Biodegradable polymer—bioactive moiety conjugates
The invention relates to a biodegradable polymer comprising a plurality of releasable bioactive moieties, the releasable bioactive moieties being pendant from and covalently bonded to the biodegradable polymer backbone, wherein the biodegradable polymer backbone is formed from monomeric units that are each coupled via a biodegradable moiety, and wherein the bioactive moieties are capable of being released at a rate equal to or faster than the rate of biodegradation of the polymer backbone.
1. A biodegradable fluoroquinolone-polymer conjugate which is a polymer of a monomer of formula (II):
where:
X′ and Y′ are each terminal reactive functional groups capable of reacting with functional groups of one or more monomers;
R represents a linear or branched optionally substituted hydrocarbon;
Z is a spacer moiety; and
D is selected from fluoroquinolone antibiotics;
with at least one monomer comprising compatible chemical functionality.
2. The fluoroquinolone-polymer conjugate of claim 1 , wherein the bioactive moiety (D) is selected from the group consisting of alatrofloxacin, balofloxacin, ciprofloxacin, clinafloxacin, danofoxacin, delafloxacin, dextrofloxacin, difloxacin, enoxacin, enrofloxacin, garenoxacin, gatifloxacin, gemifloxacin, grepafloxacin, levofloxacin, lomefloxacin, marbofloxacin, moxifloxacin, nadifloxacin, norfloxacin, ofloxacin, orbifloxacin, pefloxacin, sitafloxacin, sparfloxacin, temafloxacin, tosufloxacin, tosulfloxacin and trovafloxacin.
3. The fluoroquinolone-polymer conjugate of claim 1 , wherein X′ and Y′ are each hydroxyl and the fluoroquinolone-polymer conjugate is a copolymer formed with at least one comonomer.
4. The fluoroquinolone-polymer conjugate of claim 3 , wherein the fluoroquinolone-polymer conjugate comprises a polyurethane polymer which is a copolymer of the bioactive moiety conjugate of formula (II) formed with at least one polyisocyanate, optionally in the presence of one or more polyol co-monomers.
5. The fluoroquinolone-polymer conjugate of claim 4 , wherein the polyisocyanate is selected from the group consisting of m-phenylene diisocyanate, p-phenylene diisocyanate, 2,4-toluene diisocyanate, 2,6-toluene diisocyanate, 1,6-hexamethylene diisocyanate, 1,4-hexamethylene diisocyanate, 1,3-cyclohexane diisocyanate, 1,4-cyclohexane diisocyanate, hexahydro-toluene diisocyanate and its isomers, isophorone diisocyanate, dicyclo-hexylmethane diisocyanates, 1,5-napthylene diisocyanate, 4,4′-diphenylmethane diisocyanate, 2,4′ diphenylmethane diisocyanate, 4,4′-biphenylene diisocyanate, 3,3′-dimethoxy-4,4′-biphenylene diisocyanate, 3,3′-dimethyl-diphenylpropane-4,4′-diisocyanate, 2,4,6-toluene triisocyanate, 4,4′-dimethyl-diphenylmethane-2,2′,5,5′-tetraisocyanate, and alkyl esters of lysine diisocyanate.
6. The fluoroquinolone-polymer conjugate of claim 5 , wherein the polyisocyanate is an alkyl ester of lysine diisocyanate.
7. The fluoroquinolone-polymer conjugate of claim 4 , wherein the copolymer is a copolymer of the monomer of formula (II) with a polyisocyanate and one or more polyol co-monomers.
8. The fluoroquinolone-polymer conjugate of claim 7 , wherein the polyol co-monomer is a polyester polyol.
9. A fluoroquinolone-polymer conjugate according to claim 8 wherein the polyester polyol is selected from the group consisting of polycaprolactone diol, poly(DL lactide), poly(lactic acid-co-glycolic acid) and combinations thereof.
10. The fluoroquinolone-polymer conjugate of claim 1 wherein D is coupled through Z to R by a functional group selected from the group consisting of an ester, amide, thiol, anhydride, imide, carbonate, peroxide, peroxyester, phosphate ester, thioester, sulphate ester, carbamate, azo and boronate ester moiety.
