Search Images Maps Play YouTube News Gmail Drive More »
Sign in
Screen reader users: click this link for accessible mode. Accessible mode has the same essential features but works better with your reader.

Patents

  1. Advanced Patent Search
Publication numberUSRE39480 E1
Publication typeGrant
Application numberUS 09/912,472
Publication dateJan 23, 2007
Filing dateJul 24, 2001
Priority dateAug 8, 1997
Fee statusPaid
Also published asCA2297834A1, CA2297834C, CN1273531A, DE69831576D1, DE69831576T2, EP1001793A1, EP1001793B1, WO1999007387A1
Publication number09912472, 912472, US RE39480 E1, US RE39480E1, US-E1-RE39480, USRE39480 E1, USRE39480E1
InventorsMark F. McCarty
Original AssigneeNutrition 21, Inc.
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Chromium/biotin treatment of type II diabetes
US RE39480 E1
Abstract
A method for treating Type II diabetes by administering to an affected individual a combination of chromic tripicolinate and biotin. The two compounds are administered orally or parenterally at in daily dosages which provide between 50 and 1,000 μg of chromium and between 25 μg and 200 mg biotin, the amounts of chromium and biotin being selected together to provide a greater than additive effect.
Images(4)
Previous page
Next page
Claims(26)
1. A method for reducing hyperglycemia and stabilizing the level of serum glucose comprising administering to an individual in need thereof between about 50 to 1,000 micrograms per day of chromium as synthetic chromic tripicolinate in combination with between about 25 μg and 200 mg per day of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a greater than additive effect.
2. The method of claim 1, comprising administering between about 500 and 1,000 micrograms per day of chromium as synthetic chromic tripicolinate.
3. The method of claim 1, comprising administering between about 1 mg and 100 mg biotin per day.
4. The method of claim 1, wherein said chromic tripicolinate is in a pharmaceutically acceptable carrier.
5. The method of claim 1, wherein said biotin is in a pharmaceutically acceptable carrier.
6. The method of claim 1, wherein said chromic tripicolinate is orally administered.
7. The method of claim 1, wherein said biotin is orally administered.
8. The method of claim 1, wherein said chromic tripicolinate is parenterally administered.
9. The method of claim 1, wherein said biotin is parenterally administered.
10. A pharmaceutical composition comprising chromium as synthetic chromic tripicolinate and biotin, wherein the ratio of chromium to biotin is between about 2:1 and 1:200 (w/w), wherein the amounts of chromic tripicolinate and biotin are selected together to provide a greater than additive effect.
11. A method for reducing blood glucose levels comprising administering to an individual in need thereof between about 50 and 1,000 micrograms per day of chromium as synthetic chromic tripicolinate in combination with between about 25 μg and 200 mg per day of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
12. A method for reducing blood glucose levels comprising administering to an individual in need thereof a composition consisting essentially of between about 50 and 1,000 micrograms per day of chromium as synthetic chromic tripicolinate in combination with between about 25 micrograms and 200 milligrams per day of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
13. The method of claim 12, wherein the individual is a human.
14. The method of claim 12, comprising administering between about 500 and 1,000 micrograms per day of chromium as synthetic chromic tripicolinate.
15. The method of claim 12, comprising administering between about 1 milligram and 100 milligrams biotin per day.
16. The method of claim 12, comprising administering about 600 micrograms of chromium as synthetic chromic tripicolinate and about 300 micrograms of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
17. The method of claim 12, comprising administering about 400 micrograms of chromium as synthetic chromic tripicolinate and about 200 micrograms of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
18. The method of claim 12, wherein said chromic tripicolinate is in a pharmaceutically acceptable carrier.
19. The method of claim 12, wherein said biotin is in a pharmaceutically acceptable carrier.
20. The method of claim 12, wherein said chromic tripicolinate is orally administered.
21. The method of claim 12, wherein said biotin is orally administered.
22. The method of claim 12, wherein said chromic tripicolinate is parenterally administered.
23. The method of claim 12, wherein said biotin is parenterally administered.
24. A pharmaceutical composition consisting essentially of chromium as synthetic chromic tripicolinate and biotin, wherein the ratio of chromium to biotin is between about 2:1 and 1:200 (w/w), wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
25. A pharmaceutical composition comprising about 600 micrograms/day of chromium as synthetic chromic tripicolinate and about 300 micrograms/day of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
26. A pharmaceutical composition consisting essentially of about 600 micrograms/day of chromium as synthetic chromic tripicolinate and about 300 micrograms/day of biotin, wherein the amounts of chromic tripicolinate and biotin are selected together to provide a synergistic effect in reducing blood glucose levels.
Description
RELATED APPLICATIONS

