AU2001237809A1 - Pharmaceutical composition for muscular anabolism - Google Patents
Pharmaceutical composition for muscular anabolismInfo
- Publication number
- AU2001237809A1 AU2001237809A1 AU2001237809A AU2001237809A AU2001237809A1 AU 2001237809 A1 AU2001237809 A1 AU 2001237809A1 AU 2001237809 A AU2001237809 A AU 2001237809A AU 2001237809 A AU2001237809 A AU 2001237809A AU 2001237809 A1 AU2001237809 A1 AU 2001237809A1
- Authority
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- Australia
- Prior art keywords
- pharmaceutical composition
- protein
- daily dose
- per daily
- anabolic
- Prior art date
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Links
Description
PHARMACEUTICAL COMPOSITION FOR MUSCULAR ANABOLISM
Field of the invention
[0001] The invention is concerned with pharmaceutical or nutritional compositions suitable for increasing muscular mass ("lean body mass"), e.g. for athletes, and for preventing loss of lean body mass that may occur in periods of rest and during recovery from disease.
Background
[0002] Products intended for increasing muscle mass are commercially available, such as the product Phosphagain. A review of nutritional supplements for increasing muscle mass has been presented by Clarkson and Rawson in Crit. Rev. Food Sci. Nutr. 39 (1999) 317-328. They conclude that many claims of this effect are unsupported, and that the weight gain following of creatine ingestion is most likely water retention but that it could also be due to some new muscle protein. From this review, we learn that very little evidence exists that ergogenic components indeed improve athletic performance.
[0003] According to US 5,726,146, lean body mass can be increased without increase body fat by administration of a supplement containing creatine, taurine, and ribonucleic acid, optionally with carbohydrate for enhancing cellular uptake of these ingredients.
[0004] WO 98/43617 discloses a dietary supplement comprising L-carnitine, coenzyme Q10 and taurine useful in the correction of the abnormality in mitochondrial energetics occurring in cardiac failure and certain other diseases. It further discloses a high protein, high calorie nutritional feeding supplement comprising these three nutrients together with cysteine, vitamin E, vitamin C, selenium, and thiamine. The protein fraction can comprise of normal (i.e. denatured) whey proteins, 1 : 1 with casein. [0005] WO 95/10192 discloses a nutritional drink containing colostrum, for the purpose of improving physical performance and recovery. The colostrum is defatted and de- caseinated, and sterilised by filtration.
[0006] WO 99/56758 describes a food composition for use in changing body composition (increased lean tissue) and/or physical work capacity, which contains undenatured colostrum, in particular colostrum derived growth factors and colostrum- derived casein. The composition may further contain vitamins minerals, amino acids, and carbohydrates.
[0007] There is a need for i nutritional and/or pharmaceutical preparation that indeed helps to increase muscle strength during training. During periods when training efforts have to be stopped, e.g. becεuse of injuries or holidays, it is frequently observed that muscle mass that was built up during exercise rapidly decreases, and a lot of time is normally required to regain the level that was previously present. Losses in lean body mass are also observed frequently in persons that have to be inactive for quite a while, e.g. because they have to stay in bed due to injury, disease or other disorders. Thus, there is also a need for effective formulations, and especially nutritional formulations, that help prevent losses of body mass during these periods. [0008] Muscle consists of proteins, like myosine and actin, lipids and carbohydrates. Skeletal muscle tissue is continuously broken off and replaced in a dynamic process that depends on mechanical damage, exercise and feeding status at a particular point in time.
Description of the invention
[0009] It has now been found that the simultaneous or sequential administration of 1 - component that triggers anabolism (initiators),
2 - components that provide building blocks (substrates) for biosynthesis of muscle tissue, and
3 - components that facilitate biosynthetic processes (facilitators) increases, for a certain period of time, lean body mass and/or can prevent catabolism in periods of rest.
[0010] Sequential use means that the different components can be administered separately during the day, but they must be consumed during the same day. In this way, for example a product with one or more facilitators is consumed first, followed by consumption, e.g. 2 hours after consumption of the first product, of an effective amount of substrate and initiator in the same product. However, preferably all three types of components are consumed simultaneously in one product.
[0011] The invention pertains to pharmaceutical and/or nutritional compositions suitable for enhancing muscular anabolism, i.e. production of muscle tissue or reduction of loss of muscle tissue. The compositions according to the invention comprise an initiator for muscular tissue production, a facilitator for biosynthesis, and a substrate. They furthermore comprise a facilitator, including creatine or a functional equivalent, and
optionally further components facilitating tissue production, and also a substrate comprising e.g. carbohydrates, amino acids etc.
