Claims:1. A method for preparing an herbal spray with novel medicinal composition, comprising the steps of:
applying, the substance through the nose in a maximum amount that is insufficient to immediately stimulate an excretory response that would clear a significant portion of the substance from nasal and sinus passages and within a predetermined time period, repeating the application of the substance, through the nose in a maximum amount that is insufficient to immediately stimulate an excretory response that would clear a significant portion of the substance from nasal and sinus passages, at least once and at a minimum a sufficient number of times to provide an effective total dose of the substance.
2. The hydrophobic formulation claimed in claim 1, wherein the herbal spray and cleaning composition comprising per 100 ml. of water, 2.1 grams sodium chloride, 0.8 ml. methyl cylate 0.4 ml tea tree oil, 0.042 grams gum benzoin or balsam tolu, 0.043 grams camphor, or, 0.01 grams camphor, 0.01 grams menthol or peppermint oil, 20 ml. glycerin, 1.2 grams potassium alum, 1 gram zinc sulfate, 0.3 grams n-acetyl 1. cystine and 1 gram of alcohol.
3. The hydrophobic formulation as claimed in claim 1, wherein the 25-40% by volume of a vitamin component blend consisting of vitamin C, rose hips, acerola and lemon bioflavenoids; 8-12% by volume of a mineral component blend consisting of zinc, potassium, calcium and magnesium; 8-12% by volume aloe vera and 45-60% by volume of a water-based solvent.
4. The hydrophobic formulation claimed in claim 1, wherein the herbal spray and cleaning further composition comprising the aqueous nasal composition comprises an aqueous infusion, extract, tea, and/or other galenical preparation prepared from one or more plant products, containing caffeine.
5. The hydrophobic formulation as claimed in claim 1, wherein the herbal spray and cleaning further composition comprising the amount of caffeine which is effective to elicit a systemic therapeutic response, said caffeine being in an isotonic aqueous buffer at a pH of from about 3 to 7.
6. The hydrophobic formulation as claimed in claim 1, wherein the herbal spray and cleaning composition comprising in the form of drops, spays, and/or rinses for use for preparing an agent for treating irritations of the nasal mucosa by a cold, by hay fever, a dry nose and/or sympathomimetic dependence, characterized by comprising menthol, mint oil and/or camphor as well as at least one humectant comprising water-soluble or water-dispersible natural or synthetic polymers that form gels or viscous solutions in aqueous systems, polyhydric alcohols, mono-, di- and/or polysaccharides.
7. The hydrophobic formulation as claimed in claim 1, wherein the polymers are selected from collagen derivatives, polyalkylene glycols, especially polyethylene glycols, polyglycerols, alginates, carrageenan, pectins, gums, cellulose derivatives, polyvinyl alcohols, polyvinyl pyrrolidones and derivatives thereof, and/or dextran.
, Description:[001] The present invention relates to the person's nostrils and sinus cavities, using an inhaler or other suitable means, for cleansing, freshening and deodorizing the named areas for controlling halitosis. The invention more particularly relates to an herbal spray with novel medicinal composition and preparation method thereof.
BACKGROUND OF THE INVENTION
[002] Conventional control of halitosis or “bad breath”, as it is often known, is presently accomplished through the use of mouthwashes, breath mints, candy, chewing gum, brushing and flossing teeth, and other such means that are taken by mouth. Recent developments and research in this field have focused on the theory that the digestive organs could be responsible for objectionable odors that are produced from consuming certain foods or liquids.
[003] Numerous problems have been associated with inadequate cleansing of the nasal and sinus cavities, says for examples, but not limited to, smokers of cigars and cigarettes often have a particular form of fetid breath known as “smoker's breath.” Further, other individuals suffering from problems associated with the nasal passages and sinus cavities become addicted to over-the-counter medicated nasal and sinus sprays. Active ingredients in these sprays alter normal body functions in order to achieve short-term results. Prolonged use of medicated sprays frequently results in user dependency. In many cases this occurs long after the original symptoms for which the sprays were intended have run their course.
