Embodiments of the present invention were conceived and reduced to practice without Federal sponsorship or funding.
Embodiments of the present invention are directed to articles of manufacture in the form of formulations and methods of treatment of morning sickness.
Morning sickness is a condition in which pregnant women experience nausea especially in the first trimester of pregnancy. A number of medicaments have also been used in the past to treat deficiencies of mother and fetus during pregnancy. These include folic acid. These medicaments are also associated with nausea and upset stomach.
There is a need for improved formulations which do not cause gastric distress and nausea.
Embodiments of the present invention are directed to formulations and methods of treating morning sickness and folic acid deficiency. One embodiment of the present invention is directed to a dosage form for the treatment of folic acid deficiency and morning sickness. The dosage form has an effective amount of folic acid with an effective amount of a gingerol composition to suppress nausea and/or gastric distress. The folic acid is selected from the group comprising of natural and synthetic forms of Vitamin B-9, one of the B-complex vitamins. The gingerol composition is selected from the group of gingerol compounds comprising 6-gingerol, 8-gingerol, 10-gingerol, 12-gingerol, 6-shogaol, 8-shogaol and 10-shogaol as single compositions and mixtures thereof.
One dosage form of the present invention further comprises an oil base wherein the folic acid is dispersed as a solid suspension in such oil base and said gingerol composition is dissolved in the oil base. The oil base with the folic acid and gingerol composition can be administered orally as a liquid or held in a gel cap.
Other embodiments of the present invention feature tablets and capsules formulations. By way of example without limitation, one dosage form features a gingerol composition that is used to wet a powder of the folic acid to form a gingerol wetted folic acid powder. The gingerol wetted folic acid powder is pressed into a tablet or loaded into a capsule.
Another embodiment features a dosage form wherein said folic acid and gingerol are dissolved or suspended in a solution. This solution is administered orally as a liquid.
The gingerol composition may be synthesized or is an extract from a ginger compound containing natural source. For example, without limitation, a preferred ginger compound comprises gingerols and shogoals found in an extract from Zingibier officinale. A preferred gingerol composition is present in an amount effective to promote hematopoiesis.
The folic acid is present in 400 to 800 micrograms (mcg) of folic acid for dosage forms.
A further embodiment of the present invention is directed to a method of treating folic acid deficiency and morning sickness comprising the step of administering a dosage form comprising an effective amount of folic acid with an effective amount of a gingerol composition to suppress nausea and/or gastric distress. The gingerol composition is selected from the group of gingerol compounds comprising 6-gingerol, 8-gingerol, 10-gingerol, 12-gingerol, 6-shogaol, 8-shogaol and 10-shogaol as single compositions and mixtures thereof. The folic acid is selected from the group comprising of natural and synthetic forms of Vitamin B-9, one of the B-complex vitamins.
The dosage form may take many different forms including an emulsion, dispersion or solution in oil base for administration as an oral liquid or held in gel caps. The dosage form may comprise capsules and tablets.
The dosage form preferably has, for adults, 400 to 800 mcg of folic acid.
A preferred gingerol composition is present in an amount effective to promote hematopoiesis. Thus, the gingerol composition addresses the nausea and gastric distress of folic acid and synergistically promotes hematopoiesis to treat morning sickness.
These and other features and advantages of the present invention will be apparent to those skilled in the an upon viewing the figures and reading the detailed description that follow.
Embodiments of the present invention will now be described in detail with respect to formulations and methods of treating folic acid deficiency and morning sickness as to the inventors' present best mode to practice the invention. This best mode may change over time as new considerations become known or available. Embodiments of the present invention are also subject to alterations and modifications such that the present teaching and description should not be considered limiting.
One embodiment of the present invention is directed to a dosage form for the treatment of folic acid deficiency and morning sickness. Dosage forms embodying features of the present invention are, designated by the numerals 61a, 61b, and 61c, are depicted in
Each dosage form, tablet 61a, gel cap 61b, and solution 61c, has an effective amount of folic acid with an effective amount of a gingerol composition to suppress nausea and/or gastric distress. The folic acid is selected from the group comprising of natural and synthetic forms of Vitamin B-9, one of the B-complex vitamins. Methods of making folic acid are known and the compositions can be acquired from numerous sources. The dosage form preferably has, for adults, 400 to 800 micrograms of folic acid.