This is a continuation-in-part of allowed U.S. application Ser. No. 08/908,819, filed Aug. 8, 1997, now U.S. Pat. No. 5,789,401 the entire contents of which are hereby incorporated by reference.

FIELD OF THE INVENTION

The present invention relates to the treatment of adult-onset non-insulin dependent (Type II) diabetes. More specifically, the invention relates to the treatment of Type II diabetes by administering chromic picolinate and biotin.

BACKGROUND OF THE INVENTION

Diabetes mellitus is known to affect at least 10 million Americans, and millions more may unknowingly have the disease. In the form of this disease known as Type II, non-insulin dependent or adult-onset (as opposed to juvenile diabetes or Type I), the pancreas often continues to secrete normal amounts of insulin. However, this insulin is ineffective in preventing the symptoms of diabetes which include hyperglycemia, impaired carbohydrate metabolism, glycosuria and decreased insulin sensitivity. These symptoms, if left untreated, often lead to severe complications.

Current drugs used for managing Type II diabetes fall within two classes of compounds: the biguanides and the sulfonylureas. The biguanides, e.g. metformin, are believed to prevent excessive hepatic gluconeogenesis. The sulfonylureas, e.g. tolbutamide and glyburide, lower plasma glucose primarily by stimulating insulin secretion, by enhancing insulin effects in some target tissues and by inhibiting hepatic glucose synthesis.

U.S. Pat. No. 4,315,927 discloses that when selected essential metals are administered to mammals as exogenously synthesized coordination complexes of picolinic acid, they are directly available for absorption without competition from other metals. These complexes are safe, inexpensive, biocompatible and easy to produce.

U.S. Pat. No. 5,087,623 describes the administration of chromic tripicolinate for the treatment of Type II diabetes in doses which provide between 50 and 500 μg of chromium. The U.S. Recommended Daily Allowance for chromium is 50-200 μg. Although a small decrease in glycosylated hemoglobin, an accurate indicator of blood glucose levels, was observed, the 10.4% value obtained after chromic tripicolinate treatment was still will within the diabetic range.

International Patent Application No. PCT/US96/06493 discloses the administration of high (“supranutritional”) doses of chromium (1,000 to 10,000 μg/day) to individuals with Type II diabetes. Individuals who received 1,000 μg chromium per day as chromic tripicolinate exhibited a 30% decrease in glycosylated hemoglobin and a similar reduction in fasting and postprandial glucose levels.

Biotin is the prosthetic group for a number of carboxylation reactions, the most notable being pyruvate carboxylase which is involved in gluconeogenesis and replenishment of the citric acid cycle, and acetyl CoA carboxylase which plays a role in fatty acid biosynthesis. The safe and adequate recommended daily intake of biotin is 100-300 μg, although no side effects or toxicities were noted in previous clinical studies with oral biotin intakes of up to 200 mg daily (Mock et al, in Present Knowledge in Nutrition, seventh edition, Ziegler, E. et al., eds., ILSI Press, Washington, D.C., 1996, pp. 220-235). Supranutritional doses of biotin have been shown to have therapeutic utility in diabetes. High-dose oral or parenteral biotin has been shown to improve oral glucose tolerance in diabetic KK mice (Reddi et al., Life Sci., 42:1323-1330, 1988), rats made diabetic by injection with streptozotocin (Zhang et al., 16th International Congress of Nutrition, Montreal, 1997, abstract book, p. 264) and in pre-diabetic Otsuka Long-Evans Tokushima Fatty rats (Zhang et al., J Nutr. Sci. Vitaminol. 42:517-526, 1996).

