CRYSTALLINE FORM IV OF LlNEZOLID Cross-reference to Related Applications
This application claims the benefit of provisional applications Serial Numbers 60/584,371, filed June 29,2004; 60/584,283, filed June 30,2004; 60/601,086, filed August 12,2004; 60/602,227, filed August 17,2004; 60/633,887, filed December 7, 2004; 60/656,646, filed February 24,2005; 60/656,778, filed February 24,2005; 60/678,440, filed May 5,2005; and 60/684,410, filed May 24,2005; which are incorporated herein by reference.
Field of the Invention
The present invention relates to a novel crystalline form of Unezolid (Form IV) as well as to novel methods of preparing and using Form IV.
Background of the Invention
Linezoh'd[(S)-N~[[3-(3-Fraoro-4-morpholmyl^^
acetamide] is an antimicrobial agent. Linezolid is an oxazolidinone, having the
Linezolid is described in The Merck Index (13th edition. Monograph number: 05526, CAS Registry Number: 165800-03-3) as white crystals, with a melting point of 181.5-
empirical formula CigHaoFNaCU and the following structure:
(Figure Remove)182.5°. Linezolid, as well as a process for its preparation, is disclosed in U.S. Patent No. 5,688,792 (Example 5), European Patent No. 717738, Israeli Patent No. 110,802, Canadian Patent No. 2,168,560, and International Patent Publication WO 95/07271.
Crystalline Form n linezolid is disclosed in U.S. Patent No. 6,559,305.
Linezolid is marketed in the United States by Pfizer, Inc. as an injection, tablets, and oral suspension under the name ZYVOX®. Its main indications are nosocomial pneumonia, skin and skin-structure infections, and vancomycin-resistant Enterococcus faecium infections.
The present invention relates to the solid state physical properties of Linezolid. These properties can be influenced by controlling the conditions under which Linezolid is obtained hi solid form. Solid state physical properties include, for example, the flowability of the milled solid. Flowability affects the ease with which me material is handled during processing into a pharmaceutical product. Gfidants are often added to improve the flowability of a non-compacted solid composition and to improve the accuracy of dosing. When particles of the powdered compound do not flow past eaich other easily, a formulation specialist must take that fact into account hi developing a tablet or capsule formulation, which may necessitate the use of glidants such as colloidal silicon dioxide, talc, starch or tribasic calcium phosphate.
Crystal forms with platelet shape have better flowability than crystals with needle shape (M Rouhi, The Right Stuff; Chemical & Engineering News; 24* Feb. 2003). Crystals with plate shape are more advantageous than those with needle shape for injection. A suspension of plate-shaped crystals may be injected through a smaller needle with greater ease than a suspension of needle-shaped crystals. (S.R. Bym et al. Solid-State Chemistry of Drugs 2nd Edition pg.4).
Another important solid state property of a pharmaceutical compound is its rate of dissolution in aqueous fluid, The rate of dissolution of an active ingredient in a patient's stomach fluid can have therapeutic consequences since it imposes an upper limit on the rate at which an orally-administered active ingredient can reach the
patient's bloodstream. The rate of dissolution is also a consideration in formulating syrups, elixirs and other liquid medicaments. The solid state form of a compound may also affect its behavior oh compaction and its storage stability.
These practical physical characteristics are influenced by the conformation and orientation of molecules in the unit cell, which defines a particular polymorphic form of a substance. These conformational and orientation factors in turn result in particular intramolecular interactions such that different polymorphic forms may give rise to distinct spectroscopic properties that may be detectable by powder X-ray diffraction, solid state 13C NMR spectrometry and infrared spectrometry. A particular polymorphic form may also give rise to thermal behavior different from that of the amorphous material or another polymorphic form. Thermal behavior is measured in the laboratory by such techniques as capillary melting point, thennogravimetric analysis (TGA) and differential scanning calorimetry (DSC) and can be used to distinguish some polymorphic forms from others.
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 additional polymorphic forms of Lmezolid.
Summary of the Invention
The present invention provides linezolid crystalline Form IV. Form IV is characterized by a powder X-ray diffraction (PXRD) pattern with peaks at about 13.5, 18.0,21.1,22.2 and 25.4 ±0.2 degrees 2 theta. Form IV may be further characterized by PXRD peaks at about 7.5,18.7,19.9,27.7 and 28.4 ±0.2 degrees 2 theta. Form TV maybe further characterized by a PXRD pattern substantially as depicted hi Figure 1.