The gingerol composition is selected from the group of gingerol compounds comprising 6-gingerol, 8-gingerol, 10-gingerol, 12-gingerol, 6-shogaol, 8-shogaol and 10-shogaol as single compositions and mixtures thereof. One preferred extract has 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol, in which 6-shogaol and 6-gingerol define a ratio and the ratio of 6-shogaol to 6-gingerol is 0.04 to 0.40. Although the applicant does not wish to be bound to any theory, it is believed this ratio of 6-shogaol to 6-gingerol improves the efficacy of the extract for the treatment of nausea.
A further aspect of the invention is directed to an extract of ginger rhizome wherein the ginger rhizome has a starting mass and the extract has a mass associated with one or more of the following 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol. The ratio of 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol total mass to starting mass is 20-40%.
A further aspect of the invention is directed to an extract having 15-25% 6-gingerol, 1-5% 8-gingerol, 1-5% 10-gingerol and 1-5% 6-shogaol.
Each dosage form, such as tablet 61a, gel cap 61b, and solution 61c, has a dosage of a gingerol composition and in one aspect the dosage is in a range of 20-40 mg of the extract of ginger rhizome. This amount of extract preferably has 4.00-14 mg of combined gingerols and shogaol.
An effective amount of folic acid and an effective amount of gingerol composition can be divided into two or more dosage forms to address specific needs for greater amounts of folic acid. For example, without limitation, a person with greater needs for folic acid may take two dosage forms, such as tablet 61a, gel cap 61b and solution 61c. The amount of gingerol composition is preferably an amount to address the normal nausea and gastric distress associated with folic acid therapy. Gingerol compositions may also be present in an effective amount to promote hematopoiesis.
Turning now to
Turning now to
One embodiment features an oil with an antioxidant, that is, the antioxidant is dissolved in or suspended in the oil. One antioxidant is tocopherol. A preferred formulation has an oil having one or more emulsifying agents. The emulsifying agents facilitate bioavailability and maintain the other components of the formulation in the oil base. A preferred emulsifying agent is selected from one or more of the following agents: lecithin, and short chain, medium chain and long chain triglycerides. A preferred oil is olive oil.
Processes and methods for loading the oil with the suspended folic acid and dissolved gingerol composition are known in the art.
Turning next to
Each dosage form is used to treat morning sickness and folic acid deficiency by orally taking the dosage form, such as tablet 11a, gel cap 11b and solution 11c, to provide folic acid. Folic acid is commonly ingested one to three times daily. The gingerol compound prevents nausea and gastric distress and promotes hematopoiesis. Wetting the folic acid with the oil base and/or the gingerol composition delays absorption leading to less gastric distress and prevents oxidation of the folic acid composition.
One preferred gingerol composition is formed from a dried powdered biomass of ginger rhizome. This dried biomass is placed in a vessel with carbon dioxide under supercritical, near-critical or critical conditions to form a saturated biomass powder. The carbon dioxide is separated from the biomass to form a carbon dioxide fluid extract containing the composition of gingerols and shogaol.
Preferably, the carbon dioxide is held at a temperature of 20-50 degrees Celsius, at a pressure of 1000 to 4000 psi. Preferably, the carbon dioxide has a modifier, in the sense that the modifier is carried in the carbon dioxide in the nature of a dissolved constituent. A preferred modifier is an alcohol, such as ethanol.
Aspects of the present invention employ materials known as supercritical, critical or near-critical fluids. A material becomes a critical fluid at conditions which equal its critical temperature and critical pressure. A material becomes a supercritical fluid at conditions which equal or exceed both its critical temperature and critical pressure. The parameters of critical temperature and critical pressure are intrinsic thermodynamic properties of all sufficiently stable pure compounds and mixtures. Carbon dioxide, for example, becomes a supercritical fluid at conditions which equal or exceed its critical temperature of 31.1° C. and its critical pressure of 72.9 atm (1,070 psig). In the supercritical fluid region, normally gaseous substances such as carbon dioxide become dense phase fluids which have been observed to exhibit greatly enhanced solvating power. At a pressure of 3,000 psig (204 atm) and a temperature of 40° C., carbon dioxide has a density of approximately 0.845 g/cc and behaves much like a nonpolar organic solvent, having a dipole moment of zero Debyes.