[0012] The products can have a powdered structure, packed in sachets or cans or similar reservoirs. Other dry forms that are equally suitable are cereals and bars. The product can also have the form of a drink, e.g. based on a dairy drink (milk, whey) or fruit juice (orange, apple, grape). For liquid products it is advantageous to let it have a pH below 4.2 in order to stabilize some of the active components. The product can also have the form of a paste or spread or sauce.
Initiators [0013] The initiators (also referred to as triggering substances or triggers) to be used in the compositions of the invention are components that start up the anabolic processes. Examples are anabolic growth factors like Insulin-Like Growth Factor (IGF-1). These must be present as part of an extract of a protein-rich food ingredient, in particular in an extract from a proteinaceous material of animal origin, like milk, blood or egg. Undenatured whey and especially undenatured colostrum in particular bovine colostrum comprises a variety of anabolic trigger substances. The high effectivity of whey and colostrum that was found may also be explained by the presence of components that increase the bioavailability of the initiator components. In case of anabolic growth factors, such components are binding proteins. [0014] Specific extracts of animal origin may be used as a source of triggers for anabolism, providing that the extraction procedures do not affect the trigger components. The Fo value, defined in the Manual of Common Methods, defines decimal reductions of germs as a result of heat treatment of food products. Thus an F0 value of 3.0 defines a thousand-fold reduction of germs and is achieved by treatment at 121°C with a Z value of 10. A heat treatment above F0 = 3.0 normally destroys most of these trigger components. Thus the extracts should not have been subjected to a heat treatment with an F0 of 3.0 or higher, and preferably any heat treatment should have an F0 of less than 2.4. Most preferably, a heat treatment, if any, should not have an F0 of more than 0.2.
[0015] Suitable methods for obtaining such products avoiding substantial heat treatment are described in the art and include filtration and centrifugal techniques. The amount of extract can be as low as 5 mg per daily dose, if a high degree of purification of the triggering substances from the proteinaceous material is obtained. However, when bovine
colostrum is used as sole source for triggering substances, at least 5 g of the product, that is obtained by using the method disclosed in WO 97/16977, should be included in a daily dose according to the invention.
[0016] The inclusion of insulinotrophic components like digestible carbohydrates and arginine and lysine can further enhance the triggering activity of extracts of animal proteins. Arginine and lysine should be included in amounts of more than 1.0 g and preferably more than 1.5 g per daily dose. Carbohydrates are preferably glucose polymers like maltodextrins and should be present in an amount of more than 4 g and preferably more than 8 g. Substrates
[0017] In order to allow an adequate rate of biosynthesis of muscle tissue, the presence of sufficient amounts of substrate in the form of a variety of amino acids is required. It appears that requirements for protein in athletes are higher than in non-athletes. Daily requirements in strength athletes are above 120g protein and in endurance athletes above 1 OOg protein. Though it appeared that some amino acids become rate-limiting earlier in biosynthesis of muscle tissue than other ones, a mixture of all amino acids, including the essential amino acids is preferably provided according to the invention. These amino acids should be provided as protein or hydrolysate thereof; it is especially preferred to use intact protein for taste reasons and because the amino acids will then be released more slowly. The latter ensures a constant but sufficient provision of the substrate amino acids to the tissues and where the amino acids are insulinotrophic, a longer increase of plasma insulin levels.
[0018] In order to provide sufficient amounts of amino acids, typically more than 5g protein and especially more than 10 or even more than 20g protein is included in the formulations. Suitable proteins are all proteins that comprise high amounts of essential amino acids, especially leucine, lysine and methionine, such as casein, soy, pea, potato, egg and whey proteins. However, when undenatured proteins of animal origin like colostrum or whey from mammal milk, blood or eggs are used, these ingredients also comprise triggering components for anabolism. [0019] Proteins and amino acids can be expressed as protein equivalents (PE). One PE can be calculated by multiplying the Kjeldahl nitrogen content of the substrate by the factor 6.25.
