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Omega-3 pentaenoic acid compositions and methods of use

A composition and technology of eicosapentaenoic acid, applied in the direction of drug combination, active ingredient of heterocyclic compound, application, etc., can solve problems such as unmet medical needs

Inactive Publication Date: 2015-09-23
MATINAS BIOPHARMA
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, with the increasing popularity of omega-3 fatty acid concentrates, there is an unmet need for omega-3 fatty acid-containing compositions with improved bioavailability and a more optimal ratio of TG-lowering potency to resulting cholesterol profile. medical need

Method used

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  • Omega-3 pentaenoic acid compositions and methods of use
  • Omega-3 pentaenoic acid compositions and methods of use
  • Omega-3 pentaenoic acid compositions and methods of use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0188] Intermediates MEGAPEX E90D00EE (90% EPA ethyl ester) and MAXOMEGA DPA95FFA (≥95% DPA synthetic fatty acid made from EPA ethyl ester concentrate) converted to ethyl esters respectively by mixing and homogenizing in a ratio of 98:2 to prepare the composition of the present invention. These intermediates are prepared and sold commercially by Chemport Korea (MEGAPEX) and Equateq Ltd (MAXOMEGA) from Scotland, UK. The relative amounts of fatty acids present in the starting intermediates and the resulting novel compositions are listed in Table 1 below. The resulting novel composition comprises 89.10% EPA, 1.95% DPA, 0.19% HPA, 91.24% omega-3-pentaenoic acid, less than 0.01% DHA, 91.24% omega-3-pentaenoic acid, 93.09% of total omega-3 fatty acids, 3.15% ARA and 3.57% omega-6 fatty acids (all area %).

[0189] Table 1. The intermediate of embodiment 1 and the fatty acid composition (area %) of novel composition

[0190]

Embodiment 2

[0192] Intermediates MEGAPEX E90D00EE (90% EPA ethyl ester) and MAXOMEGA DPA95FFA (≥95% DPA synthetic fatty acid made from EPA ethyl ester concentrate) converted to ethyl esters respectively by mixing and homogenizing in a ratio of 96:4 to prepare the composition of the present invention. These intermediates are prepared and sold commercially by Chemport Korea (MEGAPEX) and Equateq Ltd (MAXOMEGA) from Scotland, UK. The relative amounts of fatty acids present in the starting intermediates and the resulting novel compositions are listed in Table 2 below. The resulting novel composition contained 87.28% EPA, 3.89% DPA, 0.18% HPA, 91.35% omega-3-pentaenoic acid, less than 0.01% DHA, 93.17% total omega-3 fatty acids, and 3.49% omega -6 fatty acids (both area %).

[0193] Table 2. The intermediate of embodiment 2 and the fatty acid composition (area %) of novel composition

[0194]

Embodiment 3

[0196] Intermediates MEGAPEX E90D00EE (90% EPA ethyl ester) and MAXOMEGA DPA95FFA (≥95% DPA synthetic fatty acid made from EPA ethyl ester concentrate) converted to ethyl esters respectively by mixing and homogenizing in a ratio of 94:6 to prepare the composition of the present invention. These intermediates are prepared and sold commercially by Chemport Korea (MEGAPEX) and Equateq Ltd (MAXOMEGA) from Scotland, UK. The relative amounts of fatty acids present in the starting intermediates and the resulting novel compositions are listed in Table 3 below. The resulting novel composition contained 85.46% EPA, 5.84% DPA, 0.18% HPA, 91.48% omega-3-pentaenoic acid, less than 0.01% DHA, 93.26% total omega-3 fatty acids, 3.02% ARA and 3.42% omega-6 fatty acids (both area %).

[0197] Table 3. The intermediate of embodiment 3 and the fatty acid composition (area %) of novel composition

[0198]

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Abstract

The present invention relates to methods of reducing lipid parameters, such as triglycerides, total cholesterol, low density lipoprotein (LDL) cholesterol, non-HDL cholesterol, free fatty acids, and other lipids, comprising administration of omega-3 docosapentaenoic acid.

Description

[0001] related application [0002] This application claims the benefit of U.S. Provisional Patent Application No. 61 / 734,331, filed December 6, 2012, and U.S. Provisional Patent Application No. 61 / 780,948, filed March 13, 2013, the contents of which are incorporated herein by reference. field of invention [0003] The present invention relates to a method comprising administering an omega-3 fatty acid composition to reduce fasting lipid parameters such as triglycerides, total cholesterol, low density lipoprotein (LDL) cholesterol, free fatty acids and other lipids. The present invention also relates to a method comprising administering an omega-3 fatty acid composition to raise high-density lipoprotein (HDL) cholesterol. The method of the invention can be used to treat a condition selected from the group consisting of hypertriglyceridemia; hypercholesterolemia; mixed dyslipidemia; coronary heart disease (CHD); Arterial syndromes; atherosclerotic disease and related condition...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12P7/64A23D9/00
CPCC11B5/0007A23D9/00A23D9/06A61K31/202A61K31/40A61K2300/00A61K9/4825A61K9/4858A61P25/00A61P29/00A61P3/06A61P9/10A61P3/10A61K9/4875A61K47/22
Inventor 乔治·博博泰斯阿卜杜勒·阿齐兹·法齐
Owner MATINAS BIOPHARMA