Cancer treating composition containing copper-silver-phosphate nanoparticles

Patent metadata

Field	Value
Publication number	US-12357658-B2
Application number	US-202318343812-A
Country	US
Kind code	B2
Filing date	Jun 29, 2023
Priority date	Jan 19, 2022
Publication date	Jul 15, 2025
Grant date	Jul 15, 2025

Abstract

A method of making Cu—Ag3PO4 nanoparticles is provided. The method includes forming a mixture of at least one silver salt, at least one phosphate salt, and at least one copper (II) salt. The method further includes dissolving the mixture in water. The method further includes sonicating the mixture. The method further includes precipitating the Cu—Ag3PO4 nanoparticles or “nanoparticles”. The copper is present in the nanoparticles in an amount of 2 to 23 weight percent (wt. %) based on the total weight of the Cu—Ag3PO4. The nanoparticles of the present disclosure find application in treating cervical cancer, and colorectal cancer. The nanoparticles may also be used in photodegrading environmental pollutants.

First claim

The invention claimed is:

1. A cancer treating composition, comprising:
Cu—Ag 3 PO 4 nanoparticles comprising Cu in a range of from 2 to 10 wt. %, based on a total weight of the Cu—Ag 3 PO 4 nanoparticles, the cancer treating composition having an IC 50 in a range of from 45 to 105 μg/mL for HeLa cells or in a range of from 35 to 68 μg/mL for HCT-116 cells,
wherein the cancer is cervical cancer or colorectal cancer;
wherein the Cu—Ag 3 PO 4 nanoparticles are made by a method comprising:
forming a mixture of at least one silver salt, at least one phosphate salt, and at least one copper (II) salt;
dissolving the mixture in water;
sonicating the mixture; and
precipitating the Cu—Ag 3 PO 4 nanoparticles; and
wherein the Cu—Ag 3 PO 4 nanoparticles comprise CuO particles and Ag 3 PO 4 particles,
wherein the Cu—Ag 3 PO 4 nanoparticles are spherical and
wherein the Cu—Ag 3 PO 4 nanoparticles have a mean particle size in a range of from 100 to 1000 nm.

2. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles comprise Cu in a range of from 2 to 7 wt. %, based on the total weight of the Cu—Ag 3 PO 4 nanoparticles, and
wherein the cancer treating composition has an IC 50 in a range of from 69 to 73 μg/mL for HeLa cells or in a range of from 66 to 68 μg/mL for HCT-116 cells.

3. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles comprise Cu in a range of from 8 to 10 wt. %, based on the total weight of the Cu—Ag 3 PO 4 nanoparticles, and
wherein the cancer treating composition has an IC 50 in a range of from 95 to 105 μg/mL for HeLa cells or in a range of from 35 to 45 for HCT-116 cells.

4. The cancer treating composition of claim 1 , wherein
the method of making the Cu—Ag 3 PO 4 nanoparticles further comprises:
dissolving the copper (II) salt in water to form a dissolved copper (II) salt;
mixing the silver salt into the dissolved copper (II) salt to form a solution;
dissolving the phosphate salt in water to form a phosphate mixture and dropwise mixing the phosphate mixture into the solution; and
sonicating the mixture for at least one hour.

5. The cancer treating composition of claim 1 , wherein the method of making the Cu—Ag 3 PO 4 nanoparticles further comprises:
centrifuging the mixture after the precipitating and separating precipitated Cu—Ag 3 PO 4 nanoparticles;
washing the precipitated Cu—Ag 3 PO 4 nanoparticles with ethanol and water; and
drying the washed Cu—Ag 3 PO 4 nanoparticles at a temperature less than 150° C.

6. The cancer treating composition of claim 1 , wherein the silver salt is silver nitrate;
wherein the phosphate salt is disodium hydrogen phosphate; and
wherein the copper (II) salt is copper (II) oxide (CuO).

7. The cancer treating composition of claim 1 , wherein the copper (II) salt is CuO, and
wherein the CuO is made by a method comprising:
dissolving copper nitrate trihydrate in water in a polytetrafluoroethylene (PTFE) lined autoclave to form a dissolved copper nitrate trihydrate;
mixing trisodium citrate and ammonium fluoride into the dissolved copper nitrate trihydrate at a temperature less than 23° C. to form a solution;
heating the solution in the PTFE lined autoclave at a temperature over 120° C. for more than 10 hours;
centrifuging the heated solution and removing excess liquid from a CuO precipitate;
washing the CuO precipitate with ethanol and water;
drying the washed CuO precipitate at a temperature less than 150° C.; and
calcining the dried CuO precipitate at a temperature greater than 300° C. to form the CuO.

8. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles comprise:
copper in a range of from 2 to 7 wt. %; and have
a mean surface area in a range of from 2.5 to 3.5 m 2 /g;
a mean pore size in a range of from 20 to 30 nm; and
a mean pore volume in a range of from 100 to 200 cm 3 /g.

9. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles comprise:
copper in a range of from 8 to 10 wt. %; and have
a mean surface area in a range of from 3.8 to 4.8 m 2 /g;
a mean pore size in a range of from 25 to 35 nm; and
a mean pore volume in a range of from 100 to 200 cm 3 /g.

10. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles consist essentially of CuO particles and Ag 3 PO 4 particles.

11. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles have a pore size in a range of from 25 to 30 nm and a pore volume in a range of from 0.01 to 0.15 cm 3 /g.

12. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles have a mean particle size in a range of from 200 to 900 nm.

13. The cancer treating composition of claim 1 , wherein the Cu—Ag 3 PO 4 nanoparticles have a mean particle size in a range of from 400 to 700 nm.

Assignees

• Univ Imam Abdulrahman Bin Faisal

Inventors

• Nawaz Muhammad
• Khan Firdos Alam

Classifications

• B82Y5/00

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

• C01P2006/14

  Pore volume · CPC title

• C01P2002/84

  by UV- or VIS- data · CPC title

• C01P2002/85

  by XPS, EDX or EDAX data · CPC title

• C01P2004/03

  obtained by SEM · CPC title