Embodiments described herein generally relate to medicinal compositions (e.g., compositions comprising an active pharmaceutical agent) such as those comprising liquid hydrogen and/or hydrogen gas. In certain embodiments, the composition comprises hydrogen and/or noble gas(es) in a medicinal composit
Embodiments described herein generally relate to medicinal compositions (e.g., compositions comprising an active pharmaceutical agent) such as those comprising liquid hydrogen and/or hydrogen gas. In certain embodiments, the composition comprises hydrogen and/or noble gas(es) in a medicinal composition, for example, within the aqueous phase (e.g., dissolved). For example, in some cases, the medicinal composition may comprise an active pharmaceutical ingredient and hydrogen (H2) and/or noble gas(es). The noble gas may be, for example, xenon, argon, or the like. In some embodiments, the hydrogen and/or the noble gas(es) may infuse with the composition (e.g., such that at least a portion of the hydrogen gas and/or noble gas(es) is dissolved within the composition). Such compositions comprising hydrogen gas and/or noble gas(es) may be useful, for example, for the treatment of animal and human diseases, for improvement in athletic performance, for the enhancement of the overall health of a subject, or the like. Such compositions and/or liquids described herein may be administered (e.g., orally, intravenously, inhaled) to/by a subject.
대표청구항▼
1. An article, comprising: a sealed container containing an aqueous solution comprising (a) dissolved H2 at a concentration of at least 1 ppm by mass, and (b) one or more cannabinoids selected from the group consisting of tetrahydrocannabinol and cannabidiol. 2. The article of claim 1, wherein the c
1. An article, comprising: a sealed container containing an aqueous solution comprising (a) dissolved H2 at a concentration of at least 1 ppm by mass, and (b) one or more cannabinoids selected from the group consisting of tetrahydrocannabinol and cannabidiol. 2. The article of claim 1, wherein the container has an internal pressure of at least 1 psi greater than atmospheric pressure. 3. The article of claim 1, wherein the aqueous solution comprises dissolved H2 at a concentration of at least 3 ppm. 4. The article of claim 1, wherein the aqueous solution comprises tetrahydrocannabinol. 5. The article of claim 1, wherein the aqueous solution comprises cannabidiol. 6. The article of claim 1, wherein the one or more cannabinoids are present at at least 1 wt % of the solution. 7. The article of claim 1, wherein the aqueous solution further comprises flavoring. 8. The article of claim 1, wherein the aqueous solution comprises at least 90% water by mass. 9. The article of claim 1, wherein the container is a can. 10. The article of claim 1, wherein the container is an aluminum can. 11. The article of claim 1, wherein the container is a bottle. 12. A method, comprising: unsealing a sealed container containing an aqueous solution comprising (a) dissolved H2 at a concentration of at least 1 ppm by mass, and (b) one or more cannabinoids selected from the group consisting of tetrahydrocannabinol and cannabidiol; anddrinking the aqueous solution. 13. The method of claim 12, wherein the sealed container has an internal pressure of at least 1 psi greater than atmospheric pressure. 14. The method of claim 12, wherein the aqueous solution comprises dissolved H2 at a concentration of at least 3 ppm. 15. The method of claim 12, wherein the aqueous solution comprises tetrahydrocannabinol. 16. The method of claim 12, wherein the aqueous solution comprises cannabidiol. 17. The method of claim 12, wherein the one or more cannabinoids are present at at least 1 wt % of the solution. 18. The method of claim 12, wherein the aqueous solution comprises at least 90% water by mass. 19. The method of claim 12, wherein the container is a can. 20. The method of claim 12, wherein the container is a bottle.
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