A supercritical fluid displays a wide spectrum of solvation power as its density is strongly dependent upon temperature and pressure. Temperature changes of tens of degrees or pressure changes by tens of atmospheres can change a compound solubility in a supercritical fluid by an order of magnitude or more. This feature allows for the fine-tuning of solvation power and the fractionation of mixed solutes. The selectivity of nonpolar supercritical fluid solvents can also be enhanced by addition of compounds known as modifiers (also referred to as entrainers or cosolvents). These cosolvents are typically somewhat polar organic solvents such as acetone, ethanol, methanol, methylene chloride or ethyl acetate. Varying the proportion of cosolvent allows wide latitude in the variation of solvent power.
Supercritical, near critical and critical fluids can exhibit liquid-like density yet still retain gas-like properties of high diffusivity and low viscosity. The latter increases mass transfer rates, significantly reducing processing times. Additionally, the ultra-low surface tension of supercritical fluids allows facile penetration into microporous materials, increasing extraction efficiency and overall yields.
A material at conditions that border its supercritical state will have properties that are similar to those of the substance in the supercritical state. These so-called “near-critical” fluids are also useful for the practice of this invention. For the purposes of this invention, a near-critical fluid is defined as a fluid which is (a) at a temperature between its critical temperature (TC) and 75% of its critical temperature and at a pressure at least 75% of its critical pressure, or (b) at a pressure between its critical pressure (PC) and 75% of its critical pressure and at a temperature at least 75% of its critical temperature. In this definition, pressure and temperature are defined on absolute scales, e.g., Kelvin and psia. To simplify the terminology, materials which are utilized under conditions which are supercritical, near-critical or exactly at their critical point with or without polar cosolvents will jointly be referred to as “SCCNC” fluids or referred to as “SFS.”
SCCNC fluids can be used for the fractional extraction and manufacturing of highly purified gingerols and shogaols.
Embodiments of the present invention are directed to methods of using supercritical fluids for isolating and manufacturing gingerols for use as a therapeutic to treat nausea and emesis.
The present method and apparatus will be described with respect to
Polarity-guided SCCNC fractionation can be carried out on the dried and fresh ginger powder. SCCNC CXF fractionations can be carried out on an automated extractor or a manual version of the same. As shown in
After loading ginger powder into a cartridge on the cartridge holder 13, the fractionation procedure can start. For example, the system will be brought to 3,000 psig and 40° C., and extracted for 10 minutes with pure CO2. This fraction will be collected in ethanol in a glass vial, numbered 19 in
Biomass: Zingiber officinale biomass, both fresh and dried, was obtained from reputable suppliers in Brazil. The material was shipped on ice by overnight freight to our facilities in Woburn, Mass. On receipt, the biomass samples were logged in; dried biomass was stored in dry, low humidity conditions and the fresh biomass will be stored at 4° C. Samples were ground to a fine powder and extracted with different solvents—ethanol, methylene chloride, chloroform and hexane—to define the gingerol content of the material by HPLC analytical techniques. Samples of the underground biomass were used for cultivar identification and sent to outside contractors for heavy metals, herbicides and pesticides analyses. Small voucher samples were retained.
Ginger Powder: The dried ginger root was cut into chunks and dried in a convective oven at 37° C. for 24 hours to remove moisture. The biomass was then ground into a fine powder in a plate and hammer mill. A sample of this fine powder was also extracted by conventional techniques to re-establish the gingerols and shogaol content of the dried and ground Zingiber officinale biomass. The biomass powder was labeled and stored at −20° C.
The fresh ginger root was also cut into chunks and dried in a VirTis shelf freeze-dryer over a 24-hour period to remove all water and moisture. The biomass was then ground into a fine powder in a plate and hammer mill. A sample of this fine powder was also extracted by conventional techniques to re-establish the gingerols and shogaol content of the dried and ground Zingiber officinale biomass. The biomass powder was labeled and stored at −20° C.
