COMPOSITIONS OF STATINS AND OMEGA-3 FATTY ACIDS
The present disclosure provides pharmaceutical compositions of statins and polyunsaturated fatty acids (PUFAs), in which the statins are dissolved in the PUFAs, the PUFA species being present substantially in the free acid form. Also provided are oral unit dosage forms of the disclosed pharmaceutical compositions and methods of treating blood lipid disorders using the compositions and oral unit dosage forms.
This application claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Application No. 61/643,764, filed May 7, 2012, the content of which is incorporated herein by reference in its entirety.
2. BACKGROUNDPharmaceutical compositions rich in omega-3 polyunsaturated fatty acids (PUFAs) have been developed to treat a variety of clinical indications, including various disorders of blood lipids, including hypertriglyceridemia and mixed dyslipidemias. Statin monotherapy is widely used to treat hypercholesterolemia and other blood lipid disorders.
Numerous studies have reported on the increased benefits of combined treatment with statins and omega-3 PUFAs in various cardiovascular disorders (See Nakamura et al., 1999, Int. J. Clin. Lab Res. 29:22-25 and Davidson et al., 1997, Am J Cardiol 80:797-798). To improve patient convenience and compliance, dual compositions comprising statins and omega-3 PUFAs in esterified form have been described, but some statins are known to be poorly soluble in such formulations (see, e.g., U.S. Pat. No. 7,642,287), and no such dual composition is commercially available.
Therefore, there is a need in the art for compositions that combine statins and omega-3 PUFAs in a single oral unit dosage form, and that provide enhanced solubility and bioavailability. Such pharmaceutical compositions would improve patient convenience, and may allow for treatment with improved effectiveness, fewer excipients, and better patient compliance, than is provided by the administration of the two actives in separate unit dosage forms.
3. SUMMARYThe inventors have discovered that certain statins have unexpectedly greater solubility in a PUFA free acid solvent system, a PUFA composition in which each of the PUFA species is present substantially in the free acid form, as compared to their solubility in a PUFA ethyl ester solvent system, a PUFA composition in which each of the PUFA species is present substantially in esterified form. Accordingly, the present disclosure provides pharmaceutical compositions, oral unit dosage forms, dosage kits, and methods of treatment comprising at least one statin dissolved in a PUFA free acid solvent system. In typical embodiments, the statin is rosuvastatin. In some embodiments, the statin is atorvastatin, pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, or pitavastatin.
In a first aspect, pharmaceutical compositions comprising at least one statin dissolved in a PUFA free acid solvent system are provided.
In various embodiments, at least 90% of the total polyunsaturated fatty acid in the PUFA free acid solvent system is present in the free acid form. In certain embodiments, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, even at least 99% of the total polyunsaturated fatty acid in the PUFA free acid solvent system is present in the free acid form.
In typical embodiments, the PUFA free acid solvent system comprises at least one, typically a plurality of, omega-3 PUFA species, wherein each of the omega-3 PUFA species is present substantially in the free acid form. In various embodiments, the composition comprises EPA, DHA, and DPA (n-3), each substantially in free acid form.
In some embodiments, at least 80% by weight of the statin is dissolved in the PUFA free acid solvent system (less than 20% by weight of the statin is undissolved in the solvent system), while in particular embodiments, at least 90% by weight of the statin is dissolved in the PUFA free acid solvent system (less than 10% by weight of the statin is undissolved in the solvent system).
In various embodiments, the one or more statins is dissolved in the PUFA free acid solvent system in an amount that permits administration of a therapeutic amount of statin in a convenient number of oral unit doses, which number of oral unit doses also suffices to deliver a therapeutic dose of omega-3 PUFAs.
In certain embodiments, the one or more statins is present in the pharmaceutical composition in an amount, per ml or per g of PUFA free acid solvent system, of at least about 5 mg, at least about 10 mg, at least about 15 mg, at least about 20 mg, at least about 25 mg, at least about 30 mg, at least about 40 mg, at least about 50 mg, at least about 60 mg, at least about 70 mg, at least about 80 mg, at least about 90 mg, even at least about 100 mg, at least about 110 mg, and in certain embodiment, at least about 120 mg.
In selected embodiments, one or more statins is present in the pharmaceutical composition in an amount, per ml or per g of PUFA free acid solvent system, of from about 2 mg to about 80 mg, from about 5 mg to about 60 mg, or from about 10 mg to about 40 mg, or from about 20 mg to about 30 mg. In various embodiments, the at least one statin is selected from the group consisting of rosuvastatin, pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, and pitavastatin.
In another aspect, oral unit dosage forms comprising the pharmaceutical compositions of the disclosure are provided. In some embodiments, the pharmaceutical composition is encapsulated in a soft gelatin capsule. In various embodiments, the oral unit dosage form further comprises at least one coating on the exterior of the soft gelatin capsule. In some embodiments, each of the at least one coatings is selected from the group consisting of: cellulose acetate trimellitate, cellulose acetate phthalate and poly(ethylacrylate-methylacrylate).
In some embodiments, the soft gelatin capsule encapsulates 1-100 mg of a statin dissolved in about 250 mg, about 500 mg, or about 1000 mg of a PUFA free acid solvent system. In certain embodiments, the soft gelatin capsule encapsulates 2-40 mg of a statin dissolved in about 250 mg, about 500 mg, or about 1000 mg of a PUFA free acid solvent system.
