Its chemical name is 4-amino-1-[3,3-difluoro-4-hydroxy-5-(hydroxymethyl) tetrahydrofuran-2-yl]-1H-pyrimidin-2-one, chemical formula is: C 9 H 11 F 2 N 3 O 4 ; molecular weight is 263.198 g/mol.

The discovery of new polymorphic forms of a pharmaceutically useful compound provides a new opportunity to improve the performance characteristics of a pharmaceutical product. It enlarges the repertoire of materials that a formulation scientist has available for designing, for example, a pharmaceutical dosage form of a drug with a targeted release profile or other desired characteristic.

There is a need in the art for various polymorphic forms of gemcitabine.

›SUMMARY OF THE INVENTION · 1 of 2

The present application provides several crystalline forms of gemcitabine base, i.e., Forms A-F.

In accordance with one embodiment, crystalline Form A of gemcitabine base is characterized by a powder x-ray diffraction pattern with peaks at about 27.6 and 9.4±0.2 degrees two-theta; preferably, Form A is further characterized by a powder x-ray diffraction pattern with peaks at about 16.1 and 20.7±0.2 degrees two-theta; more preferably, Form A is further characterized by a powder x-ray diffraction pattern with peaks at about 6.8, 15.7, 16.7, and 24.3±0.2 degrees two-theta. As a preferred embodiment, crystalline Form A is further characterized by a powder x-ray diffraction pattern as depicted in FIG. 1( a ).

Preferably, crystalline Form A of claim 1 is further characterized by a DSC thermogram as depicted in FIG. 1( b ).

Preferably, the crystalline Form A is further characterized by an infrared spectrum having bands at about 781, 1094, 1523, 1660, 1696, and 3404 (cm 1 ). More preferably, crystalline Form A is further characterized by an infrared spectrum as depicted in FIG. 1( c ).

In accordance with another embodiment, crystalline Form B of gemcitabine base is characterized by a powder x-ray diffraction pattern with peaks at about 20.8 and 23.5±0.2 degrees two-theta; preferably, crystalline Form B is further characterized by a powder x-ray diffraction pattern with peaks at about 11.8, 27.8, and 30.1±0.2 degrees two-theta; more preferably, crystalline Form B is further characterized by a powder x-ray diffraction pattern with peaks at about 10.5, 15.8, 22.0, and 33.0±0.2 degrees two-theta. As a preferred embodiment, crystalline Form B is further characterized by a powder x-ray diffraction pattern as depicted in FIG. 2( a ).

Preferably, crystalline Form B is characterized by a DSC thermogram as depicted in FIG. 2( b ).

Preferably, crystalline Form B is characterized by an infrared spectrum having bands at about 547, 661, 715, 781, 1065, 1196, 1296, 1514, 1656, and 3217 (cm −1 ); more preferably, crystalline Form B is characterized by an infrared spectrum as depicted in FIG. 2( c ).

In accordance with yet another embodiment, crystalline Form C of gemcitabine base is characterized by a powder x-ray diffraction pattern with peaks at about 15.6 and 22.3±0.2 degrees two-theta; preferably, crystalline Form C is further characterized by a powder x-ray diffraction pattern with peaks at about 14.4, 23.6, and 24.4±0.2 degrees two-theta; more preferably, crystalline Form C is further characterized by a powder x-ray diffraction pattern with peaks at about 12.1, 18.8, 23.0, 29.1, 34.5 and 34.8±0.2 degrees two-theta. As a preferred embodiment, crystalline Form C is characterized by a powder x-ray diffraction pattern as depicted in FIG. 3( a ).

Preferably, crystalline Form C is characterized by a DSC thermogram having a sharp endothermic peak at about 221.61-223.73° C. More preferably, crystalline Form C is characterized by a DSC thermogram as depicted in FIG. 3( b ).

Preferably, crystalline Form C is characterized by an infrared spectrum having bands at about 523, 781, 1086, 1199, 1297, 1492, 1656, and 3199 (cm −1 ). More preferably, crystalline Form C is further characterized by an infrared spectrum as depicted in FIG. 3( c ).

In accordance with yet another embodiment, crystalline Form D of gemcitabine base is characterized by a powder x-ray diffraction pattern with peaks at about 14.1 and 20.7±0.2 degrees two-theta; preferably, crystalline Form D is further characterized by a powder x-ray diffraction pattern with peaks at about 10.6, 14.9, 24.4, 27.8, and 30.3±0.2 degrees two-theta; more preferably, crystalline Form D is further characterized by a powder x-ray diffraction pattern with peaks at about 10.1, 17.3, 19.0, 19.7, 22.2, 23.0, 12.1, 18.8, 23.0, and 32.2±0.2 degrees two-theta. As a preferred embodiment, crystalline Form D is characterized by a powder x-ray diffraction pattern as depicted in FIG. 4( a ).