Ginger Extract: Polarity-guided SCCNC fractionation was carried out on the dried and fresh ginger powder. As shown in
The data suggests that the following percentages of gingerol and shogaol were obtained. 6-shogaol and 6-gingerol define a ratio and the ratio of 6-shogaol to 6-gingerol is 0.04 to 0.40. Although the applicant does not wish to be bound to any theory, it is believed this ratio of 6-shogaol to 6-gingerol improves the efficacy of the extract for the treatment of nausea.
The ginger rhizome has a starting mass and the extract has a mass associated with one or more of the following 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol. The ratio of 6-gingerol, 8-gingerol, 10-gingerol, and 6-shogaol total mass to starting mass is 20-40%.
The extracts are characterized as having 15-25% 6-gingerol, 1-5% 8-gingerol, 1-5% 10-gingerol and 1-5% 6-shogaol. The extracted gingerols and shogaols define a percentage of the total biomass ranging from about 10-15% to about 25-35%.
This example will present a tablet formulation for folic acid and a gingerol compound.
Each tablet to contain:
Folic acid 500 mcg
Gingerol Extract 4.0 to 14 mg
Olive oil ( in an amount to solubilize gingerol extract)
Sterotex (in an amount to bind folic acid) approximately 2.00 mg
Gingerol extract is combined with olive oil to produce solution, slowly combined and mixed with folic acid powder and Sterotex to form a compressible solid mass and the compressible solid mass is pressed into tablet form.
Each gel cap to contain.
Folic acid 500 mcg
Gingerol Extract 4.0 to 14 mg
Olive oil (in an amount to solubilize gingerol extract)
Tocopherols (as a preservative)
Lecithin
Medium chain triglycerides
Gingerol extract, desired tocopherols. lecithin and medium chain triglycerides are solubilized in olive oil to form a gingerol-olive oil product. Folic acid, as a fine powder, is dispersed within the gingerol-olive oil product to form a folic acid suspension. The folic acid suspension is loaded into a gel cap as known in the art.
Each liquid dose (five milliliters) of solution to contain:
Folic acid 500 mcg
Gingerol Extract 4.0 to 14 mg
Olive oil (in an amount to solubilize gingerol extract)
Tocopherols (as a preservative)
Lecithin
Medium chain triglycerides
Gingerol extract, desired tocopherols, lecithin and medium chain triglycerides are solubilized in olive oil to form a gingerol-olive oil product. Folic acid, as a fine powder, is dispersed within the gingerol-olive oil product to form a folic acid suspension. Folic acid suspension is placed in suitable liquid dispensing vessel, with instructions to shake well.
This example will present a capsule formulation for folic acid and a gingerol compound.
Folic acid 500 mcg
Gingerol Extract 4.0 to 14 mg
Olive oil (in an amount to solubilize gingerol extract)
Sterotex (in an amount to bind folic acid) approximately 2.00 mg
Gingerol extract is combined with olive oil to produce solution, slowly combined and mixed with folic acid powder and Sterotex to form a powder mass and the powder mass is loaded into an appropriately sized capsule in a manner known in the art.
In each of the above example directed to a dosage form, folic acid, in whole or in part, can be readily substituted with an equivalent amount of 400-800 micrograms folic acid.
The dosage forms are subject to many alterations and modification for special needs. Other dosage forms may favor liquids to be administered in lower dosages of folic acid by dropper or the like. The oil base containing the gingerol composition or the gingerol composition without an oil base may lie emulsified and the emulsion held in an aqueous medium.
Particularly for dosage forms intended to be administered as liquid, it is useful to use flavoring agents to improve patient acceptance.
Thus, the present invention has been described in detail in which a dosage form has a gingerol composition addresses the nausea and gastric distress of folic acid and synergistically promotes hematopoiesis to treat morning sickness. The description is directed to the best mode presently contemplated and the inventor's opinion as to such best mode may change in time and embodiments of the present invention are subject to alteration and modification. Therefore, this description should not be considered limiting and the invention should comprise the subject matter of the claims which follow and their equivalents.
It is intended that the matter contained in the preceding description be interpreted in an illustrative rather than a limiting sense.
This application claims priority to U.S. Provisional Patent Application No. 62/777,099 filed on Dec. 8, 2018.
Filing Document | Filing Date | Country | Kind |
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PCT/US2019/064744 | 12/5/2019 | WO | 00 |
Number | Date | Country | |
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62777099 | Dec 2018 | US |