In other aspects, the disclosure provides methods of treating a blood lipid disorder, comprising administering an effective amount of a pharmaceutical composition of the disclosure. The blood lipid disorder is selected, in certain embodiments, from the group consisting of: hypertriglyceridemia, hypercholesterolemia, coronary heart disease (CHD), hypertriglyceridemia, mixed dyslipidemias, heart failure, myocardial infarction, cardiac arrhythmias, ischemic dementia, hypertension, nephropathy, retinopathy, vascular disease, and atherosclerotic disease.
Statins are known to be poorly soluble in compositions of omega-3 PUFAs in which the PUFAs are present substantially in esterified form (“PUFA ethyl ester solvent systems”). See, e.g., U.S. Pat. No. 7,642,287. The present inventors have now discovered that certain statins unexpectedly have significantly greater solubility in PUFA compositions in which each of the PUFA species is present substantially in the free acid form (“PUFA free acid solvent system”), as compared to their solubility in a PUFA ethyl ester solvent system. Accordingly, the present disclosure provides pharmaceutical compositions, oral unit dosage forms, and dosage kits comprising at least one statin dissolved in a PUFA free acid solvent system, and methods of using these compositions and unit oral dosage forms for treatment of blood lipid disorders. In typical embodiments, the statin is rosuvastatin. In some embodiments, the statin is atorvastatin, pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, or pitavastatin.
5.2. Pharmaceutical CompositionsIn a first aspect, pharmaceutical compositions comprising at least one statin dissolved in a PUFA free acid solvent system are provided. In typical embodiments, the PUFA free acid solvent system comprises at least one, typically a plurality of, omega-3 PUFA species, wherein each of the omega-3 PUFA species is present substantially in the free acid form. In some embodiments, the statin is rosuvastatin. In various embodiments, the statin is atorvastatin, pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, or pitavastatin.
In some embodiments of the pharmaceutical composition, the statin is dissolved in the PUFA free acid solvent system to provide a substantially homogeneous composition.
In some embodiments, the statin is completely dissolved in the PUFA free acid solvent system. In various embodiments, the statin is substantially dissolved (i.e., at least about 90% of the statin is dissolved in the PUFA free acid solvent system, with about 10% or less of the statin is undissolved in the PUFA free acid solvent system). In certain embodiments, at least about 70% of the statin is dissolved in the PUFA free acid solvent system. In some embodiments, at least about 80%, 85%, 90%, 95%, even at least about 96%, 97%, 98%, 99%, even at least about 99.5% of the statin is dissolved in the PUFA free acid solvent system. In some embodiments, the statin is less than 30%, less than 20%, less than 15%, less than 10%, or less than 5% undissolved in the PUFA free acid solvent system.
In some embodiments, the pharmaceutical composition does not require significant amounts of compounds other than polyunsaturated fatty acids—such as surfactants, hydrophilic or hydrophobic solvents, oils or combinations thereof (individually and collectively, “non-PUFA solubilizers”)—to dissolve the statin in the PUFA free acid solvent system.
Preferably, the statin is dissolved in the pharmaceutical composition without the use of any non-PUFA solubilizers.
If present, non-PUFA solubilizers are present in amounts of 50% or less (w/w) based on the total weight of the PUFA free acid solvent system, 40% or less, 30% or less, 20% or less, 10% or less, or 5% or less. In various embodiments, the weight ratio of polyunsaturated fatty acids to non-PUFA solubilizers is at least about 1:1, at least 5:1, or at least 10:1. In some embodiments, the PUFA free acid solvent system contains no non-PUFA solubilizers.
Various embodiments of the pharmaceutical composition comprise a statin dissolved in a PUFA free acid solvent system, wherein the statin is present in the PUFA free acid solvent system in a weight-to-volume (w/v) ratio of about 1:5,000; about 1:4,500; about 1:4,000; about 1:3,50; about 1:3,000; about 1:2,500; about 1:2,000; about 1:1,500; about 1:1,000; about 1:800; about 1:700; about 1:500; about 1:400: about 1:300; about 1:250, about 1:125, about 1:100; about 1:80; about 1:50; or ratios intermediate the above-recited values.
In a variety of embodiments, at least one statin is dissolved in the PUFA free acid solvent system, wherein the statin is present in a weight-to-weight (w/w) ratio with respect to the PUFA free acid solvent system of about 1:5,000; about 1:4,500; about 1:4,000; about 1:3,500; about 1:3,000; about 1:2,500; about 1:2,000; about 1:1,500; about 1:1,000; about 1:800; about 1:700; about 1:500; about 1:400: about 1:300; about 1:250, about 1:125, about 1:100; about 1:80; about 1:50, or ratios intermediate these values.