11. The fluoroquinolone-polymer conjugate of claim 1 , wherein Z is selected from the group consisting of —O—; —C(O)—; and optionally substituted: —OC(O)—C 1-18 alkylene-C(O)—; —C(O)O—C 1-18 alkylene-C(O)—; —NR a C(O)—C 1-18 alkylene-C(O)—; —C(O)O—C 1-18 alkylene-O—; —O—C 1-18 alkylene-O—; —O—C 1-18 alkylene-NR a —; —OC(O)—C 1-18 alkylene-NR a —; —C(O)—C 1-18 alkylene-NR a —; —OC(O)—C 1-18 alkylene-O—; —C(O)—C 1-18 alkylene-O—; and —C(O)NR a —C 1-18 alkylene-NR a — where R a is selected from hydrogen, C 1-18 alkyl, C 1-18 alkenyl, C 1-18 alkynyl, C 6-18 aryl, C 3-18 -carbocyclyl, C 3-18 heteroaryl, C 3-18 heterocyclyl, and C 7-18 arylalkyl.
12. The fluoroquinolone-polymer conjugate of claim 1 , wherein R is a linear or branched optionally substituted hydrocarbon having from 1 to 12 carbon atoms.
13. The fluoroquinolone-polymer conjugate of claim 12 wherein R is a linear or branched hydrocarbon of from 1 to 6 carbon atoms.
14. The biodegradable fluoroquinolone-polymer conjugate according to claim 1 comprising as part of its polymer backbone a plurality of moieties of general formula (I):
where:
A and B, which are the same or different, represent the remainder of the polymer backbone and (i) comprise one or more —X—R(ZD)-Y— as shown in formula (I), and (ii) are each formed from monomeric units that are coupled via a biodegradable moiety, wherein each X, Y, R, Z and D in a given —X—R(ZD)-Y— moiety of the biodegradable polymer is the same or different;
X and Y are each independently selected from an ester and a carbamate moiety;
R represents a linear or branched optionally substituted hydrocarbon;
Z is a spacer moiety; and
D is a fluoroquinolone antibiotic.
15. The fluoroquinolone-polymer conjugate of claim 14 wherein Z is selected from the group consisting of —O—; —C(O)—; and optionally substituted: —OC(O)—C 1-18 alkylene-C(O)—; —C(O)O—C 1-18 alkylene-C(O)—; —NR a C(O)—C 1-18 alkylene-C(O)—; —C(O)O—C 1-18 alkylene-O—; —O—C 1-18 alkylene-O—; —O—C 1-18 alkylene-NR a —; —OC(O)—C 1-18 alkylene-NR a —; —C(O)—C 1-18 alkylene-NR a —; —OC(O)—C 1-18 alkylene-O—; —C(O)—C 1-18 alkylene-O—; and —C(O)NR a —C 1-18 alkylene-NR a — where R a is selected from hydrogen, C 1-18 alkyl, C 1-18 alkenyl, C 1-18 alkynyl, C 6-18 aryl, C 3-18 carbocyclyl, C 3-18 heteroaryl, C 3-18 heterocyclyl, and C 7-18 arylalkyl.
16. A biodegradable fluoroquinolone-polymer conjugate comprising as part of its polymer backbone a plurality of moieties of general formula (I):
where:
A and B, which are the same or different, represent the remainder of the polymer backbone and (i) comprise one or more —X—R(ZD)-Y— as shown in formula (I), and (ii) are each formed from monomeric units that are coupled via a biodegradable moiety, wherein each X, Y, R, Z and D in a given —X—R(ZD)-Y— moiety of the biodegradable polymer is the same or different;
X and Y are each independently selected from an ester and a carbamate moiety;
R represents a linear or branched optionally substituted hydrocarbon;
Z is a spacer moiety; and
D is a fluoroquinolone antibiotic.
17. The biodegradable polymer according to claim 16 , wherein A and B comprise a copolymer of polyurethane and polyester.
18. The biodegradable polymer according to claim 16 comprising as part of its polymer backbone plurality of moieties of general formula (Id):
wherein:
A and B, which may be the same or different, represent the remainder of the polymer backbone and are selected from a copolymer of polyurethane and polyester;
R represents a linear or branched optionally substituted hydrocarbon;
Z is a linking group; and
D is a fluoroquinolone antibiotic.