The crystalline linezolid Form IV of the present invention is polymorphically pure, i.e., contains less than about 10% Form n, preferably less than about 5% Form n, and
even more preferably less than about 1% Form H, and most preferably, less than about 0.5% Form H (by weight).
The crystalline linezolid Form IV of the present invention is anhydrous, and is stable against transformation into Form n upon storage at a relative humidity of about 0% to about 100% at room temperature for at least 10 days.
The present invention also provides crystalline linezolid Form IV that is enantiomerically pure with respect to its R-enantiomer, i.e., containing less than about 0.1% area by HPLC of the R-enantiomer, preferably less than about 0.02% area by HPLC of the R-enantiomer.
In one embodiment, the novel crystalline linezolid Form IV is in the form of irregular plate crystals when observed under the microscope.
Another embodiment of the present invention is a novel method of making crystalline linezolid Form IV that comprises spray-drying a solution of linezolid at a temperature ofatleast50°C.
Also described in the present invention is another process for preparing crystalline linezolid Form IV comprising the step of heating crystalline linezolid Form JL
Form IV may also be prepared comprising the step of heating a slurry of form H in an aromatic solvent
Another aspect of the present invention is the preparation of Form n from a slurry of Form IV in water or an organic solvent
In another embodiment, the crystalline linezolid Form IV provided by the present invention has a preferred maximum particle size of 500 Jim.
Another embodiment of the present invention is a pharmaceutical formulation xnnprising a therapeuticaHy effective amount of crystalline linezolid Form TV, xanbined with a pharmaceutically acceptable excipient or carrier.
A further embodiment of me present invention is a method for treating a patient suffering from a gram positive bacterial infection, using a formulation containing a therapeutically effective amount of crystalline linezolid Form IV.
Figures
Figure 1 is a powder X-Ray diflractogram of crystalline linezolid Form IV.
Figure 2a-2c is an FTIR spectrum of crystalline Hnezolid Form IV obtained with the mineral oil mull technique.
Figure 2d-2f is an FTIR spectrum of crystalline Linezolid Form IV obtaind with the DRIFT technique.
Figure 3 is a DSC thermogram of crystalline linezolid Form IV. Figure 4a-4d is an FTRaman spectrum of crystalline linezolid Form IV.
Figure 5 shows the needle shape of crystals of crystalline linezolid Form n as seen through a microscope.
Figure 6 shows the plate shape of crystals of crystalline linezolid Form IV as seen through a microscope.
Figure 7 also shows the plate shape of crystals of crystalline linezolid Form W as seen through a microscope.
Figure 8 is a DSC thermogram of crystalline linezolid Form n. Detailed Description of the Invention
The term "spray drying" broadly refers to processes involving breaking up liquid mixtures into small droplets (atomization) and rapidly removing solvent from the mixture, m a typical spray-drying apparatus, there is a strong driving force for evaporation of solvent from the droplets, which may be provided by a heated drying gas. Spray-drying processes and equipment are described in Perry's Chemical Engineer's Handbook, pgs. 20-54 to 20-57 (Sixth Edition 1984).
By way of non-limiting example only, the typical spray-drying apparatus comprises a drying chamber, atomizing means for atomizing a solvent-containing feed into the drying chamber, a source of heated drying gas mat flows into the drying chamber to remove solvent from the atomized-solvent-containing feed, an outlet for the products of drying, and product collection means located downstream of the drying chamber. Examples of such apparatuses include Niro Models PSD-1, PSD-2 and PSD-4 (Niro A/S, Soeborg, Denmark). Typically, the product collection means includes a cyclone connected to the drying apparatus. In the cyclone, the particles produced during spray-drying are separated from the drying gas and evaporated solvent, allowing the particles to be collected. A filter may also be used to separate and collect the particles produced by spray-drying. The process of the invention is not limited to the use of such drying apparatuses as described above.
Therapeutically effective amount" means the amount of a crystalline form that, when administered to a patient for treating a disease or other undesirable medical condition, is sufficient to have a beneficial effect with respect to that disease or condition. The "therapeutically effective amount" will vary depending on me crystalline form, the disease or condition and its severity, and the age, weight, etc., of the patient to be treated. Determining the therapeutically effective amount of a given crystalline form is within the ordinary skill of the art and requires no more than routine experimentation.