In certain embodiments, the pharmaceutical composition comprises a statin dissolved in a PUFA free acid solvent system, wherein the statin is dissolved in the PUFA free acid solvent system at a concentration of at least about 0.1 mg/ml solvent system, 0.2 mg/ml, 0.5 mg/ml, 1 mg/ml, 2 mg/ml, 5 mg/ml, 7.5 mg/ml, 10 mg/ml, 15 mg/ml, 20 mg/ml, 30 mg/ml, 40 mg/ml, 50 mg/ml, 75 mg/ml, 100 mg/ml, 120 mg/ml, 150 mg/ml, or 200 mg/ml, or in concentrations intermediate these values. In various embodiments, the pharmaceutical composition comprises a statin dissolved in a PUFA free acid solvent system, wherein the statin is dissolved in the PUFA free acid solvent system at a concentration of at least about 0.1 mg/g solvent system, 0.2 mg/g solvent system, 0.5 mg/g solvent system, 1 mg/g solvent system, 2 mg/g solvent system, 5 mg/g solvent system, 7.5 mg/g solvent system, 10 mg/g solvent system, 15 mg/g solvent system, 20 mg/g solvent system, 30 mg/g solvent system, 40 mg/g solvent system, 50 mg/g solvent system, 75 mg/g solvent system, 100 mg/g solvent system, 120 mg/g solvent system, 150 mg/g solvent system, or 200 mg/g solvent system, or in concentrations intermediate these values.
5.2.1. PUFA Free Acid Solvent System
The PUFA free acid solvent system comprises at least one, typically a plurality of, species of omega-3 PUFAs, each present substantially in the free acid form.
In typical embodiments, the PUFA free acid solvent system comprises eicosapentaenoic acid (C20:5 n-3) (“EPA,” also known as timnodonic acid) substantially in free acid form. In various embodiments, the PUFA free acid solvent system comprises docosahexaenoic acid (C22:6 n-3) (“DHA,” also known as cervonic acid) substantially in free acid form. In selected embodiments, the PUFA free acid solvent system comprises docosapentaenoic acid (C22:5 n-3) (“DPA,” also known as clupanodonic acid), substantially in free acid form.
In characteristic embodiments, the PUFA free acid solvent system comprises EPA, substantially in free acid form, in an amount, calculated as a percentage by area on GC chromatogram of all fatty acids in the PUFA free acid solvent system, of at least about 40% (“40% (a/a)”). In various embodiments, the PUFA free acid solvent system comprises EPA in an amount of at least about 41% (a/a), 42% (a/a), 43% (a/a), 44% (a/a), 45% (a/a), 46% (a/a), 47% (a/a), 48% (a/a), 49% (a/a), or at least about 50% (a/a). In certain embodiments, the PUFA free acid solvent system comprises EPA, substantially in free acid form, in an amount of at least about 51% (a/a), at least about 52% (a/a), at least about 53% (a/a), at least about 54% (a/a), at least about 55% (a/a), at least about 56% (a/a), at least about 57% (a/a), at least about 58% (a/a), even at least about 59% (a/a), at least about 60% (a/a), at least about 61% (a/a), 62% (a/a), 63% (a/a), 64% (a/a), or 65% (a/a).
In a variety of embodiments, the PUFA free acid solvent system comprises EPA, substantially in free acid form, in an amount of at least about 70% (a/a), at least about 75% (a/a), at least about 80% (a/a), at least about 85% (a/a), 90% (a/a), 91% (a/a), 92% (a/a), 93% (a/a), 94% (a/a), even at least about 95% (a/a), 96% (a/a), 97% (a/a), 98% (a/a), or 99% (a/a).
In certain embodiments, the PUFA free acid solvent system comprises EPA, substantially in free acid form, in an amount of about 45 to about 65% (a/a). In particular embodiments, EPA is present, substantially in free acid form, in an amount of about 50 to about 60% (a/a). In various embodiments, EPA is present, substantially in free acid form, in an amount of about 52 to about 58.0% (a/a). In some embodiments, EPA is present, substantially in free acid form, in an amount of about 55% (a/a) to about 56% (a/a). In some embodiments, EPA is present in an amount of about 55% (a/a).
In various embodiments, the PUFA free acid solvent system comprises EPA, substantially in free acid form, in an amount, calculated as a percentage by mass of all fatty acids in the PUFA free acid solvent system (“% (m/m)”), of about 50% (m/m) to about 60% (m/m). In certain embodiments, EPA is present, substantially in free acid form, in an amount of about 55% (m/m).
In certain embodiments, the PUFA free acid solvent system comprises DHA, substantially in free acid form, in an amount of at least about 13% (a/a). In various embodiments, the PUFA free acid solvent system comprises DHA, substantially in free acid form, in an amount of at least about 14% (a/a), at least about 15% (a/a), at least about 16% (a/a), at least about 17% (a/a), at least about 18% (a/a), at least about 19% (a/a), or at least about 20% (a/a). In selected embodiments, the PUFA free acid solvent system comprises DHA, substantially in free acid form, in an amount of at least about 21% (a/a), at least about 22% (a/a), at least about 23% (a/a), at least about 24% (a/a), even at least about 25% (a/a).
In a variety of embodiments, the PUFA free acid solvent system comprises DHA, substantially in free acid form, in an amount of at least about 30% (a/a), 35% (a/a), even at least about 40% (a/a).