[0020] In order to increase the amount of the amino acids that are most critical to muscle building, methionine, lysine and leucine, additional amounts of these amino acids can be included. This can be done by including peptides, or amino acid complexes or free amino acids in the formula. Preferably free amino acids are used, especially those in the L-form. The amounts of methionine that are included per daily serving should exceed 0.2 g (9.4% N: 0.12 g PE) and preferably exceed 0.5 g; the preferred range is 1-6 g Met. Preferably the amount of methionine is more than 2.8 g per 100 g protein equivalents and in particular in the range 3.0-5.0. The amount of lysine per daily serving should be more than 1.0 g (19.6% N: 1.3 g PE) and preferably more than 2.0 g, e.g. 2.5 - 15.0 g. Calculated per lOOg protein equivalents, the amount of lysine should be more than 8.3 g, and in particular in the range 8.5-11. The amount of leucine per daily serving should be more than 2.0 g (10.4% N: 1.3 g PE) and preferably more than 3.0 g, e.g. 3.5 - 20 g.
[0021] Sleeping disorders are often experienced, especially in those persons that consume large amounts of branched chain amino acids (BCAA: valine, isoleucine, leucine). This is especially undesirable when one wants to maintain anabolism during a longer period of time. For this reason it is important that the ratio of L-leucine/BCAA is relatively high. This ratio should be higher than 0.46 and in particular be in the range 0.5- 3.0.
[0022] In addition the amount of L-tryptophan should be relatively high. The ratio Trp/BCAA should be higher than 0.055, preferably in the range of 0.06-0.2 and in particular be in the range of 0.07-0.13. Also persons that suffer from disease frequently appear to experience problems with maintaining nitrogen balance. By consuming the above-mentioned types and amounts of substrates their capacity to synthesise muscle tissue is maximally supported. Facilitator
[0023] According to the invention, lean body tissue can only be synthesised when sufficient energy is available and sufficient amounts of cofactors are available as facilitator of the anabolic biochemical processes. Intracellular energy should be available in the form of adenosine tri-phosphate (ATP). Creatine phosphate (CP) is able to provide "energised phosphate" to ADP, which restores ATP levels once they have been used for labour or biochemical processes. It is therefore especially advantageous to include in the formulation a source of both energy, in the form of digestible carbohydrates, and creatine.
Instead of creatine, Krebs eye le intermediates such as citrate and Krebs cycle precursors, such as pyruvate, glutamate, j lutamine, can be used.
[0024] The amount of digestible carbohydrates should be above 4 g per daily dose and preferably more than 10 g per cay. That of creatine should be above 1.0 g per daily dose and preferably more than 2.0 g, for example 8 g. Suitable carbohydrates are malto- dextrins, e.g. the one having DE = 19, lactose, ribose, sucrose or mixtures thereof. Creatine can be the salt creatine, creatine phosphate, or functional and stable equivalents thereof, including acid addition salts, metal and ammonium salts, hydrolysable esters etc.
[0025] Because of the high amounts of protein that are digested, consumption of extra amounts of minerals and vitamins in the diet is desirable. Especially vitamin B6 should be fortified to ensure a consumption of at least 1.8 mg vit. B6 per lOOg protein that is consumed. The high volume of protein that is normally consumed by body builders ensures a load of methionine that should be handled appropriately in order to have only moderate increases in plasma levels of homocysteine. It is therefore recommended to include folic acid, vitamin B12, vitamin B6, zinc and magnesium in the formula, because deficiencies of one or more of these components frequently occur, while they are mandatory for homeostasis of homocysteine loads. The levels should be at least 1 mg vitamin B6, 200 μg folic acid, 1 μg cyanocobalamine, 40 mg magnesium and 5 mg zinc or the functional equivalents of these components per daily serving. The prior art discloses which forms of these components can be advantageously used for nutritional purposes. Vitamin B6 can e.g. have the form of pyridoxine or pyridoxal; folic acid can be in the monoglutamate form; zinc can be administered as salt, e.g. as zinc carbonate; magnesium can have the form of an inorganic salt like magnesium carbonate.
[0026] A further improvement of the product can be obtained by including in the product one of the metabolites of leucine, especially beta-hydroxy-beta-methylbutyrate (HMB). The latter compound can be included in an amount of 1-20 g per daily serving, in particular in the range 2-5 g per day. The component can be included as pure substance or as inorganic salt such as the calcium salt, or any other functional equivalent. Other components like yeast, carnitine, pyruvate, dihydroxyacetone, glutamine, ubiquinone (especially CoQIO) and other vitamins and minerals can be included as well. It is especially preferred to include melatonin, which supports the anabolic function of the composition.
