US20050025791A1 - Pharmaceutical compositions with improved dissolution - Google Patents

Pharmaceutical compositions with improved dissolution Download PDF

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Publication number
US20050025791A1
US20050025791A1 US10/601,092 US60109203A US2005025791A1 US 20050025791 A1 US20050025791 A1 US 20050025791A1 US 60109203 A US60109203 A US 60109203A US 2005025791 A1 US2005025791 A1 US 2005025791A1
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United States
Prior art keywords
celecoxib
pharmaceutical composition
excipient
pharmaceutical
salt
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Abandoned
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US10/601,092
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English (en)
Inventor
Julius Remenar
Matthew Peterson
Orn Almarsson
Hector Guzman
Hongming Chen
Mark Tawa
Mark Oliveira
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Transform Pharmaceuticals Inc
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Transform Pharmaceuticals Inc
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Application filed by Transform Pharmaceuticals Inc filed Critical Transform Pharmaceuticals Inc
Priority to US10/601,092 priority Critical patent/US20050025791A1/en
Priority to US10/660,202 priority patent/US7927613B2/en
Priority to JP2005508617A priority patent/JP5021934B2/ja
Priority to EP10193736A priority patent/EP2339328A3/en
Priority to AU2003303591A priority patent/AU2003303591A1/en
Priority to US10/541,216 priority patent/US8362062B2/en
Priority to EP03808567A priority patent/EP1579198A1/en
Priority to CA2511881A priority patent/CA2511881C/en
Priority to PCT/US2003/041273 priority patent/WO2004061433A1/en
Priority to PCT/US2003/041642 priority patent/WO2004060347A2/en
Priority to AU2003300452A priority patent/AU2003300452A1/en
Priority to US10/747,742 priority patent/US7790905B2/en
Priority to JP2006508979A priority patent/JP2007524596A/ja
Priority to PCT/US2004/006288 priority patent/WO2004078163A2/en
Priority to US10/546,963 priority patent/US20070059356A1/en
Priority to EP04715190A priority patent/EP1631260A2/en
Priority to CA002514733A priority patent/CA2514733A1/en
Priority to US10/551,014 priority patent/US20060223794A1/en
Priority to US10/926,842 priority patent/US7446107B2/en
Assigned to TRANSFORM PHARMACEUTICALS, INC. reassignment TRANSFORM PHARMACEUTICALS, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: ALMARSSON, ORN, CHEN, HONGMING, GUZMAN, HECTOR, OLIVEIRA, MARK, PETERSON, MATTHEW, REMENAR, JULIUS, TAWA, MARK
Publication of US20050025791A1 publication Critical patent/US20050025791A1/en
Priority to US12/234,420 priority patent/US20090088443A1/en
Priority to US12/792,415 priority patent/US20100311701A1/en
Abandoned legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605—Excipients; Inactive ingredients
    • A61K9/1629—Organic macromolecular compounds
    • A61K9/1652—Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/18—Sulfonamides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/365—Lactones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/63—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide
    • A61K31/635—Compounds containing para-N-benzenesulfonyl-N-groups, e.g. sulfanilamide, p-nitrobenzenesulfonyl hydrazide having a heterocyclic ring, e.g. sulfadiazine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/145—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

Definitions

  • Celecoxib (4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide) is a substituted pyrazolylbenzenesulfonamide represented by the structure:
  • Celecoxib belongs to the general class of non-steroidal anti-inflammatory drugs (NSAIDs). Unlike traditional NSAIDs, celecoxib is a selective inhibitor of cyclooxygenase II (COX-2) that causes fewer side effects when administered to a subject.
  • COX-2 cyclooxygenase II
  • the synthesis and use of celecoxib are further described in U.S. Pat. Nos. 5,466,823, 5,510,496, 5,563,165, 5,753,688, 5,760,068, 5,972,986, and 6,156,781, the contents of which are incorporated by reference in their entirety. Orally deliverable liquid formulations of celecoxib are discussed in U.S. Patent Application Publication No.
  • Cox-2 inhibitory drugs are related to celecoxib, which form part of a larger group of drugs, all of which are benzene sulfonamides.
  • deracoxib which is 4-[3-fluoro-4-methoxyphenyl)-3-difluoromethyl-1H-pyrazol-1-yl]benzene sulfonamide
  • valdecoxib which is 4-[5-methyl-3-phenyl isoxazol-4-yl]benzene sulfonamide
  • rofecoxib which is 3-phenyl-4-[-(methylsulfonyl)phenyl]-5H-furan-2-one
  • etoricoxib which is 5-chloro-3-(4-methylsulfonyl)phenyl-2-(2-methyl-5-pyridinyl)pyridine.
  • celecoxib In its commercially available form as CELEBREXTM, celecoxib is a neutral molecule that is essentially insoluble in water. Celecoxib typically exists as needle-like crystals, which tend to aggregate into a mass. Aggregation occurs even when celecoxib is mixed with other substances, such that a non-uniform mixture is obtained. These properties are shared by other pyrazolylbenzenesulfonamides and present significant problems in preparing pharmaceutical formulations of the drugs, particularly oral formulations.
  • the celecoxib compositions of the present invention have a greater solubility, dissolution, total bioavailability (area under the curve or AUC), lower T max , the time to reach peak blood serum levels, and higher C max, , the maximum blood serum concentration, than neutral celecoxib.
  • the celecoxib compositions of the present invention also include compounds that are less hygroscopic and more stable.
  • the celecoxib salts of the present invention when in crystalline form convert to either an amorphous free form of celecoxib upon neutralization of the salt, which subsequently converts to a neutral metastable crystalline form or directly to a neutral metastable crystalline form.
  • These amorphous and metastable crystalline forms of neutral celecoxib are more readily available forms of the api than is presently-marketed neutral celecoxib.
  • Neutral crystalline celecoxib is presently-marketed as CELEBREXTM, and is designated as “neutral” to distinguish it from the ionized salt form of celecoxib.
  • An aspect of the present invention relates to methods of increasing dissolution, solubility, and or the time a pharmaceutical (the terms pharmaceutical and drug are used herein interchangeably), can be maintained, upon dissolution, as a supersaturated solution, before precipitating out of solution.
  • the increase in dissolution results in, and thus can be represented by an increase in bioavailability, AUC, reduced time to Tmax or increased Cmax.
  • the methods comprise the steps of making a salt or co-crystal of a free acid api and combining the salt or co-crystal with a recrystallization or precipitation retardant and optionally, a recrystallization/precipitation retardant enhancer (referred to as enhancer hereafter).
  • the salt may be amorphous or crystalline, but is preferably crystalline. Normally the salt or co-crystal form used is in a crystalline form which dissolves and then recrystallizes and precipitates out of solution, which is why the term “re”crystallization retardant is used. It is noted however, that one could begin with an amorphous form of the salt so the term is used when beginning with either a crystalline or amorphous form.
  • the term “recrystallization” can also be interchanged with the term “precipitation” which refers to either a crystalline or amorphous solid form separating or “coming out of” the solution.
  • Crystalline salts are superior to amorphous salts as the initial compound, with an amorphous salt being superior to a neutral amorphous or crystalline form.
  • Free acid forms are not preferred initial compounds unless first solubilized in a solubilizer resulting in a liquid formulation comprising a precipitation retardant and optional enhancer.
  • the recrystallization/precipitation retardant is often a surfactant, preferably a surfactant with an ether functional group, preferably a repeating ether group, e.g., an ether group repeated at least two or three times wherein the oxygen atom is separated by 2 carbon atoms.
  • Further preferred surfactants have an interfacial tension of less than 10 dynes per centimeter when measured at a concentration of 0.1% w/w in water as compared to mineral oil at 25° C. and/or the surface tension of the recrystallization retardant (e.g., poloxamers) is less than 42 dynes/cm when measured as a concentration of 0.1% w/w in water at 25° C.
  • the recrystallization retardant e.g., poloxamers
  • the combination of salt or co-crystal, recrystallization/precipitation retardant and an optional enhancer preferably prevents or delays precipitation of a supersaturated solution by about 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, or 60 minutes or greater than 1 hour in an aqueous solution, preferably water or gastric fluid conditions such as the gastric fluids of an average human stomach fasted for 12 hours or simulated gastric fluid (SGF).
  • the solution remain supersaturated for more than 15, 20, or 30 minutes to allow the composition to move out of the stomach and into an environment with a higher pH.
  • the SGF may be diluted by 2, 3, 4, 5 6, 7, 8, 9, 10 fold to represent water intake.
  • the SGF may be diluted 5 fold to represent a patient drinking a glass of water at the time a composition of the present invention is taken orally.
  • the degree of increase in solubility, dissolution, and/or supersaturation may be specified, such as by 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100%, or by 3, 4, 5,6, 7, 8, 9, 10, 15, 20, 25, 30, 40, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, 400, 500, 1000, 10,000, or 100,000 fold greater than neutral celecoxib (e.g., free acid) in the same solution.
  • the increase in dissolution may be further specified by the time the composition remain supersaturated.
  • the enhancer preferably comprises a cellulose ester such as hydroxypropylcellulose (HPC) or hydroxyproplymethylcellulose (HPMC).
  • HPC hydroxypropylcellulose
  • HPMC hydroxyproplymethylcellulose
  • the enhancer does not improve the length of time the api can remain supersaturated without the additional pressure of the recrystallization/precipitation retardant.
  • the methods of the present invention are used to make a pharmaceutical drug formulation with greater solubility, dissolution, and bioavailability, AUC, reduced time to T max , the time to reach peak blood serum levels, and higher C max , the maximum blood serum concentration, when compared to the neutral form or salt alone.
  • AUC is the area under the plot of plasma concentration of drug (not logarithm of the concentration) against time after drug administration.
  • the area is conveniently determined by the “trapezoidal rule”: the data points are connected by straight line segments, perpendiculars are erected from the abscissa to each data point, and the sum of the areas of the triangles and trapezoids so constructed is computed.
  • the AUC from t n to infinite time is estimated by C n /k el .
  • the invention further relates to wherein a recrystallization/precipitation retardant and an optional, enhancer is combined with a pharmaceutical that is already in a salt or co-crystal form.
  • the invention further relates to wherein a recrystallization/precipitation retardant and an optional enhancer is combined with a pharmaceutical that is a solvate, desolvate, hydrate, dehydrate, or anhydrous form of a salt or co-crystal form.
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising:
  • the present invention provides a pharmaceutical composition comprising
  • the present invention provides a process for producing a pharmaceutical composition for delivering a supersaturated concentration of a drug having low aqueous dissolution, preferably in gastric fluid conditions, which process comprises intimately mixing together the components of the above aspects or elsewhere herein.
  • the surfactant is at a concentration of less than 5%, 4%, 3%, 2%, 1%, 0.9%, 0.8%, 0.7%, 0.6%, 0.5%, 0.4%, 0.3%, 0.2%, or 0.1% or at a concentration of 0.1% (w/w).
  • the present invention further provides a process for producing a pharmaceutical composition, which comprises:
  • those excipients or other properties of the combination can be chosen for the production of a pharmaceutical composition in which the api remains in solution for a sufficient time after administration to a subject.
  • pharmaceutical compositions which attain at least a minimum bioavailability of the api may be readily produced based on a straightforward in vitro screening.
  • api pharmaceutical compound
  • properties include the identity or amount of the excipient and the identity or amount of the pharmaceutical compound in the composition.
  • Other properties may include the amount of other diluents or carriers such as salts or buffering compounds.
  • the pharmaceutical compound itself may be screened in a variety of different forms if it is capable of polymorphism. Additionally, different salt, solvate, hydrate, co-crystal and other forms of the api may be screened in accordance with the invention.
  • the present invention provides a process for producing a pharmaceutical composition, which comprises:
  • excipient which is varied. Different excipients may be used in different containers and may be present as a single excipient or in a combination of a plurality of excipients, for example, a binary, ternary, tertiary or higher order combination.
  • the present invention provides a pharmaceutical composition obtained by processes according to the invention.
  • the pharmaceutical composition may comprise a further excipient, diluent or carrier.
  • the pharmaceutical composition is formulated for oral administration.
  • the invention further provides a method for assessing excipient-mediated retardation of solid-state nucleation or precipitation of a pharmaceutical compound, which method comprises:
  • the present invention provides a method for screening excipients that retard solid-state nucleation or precipitation of a pharmaceutical compound, which method comprises:
  • the pharmaceutical compound of the invention is an active pharmaceutical ingredient (API) typically capable of existing as a supersaturated solution, preferably in an aqueous-based medium.
  • the api may be a free acid, free base, co-crystal or salt, or a solvate, hydrate or dehydrate thereof.
  • the invention is particularly applicable to such pharmaceutical compositions which, when in contact with a body fluid such as gastric juices or intestinal fluids, would be likely to precipitate or crystallize from solution in a nucleation event. Accordingly, the invention is particularly applicable to pharmaceutical compounds which may have relatively low solubility, as defined herein, when in contact with bodily fluids but possibly relatively high solubility in appropriate in vitro conditions.
  • the compound solution is a solution wherein the compound is solubilized and may be a non-aqueous solution or an aqueous solution with a pH adjusted to accommodate the compound.
  • a free base-type compound would be dissolved in aqueous solution at acidic pH whereas a free acid-type compound would be dissolved in an aqueous solution of basic pH.
  • the compound solution may therefore be, and preferably is, a supersaturated solution when compared to water, gastric fluids or intestinal fluids. It would also be preferred for the excipient to be formed in a solution comprising water, usually deionised water, or another aqueous based solution.
  • the mixture simulates gastric juices (SGF) or intestinal fluids (SIF, 0.68% monobasic potassium phosphate, 1% pancreatin, and sodium hydroxide where the pH of the final solution is 7.5.) and in this aspect it is preferred that the excipient is added in a solution simulating those body fluids. Alternatively, further additives, usually in solution, may be added to form the mixtures creating an environment appropriate for the screening to be undertaken.