In various embodiments, the PUFA free acid solvent system comprises DHA, substantially in free acid form, in an amount of about 13% (a/a) to about 25% (a/a). In certain embodiments, DHA is present, substantially in free acid form, in an amount of about 15% (a/a) to about 25% (a/a). In several embodiments, DHA is present, substantially in free acid form, in an amount of about 17% (a/a) to about 23% (a/a). In certain embodiments, DHA is present, substantially in free acid form, in an amount of about 19% (a/a) to about 20% (a/a).
In various embodiments, the PUFA free acid solvent systems comprise DHA, substantially in free acid form, in an amount of about 15% (m/m) to about 25% (m/m). In certain embodiments, DHA is present, substantially in free acid form, in an amount of about 17% (m/m) to about 23% (m/m). In certain embodiments, DHA is present, substantially in free acid form, in an amount of about 20% (m/m).
In certain embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of at least about 1% (a/a). In various embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of at least about 1.5% (a/a), 2% (a/a), 2.5% (a/a), 3% (a/a), 3.5% (a/a), 4% (a/a), 4.5% (a/a), even at least about 5% (a/a). In selected embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of at least about 6% (a/a), at least about 7% (a/a), at least about 8% (a/a), or at least about 9% (a/a).
In a variety of embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of about 1% (a/a) to about 8% (a/a). In certain embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of about 2% (a/a) to about 7% (a/a). In selected embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of about 3% (a/a) to about 6% (a/a). In particular embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of about 4% (a/a) to about 5% (a/a).
In various embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of no less than about 1% (m/m). In various embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of about 1% (m/m) to about 8% (m/m). In particular embodiments, the PUFA free acid solvent system comprises DPA, substantially in free acid form, in an amount of no more than about 10% (m/m).
In a variety of embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form.
In various embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form, in a total amount of at least about 60% (a/a). In various embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form, in a total amount of at least about 61% (a/a), 62% (a/a), 63% (a/a), 64% (a/a), 65% (a/a), 66% (a/a), 67% (a/a), 68% (a/a), 69% (a/a), or at least about 70% (a/a). In particular embodiments, the PUFA free acid solvent system comprise EPA and DHA, each substantially in free acid form, in a total amount of at least about 71% (a/a), 72% (a/a), 73% (a/a), 74% (a/a), 75% (a/a), 76% (a/a), 77% (a/a), 78% (a/a), 79% (a/a), even at least about 80% (a/a). In certain embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form, in total amount of at least about 81% (a/a), 82% (a/a), at least about 83% (a/a), 84% (a/a), even at least about 85% (a/a).
In various embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form, in a total amount of about 70% (m/m) to about 80% (m/m). In certain embodiments, the PUFA free acid solvent system comprises about 75% (m/m) EPA plus DHA, each substantially in free acid form.
In certain embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form, in mass ratios of at least about 2:1, 2.1:1, 2.2:1, 2.3:1, 2.4:1, 2.5:1, 2.6:1, 2.7:1, 2.8:1, 2.9:1, even at least about 3:1. In certain embodiments, the PUFA free acid solvent system comprises EPA and DHA, each substantially in free acid form, in a mass ratio of about 2.75:1.
In various embodiments, the PUFA free acid solvent system comprises EPA, DHA, and DPA, each substantially in free acid form, in a total amount of at least about 61% (a/a). In typical embodiments, the PUFA free acid solvent system comprises EPA, DHA, and DPA, each substantially in free acid form, in a total amount of at least about 62% (a/a), 63% (a/a), 64% (a/a), 65% (a/a), 66% (a/a), at least about 67% (a/a), at least about 68% (a/a), at least about 69% (a/a), or at least about 70% (a/a). In certain embodiments, the PUFA free acid solvent system comprises EPA, DHA, and DPA, each substantially in free acid form, in a total amount of at least about 71% (a/a), 72% (a/a), 73% (a/a), 74% (a/a), 75% (a/a), 76% (a/a), 77% (a/a), 78% (a/a), 79% (a/a), 80% (a/a), even at least about 81% (a/a), 82% (a/a), 83% (a/a), 84% (a/a), 85% (a/a), 86% (a/a), 87% (a/a), even at least about 88% (a/a).
In various embodiments, the PUFA free acid solvent system comprises EPA, DHA, and DPA, each substantially in free acid form, in a total amount of between about 70% (a/a) to about 90% (a/a).
In a particular series of embodiments, EPA, substantially in free acid form, is present in an amount of about 55% (a/a) to about 56% (a/a); DHA, substantially in free acid form, is present in an amount of about 19% (a/a) to about 20% (a/a); and DPA, substantially in free acid form, is present in an amount of about 4% (a/a) to about 5% (ala). In certain embodiments, EPA, substantially in free acid form, is present in an amount of about 55% (m/m) to about 56% (m/m); DHA, substantially in free acid form, is present in an amount of about 19% (m/m) to about 20% (m/m); and DPA, substantially in free acid form, is present in an amount of about 4% (m/m) to about 5% (m/m).
In certain embodiments, the PUFA free acid solvent system is a complex mixture comprising a plurality of species of omega-3 PUFAs and a plurality of species of omega-6 PUFAs, each present substantially in free acid form.