[0027] Table 1 shows the scope of the products according to the invention. Table 1: Components according to the invention
Examples
Example 1. Bar for body building purposes An extract for isolating anabolic components from colostrum is prepared by applying the centrifugation process as described in WO 97/16977. The liquid phase is consequently purified by elution over a strong anionic exchanger. The liquid is then freeze-dried. The bar is prepared by using methods that are known in the art that ensure that per bar of 30g weight is present: 100 mg of colostrum powder produced as given above,
5 g soy protein
2 g L-leucine
1.5 g L-lysine
0.6 g L-methionine 2.0 g creatine
13.6 g glucose syrup
2.0 mg vitamin B6
0.2g L-tryptophan
Example 2. Powdered formula in can of 900 g. Twenty grams of powder are dissolved in
200 ml milk.
Per lOOg powder the formula contains:
50 g undenatured colostrum powder 40 g maltodextrin DE 19
10 g creatine Per day about 40-100 g of the powder is consumed.
Example 3. Powder packed as in example 2, consisting per lOOg formula of: 33 g undenatured egg white powder
50 g maltodextrin DE 25 12 g creatine 2 g melatonine
5 g of a mineral/vitamin premix that comprises 1250 ug folic acid, 10 mg pyridoxine, 7.5 ug cyanocobalamine, 75 mg zinc, 10 mg copper and 400 mg magnesium Per day about 25 g of powder is consumed e.g. suspended in 200 ml orange juice.
Example 4. Powdered product for body building, that consists per 100 g formula of 72 g undenatured whey protein powder, providing 43 g protein and 21 g lactose
5 g sucrose 8 g creatine
1 g L-methionine 1 g L-tryptophan 1 g melatonine
6 g of the mineral/vitamin premix described in example 3 4 g HMB
4 g L-leucine Per day about 50 g formula is consumed, e.g. by dissolving this amount of powder in milk together with the breakfast cereal.
Example 5. Liquid product obtained by preblending the powder of example 3 in orange juice.
Example 6. Supplement
The following components were combined an the amounts indicated for a daily dose:
30 g bovine colostrum
120 g carbohydrates 5 g creatine
6 g of essential L-amino acids (Lys, Leu, Val, Phe, Thr. His, He, Met) methionine module: Zn, Vit. B6, folic acid
Example 7. Supplement The following components were combined an the amounts indicated for a daily dose: 30 g bovine colostrum 36 g carbohydrates
5 g creatine
6 g of essential L-amino acids (Lys, Leu, Val, Phe, Thr. His, He, Met) methionine module: Zn, Vit. B6, folic acid
Example 8. Supplement
The following components were combined an the amounts indicated for a daily dose: 30 g bovine colostrum 6 g carbohydrates
5 g creatine
Claims
1. A pharmaceutical composition containing, per daily dose, at least 5 mg of anabolic initiators comprising anabolic growth factors, at least 0.12 g of protein equivalents as anabolic substrates, and at least 3 g of anabolic facilitators comprising at least 1 g of creatine or its functional equivalent.
2. The pharmaceutical composition of claim 1, wherein the anabolic initiators comprise at least 5 g of a non-denatured animal protein, non-denatured being defined as having an F0 of less than 3.0.
3. The pharmaceutical composition of claim 1 or 2, wherein the animal protein is selected form milk protein, egg protein and blood protein.
4. The pharmaceutical composition of claim 2, wherein the milk protein comprises colostrum.
5. The pharmaceutical composition of any one of claims 1-4, comprising digestible carbohydrates at a level of at least 4 g per daily dose.
6. The pharmaceutical composition of claim 5, comprising digestible carbohydrates at a level of at least 8 g per daily dose.
7. The pharmaceutical composition of any one of claims 1-6, comprising total proteins at a level of more than 10 g per daily dose.
8. The pharmaceutical composition of any one of claims 1-7, comprising one or more of the following per daily dose: more than 0.2 g methionine, more than 1.0 g lysine, more than 2.0 g leucine, and more than 0.2 g tryptophan.
9. The pharmaceutical composition of any one of claims 1-8, in which the weight ratio of leucine to branched-chain amino acids is between 0.46 and 0.8 and the weight ratio of tryptophan to branched-chain amino acids is between 0.055 and 0.2.
10. The pharmaceutical composition of any one of claims 1-9, further comprising at least one component selected from the group consisting of vitamin B6, vitamin B12, folic acid, magnesium and zinc.
11. The pharmaceutical composition of any one of claims 1-10, further comprising 1-20 g of β-hydroxy-β-methylbutyrate and/or 0.5-10 g melatonine per daily dose.
