Contact lens packaging solutions

Patent metadata

Field	Value
Publication number	US-12171871-B2
Application number	US-202117392448-A
Country	US
Kind code	B2
Filing date	Aug 3, 2021
Priority date	Aug 11, 2020
Publication date	Dec 24, 2024
Grant date	Dec 24, 2024

Abstract

The present invention relates to a method to load a water insoluble phospholipid as nanoparticles to load into a hydrogel contact lens in autoclaving process during the hydrogel contact lens manufacturing process without an extra manufacturing step and without swelling the hydrogel contact lens with an organic solvent. The phospholipid nanoparticles loaded in hydrogel contact lens subsequently releases to the eye upon wearing.

First claim

What is claimed is:

1. A method for making a soft contact lens capable of releasing phosphatidylcholine nanoparticles comprising the steps of:
a) providing a phosphatidylcholine,
b) providing a nonionic surfactant,
c) mixing the phosphatidylcholine, the nonionic surfactant with an aqueous solution to form a mixture, wherein the aqueous solution is free of an organic solvent,
d) high-energy treating the mixture of step c) to form a phosphatidylcholiner nanoparticle in the mixture with a first concentration in the mixture,
e) diluting the mixture of step d) with a buffered saline solution to form a packaging solution, wherein the packaging solution has phosphatidylcholiner nanoparticle with a second concentration,
f) packaging a hydrogel contact lens in a container containing the packaging solution,
g) autoclaving the hydrogel contact lens in the packaging solution to load the phosphatidylcholine nanoparticle into the hydrogel contact lens, wherein the packaging solution has a pH of from about 6.0 to about 8.0, an osmolality of from about 200 to about 450 mOsm/kg, wherein the first concentration of the phosphatidylcholine nanoparticle is higher than the second concentration of the phosphatidylcholine nanoparticle.

2. The method of claim 1 , wherein the aqueous solution is a de-ionized water or a buffered saline.

3. The method of claim 1 , wherein the first concentration of a phosphatidylcholiner nanoparticle in step d) is 1000-50000 ppm.

4. The method of claim 1 , wherein the second concentration of the phosphatidylcholiner nanoparticle in step e) is 50 ppm-2000 mg/ml.

5. The method of claim 1 , wherein the phosphatidylcholine comprises at least one member selected from the group consisting of 1,2-Didecanoyl-sn-glycero-3-phosphocholine (DDPC), 1,2-Dilauroyl-sn-glycero-3-phosphorylcholine (DLPC), Dimyristoylphosphatidylcholine (DMPC), Dipalmitoylphosphatidylcholine (DPPC), 1,2-Distearoyl-sn-glycero-3-phosphocholine (DSPC), 1,2-Dioleoyl-sn-Glycero-3-Phosphocholine (DOPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC), 1,2-Dierucoyl-sn-Glycero-3-Phosphatidylcholine (DEPC).

6. The method of claim 5 , wherein the phosphatidylcholine is Dimyristoylphosphatidylcholine (DMPC) or Dipalmitoylphosphatidylcholine DPPC.

7. The method of claim 1 , wherein the nonionic surfactant having a HLB vales at least 8.

8. The method of claim 1 , wherein the nonionic surfactant having a HLB between 10 to 18.

9. The method of claim 8 , wherein the nonionic surfactant at least one member selected from the group consisting of a poloamine, a poloxamer and a polyethylene glycol ester.

10. The method of claim 1 , wherein high-energy treating is select from the group consisting of a high speed stirring with at least 800 rpm, a high pressure homogenizer or sonicating.

11. The method of claim 1 , wherein the hydrogel contact lens is a silicone hydrogel contact lens.

12. The method of claim 11 , wherein the hydrogel contact lens has a load of phosphatidylcholine nanoparticle from 10 μg/lens to 100 μg/lens.

Assignees

• Alcon Inc

Inventors

• Ge Junhao
• Zhang Steve Yun
• Wu Daqing
• Cheng Jing
• Chang Yuan
• Jing Feng
• Chiou Jang-Shing
• Perreault Stephen Raymond

Classifications

• B65B25/008

  packaging of contact lenses · CPC title

• A61L12/04

  Heat (A61L12/06 takes precedence) · CPC title

• A61K31/685

  one of the hydroxy compounds having nitrogen atoms, e.g. phosphatidylserine, lecithin · CPC title

• A61K9/5192

  Processes · CPC title

• A61K9/5146

  obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyamines, polyanhydrides · CPC title