A. Field of Invention
The present invention generally relates to dietary supplements. In particular, the present invention is for a dietary supplement and method of delivery of dietary supplements that improves effectiveness in joint support. The invention is a method of delivering a supplement containing two specialized dietary supplements (a Glucosamine Sulfate or Glucosamine Hydrochloride based and a Chondroitin Sulfate) aimed at providing joint support and intended to be taken following the scheduled administration system.
B. Description of the Related Art
Joints are where bones, connective tissue and cartilage all come together in a body to promote movement. The joint support system is responsible for sustaining the area around muscles and bones, where they provide shock absorption and support a body's internal structure.
There are many ways to encourage healthy joint function, like maintaining a healthy weight and enhancing a diet with established joint care supplements and ingredients such as Glucosamine and Chondroitin.
Glucosamine is naturally found within the joints, making it a good supplement for supporting healthy joints and connective tissue. Commonly sold forms of glucosamine are glucosamine sulfate, glucosamine hydrochloride, and N-acetylglucosamine. Glucosamine lubricates the joints to support mobility and flexibility. Glucosamine is naturally present in the shells of shellfish, animal bones, bone marrow, and fungi. In addition, Glucosamine can be sourced from Vegetarian material.
Chondroitin is a naturally occurring nutrient found in connective tissue, and in supplement form, it helps promote healthy cartilage and support the structural framework of joints. It is a chemical that is normally found in cartilage around joints in the body. Chondroitin sulfate is manufactured from animal sources and is typically made from extracts of cartilaginous tissue from cow cartilage, pig, shark, fish, chickens and birds.
Current treatment methods for joint support include administering supplements that contain a blend of Glucosamine and Chondroitin in a single dose, or contain Glucosamine or Chondroitin separately, in a single dose. While the rate of absorption of Chondroitin and Glucosamine by itself may be considered adequate, when the two ingredients are combined, their absorption and overall bioavailability rates drop. Further, while the current treatment methods are considered to be adequate, the efficacy of the supplements can be greatly improved. Additionally, following the instant regimen, the formulations are optimized and the amount of necessary supplements to be taken can be reduced, thus minimizing the financial burden and expense of purchasing supplements and ultimately reducing the long term and/or aggregate unwanted effects associated with the supplements.
The instant inventor has discovered that the absorption rate and or effectiveness of Glucosamine, the primary joint supplement, is increased when followed by a dose of Chondroitin, the secondary joint supplement, at a predetermined time interval, and vice versa. As a result, the efficacy of the supplements in providing joint support is improved.
Studies show that Chondroitin Sulfate absorbs effectively by itself and Glucosamine absorbs effectively by itself. When the two ingredients are combined however, their absorption rates drop. A purpose of the instant invention is to solve this issue. By separating the ingredients via a scheduled administration system, the absorption rates will remain similar to when the products are taken by themselves.
In addition, the secondary administration will be more effective once some of the primary administration loses effectiveness through the day. By dosing two individual formulations rather than one formulation, such novelty includes separation, never before done in the same joint supplement before. Current supplements are broken into three categories based on the main active ingredient(s): supplements that blend glucosamine and chondroitin into a single dose, glucosamine supplements, and Chondroitin sulfate supplements. By taking these active ingredients (glucosamine and chondroitin) separately (specifically 6 to 18 hours apart) and at two separate time intervals, the results include an improved effectiveness of both active ingredients without the pitfall of absorption rates that blended supplements fall into.
The accompanying drawing illustrates the related time tables and efficacy related to the subject invention. In such drawings,
As shown in the accompanying drawings, for purposes of illustration, and explained herein, the present invention resides in dietary supplements (primary and secondary formulations or dosages) and methods of delivery thereof for providing joint support.
In an embodiment, the primary joint supplement can be either Glucosamine, Glucosamine Hydrochloride, Glucosamine Sulfate and/or N-Acetylglucosamine and the secondary joint supplement, administered in accordance with the instant invention can be Chondroitin Sulfate and the lecticans, components of the extracellular matrix. In another embodiment, the order of the primary and secondary supplements as indicated above may be reversed.
It has been discovered that the rate of absorption of Glucosamine will be maximized over time, defined by cycles, when a first cycle is defined by an initial dose of a primary joint supplement at time, t0, followed by a dose of a secondary joint supplement that is administered during a critical time range after, t0c. Then, following completion of a first cycle, a subsequent dose of a primary joint supplement is introduced thereafter, defining a second cycle, which is administered at a critical time range, t1c, followed by a dose of a secondary joint supplement that is administered during a critical time range, t2c. The cycles repeat, whereby subsequent, alternating doses (primary-to-secondary) are administered at critical times, until optimum results are realized.
It should be understood that the instant invention includes the embodiment where the first cycle may also be defined by an initial dose of a secondary joint supplement at time, t0, followed by a dose of a primary joint supplement that is administered during a critical time range after, t0c. Then, following completion of a first cycle, a subsequent dose of a secondary joint supplement is introduced thereafter, defining a second cycle, which is administered at a critical time range, t1c, followed by a dose of a primary joint supplement that is administered during a critical time range, t2c.
As shown in
As provided for herein, an example of the suggested administration of supplements according to the instant invention include,
The above example of the suggested administration of supplements according to the instant invention can be reversed to include,
ti+1c: administering dose of secondary joint supplement, whether it be Glucosamine, Glucosamine Hydrochloride, Glucosamine Sulfate, and or N-Acetylglucosamine. In addition, any ingredients from
The inventor of the instant invention has discovered that the amount of Glucosamine to be administered per dose may be between the range of about 500 mg to about 2000 mg, and that the subsequent critical time to administer the secondary joint supplement may generally be in the range of about 6 hours to about 18 hours after dose.
The inventor of the instant invention has discovered that the amount of chondroitin sulfate to be administered per dose may be between the range of about 400 mg to about 1200 mg, and that the subsequent critical time to administer the primary joint supplement may generally be in the range of about 6 hours to about 18 hours after dose.
By attending to the regimen as disclosed herein, efficacy of Glucosamine and Chondroitin in joint treatment will be appreciatively improved. Additionally, by alternating primary and secondary supplements, it is understood that the instant invention maximize the effectively of the supplements and that with time less supplements will ultimately be required, thus reducing long term and/or aggregate effects.
This is a non-provisional application claiming priority under 35 USC 119(e) to provisional Application Ser. No. 62/091,859 filed on Dec. 15, 2014, reference of which is incorporated herein in its entirety.
Number | Date | Country | |
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62091859 | Dec 2014 | US |