Therapeutic, radiolabeled nanoparticles and methods of use thereof

Patent metadata

Field	Value
Publication number	US-2023398243-A1
Application number	US-202118035174-A
Country	US
Kind code	A1
Filing date	Nov 3, 2021
Priority date	Nov 3, 2020
Publication date	Dec 14, 2023
Grant date	—

Abstract

Provided herein are therapeutic nanoparticles including a radiolabel, a chelator that is covalently linked to the therapeutic nanoparticle and to the radiolabel, and a nucleic acid molecule that is covalently linked to the therapeutic nanoparticle. The therapeutic nanoparticle has a diameter between about 10 nanometers (nm) to about 30 nm, and the therapeutic nanoparticle is magnetic. Also provided are pharmaceutical compositions containing these therapeutic nanoparticles. Also provided herein are methods of decreasing cancer cell invasion or metastasis in a subject having a cancer and methods of treating a metastatic cancer in a lymph node in a subject that require the administration of these therapeutic nanoparticles to a subject. Also provided herein are methods of detecting, diagnosing, and/or monitoring a metastatic cancer tissue in a subject. Also provided herein are methods of preparing these therapeutic nanoparticles.

First claim

1 . A therapeutic nanoparticle comprising:
a radiolabel; a chelator that is covalently linked to the therapeutic nanoparticle and to the radiolabel; and a nucleic acid molecule that is covalently linked to the therapeutic nanoparticle, wherein the therapeutic nanoparticle has a diameter between about 10 nanometers (nm) to about 30 nm, and wherein the therapeutic nanoparticle is magnetic.

2 . The therapeutic nanoparticle of claim 1 , wherein the chelator is covalently-linked to the therapeutic nanoparticle through a chemical moiety comprising a secondary amine.

3 . The therapeutic nanoparticle of claim 1 , wherein the chelator comprises 1,4,7-triazacyclononane, 1-glutaric acid-4,7-acetic acid (NODAGA).

4 . The therapeutic nanoparticle of claim 1 , wherein the chelator comprises DOTA, DOTA-GA, p-SCN-Bn-DOTA, CB-TE2A, CB-TE1A1P, AAZTA, MeCOSar, p-SCN-Bn-NOTA, NOTA, HBED-CC, THP, MASS, DFO, or any combination thereof.

5 . The therapeutic nanoparticle of claim 1 , wherein the radiolabel comprises copper-64 (Cu-64).

6 . The therapeutic nanoparticle of claim 1 , wherein the radiolabel comprises copper-67 (Cu-67), yttrium-90 (Y-90), terbium-161 (Tb-161), lutetium-177 (Lu-177), bismuth-231(Bi-213), lead-212 (Pb-212), actinium-225 (Ac-225), zirconium-89 (Zr), or any combination thereof.

7 . The therapeutic nanoparticle of claim 1 , wherein the nucleic acid molecule comprises at least one modified nucleotide.

8 . The therapeutic nanoparticle of claim 7 , wherein the at least one modified nucleotide is a locked nucleotide.

9 . The therapeutic nanoparticle of claim 1 , wherein the nucleic acid molecule is an antagomir.

10 . The therapeutic nanoparticle of claim 9 , wherein the antagomir inhibits microRNA-10b (miR-10b).

11 . The therapeutic nanoparticle of claim 1 , wherein the nucleic acid molecule is covalently-linked to the nanoparticle through a chemical moiety comprising a disulfide bond.

12 . The therapeutic nanoparticle of claim 1 , wherein the therapeutic nanoparticle comprises an iron oxide core.

13 . The therapeutic nanoparticle of claim 1 , wherein the nanoparticle further comprises a polymer coating.

14 . The therapeutic nanoparticle of claim 13 , wherein the polymer coating comprises dextran.

15 . A pharmaceutical composition comprising the therapeutic nanoparticle of claim 1 .

16 . The pharmaceutical composition of claim 15 , further comprising at least one pharmaceutically acceptable carrier or diluent.

17 . The pharmaceutical composition of claim 15 , wherein the pharmaceutical composition is formulated into a dosage form that is an injectable, a tablet, a lyophilized powder, a suspension, or any combination thereof.

18 . A method for decreasing cancer cell invasion or metastasis in a subject having a cancer, the method comprising administering a therapeutic nanoparticle of claim 1 to the subject having the cancer, wherein the therapeutic nanoparticle is administered in an amount sufficient to decrease cancer cell invasion or metastasis in the subject.

19 . The method of claim 18 , wherein the therapeutic nanoparticle is administered to the subject at a dose that is less than about 0.014 mg/kg.

20 . The method of claim 18 , wherein the cancer cell metastasis is from a primary tumor to a lymph node in the subject or is from a lymph node to a secondary tissue in a subject.

21 - 35 . (canceled)

Assignees

• Massachusetts Gen Hospital

Inventors

• Medarova Zdravka
• Shuvaev Sergey
• Caravan Peter
• Le Fur Mariane
• Yoo Byunghee

Classifications

• A61K51/1244 Primary

  microparticles or nanoparticles, e.g. polymeric nanoparticles · CPC title

• A61P35/04

  specific for metastasis · CPC title

• A61K51/0491

  Sugars, nucleosides, nucleotides, oligonucleotides, nucleic acids, e.g. DNA, RNA, nucleic acid aptamers · CPC title

• A61K51/0482

  chelates from cyclic ligands, e.g. DOTA · CPC title

• B82Y5/00

  Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery · CPC title