Method of forming inorganic nanocages

Patent metadata

Field	Value
Publication number	US-10688556-B2
Application number	US-201715477601-A
Country	US
Kind code	B2
Filing date	Apr 3, 2017
Priority date	Apr 1, 2016
Publication date	Jun 23, 2020
Grant date	Jun 23, 2020

Abstract

Nanocages are formed by etching nancubes. The nanocubes are added to an aqueous system having an amphiphilic lipid dissolved in an organic solvent (e.g. a hydrophobic alcohol) to form reverse micelles. As the water evaporates the micelles shrink as etching of the flat surface of the nanocubes occurs. In this fashion hollow nanocages are produced. In one embodiment, the nanocage is covalently attached to a polymer shell (e.g. a dextran shell).

First claim

The invention claimed is:

1. A method of forming a nanocage, the method comprising sequential steps of:
forming a reverse micelle system comprising an inorganic nanocube consisting of palladium, the inorganic nanocube having a diameter of 15 nm or less, the reverse micelle system further comprising an amphiphilic lipid, water and an organic solvent that is immiscible with water and has a boiling point greater than 100° C.,
removing the water by evaporation, the step of removing causing the inorganic nanocube to undergo atomic desorption in an etchant-free environment to form a nanocage, wherein the nanocage has a diameter less than the diameter of the inorganic nanocube;
isolating the nanocage;
attaching a dextran polymer to the nanocage thereby forming a nanocage-polymer complex that has a diameter of less than 50 nm.

2. The method as recited in claim 1 , wherein the nanocage is covalently attached to the dextran polymer shell by a dopamine linking group.

3. The method as recited in claim 1 , wherein the dextran polymer comprises an aminodextran.

4. The method as recited in claim 1 , wherein the amphiphilic lipid is selected from a group consisting of cetyl-trimethylammonium bromide, hexadecyl trimethyl ammonium chloride, sodium dodecyl sulfate, sodium dodecyl benzene sulfonate, oleic acid and oleylamine.

5. The method as recited in claim 1 , wherein the organic solvent is octanol.

6. The method as recited in claim 1 , wherein
the amphiphilic lipid is cetyl-trimethylammonium bromide;
the organic solvent is octanol.

7. A method of forming a nanocage, the method comprising sequential steps of:
forming a reverse micelle system comprising an inorganic nanocube consisting of iron oxide having a diameter of 15 nm or less, the reverse micelle system further comprising an amphiphilic lipid, water and an organic solvent that is immiscible with water and has a boiling point greater than 100° C.;
removing the water by evaporation, the step of removing causing the inorganic nanocube to undergo atomic desorption in an etchant-free environment to form an iron oxide nanocage, wherein the iron oxide nanocage has a diameter less than the diameter of the inorganic nanocube;
isolating the nanocage;
attaching a dextran polymer to the iron oxide nanocage to form a nanocage-polymer complex with a diameter of less than 50 nm and the iron oxide nanocage is attached to the dextran polymer shell by a catechol linking group.

8. The method as recited in claim 7 , wherein the catechol is a dopamine.

9. The method as recited in claim 7 , wherein the dextran comprises an aminodextran.

Assignees

• Univ City New York Res Found

Inventors

• Matsui Hiroshi
• Wei Zengyan
• Fang Justin

Classifications

• B22F1/102

  Metallic powder coated with organic material · CPC title

• B22F1/145

  Chemical treatment, e.g. passivation or decarburisation · CPC title

• B22F1/0553

  Complex form nanoparticles, e.g. prism, pyramid, octahedron · CPC title

• B22F1/054 Primary

  Nanosized particles · CPC title

• C09C1/24

  Oxides of iron · CPC title