Deposition products, composite materials and processes for the production thereof

• US 7,300,673 B2
• Filed: 04/23/2004
• Issued: 11/27/2007
• Est. Priority Date: 05/16/2003
• Status: Active Grant

• Current Assignee: Argent Limited Partnership
• Original Assignee: Exciton Technologies Inc.
• Inventors: Djokic, Stojan
• Primary Examiner(s): Richter; Johann R.
• Assistant Examiner(s): Arnold; Ernst V
• Application Number:
  US10/830,574
• Publication Number:
  US 20040229034A1
• Time in Patent Office: 1,313 Days
• Field of Search: 514/495, 514/709, 424/613, 424/618, 424/443, 424/445, 424/703
• US Class Current: 424/618
• CPC Class Codes: A01N 2300/00 Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
• CPC Class Codes: A01N 25/34 Shaped forms, e.g. sheets, not provided for in any other sub-group of this main group
• CPC Class Codes: A01N 59/00 Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
• CPC Class Codes: A01N 59/02 Sulfur; Selenium; Tellurium; Compounds thereof
• CPC Class Codes: A01N 59/16 Heavy metals; Compounds thereof
• CPC Class Codes: A61L 15/18 containing inorganic materials
• CPC Class Codes: A61L 15/46 Deodorants or malodour counteractants, e.g. to inhibit the formation of ammonia or bacteria
• CPC Class Codes: A61L 17/005 containing a biologically active substance, e.g. a medicament or a biocide
• CPC Class Codes: A61L 2300/104 Silver, e.g. silver sulfadiazine
• CPC Class Codes: A61L 2300/404 Biocides, antimicrobial agents, antiseptic agents
• CPC Class Codes: A61L 27/54 Biologically active materials, e.g. therapeutic substances A61L27/227 takes precedence
• CPC Class Codes: A61L 29/16 Biologically active materials, e.g. therapeutic substances A61L29/048 takes precedence
• CPC Class Codes: A61L 31/16 Biologically active materials, e.g. therapeutic substances A61L31/047 takes precedence
• CPC Class Codes: B05D 1/18 performed by dipping
• CPC Class Codes: B05D 5/00 Processes for applying liquids or other fluent materials to surfaces to obtain special surface effects, finishes or structures
• CPC Class Codes: B05D 7/02 to macromolecular substances, e.g. rubber treatment or coating of shaped articles made of macromolecular substances C08J7/00
• CPC Class Codes: C23C 18/1646 Characteristics of the product obtained
• CPC Class Codes: C23C 18/42 Coating with noble metals
• CPC Class Codes: Y10T 428/256 Heavy metal or aluminum or compound thereof
• CPC Class Codes: Y10T 428/2949 Glass, ceramic or metal oxide in coating

Abstract

Methods for the production of deposition products including an oxidized metal species under both acidic and alkaline conditions, methods for the production of composite materials including a substrate and the deposition product, and products in the nature of deposition products and composite materials. The methods are particularly suited for depositing a very thin layer of a deposition product on a substrate and may be used to produce composite materials for use in many applications, including but not limited to electronics, materials engineering and medical applications. In a preferred embodiment, the metal is silver, the substrates are medical devices or components of medical devices and the deposition product includes an antimicrobially active oxidized silver species.

Claims

1. A method for producing a composite material comprising a substrate and a deposition product, the method comprising the following steps:

(a) providing a deposition solution comprising an amount of an aqueous solution of a silver salt comprised of an amount of silver ions and an amount of an oxidizing agent, wherein the silver salt is comprised of silver nitrate, wherein the oxidizing agent is comprised of a persulfate, wherein a concentration of the silver salt in the deposition solution is between about 1 gram per liter and about 20 grams per liter, wherein a concentration of the oxidizing agent in the deposition solution is between about 1 gram per liter and about 50 grams per liter, and wherein the deposition solution has a pH below 7;

(b) producing the deposition product by facilitating a chemical reaction in the deposition solution between the silver ions and the oxidizing agent while maintaining the deposition solution at a temperature of between about 2 degrees Celsius and about 40 degrees Celsius, wherein the deposition product consists essentially of at least one oxidized silver species, and wherein the deposition product is comprised of a compound having the formula Ag₇O₈X, where X is an anion;

(c) providing the substrate, wherein the substrate is a medical device; and

(d) contacting the substrate with the deposition solution during the deposition product producing step (b), thereby producing the composite material.

