IP Library Granted Patent US 8,372,944
Granted Patent B1
US 8,372,944 · App. 12/417,017 · Granted Feb 12, 2013

Synthesis of hyperbranched amphiphilic polyester and theranostic nanoparticles thereof

Inventors: J. Manuel Perez (Orlando, FL); Santimukul Santra (Orlando, FL)
Assignee: University of Central Florida Research Foundation, Inc.
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Quick Facts
Patent No.
US 8,372,944
App. No.
12/417,017
Granted
Feb 12, 2013
Kind
B1
Abstract

A method of making a hyperbranched amphiphilic polyester compound includes drying under vacuum a mixture of 2-(4-hydroxybutyl)-malonic acid and p-toluene sulphonic acid as catalyst. The vacuum is then released with a dry inert gas after drying. The dried mixture is heated under the inert gas at a temperature sufficient for polymerization. The inert gas is evacuated while continuing to heat the mixture. The formed polymer is then dissolved in dimethylformamide and precipitated out by adding methanol. Modifications of the method yield nanoparticles of polyesters having properties suited for coencapsulating fluorescent dyes together with therapeutic drugs, resulting in theranostic nanoparticles, that is, nanoparticles useful in both therapeutic treatments and diagnostic methods.

Claims (41)

1. A method of making a hyperbranched amphiphilic polyester compound, the method comprising:

drying under vacuum a mixture of 2-(4-hydroxybutyl)-malonic acid and p-toluene sulphonic acid as catalyst;

releasing the vacuum with a dry inert gas after drying;

heating the dried mixture under the inert gas at a temperature sufficient for polymerization;

evacuating the inert gas while continuing to heat the mixture;

dissolving the formed polymer in dimethylformamide; and

precipitating the dissolved polymer by adding methanol.

2. The method of claim 1 , wherein drying comprises a mixture of 2-(4-hydroxybutyl)-malonic acid and p-toluene sulphonic acid in approximately a 100:1 molar ratio.

3. The method of claim 1 , wherein drying under vacuum is conducted at approximately 0.2 mmHg.

4. The method of claim 1 , wherein the inert gas is argon gas.

5. The method of claim 1 , wherein heating is at a temperature of approximately 150° C.

6. The method of claim 1 , wherein heating continues for approximately two hours.

7. The method of claim 1 , wherein evacuating is conducted at approximately 0.2 mmHg for about one hour while maintaining the polymerization temperature.

8. The method of claim 1 , further comprising purifying the polymer by separating the precipitate, washing with methanol and drying in a vacuum.

9. The method of claim 1 , further comprising:

dissolving the precipitated polymer in anhydrous dimethylformamide (DMF);

adding 1,1′-carbonyldiimidazole drop-wise to form a reaction mixture;

incubating the reaction mixture at room temperature for approximately one to two hours;

adding ethylenediamine in anhydrous DMF drop-wise and continue incubation of the reaction mixture at room temperature for approximately 24 hours; and

precipitating the reaction mixture in methanol, separating the precipitate and drying in a vacuum to obtain a purified hyperbranched polyester amine.

10. The method of claim 1 , further comprising:

dissolving the precipitated polymer in anhydrous dimethylformamide (DMF);

adding 1,1′-carbonyldiimidazole drop-wise to form a reaction mixture;

incubating the reaction mixture at room temperature for approximately one to two hours;

adding propargyl chloride in anhydrous DMF drop-wise and continue incubation of the reaction mixture at room temperature for approximately 24 hours; and

precipitating the reaction mixture in methanol, separating the precipitate and drying in a vacuum to obtain a purified hyperbranched propargylated polyester amine.

11. A method of making a hyperbranched amphiphilic polyester compound, the method comprising:

drying a mixture of 2-(4-hydroxybutyl)-malonic acid and a p-toluene sulphonic acid catalyst under vacuum;

heating the vacuum-dried mixture in the presence of an inert gas to a polymerization temperature and maintaining the polymerization temperature for a predetermined period of time;

evacuating the inert gas while continuing to heat the vacuum-dried mixture;

producing the hyperbranched amphiphilic polyester compound during heating, the polyester compound having a butyl group core from which a plurality of polyester branches extend, the polyester branches terminating in at least one carboxylic acid group;

purifying the hyperbranched amphiphilic polyester compound by dissolving the hyperbranched amphiphilic polyester in a first solvent; and

precipitating the hyperbranched amphiphilic polyester compound in a second solvent.

12. A method of making a hyperbranched amphiphilic polyester compound, the method comprising:

drying a mixture of 2-(4-hydroxybutyl)-malonic acid and a p-toluene sulphonic acid catalyst under vacuum;

introducing an inert gas to the dried mixture;

heating the dried mixture under the inert gas at a temperature sufficient for polymerization;

evacuating the inert gas while continuing to heat the dried mixture;

generating the hyperbranched amphiphilic polyester compound from the dried mixture, the hyperbranched amphiphilic polyester compound having a hydrophilic periphery surrounding a hydrophobic interior, the hydrophobic interior having a plurality of polyester branches that extend from a common butyl core, the periphery having a plurality of carboxylic acid groups that are attached to the terminal ends of the polyester branches; and

purifying the hyperbranched amphiphilic polyester compound by dissolving the hyperbranched amphiphilic polyester compound in a first solvent; and

precipitating the hyperbranched amphiphilic polyester compound in a second solvent.

Assignments (2)
CONFIRMATORY LICENSE Recorded Aug 27, 2013
From: UNIVERSITY OF CENTRAL FLORIDA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031087/0927 →
NUNC PRO TUNC ASSIGNMENT Recorded Apr 15, 2011
From: PEREZ, J. MANUEL; SANTRA, SANTIMUKUL
To: UNIVERSITY OF CENTRAL FLORIDA RESEARCH FOUNDATION, INC.
Reel/Frame 026135/0013 →
Continuity (1)
Provisional Application 61041624 · Apr 2, 2008