The present invention provides crystalline linezolid Form IV, characterized by a powder X-ray diffraction (PXRD) pattern with peaks at about 13.5,18.0,21.1,22.2, and 25.4 ±0.2 degrees 2 theta. Form IV may be further characterized by PXRD peaks at about 7.5,18.7,19.9,27.7, and 28.4 ±0.2 degrees 2 theta. Form IV may be further characterized by a PXRD pattern substantially as depicted in Figure 1.
Crystalline liuezolid Form IV may be further characterized by an FTIR spectrum with peaks at about 3333,2817,1732,1661,1540,1515,1335,1256,1229,1200,1213, 1148,1080,1059,1050,903,825,755, and 662 era1. Crystalline linezolid Form IV maybe further characterized by an FTIR spectrum substantially as depicted in Figure 2a-2c or in Figure 2d-2f. The most characteristic FTIR peaks are 2817,1335,1229, 1200, and 662 cm"1.
Crystalline linezolid Form IV may also be characterized by a differential scanning calorimetry (DSC) thermogram substantially as depicted in Figure 3, Form IV has a characteristic DSC thermogram compared to the DSC thermogram of Form H (Figure 8). Form n has a sharp endothermic peak around 155*C, followed by a sharp exothermic peak at around 160°C, and another sharp endothermic peak at around 180°C, which corresponds to the final melting of linezolid. Form IV has only one sharp endothermic peak, which corresponds to the final melting of linezolid.
Crystalline linezolid Form IV may be further characterized by an FTRaman spectrum having peaks at about 2975,2930,2865,1083, and 750 cm"1. Crystalline linezolid Form IV may be farther characterized by an FTRaman spectrum substantially as depicted in Figure 4a-4d,
The invention also provides crystalline linezolid Form IV, which has about 0.1% water by weight. Form IV may also be characterized by a weight loss measured by thermal gravimetric analysis (TGA) of about 0,1% by weight. This embodiment of Form IV is anhydrous. Thus, the present invention includes crystalline linezolid Form IV which has about 0.1 % or less water by weight.
The crystalline linezolid Form IV of the present invention can be made in the form of irregular plate crystals. The previously known crystalline linezolid Form n forms needle shaped crystals. The flowability of crystals with an irregular plate shape of the present invention is much better than the flowability of crystals with needle shape. Another advantage of the irregular plate crystals is that they are easier to work with than needle shaped linezolid of the prior art The bulk properties of the crystalline linezolid Form IV of the present invention are advantageous compared to those of the
prior art linezolid. The difference between the needle-shaped crystals of Form II and the plate-shaped crystals of Form IV can be appreciated by a comparison of Figure 5 (Form If) with Figure 6 (Form IV) or Figure 7 (also Form IV)-
The crystalline linezolid Form IV provided in the present invention is enantiomerically pure. Enantiomerically pure linezolid Form IV contains the unwanted R-enantiomer at a level of less man about 0.1% area by HPLC. Preferably, the enantiomerically pure linezolid Form IV of the present invention contains less than about 0.02% area by HPLC of the R-enantiomer.
The crystalline linezolid Form IV of the present invention is also polymorphically pure. Thus, it contains less than about 10% Form n, preferably less than about 5% Form n, and even more preferably less than about 1% Form n, and most preferably, less man about 0.5% Form H (by weight).
The present invention provides a novel method of making crystalline linezolid Form IV by spray-drying a solution of linezolid at a temperature of at least 50°C. This method comprises dissolving linezolid in a polar organic solvent at about room temperature, pumping the obtained solution into a spray dryer and contacting it with a nitrogen gas at a temperature of at least 50°C until Form IV is obtained. Preferably, the polar organic solvent is methanol.
The present invention provides another process for preparing crystalline linezolid Form IV comprising the step of heating crystalline linezolid Form n to a temperature of at least 85°C, preferably for at least one hour.
Form IV may also be prepared by heating a slurry of Form n in an organic solvent The slurry is produced by combining Form n with an aromatic solvent at room temperature, followed by heating for one hour to induce partial dissolution. The partially clear slurry is then filtered and the obtained solid is dried, providing crystals that were analyzed by PXRD and shown to be linezolid Form IV.
Preferred organic solvents are aromatic solvents and more preferably, xylene and toluene. Another preferred solvent is a silicon fluid.
Enantiomerically pure Form IV is prepared by slurrying Form H in an organic solvent, as described above, and using Form n that contains a maximum of 0.1 % of the R-enantiomer. Preferably, the Form n contains less than about 0.02% of the R-enantiomer.