In certain embodiments, the PUFA free acid solvent system comprises EPA, DHA, DPA, and further comprises one or more omega-3 polyunsaturated fatty acid species selected from the group consisting of α-linolenic acid (C18:3 n-3), moroctic acid (C18:4 n-3, also known as stearidonic acid), eicosatrienoic acid (C20:3 n-3), eicosatetraenoic acid (C20:4 n-3), and heneicosapentaenoic acid (C21:5 n-3), each substantially in the free acid form.
In particular embodiments, the PUFA free acid solvent system comprises EPA, DHA, DPA, and moroctic acid, each substantially in the free acid form. In a variety of embodiments, the PUFA free acid solvent system comprises EPA, DHA, DPA, moroctic acid, and heneicosapentaenoic acid, each substantially in the free acid form. In specific embodiments, the PUFA free acid solvent system comprises EPA, DHA, DPA, moroctic acid, heneicosapentaenoic acid, and eicosatetraenoic acid, each substantially in the free acid form. In selected embodiments, the PUFA free acid solvent system comprises EPA, DHA, DPA, α-linolenic acid (C18:3 n-3), moroctic acid (C18:4 n-3), eicosatrienoic acid (C20:3 n-3), eicosatetraenoic acid (C20:4 n-3), and heneicosapentaenoic acid (C21:5 n-3), each substantially in the free acid form.
In various embodiments, total omega-3 fatty acids—defined as the sum of alpha-linolenic acid (C18:3 n-3), moroctic acid (C18:4 n-3), eicosatrienoic acid (C20:3 n-3), eicosatetraenoic acid (C20:4 n-3), eicosapentaenoic acid (EPA) (C20:5 n-3), heneicosapentaenoic acid (C21:5 n-3), docosapentaenoic acid (C22:5 n-3) and docosahexaenoic acid (DHA) (C22:6 n-3), each present substantially in the free acid form—constitute from about 80% (a/a) to about 95% (a/a) of all fatty acids in the PUFA free acid solvent system. In a variety of embodiments, total omega-3 fatty acids constitute from about 80-about 95% (m/m) of all fatty acids in the PUFA free acid solvent system.
In various embodiments, the PUFA free acid solvent system further comprises one or more species of omega-6 PUFA, each present substantially in the free acid form.
In certain embodiments, the PUFA free acid solvent system comprises one or more species of omega-6 PUFA selected from the group consisting of linoleic acid (C18:2 n-6), gamma-linolenic acid (C18:3 n-6), eicosadienoic acid (C20:2 n-6), dihomo-gamma-linolenic acid (C20:3 n-6) (“DGLA”), arachidonic acid (C20:4 n-6) (“AA”), and docosapentaenoic acid (C22:5 n-6, also known as osbond acid).
In particular embodiments, the PUFA free acid solvent system comprises linoleic acid (C18:2 n-6), gamma-linolenic acid (C18:3 n-6), eicosadienoic acid (C20:2 n-6), dihomo-gamma-linolenic acid (C20:3 n-6) (“DGLA”), arachidonic acid (C20:4 n-6) (“AA”), and docosapentaenoic acid (C22:5 n-6), each present substantially in the free acid form.
In various embodiments, AA, substantially in free acid form, is present in an amount of no more than about 5% (a/a) of the fatty acids in the PUFA free acid solvent system. In certain embodiments, AA, substantially in free acid form, comprises no more than about 4.5% (a/a) of the fatty acids in the PUFA free acid solvent system. In particular embodiments, AA, substantially in free acid form, is present in an amount of no more than about 4% (a/a) of the fatty acids in the PUFA free acid solvent system.
In certain embodiments, AA, substantially in the form of the free acid, is present in an amount of no more than about 5% (m/m) of the fatty acids in the PUFA free acid solvent system. In certain embodiments, AA substantially in free acid form comprises no more than about 4.5% (m/m) of the fatty acids in the PUFA free acid solvent system. In particular embodiments, AA is present substantially in free acid form in an amount of no more than about 4% (m/m) of the fatty acids in the PUFA free acid solvent system.
In certain embodiments, total omega-6 polyunsaturated fatty acids—defined as the sum of linoleic acid (C18:2 n-6), gamma-linolenic acid (C18:3 n-6), eicosadienoic acid (C20:2 n-6), dihomo-gamma-linolenic acid (C20:3 n-6), arachidonic acid (C20:4 n-6) and docosapentaenoic acid (C22:5 n-6), each present substantially in the free acid form—comprise no more than about 10% (a/a) of the fatty acids in the PUFA free acid solvent system. In certain embodiments, total omega-6 polyunsaturated fatty acids comprise no more than about 10% (m/m) of the fatty acids in the PUFA free acid solvent system.
In specific embodiments, the PUFA free acid solvent system is given by Table 1, with each species of PUFA identified therein present substantially in free acid form and within the range of about −3 SD to about +3 SD of the respectively recited average. In certain embodiments, each species of PUFA identified therein is present substantially in free acid form and within the range of about −2 SD to about +2 SD of the respectively recited average. In certain embodiments, each species of PUFA identified therein is present substantially in free acid form and within the range of about −1 SD to about +1 SD of the respectively recited average. In selected embodiments, each species of PUFA identified therein is present substantially in free acid form and in an amount approximating the average amount respectively recited in Table 1.