  • the plurality of containers may be presented in a multiple well plate format or block and tube format such that at least 24, 48, 96, 384, or 1536 samples are assayed in parallel.
  • Multiple block and tubes or multiwell plates may be assayed such that at least 1000, 3000, 5000, 7000, 10000, 20000, 30000, 40000, 50000, 60000, 70000, 80000, 90000, or 100000 samples are assayed.
  • This is advantageous because the process may be operated in a semi-automated or automated way using existing multiple well plate format-based apparatus. At least the step of dispensing may be performed with automated liquid handling apparatus. Accordingly, it is possible to operate the process as a high throughput screen.
  • each sample may contain less than 100 mg, 50 mg, 25 mg, 10, mg, 5 mg, 750 ug, 500 ug, 250, ug, 100 ug, 75 ug, 50 ug, 25 ug, 10 ug, 1 ug, 750 ng, 500 ng, 250 ng, 100 ng, or less than 50 ng, depending on the api, sample size, etc.
  • This therefore minimises the amount of active pharmaceutical ingredient material which is needed to identify excipients or properties of the combination of pharmaceutical compound and excipient that retard onset of nucleation. In this way, improved speed and relatively low cost are advantages.
  • the intimate mixture formed in the process may be achieved by any conventional method, including the use of a mixer during or after dispensing of the solutions. Once the mixture has been formed, it is generally advantageous to incubate the mixture at a constant temperature, such as approximately 37° C., to simulate in vivo conditions.
  • Measurement of onset of solid-state nucleation or precipitation may be determined by measuring light scattering of a mixture. This may be achieved by any conventional light scattering measurement, such as the use of a nephelometer. It is also possible to include a further step in which the crystallinity of the products of the solid-state nucleation or precipitation is determined. This step is conveniently performed before selecting the pharmaceutical compound/excipient combination for use in the pharmaceutical composition. Crystallinity may be determined, e.g., by birefringence screening.
  • Neither the light scattering measurement nor the birefringence screening are invasive measurement techniques.
  • a portion or all of the sample solution does not need to be transferred to a second container and the containers or wells can be sealed with a transparent seal to allow use of these techniques.
  • the pharmaceutical composition is formulated for oral administration.
  • Drugs according to the invention may be prepared in a form having reduced time to onset of therapeutic effectiveness (the time when an effect for which the drug is administered can be identified or measured, e.g., the point in time when a reduction in fever or pain felt by a patient begins to occur) or increased bioavailability.
  • the pharmaceutical compositions according to the invention are therefore particularly suitable for administration to human subjects.
  • FIG. 1 shows a differential scanning calorimetry trace of the sodium salt of celecoxib prepared by Example 1 between 50° C. and 110° C.
  • FIG. 2 shows a thermogravimetric analysis of the sodium salt of celecoxib prepared by Example 1, which was conducted from about 30° C. to about 160° C.
  • FIG. 3 shows a powder x-ray diffraction plot of the sodium salt of celecoxib prepared by Example 1.
  • FIGS. 4A and 4B show pharmacokinetics in male Sprague-Dawley rats after 5 mg/kg oral doses of the celecoxib crystal form used in the marketed formulations and the sodium salt of 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide, as obtained following the protocol described in Example 4.
  • FIG. 5 shows the mean pharmacokinetic parameters (and standard deviations therefor) of celecoxib in the plasma of male dogs following a single oral or single intravenous dose of celecoxib or celecoxib sodium.
  • the maximum serum concentration and bioavailability of orally-administered celecoxib sodium was about three- and two-fold greater, respectively, than a roughly equal dose of orally-administered celecoxib, and the maximum serum concentration of celecoxib sodium was reached 40% faster than for celecoxib.
  • FIG. 6 shows the mean concentrations of celecoxib in plasma following the administration of a single oral dose of celecoxib or celecoxib sodium or a single intravenous dose of celecoxib in male dogs.
  • FIG. 7 shows the effect of varying ratios of ethylene glycol to propylene glycol subunits in poloxamers on the concentration of celecoxib sodium in solution.
  • FIG. 8 shows the effect of different celluloses on the dissolution of various composition
  • cellulose hydroxypropylcellulose (HPC, 100,000 kDa), low-viscosity hydroxypropylmethylcellulose (ld HPMC, viscocity was 80-120 cps), high-viscosity hydroxypropylmethylcellulose (hd HPMC, viscosity was 15,000 cps), microcrystalline cellulose (Avicel PH200)), d-alpha-tocopherol polyethylene glycol-1000 succinate (vitamin E TGPS), and celecoxib sodium.
  • HPC hydroxypropylcellulose
  • ld HPMC low-viscosity hydroxypropylmethylcellulose
  • hd HPMC high-viscosity hydroxypropylmethylcellulose
  • microcrystalline cellulose Avicel PH200
  • d-alpha-tocopherol polyethylene glycol-1000 succinate vitamin E TGPS
  • celecoxib sodium d-alpha-tocopherol polyethylene glycol
  • FIG. 9 shows the dissolution at 37° C. for compositions comprising various weight ratios of d-alpha-tocopherol polyethylene glycol-1000 succinate (vitamin E TGPS), hydroxypropylcellulose and celecoxib sodium.
  • FIG. 10 shows the dissolution profile of celecoxib sodium in simulated gastric fluid (SGF) from solid mixtures with excipients at room temperature.
  • SGF gastric fluid
  • the legend indicates the excipient and the weight ratio of excipient to celecoxib sodium (if unmarked, 1:1).
  • Excipients include polyvinylpyrrolidone (PVP), poloxamer 188 (P188), poloxamer 237 (P237), d-alpha-tocopherol polyethylene glycol-1000 succinate (vit E TGPS), and GelucireTM 50/13.
  • FIG. 11 shows the effect of Avicel microcrystalline cellulose and silica gel on the dissolution of mixtures of celecoxib sodium, d-alpha-tocopherol polyethylene glycol-1000 succinate (vit E TGPS), and hydroxypropylcellulose (HPC) mixtures in simulated gastric fluid (SGF) at 37° C.
  • the legend indicates the weight ratios of the components.
  • FIG. 12 shows the dissolution of celecoxib sodium (TPI336Na) in 5-times diluted simulated gastric fluid, with excipients including d-alpha-tocopherol polyethylene glycol-1000 succinate (vitamin E TGPS), hydroxypropylcellulose (HPC), and poloxamer 237.
  • the legend indicates the weight ratios of the components.
  • FIGS. 13A and 13B shows the particle-induced x-ray diffraction (PXRD) and raman spectra, respectively, of the sodium salt of celecoxib prepared by the method of Example 6.
  • FIG. 14 shows a differential scanning calorimetry analysis of celecoxib lithium salt MO-116-49B.
  • FIG. 15 shows a thermogravimetric analysis of celecoxib lithium salt MO-116-49B.
  • FIG. 16 shows the RAMAN spectrum of celecoxib lithium salt MO-116-49B.
  • FIG. 17 shows the PXRD spectrum of celecoxib lithium salt MO-116-49B.
  • FIG. 18 shows a differential scanring calorimetry analysis of celecoxib potassium salt MO-116-49A.
  • FIG. 19 shows a thermogravimetric analysis of celecoxib potassium salt MO-116-49A.
  • FIG. 20 shows the RAMAN spectrum of celecoxib potassium salt MO-116-49A.
  • FIG. 21 shows the PXRD spectrum of celecoxib potassium salt MO-116-49A.
  • FIG. 22 shows a thermogravimetric analysis of celecoxib potassium salt MO-116-55D.
  • FIG. 23 shows the RAMAN spectrum of celecoxib potassium salt MO-116-55D.
  • FIG. 24 shows the PXRD spectrum of celecoxib potassium salt MO-116-55D.
  • FIG. 25 shows a thermogravimetric analysis of celecoxib calcium salt MO-116-62A.
  • FIG. 26 shows the RAMAN spectrum of celecoxib calcium salt MO-116-62A.
  • FIG. 27 shows the PXRD spectrum of celecoxib calcium salt MO-116-62A.
  • FIG. 28 shows the PXRD spectrum of commercially-available celecoxib.
  • FIG. 29 shows the RAMAN spectrum of commercially-available celecoxib.
  • FIG. 30 shows crystal retardation time for celecoxib as a function of excipient in simulated gastric fluid (SGF).
  • FIG. 31 shows interfacial tension of selected PLURONIC excipients in water.
  • FIG. 32 shows dissolution of celecoxib sodium hydrate from compositions containing PLURONIC P123 and F127.
  • FIG. 33 shows dissolution of celecoxib sodium hydrate from PLURONIC P123, F127 and F87, in the presence of HPC.
  • FIG. 34 shows dissolution of celecoxib sodium hydrate using PLURONIC F1 27, HPC and a granulating fluid.
  • FIG. 35 shows dissolution of celecoxib sodium hydrate using PLURONIC F127 and HPC in a compact formulation.
  • FIG. 36 shows a flowchart outlining a process according to the invention.
  • FIG. 37 shows a platemap for an automated liquid dispenser.
  • FIG. 38 shows a trace of light scatter against time in an assay according to the invention.
  • FIG. 39 shows a thermogravimetric analysis of a propylene glycol solvate of a celecoxib sodium salt.
  • FIG. 40 shows the PXRD spectrum of a propylene glycol solvate of a celecoxib sodium salt.
  • FIG. 42 shows the PXRD spectrum of a propylene glycol solvate of a celecoxib potassium salt.
  • FIG. 43 shows a thermogravimetric analysis of a propylene glycol solvate of a celecoxib lithium salt.
  • FIG. 44 shows a thermogravimetric analysis of the sodium salt propylene glycol trihydrate of celecoxib prepared by Example 21.
  • FIG. 46 shows a thermogravimetric analysis of the sodium salt propylene glycoltrihydrate of celecoxib prepared by Example 21b.
  • FIG. 47 shows a powder X-ray diffraction plot of the sodium salt propylene glycol trihydrate of celecoxib prepared by Example 21b.
  • FIG. 48 show a DSC trace of the sodium salt isopropyl alcohol solvate of celecoxib prepared by Example 22.
  • FIG. 50 shows a powder X-ray diffraction plot of the sodium salt of isopropyl alcohol solvate of celecoxib prepared by Example 22.
  • Such metal salts include alkali metal or alkaline earth metal salts, preferably sodium, potassium, lithium, calcium and magnesium salts.
  • the precipitation retardant used in the present invention can be chosen from a wide range of surfactants (see e.g., FIG. 30 ). Embodiments include where the surfactant is non-ionic or wherein the surfactant is ionic. In embodiments of the present invention, the interfacial tension of the recrystallization/precipitation retardant (e.g., poloxamers) is less than 10 dyne/cm when measured as a concentration of 0.1% w/w in water as compared to mineral oil at 25° C.
  • the recrystallization/precipitation retardant e.g., poloxamers
  • a poloxamer comprises an ethylene oxide-propylene oxide block copolymer, which preferably has the structure (PEG) x -(PPG) y -(PEG) z , where x, y and z are integers and x is usually equal to z.
  • a preferred form of poloxamer are those obtainable from BASF designated “PLURONIC”®. The invention is not, however, limited to the PLURONIC series as similar poloxamers obtainable from other sources may be used.
  • PLURONIC poloxamers examples include PLURONIC L122, PLURONIC P123, PLURONIC F127 (Poloxamer 407), PLURONIC L72, PLURONIC P105, PLURONIC LP2, PLURONIC P104, PLURONIC F108 (Poloxamer 338), PLURONIC P103, PLURONIC L44 (Polaxamer 124), PLURONIC F68 (Poloxamer 188), and PLURONIC F87 (Poloxamer 237).
  • a specific poloxamer and its corresponding PLUROIC i.e., the generic and tradename, may be used interchangeably throughout.
  • the optional third component of the pharmaceutical composition according to the present invention comprises a recrystallization/precipitation retardant enhancer.
  • An enhancer is a compound capable of increasing the effectiveness of the recrystallization/precipitation retardant in inhibiting, preventing or at least reducing the extent of crystallization or precipitation of the drug of low aqueous solubility, usually when diluted such as following oral administration.
  • the enhancer does not act as a recrystallization/precipitation retardant alone.
  • the enhancer has no affect or a negative affect in an in vitro recrystallization/precipitation assay, but increases the effectiveness of the recrystallization/precipitation retardant in an in vitro or in situ dissolution assay.
  • Cellulose esters such as hydroxypropyl cellulose are particularly useful enhancer according to the present invention.
  • Cellulose esters vary in the chain length of their cellulosic backbone and consequently, in their viscosity as measured for example at a 2% by weight concentration in water at 20 degrees C. Lower viscosities are normally preferred to higher viscosities in the present invention.
  • the cellulose ester such as HPC, has a viscosity, 2% in water, of about 100 to about 100,000 cP or about 1000 to about 15,000 cP. In other embodiments the viscosity is less than 1,500,000, 1,000,000, 500,000, 100,000, 75,000, 50,000, 35,000, 25,000, 20,000, 17,500, 15,000, 12,500.
  • Enhancers are also useful in delaying the Tmax and/or increasing the amount of time the api concentration is above 1 ⁇ 2 Tmax, thus acting to smooth out the curve.
  • Preferred enhancers increase the amount of time the api concentration is above 1 ⁇ 2 Tmax by 25%, 50%, 75%, 100%, three fold or more than three fold.
  • the composition has both a reduced time to Tmax and remains at 1 ⁇ 2 Tmax longer than the free acid or in the same composition except the salt or co-crystal is replaced by the free acid.
  • the ratio of component a:b:c (api: recrystallization/precipitation retardant;enhancer) as exemplified herein is approximately 1:1:1 (+/ ⁇ 0.2 for the recrystallization/precipitation retardant and enhancer).
  • the ratio can be adjusted to suit the application.
  • the amount of recrystallization/precipitation retardant or enhancer may need to be decreased, and even decreased below the optimum concentration in order to decrease the amount of excipients in the administered form of the composition, such as a tablet or capsule.
