PLASMA POLYMER NANOPARTICLES CARRYING AGENTS
The present disclosure relates to the field of nanoparticles, conjugates thereof and their use in methods of treatment or prevention of vascular inflammation. The present disclosure also relates to methods of delivering an agent to a region of a blood vessel in a patient, comprising: a) conjugating the agent to a nanoparticle to produce a conjugate; and b) delivering the conjugate to the region of the blood vessel.
1 . A method of delivering an agent to a region of a blood vessel in a patient, comprising:
a) conjugating the agent to a nanoparticle to produce a conjugate; and
b) delivering the conjugate to the region of the blood vessel.
2 . The method of claim 1 , wherein the agent is a biologically active agent or an imaging agent.
3 . A method of regulating inflammation or promoting healing in a region of a blood vessel in a patient, comprising:
a) conjugating a biologically active agent to a nanoparticle to produce a conjugate; and
b) delivering the conjugate to the region of the blood vessel.
4 . The method according to claim 1 , wherein the conjugate is retained in the region of the blood vessel for a period greater than the period unconjugated biologically active agent would be retained in the region of the blood vessel.
5 . The method according to claim 4 , wherein the conjugate is retained at the site of delivery in the blood vessel for at least 1 day, for at least 5 days, or for at least 14 days.
6 . (canceled)
7 . (canceled)
8 . The method according to claim 1 , wherein the biologically active agent is an anti-inflammatory cytokine; an anti-inflammatory drug; a limus drug; a statin drug or an anti-proliferative drug.
9 . The method according to claim 8 , wherein the biologically active agent is an anti-inflammatory cytokine.
10 . The method according to claim 9 , wherein the anti-inflammatory cytokine is interleukin-4 or interleukin-10.
11 . The method according to claim 8 , wherein
the anti-inflammatory drug is sulindac; or wherein
the statin drug is simvastatin; or wherein
the anti-proliferative drug is paclitaxel, Sirolimus or an mTOR inhibitor.
12 . The method according to claim 3 , wherein the regulation of inflammation is through macrophage polarization.
13 . A method of retaining a biologically active agent to a region in a blood vessel in a patient for a period of at least 14 days comprising:
a) conjugating the biologically active agent to a nanoparticle to produce a conjugate; and b) delivering the conjugate to the blood vessel.
14 . The method according to claim 1 , wherein the conjugate is delivered to the blood vessel using a catheter.
15 . The method according claim 14 , wherein the catheter is an occlusion perfusion catheter or a sweating balloon catheter.
16 . The method according to claim 1 , wherein the patient is receiving or has received an endovascular intervention.
17 . A conjugate comprising:
a nanoparticulate polymer with a mean diameter of about 1 nm to about 50 nm and formed from a plasma comprising at least one monomer selected from: an alkene, an alkyne, a cycloalkene, a cycloalkyne, or a mixture thereof; or an aggregate comprising two or more of the nanoparticulate polymers, wherein the aggregate has a mean diameter of about 5 nm to about 500 nm;
and a biologically active agent selected from the group consisting of: an anti-inflammatory cytokine; anti-inflammatory drug; a statin drug and an anti-proliferative drug.
18 . The conjugate according to claim 17 , wherein the biologically active agent is an anti-inflammatory cytokine.
19 . The conjugate according to claim 18 , wherein the anti-inflammatory cytokine is interleukin-4 or interleukin-10.
20 . The conjugate according to claim 17 , wherein
the anti-inflammatory drug is Sulindac; or wherein
the statin drug is simvastatin; or wherein
the anti-proliferative drug is paclitaxel, Sirolimus or an mTOR inhibitor.
21 . A conjugate comprising:
a nanoparticulate polymer with a mean diameter of about 1 nm to about 50 nm and formed from a plasma comprising at least one monomer selected from: an alkene, an alkyne, a cycloalkene, a cycloalkyne, or a mixture thereof; or an aggregate comprising two or more of the nanoparticulate polymers, wherein the aggregate has a mean diameter of about 100 nm to about 200 nm; and
i) interleukin-10; or
ii) Sulindac; or
iii) Sirolimus.
22 . A method of treating or preventing vascular injury or vascular disease comprising delivering the conjugate according to claim 17 to a region of a blood vessel in a patient in need thereof.
23 . The method according to claim 22 , wherein the conjugate is delivered to the region of the blood vessel using a catheter.
24 . (canceled)
25 . The method according to claim 22 , wherein the vascular injury is a result of endovascular intervention.
26 . The method according to claim 22 , wherein the vascular injury is neointimal hyperplasia or restenosis.
27 . The method according to claim 22 , wherein the vascular disease is artherosclerosis.
28 . (canceled)