In certain embodiments, the PUFA free acid solvent system is given by Table 2, with each species of PUFA identified therein present substantially in free acid form and within the range of about −3 SD to about +3 SD of the respectively recited average. In certain embodiments, each species is present substantially in free acid form and within the range of about −2 SD to about +2 SD of the respective average recited in Table 2. In certain embodiments, each PUFA species is present substantially in free acid form and within the range of about −1 SD to about +1 SD of the respectively recited average. In selected embodiments, each species of PUFA identified therein is present substantially in free acid form and in an amount approximating the average amount respectively recited in Table 2.
In certain embodiments, polyunsaturated fatty acids other than omega-3 and omega-6 polyunsaturated fatty acids are present in an amount of no more than about 5% (a/a). In various embodiments, polyunsaturated fatty acids other than omega-3 and omega-6 polyunsaturated fatty acids are present in an amount of no more than about 5% (m/m).
In a variety of embodiments, at least about 90% of each species of omega-3 PUFA present in the PUFA free acid solvent system is present in the free acid form. In certain embodiments, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, even at least 99% of each species of omega-3 PUFA present in the PUFA free acid solvent system is present in the free acid form. In exemplary embodiments, at least 90% of the total omega-3 polyunsaturated fatty acid content in the PUFA free acid solvent system is present in the free acid form. In certain embodiments, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, even at least 99% of the total omega-3 polyunsaturated fatty acid content in the PUFA free acid solvent system is present in the free acid form.
In various embodiments, at least 90% of each species of omega-6 PUFA present in the PUFA free acid solvent system is present in the free acid form. In certain embodiments, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, even at least 99% of each species of omega-6 PUFA in the PUFA free acid solvent system is present in the free acid form. In exemplary embodiments, at least 90% of the total omega-6 polyunsaturated fatty acid content in the PUFA free acid solvent system is present in the free acid form.
In various embodiments, at least 90% of the total polyunsaturated fatty acid content in the PUFA free acid solvent system is present in the free acid form. In certain embodiments, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, even at least 99% of the total polyunsaturated fatty acid in the PUFA free acid solvent system is present in the free acid form.
The PUFA free acid solvent system comprises, in typical embodiments, no more than about 3% (a/a) saturated fatty acids and no more than about 5% (a/a) mono-unsaturated fatty acids. In various embodiments, the PUFA free acid solvent system comprises no more than about 3% (m/m) saturated fatty acids and no more than about 5% (m/m) mono-unsaturated fatty acids.
In typical embodiments, the PUFA free acid solvent system usefully further comprises an antioxidant. In certain embodiments, the antioxidant is butylated hydroxyanisole (BHA). In some embodiments, the antioxidant is alpha-tocopherol. In some embodiments, alpha-tocopherol is present in an amount of about 0.20-about 0.40% (m/m). In various embodiments, alpha-tocopherol is present in an amount of about 0.25-about 0.35% (m/m). In particular embodiments, alpha-tocopherol is present in an amount of about 0.27-about 0.33% (m/m). In typical embodiments, the PUFA free acid solvent system comprises no more than about 0.1 ppm ethyl carbamate. In some embodiments, the PUFA free acid solvent system comprises no more than 0.1 ppm ethyl carbamate. In various embodiments, the PUFA free acid solvent system comprises less than 0.1 ppm ethyl carbamate.
5.2.2. Statins
In various embodiments, at least one statin is present in the pharmaceutical composition in an amount, per ml or per g of PUFA free acid solvent system, of at least about 2 mg, at least about 2.5 mg, at least about 5 mg, at least about 10 mg, at least about 15 mg, at least about 20 mg, at least about 25 mg, at least about 30 mg, at least about 40 mg, at least about 50 mg, at least about 60 mg, at least about 70 mg, at least about 80 mg, at least about 90 mg, even at least about 100 mg, at least about 110 mg, and in certain embodiment, at least about 120 mg.
In selected embodiments, at least one statin is present in the pharmaceutical composition in an amount, per ml or per g of PUFA free acid solvent system, of from about 2 mg to about 80 mg, from about 5 mg to about 60 mg, or from about 10 mg to about 40 mg, or from about 20 mg to about 30 mg.
In various embodiments, the at least one statin is selected from the group consisting of rosuvastatin, pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, and pitavastatin.
In typical embodiments, the at least one statin is dissolved in the PUFA free acid solvent system in an amount that permits administration of a therapeutic amount of statin in a convenient number of oral unit doses, which number of oral unit doses also suffices to deliver a therapeutic dose of omega-3 PUFAs.
Rosuvastatin is marketed under the name Crestor® by Astra Zeneca, Wilmington, Del. In typical embodiments, rosuvastatin is dissolved in the PUFA free acid solvent system in an amount that permits daily administration, in a convenient number of oral doses, of 5 mg, 10 mg, 20 mg, 30 mg, 40 mg, 50 mg, 60 mg, 70 mg, 80 mg, even 90 mg or 100 mg. In particular embodiments, rosuvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, rosuvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
Atorvastatin, which is marketed under the name Lipitor® by Pfizer, New York, N.Y., is hydrophobic and is known as a synthetic statin. In some embodiments, atorvastatin is dissolved in the PUFA free acid solvent system in an amount that permits daily administration, in a convenient number of oral doses, of from 2.5 to 100 mg, from 5 to 80 mg, and from 10 to 40 mg.
