US2022296632A1PendingUtilityA1

Mrna functionalization method

Assignee: UNIV TOKYOPriority: Dec 27, 2016Filed: May 16, 2022Published: Sep 22, 2022
Est. expiryDec 27, 2036(~10.4 yrs left)· nominal 20-yr term from priority
A61K 48/005A61K 31/7115A61P 33/00A61K 47/6911A61K 2039/53A61K 47/549A61K 48/00A61K 2039/6025A61P 31/10A61K 47/50C12N 15/117A61K 31/7088A61K 39/0001A61K 39/39A61K 39/0003A61P 37/04A61P 35/00A61P 31/04A61P 31/12A61K 39/0011A61K 2039/5154A61K 39/00A61K 31/713A61K 48/0008Y02A50/30
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Claims

Abstract

The present invention provides a functionalized mRNA including mRNA and double-stranded RNA including at least one RNA oligomer hybridized with mRNA. Functionalized mRNA is provided according to this configuration.

Claims

exact text as granted — not AI-modified
1 . A method for stabilizing a carrier, which comprises:
 allowing a carrier to load therein an mRNA encoding a target gene and at least one RNA oligomer hybridizing with the mRNA, wherein   the RNA oligomer comprises:   (a) an RNA sequence consisting of a sequence of 12 to 40 nucleotides complementary to the sequence of the mRNA, or   (b) an RNA sequence having an identity of 90% or more to a sequence of 12 to 40 nucleotides complementary to the sequence of the mRNA, and hybridizing with the mRNA,   and the RNA oligomer is chemically unmodified or is chemically modified.   
     
     
         2 . The method of  claim 1 , wherein the RNA sequence consists of a sequence of 15 to 23 nucleotides. 
     
     
         3 . The method of  claim 1 , wherein the RNA sequence consists of a sequence of 17 nucleotides. 
     
     
         4 . The method of  claim 1 , wherein the RNA oligomer comprises said RNA sequence (a) or (b) that is chemically modified. 
     
     
         5 . The method of  claim 4 , wherein the chemical modification is performed on the 5′-terminus or 3′-terminus of the sequence of the RNA oligomer via an overhang sequence consisting of 1 to 5 nucleotides. 
     
     
         6 . The method of  claim 5 , wherein the overhang sequence is a sequence consisting of 2 nucleotides. 
     
     
         7 . The method of  claim 4 , wherein the chemical modification is modification with a hydrophobic group. 
     
     
         8 . The method of  claim 4 , wherein the modification with a hydrophobic group is cholesterol modification. 
     
     
         9 . The method of  claim 4 , wherein the chemical modification is polyethylene glycol modification. 
     
     
         10 . The method of  claim 1 , wherein the carrier is a polymeric micelle or a lipidic mRNA carrier.

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