US2015004206A1PendingUtilityA1
Microparticles comprising pcl and uses thereof
Est. expiryJul 26, 2027(~1 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 11/04A61P 17/02A61P 11/00A61P 23/00A61P 13/10A61P 1/04A61P 15/10A61P 17/00A61P 1/00A61Q 19/00A61K 9/0019A61K 31/445A61K 2800/654A61K 31/167A61K 9/1647A61K 2800/412A61K 8/85A61K 8/042A61K 2800/54A61L 27/52A61K 9/14A61K 9/06A61Q 19/08A61K 8/025A61K 2800/91A61K 9/5031A61L 27/18A61K 31/245A61K 31/765A61K 9/0024A61K 31/05
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Claims
Abstract
The invention relates to a process for preparing PCL-comprising microparticles, to microparticles obtainable by said process, to gel hence obtained and to several uses of the gel such as for the preparation of a medicament for treating a skin abnormality or disfigurement, and/or for controlling bladder function and/or controlling gastric reflux and/or for treating erectile dysfunction and/or for treating vocal cords. The gel may also be used for cosmetic applications.
Claims
exact text as granted — not AI-modified1 - 15 . (canceled)
16 . A process for preparing polycaprolactone (PCL)-comprising microparticles, wherein the process comprises:
(a) solubilizing a PCL polymer in a solvent to form a PCL polymer solution, (b) mixing the PCL polymer solution with a liquid comprising a surfactant, said liquid having a viscosity between about 20 and about 10,000 cP, (c) forming PCL-comprising microparticles from the solution.
17 . The process according to claim 16 , wherein the viscosity is between about 40 and about 1,000 cP.
18 . The process according to claim 17 , wherein the viscosity is between about 75 and about 300 cP.
19 . The process according to claim 16 , wherein the solvent comprises a halogen containing compound.
20 . The process according to claim 19 , wherein the solvent is dichloromethane.
21 . The process according to claim 16 , wherein the forming step comprises extracting the solvent from the PCL-comprising microparticles dispersed in the liquid by extraction evaporation.
22 . The process according to claim 16 , wherein the surfactant is methyl cellulose.
23 . The process according to claim 22 , wherein the methyl cellulose has a Mn between 41000 and 88000.
24 . The process according to claim 22 , wherein the methyl cellulose has a concentration between about 0.5 and about 2.5 w/w %.
25 . The process according to claim 24 , wherein the methyl cellulose has a concentration between about 0.8 and about 1.1 w/w %.
26 . The process according to claim 16 , wherein the PCL polymer is a linear polymer, a copolymer, a terpolymer or a blend of different types of homo/co/ter-polymers.
27 . PCL-comprising microparticles having:
i) a diameter between 5 and 200 μm, ii) homogenous density, form and content, iii) essentially spherical and smooth surfaces, and iv) optionally, an active ingredient.
28 . The microparticles according to claim 27 , wherein the PCL-comprising polymer does not comprise a second monomer selected from the group consisting of glycolide, dioxanone, trimethylene carbonate and the lactides, and combinations thereof.
29 . The microparticles according to claim 27 , wherein the PCL-comprising polymer is a PCL homopolymer.
30 . A biodegradable, injectable gel comprising microparticles according to claim 27 .
31 . The gel according to claim 30 , comprising an anesthetic as the active ingredient.
32 . The gel according to claim 30 , which is an implant or a filler.
33 . A medicament comprising (1) an active ingredient and (2) microparticles having:
i) a diameter between 5 and 200 μm, ii) homogenous density, form and content, iii) essentially spherical and smooth surfaces.
34 . The medicament according to claim 33 which is a cosmetic.
35 . A method of treating a skin abnormality or disfigurement, for controlling bladder function, for controlling gastric reflux, for treating erectile dysfunction, and/or for treating vocal cords, comprising administering to a patient in need thereof a biodegradable, injectable gel comprising microparticles according to claim 27 .Join the waitlist — get patent alerts
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