  • the unit dosage form comprises an amount of precipitation retardant sufactant that is at or above an amount needed for the retardant to reach its critical micell concentration (CMC) in 100 ml in 500 ml H 2 O or SGF, or H 2 O or SGF or in 1L H 2 O or SGF.
  • CMC critical micell concentration
  • the poloxamers may not form true micells but do form analogous structures which are considered micells for the purpose of the present invention.
  • the composition may further comprise a pharmaceutically-acceptable diluent, excipient or carrier and such additional components are discussed in further detail below.
  • a pharmaceutically-acceptable diluent, excipient or carrier and such additional components are discussed in further detail below.
  • One such additional component comprises a granulating fluid-like liquid, such as poloxamer 124, PEG 200 or PEG 400, that forms an intimate contact between the api, recrystallization/precipitation retardant and optional enhancer by binding or partially dissolving them.
  • the composition remains in a solid, semi-solid or paste, although an embodiment is drawn to wherein the composition is at least 25%, 50%, 75% or nearly or fully dissolved Any pharmaceutically acceptable liquid may be used as long as it does not cause conversion of the salt or co-crystal form to the free form in the solid state.
  • Some non-limiting examples include methanol, ethanol, isopropanol, higher alcohols, propylene glycol, ethyl caprylate, propylene glycol laurate, PEG, diethyl glycol monoethyl ether (DGME), tetraethylene glycol dimethyl ether, triethylene glycol monoethyl ether, and polysorbate 80.
  • the presence of the granulated fluid-like liquid increases the dissolution of the api, possibly by delaying the contact between the api and the dissolution medium until the surfactant dissolves to a significant extent, thus delaying recrystallization/precipitation.
  • the use of a granulating fluid-like liquid is particularly useful when the api and recrystallization/precipitation retardant are solids.
  • the pharmaceutical composition is in the form of a compact whereby, during the process of producing the pharmaceutical composition, the components are compacted together.
  • Compaction may perform a similar role to that performed by the granulating fluid.
  • Retarded dissolution or a smoothing out of the curve may be limited, if required, by using a disintegrant in the compact.
  • the api and crystallization/precipitation retardant (and optional enhancer), when mixed forms a paste or non-aqueous solution.
  • An adherent mass of components may be produced if a paste is used which is thought to delay dissolution of the api by allowing the surfactant to dissolve first. This is thought to promote dissolution of the api.
  • the compound(s)s and the api of the present invention are in intimately associated as a pharmaceutical composition.
  • An “intimate association” in the present context includes, for example, the pharmaceutical admixed with the recrystallization/precipitation retardant inhibitor, the pharmaceutical embedded or incorporated in the retardant, the compound forming a coating on particles of the pharmaceutical or vice versa, and a substantially homogeneous dispersion of the pharmaceutical throughout the compound(s).
  • the pharmaceutical composition includes a Cox-2 inhibitor
  • a method of treating a subject in a further aspect of the invention, in which the subject may be suffering from pain, inflammation, cancer or pre-cancer such as intestinal or colonic polyps.
  • the method comprises administering to the subject a pharmaceutical composition as described herein.
  • the pharmaceutical composition is formulated for oral administration.
  • Drugs according to the invention may be prepared in a form having an increased time to onset of therapeutic effectiveness and likely having increased bioavailability.
  • the pharmaceutical compositions according to the invention are therefore particularly suitable for administration to human subjects.
  • the methods and compositions of the present invention relate to improving solubility, dissolution and bioavailability of pharmaceuticals.
  • the present invention further relates to improving the performance of pharmaceutical compounds that are free acids in their neutral state or that initially dissolve but then recrystallize in gastric fluid conditions.
  • Further embodiments relate to pharmaceuticals with an aminosulfonyl functional group.
  • aminosulfonly functional group herein refers to a functional group having the following structure: Wherein the wavy line represents a bond by which the functional group is attached to the rest of the drug molecule; and R is hydrogen or a substituent that preserves ability of polyethylene glycol or a polyethylene glycol degradation product to react with the amino group adjacent to R to form an addition compound.
  • substituents include partially unsaturated hereocyclyl, hereoaryl, cycloalkenyl, aryl, alkylcarbonyl, formyl, halo, alkyl, haloalkyl, oxo, cyano, nitro, carboxyl, phenyl, alkoxy, aminocarbonyl, alkoxycarbonyl, carboxyalkyl, cyanoalkyl, hydroxyalkyl, hydroxyl, alkoxyalkyloxyalkyl, haloalkylsulfonyloxy, carboxyalkoxyalkyl, cycloalkylalkyl, alkynyl, heterocyclyloxy, alkylthio, cycloalkyl, heterocyclyl, cycloalkenyl, aralkyl, heterocyclylalkyl, heteroarylcarbonyl, alkylthioalkyl, arylcarbonyl, alkylthioalkyl, arylcarbonyl, alky
  • Non-limiting illustrative examples of aminosulfonyl-comprising drugs include ABT-751 of Eisai (N-(2-(4-hydroxyphenyl)amino)-3-pyridyl)4-methoxybenzenesulfonamide); alpiropride; amosulalol; amprenavir; ainsacrine; argatroban; asulacrine; azosemide; BAY-38-4766 of Bayer (N-[4-[[[[5-(dimethylamino)-1-naphthalenyl]sulfonyl]amino]phenyl]-3-hydroxy-2,2-dimethylpropanamide); bendroflumethiazide; BMS-193884 of Bristol Myers Squibb (N-(3,4-dimethyl-5-isoxazolyl)-4 1 -(2-oxazolyl)-[1,1 1 -biphenyl]-2-sulfonamide
  • the aminosulfonyl-comprising drug is a selective COX-2 inhibitory drug of low water solubility.
  • Suitable selective COX-2 inhibitory drugs are compounds having the formula (IV): wherein:
  • Particularly suitable selective COX-2 inhibitory drugs are compounds having the formula (V): where R 4 is hydrogen or a C 1-4 alkyl or alkoxy group, X is N or CR 5 where R 5 is hydrogen or halogen, and Y and Z are independently carbon or nitrogen atoms defining adjacent atoms of a five-to-six-membered ring that is unsubstituted or substituted at one or more positions with oxo, halo, methyl, or halomethyl groups.
  • Preferred such five-to six-membered rings are cyclopentenone, furanone, methylpyrazole, isoxazole and pyridine rings substituted at no more than one position.
  • compositions of the invention are suitable for celecoxib, deracoxib, valdecoxib and JTE-522, more particularly celecoxib, paracoxib and valdecoxib.
  • suitable compositions include Acetazolamide CAS Registry Number: 59-66-5, Acetohexamide CAS Registry Number: 968-81-0, Alpiropride CAS Registry Number: 81982-32-3, Althiazide CAS Registry Number: 5588-16-9, Ambuside CAS Registry Number: 3754-19-6,Amidephrine CAS Registry Number: 3354-67-4, Amosulalol CAS Registry Number: 85320-68-9, Amsacrine CAS Registry Number: 51264-14-3, Argatroban CAS Registry Number: 74863-84-6, Azosemide CAS Registry Number: 27589-33-9, Bendroflumethiazide CAS Registry Number: 73-48-3, Benzthiazide CAS Registry Number: 91-33-8, Benz
  • the pharmaceutical compositions of the present invention comprise a salt of celecoxib, (e.g., sodium, lithium, potassium or calcium salt).
  • the salt may be significantly more soluble in water than presently-marketed neutral celecoxib. Due to the high pK a of celecoxib (approximately 11), salts only form under strongly basic conditions. Typically, more than about one equivalent of a base is required to convert celecoxib to its salt form.
  • a suitable aqueous solution for converting celecoxib to a salt has a pH of about 11.0 or greater, about 11.5 or greater, about 12 or greater, or about 13 or greater. Typically, the pH of such a solution is about 12 to about 13.
  • the invention includes other pharmaceutical drugs with a pKa greater than 9, 9.5, 10, 10.5, 11, 11.5, 12, 12.5, or 13. The drug may normally be in a neutral form or a salt form may already exist.
  • Salts of the pharmaceutical are formed by reaction of the pharmaceutical with an acceptable base.
  • Acceptable bases include, but are not limited to, metal hydroxides and alkoxides.
  • Metals include alkali metals (sodium, potassium, lithium, cesium), alkaline earth metals (magnesium, calcium), zinc, aluminum, and bismuth.
  • Alkoxides include methoxide, ethoxide, n-propoxide, isopropoxide and t-butoxide.
  • Sodium hydroxide and sodium ethoxide are preferred bases.
  • the amount of base used to form a salt is typically about one or more, about two or more, about three or more, about four or more, about five or more, or about ten or more equivalents relative to the pharmaceutical.
  • about three to about five equivalents of one or more bases are reacted with the pharmaceutical to form a salt.
  • a pharmaceutical salt can be transformed into a second pharmaceutical salt by transmetallation or another process that replaces the cation of the first pharmaceutical salt.
  • a sodium salt of pharmaceutical is prepared and is subsequently reacted with a second salt such as an alkaline earth metal halide (e.g., MgBr 2 , MgCl 2 , CaCl 2 , CaBr 2 ), an alkaline earth metal sulfate or nitrate (e.g., Mg(NO 3 ) 2 , Mg(SO 4 ) 2 , Ca(NO 3 ) 2 , Ca(SO 4 ) 2 ), or an alkaline metal salt of an organic acid (e.g. calcium formate, magnesium formate, calcium acetate, magnesium acetate, calcium propionate, magnesium propionate) to form an alkaline earth metal salt of the pharmaceutical.
  • an alkaline earth metal halide e.g., MgBr 2 , MgCl 2 , CaCl 2 , CaBr
  • the pharmaceutical salts are substantially pure.
  • a salt that is substantially pure can be greater than about 80% pure, greater than about 85% pure, greater than about 90% pure, greater than about 95% pure, greater than about 98% pure, or greater than about 99% pure. Purity of a salt can be measured with respect to the amount of salt (as opposed to unreacted neutral pharmaceutical or base) or can be measured with respect to a specific polymorph, co-crystal, solvate, desolvate, hydrate, dehydrate, or anhydrous form of a salt.
  • a pharmaceutical salt as described herein may be significantly more soluble in water than the existing neutral form, such as the presently-marketed neutral celecoxib, and is typically at least about twice, at least about three times, at least about five times, at least about ten times, at least about twenty times, at least about fifty times, or one at least about hundred times more or soluble in water or SGF than the neutral form, such as celecoxib marketed by Pfizer Inc. and G. D. Searle & Co. (Pharmacia Corporation), and described at pages 2676-2680 and 2780-2784 of the 2002 edition of the Physicians Desk Reference (also referred to herein as presently-marketed celecoxib).
  • the solubility depends on whether the salt is tested alone, or as a formulation further comprising the recrystallization/precipitation retardants and enhancers of the invention.
  • the salt can be neutralized by an acid or by dissolved gases such as carbon dioxide.
  • the pH of such a solution is 11 or less, 10 or less, or 9 or less.
  • Neutralizing the salt results in precipitation of an amorphous or metastable crystalline form of neutral celecoxib.
  • neutralizing a pharmaceutical salt includes protonating the majority of negatively charged anions. For celecoxib, protonation results in the formation of amorphous and/or metastable crystalline celecoxib, which are “neutral” (i.e., predominantly uncharged).
  • the neutral pharmaceutical (including amorphous and/or metastable crystalline forms thereof, such as celecoxib) comprises 10% mol or less of charged molecules.
  • amorphous and/or metastable crystalline forms thereof such as celecoxib
  • solutions of the sodium salt of celecoxib precipitate immediately as an amorphous form of neutral celecoxib.
  • the amorphous form converts to a neutral metastable crystalline form, which subsequently becomes the stable, needle-like, insoluble form of neutral celecoxib.
  • amorphous neutral celecoxib formed from the salts of the present invention e.g., the sodium salt of Example 1, converts to metastable crystalline neutral celecoxib over about 5 to about 10 minutes.
  • Amorphous neutral celecoxib converts to the same more rapidly.
  • Amorphous neutral celecoxib can be characterized by a lack of a regular crystal structure, while metastable crystalline neutral celecoxib can be distinguished from typical crystalline neutral celecoxib by the PXRD pattern of isolated material.
  • Amorphous and metastable crystalline forms of neutral celecoxib are more soluble and likely more readily absorbed by a subject than stable crystalline forms of neutral celecoxib, because the energy required for a drug molecule to escape from a stable crystal is greater than the energy required for the same drug molecule to escape from a non-crystalline, amorphous form or a metastable crystalline form.
  • the instability of neutral amorphous and neutral metastable crystalline forms makes them difficult to formulate as pharmaceutical compositions. As is described in U.S. Publication No.
  • liquid formulations of compounds of the present invention e.g. celecoxib
  • the drug is solubilized either directly with the precipitation retardant or with a solubilizer or solvent.
  • Preferred solubilizers are polyethylene oxides. More preferably, the polyethylene oxide is a surfactant. Preferred ethylene oxides comprise the functional group —(C 2 H 4 O) n — where n ⁇ 2.
  • polyethylene oxides are poloxamers having the general formula HO(C 2 H 4 O)a(C 3 H 6 O)b(C 2 H 4 O)aH where a ⁇ 2, where a ⁇ 3, where a ⁇ 2 and b ⁇ 30, where a ⁇ 2 and b ⁇ 4, where a ⁇ 2 and b ⁇ 50, where a ⁇ 2 and b ⁇ 60.
  • the precipitation retardant compounds preferably surfactants, have the following physical properties or characteristics:
  • the retardant molecule comprises at least one, preferably two, 10, 25, 40, 50, 60, 80, 100 or more functional interacting groups, wherein a functional interacting group comprises two oxygen atoms, with each of the two oxygen atoms interacting (e.g., hydrogen bonding) with the api.
  • the two oxygen atoms interact with the aminosulfonyl group of the api.
  • the aminosulfonyl group is —SO 2 NH 2 .
  • the two interacting oxygen atoms are preferably separated by between about 3.6 angstroms to about 5.8 angstroms, about 3.9 angstroms to about 5.5 angstroms, 4.3 to about 5.2 angstroms, 4.6 to about 5.0 angstroms, or about 4.7 to about 4.9 angstroms.
