Polymeric depots for localization of agent to biological sites
Provided herein are polymeric particles and compounds and processes that can be used to prepare polymer-based particles and methods of using those particles to localize or concentrate a subsequently delivered agent to an in vivo site.
1. A method of administering an agent to a tissue location in a subject, the method comprising administering to the subject polymeric particle prior to, or after administering said agent to the subject, wherein said agent is administered without the polymeric particle and the polymeric particle does not include any therapeutic agent or diagnostic agent when the polymeric particle is administered,
wherein the polymeric particle comprises an oligomer or a polymer comprising a monomer represented by Formula XX:
wherein:
Q is selected from the group consisting of O, S, Se, and NH;
G is selected from the group consisting of the following structures:
R 2 is selected from the group consisting of hydrogen, a straight or branched alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, arylalkyl, and fluorocarbon chain of 1-50 carbons, wherein each alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, arylalkyl, or fluorocarbon chain is optionally substituted internally or terminally by one or more hydroxyl, hydroxyether, carboxyl, carboxyester, carboxyamide, amino, mono- or di-substituted amino, thiol, thioester, sulfate, phosphate, phosphonate, or halogen substituents;
one R 3 is selected from the group consisting of methoxy, ethoxy, amino, nitro, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, and arylalkyl chain of 1-10 carbons;
and the remaining R 3 are each independently selected from the group consisting of hydrogen, methoxy, ethoxy, amino, a straight and branched alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, and arylalkyl chain of 1-10 carbons;
R 4 , R 5 , and R 6 are each independently selected from the group consisting of a straight or branched alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, and arylalkyl chain of 1-10 carbons; and
R 7 and R 8 are each independently selected from the group consisting of hydrogen, a straight or branched alkyl, cycloalkyl, aryl, olefin, alkylaryl, and arylalkyl chain of 1-50 carbons, wherein each alkyl, cycloalkyl, aryl, olefin, alkylaryl, or arylalkyl chain is optionally substituted internally or terminally by one or more hydroxyl, hydroxyether, carboxyl, carboxyester, carboxyamide, amino, mono- or di-substituted amino, thiol, thioester, sulfate, phosphate, phosphonate, or halogen substituents.
2. The method of claim 1 , wherein the agent is a therapeutic agent or a diagnostic agent.
3. The method of claim 2 , wherein the agent is selected from anticancer agents, immune modulator agents, anti-inflammatory agents, antibiotics, and any combinations thereof.
4. The method of claim 1 , wherein the oligomer or the polymer comprises the monomer
5. The method of claim 1 , wherein the polymeric particle further comprises a microparticle or a nanoparticle.
6. The method of claim 1 , wherein the subject is in need of treatment for cancer, recurrence of a malignancy, lymph node metastasis, inflammation, infection, wound healing, abnormal scar formation, a chronic condition, or post-operative pain.
7. A method of treating a cancer or tumor in a subject, the method comprising administering to the subject in need thereof polymeric particle prior to, or after administering an anti-cancer agent, wherein said anti-cancer agent is administered without the polymeric particle and the polymeric particle does not include any therapeutic agent or diagnostic agent when the polymeric particle is administered, wherein the polymeric particle comprises an oligomer or a polymer comprising a monomer represented by Formula XX:
wherein:
Q is selected from the group consisting of O, S, Se, and NH;
G is selected from the group consisting of the following structures:
R 2 is selected from the group consisting of hydrogen, a straight or branched alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, arylalkyl, and fluorocarbon chain of 1-50 carbons, wherein each alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, arylalkyl, or fluorocarbon chain is optionally substituted internally or terminally by one or more hydroxyl, hydroxyether, carboxyl, carboxyester, carboxyamide, amino, mono- or di-substituted amino, thiol, thioester, sulfate, phosphate, phosphonate, or halogen substituents;
one R 3 is selected from the group consisting of methoxy, ethoxy, amino, nitro, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, and arylalkyl chain of 1-10 carbons;
and the remaining R 3 are each independently selected from the group consisting of hydrogen, methoxy, ethoxy, amino, a straight and branched alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, and arylalkyl chain of 1-10 carbons;
R 4 , R 5 , and R 6 are each independently selected from the group consisting of a straight or branched alkyl, cycloalkyl, aryl, olefin, silyl, alkylsilyl, arylsilyl, alkylaryl, and arylalkyl chain of 1-10 carbons; and
R 7 and R 8 are each independently selected from the group consisting of hydrogen, a straight or branched alkyl, cycloalkyl, aryl, olefin, alkylaryl, and arylalkyl chain of 1-50 carbons, wherein each alkyl, cycloalkyl, aryl, olefin, alkylaryl, or arylalkyl chain is optionally substituted internally or terminally by one or more hydroxyl, hydroxyether, carboxyl, carboxyester, carboxyamide, amino, mono- or di-substituted amino, thiol, thioester, sulfate, phosphate, phosphonate, or halogen substituents.
8. The method of claim 7 , wherein the tumor is a malignant tumor, a benign tumor, a primary tumor or a metastatic tumor.
9. The method of claim 7 , wherein the polymeric particle comprises an oligomer or a polymer comprising the monomer
10. The method of claim 1 , wherein the polymeric particle comprises an oligomer or polymer comprising the cross linker:
11. The method of claim 1 , wherein the polymeric particle comprises an oligomer or polymer comprising a monomer of formula:
and a cross-linker monomer of formula:
12. The method of claim 9 , wherein the polymeric particle comprises an oligomer or polymer comprising the cross linker:
13. The method of claim 7 , wherein the polymeric particle comprises an oligomer or polymer comprising a monomer of formula:
and a cross-linker monomer of formula: