper amount of insulin. Hence the sugar is not properly metabolized to produce energy. As a result, diabetic patient experience an elevated levels of sugar in the blood. The diabetes can be broadly categorized into IDI ).\1 and N1DDM. Roughly "IDDM" refers to insulin dependent diabetes mellitus or type I wherein, anti-bodies destroy .beta.-cells of islets of Langerhans which produce insulin and hence very low and no insulin levels in the circulation. In NIDDM there is no loss or moderate reduction in .beta.-cell mass and is due to abnormality in gluco-receptor of .beta.-cells, reduced sensitivity of peripheral tissues to insulin. The conventional treatment of IDDM involves the administration of insulin to a patient typically by means of injections. These injections must be performed on a regular basis and are normally administered by an hypodermic needle. This is inconvenient to a patient since the administration of insulin using hypodermic needle requires both a suitable place and time to perform the injection, apart from a great deal discomfort to the patient. Also, if the amount of insulin is excessive for amount of sugar in the blood, the patient can undergo insulin shock. If a patient is unwilling or not able to accept insulin injections, pharmaceutical preparations containing oral antidiabetic drugs such as sulfonylureas (Glibinclamide, Gliquidone etc.) or biguanides (metformin, phenformin) or insulin sensitizers such as troglitozones could be taken. All in all, the patient is constantly on the narrow edge of either too much or insufficient medication and frequently is not able to tolerate such medication because of its side effects. To control proper blood sugar levels there by controlling this dysfunction so as prevent eventual complications, insulin independent diabetics must maintain a regulated diet control and exercise. Unfortunately most of the diabetics experience to great of difficulty to follow such restrictions leading to worsening of associated complications. Further more, treating with insulin never cures this disorder and there is an urgent need to treat this disease with natural products, which have the advantages of patient compliance and least side effects compared to synthetic medicines. The usage of herbs in the treatment of medical ailments has been a tradition in many countries like India, china etc for so many years, and several diseases can be cured without any side effects. Hypoglycemic efficacy of different parts of Azadirachta indica was evaluated by different researchers (Sonia & Srinivas, 1999, Santoshkumari and Devi, 1990, Murty et.al., 1978, Dixit et.al., 1986, Shukla et.al., 1973, Jain, 1984). Hypoglycemic effects of (-)-epicatchin (Chakravarthy et. al. 1982), Gymnesma sylvestre (Asha et. al. 1981), Trigonella foenum graecum (Khosla et. al. 1995) have been reported. Herbal composition containing different compositions of Trigonella foenum graecum, Nigella saliva, Orgnanum vulgare, Rosmarinus officinalis, Lupinusterms, Lawsonia inermis and Foemiculum vulgare and methods to treat diabetes mellitus were described in USPTO 6,042,834 (Baraka,2000). Hypoglycemic extracts for treating diabetes which were obtained from different species of genus Eugena of myrtaceae family were disclosed in USPTO Pub. No. US 2001/0021401 Al (Sharma et.al. 2001). Similarly medicinal compositions, described as pancreas tonic, containing Epicatechin (pterocarpus marsupium), gymnemic acid (gymnema sylvestre) along with other plant products such as Cinnamomum tamala, Momardica charantia, Aegle marelose, Syzygium cumini, Trigunella foenum graceum and Azadirachta indica, Tinospora cordifolia, Ficus racemosa was described in US application 5,886,029 (Dhaliwal,1999). A different herbal edible composition containing Syzygim cumini, Gymne sylvestre, Momordica charantia and Solanum melogena was described in US PTO 5,900,240 (Tomer et.al. 1999). Patent Documents : 1. Dhaliwal, K.S. 1999. Method and composition for treatment of diabetes. US PTO 5, 886, 029. 2. Baraka,M.W. 2000. Herbal composition for diabetes and method of treatment. US PTO 6, 042, 834. 3. Tomer, O.S., Peter Glomski, Kripanath Borah, 1999. Herbal compositions their use as hypoglycemic agents. US PTO 5, 900, 240. 4. Sharma, Suman Bala., Pothapragada Suryanarayana, Kurthy, Krishan Madhav Prabhu, Afreena Nasir, 2001. Process for the preparation of an herbal-therapeutic product extracted from the pulp of a species Eugenia jambolana. US Pub. No. 2001/0021401 Al. References: 1. Asha N. Baimi. Studies on Protein-Bound Polysaccharide Components & Glycosaminoglycans in Experimental Diabetes—Effect on Gymnema sylvestre. Ind. J. Exp. Biol. 1981, 19 : 715-721. 2. Chakravarthy, B.K. Functional Beta Cell Regeneration in the Islets of Pancreas in Alloxan Induced Diabetic Rats by (-)-Epicatechin. Life Sciences. 1982, 31 : 2693-2697. 3. Dixit, V.P., Sinha R., Jank R. Effect of Neem seed oil on the blood glucose concentration of normal and alloxan induced diabetic rats. J. Ethnopharmacol. 1986, 17 : 95 - 8. 4. Jain, G. Pharmacological profile of Azadirachta indica : A study. M. Pharm. Thesis. Delhi Universit. 1984. 5. Khosla P. Effect of Trigonella foenum graecum (Fenugreek) on Blood Glucose in Norman and Diabetic Rats. Ind. J. Phy. Pharma. 1995, 39 (2), 173-174. 6. Murty, K.S., Rao, D.N.I., Rao, O.K., Murty, L.B.G. A preliminary study on hypoglycaemic and anti hyperglycaemic effect of Azadirachta indica. Indian J. Pharmacol. 1978, 10 : 247 - 50. 