  • the two oxygen atoms are separated by at least three atoms. In another embodiment, the two oxygen atoms are separated by 5 atoms.
  • the two oxygen atoms are separated by 4 carbons and one oxygen atom.
  • the order of the 5 atoms is —C—C—O—C—C—, whereby a single unit of the functional interacting group (including the two interacting oxygen atoms), is —O—C—C—O—C—C—O—.
  • Glycol ethers can also be used as solubilizers of neutral or other forms of celecoxib include those that conform with the formula: R 1 —O—((CH 2 ) m O) n —R 2 (VII) Wherein R 1 and R 2 are independently hydrogen or C 1-6 alkyl, C 1-6 alkenyl, phenyl or benzyl groups, but no more than one of R 1 and R 2 is hydrogen; m is an integer of 2 to about 5; and n is an integer of 1 to about 20.
  • one of R 1 and R 2 is a C 1-4 alkyl group and the other is hydrogen or a C 1-4 alkyl group; more preferably at least one of R 1 and R 2 is a methyl or ethyl group. It is preferred that m is 2. It is preferred that n is an integer of 1 to about 4, more preferably 2. Glycol ethers, including those of the above formula, can also be specifically excluded from the present invention. Preferably, the glycol ethers are surfactants.
  • compositions of the present invention optionally comprise one or more pharmaceutically acceptable co-solvents.
  • co-solvents suitable for use in compositions of the present invention include any glycol ether listed above; alcohols, for example ethanol and n-butanol; glycols not listed above; for
  • Celecoxib salts are preferred because they are stable, such that they can be formulated as pharmaceutical compositions and stored before administration to a subject. Only after dissolution and subsequent neutralization do the celecoxib salts precipitate as or transform into substantially amorphous neutral and then substantially metastable crystalline neutral forms. Preferably, dissolution and neutralization of celecoxib salts occur in situ in the gastrointestinal tract of a subject (e.g., stomach, duodenum, ileum), such that a maximal amount of amorphous and/or metastable crystalline neutral celecoxib is present after administration (e.g., in vivo), rather than before administration.
  • a subject e.g., stomach, duodenum, ileum
  • Dissolution rate K S ( C s ⁇ C ) where K is dissolution rate constant, S is the surface area, C s is the apparent solubility, and C is the concentration of api in the dissolution media. For rapid api absorption, C s ⁇ C is approximately equal to C s
  • the dissolution rate of apis may be measured by conventional means known in the art.
  • the increase in the dissolution rate of a composition of the present invention, as compared to the neutral free form, may be specified, such as by 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100%, or by 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 40, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, 400, 500, 1000, 10,000, or 100,000 fold greater than the free form in the same solution.
  • Conditions under which the dissolution rate is measured is the same as discussed above
  • the increase in dissolution may be further specified by the time the composition remains supersaturated.
  • compositions with a dissolution rate, at 37 degrees C. and a pH of 7.0, that is increased at least 5 fold over the neutral free form compositions with a dissolution rate in SGF that is increased at least 5 fold over the neutral free form
  • compositions with a dissolution rate in SIF that is increased at least 5 fold over the neutral free form.
  • the present invention demonstrates that the length of time in which celecoxib or other apis remains in solution can be increased to a surprising high degree by using a salt or co-crystal form with the presence of a recrystallization/precipitation retardant, normally a surfactant (e.g., poloxamer, TPGS, SDS, etc.) and an optional enhancer (e.g., hydroxypropyl cellulose) as discussed herein.
  • a recrystallization/precipitation retardant normally a surfactant (e.g., poloxamer, TPGS, SDS, etc.) and an optional enhancer (e.g., hydroxypropyl cellulose) as discussed herein.
  • a surfactant e.g., poloxamer, TPGS, SDS, etc.
  • an optional enhancer e.g., hydroxypropyl cellulose
  • the present invention is drawn compositions that can be maintained for a period of time (e.g., 15, 30, 45, 60, mins and longer) as supersaturated solutions at concentrations 2, 3, 5, 7, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100%, or by 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30 40, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, 400, 500, 1000, 10,000, or 100,000 fold greater than the solubility of the neutral free form in the same solution (e.g., water or SGF).
  • a period of time e.g., 15, 30, 45, 60, mins and longer
  • concentrations 2, 3, 5, 7, 10, 20, 30, 40, 50, 60, 70, 80, 90, or 100% or by 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30 40, 50, 75, 100, 125, 150, 175, 200, 250, 300, 350, 400, 500, 1000, 10,000, or 100,000 fold greater than the solubility of the neutral free form in the same solution (e.g
  • the amount of recrystallization/precipitation inhibitor or enhancer may each or together be less than 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 70, 80, or 90% w/w (recrystallization/precipitation inhibitor or enhancer/pharmaceutical).
  • the % w/w for either or both recrystallization/precipitation inhibitor or enhancer may also be in a range represented by any two integers of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55, 60, 70, 80, or 90.
  • Celecoxib salts of the present invention are typically stable (i.e., more than 90% of the celecoxib salt does not change in composition or crystalline structure) for at least about one week, at least about one month, at least about two months, at least about three months, at least about six months, at least about nine months, at least about one year, or at least about two years at room temperature in the absence of moisture.
  • Room temperature typically ranges from about 15° C. to about 30° C.
  • the absence of moisture, as defined herein, refers to celecoxib salts not contacting quantities of liquid, particularly water or alcohols.
  • gases such as water vapor are not considered to be moisture.
  • compositions of the present invention including the active pharmaceutical ingredient (api) and formulations comprising the api, are suitably stable for pharmaceutical use.
  • the api or formulations thereof of the present invention are stable such that when stored at 30 deg. C. for 2 years, less than 0.2% of any one degradant is formed.
  • degradant refers herein to product(s) of a single type of chemical reaction. For example, if a hydrolysis event occurs that cleaves a molecule into two products, for the purpose of the present invention, it would be considered a single degradant. More preferably, when stored at 40 deg. C. for 2 years, less than 0.2% of any one degradant is formed. Alternatively, when stored at 30 deg. C.
  • the relative humidity (RH) may be specified as ambient (RH), 75% (RH), or as any single integer between 1 to 99%
  • the methods of the present invention are used to make a pharmaceutical api formulation with greater solubility, dissolution, and bioavailability, AUC, reduced time to T max , the time to reach peak blood serum levels, and higher C max, , the maximum blood serum concentration, when compared to the neutral free form.
  • AUC is the area under the plot of plasma concentration of api (not logarithm of the concentration) against time after api administration.
  • the area is conveniently determined by the “trapezoidal rule”: the data points are connected by straight line segments, perpendiculars are erected from the abscissa to each data point, and the sum of the areas of the triangles and trapezoids so constructed is computed.
  • the AUC is of particular use in estimating bioavailability of apis, and in estimating total clearance of apis (Cl T ).
  • the present invention provides a process for modulating the bioavailability of an api when administered in its normal and effective dose range, whereby the AUC is increased, the time to T max is reduced, or C max is increased, which process comprises:
  • compositions with a time to T max that is reduced by at least 10% as compared to the neutral free form compositions with a time to T max that is reduced by at least 20% over the free form, compositions with a time to T max that is reduced by at least 40% over the free form, compositions with a time to T max that is reduced by at least 50% over the free form, compositions with a T max that is reduced by at least 60% over the free form, compositions with a T max that is reduced by at least 70% over the free form, compositions with a T max that is reduced by at least 80% over the free form, compositions with a C max that is increased by at least 20% over the free form, compositions with a C max that is increased by at least 30% over the free form, compositions with a C max that is increased by at least 40% over the free form, compositions with a C max that is increased by at least 50% over the free form, compositions with a C max that is increased by at least 60% over the free form, compositions with a C
  • compositions with a more rapid onset to therapeutic effect typically reach a higher maximum blood serum concentration (C max ) a shorter time after oral administration (T max ).
  • compositions, preferably including salts, of the present invention have a higher C max and/or a shorter T max than presently-marketed celecoxib.
  • the Tmax for the compositions of the present invention may occurs within about 60 minutes, 55 minutes, 50 minutes, 45 minutes, 40 minutes, 35 minutes, 30 minutes, 25 minutes, 20 minutes, 15 minutes, 10 minutes, or within about 5 minutes of administration (e.g., oral administration).
  • compositions of the present invention begin to occur within about 60 minutes, 55 minutes, 50 minutes, 45 minutes, 40 minutes, 35 minutes, 30 minutes, within about 25 minutes, within about 20 minutes, within about 15 minutes, within about 10 minutes, or within about 5 minutes of administration (e.g., oral administration).
  • compositions of the present invention have a bioavailability greater than the neutral celecoxib and currently marketed CELEBREXTM.
  • the compositions of the present invention have a bioavailability of at least 50%, 60%, 65%, 70%, 75%, 80%, 85%, 87%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99%.
  • the present invention provides a process for improving the dose response of an api, by making a composition of the present invention.
  • Dose response is the quantitative relationship between the magnitude of response and the dose inducing the response and may be measured by conventional means known in the art.
  • the curve relating effect (as the dependent variable) to dose (as the independent variable) for an api-cell system is the “dose-response curve”.
  • the dose-response curve is the measured response to an api plotted against the dose of the api (mg/kg) given.
  • the dose response curve can also be a curve of AUC against the dose of the api given.
  • the dose-response curve for presently-marketed celecoxib is nonlinear.
  • the dose-response curve for celecoxib salts and co-crystal composition of the present invention are linear or contains a larger linear region than presently-marketed celecoxib.
  • the absorption or uptake of presently-marketed celecoxib depends in part on food effects, such that uptake of celecoxib increases when taken with food, especially fatty food.
  • uptake of celecoxib salts of the present invention exhibits a decreased dependence on food, such that the difference in uptake of celecoxib salts when taken with food and when not taken with food is less than the difference in uptake of presently-marketed celecoxib.
  • the present invention provides for apis with decreased hygroscopicity and a method for decreasing the hygroscopicity of an api by making the same.
  • An aspect of the present invention provides a pharmaceutical composition of an api that is less hygroscopic than amorphous or crystalline free form.
  • Hygroscopicity can be assessed by dynamic vapor sorption analysis, in which 5-50 mg of the compound is suspended from a Cahn microbalance.
  • the compound being analyzed should be placed in a non-hygroscopic pan and its weight should be measured relative to an empty pan composed of identical material and having nearly identical size, shape, and weight.
  • platinum pans should be used.
  • the pans should be suspended in a chamber through which a gas, such as air or nitrogen, having a controlled and known percent relative humidity (%RH) is flowed until eqilibrium criteria are met.
  • a gas such as air or nitrogen
  • Typical equilibrium criteria include weight changes of less than 0.01% change over 3 minutes at constant humidity and temperature.
  • the relative humidity should be measured for samples dried under dry nitrogen to constant weight ( ⁇ 0.01% change in 3 minutes) at 40° C. unless doing so would de-solvate or otherwise convert the material to an amorphous compound.
  • the hygroscopicity of a dried compound can be assessed by increasing the RH from 5 to 95% in increments of 5% RH and then decreasing the RH from 95 to 5% in 5% increments to generate a moisture sorption isotherm.
  • the sample weight should be allowed to equilibrate between each change in %RH.
  • the experiment should be repeated with a fresh sample and the relative humidity range for the cycling should be narrowed to 5-75% RH or 10-75% RH instead of 5-95%RH. If the sample cannot be dried prior to testing due to lack of form stability, than the sample should be studied using two complete humidity cycles of either 10-75% RH or 5-95% RH, and the results of the second cycle should be used if there is significant weight loss at the end of the first cycle.
  • Hygroscopicity can be defined using various parameters.
  • a non-hygroscopic molecule should not gain or lose more than 1.0%, or more preferably, 0.5% weight at 25degrees C. when cycled between 10 and 75% RH (relative humidity at 25 degrees C.).
  • the non-hygroscopic molecule more preferably should not gain or lose more than 1.0%, or more preferably, 0.5% weight when cycled between 5 and 95%RH at 25 degrees C., or more than 0.25% of its weight between 10 and 75% RH.
  • Most preferably, a non-hygroscopic molecule will not gain or lose more than 0.25% of its weight when cycled between 5 and 95% RH.
  • hygroscopicity can be defined using the parameters of Callaghan et al., Equilibrium moisture content of pharmaceutical excipients, in Api Dev. Ind. Pharm., Vol. 8, pp. 335-369 (1982). Callaghan et al. classified the degree of hygroscopicity into four classes. Class 1: Essentially no moisture increases degrees Non-hygroscopic occur at relative humidities below 90%. Class 2: Essentially no moisture increases degrees Slightly hygroscopic occur at relative humidities below 80%. Class 3: Moisture content does not increase more than Moderately hygroscopic 5% after storage for 1 week at relative humidities below 60%. Class 4: Moisture content increase may degrees occur Very hygroscopic at relative humidities as low as 40 to 50%.
  • hygroscopicity can be defined using the parameters of the European Pharmacopoeia Technical Guide (1999, p. 86) which has defined hygrospocity, based on the static method, after storage at 25° C. for 24 h at 80 percent RH:
  • compositions of the present invention can be set forth as being in Class 1, Class 2, or Class 3, or as being Slightly hygroscopic, Hygroscopic, or Very Hygroscopic. Composition of the present invention can also be set forth based on their ability to reduce hygroscopicity. Thus, preferred composition of the present invention are less hygroscopic than the neutral free form. Further included in the present invention are composition that do not gain or lose more than 1.0% weight at 25 degrees C. when cycled between 10 and 75% RH, wherein the reference compound gains or loses more than 1.0% weight under the same conditions. Further included in the present invention are composition that do not gain or lose more than 0.5% weight at 25 degrees C.
