US2018103645A1PendingUtilityA1
Methods for forming stabilized metal salt particles
Assignee: JOHNSON & JOHNSON VISION CAREPriority: Oct 8, 2007Filed: Dec 14, 2017Published: Apr 19, 2018
Est. expiryOct 8, 2027(~1.2 yrs left)· nominal 20-yr term from priority
G02B 1/043C01P 2004/64A01N 59/16C01G 9/006C01P 2006/80A61L 12/088C01P 2006/82
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Claims
Abstract
The present invention relates to a process for forming stabilized metal salt particles.
Claims
exact text as granted — not AI-modified1 . A process comprising
a. forming a first solution comprising at least one sodium iodide salt precursor; b. forming a second solution comprising a complex formed from at least one silver acetate metal agent and a polyvinyl pyrrolidone dispersing agent in a particle size stabilizing effective amount; c. adding said second solution to said first solution at a rate sufficient to maintain a clear solution throughout addition and to form a product solution comprising stabilized metal salt particles having a mean particle size of less than about 200 nm; d. drying said product solution to form an antimicrobial metal salt powder comprising 0.01 to about 10 weight % metal in the antimicrobial metal salt powder.
2 . The process of claim 1 wherein said second solution has a metal agent concentration of at least about 1500 ppm.
3 . The process of claim 1 wherein the dispersing agent is present in said second solution in a concentration between about 20 and about 50 w/w%.
4 . The process of claim 1 wherein said first solution has a salt precursor concentration of at least about 1500 ppm.
5 . The process of claim 1 wherein said first solution has a salt precursor concentration of at least about 5000 ppm.
6 . The process of claim 1 wherein said first solution has a salt precursor concentration of about 5000 ppm to about 50,000 ppm.
7 . The process of claim 1 wherein said mean particle size is less than about 100 nm.
8 . The process of claim 1 wherein said mean particle size is less than about 50 nm.
9 . The process of claim 1 wherein said first and second solutions are aqueous solutions.
10 . The process of claim 1 wherein said product solution has a viscosity of less than about 50 cps.
11 . The process of claim 1 wherein said first solution is stirred as said second solution is added.
12 . The process of claim 9 wherein said solutions are maintained at a pressure between about ambient and about 40 mbar during said adding step.
13 . (canceled)
14 . The process of claim 1 wherein at least one of said first and second solution comprises at least one solvent and said powder comprises less than about 10 wt % of said solvent.
15 . The process of claim 14 wherein said powder comprises less than about 5% of said solvent.
16 . The process of claim 14 wherein said solvent comprises water.
17 - 18 . (canceled)
19 . The process of claim 1 wherein said polyvinyl pyrrolidone and metal agent are present in said second solution in a molar ratio of at least about 1.5.
20 . The process of claim 1 wherein said metal salt powder comprises at least one metal salt having a K sp of less than about 2×10 −10 in pure water at 25° C.
21 . (canceled)
22 . The process of claim 1 wherein said second solution has a metal agent concentration of at least about 5000 ppm.
23 . The process of claim 1 wherein said second solution has a metal agent concentration of about 5000 ppm to about 50,000 ppm.
24 . A process comprising
a. forming a first solution comprising Nal; b. forming a second solution comprising a complex formed from silver acetate and polyvinyl pyrrolidone in a particle size stabilizing effective amount; c. adding said second solution to said first solution at a rate sufficient to maintain a clear solution throughout addition and to form a product solution comprising stabilized Agl particles having a mean particle size of less than about 200 nm; d. drying said product solution to form an antimicrobial Agl powder comprising 0.01 to about 10 weight % Ag in the antimicrobial Agl powder.Join the waitlist — get patent alerts
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