7. Santoshkumari, K.S., Devi, K.S. Hypoglycaemic effects of medicinal plants. Ancient Sci. Life. 1990, 9 : 221 -3. 8. Shukla, R., Singh, S., Bhandari, C.R. Preliminary clinical trials on antidiabetic actions of Azadirachta indica. Medicine and Surgery. 1973, 134: 11-2. Sonia Bajaj, Srinivasan, B.P. Investigations into the anti-diabetic activity of Azadirachta indica. Ind. J. Pharmacol. 1999, 31 : 138 - 141. Objects of the invention: The main object of the present invention is to provide a herbal composition of medicinal or edible nature to treat diabetic patients for controlling diabetes mellitus without any side effects. Another object is to provide a herbal composition which is inexpensive and easily digestible. Summary of the invention: The invention provides an edible therapeutic herbal composition useful as a hypoglycemic agent, comprising a mixture of at least three herbs selected from the group consisting Prunus amygdales, Ocimum sanctum, Azadirachta indica, Aegle marelose and Vitus vinefera, in therapeutically effective amounts. In an embodiment, the herbal composition comprises 15-40% w/w of each of the three herbs. In another embodiment, the composition is formulated as oral dosage forms comprising solutions, suspensions, emulsions, gels, pastes, elixirs, viscous colloidal dispersions, tablets, capsules and / or oral control release types or such delivery forms suitable for oral route. In still another embodiment, the herbs are selected from dried fruits of Prunus amygdalus, leaves of Ocimum santum, leaves of Azaidarchta indica, leaves ofAgilo marelose and fruits of Vitus vine/era. In another embodiment, the invention provides a method of treatment for hyperglycemia in humans and animals, comprising the step of oral administration of herbal composition comprising a mixture of at least three herbs selected from the group consisting Prunus amygdales, Ocimum sanctum, Azadirachta indica, Aegle marelose and Vitus vinefera, in therapeutically effective amounts. In yet another embodiment, the herbal composition is administered before food. In another embodiment, the herbal composition may be administered along with diet of the patient. In still another embodiment, the composition is administered in a dosage form containing 0.01-0.5 gm/Kg. of the composition. In another embodiment, the invention provides a method for reducing the blood glucose level in a mammal which comprises of a therapeutically effective amount of the composition of the invention. Detailed description of the invention: The present invention provides a composition consisting of five different herbs for treatment and controlling diabetes mellitus, more particularly to non-insulin dependent diabetics. This herbal composition consists of Prunus amygdales, Ocimum sanctum, Azadirachta indica, Aegle marelose and Vitus vinefera. These plants may be found in various places in the world. The composition containing mixture (Composition Fl in Table 1) of dried form of leaves of Azadirachta indica, leaves of Ocimum sanctum, fruit of Prunus amygdalus, leaves of Aegle marelose and fruit of Vitus vinefera is particularly preferred. In another embodiment of the present invention, the active ingredients are taken from the any parts of the plants mentioned as above. The ratio of each ingredient is not very critical and 15-40% w/w of one ingredient is taken and is balanced with the ingredients of at least two to all four herbs. The dietary compositions are made with dried plant parts after proper milling to get fine powder and formulated to suitable oral dosage forms. By using these five different herbs, various compositions (F1-F9) were prepared comprises compositions with 15-40% w/w of all or at least three herbs. The plant ingredients are either in raw form or as medicinal extract of plant parts, and are administered to experimental subjects (both diabetic and normal rats with elevated blood glucose levels and non-insulin dependent diabetic humans) at a dose of 0.01 - 0.5 gm/Kg body weight. The dosage to be administered is not critical and could be varied depending on status of the disease, diet of the subjects and nature of the subjects (animal or human), age, sex, bodyweight, and physical condition. The dose of dietary compositions made of raw ingredients is little higher than those obtained by extraction procedures, and overdoses of these dietary compositions is not a problem. The extraction methods are known to the person skilled in the art. Generally a subject receives their own dose after some initial dosing to maintain normoglycaemia and then such doses will be continued until some steady states are obtained. The herbal compositions were preferably in suspension form. The herbs were milled to fine powder, mixed and then prepared suspension with distilled water. The powder can be used to prepare different oral dosage forms. Although ingredients of compositions itself has good product stability characteristics, the herbal composition may contain some inert ingredients as required for oral dosage forms. Although, suitable oral dosage forms are formulated and administered, the preferable dosage form is a suspension of the said herbal composition. The mechanism by which the herbal composition of the invention operates is not exactly understood. However it is assumed that the herbal composition stimulates the pancreas to make its own insulin or assists in some healing mechanism of the diseased pancreatic tissue. The herbs