  • compositions that have a hygroscopicity (according to Callaghan et al.) that is at least one class lower than the reference compound or at least two classes lower than the reference compound. Included are a Class 1 composition of a Class 2 reference compound, a Class 2 composition of a Class 3 reference compound, a Class 3 composition of a Class 4 reference compound, a Class 1 composition of a Class 3 reference compound, a Class 1 composition of a Class 4 reference compound, or a Class 2 composition of a Class 4 reference compound.
  • compositions that have a hygroscopicity that is at least one class lower than the reference compound or at least two classes lower than the reference compound.
  • Non-limiting examples include; a Slightly hygroscopic composition of a Hygroscopic reference compound, a Hygroscopic composition of a Very Hygroscopic reference compound, a Very Hygroscopic composition of a Deliquescent reference compound, a Slightly hygroscopic composition of a Very Hygroscopic reference compound, a Slightly hygroscopic composition of a Deliquescent reference compound, a Hygroscopic composition of a Deliquescent reference compound.
  • a celecoxib salt can be characterized by differential scanning calorimetry (DSC).
  • DSC differential scanning calorimetry
  • the sodium salt of celecoxib prepared in Example 1 is characterized by at least 3 overlapping endothermic transitions between 50° C. and 110° C. ( FIG. 1 ).
  • Conditions for DSC can be found in Example 1.
  • Celecoxib salts can be characterized by thermogravimetric analysis (TGA).
  • TGA thermogravimetric analysis
  • the sodium salt product prepared by Example 1 was characterized by TGA, and had about 3 loosely bound equivalents of water that evaporated between about 30° C. and about 40° C., one more tightly bound equivalent of water that evaporated between about 40° C. and about 100° C., and one very tightly bound equivalent of water that evaporated between about 140° C. and about 160° C. ( FIG. 2 ).
  • TGA thermogravimetric analysis
  • the sodium salt product prepared by Example 1 was characterized by TGA, and had about 3 loosely bound equivalents of water that evaporated between about 30° C. and about 40° C., one more tightly bound equivalent of water that evaporated between about 40° C. and about 100° C., and one very tightly bound equivalent of water that evaporated between about 140° C. and about 160° C.
  • the sodium salt can exist at different states of hydration depending on the humidity, temperature, and other conditions. Conditions for TGA can
  • Celecoxib salts of the present invention can also be characterized by powder X-ray diffraction (PXRD).
  • the sodium salt of celecoxib prepared by Example 1 had an intense reflection or peak at a 2-theta angle of 6.40°, and other reflections or peaks at 7.01°, 16.73°, and 20.93° ( FIG. 3 ).
  • Conditions for PXKD can be found in Example 1.
  • Celecoxib salts may comprise solvate molecules and can occur in a variety of solvation states, also known as solvates.
  • celecoxib salts can exist as crystalline polymorphs. Polymorphs are different crystalline forms of the same drug substance, and in the present use of the term include solvates and hydrates.
  • different polymorphs of a celecoxib salt can be obtained by varying the method of preparation (compare Examples). Crystalline polymorphs typically have different solubilities, such that a more thermodynamically stable polymorph is less soluble than a less thermodynamically stable polymorph.
  • Pharmaceutical polymorphs can also differ in properties such as shelf-life, bioavailability, morphology, vapor pressure, density, color, and compressibility.
  • Suitable solvate molecules include water, alcohols, other polar organic solvents, and combinations thereof.
  • Alcohols include methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, propylene glycol and t-butanol.
  • Propylene glycol solvates are particularly preferred because they are more stable and less hygroscopic than other forms.
  • Alcohols also include polymerized alcohols such as polyalkylene glycols (e.g., polyethylene glycol, polypropylene glycol).
  • water is the solvent.
  • a celecoxib salt contains about 0.0%, less than 0.5%, 0.5, 1, less than 1%, 1.5, less than 1.5%, 2, less than 2%, 2.5, 3, 3.5, 4, 4.5, 5, 5.5 or about 6 equivalents, or about 1 to about 6, 2 to about 5, 3 to about 6, 3 to about 5, 1 to about 4, 2 to about 4, 1 to about 3, 2 to about 3, 0 to about 3, 0.5 to about 3, 0 to about 2, 0.5 to about 2, 0 to about 1.5, 0.5 to about 1.5, 1 to about 1.5, or 0.5 to about 1 equivalents of water per equivalent of salt.
  • Solvate molecules can be removed from a crystalline salt, such that the salt is either a partial or complete desolvate.
  • co-crystal as used herein means a crystalline material comprised of two or more unique solids at room temperature, each containing distinctive physical characteristics, such as structure, melting point and heats of fusion. Solvates of api compounds that do not further comprise a co-crystal forming compound are not co-crystals according to the present invention.
  • the co-crystals may however, include one or more solvent molecules in the crystalline lattice.
  • hydrogen-bonding is the dominant interaction in the formation of the co-crystal, whereby a non-covalent bond is formed between a hydrogen bond donor of one of the moieties and a hydrogen bond acceptor of the other.
  • An alternative embodiment provides for a co-crystal wherein the co-crystal former is a second api. In another embodiment, the co-crystal former is not an api.
  • the pharmaceutical is a co-crystal.
  • the co-crystal formers are selected from one or two (for ternary co-crystals) of the following: saccharin, nicotinamide, pyridoxine (4-pyridoxic acid), acesulfame, glycine, arginine, asparagine, cysteine, glutamine, histidine, isoleucine, lysine, methionine, phenylalanine, proline, threonine, tyrosine, valine, aspartic acid, glutamic acid, tryptophan, adenine, acetohydroxamic acid, alanine, allopurinaol, 4-aminobenzoic acid, cyclamic acid, 4-ethoxyphenyl urea, 4-aminopyridine, leucine, nicotinic acid, serine, tris, vitamin k5, xylito
  • bases can either be dissolved in a solvent, which can be either the solvent already contacting celecoxib or a different solvent, can be added as a neat solid or liquid, or a combination thereof.
  • a solvent which can be either the solvent already contacting celecoxib or a different solvent
  • Sodium hydroxide and sodium ethoxide are preferred bases.
  • the amount of base required is discussed above.
  • the solvent can be evaporated to obtain crystals of the celecoxib salt, or the celecoxib salt may precipitate and/or crystallize independent of evaporation. Crystals of a celecoxib salt can be filtered to remove bulk solvent. Methods of removing solvated solvent molecules are discussed above.
  • a pharmaceutical composition of the invention contains a desired amount of celecoxib per dose unit and, if intended for oral administration, can be in the form, for example, of a tablet, a caplet, a pill, a hard or soft capsule, a lozenge, a cachet, a dispensable powder, granules, a suspension, an elixir, a dispersion, a liquid, or any other form reasonably adapted for such administration. If intended for parenteral administration, it can be in the form, for example, of a suspension or transdermal patch. If intended for rectal administration, it can be in the form, for example, of a suppository. Presently preferred are oral dosage forms that are discrete dose units each containing a predetermined amount of the drug, such as tablets or capsules.
  • Non-limiting examples follow of excipients that can be used to prepare pharmaceutical compositions of the invention.
  • Such carriers or diluents constitute in total about 5% to about 99%, preferably about 10% to about 85%, and more preferably about 20% to about 80%, of the total weight of the composition.
  • the carrier, carriers, diluent, or diluents selected preferably exhibit suitable flow properties and, where tablets are desired, compressibility.
  • the use of extragranular microcrystalline cellulose that is, microcrystalline cellulose added to a granulated composition) can be used to improve hardness (for tablets) and/or disintegration time.
  • Lactose, especially lactose monohydrate is particularly preferred.
  • Lactose typically provides compositions having suitable release rates of celecoxib, stability, pre-compression flowability, and/or drying properties at a relatively low diluent cost. It provides a high density substrate that aids densification during granulation (where wet granulation is employed) and therefore improves blend flow properties and tablet properties.
  • Disintegrants may be added at any suitable step during the preparation of the composition, particularly prior to granulation or during a lubrication step prior to compression. Such disintegrants, if present, constitute in total about 0.2% to about 30%, preferably about 0.2% to about 10%, and more preferably about 0.2% to about 5%, of the total weight of the composition.
  • Croscarmellose sodium is a preferred disintegrant for tablet or capsule disintegration, and, if present, preferably constitutes about 0.2% to about 10%, more preferably about 0.2% to about 7%, and still more preferably about 0.2% to about 5%, of the total weight of the composition. Croscarmellose sodium confers superior intragranular disintegration capabilities to granulated pharmaceutical compositions of the present invention.
  • Suitable binding agents and adhesives include, but are not limited to, either individually or in combination, acacia; tragacanth; sucrose; gelatin; glucose; starches such as, but not limited to, pregelatinized starches (e.g., NationalTM 1511 and NationalTM 1500); celluloses such as, but not limited to, methylcellulose and carmellose sodium (e.g., TyloseTM); alginic acid and salts of alginic acid; magnesium aluminum silicate; PEG; guar gum; polysaccharide acids; bentonites; povidone, for example povidone K-15, K-30 and K-29/32; polymethacrylates; HPMC; hydroxypropylcellulose (e.g., KlucelTM of Aqualon); and ethylcellulose (e.g., EthocelTM of the Dow Chemical Company).
  • Such binding agents and/or adhesives if present, constitute in total about 0.5% to about 25%, preferably about 0.75% to about 15%, and more preferably about 1%
  • binding agents are polymers comprising amide, ester, ether, alcohol or ketone groups and, as such, are preferably included in pharmaceutical compositions of the present invention.
  • Polyvinylpyrrolidones such as povidone K-30 are especially preferred.
  • Polymeric binding agents can have varying molecular weight, degrees of crosslinking, and grades of polymer.
  • Polymeric binding agents can also be copolymers, such as block co-polymers that contain mixtures of ethylene oxide and propylene oxide units. Variation in these units' ratios in a given polymer affects properties and performance. Examples of block co-polymers with varying compositions of block units are Poloxamer 188 and Poloxamer 237 (BASF Corporation).
  • compositions of the invention optionally comprise one or more pharmaceutically acceptable wetting agents as excipients.
  • wetting agents are preferably selected to maintain the celecoxib in close association with water, a condition that is believed to improve bioavailability of the composition.
  • Such wetting agents can also be useful in solubilizing or increasing the solubility of metal salts of celecoxib.
  • Non-limiting examples of surfactants that can be used as wetting agents (not necessarily as the recrystallization/precipitation retardant) in pharmaceutical compositions of the invention include quaternary ammonium compounds, for example benzalkonium chloride, benzethonium chloride and cetylpyridinium chloride, dioctyl sodium sulfosuccinate, polyoxyethylene alkylphenyl ethers, for example nonoxynol 9, nonoxynol 10, and octoxynol 9, poloxamers (polyoxyethylene and polyoxypropylene block copolymers), polyoxyethylene fatty acid glycerides and oils, for example polyoxyethylene (8) caprylic/capric mono- and diglycerides (e.g., LabrasolTM of Gattefosse), polyoxyethylene (35) castor oil and polyoxyethylene (40) hydrogenated castor oil; polyoxyethylene alkyl ethers, for example polyoxyethylene (20) cetostearyl ether, polyoxyethylene fatty
  • Sodium lauryl sulfate is a particularly preferred wetting agent.
  • Sodium lauryl sulfate if present, constitutes about 0.25% to about 7%, more preferably about 0.4% to about 4%, and still more preferably about 0.5% to about 2%, of the total weight of the pharmaceutical composition.
  • compositions of the invention optionally comprise one or more pharmaceutically acceptable lubricants (including anti-adherents and/or glidants) as excipients.
  • suitable lubricants include, but are not limited to, either individually or in combination, glyceryl behapate (e.g., CompritolTM 888 of Gattefosse); stearic acid and salts thereof, including magnesium, calcium and sodium stearates; hydrogenated vegetable oils (e.g., SterotexTM of Abitec); colloidal silica; talc; waxes; boric acid; sodium benzoate; sodium acetate; sodium fumarate; sodium chloride; DL-leucine; PEG (e.g., CarbowaxTM 4000 and CarbowaxTM 6000 of the Dow Chemical Company); sodium oleate; sodium lauryl sulfate; and magnesium lauryl sulfate.
  • Such lubricants if present, constitute in total about 0.1% to about 10%, preferably about
  • Magnesium stearate is a preferred lubricant used, for example, to reduce friction between the equipment and granulated mixture during compression of tablet formulations.
  • Suitable anti-adherents include, but are not limited to, talc, cornstarch, DL-leucine, sodium lauryl sulfate and metallic stearates.
  • Talc is a preferred anti-adherent or glidant used, for example, to reduce formulation sticking to equipment surfaces and also to reduce static in the blend.
  • Talc if present, constitutes about 0.1% to about 10%, more preferably about 0.25% to about 5%, and still more preferably about 0.5% to about 2%, of the total weight of the pharmaceutical composition.
  • Glidants can be used to promote powder flow of a solid formulation. Suitable glidants include, but are not limited to, colloidal silicon dioxide, starch, talc, tribasic calcium phosphate, powdered cellulose and magnesium trisilicate. Colloidal silicon dioxide is particularly preferred. Other excipients such as colorants, flavors and sweeteners are known in the pharmaceutical art and can be used in pharmaceutical compositions of the present invention. Tablets can be coated, for example with an enteric coating, or uncoated. Compositions of the invention can further comprise, for example, buffering agents.
  • one or more effervescent agents can be used as disintegrants and/or to enhance organoleptic properties of pharmaceutical compositions of the invention.
  • one or more effervescent agents are preferably present in a total amount of about 30% to about 75%, and preferably about 45% to about 70%, for example about 60%, by weight of the pharmaceutical composition.
  • an effervescent agent present in a solid dosage form in an amount less than that effective to promote disintegration of the dosage form, provides improved dispersion of the celecoxib in an aqueous medium.
  • the effervescent agent is effective to accelerate dispersion of celecoxib from the dosage form in the gastrointestinal tract, thereby further enhancing absorption and rapid onset of therapeutic effect.
  • an effervescent agent is preferably present in an amount of about 1% to about 20%, more preferably about 2.5% to about 15%, and still more preferably about 5% to about 10%, by weight of the pharmaceutical composition.
