IP Library Granted Patent US 7,220,414
Granted Patent B2
US 7,220,414 · App. 09/949,162 · Granted May 22, 2007

Degradable polyacetal polymers

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Quick Facts
Patent No.
US 7,220,414
App. No.
09/949,162
Granted
May 22, 2007
Kind
B2
Abstract

Degradable polyacetal polymers and functionalized degradable polyacetal polymers have properties favorable for use in pharmaceutical and biomedical applications. The degradable polyacetal polymers are relatively stable at physiological pH with favorable biodistribution profiles, and degrade readily in low pH conditions. Conjugates of the polymers with drugs, especially anticancer drugs, and methods of treatment of cancer.

Claims (40)

1. A polymer-drug conjugate comprising a polymer of Formula (I)

wherein

R and R1 are independently selected from the group consisting of hydrogen, C 1-18 alkyl, C 2-18 alkenyl, C 2-18 alkynyl, C 6-18 aryl, C 7-18 alkaryl and C 7-18 aralkyl groups;

X is selected from the groups (IV)–(VIII)

wherein

R 2 and R 3 are selected from covalent bonds or C 1-18 alkanediyl groups;

R 12 are selected from synthetic or natural amino acid side chains;

R 4 is selected from the group consisting of hydrogen, activating/protecting groups, and the groups (IX), (X), (XI) and (XII),

R 5 and R 6 are selected from the group consisting of —NH 2 , —NHR 13 , —OR 14 ;

R 13 and R 14 are selected from activating/protecting groups consisting of N-succinimidyl, pentachlorophenyl, pentafluorophenyl, para-nitrophenyl, dinitrophenyl, N-phthalimido, N-norbonyl, cyanomethyl, pyridyl, trichlorotriazine, 5-chloroquinilino, and protecting groups such as N-(9-fluorenyl-methoxycarbonyl) (Fmcx), carbobenzyloxy (Cbz), 1-(4,4-dimethyl-2,6-dioxocyclohexyldene)-ethyl (Dde) and imidazolyl; and

m is an integer of 0-20; wherein X is covalently conjugated to a drug via a peptidic or a hydrolytically-labile bond;

Y is —(C n H 2n O) q , C n H 2n- , wherein n is an interger of 2–10 and q is an interger of 1 to 200.

2. The polymer-drug conjugate of claim 1 wherein the drug is an anti-cancer agent selected from a group consisting of doxorubicin, daunomycin, paclitaxel, and taxotere.

3. The polymer-drug conjugate of claim 2 wherein the drug is doxorubicin.

4. A process for the preparation of a polymer-drug conjugate comprising a polymer of Formula (I)

wherein

R and R1 are independently selected from the group consisting of hydrogen, C 1-18 alkyl, C 2-18 alkenyl, C 2-18 alkynyl, C 6-18 aryl, C 7-18 alkaryl and C 7-18 aralkyl groups;

X is selected from the groups (IV)–(VIII)

wherein

R 2 and R 3 are selected from covalent bonds or C 1-18 alkanediyl groups;

R 12 are selected from synthetic or natural amino acid side chains;

R 4 is selected from the group consisting of hydrogen, activating/protecting groups, and the groups (IX), (X), (XI) and (XII),

R 5 and R 6 are selected from the group consisting of —NH 2 , —NHR 13 , —OR 14 ;

R 13 and R 14 are selected from activating/protecting groups consisting of N-succinididy, pentachlorophenyl, pentafluorophenyl, para-nitrophenyl, dinitrophenyl, N-phthalimido, N-norbomyl, cyanomethyl, pyridyl, trichlorotriazine, 5-chloroquinoline, and protecting groups such as N-(9-fluoroenyl-methoxycarbonyl) (Fmox), carbobenzyloxy (Cbz), 1-(4,4-dimethyl-2,6-dixoycyclohexyldene)-ethyl (Dde) and imidazolyl; and

m is an integer of 0–20, wherein X is covalently conjugated to a drug via a peptidic or a hydrolytically-labile bond;

Y is —(C n H 2n O) q , C n H 2n- , wherein n is an interger of 2–10 and q is an interger of 1 to 200.

5. The process of claim 4 wherein the drug is an anti-cancer agent selected from a group consisting of doxorubin, daunomycin, paclitaxel and taxotere.

6. A pharmaceutical composition comprising a polymer-drug conjugate comprising a polymer of Formula (I)

wherein

R and R 1 are independently selected from the group consisting of hydrogen, C 1-18 alkyl, C 2-18 alkenyl, C 2-18 alkynyl, C 6-18 aryl, C 7-18 alkaryl and C 7-18 aralkyl groups;

X is selected from the groups (IV)–(VIII)

wherein

R 2 and R 3 are selected from covalent bonds or C 1-18 alkanediyl groups;

R 12 are selected from synthetic or natural amino acid side chains;

R 4 is selected from the group consisting of hydrogen, activating/protecting groups, and the groups (IX), (X), (XI) and (XII),

R 5 and R 6 are selected from the group consisting of —NH 2 , —NHR 13 , —OR 14 ;

R 13 and R 14 are selected from activating/protecting groups consisting of N-succinididy, pentachlorophenyl, pentafluorophenyl, para-nitrophenyl, dinitrophenyl, N-phthalimido, N-norbomyl, cyanomethyl, pyridyl, trichlorotriazine, 5-chloroquinoline, and protecting groups such as N-(9-fluoroenyl-methoxycarbonyl) (Fmoc), carbobenzyloxy (Cbz), 1-(4,4-dimethyl-2,6-dixoycyclohexyldene)-ethyl (Dde) and imidazolyl; and

m is an integer of 0–20, wherein X is covalently conjugated to a drug via a peptidic or a hydrolytically-labile bond;

Y is —(C n H 2n O) q , C n H 2n- , wherein n is an interger of 2–10 and q is an interger of 1 to 200.

7. The pharmaceutical composition of claim 6 wherein the drug is an anti-cancer agent selected from a group consisting of doxorubin, daunomycin, paclitaxel and taxotere.

Assignments (2)
RELEASE OF SECURITY INTEREST IN PATENTS RECORDED AT REEL 026177/FRAME 0874 Recorded Sep 27, 2023
From: TANG CAPITAL PARTNERS, LP
To: HERON THERAPEUTICS, INC. (F/K/A A.P. PHARMA, INC.)
Reel/Frame 065045/0730 →
CHANGE OF NAME Recorded Feb 3, 2014
From: A.P. PHARMA, INC.
To: HERON THERAPEUTICS, INC.
Reel/Frame 032153/0273 →