Platinum complexes as antitumor agents in combination with biochemical modulation
View Patent ↗The present invention concerns the use of methods and compositions for the treatment of cancer and other hyperproliferative diseases. In certain embodiments, methods are described for the treatment of cancer and/or hyperproliferative diseases by administration of compositions containing at least one platinum complex alone or in combination with a modulator of glutathione. In particular, the methods may be used to treat cisplatin or carboplatin resistant tumor cells.
1. A composition comprising a compound represented by the structural formula
or salts thereof, and a negative modulator of glutathione.
2. The composition of claim 1 , wherein the negative modulator of glutathione is an inhibitor of glutathione synthesis.
3. The composition of claim 2 , wherein the inhibitor of glutathione synthesis is an inhibitor of γ-glutamylcysteine synthetase.
4. The composition of claim 2 , wherein the negative modulator of glutathione synthesis is L-buthionine-sulfoximine.
5. The composition of claim 1 , wherein the negative modulator of glutathione is an inhibitor of glutathione transferase.
6. A composition comprising a compound represented by the structural formula
or salts thereof, and a negative modulator of glutathione.
7. The composition of claim 6 , wherein the negative modulator of glutathione is an inhibitor of glutathione synthesis.
8. The composition of claim 7 , wherein the inhibitor of glutathione synthesis is an inhibitor of γ-glutamylcysteine synthetase.
9. The composition of claim 7 , wherein the negative modulator of glutathione synthesis is L-buthionine-sulfoximine.
10. The composition of claim 6 , wherein the negative modulator of glutathione is an inhibitor of glutathione transferase.
11. A composition comprising a compound represented by the structural formula
or salts thereof, and a negative modulator of glutathione.
12. The composition of claim 11 , wherein the negative modulator of glutathione is an inhibitor of glutathione synthesis.
13. The composition of claim 12 , wherein the inhibitor of glutathione synthesis is an inhibitor of γ-glutamylcysteine synthetase.
14. The composition of claim 12 , wherein the negative modulator of glutathione synthesis is L-buthionine-sulfoximine.
15. The composition of claim 11 , wherein the negative modulator of glutathione is an inhibitor of glutathione transferase.
16. A composition comprising a compound represented by the structural formula
or salts thereof, and a negative modulator of glutathione.
17. The composition of claim 16 , wherein the negative modulator of glutathione is an inhibitor of glutathione synthesis.
18. The composition of claim 17 , wherein the inhibitor of glutathione synthesis is an inhibitor of γ-glutamylcysteine synthetase.
19. The composition of claim 17 , wherein the negative modulator of glutathione synthesis is L-buthionine-sulfoximine.
20. The composition of claim 16 , wherein the negative modulator of glutathione is an inhibitor of glutathione transferase.
21. A pharmaceutical composition comprising (a) a platinum complex selected from the group consisting of ammine/cycloheptylamine-dichloro-platinum(II), ammine/piperidine-dichloro-platinum(II), ammine/hexamethyleneimine-dichloro-platinum(II), and ammine/hexamethyleneimine-tetrachloro-platinum(IV), and (b) a negative modulator of glutathione.
22. The pharmaceutical composition of claim 21 , wherein the concentration of a selected platinum complex is in the approximate range of 0.1 mM to 20 mM.
23. The pharmaceutical composition of claim 21 , wherein the concentration of a selected platinum complex is in the approximate range of 1 mM to 10 mM.
24. The pharmaceutical composition of claim 21 , wherein the concentration of a selected platinum complex is in the approximate range of 1 mM to 5 mM.
25. The pharmaceutical composition of claim 21 , wherein the negative modulator of glutathione is an inhibitor of glutathione synthesis.
26. The pharmaceutical composition of claim 25 , wherein the inhibitor of glutathione synthesis is an inhibitor of γ-glutamylcysteine synthetase.
27. The pharmaceutical composition of claim 25 , wherein the inhibitor of glutathione synthesis is L-buthionine-sulfoximine.
28. The pharmaceutical composition of claim 25 , wherein the concentration of L-buthionine-sulfoximine is in the approximate range of 1 μM to 300 μM.
29. The pharmaceutical composition of claim 25 , wherein the concentration of L-buthionine-sulfoximine is in the approximate range of 10 μM to 200 μM.
30. The pharmaceutical composition of claim 25 , wherein the concentration of L-buthionine-sulfoximine is in the approximate range of 20 μM to 100 μM.
31. The pharmaceutical composition of claim 21 , further defined as an intravenous pharmaceutical composition.
32. The pharmaceutical composition of claim 21 , wherein the negative modulator of glutathione is an inhibitor of glutathione transferase.