Form n and the solvents used m the slurrying processes are preferably combined at 25°C, providing a slurry that is heated, preferably to reflux, when an aromatic solvent is used, and more preferably, to 140°C, when a silicon fluid is used. The isolated linezolid Form IV is dried, preferably in an oven, preferably by heating to a temperature of 50°C.
The invention encompasses a process for the transformation of Form IV into Form H comprising combining Form IV at room temperature with water or with an organic solvent selected from the group consisting of aketone, a straight or branched Ci-Q alcohol, an ester, an aromatic solvent, and a nitrile, to obtain a slurry, and maintaining the slurry for at least about one hour. The slurry is then filtered, providing crystals of Form H, which are then dried and analyzed by PXRD.
The temperature of the reaction is preferably room temperature. The slurry is maintained for at least about one hour, preferably for about one hour to about 24 hours.
The stability of linezolid Form TV was tested by storing it for 10 days at a relative humidity of between 0 and 100% at room temperature. The results are summarized in Table 1.
Form IV has proven to be stable and non-hygroscopic between 0-100 % RH.
The long term stability of linezolid Form IV was tested by storing it at room temperature and under accelerated conditions at 40'C and 55'C. The results are summarized in Table 2.

Form IV has proven to be stable at 25*C, 40*C, and 55*C for a mininurm of 3 months
The particle size distribution (PSD) of the active ingredient is one of the key parameters of a fonnalation. For measuring particle size, the following main methods maybe employed: sieves, sedimentation, electrozone sensing (coulter counter), microscopy, Low Angle Laser Light Scattering (LALLS). The crystalline linezolid Form IV of the present invention has a preferred maximum particle size of 500 um. Preferably, the particle size is less than 300 um, less man 200 urn, less than 100 urn, or even less than 50 urn.
Another embodiment of the present invention is a pharmaceutical formulation comprising a therapeutically effective amount of crystalline linezolid Form IV, combined with a pharmaoeutically acceptable excipient or carrier.
Another embodiment of the present invention is a method for treating a patient suffering from a gram positive bacterial infection, comprising the step of administering to the patient the pharmaceutical formulation comprising a therapeutically effective amount of crystalline linezolid Form IV.
The crystalline linezolid Form IV of the present invention used to prepare pharmaceutical formulations may be substantially pure with respect to other crystalline forms, i.e., the pharmaceutical formulations may contain less than about 10%, preferably less than about 5%, and even more preferably less than about 1% (by weight) of other crystalline forms of linezolid. In particular, the pharmaceutical formulations may contain less than about 10%, preferably less than about 5%, and more preferably less than about 1%, and even more preferably less than 0.5% (by weight) of crystalline linezolid Form ft In certain embodiments, the pharmaceutical formulations may contain less than about 10%, preferably less than about 5%, and even more preferably less than about 1% (by weight) of amorphous linezolid.
In other embodiments, pharmaceutical formulations of the present invention may contain crystalline linezolid Form IV in a mixture with other forms of linezolid.
In addition to the active ingredients), the pharmaceutical formulations of the present invention may contain one or more excipients. Excipients are added to the formulation for a variety of purposes.
Diluents may be added to the formulations of the present invention. Diluents increase the bulk of a solid pharmaceutical composition, and may make a pharmaceutical dosage form containing the composition easier for the patient and care giver to handle. Diluents for solid compositions include, for example, microcrystalline cellulose (e.g., AV1CEL®), microfine cellulose, lactose, starch, pregelatinized starch, calcium carbonate, calcium sulfate, sugar, dextrates, dextrin, dextrose, dibasic calcium phosphate dihydrate, tribasic calcium phosphate, kaolin,
magnesium carbonate, magnesium oxide, maltodextrin, xoannitol, polymethaciyiates ' (e.g., EUDRAGIT®), potassium chloride, powdered cellulose, sodium chloride, sorbitol, and talc.
Solid pharmaceutical compositions that are compacted into a dosage form, such as a tablet, may include excipients whose functions include helping to bind the active ingredient and other excipients together after compression. Binders for solid pharmaceutical compositions include acacia, algmic acid, carbomer (e.g., carbopol), carboxymethylcellulose sodium, dextrin, ethyl cellulose, gelatin, guar gum, hydrogenated vegetable oil, hydroxyethyl cellulose, hydroxypropyl cellulose (e.g., KLUCEL®), hydroxypropyl methyl cellulose (e.g., METHOCEL®), liquid glucose, magnesium aluminum silicate, maltodextrin, methylcellujose, polymetnacrylates, povidone (e.g., KOLLIDON®, PLASDONE®), pregektinized starch, sodium algmate, and starch.
