IP Library Granted Patent US 11,292,878
Granted Patent B2
US 11,292,878 · App. 16/277,781 · Granted Apr 5, 2022

Poly(L-lysine isolphthalamide) (PLP) polymers with hydrophobic pendant chains

Inventors: Rongjun Chen (London, GB); Siyuan Chen (Huzhou, CN); Liwei Wu (Chengdu, CN)
Assignee: Rongjun Chen
C08G69/48A61K47/34A61K47/645C08G69/10C12Q1/025
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Quick Facts
Patent No.
US 11,292,878
App. No.
16/277,781
Granted
Apr 5, 2022
Kind
B2
Abstract

The present disclosure relates to the provision of novel biodegradable amphiphilic peptides and peptide analogues based derivatives comprising hydrophobic chains and their use in the permeabilization of mammalian cells and delivery of agents, for example therapeutic agents, imaging agents and cell preservation agents.

Claims (69)

1. A poly(lysine isophthalamide) derivative comprising general formula (I):

wherein R comprises

NR 1 R 2 or OH wherein at least one of R are NR 1 R 2 ;

R 1 and R 2 each independently comprises:

H;

C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl, C 6-10 aryl or C 5-10 heteroaryl; wherein

Alkyl, alkenyl and alkynyl groups R 1 and R 2 are optionally substituted with one or more substituents selected from halo, cyano, nitro, diazonium, —OP(O)OR 3 OR 4 , —PR 3 R 4 , NR 3 R 4 , ═NR 3 , ═O, C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 3-7 cycloalkyl, C 3-10 heterocyclyl, C 6-14 aryl or C 4-14 heteroaryl;

wherein cycloalkyl, heterocyclyl, aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 , aryl substituted with R 3 and heteroaryl substituted with R 3 and, where chemically appropriate, ═O; and

wherein each of R 3 and R 4 is independently H or C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 6-10 aryl;

aryl and heteroaryl groups R 1 and R 2 are optionally substituted with one or more substituents selected from C 1-16 alkyl, halo, cyano, nitro, diazonium, —OP(O)OR 3 OR 4 , —PR 3 R 4 , NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 6-14 aryl, C 4-14 heteroaryl or S—CH 2 C(O)NR 5 R 6 ;

wherein alkyl groups are optionally substituted with one or more substituents selected from halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ;

wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ;

wherein R 3 and R 4 are as defined above and R 5 and R 6 are each independently H, C 1-6 alkyl optionally substituted with OR 3 or halo or C 6-14 aryl optionally substituted with C 1-6 alkyl, OH, O(C 1-6 alkyl) or O—C 6-14 aryl; or

R 1 and R 2 together with the nitrogen atom to which they are attached form a 5-12-membered heterocyclic ring optionally containing one or more additional heteroatoms selected from N, O and S and optionally substituted with one or more substituents selected from C 1-16 alkyl, C 1-16 haloalkyl, halo, cyano, nitro, diazonium, ═O, —OP(O)OR 3 R 4 , —PR 3 R 4 , NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 6-14 aryl or C 4-14 heteroaryl;

wherein alkyl and haloalkyl groups are optionally substituted with one or more substituents selected from halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ,

wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ;

wherein R 3 and R 4 are as defined above; and

n≥4.

2. A poly(lysine isophthalamide) derivative according to claim 1 wherein

R 1 and R 2 each independently comprises:

H;

C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl group optionally substituted with one or more substituents selected from halo, cyano, nitro, diazonium, —OP(O)OR 3 OR 4 , —PR 3 R 4 , NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 6-14 aryl or C 4-14 heteroaryl,

wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ; and wherein each of R 3 and R 4 is independently H or C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 6-10 aryl;

C 6-10 aryl optionally substituted with one or more substituents selected from C 1-16 alkyl, C 1-16 haloalkyl, halo, cyano, nitro, diazonium, —OP(O)OR 3 OR 4 , —PR 3 R 4 , NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 6-14 aryl or C 4-14 heteroaryl,

wherein alkyl and haloalkyl groups are optionally substituted with one or more substituents selected from halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ;

wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ;

wherein R 3 and R 4 are as defined above; or

R 1 and R 2 together with the nitrogen atom to which they are attached to form a 5-12-membered heterocyclic ring optionally containing one or more additional heteroatoms selected from N, O and S and optionally substituted with one or more substituents selected from C 1-16 alkyl, C 1-16 haloalkyl, halo, cyano, nitro, diazonium, —OP(O)OR 3 OR 4 , —PR 3 R 4 , NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 6-14 aryl or C 4-14 heteroaryl;

wherein alkyl and haloalkyl groups are optionally substituted with one or more substituents selected from halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ,

wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , azide, OP(O)OR 3 OR 4 , —PR 3 R 4 ;

wherein R 3 and R 4 are as defined above; and n≥4.

