US2021322568A1PendingUtilityA1
Virucidal Nanoparticles And Use Thereof Against Influenza Virus
Assignee: ECOLE POLYTECHNIQUE FED LAUSANNE EPFLPriority: Sep 4, 2018Filed: Sep 3, 2019Published: Oct 21, 2021
Est. expirySep 4, 2038(~12.1 yrs left)· nominal 20-yr term from priority
A61P 31/16A61K 47/549A61K 47/6929A61K 47/61A61K 47/6939A61K 47/6951A61K 47/6923
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Claims
Abstract
The invention relates to virucidal nanoparticles comprising a trisaccharide moiety and use thereof against influenza virus.
Claims
exact text as granted — not AI-modified1 . A virucidal nanoparticle comprising a core and a plurality of ligands covalently linked to the core, wherein at least a portion of said ligands comprise a trisaccharide moiety and wherein:
the core is cyclodextrin, the ligands are the same or different and are optionally substituted alkyl-based ligands, and each trisaccharide moiety is selected from 3-sialyl-N-acetyllactoseamine (3′SLN) and 6-sialyl-N-acetyllactoseamine (6′SLN).
2 . The virucidal nanoparticle of claim 1 , wherein cyclodextrin is selected from the group consisting of alpha-cyclodextrin, beta-cyclodextrin, gamma-cyclodextrin, and a combination thereof.
3 . The virucidal nanoparticle of claim 1 , wherein the ligands are optionally substituted C 4 -C 30 alkyl-based ligands.
4 . The virucidal nanoparticle of claim 1 , wherein the ligands are optionally substituted C 6 -C 15 alkyl-based ligand compounds.
5 . The virucidal nanoparticle of claim 1 , wherein some or all of said ligands comprise 3′SLN, some or all of said ligands comprise 6′SLN, and some but not all of said ligands comprise no trisaccharide moiety.
6 . A virucidal nanoparticle represented by Formula (I)
wherein
m is 2 to 8, and
n is 2 to 28 or 4 to 13.
7 . The virucidal nanoparticle of claim 6 , wherein cyclodextrin is selected from the group comprising alpha-cyclodextrin, beta-cyclodextrin, and gamma-cyclodextrin.
8 . The virucidal nanoparticle of claim 6 , wherein m is 3 or 4.
9 . A virucidal nanoparticle represented by Formula (II)
wherein:
each R, independently, is an optionally substituted alkyl-based ligand, wherein at least two of said ligands have a trisaccharide moiety selected from the group comprising 3-sialyl-N-acetyllactoseamine (3′SLN) and 6-sialyl-N-acetyllactoseamine (6′SLN), or wherein at least one of said ligands has 3′SLN and another has 6′SLN;
each R′, independently, is H, —(CH 2 ) y —COOH, —(CH 2 ) y —SO 3 − , a polymer or a water solubilizing moiety;
x is 6, 7 or 8; and
y is an integer from 4 to 20,
or a pharmaceutically acceptable salt thereof.
10 . The virucidal nanoparticle of claim 9 , wherein R′ is H.
11 . The virucidal nanoparticle of claim 9 , wherein said alkyl-based ligands are optionally substituted C 4 -C 30 alkyl-based ligands.
12 . The virucidal nanoparticle of claim 9 , wherein the alkyl-based ligands are optionally substituted C 6 -C 15 alkyl-based ligands comprising 6′SLN.
13 . A pharmaceutical composition comprising an effective amount of one or more virucidal nanoparticles of claim 1 and at least one pharmaceutically acceptable excipient, carrier and/or diluent.
14 . A method of treating and/or preventing an influenza virus infection and/or a disease associated with an influenza virus, the method comprising administering to a subject in need thereof a therapeutically effective amount of one or more virucidal nanoparticles of claim 1 .
15 . A virucidal composition comprising an effective amount of one or more virucidal nanoparticles of claim 1 and optionally at least one suitable aerosol carrier.
16 . A method of disinfection and/or sterilization comprising contacting a surface with the virucidal nanoparticle of claim 1 .
17 . A device comprising one or more virucidal nanoparticles of claim 1 and means for applying or dispensing the virucidal nanoparticles.
18 . (canceled)Join the waitlist — get patent alerts
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