The dissolution rate of a compacted solid pharmaceutical composition in the patient's stomach may be increased by the addition of a disintegrant to the composition. Disintegrants include algmic acid, carboxymethylcelMose calcium, carboxymethylceUulose sodium (e.g., AC-DI-SOL®, PRIMELLOSE®), colloidal sih'con dioxide, croscatmeflose sodium, crospovidone (e.g., KOLLIDON®, POLYPLASDONE®), guar gum, magnesium aluminum silicate, methyl cellulose, microcrystalline cellulose, polacrilin potassium, powdered cellulose, pregektinized starch, sodium alginate, sodium starch glycolate (e.g., EXPLOTAB®), and starch.
Glidants can be added to improve the flowability of a non-compacted solid composition and to improve the accuracy of dosing. Excipients that may function as glidants include colloidal silicon dioxide, magnesium trisilicate, powdered cellulose, starch, talc, and tribasic calcium phosphate.
When a dosage form such as a tablet is made by the compaction of a powdered composition, the composition is subjected to pressure from a punch and dye. Some excipients and active ingredients have a tendency to adhere to the surfaces of the punch and dye, which can cause the product to have pitting and other surface irregularities. A lubricant can be added to the composition to reduce adhesion and
ease the release of the product from the dye. Lubricants include magnesium stearate, calcium stearate, glycerylmonostearate, glyceryl palrnitostearate, hydrogenated castor oil, hydrogenated vegetable oil, mineral oil, polyethylene glycol, sodium benzoate, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc, and zinc stearate.
Flavoring agents and flavor enhancers make the dosage form more palatable to the patient Common flavoring agents and flavor enhancers for pharmaceutical products that may be included in the composition of the present invention include maltol, vanillin, ethyl vanillin, menthol, citric acid, fumaric acid, ethyl maltol, and tartaric acid.
Solid and liquid compositions may also be dyed using any pharmaceuticaDy acceptable colorant to improve their appearance and/or facilitate patient identification of the product and unit dosage level.
The present invention is not intended to 'encompass true solutions of crystalline linezolid Form IV whereupon the crystal structure of the novel Form IV and the properties that characterize the novel crystalline form of the present invention are lost. However, the use of the novel form to prepare such solutions (e.g., so as to deliver linezolid in a liquid pharmaceutical formulation) is considered to be within the rontemplation of the invention.
In liquid pharmaceutical, compositions prepared using Form IV of the present nvention, Form IV and any other solid excipients are dissolved or suspended in a iquid carrier such as water, vegetable oil, alcohol, polyethylene glycol, propylene jlycol, or glycerin.
Liquid pharmaceutical compositions may contain emulsifying agents to disperse uniformly throughout the composition an active ingredient or other excipient that is not soluble in the liquid carrier. Emulsifying agents that may be useful in liquid compositions of the present invention include, for example, gelatin, egg yolk, casein, cholesterol, acacia, tragacanth, chondrus, pectin, methyl cellulose, carbomer, cetostearyl alcohol, and cetyl alcohol.
liquid pharmaceutical compositions may also contain a viscosity enhancing agent to improve the mouth-feel of the product and/or coat the lining of the gastrointestinal tract. Such agents include acacia, alginic acid bentonite, carbomer, carboxymethylcellulose calcium or sodium, cetostearyl alcohol, methyl cellulose, ethylcellulose, gelatin guar gum, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, maltodextrin, polyvinyl alcohol, povidone, propylene carbonate, propylene glycol alginate, sodium alginate, sodium starch glycolate, starch tragacanth, and xanthan gum.
Sweetening agents such as sorbitol, saccharin, sodium saccharin, sucrose, aspartame, fructose, mannitol, and invert sugar maybe added to improve the taste.
Preservatives and chelating agents such as alcohol, sodium benzoate, butylated hydroxyl toluene, butylated hydroxyanisole, and ethylenediamine tetraacetic acid may be added at levels safe for ingest* on to improve storage stability,
A liquid composition may also contain a buffer such as guconic acid, lactic acid, citric acid or acetic acid, sodium guconate, sodium lactate, sodium citrate, or sodium acetate. Selection of excipients and the amounts used may be readily determined by the formulation scientist based upon experience and consideration of standard procedures and reference works in the field.