12. The pharmaceutical composition of any one of claims 1-11, which is a supplement.
13. A method of improving muscular anabolism comprising administering to a subject in need of muscular anabolism an effective amount of at least 1 g of biosynthesis facilitators and at least 5 g of non-denatured animal protein per day.
14. Use of at least 1 g of biosynthesis facilitators and at least 5 g of non-denatured animal protein per daily dose for preparing a pharmaceutical or nutritional composition for improving muscular anabolism.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/500,802 | 2000-02-10 | ||
| US09/500,802 US6521591B1 (en) | 2000-02-10 | 2000-02-10 | Pharmaceutical composition for muscular anabolism |
| PCT/NL2001/000112 WO2001058284A1 (en) | 2000-02-10 | 2001-02-12 | Pharmaceutical composition for muscular anabolism |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2001237809A1 true AU2001237809A1 (en) | 2001-11-01 |
| AU2001237809B2 AU2001237809B2 (en) | 2005-04-07 |
Family
ID=23990994
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2001237809A Ceased AU2001237809B2 (en) | 2000-02-10 | 2001-02-12 | Pharmaceutical composition for muscular anabolism |
| AU3780901A Pending AU3780901A (en) | 2000-02-10 | 2001-02-12 | Pharmaceutical composition for muscular anabolism |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU3780901A Pending AU3780901A (en) | 2000-02-10 | 2001-02-12 | Pharmaceutical composition for muscular anabolism |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6521591B1 (en) |
| EP (1) | EP1253830B1 (en) |
| AT (1) | ATE447858T1 (en) |
| AU (2) | AU2001237809B2 (en) |
| CA (1) | CA2398990C (en) |
| DE (1) | DE60140426D1 (en) |
| ES (1) | ES2336764T3 (en) |
| HK (1) | HK1048050B (en) |
| WO (1) | WO2001058284A1 (en) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10032964B4 (en) * | 2000-07-06 | 2017-10-12 | Beiersdorf Ag | Use of creatine in cosmetic or dermatological preparations |
| US7744930B2 (en) * | 2002-11-22 | 2010-06-29 | Shaklee Corporation | Compositions, methods and kits for enhancing weight loss while inhibiting loss of lean body mass |
| US7288570B2 (en) * | 2002-12-20 | 2007-10-30 | Nutricia N.V. | Stimulation of in vivo production of proteins |
| US20050143343A1 (en) * | 2003-12-30 | 2005-06-30 | Nerenberg Arnold P. | Nutritional supplement for enhancing the production and effect of natural human growth hormone |
| MXPA06009377A (en) * | 2004-02-20 | 2007-03-07 | Lifescape Biosciences Inc | Compositions and methods for sleep regulation. |
| US20050215640A1 (en) | 2004-03-26 | 2005-09-29 | Baxter Jeffrey H | HMB compositions and uses thereof |
| US20060013889A1 (en) * | 2004-07-16 | 2006-01-19 | Playford Raymond J | Colostrum-based treatment for irritable bowel syndrome |
| MX2007002209A (en) * | 2004-08-25 | 2007-11-08 | Multi Formulations Ltd | Compositions and methods for activating protein synthesis and deactivating catabolic processes in skeletal muscle. |
| US7426440B2 (en) * | 2004-09-24 | 2008-09-16 | Nutritional Bioscience Ltd. | Repair and protection factor scoring method for bioactive agents |
| US20060068022A1 (en) * | 2004-09-29 | 2006-03-30 | Playford Raymond J | Bioactive agent compositions for repair of cell injuries |
| CA2537647A1 (en) * | 2005-03-01 | 2006-09-01 | Six Star Formulations Ltd. | Supplemental dietary composition for supporting muscle growth, recovery and strength |
| DE102005028446A1 (en) * | 2005-06-17 | 2006-12-28 | Sibylle E. Bauer | Composition, preferably dietary supplements or dietetic food, useful e.g. to increase the efficiency and well-being of a healthy person, comprises colostrum and at least a ketocarboxylic acid |
| US20080317886A1 (en) * | 2005-11-03 | 2008-12-25 | Sparkman Dennis R | Compositions for Preventing and Reducing Delayed Onset Muscle Soreness |
