US2009011075A1PendingUtilityA1
Polar Lipid Mixtures, their Preparation and Uses
Est. expiryApr 28, 2025(expired)· nominal 20-yr term from priority
A61P 25/28A61P 25/00A23J 7/00A23V 2002/00A23L 33/115
47
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Claims
Abstract
Disclosed herein are polar lipid mixtures, comprising glycerophospholipids such as phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylserine (PS) and phosphatidyl-inositol (PI), and sphingolipids such as sphyngomyelin (SM). Most importantly, the ratio of phospholipids in said mixture is comparable to that of HMF, and is represented by SM>PC>PE>PS>PI or SM=PC>PE>PS>PI. Processes for the preparation of said mixtures and uses thereof are also described herein.
Claims
exact text as granted — not AI-modified1 - 56 . (canceled)
57 . A man-made lipid preparation comprising a mixture of glycerophospholipids being phosphatidylcholine (PC), phosphatidylethanolamine (PE), phosphatidylserine (PS) and phosphatidyl-inositol (PI), and optionally comprising a sphingolipid or a precursor or metabolite thereof, wherein the level of each of said PC, PE, PS and PI is at least 1% w/w, the ratio between said glycerophospholipids is PC>PE>PS>PI, and said glycerophospholipids are derived from a natural non-brain animal lipid source.
58 . The lipid preparation of claim 57 , wherein said sphingolipid is sphingomyelin (SM).
59 . The lipid preparation of claim 58 , comprising sphingomyelin, wherein the ratio between said glycerophospholipids is SM>PC>PE>PS>PI.
60 . The lipid preparation of claim 57 , wherein said glycerophospholipids are obtained from said natural non-brain animal lipid source by fractionation and/or extraction.
61 . The lipid preparation of claim 57 , wherein the level of PC is at least 5% w/w, the level of PS is at least 2% w/w, the level of PE is at least 4% w/w, and the level of PI is at least 2% w/w.
62 . The lipid preparation of claim 59 comprising at least 2% w/w SM.
63 . A process for the preparation of a lipid preparation comprising a mixture of glycerophospholipids being phosphatidyl-choline (PC), phosphatidylethanolamine (PE), phosphatidylserine (PS) and phosphatidyl-inositol (PI), and optionally comprising a sphingolipid or a precursor or metabolite thereof preferably sphingomyelin, wherein the ratio between said glycerophospholipids is PC>PE>PS>PI, from a natural non-brain animal lipid source, comprising isolating said lipid mixture from said natural non-brain animal lipid source by methods which do not involve transphosphatidylation.
64 . The process of claim 63 , wherein said sphingolipid is sphyngomyelin.
65 . The process of claim 64 , wherein said glycerophospholipid mixture comprises sphingomyelin from a natural non-brain animal lipid source, wherein the ratio between said glycerophospholipids is SM>PC>PE>PS>PI.
66 . The process of claim 63 , wherein said isolation comprises the steps of:
(a) providing a natural non-brain animal lipid source which has a substantially low content of polar lipids; (b) removing non-lipid material from said lipid source, dispersing the lipids, preferably with agitation, in a suitable organic solvent or a mixture of organic solvents; (c) separating the dissolved lipid fraction obtained in step (b) and removing the organic solvent therefrom to give a lipid fraction; (d) de-oiling said lipid fraction obtained in step (c) at least once to remove any non-polar lipids; (e) filtering and drying said polar lipids obtained in step (d); and
further optionally comprising a step of treating said lipid source with an aqueous medium, either before or after step (b).
67 . The process of claim 66 , wherein said glycerophospholipids mixture comprises sphingomyelin from a natural non-brain animal lipid source, wherein the ratio between said glycerophospholipids in said preparation is SM>PC>PE>PS>PI, comprising the steps of:
(a) providing a natural non-brain animal lipid source which has a substantially low content of polar lipids; (b) removing non-lipid material from said lipid source, dispersing the lipids, preferably with agitation, in a suitable organic solvent or a mixture of organic solvents, (c) separating the dissolved lipid fraction obtained in step (b) and removing the organic solvent therefrom to give a lipid fraction; (d) de-oiling said lipid fraction obtained in step (c) at least once to remove any non-polar lipids; (e) filtering and drying said polar lipids obtained in step (d); and
further optionally comprising a step of treating said lipid source with an aqueous medium, either before or after step (b).
68 . The process of claim 66 , wherein said natural lipid source is derived from bovine milk, and contains up to 5% w/w, preferably 10% w/w, more preferably 25% w/w, even more preferably 35% w/w of total lipids, and optionally contains sphingomyelin, in addition to other constituents including proteins and carbohydrates, and wherein about 20%, preferably 30%, more preferably 50%, most preferably 70% of said total lipids are polar lipids.
69 . The process of claim 64 , said process comprising further subjecting said preparation to a step of any one of alkaline hydrolysis, enzymatic hydrolysis, preparative chromatography or polar lipid extraction, whereby the lipid preparation obtained is enriched with sphingomyelin (SM).
70 . A dietary supplement comprising a lipid preparation as defined in claim 57 .
71 . The dietary supplement of claim 70 , for use as an ingredient of a lipid constituent of infant formulas or as an ingredient of infant formulas.
72 . A method for the enhancement of infants and/or children development, comprising administering to said infant or child a lipid preparation as defined in claim 57 .
73 . The method of claim 72 , wherein said development is cognitive development or vision development.
74 . A food article comprising the dietary supplement of claim 70 .
75 . The food article of claim 74 , wherein said food article is an infant formula.
76 . The process of claim 63 , further comprising the step of isolating SM from the polar lipid fraction.
77 . A method for the treatment of brain related illnesses or disorders or for improving cognitive functions or for treating, preventing or ameliorating myelin-related disorders or diseases, particularly de-myelination related disorders in a subject in need of such treatment, comprising administering to said subject the lipid preparation as defined in claim 57 .
78 . The method of claim 77 , wherein said brain-related disorder is one of mood-, memory-, stress-, or age-related disorders, dementia, Alzheimer's disease, said cognitive function is one of memory loss, problems of concentration and attention and learning capabilities, and said de-myelination related disorder is MS.
79 . A method of supporting and enhancing in a subject, the normal or improved development of myelin sheath and other sphingomyelin-related tissues comprising administering to said subject the lipid preparation of claim 58 .Cited by (0)
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