2. The method as claimed in claim 1 wherein the persulfate is selected from the group of persulfates consisting of potassium persulfate, sodium persulfate, ammonium persulfate and mixtures thereof.

3. The method as claimed in claim 2 wherein the persulfate is comprised of potassium persulfate.

4. The method as claimed in claim 1 wherein the amount of the oxidizing agent is selected to be a stoichiometrically appropriate amount relative to the amount of the silver ions.

5. The method as claimed in claim 2, further comprising the step of adding an amount of a source of anions to the deposition solution for combining with the silver ions in order to produce the deposition product.

6. The method as claimed in claim 5 wherein the source of anions is comprised of at least one acid.

7. The method as claimed in claim 6 wherein the acid is selected from the group of acids consisting of carbonic acid, nitric acid, perchloric acid, sulfuric acid, acetic acid, fluoroboric acid, citric acid, acetylsalicylic acid and mixtures thereof.

8. The method as claimed in claim 5 wherein the amount of the source of anions is selected to be a stoichiometrically appropriate amount relative to the amount of the silver ions.

9. The method as claimed in claim 2 wherein the deposition product producing step is comprised of maintaining the deposition solution at a temperature of between about 10 degrees Celsius and about 25 degrees Celsius.

10. The method as claimed in claim 2 wherein the deposition product producing step is comprised of agitating the deposition solution during at least a portion of the deposition product producing step.

11. The method as claimed in claim 1 wherein the substrate contacting step is performed for at least about 1 minute.

12. The method as claimed in claim 11 wherein die substrate contacting step is performed for between about 1 minute and about 60 minutes.

13. The method as claimed in claim 12 wherein the substrate contacting step is performed for between about 1 minute and about 20 minutes.

14. The method as claimed in claim 13 wherein the substrate contacting step is performed for between about 2 minutes and about 10 minutes.

15. The method as claimed in claim 1, further comprising the step, following the substrate contacting step, of washing the composite material.

16. The method as claimed in claim 1, further comprising the step, prior to the substrate contacting step, of etching the substrate by immersing the substrate in an etching solution.

17. The method as claimed in claim 16 wherein the etching solution is comprised of a mixture of an alcohol and an aqueous solution of a hydroxide compound.

18. The method as claimed in claim 17 wherein the hydroxide compound is selected from the group of hydroxide compounds consisting of sodium hydroxide, potassium hydroxide and mixtures thereof.

19. The method as claimed in claim 17 wherein the hydroxide compound is comprised of sodium hydroxide.

20. The method as claimed in claim 17 wherein the etching step is performed for between about 5 minutes and about 20 minutes.

21. The method as claimed in claim 17, further comprising the step, following the etching step, of washing the substrate to remove residual alkali from the substrate.

22. The method as claimed in claim 1, further comprising the step, following the substrate contacting step, of immersing the composite material in boiling water.

23. The method as claimed in claim 22 wherein the immersing step is performed for at least about 1 minute.

24. The method as claimed in claim 1 wherein the substrate is comprised of a wound dressing.

25. The method as claimed in claim 24 wherein the substrate is comprised of a high density polyethylene material.

26. The method as claimed in claim 25 wherein the substrate is comprised of a skin adhesive layer, wherein the skin adhesive layer is comprised of a cross-linked silicon gel, and wherein the deposition product is deposited on the skin adhesive layer.

27. The method as claimed in claim 26 wherein the skin adhesive layer has adhesive properties and wherein the deposition product does not materially interfere with the adhesive properties of the skin adhesive layer.

28. The method as claimed in claim 1 wherein the deposition product is further comprised of Ag₂SO₄.

29. The method as claimed in claim 1 wherein the deposition product is further comprised of at least one silver oxide selected from the group of silver oxides consisting of monovalent silver oxide, bivalent silver oxide, trivalent silver oxide and mixtures thereof.

30. The method as claimed in claim 1 wherein X is derived from an acid.

31. The method as claimed in claim 1 wherein the deposition product is comprised of a plurality of valent states of silver.

32. The method as claimed in claim 1 wherein X is selected from the group of anions consisting of HCO₃⁻

, CO₃²⁻

, NO₃⁻

, ClO₄⁻

, SO₄²⁻

, F⁻

, and mixtures thereof.

33. The method as claimed in claim 32 wherein X is comprised of NO₃⁻

.