[004] Other individuals having problems with nasal and sinus passages are those recovering from post operative medical care that are frequently required to visit an ear, nose and throat specialist (ENT) for sinus and nasal irrigation procedures. In these procedures, solutions are forced, under pressure, into the patient's affected areas for cleansing.
[005] The present invention is an herbal spray with novel medicinal composition and preparation method thereof, which has various advantages, such as freshen breath and eliminate or mask objectionable breath odors by introducing the composition of the present invention into the nostrils and therethrough, into the sinus cavities. As a result, a better formulation and approach to fulfill the aforementioned requirements would be helpful and desired, thus overcoming the aforementioned issue and deficiencies.
SUMMARY OF THE PRESENT INVENTION
[006] Given the aforementioned drawbacks of the prior art's known types of synthesis techniques and methods for an herbal spray with novel medicinal composition that has all of the prior art's advantages and none of the drawbacks.
[007] The present invention is provided with drawn to the unique Vitamin Component of the formulation includes a large proportion of powdered buffered vitamin C (Ascorbate); Rosa Hips; Acerola; Lemon Bioflavonoids; Rustin, Hesperidin and Vitamin B6. This component makes up roughly from 25 to 40% by volume of the formulation.
[008] Further, the unique Mineral Component of the formulation includes Zinc (from chelated Zinc Gluconate or Zinc Picolinate); Potassium; Calcium; Magnesium; and Manganese. This component makes up roughly from 8 to 12% by volume of the formulation.
[009] It is further preferred that the prepared composition according to the invention, and while nasal administration of certain therapeutic agents to mammals, especially humans is known, it is not a necessary conclusion from such knowledge that all therapeutic agents can be usefully administered by this route. In fact it has been shown that many drugs cannot be usefully administered by the nasal route. It certainly is not a suggestion that the compounds of this invention can be usefully administered nasally to achieve enhanced bioavailability and sustained therapeutic blood levels.
[010] In this respect, before explaining at least one object of the invention in detail, it is to be understood that the invention is not limited in its application to the details of set of rules and to the arrangements of the various models set forth in the following description or illustrated in the working examples. The invention is capable of other objects and of being practiced and carried out in various ways, according to the need of that industry. It should also be noted that the phraseology and language used herein are for descriptive purposes only and should not be construed as limiting.
[011] These together with other objects of the invention, along with the various features of novelty which characterize the invention, are pointed out with particularity in the disclosure. Refer to the accompanying drawings and descriptive matter in which preferred embodiments of the invention are illustrated for a better understanding of the invention, its operating advantages, and the specific objects attained by its use.
DETAILED DESCRIPTION OF THE INVENTION
[012] While the present invention is described herein by way of example using embodiments and as used throughout this description, the word "may" is used in a permissive sense (i.e. meaning having the potential to), rather than the mandatory sense, (i.e. meaning must). Further, the words "a" or "an" mean "at least one” and the word “plurality” means “one or more” unless otherwise mentioned. Furthermore, the terminology and phraseology used herein is solely used for descriptive purposes and should not be construed as limiting in scope. Language such as "including," "comprising," "having," "containing," or "involving," and variations thereof, is intended to be broad and encompass the subject matter listed thereafter, equivalents, and additional subject matter not recited, and is not intended to exclude other additives, components, integers or steps. Likewise, the term "comprising" is considered synonymous with the terms "including" or "containing" for applicable legal purposes. Any discussion of documents, acts, materials, devices, articles and the like is included in the specification solely for the purpose of providing a context for the present invention. It is not suggested or represented that any or all of these matters form part of the prior art base or are common general knowledge in the field relevant to the present invention.
[013] In this disclosure, whenever a composition or an element or a group of elements is preceded with the transitional phrase “comprising”, it is understood that we also contemplate the same composition, element or group of elements with transitional phrases “consisting of”, “consisting”, “selected from the group of consisting of, “including”, or “is” preceding the recitation of the composition, element or group of elements and vice versa.