are stimulant to the pancreas and cause the cells of the pancreas to respond and to recommend production of insulin. Since this composition of present invention is holistic in nature and represent in dietary supplements and hence overdosing would not be a problem. And there are no dangers or side effects associated with treatment with this herbal remedy of the invention. The herbal composition also produces beneficial effects such as diuretic, stomachic, antiulcers. Brief description of the accompanying drawings: Figure-1. Describes the effect of herbal formulation and glibenclamide on oral glucose tolerance tests in rats. The invention is described in detail herebelow by the following examples which are meant to illustrate the invention and should not be construed as limitations Compositions Various compositions with permutations and combination were tried (Table-1) using Azadirachta indica.Prunus amygdales, Ocimum sanctum , Aegle marmelos and EXAMPLE-1 Male albino rats of wistar strains (150-200 g) were used throughout the studies. Rats were divided into eleven groups of each containing 6 rats. These animals were randomly assigned to the following groups which include (A) control group, (B) standard group (glibenclamide, 3mg/Kg) and (C) test groups (F1-F9). Diabetes was induced by injecting streptozocin (STZ) in a dose of 65 mg/kg intra venous in 0.1M citrate buffer. Rats were kept fasted overnight but were given water ad libitum. After 48 hours of STZ injection, blood samples were taken from tail vein of conscious rats. The blood was centrifuged at 5000 rpm for 10 minutes in an eppendorf tubes containing EDTA (1 mg/ml of blood). Plasma glucose estimations were done by glucose oxidase method by using Auto blood analyzer (Techinicon RA- 100, Bayer Diagnostics, Ireland). Animals with blood glucose level more than 250% of the fasting level were considered to be diabetic and were used for the experiment. Group A was given normal saline, group B was given glibenclamide and various groups of C were given herbal compositions for 15 days at least once in day. Blood was collected from tail veins of all the rats after 7 days and 15 days of treatment and glucose levels were estimated as described previously (Table 2). The statistical analysis was performed using Prism program (Graphpad software). ANOVA with post Newman - Keul test with P values was used to compare the treatment efficacy between the test groups. Significantly higher compared to control group (P Significant anti-diabetic activity was found in the compositions tested. Fl was found to be most effective out of all the composition tested, which is significantly higher than standard groups, although other groups showed considerable activity. EXAMPLE 2: GLUCOSE TOLERANCE TEST (GTT) From the above STZ induced diabetic model the composition 1 has chosen for GTT study. Male albino rats of wistar strains (150-200 g) were used. They were divided into three groups each containing 6 rats. They were randomly assigned A) control group B) standard group (glibenclamide) C) test group. Group A was given saline, group B was given glibenclamide (3 mg/Kg) and group C was given test compositions. After 2 hours all rats were loaded with glucose with a dose of 5g/kg. Blood samples were taken from tail vein of conscious rats for every 30 minutes up to 3 hours. Plasma glucose estimations were done by glucose oxidase method by using Auto Blood Analyzer as described in Figure 1. The statistical analysis was performed using Prism program (Graphpad software). Annova with post Newman - Keul test with P values was used to compare the treatment efficacy between the test groups. Although activity of the test composition is significantly higher, both composition Fl and glibenclamide showed increased (P compared to control group. EXAMPLE-3 In this example the composition-1 was tested on humans. Five non-insulin dependent diabetic male patients aged 45-55 years old and an average body weight of 68 ±5 kg were given composition Fl at a dose of 0.1 gm/Kg for 30 days daily in 3 divided doses, half and hour before breakfast, lunch and dinner. The fasting blood glucose level was monitored for every five days starting from day zero. The results of this test are shown in table-3. Considerable reduction in the blood glucose levels were observed in all the individuals although the response varied significantly. It is concluded that some changes in dosage regime and diet would give a proper control of diabetes in non-insulin dependent diabetic patients. It is assumed that, these herbal compositions could be used in type I diabetic patients along with insulin therapy as ingredients of this compositions could increased peripheral insulin sensitivity, and hence insulin dose could be reduced. We Claim: 1. An edible therapeutic herbal composition for treating hyperglycemia, comprising herbs Primus amygdalus of concentration 30% w/vv, Ocimum sanctum of concentration 20% w/w, Azadirachta indica of concentration 20% w/vv, Aegle marelose of concentration 15% w/w, and Vitus vinefera of concentration 15% w/w. 2. A composition as claimed in claim 1, wherein the herbs are selected from dried fruits of Primus amygdalus, leaves of Ocimum sanctum, leaves of A/adinicliki indica, leaves of Aegle marelose, and fruits of Vitus vinefera. 3. An edible therapeutic herbal composition for treating hyperglycemia substanliallv as herein describe with reference to examples accompanying this specification.