33. A method of making ammine/cycloheptylamine-dichloro-platinum(II) comprising:
a) treating an aqueous 20 mmol solution of K 2 PtCl 4 with 200 mmol KI with stirring for 10 minutes at room temperature; b) adding two equivalents of cycloheptylamine dropwise and stirring for 30 minutes forming a cis-Pt II (c-C 7 H 11 NH 2 ) 2 I 2 precipitate; c) filtering and washing the cis-Pt II (c-C 7 H 11 NH 2 ) 2 I 2 precipitate with water; d) recrystallizing the cis-Pt II (c-C 7 H 11 NH 2 ) 2 I 2 precipitate from a DMF/H 2 O mixture and washing with water, methanol, and ethyl ether; e) drying the cis-Pt II (c-C 7 H 11 NH 2 ) 2 I 2 precipitate in vacuo; f) suspending the dried cis-Pt II (c-C 7 H 11 NH 2 ) 2 I 2 precipitate in 50 mL of 60 to 70% HClO 4 and adding 150 mL of ethanol to the suspension with stirring at room temperature forming a brown [Pt II (c-C 7 H 11 NH 2 )I 2 ] 2 precipitate; g) filtering the brown [Pt II (c-C 7 H 11 NH 2 )I 2 ] 2 precipitate and washing the brown [Pt II (c-C 7 H 11 NH 2 )I 2 ] 2 precipitate with water; h) drying the washed brown [Pt II (c-C 7 H 11 NH 2 )I 2 ] 2 precipitate in vacuo; i) mixing 5 mmol of brown [Pt II (c-C 7 H 11 NH 2 )I 2 ] 2 precipitate with 5 mL of 1.5M NH 4 OH in 25 mL of water and stirring the mixture at room temperature overnight forming a yellow cis-Pt II (NH 3 )(c-C 7 H 11 NH 2 )I 2 precipitate; j) filtering the yellow cis-Pt II (NH 3 )(c-C 7 H 11 NH 2 )I 2 precipitate and washing with water; k) drying the washed yellow cis-Pt II (NH 3 )(c-C 7 H 11 NH 2 )I 2 precipitate in vacuo 1) mixing 4 mmol of cis-Pt II (NH 3 )(c-C 7 H 11 NH 2 )I 2 with 7.4 mmol of AgNO 3 in 200 mL of water and stirring overnight in the dark forming an AgI precipitate; m) removing AgI precipitate by filtration through celite forming a cis-Pt II (NH 3 )(c-C 7 H 11 NH 2 )NO 3 filtrate; n) adding 10 mL of concentrated HCl the cis-Pt II (NH 3 )(c-C 7 H 11 NH 2 )NO 3 filtrate and stirring the mixture for 3 h forming a yellow Pt II (NH 3 )(C 7 H 11 N)Cl 2 precipitate; o) evaporating the mixture to approximately 2 mL under reduced pressure and filtering yellow Pt II (NH 3 )(C 7 H 11 N)Cl 2 precipitate; p) washing the yellow Pt II (NH 3 )(C 7 H 11 N)Cl 2 precipitate with water and acetone, and drying the washed yellow Pt II (NH 3 )(C 7 H 11 N)Cl 2 precipitate in vacuo.
34. A method of making ammine/hexamethyleneimine-tetrachloro-platinum(IV) comprising:
a) adding 10 milliliters of H 2 O 2 to a suspension of 2.61 mmol Pt II (NH 3 )(C 6 H 13 N)Cl 2 in 200 mL of water, stirring for 15 hours, filtering the solution, concentrating to a minimum volume b) precipitating with acetone forming a yellow (Pt IV (NH 3 )(C 6 H 13 N)trans-(OH) 2 Cl 2 ) product; c) drying the yellow (Pt IV (NH 3 )(C 6 H 13 N)trans-(OH) 2 Cl 2 ) in vacuo.
d) dissolving the yellow 1.64 mmol of Pt IV (NH 3 )(C 6 H 13 N)trans-(OH) 2 Cl 2 (0.650 g; 1.64 mmol) in 100 mL of water; e) adding 20 mL of concentrated HCl and stirring for 24 hours at room temperature forming a clear yellow solution; f) filtering the clear yellow solution, concentrating the clear yellow solution to a minimum volume to form a yellow crystalline Pt IV (NH 3 )(C 6 H 13 N)Cl 4 ; and g) filtering, washing the yellow crystalline Pt IV (NH 3 )(C 6 H 13 N)Cl 4 with water, and drying under a vacuum.