In a clinical study, Coggeshall et al. (Ann. N.Y. Acad. Sci, 447:387-392, 1985) demonstrated that a daily oral dose of biotin of 16 mg lowered fasting plasma glucose levels in Type I diabetics in whom insulin injections had been temporarily discontinued. Maebashi et al. (J. Clin. Biochem. Nutr. 14:211-218, 1993) showed that administration of 3 mg biotin three times per day to poorly-controlled type II diabetics resulted in improved pancreatic beta cell function as evidenced by the fact that fasting insulin levels did not decline in biotin-treated subjects despite the sharp decline in glucose levels.

There is a constant need for effective treatments for type II diabetes. The present invention addresses this need by providing a safe, inexpensive, drug-free therapeutic agent.

SUMMARY OF THE INVENTION

One embodiment of the present invention is a method for reducing hyperglycemia and stabilizing the level of serum glucose comprising administering to an individual in need thereof between about 50 to 1,000 micrograms per day of chromium as synthetic chromic tripicolinate in combination with between about 25 μg and 200 mg per day of biotin, the amounts of chromic tripicolinate and biotin being selected together to provide a greater than additive effect. Preferably, the amount of chromium administered as synthetic chromic tripicolinate is between 500 and 1,000 micrograms per day. Advantageously, the amount of biotin administered per day is between about 1 mg and 100 mg. In one aspect of this preferred embodiment, the chromic tripicolinate is in a pharmaceutically acceptable carrier. In another aspect of this preferred embodiment, the biotin is in a pharmaceutically acceptable carrier. Preferably, the biotin is orally administered. Advantageously, the chromic tripicolinate is orally administered. Preferably, the chromic tripicolinate is parenterally administered. In another aspect of this preferred embodiment, the biotin is parenterally administered.

The present invention also provides a pharmaceutical composition comprising chromium as synthetic chromic tripicolinate and biotin, wherein the ratio of chromium to biotin is between about 2:1 and 1:200 (w/w), the amounts of chromic tripicolinate and biotin being selected together to provide a greater than additive effect.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention includes the discovery that doses of chromium from the highest RDA amount up to five times this amount, administered in the form of chromic picolinate, combined with either low or high doses of biotin, promote significant reduction in blood glucose levels and stabilize blood glucose levels in individuals with type II diabetes. This reduction is markedly greater than what would be expected when either component is administered alone, thus indicating a synergistic effect.

The synthesis of chromic picolinates is described in U.S. Pat. No. 5,087,623, the entire contents of which are hereby incorporated by reference. Chromic tripicolinate and biotin are commercially available from health food stores, drug stores and other commercial sources. In order to reduce the requirement for insulin and/or diabetic drugs and to reduce several important risk factors associated with Type II diabetes, it is anticipated that the dosage range of chromium administered to a patient in the form of chromic tripicolinate will be between about 50 and 1,000 μg/day. In a preferred embodiment, this amount is between about 500 and 1,000 μg/day. With regard to the biotin component of the combination therapy, the preferred daily dosage is between about 25 μg and 200 mg. More preferably, the daily dosage of biotin is between about 1 mg and 100 mg.

For oral administration, the chromic picolinates and biotin may be provided as a tablet, aqueous or oil suspension, dispersible powder or granule, emulsion, hard or soft capsule, syrup or elixir. Compositions intended for oral use may be prepared according to any method known in the art for the manufacture of pharmaceutically acceptable compositions and such compositions may contain one or more of the following agents: sweeteners, flavoring agents, coloring agents and preservatives. The sweetening and flavoring agents will increase the palatability of the preparation. Tablets containing chromic tripicolinate in admixture with non-toxic pharmaceutically acceptable excipients suitable for tablet manufacture are acceptable. Pharmaceutically acceptable means that the agent should be acceptable in the sense of being compatible with the other ingredients of the formulation (as well as non-injurious to the patient). Such excipients include inert diluents such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, such as corn starch or alginic acid; binding agents such as starch, gelatin or acacia; and lubricating agents such as magnesium stearate, stearic acid or talc. Tablets may be uncoated or may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period of time. For example, a time delay material such as glyceryl monostearate or glyceryl distearate alone or with a wax may be employed.

Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, such as peanut oil, liquid paraffin or olive oil.

Aqueous suspensions may contain the chromic tripicolinate complex of the invention in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients include suspending agents, dispersing or wetting agents, one or more preservatives, one or more coloring agents, one or more flavoring agents and one or more sweetening agents such as sucrose or saccharin.