3. A poly(lysine isophthalamide) derivative according to claim 1 wherein R 1 is as defined in claim 1 and R 2 is C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl, C 6-10 aryl or C 5-10 heteroaryl, any of which is optionally substituted as defined in claim 1 .

4. A poly(lysine isophthalamide) derivative according to claim 3 , wherein R 1 is H, C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl, any of which may optionally be substituted as defined in claim 1 and R 2 is C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl, any of which may optionally be substituted as defined in claim 1 .

5. A poly(lysine isophthalamide) derivative according to claim 4 wherein

R 1 is H or C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl, any of which is unsubstituted or is substituted with F, Cl, OH, SH, methoxy or ethoxy; and

R 2 is C 6-30 alkyl, C 6-30 alkenyl or C 6-30 alkynyl, any of which is unsubstituted or is substituted with F, Cl, OH, SH, methoxy or ethoxy.

6. A poly(lysine isophthalamide) derivative according to claim 5 wherein R 1 is H or unsubstituted C 6-30 alkyl, unsubstituted C 6-30 alkenyl or unsubstituted C 6-30 alkynyl; and R 2 is unsubstituted C 6-30 alkyl, unsubstituted C 6-30 alkenyl or unsubstituted C 6-30 alkynyl.

7. A poly(lysine isophthalamide) derivative according to claim 5 , wherein R 1 is H and R 2 is unsubstituted C 7-18 alkyl.

8. A poly(lysine isophthalamide) derivative according to claim 7 , wherein each of R 1 and R 2 is independently unsubstituted C 7-18 alkyl.

9. The poly(lysine isophthalamide) derivative according to claim 7 wherein R 2 is n-heptyl, n-decyl, n-tetradecyl or n-octadecyl.

10. The poly(lysine isophthalamide) derivative according to claim 9 wherein said R 2 is n-decyl.

11. The poly(lysine isophthalamide) derivative according to claim 1 wherein between 0.1-99% of the moieties R are NR 1 R 2 .

12. The poly(lysine isophthalamide) derivative according to claim 11 wherein 3-18% of the moieties R are NR 1 R 2 .

13. The poly(lysine isophthalamide) derivative according to claim 2 wherein each of R 1 and R 2 is C 7-18 alkyl, C 7-18 alkenyl or C 7-18 alkynyl, any of which may optionally be substituted as defined in claim 2 .

14. The poly(lysine isophthalamide) derivative according to claim 13 wherein each of R 1 and R 2 is C 7 -alkyl, C 8 -alkyl, C 10 alkyl, C 14 alkyl or C 18 alkyl, any of which may be optionally be substituted according to claim 2 .

15. The poly(lysine isophthalamide) derivative according to claim 1 wherein each of R 1 and R 2 is optionally substituted with one or more substituents selected from halo, cyano, nitro, azo, diazonium, phosphate, phosphate ester, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , C(O)SR 3 , C(O)NR 3 R 4 , azide, C 6-14 aryl or C 4-14 heteroaryl, wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-10 alkyl, C 1-10 haloalkyl, C 2-10 alkenyl, C 2-10 alkynyl, halo, cyano or nitro, NR 3 R 4 , C(O)OR 3 , OR 3 , SR 3 , RN 3 , phosphate, phosphate ester and wherein each of R 3 and R 4 is independently H or C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl.

16. The poly(lysine isophthalamide) derivative according to claim 2 wherein each of R 1 and R 2 is optionally substituted with one or more substituents selected from halo, cyano, nitro, NR 3 R 4 , C(O)OR 3 OR 3 SR 3 , C 6-10 aryl or heteroaryl, wherein aryl and heteroaryl groups are optionally substituted with one or more substituents selected from C 1-4 alkyl, C 1-4 haloalkyl, halo, cyano or nitro; and wherein each of R 3 and R 4 is independently H or C 1-6 alkyl.