  • an “effervescent agent” herein is an agent comprising one or more compounds which, acting together or individually, evolve a gas on contact with water.
  • the gas evolved is generally oxygen or, most commonly, carbon dioxide.
  • Preferred effervescent agents comprise an acid and a base that react in the presence of water to generate carbon dioxide gas.
  • the base comprises an alkali metal or alkaline earth metal carbonate or bicarbonate and the acid comprises an aliphatic carboxylic acid.
  • Non-limiting examples of suitable bases as components of effervescent agents useful in the invention include carbonate salts (e.g., calcium carbonate), bicarbonate salts (e.g., sodium bicarbonate), sesquicarbonate salts, and mixtures thereof. Calcium carbonate is a preferred base.
  • Non-limiting examples of suitable acids as components of effervescent agents and/or solid organic acids useful in the invention include citric acid, tartaric acid (as D-, L-, or D/L-tartaric acid), malic acid, maleic acid, fumaric acid, adipic acid, succinic acid, acid anhydrides of such acids, acid salts of such acids, and mixtures thereof.
  • Citric acid is a preferred acid.
  • the weight ratio of the acid to the base is about 1:100 to about 100:1, more preferably about 1:50 to about 50:1, and still more preferably about 1:10 to about 10:1. In a further preferred embodiment of the invention, where the effervescent agent comprises an acid and a base, the ratio of the acid to the base is approximately stoichiometric.
  • Excipients which solubilize metal salts of celecoxib typically have both hydrophilic and hydrophobic regions, or are preferably amphiphilic or have amphiphilic regions.
  • One type of amphiphilic or partially-amphiphilic excipient comprises an amphiphilic polymer or is an amphiphilic polymer.
  • a specific amphiphilic polymer is a polyalkylene glycol, which is commonly comprised of ethylene glycol and/or propylene glycol subunits. Such polyalkylene glycols can be esterified at their termini by a carboxylic acid, ester, acid anhyride or other suitable moiety.
  • excipients examples include poloxamers (symmetric block copolymers of ethylene glycol and propylene glycol; e.g., poloxamer 237), polyalkyene glycolated esters of tocopherol (including esters formed from a di- or multi-functional carboxylic acid; e.g., d-alpha-tocopherol polyethylene glycol-1000 succinate), and macrogolglycerides (formed by alcoholysis of an oil and esterification of a polyalkylene glycol to produce a mixture of mono-, di- and tri-glycerides and mono- and di-esters; e.g., stearoyl macrogol-32 glycerides).
  • poloxamers symmetric block copolymers of ethylene glycol and propylene glycol
  • polyalkyene glycolated esters of tocopherol including esters formed from a di- or multi-functional carboxylic acid; e.g., d-alpha-tocopherol
  • compositions of the present invention can comprise about 10% to about 50%, about 25% to about 50%, about 30% to about 45%, or about 30% to about 35% by weight of a metal salt of celecoxib; about 10% to about 50%, about 25% to about 50%, about 30% to about 45%, or about 30% to about 35% by weight of a an excipient which inhibits crystallization; and about 5% to about 50%, about 10% to about 40%, about 15% to about 35%, or about 30% to about 35% by weight of a binding agent.
  • the weight ratio of the metal salt of celecoxib to the excipient which inhibits crystallization to binding agent is about 1 to 1 to 1.
  • Solid dosage forms of the invention can be prepared by any suitable process, not limited to processes described herein.
  • An illustrative process comprises (i) a step of blending a celecoxib salt of the invention with one or more excipients to form a blend, and (ii) a step of tableting or encapsulating the blend to form tablets or capsules, respectively.
  • solid dosage forms are prepared by a process comprising (a) a step of blending the celecoxib salt to form a blend, (b) a step of granulating the blend to form a granulate, and (c) a step of tableting or encapsulating the blend to form tablets or capsules respectively.
  • Step (b) can be accomplished by any dry or wet granulation technique known in the art.
  • a celecoxib salt is advantageously granulated to form particles of about 1 micrometer to about 100 micrometer, about 5 micrometer to about 50 micrometer, or about 10 micrometer to about 25 micrometer.
  • One or more diluents, one or more disintegrants and one or more binding agents may be added, for example in the blending step, a wetting agent can optionally be added, for example in the granulating step, and one or more disintegrants may be added after granulating but before tableting or encapsulating.
  • a lubricant may be added before tableting.
  • Blending and granulating can be performed independently under low or high shear.
  • a process is preferably selected that forms a granulate that is uniform in drug content, that readily disintegrates, that flows with sufficient ease so that weight variation can be reliably controlled during capsule filling or tableting, and that is dense enough in bulk so that a batch can be processed in the selected equipment and individual doses fit into the specified capsules or tablet dies.
  • solid dosage forms are prepared by a process that includes a spray drying step, wherein a celecoxib salt is suspended with one or more excipients in one or more sprayable liquids, preferably a non-protic (e.g., non-aqueous or non-alcoholic) sprayable liquid, and then is rapidly spray dried over a current of warm air.
  • a spray drying step wherein a celecoxib salt is suspended with one or more excipients in one or more sprayable liquids, preferably a non-protic (e.g., non-aqueous or non-alcoholic) sprayable liquid, and then is rapidly spray dried over a current of warm air.
  • a granulate or spray dried powder resulting from any of the above illustrative processes can be compressed or molded to prepare tablets or encapsulated to prepare capsules.
  • Conventional tableting and encapsulation techniques known in the art can be employed. Where coated tablets are desired, conventional coating techniques are suitable.
  • Excipients for tablet compositions of the invention are preferably selected to provide a disintegration time of less than about 30 minutes, preferably about 25 minutes or less, more preferably about 20 minutes or less, and still more preferably about 15 minutes or less, in a standard disintegration assay.
  • Celecoxib dosage forms of the invention preferably comprise celecoxib in a daily dosage amount of about 10 mg to about 1000 mg, more preferably about 50 mg to about 100 mg, about 100 mg to about 150 mg, 150 mg to about 200 mg, 200 mg to about 250 mg, 250 mg to about 300 mg, 300 mg to about 350 mg, 350 mg to about 400 mg, 400 mg to about 450 mg 450 mg to about 500 mg, 500 mg to about 550 mg, 550 mg to about 600 mg, 600 to about 700, and 700 to about 800 mg.
  • compositions of the invention comprise one or more orally deliverable dose units.
  • Each dose unit comprises celecoxib in a therapeutically effective amount that is preferably those listed.
  • dose unit herein means a portion of a pharmaceutical composition that contains an amount of a therapeutic or prophylactic agent, in the present case celecoxib, suitable for a single oral administration to provide a therapeutic effect.
  • one dose unit, or a small plurality (up to about 4) of dose units, in a single administration provides a dose comprising a sufficient amount of the agent to result in the desired effect.
  • Administration of such doses can be repeated as required, typically at a dosage frequency of 1, 2, 3 or 4 times per day.
  • a “subject” to which a celecoxib salt or a pharmaceutical composition thereof can be administered includes a human subject of either sex and of any age, and also includes any nonhuman animal, particularly a warm-blooded animal, more particularly a domestic or companion animal, illustratively a cat, dog or horse.
  • an amount of celecoxib (measured as the neutral form of celecoxib, that is, not including counterions in a salt or water in a hydrate) relatively low in the preferred range of about 10 mg to about 1000 mg is likely to provide blood serum concentrations consistent with therapeutic effectiveness.
  • an amount of celecoxib relatively low in the preferred range of about 10 mg to about 1000 mg is likely to provide blood serum concentrations consistent with therapeutic effectiveness.
  • achievement of such blood serum concentrations of celecoxib is likely to require dose units containing a relatively greater amount of celecoxib.
  • a dose unit containing a particular amount of celecoxib can be selected to accommodate any desired frequency of administration used to achieve a desired daily dosage.
  • the daily dosage and frequency of administration, and therefore the selection of appropriate dose unit depends on a variety of factors, including the age, weight, sex and medical condition of the subject, and the nature and severity of the condition or disorder, and thus may vary widely.
  • compositions of the present invention can be used to provide a daily dosage of celecoxib of about 50 mg to about 1000 mg, preferably about 100 mg to about 600 mg, more preferably about 150 mg to about 500 mg, and still more preferably about 175 mg to about 400 mg, for example about 200 mg.
  • the daily dose can be administered in one to about four doses per day. Administration at a rate of one 50 mg dose unit four times a day, one 100 mg dose unit or two 50 mg dose units twice a day or one 200 mg dose unit, two 100 mg dose units or four 50 mg. dose units once a day is preferred.
  • oral administration herein includes any form of delivery of a therapeutic agent or a composition thereof to a subject wherein the agent or composition is placed in the mouth of the subject, whether or not the agent or composition is immediately swallowed, although each are embodiments of the invention.
  • oral administration includes buccal and sublingual as well as esophageal administration. Absorption of the agent can occur in any part or parts of the gastrointestinal tract including the mouth, esophagus, stomach, duodenum, ileum and colon.
  • oral administration includes buccal and sublingual as well as esophageal administration. Absorption of the agent can occur in any part or parts of the gastrointestinal tract including the mouth, esophagus, stomach, duodenum, ileum and colon.
  • orally deliverable herein means suitable for oral administration.
  • compositions of the invention are useful in treatment and prevention of a very wide range of disorders mediated by COX-2, including but not restricted to disorders characterized by inflammation, pain and/or fever.
  • Such pharmaceutical compositions are especially useful as anti-inflammatory agents, such as in treatment of arthritis, with the additional benefit of having significantly less harmful side effects than compositions of conventional non-steroidal anti-inflammatory drugs (NSAIDs) that lack selectivity for COX-2 over COX-1.
  • NSAIDs non-steroidal anti-inflammatory drugs
  • compositions of the invention have reduced potential for gastrointestinal toxicity and gastrointestinal irritation including upper gastrointestinal ulceration and bleeding, reduced potential for renal side effects such as reduction in renal function leading to fluid retention and exacerbation of hypertension, reduced effect on bleeding times including inhibition of platelet function, and possibly a lessened ability to induce asthma attacks in aspirin-sensitive asthmatic subjects, by comparison with compositions of conventional NSAIDs.
  • Contemplated pharmaceutical compositions are useful to treat a variety of arthritic disorders, including but not limited to rheumatoid arthritis, spondyloarthropathies, gouty arthritis, osteoarthritis, systemic lupus erythematosus and juvenile arthritis.
  • Such pharmaceutical compositions are useful in treatment of asthma, bronchitis, menstrual cramps, preterm labor, tendonitis, bursitis, allergic neuritis, cytomegalovirus infectivity, apoptosis including HIV-induced apoptosis, lumbago, liver disease including hepatitis, skin-related conditions such as psoriasis, eczema, acne, burns, dermatitis and ultraviolet radiation damage including sunburn, and post-operative inflammation including that following ophthahnic surgery such as cataract surgery or refractive surgery.
  • compositions of the present invention are useful to treat gastrointestinal conditions such as, but not limited to, inflammatory bowel disease, Crohn's disease, gastritis, irritable bowel syndrome and ulcerative colitis.
  • compositions are useful in treatment of ophthalmic diseases, such as retinitis, conjunctivitis, retinopathies, uveitis, ocular photophobia, and of acute injury to the eye tissue.
  • ophthalmic diseases such as retinitis, conjunctivitis, retinopathies, uveitis, ocular photophobia, and of acute injury to the eye tissue.
  • compositions are useful in treatment of allergic rhinitis, respiratory distress syndrome, endotoxin shock syndrome and liver disease.
  • compositions of the present invention are useful in treatment of pain, including but not limited to postoperative pain, dental pain, muscular pain, and pain resulting from cancer.
  • such compositions are useful for relief of pain, fever and inflammation in a variety of conditions including rheumatic fever, influenza and other viral infections including common cold, low back and neck pain, dysmenorrhea, headache, toothache, sprains and strains, myositis, neuralgia, synovitis, arthritis, including rheumatoid arthritis, degenerative joint diseases (osteoarthritis), gout and ankylosing spondylitis, bursitis, bums, and trauma following surgical and dental procedures.
  • the present invention is further directed to a therapeutic method of treating a condition or disorder where treatment with a COX-2 inhibitory drug is indicated, the method comprising oral administration of a pharmaceutical composition of the invention to a subject in need thereof.
  • the dosage regimen to prevent, give relief from, or ameliorate the condition or disorder preferably corresponds to once-a-day or twice-a-day treatment, but can be modified in accordance with a variety of factors. These include the type, age, weight, sex, diet and medical condition of the subject and the nature and severity of the disorder. Thus, the dosage regimen actually employed can vary widely and can therefore deviate from the preferred dosage regimens set forth above.
  • compositions can be used in combination with other therapies or therapeutic agents, including but not limited to, therapies with opioids and other analgesics, including narcotic analgesics, Mu receptor antagonists, Kappa receptor antagonists, non-narcotic (i.e. non-addictive) analgesics, monoamine uptake inhibitors, adenosine regulating agents, cannabinoid derivatives, GABA active agents, norexin neuropeptide modulators, Substance P antagonists, neurokinin-1 receptor antagonists and sodium channel blockers, among others.
