IP Library Granted Patent US 10,370,656
Granted Patent B2
US 10,370,656 · App. 15/296,387 · Granted Aug 6, 2019

Nucleic acid functionalized nanoparticles for therapeutic applications

Inventors: Chad A. Mirkin (Wilmette, IL); David A. Giljohann (Chicago, IL); Dwight S. Seferos (Toronto, CA)
Assignee: NORTHWESTERN UNIVERSITY
C12N15/113A61K9/51A61K31/7088C12N15/111C12N15/87C12N2310/11C12N2310/14C12N2310/351C12N2320/32
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Quick Facts
Patent No.
US 10,370,656
App. No.
15/296,387
Granted
Aug 6, 2019
Kind
B2
Abstract

Materials and methods for modulating cellular uptake of functionalized nanoparticles are provided. Also provided are materials and methods for modulating the effectiveness of a therapeutic agent with a functionalized nanoparticle.

Claims (17)

1. A method of modulating effectiveness of an anticancer drug comprising the step of:

administering said anticancer drug concomitantly with an oligonucleotide-functionalized nanoparticle, wherein said oligonucleotide-functionalized nanoparticle comprises an oligonucleotide comprising a sequence that modulates the effectiveness of said anticancer drug, and wherein the nanoparticle does not comprise a targeting agent.

2. The method of claim 1 wherein cellular localization of the anticancer drug is controlled by the oligonucleotide-functionalized nanoparticle.

3. The method of claim 1 wherein the oligonucleotide sequence is a chemosensitizing antisense sequence.

4. The method of claim 3 wherein the chemosensitizing antisense sequence increases the toxicity of the anticancer drug.

5. The method of claim 1 wherein the nanoparticle is non-metallic.

6. The method of claim 1 wherein the nanoparticle is metallic.

7. The method of claim 6 wherein the nanoparticle comprises gold, silver, platinum, aluminum, palladium, copper, cobalt, indium, or nickel.

8. The method of claim 1 wherein the effectiveness of the anticancer drug is altered by at least 10%, or at least 15%, or at least 20%, or at least 25%, or at least 30%, or at least 40%, or at least 50%, or at least 60%, or at least 70%, at least 80%, at least 90%, at least 95%, at least 2-fold, at least 5-fold, at least 10-fold, at least 20-fold, at least 50-fold or more compared to effectiveness of the anticancer drug in the absence of the oligonucleotide-functionalized nanoparticle.

9. The method of claim 1 wherein the oligonucleotide is from about 5 to about 100 nucleotides in length.

10. The method of claim 1 wherein the nanoparticle is from about 5 nanometers (nm) to about 50 nm in mean diameter.

11. The method of claim 1 wherein at least 20 oligonucleotides are functionalized to the nanoparticle.

12. The method of claim 1 wherein density of oligonucleotide on the surface of the nanoparticle is from about 1.5 pmol/cm 2 to about 25 pmol/cm 2 .

13. The method of claim 1 wherein density of oligonucleotide on the surface of the nanoparticle is about 4 pmol/cm 2 .

14. The method of claim 1 wherein the oligonucleotide is attached to the nanoparticle through a spacer.

15. The method of claim 1 wherein the oligonucleotide is a DNA oligonucleotide or a RNA oligonucleotide.

16. The method of claim 1 wherein the oligonucleotide-functionalized nanoparticle is associated with the anticancer drug.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2017
From: MIRKIN, CHAD A.; GILJOHANN, DAVID A.; SEFEROS, DWIGHT
To: NORTHWESTERN UNIVERSITY
Reel/Frame 044190/0852 →
Continuity (5)
Continuation 12130643 · May 30, 2008
Continuation In Part PCTUS2006022325 · Jun 8, 2006
Provisional Application 60985462 · Nov 5, 2007
Provisional Application 60940886 · May 30, 2007
Related Publication 20170137809A1 · May 18, 2017
Cited By (5)
US 12,264,344 US 12,319,711 US 12,378,560 US 12,691,166 US 12,702,719