Nutraceutical Composition Comprising C60 And Ketone Esters
a technology of ketone esters and c60, which is applied in the field of nutraceutical compositions, can solve the problems of reducing ros production and none of these references teach using fullerene, and achieve the effects of preventing and reducing inflammation, improving longevity, and improving human health
Patent Information
- Authority / Receiving Office
- US · United States
- Patent Type
- Applications(United States)
- Current Assignee / Owner
- Publication Date
- 2020-06-18
- Estimated Expiration
- Not applicable · inactive patent
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Abstract
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application claims priority to, and is a continuation in part (CIP) of, U.S. Utility application Ser. No. 16 / 220,890, titled “Nutraceutical Compositions Comprising C60 and Cox-2 Inhibitor” by the same inventor, filed on Dec. 14, 2018, which is incorporated herein by reference in its entirety.FIELD OF THE INVENTION
[0002] The field of the invention is nutraceutical compositions, especially compositions containing fullerene.BACKGROUND
[0003] The following description includes information that may be useful in understanding the present invention. It is not an admission that any of the information provided herein is prior art or relevant to the presently claimed invention, or that any publication specifically or implicitly referenced is prior art.
[0004] The human body is under constant attack from oxidative stress caused by free radicals from e.g., reactive oxygen species (ROS). Oxidative stress causes damage to cells, especially cellular pro...
Examples
Embodiment Construction
[0028]FIG. 1 shows an exemplary C60 fullerene molecule substituted with (x) number of beta-hydroxybutyrate groups, where the value of (x) can be anywhere between 1 and the maximum number that can be substituted on the fullerene molecule. The substitution can take place at any suitable position of the fullerene molecule. FIG. 1A shows the exemplary fullerene molecule in FIG. 1, substituted with one or more L-beta-hydroxybutyrate groups. FIG. 1B shows the exemplary fullerene molecule in FIG. 1, substituted with one or more D-beta-hydroxybutyrate groups.
[0029]FIG. 2 shows an exemplary C60 fullerene molecule substituted with (x) number of beta-hydroxybutyrate groups and y number of carboxylic acids (n=0-100). The value of (x) and (y) can be anywhere between 1 and the maximum number that can be substituted on the fullerene molecule. The substitution can take place at any suitable position of the fullerene molecule. FIG. 2A shows the exemplary fullerene molecule in FIG. 2, where the carbo...