19. The biodegradable polymer according to claim 18 which comprises less than 25 mol % of polymerized residues that are derived from a C 2 diol, relative to the total number of moles of polymerized diol residues.
20. The biodegradable polymer according to claim 16 , wherein the bioactive moieties (D) is selected from the group consisting of alatrofloxacin, balofloxacin, ciprofloxacin, clinafloxacin, danofoxacin, delafloxacin, dextrofloxacin, difloxacin, enoxacin, enrofloxacin, garenoxacin, gatifloxacin, gemifloxacin, grepafloxacin, levofloxacin, lomefloxacin, marbofloxacin, moxifloxacin, nadifloxacin, norfloxacin, ofloxacin, orbifloxacin, pefloxacin, sitafloxacin, sparfloxacin, temafloxacin, tosufloxacin, tosulfloxacin, and trovafloxacin.
21. The biodegradable polymer according to claim 16 , wherein D is coupled through Z to R by a functional group selected from the group consisting of an ester, amide, thiol, anhydride, imide, carbonate, peroxide, peroxyester, phosphate ester, thioester, sulphate ester, carbamate, azo or boronate ester moiety.
22. The biodegradable polymer according to claim 17 , wherein Z is selected from the group consisting of —O—; —C(O)—; and optionally substituted: —OC(O)—C 1-18 alkylene-C(O)—; —C(O)O—C 1-18 alkylene-C(O)—; —NR a C(O)—C 1-18 alkylene-C(O)—; —C(O)O—C 1-18 alkylene-O—; —O—C 1-18 alkylene-O—; —O—C 1-18 alkylene-NR a —; —OC(O)—C 1-18 alkylene-NR a —; —C(O)—C 1-18 alkylene-NR a —; —OC(O)—C 1-18 alkylene-O—; —C(O)—C 1-18 alkylene-O—; and —C(O)NR a —C 1-18 alkylene-NR a — where R a is selected from hydrogen, C 1-18 alkyl, C 1-18 alkenyl, C 1-18 alkynyl, C 6-18 aryl, C 3-18 -carbocyclyl, C 3-18 heteroaryl, C 3-18 heterocyclyl, and C 7-18 arylalkyl.
23. The biodegradable polymer according to claim 16 , wherein R is a linear or branched optionally substituted hydrocarbon having from 1 to 12 carbon atoms.
24. A method of delivering a bioactive moiety to a subject, the method comprising administering to the subject a biodegradable polymer according to claim 1 .
25. A method for preparing a biodegradable polymer according to claim 16 , said method comprising the step of polymerising a monomer-bioactive moiety conjugate of formula (II):
where:
X′ and Y′ are each independently functional groups that (a) are capable of undergoing polymerisation with monomer having compatible chemical functionality, and (b) react with the compatible chemical functionality to afford a biodegradable moiety selected from an ester and a carbamate moiety; and
R, Z and D are as defined in claim 16 ;
with at least one monomer comprising compatible chemical functionality.
26. The method according to claim 25 , wherein X′ and Y′ are both hydroxyl and the monomer-bioactive moiety conjugate is polymerised with a polyisocyanate and at least one selected from the group consisting of a polyacid, a polyester, and a polyester polyol.
27. The method according to claim 26 , wherein the monomer-bioactive moiety conjugate is polymerised with a polyisocyanate and a polyester polyol.
28. An ocular implant comprising the biodegradable polymer according to claim 16 , wherein the bioactive moiety is a fluoroquinolone antibiotic.
29. A monomer-bioactive moiety conjugate that is suitable for use in preparing a biodegradable polymer, the monomer-bioactive moiety conjugate having a structure of general formula (II):
where:
X′ and Y′ are each independently functional groups that (a) are capable of undergoing polymerisation with monomer having compatible chemical functionality so as to form a biodegradable polymer, and (b) react with the compatible chemical functionality to afford a biodegradable moiety;
R represents a linear or branched optionally substituted hydrocarbon;
Z is a spacer moiety; and
D is a fluoroquinolone antibiotic.
30. The monomer-bioactive moiety conjugate according to claim 29 , wherein X′ and Y′ are each hydroxyl.