Oil suspensions may be formulated by suspending the active ingredient in a vegetable oil, such as arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as liquid paraffin. The oil suspension may contain a thickening agent, such as beeswax, hard paraffin or cetyl alcohol. Sweetening agents, such as those set forth above, and flavoring agents may be added to provide a palatable oral preparation. These compositions may be preserved by an added antioxidant such as ascorbic acid. Dispersible powders and granules of the invention suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, a suspending agent, and one or more preservatives. Additional excipients, for example sweetening, flavoring and coloring agents, may also be present.

Syrups and elixirs may be formulated with sweetening agents, such as glycerol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative, a flavoring or a coloring agent.

The chromic tripicolinate preparations for parenteral administration may be in the form of a sterile injectable preparation, such as a sterile injectable aqueous or oleaginous suspension. This suspension may be formulated according to methods well known in the art using suitable dispersing or wetting agents and suspending agents. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, such as a solution in 1,3-butanediol. Suitable diluents include, for example, water, Ringer's solution and isotonic sodium chloride solution. In addition, sterile fixed oils may be employed conventionally as a solvent or suspending medium. For this purpose, any bland fixed oil may be employed including synthetic mono or diglycerides. In addition, fatty acids such as oleic acid may likewise be used in the preparation of injectable preparations.

The pharmaceutical compositions may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, such as olive oil or arachis oil, a mineral oil such as liquid paraffin, or a mixture thereof. Suitable emulsifying agents include naturally-occurring gums such as gum acacia and gum tragacanth, naturally occurring phosphatides, such as soybean lecithin, esters or partial esters derived from fatty acids and hexitol anhydrides, such as sorbitan mono-oleate, and condensation products of these partial esters with ethylene oxide, such as polyoxyethylene sorbitan mono-oleate. The emulsions may also contain sweetening and flavoring agents.

The amount of chromic tripicolinate/biotin that may be combined with the carrier material to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.

