Multifunctional forms of polyoxazoline copolymers and drug compositions comprising the same
The present disclosure provides copolymers of 2-substituted-2-oxazolines possessing two or three reactive functional groups which are also chemically orthogonal. The copolymers described may be random copolymers, block copolymers or a mixture of random and block copolymer configurations. Furthermore, the present disclosure provides novel methods for synthesizing the above polymers and for conjugating to molecules such as targeting, diagnostic and therapeutic agents.
1. A heterofunctional polyoxazoline derivative of the general structure:
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —Z
wherein:
R 1 is an initiating group;
R 2 is independently selected for each repeating unit from an unsubstituted or substituted alkyl, an unsubstituted or substituted alkenyl, an unsubstituted or substituted aralkyl or an unsubstituted or substituted heterocyclylalkyl group;
X is a pendent moiety containing a first functional group;
Y is a pendent moiety containing a second functional group;
Z is a terminating nucleophile;
a is ran which indicates a random copolymer or block which indicates a block copolymer;
o and m are each an integer independently selected from 1-50;
n is an integer selected from 0-1000; and
wherein the first and second functional groups are each independently an alkyne, an amine, an oxyamine, an aldehyde, a ketone, an acetal, a ketal, an ester, a carboxylic acid, an activated carboxylic acid, an active carbonate, a chloroformate, an alcohol, an azide, a vinyl sulfone, a maleimide or orthopyridyl disulfide.
2. The heterofunctional polyoxazoline derivative of claim 1 , wherein R 1 is a hydrogen, substituted or unsubstituted alkyl or substituted or unsubstituted aralkyl group.
3. The heterofunctional polyoxazoline derivative of claim 1 , wherein R 2 is an unsubstituted alkyl.
4. The heterofunctional polyoxazoline derivative of claim 1 , wherein Z is —S—U—W, wherein U is a linking group and W is a third functional group selected from the group consisting of an alkyne, an amine, an oxyamine, an aldehyde, a ketone, an acetal, a ketal, an ester, a carboxylic acid, an activated carboxylic acid, an active carbonate, a chloroformate, an alcohol, an azide, a vinyl sulfone, a maleimide, and orthopyridyl disulfide.
5. The heterofunctional polyoxazoline derivative of claim 4 , wherein W is a carboxylic acid, a protected carboxylic acid, an active ester, an amine or a protected amine and U is an alkylene linking portion.
6. The heterofunctional polyoxazoline derivative of claim 4 , wherein the first and third and second and third functional groups are chemically orthogonal to one another.
7. The heterofunctional polyoxazoline derivative of claim 4 having the structure:
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —S—(CH 2 ) p —W,
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —S—(CH 2 ) p —NH 2 or
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —S—(CH 2 ) p —CO 2 H,
wherein p is an integer from 1 to 10.
8. The heterofunctional polyoxazoline derivative of claim 1 linked to at least one target molecule, wherein the at least one target molecule is linked to the heterofunctional polyoxazoline derivative through at least one of the first or second functional groups.
9. The heterofunctional polyoxazoline derivative of claim 8 , wherein the at least one target molecule is independently selected for each of the first and second functional groups from a therapeutic moiety, a diagnostic moiety, a targeting moiety, or a combination of the foregoing.
10. The heterofunctional polyoxazoline derivative of claim 8 , wherein the at least one target molecule is independently selected from an organic molecule, a peptide, a protein, an antibody, an antibody fragment, a carbohydrate, an oligonucleotide, or a combination of the foregoing.
11. The heterofunctional polyoxazoline derivative of claim 8 , wherein the conjugate contains a therapeutic moiety and a targeting moiety, a diagnostic moiety and a targeting moiety, or a diagnostic moiety, a therapeutic moiety and a targeting moiety.
12. A heterofunctional polyoxazoline derivative of the general structure:
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —Z
wherein:
R 1 is an initiating group;
R 2 is independently selected for each repeating unit from an unsubstituted or substituted alkyl, an unsubstituted or substituted alkenyl, an unsubstituted or substituted aralkyl or an unsubstituted or substituted heterocyclylalkyl group;
X is a pendent moiety containing a first functional group;
Y is a pendent moiety containing a second functional group;
Z is a terminating nucleophile containing a third functional group;
a is ran which indicates a random copolymer or block which indicates a block copolymer;
o and m are each an integer independently selected from 1-50;
n is an integer selected from 0-1000; and
wherein the first, second and third functional groups are each independently an alkyne, an amine, an oxyamine, an aldehyde, a ketone, an acetal, a ketal, an ester, a carboxylic acid, an activated carboxylic acid, an active carbonate, a chloroformate, an alcohol, an azide, a vinyl sulfone, a maleimide or orthopyridyl disulfide and wherein the first and third and second and third functional groups are chemically orthogonal to one another.
13. The heterofunctional polyoxazoline derivative of claim 12 , wherein R 1 is a hydrogen, substituted or unsubstituted alkyl or substituted or unsubstituted aralkyl group.
14. The heterofunctional polyoxazoline derivative of claim 12 , wherein R 2 is an unsubstituted alkyl.
15. The heterofunctional polyoxazoline derivative of claim 12 , wherein Z is —S—U—W, wherein U is a linking group and W is the third functional group selected from the group consisting of an alkyne, an amine, an oxyamine, an aldehyde, a ketone, an acetal, a ketal, an ester, a carboxylic acid, an activated carboxylic acid, an active carbonate, a chloroformate, an alcohol, an azide, a vinyl sulfone, a maleimide, and orthopyridyl disulfide.
16. The heterofunctional polyoxazoline derivative of claim 15 , wherein W is a carboxylic acid, a protected carboxylic acid, an active ester, an amine or a protected amine and U is an alkylene linking portion.
17. The heterofunctional polyoxazoline derivative of claim 15 having the structure:
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —S—(CH 2 ) p —W,
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —S—(CH 2 ) p —NH 2 or
R 1 —{[N(COX)CH 2 CH 2 ] o —[N(COR 2 )CH 2 —CH 2 )] n —[N(COY)CH 2 —CH 2 )] m } a —S—(CH 2 ) p —CO 2 H,
wherein p is an integer from 1 to 10.
18. The heterofunctional polyoxazoline derivative of claim 12 linked to at least one target molecule, wherein the at least one target molecule is linked to the heterofunctional polyoxazoline derivative through at least one of the first or second functional groups.
19. The heterofunctional polyoxazoline derivative of claim 18 , wherein the at least one target molecule is independently selected for each of the first and second functional groups from a therapeutic moiety, a diagnostic moiety, a targeting moiety, or a combination of the foregoing.
20. The heterofunctional polyoxazoline derivative of claim 18 , wherein the at least one target molecule is independently selected from an organic molecule, a peptide, a protein, an antibody, an antibody fragment, a carbohydrate, an oligonucleotide, or a combination of the foregoing.
21. The heterofunctional polyoxazoline derivative of claim 18 , wherein the conjugate contains a therapeutic moiety and a targeting moiety, a diagnostic moiety and a targeting moiety, or a diagnostic moiety, a therapeutic moiety and a targeting moiety.