  • therapies with opioids and other analgesics including narcotic analgesics, Mu receptor antagonists, Kappa receptor antagonists, non-narcotic (i.e. non-addictive) analgesics, monoamine uptake inhibitors, adenosine regulating agents, cannabinoid derivatives, GABA active agents, norexin neuropeptide modulators, Substance P antagonists, neurokinin-1 receptor antagonists and sodium channel block
  • Preferred combination therapies comprise use of a composition of the invention with one or more compounds selected from aceclofenac, acemetacin, e-acetamidocaproic acid, acetaminophen, acetaminosalol, acetanilide, acetylsalicylic acid (aspirin), S-adenosylmethionine, alclofenac, alfentanil, allylprodine, alminoprofen, aloxiprin, alphaprodine, aluminum bis(acetylsalicylate), amfenac, aminochlorthenoxazin, 3-amino-4-hydroxybutyric acid, 2-amino-4-picoline, aminopropylon, aminopyrine, amixetrine, ammonium salicylate, ampiroxicam, amtolmetin guacil, anileridine, antipyrine, antipyrine salicylate, antrafenine, apazone, bendazac, benorylate, benoxapro
  • compositions of the present invention are useful in prevention and treatment of benign and malignant tumors and neoplasia including cancer, such as colorectal cancer, brain cancer, bone cancer, epithelial cell-derived neoplasia (epithelial carcinoma) such as basal cell carcinoma, adenocarcinoma, gastrointestinal cancer such as lip cancer, mouth cancer, esophageal cancer, small bowel cancer, stomach cancer, colon cancer, liver cancer, bladder cancer, pancreatic cancer, ovarian cancer, cervical cancer, lung cancer, breast cancer, skin cancer such as squamous cell and basal cell cancers, prostate cancer, renal cell carcinoma, and other known cancers that effect epithelial cells throughout the body.
  • cancer such as colorectal cancer, brain cancer, bone cancer, epithelial cell-derived neoplasia (epithelial carcinoma) such as basal cell carcinoma, adenocarcinoma, gastrointestinal cancer such as lip cancer, mouth cancer, esophageal cancer, small bowel cancer,
  • Neoplasias for which compositions of the invention are contemplated to be particularly useful are gastrointestinal cancer, Barrett's esophagus, liver cancer, bladder cancer, pancreatic cancer, ovarian cancer, prostate cancer, cervical cancer, lung cancer, breast cancer and skin cancer.
  • Such pharmaceutical compositions can also be used to treat fibrosis that occurs with radiation therapy.
  • These pharmaceutical compositions can be used to treat subjects having adenomatous polyps, including those with familial adenomatous polyposis (FAP).
  • FAP familial adenomatous polyposis
  • pharmaceutical compositions of the present invention can be used to prevent polyps from forming in subjects at risk of FAP.
  • compositions inhibit prostanoid-induced smooth muscle contraction by inhibiting synthesis of contractile prostanoids and hence can be of use in treatment of dysmenorrhea, premature labor, asthma and eosinophil-related disorders. They also can be of use for decreasing bone loss particularly in postmenopausal women (i.e., treatment of osteoporosis), and for treatment of glaucoma.
  • the sample was either left in the glass vial in which it was processed or an aliquot of the sample was transferred to a glass slide.
  • the glass vial or slide was positioned in the sample chamber.
  • the measurement was made using an AlmegaTM Dispersive Raman (AlmegaTM Dispersive Raman, Thermo-Nicolet, 5225 Verona Road, Madison, Wis. 53711-4495) system fitted with a 785 nm laser source.
  • the sample was manually brought into focus using the microscope portion of the apparatus with a 10 ⁇ power objective (unless otherwise noted), thus directing the laser onto the surface of the sample.
  • the spectrum was acquired using the parameters outlined in Table 1. (Exposure times and number of exposures may vary; changes to parameters will be indicated for each acquisition.)
  • All x-ray powder diffraction patterns were obtained using the D/Max Rapid X-ray Diffractometer (D/Max Rapid, Contact Rigaku/MSC, 9009 New Trails Drive, The Woodlands, Tex., USA 77381-5209) equipped with a copper source (Cu/K ⁇ 1.5406), manual x-y stage, and 0.3 mm collimator.
  • the sample was loaded into a 0.3 mm boron rich glass capillary tube (e.g., Charles Supper Company, 15 Tech Circle, Natick Mass. 01760-1024) by sectioning off one end of the tube and tapping the open, sectioned end into a bed of the powdered sample or into the sediment of a slurried precipitate.
  • precipitate can be amorphous or crystalline.
  • the loaded capillary was mounted in a holder that was secured into the x-y stage.
  • a diffractogram was acquired (e.g., Control software: RINT Rapid Control Software, Rigaku Rapid/XRD, version 1.0.0, ⁇ 1999 Rigaku Co.) under ambient conditions at a power setting of 46 kV at 40 mA in reflection mode, while oscillating about the omega-axis from 0-5 degrees at 1 degree/s and spinning about the phi-axis at 2 degrees/s.
  • the exposure time was 15 minutes unless otherwise specified.
  • the diffractogram obtained was integrated over 2-theta from 2-60 degrees and chi (1 segment) from 0-360 degrees at a step size of 0.02 degrees using the cyllnt utility in the RINT Rapid display software (Analysis software: RINT Rapid display software, version 1.18, Rigaku/MSC.) provided by Rigaku with the instrument.
  • the dark counts value was set to 8 as per the system calibration (System set-up and calibration by Rigaku); normalization was set to average; the omega offset was set to 180°; and no chi or phi offsets were used for the integration.
  • the analysis software JADE XRD Pattern Processing, versions 5.0 and 6.0 (( 8 1995-2002, Materials Data, Inc. was also used.
  • the relative intensity of peaks in a diffractogram is not necessarily a limitation of the PXRD pattern because peak intensity can vary from sample to sample, e.g., due to crystalline impurities. Further, the angles of each peak can vary by about +/ ⁇ 0.1 degrees, preferably +/ ⁇ 0.05. The entire pattern or most of the pattern peaks may also shift by about +/ ⁇ 0.1 degree due to differences in calibration, settings, and other variations from instrument to instrument and operator to operator.
  • sample pan e.g., Pan part #900786.091; lid part #900779.901; TA Instruments, 109 Lukens Drive, New Castle, Del. 19720
  • the sample pan was sealed either by crimping for dry samples or press fitting for wet samples (e.g., hydrated or solvated samples).
  • the sample pan was loaded in to the apparatus (DSC: Q1000 Differential Scanning Calorimeter, TA Instruments, 109 Lukens Drive, New Castle, Del.
  • thermogram was obtained by individually heating the sample (e.g., Control software: Advantage for QW-Series, version 1.0.0.78, Thermal Advantage Release 2.0, ⁇ 2001 TA instruments—Water LLC) at a rate of 10° C./min from T min (typically 20° C.) to T max (typically 300° C.) (Heating rate and temperature range may vary, changes to these parameters will be indicated for each sample) using an empty aluminum pan as a reference.
  • Dry nitrogen e.g., Compressed nitrogen, grade 4.8, BOC Gases, 575 Mountain Avenue, Murray Hill, N.J. 07974-2082
  • Heating rate and temperature range may vary, changes in parameters will be indicated for each sample
  • dry nitrogen e.g., Compressed nitrogen, grade 4.8, BOC Gases, 575 Mountain Avenue, Murray Hill, N.J. 07974-2082
  • sample purge flow rate 60 ml/min
  • balance purge flow rate 40 ml/min.
  • Thermal transitions e.g. weight changes
  • the resulting material was analyzed by powder x-ray diffraction (PXRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA), the results of which are seen in FIGS. 1-3 .
  • the product was found to contain about 4.1 equivalents of water per equivalent of salt, although most of all of the water could be contained in the NaOH that co-precipitated with the salt.
  • the purge gas used was dry nitrogen
  • the reference material was an empty aluminum pan that was crimped
  • the sample purge was 50 mL/minute.
  • DSC analysis of the sample was performed by placing 2.594 mg of sample in an aluminum pan with a crimped pan closure.
  • the starting temperature was 20° C. with a heating rate of 10° C./minute
  • the ending temperature was 200° C.
  • the resulting DSC analysis is shown in FIG. 1 .
  • the transitions observed include a melt/dehydration process between about 40 and about 70 C, another transition between about 70 and about 100 C possibly resulting from a recrystallization/precipitation event and a second melt/dehydration transition between about 100 and about 110 C.
  • the purge gas used was dry nitrogen, the balance purge was 40 mL/minute N 2 , and the sample purge was 60 mL/minute N 2 .
  • TGA of the sample was performed by placing 2.460 mg of sample in a platinum pan. The starting temperature was 20° C. with a heating rate of 10° C./minute, and the ending temperature was 300° C. The resulting TGA analysis is shown in FIG. 2 .
  • the TGA shows a mass loss of about 12.5% between about 30 and about 50° C., attributed to the loss of about 2.8 water molecules. A second mass loss of about 2.0% between about 71 and 85° C., attributed to the loss of about 0.5 water molecules. Finally, a mass loss of about 4.0% between about 148 and 170° C. attributed to either the loss of about 1 water molecule or some decomposition of the drug compound.
  • the hydration state of the salt can vary depending on the humidity, temperature and other conditions.
  • the PXRD pattern for the compound prepared above is shown in FIG. 3 .
  • the PXRD pattern has characteristic peaks that can be used to characterize the salt comprising any one, or any combination of any two, any three or any four peaks or any other combination of peaks at a 2-theta angle of FIG. 3 including for example, the peaks at 6.40°, 7.01°, 16.73°, and 20.93°.
  • the slurry was filtered by suction filtration and rinsed with 2 mL of isopropanol. The solid was allowed to air dry before being gently ground to a powder.
  • the product was analyzed by PXRD, DSC, and TGA as in Example 1, but a 0.5 mm capillary was used to hold the sample in the PXRD experiment.
  • the compound lost 17.35% weight between room temperature and 120° C.
  • the DSC trace shows a broad endothermic region, which is consistent with a loss of volatile components with increasing temperature. The endotherm peaks at 66° C.
  • the PXRD pattern peaks that can be used to characterize the salt include any one or combination comprising any two, any three, any four, any five, any six, any seven, any eight, any nine, any ten, any eleven, any twelve, or all thirteen 2-theta angles of 4.09°, 4.99°, 6.51°, 7.07°, 9.99°, 11.59°, 16.53°, 17.69°, 18.47°, 19.13°, 20.11°, 20.95°, 22.67°, or any one or combination of 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, or 13 peaks of FIG. 62 .
  • the sodium salt form (from Example 6) was compared with CELEBREX powder in terms of absorption in rats ( FIGS. 4A and 4B ).
  • Crystalline neutral celecoxib did not dissolve when added to aqueous polyvinylpyrrolidone or when water was added to a dry blend of neutral crystalline celecoxib and polyvinylpyrrolidone.
  • Raman shift (cm ⁇ 1 ) peaks occur at positions including, but not limited to, any one, any two, any three, any four, all five of 1617.11, 1446.20, 1373.73, 975.02 and 800.15, or any combinations 2, 3, 4, 5 or more peaks of FIG. 13B .
  • the celecoxib salt of Example 6 was administered to dogs and compared to administration of commercially available celecoxib.
  • Six male beagle dogs aged 2-4 years old and weighing 8-12 kg were food-deprived but were given water.
  • Each of the dogs was administered 3 test doses as described below and allowed a one week washout period between doses.
  • test doses were: (1) commercially available celecoxib in the form of CELEBREX® at 1 milligrams per kilograms (mpk) combined with 70/30 PEG400/water which was administered IV, (2) oral dose of commercially available celecoxib in the form of CELEBREX® at 5 mpk adjusted for each dog's weight in size 4 gelatin capsules, and (3) oral dose of the sodium salt of the instant invention as prepared according to Example 6 at 5 mpk adjusted for each dog's weight in size 4 gelatin capsules.
  • Blood samples of approximately 2 ml in sodium heparin were obtained by jugular venipuncture at 0.25, 0.5, 1, 3, 4, 6, 8, 12, and 24 hours post-dose.
  • Plasma samples were obtained predose and at 0.08 hr for the IV study. Blood samples were immediately placed on ice and centrifuged within 30 min of collection at 3200 g at 4 degrees C. nominal for 10 minutes. Plasma samples ( ⁇ 1.0 ml) were harvested and stored in 4 aliquots of 0.25 ml at ⁇ 20 degrees C. Plasma samples were analyzed for celecoxib using a LC-MS/MS assay with a lower limit of quantitation of 5 ng/ml. Pharmacokinetic profiles of celecoxib in plasma were analyzed using the PhAST software Program (Version 2.3, Pheonix Life Sciences, Inc.). The absolute biovavailability (F) is reported for oral doses relative to the IV dose.
  • FIG. 5 shows the mean pharmacokinetic parameters (and standard deviations therefore) of celecoxib in the plasma of male dogs following a single oral or single intravenous dose of celecoxib or celecoxib sodium.
  • the maximum serum concentration and bioavailability of orally-administered celecoxib sodium was about three- and two-fold greater, respectively, than a roughly equal dose of orally-administered celecoxib, and the maximum serum concentration of celecoxib sodium was reached 40% faster than for celecoxib.
  • Results of Raman spectroscopy show multiple spectral peaks that can be used to characterize the salt. These include any one, any two, any three, any four, any five, any six, any seven, any eight, any nine, any ten, or and any other combination of peaks of FIG. 16 , e.g., 1617.10, 1596.95, 1449.56, 1374.03, 1115.24, 1062.85, 976.50, 800.67, 740.91 and 633.94.
  • PXRD peaks that can be used to characterize the salt include any one, or combination of any two, any three, any four, any five, any six, any seven, any eight, any nine, any ten or any other combination of peaks from FIG. 17 , e.g., 4.18, 9.04, 10.705, 12.47, 15.75, 18.71, 19.64, 20.52, 21.55 and 23.0.
  • Celecoxib-Potassium Salt Preparation Method MO-116-49A
  • Celecoxib (Fako Ilaclari A.S.) was dissolved in a 0.35M KOH(aq) solution (Potassium Hydroxide—Spectrum, Cat#P0180, Lot#PN0690) with a Potassium:Celecoxib ratio of 1.40:1 in a vial with a Teflon coated silicon rubber septum cap.
  • the resulting solution was gently warmed during dissolution with occasional swirling until all solids dissolved. After all solids were dissolved, the solution was dried by flowing dry nitrogen over the solution for 2 days through stainless steel needles inserted into the septum cap. Analysis of the resulting product was performed. Characterization of the product was achieved via DSC ( FIG. 18 ,) TGA ( FIG. 19 ), Raman spectroscopy ( FIG. 20 ) and PXRD ( FIG. 21 ).