The solid compositions of the present invention include powders, granulates, aggregates and compacted compositions. The dosages include dosages suitable for oral, buccal, rectal, parenteral (including subcutaneous, intramuscular, and intravenous), inhalant, and ophthalmic administration. Although the most suitable administration in any given case will depend on the nature and severity of the condition being treated, the most preferred route of the present invention is oral. The dosages may be conveniently presented in unit dosage form and prepared by any of the methods well-known in the pharmaceutical arts.
Dosage forms include solid dosage forms like tablets, powders, capsules, suppositories, sachets, troches and lozenges, as well as liquid syrups, suspensions and elixirs.
The dosage of GEODON may be used as guidance. The oral dosage form of the present invention is preferably in the form of an oral capsule having a dosage of about 10 mg to about 160 mg, more preferably from about 20 mg to about 80 mg, and most preferably capsules of 20,40,60 and 80 mg. Daily dosages may include 1,2, or more capsules per day.
The dosage form of the present invention may be a capsule containing the composition, preferably a powdered or granulated solid composition of the invention, within either a hard or soft shell The shell may be made from gelatin and optionally contain a plasticizer such as glycerin and sorhitol, and an opacifying agent or colorant
A composition for tableting or capsule filling may be prepared by wet granulation. In wet granulation, some or all of the active ingredients and excipients in powder form are blended and then further mixed in the presence of a liquid, typically water, that causes the powders to clump into granules. The granulate is screened and/or milled, dried and then screened and/or milled to the desired particle size. The granulate may then be tableted, or other excipients may be added prior to tableting, such as a glidant and/or a lubricant
A tableting composition may be prepared conventionally by dry blending. For example, the blended composition of the actives and excipients may be compacted into a slug or a sheet and then comminuted into compacted grannies. The compacted granules may subsequently be compressed into a tablet
As an alternative to dry granulation, a blended composition may be compressed directly into a compacted dosage form using direct compression techniques. Direct compression produces a more uniform tablet without granules. Excipients that are particularly well suited for direct compression tableting include microcrystaUine cellulose, spray dried lactose, dicalcium phosphate dihydrate and colloidal silica. The proper use of these and other excipients in direct compression tableting is known to those in the art with experience and skill in particular formulation challenges of direct compression tableting.
A capsule filling of the present invention may comprise any of the aforementioned blends and granulates that were described with reference to tabletmg, however, they are not subjected to a final tableting step.
The active ingredient and excipients may be formulated into compositions and dosage forms according to methods known in the art.
The crystalline linezolid Form IV of the present invention may be used in pharmaceutical formulations or compositions as a single active ingredient or as a mixture together with other crystalline forms of linezolid or with amorphous linezolid. However, it is preferred that the pharmaceutical formulations or compositions of the present invention contain 25-100% by weight, especially 50-100% by weight, of crystalline linezolid Form IV, based on the total amount of linezolid in the formulation or composition. Preferably, such an amount of crystalline linezolid Form IV is 75-100% by weight, especially 90-100% by weight Highly preferred is an amount of 95-100% by weight.
Having described the invention with reference to certain preferred embodiments, other embodiments will become apparent to one skilled in the art from consideration of the specification. The invention is further defined by reference to the following examples describing in detail the preparation of the composition and methods of use of the invention. It will be apparent to those skilled in the art that many modifications, both to materials and methods, may be practiced without departing from the scope of the invention.
Examples
Microscopic samples were prepared in mineral oil suspension and placed between slides.
Powder X-ray diffraction
Powder X-ray diffraction data were obtained by methods known in the art using a SCINTAG® powder X-ray diffiactometer model XTRA® equipped with a solid state
detector. Copper radiation of 1.5418 A was used. A round aluminum sample holder with round zero background quartz plate was used, with cavity of 25(diameter)* 0.5(depth) mm. The obtained characteristic peaks were in the range of 2-40 degrees twotheta.
DSC analysis was done using a Mettler 821 Star0. The weight of the samples was about 5 mg; the samples were scanned at a rate of 10°C/min from 30°C to 250°C, The oven was constantly purged with nitrogen gas at a flow rate of 40 ml/min. Standard 70 ul alumina crucibles covered by lids with 1 hole were used.
