Blood filtration system containing mannose coated substrate

a filtration system and substrate technology, applied in the direction of filtration separation, moving filter element filter, separation process, etc., can solve the problems of drug-resistant pathogens threatening the healthcare system, current antibiotics becoming less effective, and the current market for new anti-infective drugs is relatively small in comparison to their significant regulatory and development costs, so as to improve overall safety

Inactive Publication Date: 2016-04-14
EXTHERA MEDICAL
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0008]The present invention provides methods to functionalize the surface of a media with mannose. In certain instances, mannose media and heparinized media can be combined or mixed together to create a single...

Problems solved by technology

The emergence of drug-resistant pathogens is a growing threat to the healthcare system.
Not only are current antibiotics becoming less effective, large pharmaceutical companies are shifting focus from new antimicrobial development to more lucrative drug discovery programs such as cancer therapeutics.
Although it is recognized that “superbugs” are a major concern, the current market for new anti-infective drugs is relatively small in comparison to their significant regulatory and development costs.
Resistance of CREs to even the strongest available antibiotics leaves clinicians with few treatment options.
This is a major challenge as some of...

Method used

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  • Blood filtration system containing mannose coated substrate
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  • Blood filtration system containing mannose coated substrate

Examples

Experimental program
Comparison scheme
Effect test

example 1

End-Point Attachment of Intact Mannan from Sacchromyces Cerevisiae to Aminated Beads Via the Reducing Terminal Residue

[0101]Oligomers of mannose are reductively coupled to primary amines on aminated beads by reductive amination. Coupling of the open aldehyde form to the bead results in a stable secondary amine and the reaction is as set forth below in Reaction Scheme 1.

[0102]In water, the aldehyde function of the D-mannopyranose below is in equilibrium with the α and β forms, formed, by ring closure with the hydroxyl function on carbon atom 5, thus forming a six membered ring. A small proportion of the open free aldehyde form is always present in the equilibrium. The latter react with primary amines and Schiff's bases are formed. By reduction, these bases are irreversible converted to stable secondary amines. Thus, even if the open aldehyde form is less than 1% in the equilibrium the coupling yields are satisfactory.

[0103]Mannan from Saccharomyces cerevisiae is coupled to primary am...

example 2

End-Point Attachment of Low Molecular Weight Oligo-Mannose (LMV-Mannose)

[0109]The reaction scheme is essentially the same as described in Example 1.

[0110]Sodium chloride, 0.37 g. (Sigma-Aldrich, Lot no. BCBG1923V) was dissolved in 12.5 ml of DI water with magnetic stirring. LMV-Mannose, 5.0 mg. was dissolved in the water solution also with stirring.

[0111]Aminated beads, 5.0 g, (ExThera Medical, Lot no. 1120341) were added to the solution and the pH was adjusted to 3.9 with 0.1 M hydrochloric acid. The acid used to make the 0.1 M hydrochloric acid was 2M HCL (ExThera AB, Lot no. 121204) diluted with purified water (1:19).

[0112]A solution of Sodium cyanoborohydride, 5.0 mg, (Acros Organics, Lot no. A0240008) in 0.5 mL purified water was added to the mixture. The mixture was heated to 60° C. for the duration of 24 hours.

[0113]The pH was controlled for 1 hour and was subsequently adjusted down to 3.9 with 0.1M HCl from approximately 5.8. After 24 hours pH increased to approx. 5.7. The b...

example 3

End-Point Attachment of Middle Molecular Weight Oligo-Mannose to Aminated Beads Via the Reducing Terminal Residue (MMV-Mannose)

[0114]The reaction schemes are essentially the same as described in Example 1.

[0115]Oligomers of mannose are reductively coupled to primary amines on aminated beads by reductive amination. Coupling of the open aldehyde form to the bead results in a stable secondary amine and the reaction is irreversible.

[0116]The aldehyde function of the monosaccharide unit in the reducing terminal unit is in equilibrium with the hemiacetal, formed by ring closure with the hydroxyl function on carbon atom 5 and, thus forming a six membered ring and the open free aldehyde form. The latter can be used for reductive coupling to primary amines by the use of NaBH3CN. Sodium chloride, 0.37 g. (Sigma-Aldrich, Lot no. BCBG1923V) was dissolved in 12.5 mL of DI water with magnetic stirring. MMV-Mannose, 5.0 mg. was dissolved in the water solution also with stirring.

[0117]Aminated bead...

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Abstract

A blood filtration method, system, device and media for removing gram negative bacteria from the blood wherein the media includes a substrate coated with mannose optionally in constitution with substrate coated with heparin.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS[0001]The present application is a continuation of PCT / US2014 / 043358, filed Jun. 20, 2014, which application claims priority to U.S. Provisional Patent Application No. 61 / 838,854, filed Jun. 24, 2013, the disclosures of which are hereby incorporated by reference in their entireties for all purposes.BACKGROUND OF THE INVENTION[0002]The emergence of drug-resistant pathogens is a growing threat to the healthcare system. Not only are current antibiotics becoming less effective, large pharmaceutical companies are shifting focus from new antimicrobial development to more lucrative drug discovery programs such as cancer therapeutics. Although it is recognized that “superbugs” are a major concern, the current market for new anti-infective drugs is relatively small in comparison to their significant regulatory and development costs.[0003]The CDC has recently warned of the emergence of carbapenem-resistant Enterobacteriacea (CRE). The mortality rate for ...

Claims

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Application Information

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IPC IPC(8): A61M1/34B01D39/08B01D39/16C07H1/00B01D63/08B01D65/08B01D71/08B01D39/04B01D63/10
CPCA61M1/34B01D39/04B01D39/083B01D39/1615B01D63/10A61M1/3673B01D65/08B01D71/08C07H1/00A61M2205/7518B01D63/08A61M1/3679A61M1/3687A61M2202/203A61M1/36A61M2205/33A61M2205/3334
Inventor MCCREA, KEITHWARD, ROBERTLARM, OLLEADOLFSSON, LARS
Owner EXTHERA MEDICAL
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