Abstract:
Present invention relates to a herbal composition for the treatment of urolithiasis (kidney stones), and prophylaxis of re-formation of stones after passing them, for the treatment of gout, and for inhibition of excessive amount of salts (urates, oxalates, phosphates, carbonates) in kidneys, for the treatment of dysuria phenomenon (pollakiuria, strangury, dysuria, nycturia, low urinary pressure and urinary continence), and of urinary and biliary tract spasm, spastic colitis, different poisoning types (drugs, alcohol, medications, food poisoning), for the treatment of asymptomatic bacteriuria and for the treatment of urinary tract infections (cystitis, urethritis, pyelonephritis etc.), wherein its production is disclosed by using herbal composition comprising Equisetum arvense at a concentration of 3%-67% by weight, spergularia rubra at a concentration of 2%-38% by weight, peumus boldus at a concentration of 1.5%-32% by weight, opuntia ficus indica at a concentration of 1 %-20% by weight, sideritis angustifolia at a concentration of 1 -20% by weight, rosmarinus officinalis at a concentration of 1-20% by weight, cynodon dactylon at a concentration of 1 -20% by weight and melissa officinalis at a concentration of 1 -20% by weight, and vapor distillation method.
Abstract:
The present invention relates to a method of producing Ingenol, Ingenol esters and/or Tiglian- 3-one derivatives, the method comprising the steps of: (a) culturing plant cells obtained from a plant selected from the family Euphorbiaceae in a nutrient medium in a suspension cell culture, wherein the cells produce Ingenol, one or more Ingenol esters and/or one or more Tiglian-3-one derivatives; and (b) recovering the Ingenol, the one or more Ingenol esters and/or the one or more Tiglian-3-one derivatives produced in (a). The present invention further relates to a plant suspension cell culture, wherein the cells are obtained from a plant selected from the family Euphorbiaceae, and wherein the plant cells produce Ingenol and/or one or more Ingenol ester and/or one or more Tiglian-3-one derivatives. The present invention further relates to a plant cell biomass comprising plant cells obtained from the suspension cell culture of the invention, and comprising Ingenol and/or one or more Ingenol esters and/or one or more Tiglian-3-one derivatives. Also, the present invention relates to cryopreserved cells of the plant suspension cell culture of the invention as well as to a method of producing Ingenol, Ingenol esters and/or Tiglian-3-one derivatives based on these cryopreserved cells.
Abstract:
Provided are methods of treating diarrhea, particularly malabsorption diarrhea, in neonatal, young and adult non-human animals, in which the diarrhea results from infection of the animals by Salmonella spp., such as Salmonella typhimurium, with a therapeutically effective amount of a proanthocyanidin polymer from Croton lechleri, in either enteric or non-enteric form.
Abstract:
Methods of treating adult non-human animals afflicted with diarrhea, particularly, stress-induced diarrhea, by administering to an animal in need thereof an effective amount of a pharmaceutical formulation of a proanthocyanidin polymer composition isolated from a Croton spp. or a Calophyllum spp. are provided. In particular, the adult animals include horses and camels which frequently suffer from stress-induced diarrhea and its symptoms, and the administered proanthocyanidin polymer composition is isolated from a Croton lechleri . The composition, which can be enteric or non-enteric, is administered particularly to target the intestine/gut of the animal via a mode and under conditions conducive and sufficient for providing effective treatment of diarrhea in the affected animal. Preferred modes of administration include orally providing an effective concentration of the proanthocyanidin polymer composition, e.g., via an oral paste formulation, drench, animal feed, or water bottle, to the affected animal.
Abstract:
A composition having an extract of seed of Emblica officinalis . Methods of preparing extract of seed of Emblica officinalis . An amla seed blend composition having various ratios of extracts of seeds of Emblica officinalis . Nutraceutical or pharmaceutical methods for decreasing the total cholesterol, decreasing triglyceride, decreasing blood glucose level, enhancing HDL-C levels, increasing the HDL-C level to total cholesterol ratio, lowering LDL- C levels, decreasing the CRP level, decreasing the intima media thickening, reducing hair fall in mammals especially human beings. The extract of seed of Emblica officinalis , or the amla seed blend composition is more effective compared to extracts prepared from fruits of Emblica officinalis .
Abstract:
The present invention provides a nicotine free synergistic polyherbal masticatory formulation and a process for the preparation thereof. The prepared formulation exhibits tobacco de-addiction properties and is envisaged to replace tobacco based harmful products. The formulation of the present invention is useful as a tobacco supplement or a tobacco substitute for use in smoking cessation, tobacco chewing urge and nicotine replacement therapies, which provides the user to reduce tobacco withdrawal symptoms without causing unacceptable adverse effects along with health rejuvenation being antimicrobial and antioxidant.
Abstract:
The present disclosure relates to botanical composition for treating AIDS having at least IC 50 for anti HIV-1 integrase activity of 0.1-10 microgram/milliliter, IC 50 for anti HIV-1 protease activity of 0.1 - 10 microgram/milliliter and, IC 50 for anti HIV- 1 transcriptase activity of 0.1 - 10 microgram/milliliter. The composition comprises ethanolic extracts from Antidesma acidum Retz.-root (I), Terminalia bellirica (Gaertn.) Roxb.-fruit(II) and Cyperus rotundus Linn. -rhizome (III) at a ratio of 5:4: 1 by weight. The mixture is prepared in pharmaceutical preparation as capsule, soft capsule, suspension, elixir, emulsion, tablet or film-coated tablet. When the composition is given to AIDS patients, the viral load log was found to decrease progressively within 6 months.