IR analysis was done using a Perkm Elmer SPECTRUM ONE FT-IR spectrometer in DRIFT mode or using mineral oil mull technique. The samples in the 4000-400 cm*1 interval were scanned 16 times with 4.0 cm'1 resolution.
The FTRaman analysis was performed by Broker RFS-100/S Raman spectrometer. The scanning parameters were:
Range: 3500 to 50 cm"1; ' Aperture Setting: 10.0mm; Low Pass Filter 16: 1kHz; Source Setting Laser: 9394.0 cm"1,1600 mW; Raman Laser Power: 500 mW; Scanner: Velocity5.Oat4kHz; Sample Scans: 100; and Resolution: 4.0 cm"1.
Example 1 - preparation of crystalline linezolid Form IV
A flask containing 5.5 g of (S)-N-{4-morpholmyl-3-fluorophenyl)-2-oxo-5-oxazolidinyl-methyl amine and 20 ml ammonium hydroxide in 200 ml toluene was mixed at 25°C. Triethyl amine (2 equivalents) was added. The mixture was cooled to 3°C and acetic anhydride (2.5 equivalents) was added dropwise. The reaction mixture was brought to RT. Linezolid that precipitated from the reaction mixture was filtered. The wet crystals were analyzed by PXRD and shown to be crystalline linezolid Form IV.
Example 2 - Procedure for the preparation of crystalline linezolid Form IV
This example was carried out on a Buchi Mini Spray Dryer B-290.
5 g of linezolid was dissolved in methanol (300 ml) at room temperature. The obtained solution was pumped into the spray dryer. The nitrogen was at an inlet temperature of 50°C. The evaporated solvent and nitrogen exited the spray dryer at 35°C. The obtained sample was analyzed by PXRD and shown to be linezolid Form IV.
Examples - preparation of crystalline linezolid Form IV bv heating crystalline linezolid Form n
Crystalline linezolid Form IV may be prepared by heating crystalline linezolid Form n to a temperature higher than 85°C. Crystalline linezolid Form IV is obtained by keeping crystalline linezolid Form n at a temperature of between 85-175°C. As an example, crystalline linezolid Form n was kept at a temperature of 170°C during one hour. The polymorphic form of crystalline linezolid Form n was changed to crystalline linezolid Form IV. The crystalline linezolid Form IV obtained at 170°C was chemically stable.
Example 4 - preparation of crystalline linezolid Form IV bv reslurrving Form n fa jtylene
Ciystallme(S)-N-(4-morpholrnyl-3^
acetamide (Form H having an (R)-Linezolid content of 0.02%) (2.2 g) was mixed with xylene (20 ml) at 25°C. The mixture was heated to reflux and stirred for one hour to induce partial dissolution. The clearer slurry was then filtered and the obtained crystals were dried at SO C in an oven overnight. The crystals obtained were analyzed by PXRD and shown to be linezolid Form IV, wifli the same enantiomeric content.
Example 5 - preparation of crystalline linezolid Form IV bv reslurrymg Form n in toluene
Qystalmie(S)-N-(4-morphomiyl-3'-fluorophenyl)-2-oxo-5-oxazolidinyl-methyI acetamide (Form n having an (R)-Lraezolid content of 0.02%) (2.2 g) was mixed with toluene (20 ml) at 25°C. The mixture was heated to reflux and stirred for one hour to induce partial dissolution. The clearer slurry was then filtered and the obtained crystals were dried at 50*C in an oven overnight. The crystals obtained were analyzed by PXRD and shown to be Linezolid Form IV, with the same enantiomeric content
Example 6 - preparation of crystalline liaezolid Form IV bv reslnrrvtag Form n In a silicon fluid
Grystallme(S)-N-(4-morpholmyl-3-^
acetamide (Form H having an (R)-L4nezolid content of 0.02%) (2.2 g) was mixed
with a silicon fluid (20 ml) at 25°C. The mixture was heated to 140°C and stirred for
one hour to induce partial dissolution. The clearer slurry was then filtered and the
obtained crystals were dried at 50 C in an oven overnight The crystals obtained were
analyzed by PXRD and shown to be Lmezoh'd Form TV, with the same enantiomeric
content
Example 7 - preparation of crystalline Hnezolid Form n from a slurry of Form JV
A slurry of linezolid Form IV was produced by combining linezolid Form IV (2,0 g) with one of the solvents listed below, at room temperature. The slurry was men stirred for 1 to 24 hours, followed by filtering and drying the obtained crystals. The crystals were analyzed by PXRD and shown to be Form n of Linezolid, as summarized hi the following Table 3:

AMENDED CLAIMS
[received by the International Bureau on 03 January 2006 (03.01.2006); original claims 1-7,22,23 canceled, claims 8-21 amended and renumbered]
1. Crystalline linezolid characterized by data selected from the group consisting of:
a powder X-ray diffraction pattern with peaks at about 13.5,18.0,21.1,
22.2, and 25.4 ±02 degrees 2 theta;
an FTIR spectrum with peaks at about 2817,1335,1229,1200, and 662
cm"'; and
an FTRaman spectrum with peaks at about 2975,2930,2865,1083, and
750cm-1;
and having a content of less man 0.5% (w/w) of the R-enantiomer of linezolid.
