US2020338116A1PendingUtilityA1
Modified immune-modulating particles
Assignee: COUR PHARMACEUTICALS DEV COMPANY INCPriority: Nov 12, 2010Filed: Apr 7, 2020Published: Oct 29, 2020
Est. expiryNov 12, 2030(~4.3 yrs left)· nominal 20-yr term from priority
Y02A50/30A61P 19/02A61K 9/10A61K 31/19A61P 37/06A61P 25/00A61P 31/12A61P 1/04A61P 9/08A61P 29/00A61K 9/48A61P 37/08A61K 9/0019A61K 47/50A61P 11/06A61P 9/00A61P 37/02Y10T428/2982A61K 31/765A61P 3/10A61P 17/06A61P 9/10A61K 38/16A61K 9/14A61P 9/04A61P 11/02A61P 17/00Y02A50/393
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Claims
Abstract
The current invention involves the surprising finding that when carboxylated particles, such as carboxylated poly-styrene, PLGA, or diamond particles are administered to subjects, inflammatory immune responses are ameliorated. Additionally, the present invention describes methods of treating inflammatory diseases by administering these same carboxylated particles.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A composition comprising particles having a negative surface charge, wherein the particles comprise polylactide-co-glycolide (PLGA) and a polyamino acid having a carboxyl group on the side chain.
2 . The composition of claim 1 , wherein the polyamino acid having a carboxyl group on the side chain is poly(aspartic acid) or poly(glutamic acid).
3 . The composition of claim 2 , wherein the polyamino acid having a carboxyl group on the side chain is poly(gamma-glutamic acid), poly(L-glutamic acid), poly(D-glutamic acid), or poly(D,L-glutamic acid).
4 . The composition of claim 1 , wherein the particles are microparticles or nanoparticles.
5 . The composition of claim 1 , wherein the PLGA has a molecular weight of 1,000 Da to 100,000 Da.
6 . The composition of claim 1 , wherein the particles have been modified to comprise one or more carboxyl groups on the particle's surface.
7 . The composition of claim 1 , wherein the particles an average diameter of about 0.1 μm to about 10 μm.
8 . The composition of claim 7 , wherein the particles an average diameter of about 0.2 μm to about 2 μm.
9 . The composition of claim 1 , further comprising one or more pharmaceutically acceptable excipients.
10 . The composition of claim 9 , wherein the one or more pharmaceutically acceptable excipients are selected from the group consisting of preservatives, antioxidants, moisturizers, emollients, buffering agents, solubilizing agents, penetration agents, skin protectants, surfactants, and propellants.
11 . The composition of claim 9 , wherein one of the one or more pharmaceutically acceptable excipients is a surfactant.
12 . The composition of claim 11 , wherein the surfactant is selected from the group consisting of Polyoxyl 40 Stearate, polysorbate, poloxamers, polyethylene glycol, polyvinyl alcohol, and polyvinylpyyrolidinone.
13 . The composition of claim 1 , wherein the composition does not comprise an active agent.
14 . A composition comprising particles having negative surface charges, wherein the particles comprise polylactide-co-glycolide (PLGA) and a polyamino acid having a carboxyl group on the side chain group, made by an emulsion process.
15 . The composition of claim 14 , wherein the polyamino acid having a carboxyl group on the side chain is poly(aspartic acid) or poly(glutamic acid).
16 . The composition of claim 14 , wherein the polyamino acid having a carboxyl group on the side chain is poly(gamma-glutamic acid), poly(L-glutamic acid), poly(D-glutamic acid), or poly(D,L-glutamic acid).Join the waitlist — get patent alerts
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