The above description of the invention is set forth solely to assist in understanding the invention. It is to be understood that variations of the invention, including all equivalents now known or later developed, are to be considered as falling within the scope of the invention, which is limited only by the following claims.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US4315927 *Aug 8, 1980Feb 16, 1982The United States Of America As Represented By The Secretary Of AgricultureDietary supplementation with essential metal picolinates
US5087623 *Mar 21, 1989Feb 11, 1992Nitrition 21Chromic picolinate treatment
US5336672Jul 21, 1992Aug 9, 1994Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical CollegeIncreasing egg production in poultry
US5470846Jan 14, 1994Nov 28, 1995Sandyk; ReuvenTreatment of neurological and mental disorders
US5496827Jul 15, 1994Mar 5, 1996Patrick; JayCompositions for the transdermal delivery of nutrients
US5597585Dec 26, 1995Jan 28, 1997Williams; Andrew H.Vitamin/mineral composition
US5635535Apr 5, 1996Jun 3, 1997Wagstaff; Robert K.Method for increasing blood glucose levels
US5789401 *Aug 8, 1997Aug 4, 1998Nutrition 21High-dose chromium/biotin treatment of type II diabetes
US6048846 *Feb 26, 1998Apr 11, 2000Cochran; Timothy M.Compositions used in human treatment
US6140304Dec 24, 1992Oct 31, 2000Eicotech CorporationMethod of and nutritional and pharmaceutical compositions for reduction of hyperinsulinemia
WO1991011117A2Feb 4, 1991Aug 6, 1991Univ TexasDietary supplements comprising vitamins and minerals
WO1996025939A1Nov 6, 1995Aug 29, 1996Vladimir BadmaevUse of piperine as a bioavailability enhancer
WO1996035421A1 *May 8, 1996Nov 14, 1996Nutrition 21High-dose chromic tripicolinate for the treatment of type ii diabetes
WO1999007387A1Jul 31, 1998Feb 18, 1999Nutrition 21Chromium/biotin treatment of type ii diabetes
WO2002011564A2Aug 2, 2001Feb 14, 2002Stacey J BellSupplement for type 2 diabetes or lipodystrophy
Non-Patent Citations
Reference
1Anderson, R.A. (1997) Nutritional factors influencing the glucose/insulin system: Chromium. Journal of the American College of Nutrition. 16(5):404-410.
2Cefalu et al. (1997) The effect of chromium supplementation on carbohydrate metabolism and body fat distribution. Diabetes. 46:55a.
3 *Coggeshall, et al. (1985) Biotin status and plasma glucose in diabetics. Ann. N.Y. Acad. Sci. 447:389-392.
4 *Copy of label from Multi-Vitamin suppl. "alpha-betic(TM)".
5 *Copy of label from Multi-Vitamin suppl. "Mega Men(C)".
6Maebashi et al. (1993) Therapeutic evaluation of the effect of biotin on hyperglycemia in patients with non-insulin dependent diabetes mellitus. J. Clin. Biochem, Nutr. 14:211-218.
7 *Maebashi, et al. (1993) Therapeutic evaluation of the effect of biotin on hyperglycemia in patients with non-insulin dependent diabetes mellitus. J. Clin. Biochem. Nutr. 14:211-218.
8McCarty (1991) The case for supplemental chromium and a survey of clinical studies wiht chromium picolinate. Journal of Applied Nutrition. 43(1):58-66.
9McCarty, Mark F. "Dietary glycemic index may influence cancer risk by modulating IGF-1 activity: a hypothesis." Journal of Medicinal Food. 1(2): 123-140 (1998).
10 *Mock, D. (1984) In Present Knowledge in Nutrition, 7<SUP>th </SUP>Edition, Chapter 22, pp. 220-235.
11Ravina et al. (1995) Clinical use of the trace element chromium (III) in the treatment of diabetes mellitus. The Journal of Trace Elements in Experimental Medicine. 8:183-190.
12 *Reddi, et al. (1988) Biotin supplementation improves glucose and insulin tolerances in genetically diabetic kk mice. Life Sciences. 42:1323-1330.
13 *Zhang, et al. (1996) A high biotin improves the impaired glucose tolerance of long-term spontaneously hyperglycemic rats with non-insulin-dependent diabetes mellitus. J. Nutri. Sci. Vitaminol. 42:517-526.
14 *Zhang, et al.(1997) Biotin administration improves the impaired glucose tolerance of streptozotocin-induces diabetic Wistar rats. J. Nutri. Sci. Vitaminol. 43(3):271-280.
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US8586061Dec 22, 2009Nov 19, 2013Jds Therapeutics, LlcMultiple unit dosage form having a therapeutic agent in combination with a nutritional supplement
US8933022Mar 1, 2012Jan 13, 2015Jds Therapeutics, LlcMethods and compositions for the treatment and prevention Hypoglycemia and related disorders
US9005637Apr 5, 2013Apr 14, 2015Jds Therapeutics, LlcMultiple unit dosage form having a therapeutic agent in combination with a nutritional supplement
Classifications
U.S. Classification514/188, 514/387
International ClassificationA61K33/24, A61K31/415, A61K31/381, A61K31/4188, A61P3/10, A61K31/44
Cooperative ClassificationA61K31/44, A61K33/24, A61K31/415
European ClassificationA61K31/44, A61K33/24, A61K31/415
Legal Events
DateCodeEventDescription
Feb 5, 2014ASAssignment
Owner name: NUTRITION 21, LLC, NEW YORK
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:JDS THERAPEUTICS, LLC;REEL/FRAME:032143/0720
Effective date: 20121203
Dec 10, 2012ASAssignment
Owner name: NUTRITION 21 LP, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:MCCARTY, MARK F.;REEL/FRAME:029436/0377
Effective date: 19980630
Free format text: MERGER;ASSIGNOR:AMBI, INC.;REEL/FRAME:029437/0028
Owner name: NUTRITION 21, LLC., NEW YORK
Effective date: 20000101
Jun 14, 2012ASAssignment
Owner name: JDS THERAPEUTICS, LLC, NEW YORK
Free format text: CHANGE OF NAME;ASSIGNOR:N21 ACQUISITION HOLDING, LLC;REEL/FRAME:028603/0993
Effective date: 20120201
Jan 10, 2012ASAssignment
Effective date: 20111122
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:NUTRITION 21, LLC;REEL/FRAME:027545/0097
Owner name: N21 ACQUISITION HOLDING, LLC, NEW YORK
Jan 19, 2011FPAYFee payment
Year of fee payment: 12