Preferably, crystalline Form D is characterized by a DSC thermogram as depicted in FIG. 4( b ).

Preferably, crystalline Form D is further characterized by an infrared spectrum having bands at about 598, 784, 1097, 1523, 1654, and 3407 (cm −1 ). More preferably, crystalline Form D is characterized by an infrared spectrum as depicted in FIG. 4( c ).

In accordance with yet another embodiment, crystalline Form E of gemcitabine base is characterized by a powder x-ray diffraction pattern with peaks at about 20.8 and 23.5±0.2 degrees two-theta; preferably, crystalline Form E is further characterized by a powder x-ray diffraction pattern with peaks at about 10.3, 11.8, 27.5, and 30.0±0.2 degrees two-theta; more preferably, crystalline Form E is further characterized by a powder x-ray diffraction pattern with peaks at about 10.5, 15.8, 22.0, 23.0, 24.7, 28.1, and 33.0±0.2 degrees two-theta. As a preferred embodiment, crystalline Form E is further characterized by a powder x-ray diffraction pattern as depicted in FIG. 5( a ).

Preferably, the crystalline Form E is further characterized as depicted in FIG. 5( b ).

Preferably, crystalline Form E is characterized by an infrared spectrum having bands at about 577, 782, 1096, 1523, 1662, and 3406 (cm −1 ). More preferably, crystalline Form E is characterized by an infrared spectrum as depicted in FIG. 5( c ).

In accordance with yet another embodiment, crystalline Form F of gemcitabine base is characterized by a powder x-ray diffraction pattern with peaks at about 20.8 and 27.6±0.2 degrees two-theta; preferably, crystalline Form F is characterized by a powder x-ray diffraction pattern with peaks at about 9.4, 11.8, 15.8, 24.3, and 30.1±0.2 degrees two-theta; more preferably, crystalline Form F is further characterized by a powder x-ray diffraction pattern with peaks at about 16.1, 16.8, 22.0, 28.2, and 33.0±0.2 degrees two-theta. As a preferred embodiment, crystalline Form F is characterized by a powder x-ray diffraction pattern as depicted in FIG. 6( a ).

Preferably, crystalline Form F is characterized by a DSC thermogram as depicted in FIG. 6( b ).

›SUMMARY OF THE INVENTION · 2 of 2

Preferably, crystalline Form F is characterized by an infrared spectrum having bands at about 781, 1059, 1094, 1523, 1660, and 3404 (cm −1 ). More preferably, Form F is characterized by an infrared spectrum as depicted in FIG. 6( c ).

The various features of novelty which characterize the invention are pointed out with particularity in the claims annexed to and forming a part of the disclosure. For a better understanding of the invention, its operating advantages, and specific objects attained by its use, reference should be had to the drawing and descriptive matter in which there are illustrated and described preferred embodiments of the invention.

›BRIEF DESCRIPTION OF THE DRAWINGS

In the drawings:

FIG. 1 is the X-ray powder diffraction pattern (a), the DSC pattern (b), and the Infrared spectrum (c) for crystalline Form A of gemcitabine base.

FIG. 2 is the X-ray powder diffraction pattern (a), the DSC pattern (b), and the Infrared spectrum (c) for crystalline Form B of gemcitabine base.

FIG. 3 is the X-ray powder diffraction pattern (a), the DSC pattern (b), and the Infrared spectrum (c) for crystalline Form C of gemcitabine base.

FIG. 4 is the X-ray powder diffraction pattern (a), the DSC pattern (b), and the Infrared spectrum (c) for crystalline Form D of gemcitabine base.

FIG. 5 is the X-ray powder diffraction pattern (a), the DSC pattern (b), and the Infrared spectrum (c) for crystalline Form E of gemcitabine base.

FIG. 6 is the X-ray powder diffraction pattern (a), the DSC pattern (b), and the Infrared spectrum (c) for crystalline Form F of gemcitabine base.

›DETAILED DESCRIPTION OF THE PRESENTLY PREFERRED EMBODIMENTS

The following examples are provided to illustrate, but not to limit the present invention.