In particular embodiments, atorvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, atorvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
Pravastatin, which is marketed as Pravachol® by Bristol-Myers Squibb, Princeton, N.J., is hydrophilic. Administered as monotherapy, pravastatin is best absorbed without food. In some embodiments, pravastatin is dissolved in the PUFA free acid solvent system in an amount that permits daily administration, in a convenient number of oral doses, of from 2.5 to 80 mg, from 5 to 60 mg, or from 10 to 40 mg.
In particular embodiments, pravastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, pravastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
Lovastatin, which is marketed under the name Mevacor® by Merck, Whitehouse Station, N.J., is hydrophobic. In some embodiments, lovastatin is dissolved in the PUFA free acid solvent system in an amount that permits daily administration, in a convenient number of oral doses, of from 2.5 to 100 mg, from 5 to 80 mg, or from 10 to 40 mg.
In particular embodiments, lovastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, lovastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
Simvastatin, which is marketed under the name Zocor® by Merck, Whitehouse Station, N.J., is hydrophobic. In some embodiments, simvastatin is dissolved in the PUFA free acid solvent system in an amount that permits daily administration, in a convenient number of oral doses, of from 1 to 80 mg per day, from 2 to 60 mg, or from 5 to 40 mg per day.
In particular embodiments, simvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, simvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
Fluvastatin, which is marketed under the name Lescol® by Novartis, East Hanover, N.J., is hydrophilic and is known as a synthetic statin. In various embodiments, fluvastatin is dissolved in the PUFA free acid solvent system in an amount that permits daily administration, in a convenient number of oral doses, of from 5 to 160 mg, from 10 to 120 mg, and from 20 to 80 mg.
In particular embodiments, fluvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, fluvastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
Pitavastatin is marketed under the name Livalo® by Kowa Pharmaceuticals America, Inc., Montgomery, Ala. and Lilly USA, Indianapolis, Ind. The dosage of pitavastatin in the pharmaceutical composition can be from 2.5 to 80 mg, from 2.5 to 60 mg, or from 5 to 40 mg.
In particular embodiments, pitavastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 2.5 mg, 5 mg, 10 mg, 15 mg, 20 mg, 25 mg, 30 mg, 35 mg, 40 mg, even 45 mg or 50 mg. In certain embodiments, pitavastatin is dissolved in the PUFA free acid solvent system in an amount, per ml or per g of PUFA solvent system, of 1.25 mg, 2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg, even 25 mg.
In typical embodiments, the pharmaceutical composition comprises a statin which is more soluble in a PUFA free acid solvent system than in a PUFA ethyl ester solvent system. In some embodiments, the pharmaceutical composition comprises a hydrophobic statin which is more soluble in a PUFA free acid solvent system than in a PUFA ethyl ester solvent system. In some embodiments, the pharmaceutical composition comprises a hydrophobic statin which is more soluble in a PUFA free acid solvent system than in a PUFA ethyl ester solvent system.
5.3. Oral Unit Dosage FormsIn another aspect, the pharmaceutical composition is usefully packaged in unit dosage forms for oral administration.
In particular embodiments, the dosage form is a capsule. In certain embodiments, the dosage form is a hard gelatin capsule. In other embodiments, the dosage form is a soft gelatin capsule.
In various embodiments, the capsule comprises Type A gelatin. In certain embodiments, the capsule comprises Type B gelatin. In some embodiments, the capsule comprises both Type A and Type B gelatin. Sources of collagen for the production of either type A or type B gelatin include, but are not limited to, cows, pigs and fish.
In various embodiments, the capsule is a soft gelatin capsule in which at least about 1% (w/w) of the gelatin is Type A gelatin. In certain embodiments, at least about 2% (w/w), 3% (w/w), 4%, (w/w), 5% (w/w), 6% (w/w), 7% (w/w), 8% (w/w), 9% (w/w), or at least about 10% (w/w) of the gelatin is Type A gelatin. In selected embodiments, at least about 15% (w/w), 20% (w/w), 25% (w/w), 30% (w/w), 35% (w/w), 40% (w/w), 45% (w/w), even at least about 50% (w/w), 55% (w/w), 60% (w/w), 65% (w/w), 70% (w/w), 75% (w/w), 80% (w/w), 85% (w/w), 90% (w/w), 95% or more of the gelatin is Type A gelatin.
In particular embodiments, the gelatin of the capsule consists essentially of type A gelatin.
In a selection of embodiments, sufficient Type A gelatin is present such that the capsule, when lacking an exterior coating such as those described below, disintegrates within a time period of not more than 30 minutes in purified water at 37° C. after storage for at least 3 months at 40° C. In certain embodiments, the capsule is a soft gelatin capsule comprising sufficient Type. A gelatin such that the capsule, uncoated, disintegrates within a time period of not more than 30 minutes in purified water at 37° C. after storage for at least 6 months at 40° C.