| ES2548432T3 (en) * | 2005-12-19 | 2015-10-16 | Abbott Laboratories | Use of beta-hydroxy-beta-methylbutyrate to modulate the imbalance in the production of type 1 and type 2 cytokines |
| CN101524155B (en) * | 2009-04-20 | 2012-10-10 | 北京康比特体育科技股份有限公司 | Amino acid composition |
| SG182812A1 (en) | 2010-01-29 | 2012-09-27 | Abbott Lab | Nutritional emulsions comprising calcium hmb |
| TWI519242B (en) * | 2010-01-29 | 2016-02-01 | 亞培公司 | Nutritional emulsion containing calcium HMB and soluble protein |
| BR112012018642A2 (en) * | 2010-01-29 | 2015-09-01 | Abbott Lab | Nutritional powders comprising spray dried hmb |
| WO2011094548A1 (en) | 2010-01-29 | 2011-08-04 | Abbott Laboratories | Aseptically packaged nutritional liquids comprising hmb |
| US9693577B2 (en) | 2010-01-29 | 2017-07-04 | Abbott Laboratories | Method of preparing a nutritional powder comprising spray dried HMB |
| CN101791127B (en) * | 2010-03-05 | 2012-07-18 | 北京康比特体育科技股份有限公司 | Muscle protection composite containing HMbeta |
| TWI526161B (en) | 2010-06-10 | 2016-03-21 | 亞培公司 | a substantially transparent nutrient solution comprising calcium HMB and soluble protein |
| ES2633360T3 (en) | 2014-04-02 | 2017-09-20 | Alzchem Ag | Creatine and protein matrix as well as procedure for the production of this matrix |
| AU2017217466A1 (en) | 2016-02-11 | 2018-08-23 | Nutrition 21, Llc | Chromium containing compositions for improving health and fitness |
| JOP20190146A1 (en) | 2016-12-19 | 2019-06-18 | Axcella Health Inc | Amino acid compositions and methods for the treatment of liver diseases |
| WO2019036471A1 (en) | 2017-08-14 | 2019-02-21 | Axcella Health Inc. | Amino acid for the treatment of liver disease |
| EP3810123A1 (en) | 2018-06-20 | 2021-04-28 | Axcella Health Inc. | Compositions and methods for the treatment of fat infiltration in muscle |
| TWI737987B (en) * | 2019-04-23 | 2021-09-01 | 豐華生物科技股份有限公司 | Use of lactic acid bacteria in preparaing a composition for increasing exercise performance and anti-fatigue |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5036052A (en) * | 1988-06-22 | 1991-07-30 | Morishita Pharmaceutical Co., Ltd. | Amino acid nutrient compositions |
| US5726146A (en) * | 1994-12-06 | 1998-03-10 | Natural Supplement Association, Incorporated | Non-steroidal, anabolic dietary supplement and method to increase lean mass without linked increase fat mass |
| DE69814834T2 (en) | 1997-03-27 | 2004-04-08 | Sole, Michael J., Toronto | NUTRITIONAL COMPOSITION TO IMPROVE CELL ENERGY |
| EP0875155A1 (en) | 1997-05-01 | 1998-11-04 | N.V. Nutricia | Peri-operative drink |
| AUPP327198A0 (en) * | 1998-04-30 | 1998-05-21 | Northfield Laboratories Pty Ltd | A food composition and method of using same |
| EP1094824B1 (en) | 1998-06-10 | 2006-04-05 | Albert B. Crum | Prophylactic and therapeutic nutritional supplement for creation/maintenance of health-protective intestinal microflora and enhancement of the immune system |
-
2000
- 2000-02-10 US US09/500,802 patent/US6521591B1/en not_active Expired - Lifetime
-
2001
- 2001-02-12 DE DE60140426T patent/DE60140426D1/en not_active Expired - Lifetime
- 2001-02-12 WO PCT/NL2001/000112 patent/WO2001058284A1/en not_active Ceased
- 2001-02-12 ES ES01910231T patent/ES2336764T3/en not_active Expired - Lifetime
- 2001-02-12 HK HK03100252.0A patent/HK1048050B/en not_active IP Right Cessation
- 2001-02-12 AU AU2001237809A patent/AU2001237809B2/en not_active Ceased
- 2001-02-12 AT AT01910231T patent/ATE447858T1/en not_active IP Right Cessation
- 2001-02-12 CA CA2398990A patent/CA2398990C/en not_active Expired - Fee Related
- 2001-02-12 EP EP01910231A patent/EP1253830B1/en not_active Revoked
- 2001-02-12 AU AU3780901A patent/AU3780901A/en active Pending
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