EXAMPLES

›Examples19

›Example 1

1 g Gemcitabine is dissolved in 5 mL MeOH at RT (20-30° C.). 10 mL toluene is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 2

1 g Gemcitabine is dissolved in 5 mL MeOH at RT (20-30° C.). 10 mL EA is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 3

1 g Gemcitabine is dissolved in 5 mL water and 5 mL EtOH at 40° C. 10 mL MTBE is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form B.

›Example 4

1 g Gemcitabine is dissolved in 5 mL MeOH at RT (20-30° C.). 10 mL CH 2 Cl 2 is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 5

1 g Gemcitabine is dissolved in 10 mL EtOH at reflux temp. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 6

1 g Gemcitabine is dissolved in 18 mL MeOH and 1 mL water at 70° C. 54 mL EA is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 7

1 g Gemcitabine is dissolved in 5 mL MeOH and 25 mL ACN at RT (20-30° C.). 25 mL n-heptane° is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 8

1 g Gemcitabine is dissolved in 30 mL acetone. 30 mL CH 2 Cl 2 is added to the reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form E.

›Example 9

1 g Gemcitabine is dissolved in 30 mL THF and 30 mL water at 50-60° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form B.

›Example 10

1 g Gemcitabine is dissolved in 2 mL water and 36 mL IPA at 70° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 11

1 g Gemcitabine is dissolved in 6 mL water and 60 mL ACN at 70° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form F.

›Example 12

1 g Gemcitabine is dissolved in 16 mL water 50-60° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form B.

›Example 13

1 g Gemcitabine is dissolved in 5 mL MeOH at RT (20-30° C.). 15 mL MIBK is added to reaction mixture and solid begins to precipitate out. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 14

1 g Gemcitabine is dissolved in 2 mL water and 20 mL n-butanol at 70° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form A.

›Example 15

1 g Gemcitabine is dissolved in 2 mL water and 20 mL IPA at 70° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine Form B.

›Example 16

1 g Gemcitabine is dissolved in water/IPA=95/5, 90/10, at 70° C. The reaction mixture is cooled to 0-10° C. and filtered and Gemcitabine dried for 2 hours at 60° C. under vacuum, to obtain Gemcitabine Form D.

›Example 17

1 g Gemcitabine is dissolved in water/IPA=95/5 or 90/10 at 70° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine form B. After 2 hours of drying at 60° C. under vacuum, Gemcitabine Form B is converted to Form A.

›Example 18

1 g Gemcitabine is dissolved in water/IPA=85/15, at 70° C. The reaction mixture is cooled to 0-10° C. and filtered. The solid is Gemcitabine form A+B. After 2 hours of drying at 60° C. under vacuum, Gemcitabine Form B is converted to Form A.

›Example 19

Form C is an anhydrous form from heating Form A at 200° C.

Table 1 blow summarizes production of various crystalline forms of gemcitabine in accordance with the embodiments provided above.

Table 2 below shows the solubility of Form A in different solvents.

The invention is not limited by the embodiments described above which are presented as examples only but can be modified in various ways within the scope of protection defined by the appended patent claims.

›Tables in the description — 2

TABLE 1 — Solvent system (part

Item	by Volume)	Crystal form
1	MeOH/Toluene = 5/10	A
2	MeOH/EA = 5/10	A
3	H 2 O/EtOH/MTBE = 5/5/10	B
4	MeOH/CH 2 Cl 2 = 5/10	A
5	EtOH = 10	A
6	IPA/H 2 O/EA = 18/1/54	A
7	MeOH/ACN/n-hep =	A
	5/20/10
8	Acetone/CH 2 Cl 2 = 30/30	E
9	THF/H 2 O = 30/30	B
10	IPA/H 2 O = 36/2	A
11	AcN/H 2 O = 60/6	F
12	H 2 O	B
13	MeOH/MIBK = 5/15	A
14	n-butanol/water = 20/2	A
15	IPA/H 2 O = 20/2	B
16	IPA/H 2 O = 5/95, 10/90	D
17	H 2 O/EtOH/MTBE = 5/5/10	B
18	IPA/H2O = 36/2	A

solvent	MeOH	EtOH	IPA	Butanol	Acetone	MIBK	MTBE	THF	Toluene
Solubility (mg/mL)	201.16	26.23	8.36	4.92	5.9	0.054	0	0.84	0
solvent	H 2 O	ACN	EA	n-heptane	CH 2 Cl 2	DMAC	DMSO
Solubility (mg/mL)	20.32	1.78	0.06	0	0	>468.06	217.22

Claims as granted

24 claims

Classifications

2 codes

IPC · International Patent Classification

Section C — Chemistry; metallurgy

C07H19/00

USPC · US Patent Classification

536/28.5

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