[014] The present invention discloses an herbal spray with novel medicinal composition and preparation method thereof. The herbal spray and formulation preparation method is comprised the steps of, but not limited to, applying, the substance through the nose in a maximum amount that is insufficient to immediately stimulate an excretory response that would clear a significant portion of the substance from nasal and sinus passages and within a predetermined time period, repeating the application of the substance, through the nose in a maximum amount that is insufficient to immediately stimulate an excretory response that would clear a significant portion of the substance from nasal and sinus passages, at least once and at a minimum a sufficient number of times to provide an effective total dose of the substance.
[015] the herbal spray and cleaning composition comprising per 100 ml. of water, 2.1 grams sodium chloride, 0.8 ml. methyl cylate 0.4 ml tea tree oil, 0.042 grams gum benzoin or balsam tolu, 0.043 grams camphor, or, 0.01 grams camphor, 0.01 grams menthol or peppermint oil, 20 ml. glycerin, 1.2 grams potassium alum, 1 gram zinc sulfate, 0.3 grams n-acetyl 1. cystine and 1 gram of alcohol.
[016] In accordance with an embodiment of the present invention, the 25-40% by volume of a vitamin component blend consisting of vitamin C, rose hips, acerola and lemon bioflavenoids; 8-12% by volume of a mineral component blend consisting of zinc, potassium, calcium and magnesium; 8-12% by volume aloe vera and 45-60% by volume of a water-based solvent.
Best mode & enablement of the present invention to enable person ordinary skilled in the art
[017] In another exemplary embodiment of the present invention, the herbal spray and cleaning further composition comprising the aqueous nasal composition comprises an aqueous infusion, extract, tea, and/or other galenical preparation prepared from one or more plant products, containing caffeine.
[018] In accordance with another embodiment of the present invention, the herbal spray and cleaning further composition comprising the amount of caffeine which is effective to elicit a systemic therapeutic response, said caffeine being in an isotonic aqueous buffer at a pH of from about 2 to 6.
[019] In accordance with another embodiment of the present invention, the herbal spray and cleaning composition comprising in the form of drops, spays, and/or rinses for use for preparing an agent for treating irritations of the nasal mucosa by a cold, by hay fever, a dry nose and/or sympathomimetic dependence, characterized by comprising menthol, mint oil and/or camphor as well as at least one humectant comprising water-soluble or water-dispersible natural or synthetic polymers that form gels or viscous solutions in aqueous systems, polyhydric alcohols, mono-, di- and/or polysaccharides.
[020] In accordance with another embodiment of the present invention, the polymers are selected from collagen derivatives, polyalkylene glycols, especially polyethylene glycols, polyglycerols, alginates, carrageenan, pectins, gums, cellulose derivatives, polyvinyl alcohols, polyvinyl pyrrolidones and derivatives thereof, and/or dextran.
[021] In accordance with another embodiment of the present invention, the method is further comprising the steps of, but not limited to, providing, a substrate comprises trimethyl cellulose acetate and cellulose acetate butyrate.
[022] According to another aspect of the present invention, the therapeutically effective compositions of this invention are prepared by mixing the ingredients following generally accepted procedures. For example the selected components may be simply mixed in a blender, or other standard device to produce a concentrated mixture which may then be adjusted to the final concentration and viscosity by the addition of water or thickening agent.
[023] The aforementioned characteristics make the present invention unique and creative in order to achieve reliability and performance while addressing the limitations of pre-existing processes and techniques. It should be noted that the above description is meant to be illustrative rather than limiting. The aforementioned embodiments, for example, may be utilised in combination with one another. Many additional embodiments will be obvious to those skilled in the art after reviewing the above discussion.
[024] The above examples are just a few of the many potential parameters and lab conditions that may be created using the fundamental components, and it should be noted that the recital of these compositions is not meant to restrict the scope of this invention in any manner.
[025] The benefits and advantages that the present invention may offer have been discussed above in terms of particular embodiments. These benefits and advantages, as well as any components or restrictions that may cause them to arise or become more apparent, should not be interpreted as critical, required, or essential features of any or all embodiments.
[026] While the present invention has been discussed with reference to certain embodiments, it should be understood that the embodiments are only illustrative and that the invention's scope is not limited to these implementations. There are many changes, adjustments, additions, and enhancements that may be made to the embodiments described above. These changes, alterations, additions, and enhancements are considered to be within the scope of the invention.