The present invention is generally related to the delivery nutritional supplements through the oral mucosa, specifically the storage and delivery devices needed to deliver them.
Proper hydration in athletes is essential for optimal performance, and hydration management has long been a laborious task for coaches and trainers. To that end, systems have been developed to monitor hydration in real-time by using water bottles capable of monitoring an athlete's fluid intake. This information can be collected and compared with changes in the athlete's weight to train staff to evaluate an athlete's hydration.
During exercise, the body requires more oxygen than when the body is at rest. When oxygen cannot be delivered to the muscles faster to replace the used oxygen, the muscles will begin to convert the available glucose to lactic acid. This will build up in the muscle, causing fatigue. More rapid delivery of oxygen to the system during exertion can reduce fatigue. Supplemental oxygen therapy has been demonstrated to improve athletic performance and decrease reaction times.
The benefits of proper hydration and supplemental oxygen therapy on athletic performance are demonstrable. Therefore, it is desirable to have a means of integrating the delivery of electrolytes and supplemental oxygen to a real-time hydration management system.
A beverage bottle that dispenses both a beverage, such as water, and an aerosol supplement composition is described. The aerosol supplement composition may include electrolytes and other nutritional supplements. The beverage bottle may have separate outlets for the beverage and the aerosol. The beverage bottle may contain a canister of the supplement composition under pressure. The canister may be pressurized with air or oxygen.
In one aspect, a beverage bottle with a pressurized compartment and an unpressurized compartment to integrate supplemental oxygen delivery into a hydration and electrolyte management system is described.
In one aspect, a beverage bottle system to dispense both a fluid and an aerosol supplement composition is described. The system includes a bottle configured to hold a fluid. The bottle defines an interior. A cap is configured to engage the bottle. The cap includes a dispensing opening. A canister contains a supplement composition under pressure. A cradle is configured to support the canister in the system. An outlet connects to the canister. The outlet includes an exterior opening. The exterior opening is configured to dispense an aerosol of the supplement composition. The dispensing opening is configured to dispense the fluid.
In another aspect, a beverage bottle system to dispense both a fluid and an aerosol supplement composition is described. The bottle is configured to hold a fluid. The bottle defines an interior. A cap is configured to engage over the interior of the bottle. The cap includes a dispensing opening. The dispensing opening is configured to dispense the fluid. A canister contains a supplement composition under pressure. An outlet connects to the canister. The outlet includes an exterior opening. The exterior opening is configured to dispense an aerosol of the supplement composition separate from the fluid.
In another aspect, an external supplement canister for a beverage bottle is described. The canister mounts to an exterior of a beverage bottle. An outlet connects to the canister. The outlet includes an exterior opening. The exterior opening is configured to dispense an aerosol of the supplement composition.
In another aspect, an external supplement canister for a beverage bottle is described. The canister includes a mounting bracket configured to extend around an outer circumference of a beverage bottle. The canister contains a supplement composition under pressure. The mounting bracket is configured to hold the canister. An outlet connects to the canister. The outlet includes an exterior opening. The exterior opening is configured to dispense an aerosol of the supplement composition.
For purposes of this application, any terms that describe relative position (e.g., “upper”, “middle”, “lower”, “outer”, “inner”, “above”, “below”, “bottom”, “top”, etc.) refer to an aspect of the invention as illustrated, but those terms do not limit the orientation in which the aspect can be used.
The system 100 comprises a canister 102 holding a nutritional supplement composition or matrix to enable transmucosal delivery of the nutritional supplement. Transmucosal delivery of nutrient supplements offers advantages over oral delivery when negative issues relating to the gastrointestinal tract, stomach, substance digestion, absorption, swallowing, protocol compliance, substance effectiveness, and other gastrointestinal metabolism issues are considered. The nutritional supplement composition may include (i) a nutritional supplement matrix fraction, (ii) a gas fraction, (iii) an enhancer fraction, (iv) a liquid fraction, and (v) a preservative fraction wherein the nutritional supplement matrix fraction, the gas fraction, the enhancer fraction, the liquid fraction, and the preservation fraction are all mixed or combined and treated to maintain a state of balanced suspension among the oxygen molecules for a specific duration of time before being dispensed from a canister 102. Furthermore, the supplement composition may be in a compressed state in the canister 102 before being dispensed.
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The canister 102 holds the supplement composition in a compressed or pressurized state until the supplement composition is dispensed from the system 100. The canister 102 may be fixed to or positioned in a bottle 104. With respect to
The supplement composition may be delivered to the user via an outlet 108. The outlet 108 may include tubing, hosing, ducts, or piping fluidly connecting the canister 102 and an exterior of the system 100. In certain aspects, the outlet 108 may be configured to direct the supplement composition towards the buccal mucosa. An exterior opening 128 of the outlet 108 may be integrated into the cap 110 or the dispensing opening 130. A lower opening 138 of the outlet 108 may connect with the canister 102.
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In other aspects, the bottle 104 may include a flow measurement device, such as a thermal mass flow meter, to measure the user's amount of fluid consumed.
In other aspects, the user may press directly against the exterior opening 128 of the outlet 108 to dispense the supplement composition from the system 100. In other aspects, the bottle 104 or the cap 110 may include buttons, triggers, etc. to dispense the supplement composition from the system 100.