Documents:

2183-DELNP-2004-Abstract-(15-12-2008).pdf

2183-DELNP-2004-Abstract-(27-03-2009).pdf

2183-delnp-2004-abstract.pdf

2183-DELNP-2004-Claims-(15-12-2008).pdf

2183-DELNP-2004-Claims-(27-03-2009).pdf

2183-delnp-2004-claims.pdf

2183-DELNP-2004-Correspondence-Others-(15-12-2008).pdf

2183-DELNP-2004-Correspondence-Others-(18-12-2008).pdf

2183-DELNP-2004-Correspondence-Others-(27-03-2009).pdf

2183-delnp-2004-correspondence-others.pdf

2183-DELNP-2004-Description (Complete)-(27-03-2009).pdf

2183-delnp-2004-description (complete).pdf

2183-DELNP-2004-Drawings-(27-03-2009).pdf

2183-delnp-2004-drawings.pdf

2183-DELNP-2004-Form-1-(27-03-2009).pdf

2183-delnp-2004-form-1.pdf

2183-delnp-2004-form-18.pdf

2183-DELNP-2004-Form-2-(15-12-2008).pdf

2183-DELNP-2004-Form-2-(27-03-2009).pdf

2183-delnp-2004-form-2.pdf

2183-DELNP-2004-Form-3-(15-12-2008).pdf

2183-delnp-2004-form-3.pdf

2183-delnp-2004-form-5.pdf

2183-DELNP-2004-Petition-137-(15-12-2008).pdf