2. Crystalline linezolid characterized by data selected from the group consisting of:
a powder X-ray diffraction pattern with peaks at about 13.5,18.0,21.1,
22.2, and 25.4 ±0.2 degrees 2 theta;
an FTIR spectrum with peaks at about 2817,1335,1229,1200, and 662
cm"; and
an FTRaman spectrum with peaks at about 2975,2930,2865,1083, and
750 cm"1;
and containing less than about 10% of crystalline Form E.
The crystalline linezolid of claim 2, containing less than about 5% of
crystalline Form II.
The crystalline linezolid of claim 3, containing less than about 0.5% of
crystalline Form n.
Crystalline linezolid characterized by data selected from the group consisting
of:

a powder X-ray diffraction pattern with peaks at about 13.5,18.0,21.1,
22.2, and 25.4 ±0.2 degrees 2 theta;
an FTIR spectrum with peaks at about 2817,1335,1229,1200, and 662
cm"1; and
c) an FTRaman spectrum with peaks at about 2975,2930,2865,1083, and
750cm'1;
and which is stable against transformation into Form U upon storage at a relative humidity of about 0% to about 100% at room temperature for at least 10 days.
6. A method of preparing crystalline linezolidy characterized by data selected from the group consisting of:
a powder X-ray diffraction pattern with peaks at about 13.5,18.0,21.1,
222, and 25.4 ±02 degrees 2 theta;
an FTIR spectrum with peaks at about 2817,1335,1229,1200, and 662
cm'; and
an FTRaman spectrum with peaks at about 2975,2930,2865,1083, and
750 cm"' comprising:
dissolving linezolid in a polar organic solvent to form a linezolid solution; '
spray-drying the linezolid solution at a temperature of at least 50°C.

The method of claim 6 where the dissolving is carried out at room temperature.
The method of claim 6 where the polar organic solvent is methanoL
The method of claim 6 where the spray-drying is carried out with nitrogen gas.
10. A process for preparing crystalline linezolid characterized by data selected
from the group consisting of:
a powder X-ray diffraction pattern with peaks at about 13.5,18.0,21.1,
22.2, and 25.4 ±0.2 degrees 2 theta;
an FTIR spectrum with peaks at about 2817,1335,1229,1200, and 662
cm"1; and
an FTRaman spectrum with peaks at about 2975,2930,2865,1083, and
750 cm"1 comprising heating crystalline Linezolid Form n to a temperature of
at least 85*C for at least one hor>.
11. A process for preparing crystalline linezolid Form n comprising:
combining crystalline linezolid Form IV with a solvent at room temperature
to form a slurry;
stirring the slurry for 1 to 24 hours to obtain crystalline material;
filtering and drying fee crystalline material to obtain crystalline linezolid
Form n,
12. The process of claim 1 ] where the solvent is selected from the group
consisting of: acetone, EtOH 95%, EtOAe, toluene, ACN, IP A, and H2O.
13. A process for preparing crystalline linezolid Form IV comprising:
combining crystalline linezolid Form n with a solvent at room temperature
to form a slurry,
heating the slurry;
filtering the heated slurry to obtain crystalline linezolid Form IV,
14. The process of claim 13 where the solvent is selected from the group consisting of: xylene, toluene, and a silicon fluid.
The crystalline linezolid of claim 1, having a content of less than about 0 1% of the
R-enantiomer of linezolid.
The crystalline linezolid of claim 1, having a content of less than about 0.02% of
the R-enantiomer of linezolid.