In other aspects, the system 100 may include a pod 106, which may contain a hydration supplement that is mixed with the fluid in the bottle 104 and delivered to the user through the cap 110. With respect to
In certain aspects, the system 100 may include a circular disk 114, which may contain electronics, including a programmable logic controller, a memory to store flow measurements, a transceiver to transmit the measurements, and a battery. In one aspect, the circular disk 114 may contain LED lights to convey usage statistics, schedules, or suggestions to the user, trainer, or coach. In one aspect, the circular disk 114 may contain, or communicate to a computer, a watch, a transdermal patch, or other wearable technology that may analyze the data related to the fluid and nutritional supplement matrix consumption to calculate whether the athlete should consume more or less of either the fluid or the nutritional supplement matrix. In another aspect, the system 100 may be designed to adapt to any water bottle wherein the internal components would be designed at different dimensions to fit different size water bottles. In this aspect, the circular disk 114 is mounted above the cradle 112.
The outlet 108 may pass through the circular disk 114, which may have a flow measurement device to monitor the volume and frequency of the user's intake of the contents of the canister 102.
In other aspects, the mounting bracket 116 may be configured to pair with a specific bottle 104 shapes and sizes. The mounting bracket 116 may also be adjustable to fit a variety of bottle 104 designs.
The outlet 108 may extend along an exterior surface of the bottle 104 and the cap 110. In one aspect, outlet 108 may be configured to join with the cap 110 to allow the user to take in either the contents of the canister 102 or bottle 104 from the same outlet. In one aspect, the mounting bracket 116 may position the canister 102 so that the user may easily use separate outlets for the bottle 104 and the supplement composition from the canister 102. In one aspect, outlet 108 may be configured to capture and communicate flow data related to the canister 102 contents as part of hydration and nutritional supplement management system.
The supplement composition may include any one or more of (i) a nutritional supplement fraction, (ii) a gas fraction, (iii) an enhancer fraction, (iv) a liquid fraction and (v) a preservative fraction, wherein the enhancer fraction being a mucoadhesive to ensure adhesion of the atomized droplet to the membrane maximizing absorption. Furthermore, the particles of the composition can be positively or negatively charged so that they coalesce or disperse.
The supplement fraction may include a combination of electrolytes, vitamins, or minerals. Furthermore, the nutritional supplement matrix maybe selected from or be combination of Potassium chloride, Sodium chloride, Iron, Sodium, Calcium, Magnesium, Carbohydrates, Proteins, Zinc, Molybdenum, Caffeine, Copper, Potassium, Manganese, Chlorides, Bicarbonate and Carbonate, Aluminum, Arsenic, Bromine, Cadmium, Chromium, Sodium, Potassium, Chlorine, Cobalt, Fluorine, Iodine, Citicoline, Tyrosine Phenylalanine, Taurine, Malic Acid, Glucuronolactone, Manganese, Molybdenum Nickel, Phosphorus, Selenium, Silicon, Vanadium, Amino Acids, Vitamin A, Vitamin D, Vitamin E, Vitamin K, Vitamin C, Vitamin B complex, Thiamine (Vitamin 31), Riboflavin (Vitamin 132). Niacin (Vitamin B3), Pyridoxine (Vitamin B6), Biotin, Pantothenic Acid and Pantetheine, Folic Acid, Vitamin B12, “Unofficial” B Vitamins including Choline and Inositol, Vitamin P (bioflavonoids), and flavoring agents, and/or other vital nutrients, in addition to various homeopathic/alternative substances. In one embodiment the formulation or composition of nutritional supplement matrix comprises 50 to 60 weight % of Chloride, where the chloride is from potassium chloride and sodium chloride; 30 to 40 weight % of Sodium, where the sodium is from sodium chloride; and 5 to 15 weight % of Potassium where the potassium is from potassium chloride.
The gas fraction in the above-mentioned formulation or composition comprises ambient air, oxygen, or nitrogen, wherein the gas fraction maybe in a compressed state. In one embodiment the gas fraction is comprised of oxygen wherein the concentration of oxygen is up to 95% oxygen and can mixed with other gases such as nitrogen.
The enhancer fraction in the above-mentioned formulation or composition is a mucoadhesive enhancer, an absorption enhancer, or a flavoring. Wherein the mucoadhesive enhancer fraction is selected from a group of pectin's or apple pectin's. Wherein the absorption enhancer is selected from a group of glycerin's or vegetable glycerin's. Wherein the flavoring fraction is selected from a group of natural flavoring for foods and artificial flavoring for foods.
The liquid fraction in the above-mentioned formulation or composition is selected from a group of water, distilled water, filtered water, oxygenated water or saline and where the composition is water-soluble. Wherein the amount of water is sufficient to dissolve all elements of the composition and prevent any molecules from precipitating. Furthermore, wherein the liquid fraction can be a combination of liquids and used to adjust the pH of the composition to be close to a physiological pH.
The preservative fraction in the above-mentioned formulation or composition is selected from a group of food preservatives or potassium sorbate. The food preservative fraction helps maintain and extend the shelf life of the composition.
As such, it should be understood that the disclosure is not limited to the particular aspects described herein, but that various changes and modifications may be made without departing from the spirit and scope of this novel concept as defined by the following claims. Further, many other advantages of applicant's disclosure will be apparent to those skilled in the art from the above descriptions and the claims below.
The present application claims to priority to U.S. Provisional Patent Application No. 63/209,826 filed Jun. 11, 2021, which is incorporated by reference.
Number | Date | Country | |
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63209826 | Jun 2021 | US |