Biodegradable polymers with sulfenamide bonds for drug delivery applications
The present invention provides methods for preparing polysulfenamides having a repeating unit of formula (4): wherein R 1 is selected from the group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl. Each of R 4 , R 5 and R 6 are independently selected from the group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl. Microparticles comprising polysulfenamides can be used as delivery vehicles for a variety of biological applications.
1. A method of manufacturing a polysulfenamide, comprising:
forming a mixture comprising an activated dithiol and a secondary diamine.
2. The method of claim 1 , wherein the activated dithiol is of formula (3):
X—S—R 1 —S—X (3),
wherein R 1 is selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl, and
X is selected from a group consisting of halogen, tosylate group, mesylate group, succinimidyl group, and imidyl group.
3. The method of claim 2 , wherein X is a succinimidyl group.
4. The method of claim 1 , wherein the mixture further comprises a solvent selected from a group consisting of methylene chloride (CH 2 Cl 2 ), chloroform (CHCl 3 ), CCl 4 , hexane, benzene, toluene, 1,4-dioxane, diethyl ether, tetrahydrofuran, ethyl acetate, acetone, dimethylformamide, acetonitrile, dimethyl sulfoxide, or a combination thereof.
5. The method of claim 1 , wherein the secondary diamine is a secondary diamine of formula (2):
wherein R 4 , R 5 , and R 6 are each independently selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl.
6. The method of claim 5 , wherein R 4 , R 5 , and R 6 are each independently selected from a group consisting of alkyl and ether.
7. The method of claim 5 , wherein R 5 and R 6 are part of the same cyclical moiety.
8. A polysulfenamide comprising a repeating unit of formula (4):
wherein R 1 is selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl, and
R 4 , R 5 , and R 6 are each independently selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl.
9. The polysulfenamide of claim 8 , wherein R 1 is selected from a group consisting of alkyl, cycloalkyl, ether, and cycloether.
10. The polysulfenamide of claim 8 , wherein R 4 , R 5 , and R 6 are each independently selected from a group consisting of alkyl and ether.
11. The polysulfenamide of claim 8 , wherein R 5 and R 6 are part of the same cyclic moiety.
12. A microparticle comprising a polysulfenamide, wherein the microparticle has an average size of about 0.1 μm to about 20 μm.
13. The microparticle of claim 12 , wherein the microparticle has an average size of about 1 μm to about 5 μm.
14. The microparticle of claim 12 , wherein the microparticle has an average size of about 2 μm to about 3 μm.
15. The microparticle of claim 12 , wherein the microparticle is further functionalized with an amine.
16. The microparticle of claim 12 , wherein the polysulfenamide comprises a repeating unit of formula (4):
wherein R 1 is selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl, and
R 4 , R 5 , and R 6 are each independently selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl.
17. The microparticle of claim 16 , wherein the microparticle is further functionalized with an amine.
18. A method of manufacturing a polysulfenamide, comprising:
forming a mixture comprising a disulfenamide and a secondary diamine.
19. The method of claim 18 , wherein the disulfenamide is of formula (1):
(R 2 R 3 )N—S—R 1 —S—N(R 2′ R 3′ ) (1),
wherein R 1 is selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl, and
R 2 , R 3 , R 2′ , and R 3′ are each independently selected from a group consisting of hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, cycloalkyl, ether, aryl, and heteroaryl.
20. The method of claim 18 , wherein the secondary diamine is a secondary diamine of formula (2):
wherein R 4 , R 5 , and R 6 are each independently selected from a group consisting of alkyl, alkenyl, alkynyl, haloalkyl, alkoxyalkyl, hydroxyalkyl, ether, cycloether, aryl, heteroaryl, arylalkyl, heteroarylalkyl, hydroxyaryl, arylether, cycloalkyl, heterocycloalkyl, hydroxycycloalkyl, halocycloalkyl, and aminocycloalkyl.