  • results are depicted in FIG. 20 and show characteristic Raman shift (cm ⁇ 1 ) peaks at positions including, but not limited to any one or combination of any two, any three, any four, any five or all six of the peaks: 1617.66, 1448.22, 1374.09, 976.28, 801.60, or any combinations of 2, 3, 4, 5, 6 or more peaks of FIG. 20 .
  • a small amount of collected sample was placed in a 0.3 mm glass PXRD tube.
  • the tube was placed in Rigaku D/Max Rapid PXRD set to Cu; 46 kV/40 mA; Collimeter:0.3; Omega-axis oscillation, Pos(deg) 0-5, speed 1; Phi-axis spin, Pos 360, Speed 2; Collection time was equal to 15 minutes.
  • the PXRD pattern has characteristic peaks as shown in FIG. 21 . Peaks can be seen at 2-theta angles including, but not limited to, 4.03, 12.23, 15.35, and 19.79.
  • the crystal can be characterized by any one or combination of any two, any three, or all four, of the above angles or any one or any number combination of 2-theta angles of FIG. 21 .
  • the results are depicted in FIG. 23 and show characteristic Raman shift (cm ⁇ 1 ) peaks at positions including, but not limited to any one or combination of any two, any three, any four, any five or any six, any seven, any eight, any nine, any ten, or all eleven of the peaks 1615.51, 1446.09, 1374.28, 1232.91, 1197.04, 1108.99, 1060.94, 973.01, 798.86, 739.82, 633.37 or any one or combinations of 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or more peaks of FIG. 23 .
  • a small amount of collected sample was placed in a 0.3 mm glass PXRD tube.
  • the tube was placed into a Rigaku D/Max Rapid PXRD set to Cu; 46 kV/40 mA; Collimeter:0.3; Omega-axis oscillation, Pos(deg) 0-5, speed 1; Phi-axis spin, Pos 360, Speed 2; Collection time was equal to 15 minutes.
  • the results are depicted in FIG. 24 .
  • Characteristic raman shift (cm ⁇ 1 ) peaks were observed at positions including, but not limited to, any one, any two, any three, any four, any five, and six or all seven of the peaks 16.16.99, 1598.42, 1450.05, 1376.57, 973.10, 800.62, 642.20, or any combinations of 2, 3, 4, 5, 6, 7 or more peaks of FIG. 26 .
  • a small amount of collected sample was placed into a 0.3 mm glass PXRD tube.
  • the tube was placed in Rigaku D/Max Rapid PXRD set to Cu; 46 kV/40 mA; Collimeter:0.3; Omega-axis oscillation, Pos(deg) 0-5, speed 1; Phi-axis spin, Pos 360, Speed 2; Collection time was equal to 15 minutes.
  • An intense peak was observed at 2-theta angle of 31.67 and lesser peaks at 7.82, 9.27, 20.56, and 27.35. Any one or combination of 2, 3, 4, or 5 of the preceding peaks can be used to characterize the salt, as well as, any 1, 2, 3, 4, 5, 6, or more peaks of FIG. 27 .
  • peaks of the free acid may also be found in the compositions of the present invention.
  • the peaks characteristic of the free acid as shown in FIG. 28 , may also be specifically excluded from compositions of the present invention.
  • This example demonstrates that related solid-state formulations enhance the dissolution and retard the recrystallization/precipitation of celecoxib salts as compared to the celecoxib freeacid compound.
  • the processes used to identify and test the preferred excipients in these examples are two-fold: (1) A “Crystal Retardation Assay” was used to identify excipients that supersaturate celecoxib in solution; and (2) In-vitro dissolution studies were performed on selected excipients to verify the “Crystal Retardation Assay” results.
  • 58 excipients according to Table 1 were prepared at a concentration of2 mg/ml (0.2% by weight) in simulated gastric fluid having 200 mM hydrochloric acid and dispensed in quadruplicate in 96-well plates at a volume of 150 ul.
  • Two controls were used: (a) Simulated gastric fluid lacking excipients; and (b) Simulated gastric fluid containing 2 mg/ml Vitamin E TPGS and 2 mg/ml HPC. The latter control was chosen because of prior indication that this excipient combination provides enhanced dissolution of celecoxib sodium hydrate.
  • Simulated gastric fluid was prepared by adding 2 g/L sodium chloride and 1 g/L Triton X-100 to DI H20.
  • FIG. 30 shows crystal retardation time for celecoxib as a function of excipient in simulated gastric fluid (SGF).
  • Final concentration of celecoxib was 0.5 mg/ml.
  • Black bars indicate crystal retardation time that may be greater than 60 min.
  • Excipients listed in Table I, but excluded from FIG. 30 did not show any appreciable crystal retardation time (i.e., greater than 1.5 min).
  • Vitamin E TPGS alone had a longer retardation time than in combination with HPC alone did not show any retardation time.
  • the solubility of celecoxib freeacid in Transcutol P is 350 mg/g. It was found that in contrast to enhancing solubility, Transcutol P does not enhance dissolution of the free acid. Transcutol P does extend the time to Tmax and increases the time the concentration of celecoxib is above 1 ⁇ 2 Tmax when used in combination with a recrystallization/precipitation retardant and enhancer. It was further found that dissolution of a salt form is far superior to the dissolution of composition comprising the free acid.
  • PLURONIC polyxamer
  • properties can be significantly altered (i.e., melting point, cloud point, molecular weight, HLB number, surface tension, interfacial tension, etc.) by adjusting the ratio of copolymer blocks. Further examination of these properties showed that the surface tension of these copolymers at a 0.1% concentration in water correlates with the ability to retard the crystallization of celecoxib.
  • PLURONIC excipients having low interfacial tension i.e., less than about 10 dyne/cm
  • having a surface tension less then about 42 dyne/cm were more effective at keeping celecoxib in solution than PLURONIC excipients having high interfacial tension or surface tension.
  • This observation is illustrated in FIG. 31 , along with interfacial data for PLURONICs that were not tested. Based on this correlation, the supersaturation properties of these additional PLURONICs also correlate with interfacial tension.
  • FIG. 31 shows interfacial tension of selected PLURONIC excipients in water.
  • PLURONIC excipients having low interfacial tension correlate with excipients that retard crystallization of celecoxib in simulated gastric fluid.
  • An interfacial tension threshold for crystal retardation was loosely defined as less than about 9 or 10 dyne/cm.
  • Excipient concentration in the assay was 0.18%; celecoxib concentration was 0.5 mg/ml.
  • FIG. 39 shows the results of TGA. A weight loss of about 15.6% was observed between about 65° and 200° C.
  • FIG. 40 shows the results of PXRD. Peaks, in 2-theta angles, that can be used to characterize the solvate include any 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 of the following: 3.77, 7.57, 8.21, 11.33, 14.23, 16.15, 18.69, 20.63, 22.69 and 24.77 or any one or any combination of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more peaks of FIG. 40 . The other peaks of the graphs may also be used alone or in any combination to characterize the salt.
  • a propylene glycol solvates of the sodium salt of celecoxib was prepared. To a solution of celecoxib (312 mg; 0.818 mmol) in Et 2 O (6 mL) was added propylene glycol (0.127 ml, 1.73 mmol). To the clear solution was added NaOEt in EtOH (21%, 0.275 ⁇ L, 0.817 mmol). After 1 minute, crystals began to form. After 5 minutes, the solid had completely crystallized. The solid was collected by filtration and was washed with Et 2 O (10 mL). The off-white solid was then air-dried and collected. This was a 1:1 solvate. The solid was characterized by TGA and PXRD. The results are depicted in FIGS. 39 and 40 .
  • FIG. 41 shows the results of TGA. A weight loss of about 14.94% was observed between about 65° and about 250° C.
  • FIG. 42 shows the results of PXRD. Peaks; in 2-theta angles, that can be used to characterize te solvate include any 1, 2, 3, 4, 5, 6, 7, 8 , 9 or 10 of the following: 3.75, 7.47, 11.33, 14.93, 15.65, 18.31, 20.47, 21.71, and 24.67 or any one or any combination of 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more peaks of FIG. 42 .
  • Characteristic peaks of 2-theta angles that can be used to characterize the salt include any one, or combination of any 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12 of 3.79, 7.51, 8.19, 9.83, 11.41, 15.93, 18.29, 19.19, 19.87, 20.63, 22.01, 25.09 or any one or any combination of peaks of FIG. 51 .
  • FIG. 44 shows the results of TGA where an about 9.64% weight loss was observed between room temperature and 60° C. and an about 13.6% weight loss was observed between abuot 60° C. and 175° C.
  • the PXRD pattern has characteristic peaks at 2-theta angles shown in FIG. 45 . Any 1, 2, 3, 4, 5, 6, 7, 8, 9, or more peaks can be used to characterize the solvate, including for example, peaks at 3.47, 6.97, 10.37, 13.97, 16.41, 19.45, 21.29, 22.69, 23.87 and 25.75.
  • the PXRD pattern has characteristic peaks at 2-theta angles shown in FIG. 47 . Any 1, 2, 3, 4, 5, 6, 7, 8, 9, or more peaks can be used to characterize the solvate, including for example, peaks at 3.43, 6.95, 10.25, 13.95, 16.39, 19.43, 21.21, 22.61 and 25.71.
  • FIGS. 48-50 The results of DSC, TGA and PXRD analysis are shown in FIGS. 48-50 .
  • FIG. 48 shows the results of DSC analysis where a peak endotherm was observed at 67.69° C.
  • the results of TGA, as shown in FIG. 49 revealed a weight loss of about 18.23% from about room temperature to about 120° C.
  • the PXRD pattern has characteristic peaks at 2-theta angles shown in FIG. 50 . Any 1, 2, 3, 4, 5, 6, 7, 8, 9, or more peaks can be used to characterize the solvate, including for example, peaks at 3.43, 7.03, 10.13, 11.75, 14.11, 16.61, 17.61, 18.49, 19.51, 20.97, 22.33, 22.81 and 25.93.
  • Celecoxib 100 mg, 0.26 mmol
  • Nicotinamide 32.0 mg, 0.26 mmol
  • the two solutions were mixed and the resulting mixture was allowed to evaporate slowly overnight.
  • the precipitated solid was collected and characterized.
  • Detailed characterization of the co-crystal was performed using DSC, TGA & PXRD.
  • the results of DSC showed decomposition beginning at ⁇ 150° C.
  • the results of TGA showed two phase transitions at 117.2 and 118.8° C. and a sharp endotherm at 129.7° C.
  • the results of PXRD is shown in FIG. 52 .
  • Characteristic peaks that can be used to characterize the co-crystal include any one, or any combination of any 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14 or 15 the peaks at 3.77, 7.56, 9.63, 14.76, 16.01, 17.78, 18.68, 19.31, 20.435, 21.19, 22.10, 23.80, 24.70, 25.295, and 26.73, or any one or any combination of any 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or more peaks of FIG. 52 .
  • the celecoxib sodium is a variable hydrate.
  • the celecoxib sodium salt and celecoxib sodium salt propylene glycol solvate were analyzed by PXRD under 17%, 31%, 59% and 74% constant relative humidity at room temperature.
  • the following table lists PXRD 2-theta angle peaks at the different relative humidities.

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US10/601,092 US20050025791A1 (en) 2002-06-21 2003-06-20 Pharmaceutical compositions with improved dissolution
US10/660,202 US7927613B2 (en) 2002-02-15 2003-09-11 Pharmaceutical co-crystal compositions
JP2005508617A JP5021934B2 (ja) 2002-12-30 2003-12-24 改善された溶解性を有する医薬組成物
EP10193736A EP2339328A3 (en) 2002-12-30 2003-12-24 Pharmaceutical co-crystal compositions of celecoxib
AU2003303591A AU2003303591A1 (en) 2002-12-30 2003-12-24 Pharmaceutical compositions with improved dissolution
US10/541,216 US8362062B2 (en) 2002-02-15 2003-12-24 Pharmaceutical compositions with improved dissolution
EP03808567A EP1579198A1 (en) 2002-12-30 2003-12-24 Pharmaceutical compositions with improved dissolution
CA2511881A CA2511881C (en) 2002-12-30 2003-12-24 Pharmaceutical compositions comprising a sodium salt of celecoxib with improved dissolution
PCT/US2003/041273 WO2004061433A1 (en) 2002-12-30 2003-12-24 Pharmaceutical compositions with improved dissolution
US10/747,742 US7790905B2 (en) 2002-02-15 2003-12-29 Pharmaceutical propylene glycol solvate compositions
AU2003300452A AU2003300452A1 (en) 2002-12-30 2003-12-29 Pharmaceutical propylene glycol solvate compositions
PCT/US2003/041642 WO2004060347A2 (en) 2002-09-03 2003-12-29 Pharmaceutical propylene glycol solvate compositions
CA002514733A CA2514733A1 (en) 2003-02-28 2004-02-26 Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
PCT/US2004/006288 WO2004078163A2 (en) 2003-02-28 2004-02-26 Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
US10/546,963 US20070059356A1 (en) 2002-05-31 2004-02-26 Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothiazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
EP04715190A EP1631260A2 (en) 2003-02-28 2004-02-26 Pharmaceutical co-crystal compositions of drugs such as carbamazepine, celecoxib, olanzapine, itraconazole, topiramate, modafinil, 5-fluorouracil, hydrochlorothazide, acetaminophen, aspirin, flurbiprofen, phenytoin and ibuprofen
JP2006508979A JP2007524596A (ja) 2003-02-28 2004-02-26 共結晶医薬組成物
US10/551,014 US20060223794A1 (en) 2002-02-15 2004-03-31 Novel olanzapine forms and related methods of treatment
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US12/234,420 US20090088443A1 (en) 2002-02-15 2008-09-19 Novel crystalline forms of conazoles and methods of making and using the same
US12/792,415 US20100311701A1 (en) 2002-02-15 2010-06-02 Pharmaceutical Co-Crystal Compositions

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US10/660,202 Continuation-In-Part US7927613B2 (en) 2002-02-15 2003-09-11 Pharmaceutical co-crystal compositions
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US8362062B2 (en) 2013-01-29

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