US2013216518A1PendingUtilityA1
Composition comprising a combination of at least one proteolytic enzyme and at least one lipolytic enzyme, for use in preventing triglyceride synthesis
Est. expiryOct 29, 2030(~4.3 yrs left)· nominal 20-yr term from priority
Inventors:Max Rombi
A61P 9/10A61P 3/10A61P 3/08A61P 3/06A61P 43/00A61P 3/04A61K 38/465A61K 38/482
45
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Claims
Abstract
The present invention relates to a composition comprising a combination of at least one proteolytic enzyme, such as subtilisin, and at least one lipolytic enzyme, for use in preventing triglyceride synthesis, advantageously by degrading 2-monoacylglycerol in the intestine. The invention also has as an object such a composition for use as a drug, cosmetic agent, medical device, dietary composition, dietary supplement or nutraceutical, notably for use in preventing or treating obesity, atherosclerosis, type 2 diabetes or for use in preventing or reducing excess weight.
Claims
exact text as granted — not AI-modified1 . A method for inhibiting or preventing synthesis or reformation of triglycerides in the enterocytes or cells of the intestine which comprises administering to a patient in need thereof a composition comprising a combination of at least one proteolytic enzyme and at least one lipolytic enzyme.
2 . The method of claim 1 , wherein the proteolytic enzyme is selected from the group comprising subtilisin, nagarse, nattokinase, chymotrypsin, trypsin, elastase, thermolysin, serrapeptase, and mixtures thereof.
3 . The method of claim 1 or claim 2 , wherein the composition is in the form of a drug, cosmetic agent, medical device, dietary composition, nutraceutical or dietary supplement.
4 . The method of any claim 1 , for prevention or reduction of excess weight, adipogenesis, excess cholesterol, or cellulite.
5 . The method of claim 1 , for prevention or treatment of obesity, atherosclerosis or type 2 diabetes.
6 . The method of claim 1 , wherein the composition is administered orally.
7 . The composition of claim 1 , wherein the composition is in the form of a hard or soft capsule, tablet, granule, powder or oral solution.
8 . The method of claim 7 , wherein the composition is in the form of a gelatin capsule or a gastro-resistant tablet.
9 . The method of claim 1 , wherein the administration of the composition includes a daily dose of proteolytic enzyme of 50-100 mg.
10 . The method of claim 1 , wherein the administration of the composition includes a daily dose of lipolytic enzyme of 200-300 mg.
11 . The method of claim 1 , wherein the lipolytic enzyme is selected from the group comprising a lipase extracted from Thermomyces lanuginosus, Rhizopus niveus, Penicillium roqueforti, Penicillium camemberti, Geotrichum candidum, Candida rugosa, Candida lipolytica, Candida parapsilosis, Aspergillus niger, Rhizopus oryzae, Mucor javanicus, Candida anthartica, Geotrichum candidum , oats, and mixtures thereof.
12 . The method of claim 11 , wherein the lipase is a Cal A or Cal B lipase of Candida anthartica, Geotrichum candidum, Candida rugosa , or a mixture of these lipases.
13 . A product for inhibiting or preventing synthesis or reformation of triglycerides in the enterocytes or cells of the intestine comprising:
at least one proteolytic enzyme, and at least one lipase, wherein said product is in the form of a hard or soft capsule, tablet, granule, powder or oral solution.
14 . The method of claim 1 , wherein the proteolytic enzyme and the lipolytic enzyme are administered simultaneously, separately or sequentially.
15 . The method of claim 2 , wherein the protelytic enzyme is subtilisin, nattokinase or a mixture thereof.
16 . The method of claim 15 , wherein the lipase is a Cal A or Cal B lipase of Candida anthartica, Geotrichum candidum, Candida rugosa , or a mixture of these lipases.
17 . The method of claim 1 , wherein 2-monoacylglycerol is degraded in the intestine.Join the waitlist — get patent alerts
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