US2006110379A1PendingUtilityA1
Linkage of agents using microparticles
Est. expiryJan 20, 2018(expired)· nominal 20-yr term from priority
A61Q 19/00Y10S530/812C07K 17/08A61K 9/167A61K 8/11A61P 39/02A61K 2800/412A61K 2800/94A61K 8/64A61K 2800/57
58
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Claims
Abstract
Methods, products and kits are provided for attaching agents to a skin surface via microparticles using endogenous or exogenous transglutaminase.
Claims
exact text as granted — not AI-modified1 . A method of treating a subject to attach microparticles to a skin surface of the subject comprising
contacting the skin surface with microparticles having surface available transglutaminase substrate reactive groups in an amount sufficient to attach the microparticles to the skin surface in the presence of endogenous transglutaminase, allowing the microparticles to remain in contact with the skin surface for a time sufficient to permit a layer of microparticles to covalently attach to the skin surface.
2 . The method of claim 1 , wherein the surface available transglutaminase substrate reactive groups are lysines.
3 . The method of claim 1 , wherein the surface available transglutaminase substrate reactive groups are glutamines.
4 . (canceled)
5 . The method of claim 1 , wherein the microparticles further comprise an active agent.
6 - 8 . (canceled)
9 . The method of claim 5 , wherein the active agent is not itself a substrate of transglutaminase.
10 - 13 . (canceled)
14 . The method of claim 1 , wherein the microparticles are 100 nm to 500 nm in size.
15 . The method of claim 1 , wherein the microparticles are 20 nm to 35 nm in size.
16 - 25 . (canceled)
26 . A method of treating a subject to attach microparticles to a skin surface of the subject comprising
contacting the skin surface with microparticles having surface available transglutaminase substrate reactive groups in an amount sufficient to attach the microparticles to the skin surface in the presence of exogenous transglutaminase, applying exogenous transglutaminase to the skin surface, and allowing the microparticles and exogenous transglutaminase to remain in contact with the skin surface for a time sufficient to permit a layer of microparticles to covalently attach to the skin surface.
27 . The method of claim 26 , wherein the surface available transglutaminase substrate reactive groups are lysines.
28 . The method of claim 26 , wherein the surface available transglutaminase substrate reactive groups are glutamines.
29 . (canceled)
30 . The method of claim 26 , wherein the microparticles further comprise an active agent
31 - 33 . (canceled)
34 . The method of claim 30 , wherein the active agent is not itself a substrate of transglutaminase.
35 - 38 . (canceled)
39 . The method of claim 26 , wherein the microparticles are 100 nm to 500 nm in size.
40 . The method of claim 26 , wherein the microparticles are 20 nm to 35 nm in size.
41 - 101 . (canceled)
102 . A composition comprising
a microparticle comprising an active agent and a lysine-rich or glutamine-rich polymer having transglutaminase substrate reactive groups, wherein the microparticle is non-biodegradable, and the transglutaminase substrate reactive groups are surface available.
103 - 105 . (canceled)
106 . The composition of claim 102 , wherein the active agent is not itself a substrate of transglutaminase.
107 - 109 . (canceled)
110 . The composition of claim 102 , wherein the microparticle further comprises a synthetic polymer, and wherein the lysine-rich or glutamine-rich polymer is covalently linked to the synthetic polymer.
111 - 112 . (canceled)
113 . The composition of claim 102 , wherein the microparticle is 100 nm to 500 nm in size.
114 . The composition of claim 102 , wherein the microparticle is 20 nm to 35 nm in size.
115 - 116 . (canceled)
117 . The composition of claim 102 , wherein the transglutaminase substrate reactive groups are surface available in an amount sufficient to attach the microparticle to a skin surface in the presence of endogenous or exogenous transglutaminase.
118 - 145 . (canceled)Join the waitlist — get patent alerts
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