17. The poly(lysine isophthalamide) derivative according to claim 1 wherein said peptide is associated, either directly or indirectly with an agent for intracellular delivery to a cell.

18. The poly(lysine isophthalamide) derivative according to claim 17 wherein said agent is covalently or non-covalently associated with said poly(lysine isophthalamide) derivative.

19. The poly(lysine isophthalamide) derivative according to claim 18 wherein said agent is a therapeutic agent.

20. The poly(lysine isophthalamide) derivative according to claim 18 wherein said agent is an imaging agent.

21. The poly(lysine isophthalamide) derivative according to claim 18 wherein said agent is a cell preservation agent.

22. A process for the preparation of poly(lysine isophthalamide) derivative according to claim 1 comprising the steps

i) polymerization of aqueous lysine methyl ester.2HCl with an equivalent amount of isophthaloyl chloride in acetone and subsequent hydrolysis in DMSO with ethanolic sodium hydroxide, and

ii) conjugation of R, wherein R comprises NR 1 R 2 and is defined as above onto the polymer backbone via dicyclohexylcarboiimide/dimethylaminopyridine (DCC/DMAP) coupling; or

conjugation of R is via 1-Ethyl-3-(3-dimethylaminopropyl)-carbodiimide (EDC)/N-Hydroxysuccinimide (NHS) coupling.

23. A composition comprising a poly(lysine isophthalamide) derivative according to claim 1 .

24. The composition according to claim 23 wherein the agent is a therapeutic agent and the composition is a pharmaceutical composition including a pharmaceutically acceptable carrier.

25. The composition according to claim 23 wherein said composition comprises mammalian cells or a collection of mammalian cells.

26. A composition according to claim 23 for use in the delivery of at least one agent to a mammalian cell, cellular aggregate, tissue or organ.

27. An in vitro or ex vivo method to deliver an agent to a cell comprising:

i) contacting cells or a cellular aggregate, tissue or organ comprising cells with an effective amount of a composition according to claim 23 ; and

ii) incubating said cell, cellular aggregate, tissue or organ to allow permeabilization of said mammalian cells or cellular aggregate, tissue or organ comprising cells thereby delivering said agent.

28. The method according to claim 27 wherein said cell is a mammalian cell.

29. An in vitro or ex vivo method for the preservation of a mammalian cell, cellular aggregate, tissue or organ comprising the steps:

i) providing a preparation comprising a mammalian cell preparation, mammalian cellular aggregate, tissue or organ and a composition according to claim 23 ;

ii) incubating said preparation to permeabilize the mammalian cell membranes of said mammalian cell, cellular aggregate, tissue or organ; and

iii) contacting said permeabilized cell, cellular aggregate, tissue or organ with one or more preservation agents.

30. The method according to claim 29 wherein said preservation agent is a sugar.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 5, 2022
From: CHEN, RONGJUN, DR
To: ALPHACELLS BIOTECHNOLOGIES LIMITED
Reel/Frame 059508/0760 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 12, 2019
From: IMPERIAL COLLEGE INNOVATIONS LTD
To: CHEN, RONGJUN, DR
Reel/Frame 049737/0673 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2019
From: CHEN, RONGJUN; CHEN, SIYUAN; WU, LIWEI
To: IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE
Reel/Frame 049464/0234 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2019
From: IMPERIAL COLLEGE OF SCIENCE, TECHNOLOGY AND MEDICINE
To: IMPERIAL INNOVATIONS LIMITED
Reel/Frame 049464/0400 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2019
From: IMPERIAL INNOVATIONS LIMITED
To: IMPERIAL WHITE CITY INCUBATOR LIMITED
Reel/Frame 049464/0455 →
CHANGE OF NAME Recorded Jun 13, 2019
From: IMPERIAL WHITE CITY INCUBATOR LIMITED
To: IMPERIAL COLLEGE INNOVATIONS LIMITED
Reel/Frame 049464/0506 →
Priority Claims (1)
GB 1612150 · Jul 13, 2016 · national
Continuity (3)
Continuation 16246250 · Jan 11, 2019
Continuation PCTGB2017052058 · Jul 13, 2017
Related Publication 20190248956A1 · Aug 15, 2019