In various embodiments, the capsule is a soft gelatin capsule comprising sufficient Type A gelatin such that the capsule, when uncoated, disintegrates within a time period of not more than 30 minutes in purified water at 37° C. after storage for at least 3 months at 30° C. In certain embodiments, the capsule is a soft gelatin capsule comprising sufficient Type A gelatin such that the capsule, when not coated, disintegrates within a time period of not more than 30 minutes in purified water at 37° C. after storage for at least 6 months at 30° C. In some embodiments, the capsule is a soft gelatin capsule comprising sufficient Type A gelatin such that the capsule in an uncoated state disintegrates within a time period of not more than 30 minutes in purified water at 37° C. after storage for at least 9 months at 30° C. In some embodiments, the capsule is a soft gelatin capsule comprising sufficient Type A gelatin such that the capsule, if not further coated, disintegrates within a time period of not more than 30 minutes in purified water at 37° C. after storage for at least 12 months at 30° C.
In certain embodiments, the Type A gelatin is porcine Type A gelatin.
In some embodiments, the capsule is a reduced cross-linked gelatin capsule, such as those described in U.S. Pat. No. 7,485,323, incorporated herein by reference in its entirety. In a variety of embodiments, capsules are made from substances that are not animal by-products, such as alginate, agar-agar, carrageenan, pectin, konjak, guar gum, food starch, modified corn starch, potato starch, and tapioca. Non-animal sources of materials that can be used to make capsules are described in U.S. Patent Publication No. 2011/0117180, incorporated herein by reference. In some embodiments, Vegicaps® Capsules (Catalent) are used.
In certain embodiments, the capsule comprises a chemically-modified gelatin. In various embodiments, the chemically-modified gelatin is a succinylated gelatin.
In certain capsular oral unit dosage form embodiments, the capsule is uncoated. In a variety of embodiments, the capsule is coated.
In certain coated capsule embodiments, the capsule is coated with a coating on the exterior of the capsule that causes the encapsulated pharmaceutical composition to be released in a time-dependent manner. In various embodiments, release of the pharmaceutical composition is delayed for at least 15 minutes after ingestion. In particular embodiments, release of the pharmaceutical composition is delayed for at least 30 minutes after ingestion. In other embodiments, release of the fatty acid composition is delayed for about 30 minutes-about 60 minutes after ingestion. In various coated embodiments, the coating is selected from cellulose acetate trimellitate, cellulose acetate phthalate and poly(ethylacrylate-methylacrylate). In some embodiments, the coating is a neutral polyacrylate such as poly(ethylacrylatemethylmethacrylate), such as Eudragit NE 30-D (Evonik Industries AG), which has an average molecular weight of about 800,000.
In certain embodiments, capsules are coated as described in U.S. Pat. Nos. 5,792,795 and 5,948,818, the disclosures of which are incorporated herein by reference. In certain embodiments, the dosage form is a coated soft gelatin capsule comprising porcine type A gelatin, as described in U.S. Pat. No. 7,960,370, incorporated herein by reference.
In various embodiments, the oral unit dosage form contains from about 100 mg to about 2000 mg of the pharmaceutical composition described herein. In some embodiments, the oral dosage form contains about 250 mg of the pharmaceutical composition. In some embodiments, the oral dosage form contains about 500 mg of the pharmaceutical composition. In certain embodiments, the oral dosage form contains about 750 mg of the pharmaceutical composition. In some embodiments, the oral dosage form contains about 1000 mg of the pharmaceutical composition. In other embodiments, the oral dosage form contains about 1500 mg of the pharmaceutical composition. In certain embodiments, the unit dosage form contains nonintegral weight amounts of pharmaceutical composition, typically between 100 mg and 2000 mg.
In some embodiments, the dosage form encapsulates PUFAs in an amount of about 50 mg to about 5000 mg, about 75 mg to about 2500 mg, or about 100 mg to about 1000 mg, for example about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, about 200 mg, about 225 mg, about 250 mg, about 275 mg, about 300 mg, about 325 mg, about 350 mg, about 375 mg, about 400 mg, about 425 mg, about 450 mg, about 475 mg, about 500 mg, about 525 mg, about 550 mg, about 575 mg, about 600 mg, about 625 mg, about 650 mg, about 675 mg, about 700 mg, about 725 mg, about 750 mg, about 775 mg, about 800 mg, about 825 mg, about 850 mg, about 875 mg, about 900 mg, about 925 mg, about 950 mg, about 975 mg, about 1000 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1100 mg, about 1025 mg, about 1050 mg, about 1075 mg, about 1200 mg, about 1225 mg, about 1250 mg, about 1275 mg, about 1300 mg, about 1325 mg, about 1350 mg, about 1375 mg, about 1400 mg, about 1425 mg, about 1450 mg, about 1475 mg, about 1500 mg, about 1525 mg, about 1550 mg, about 1575 mg, about 1600 mg, about 1625 mg, about 1650 mg, about 1675 mg, about 1700 mg, about 1725 mg, about 1750 mg, about 1775 mg, about 1800 mg, about 1825 mg, about 1850 mg, about 1875 mg, about 1900 mg, about 1925 mg, about 1950 mg, about 1975 mg, about 2000 mg, about 2025 mg, about 2050 mg, about 2075 mg, about 2100 mg, about 2125 mg, about 2150 mg, about 2175 mg, about 2200 mg, about 2225 mg, about 2250 mg, about 2275 mg, about 2300 mg, about 2325 mg, about 2350 mg, about 2375 mg, about 2400 mg, about 2425 mg, about 2450 mg, about 2475 mg or about 2500 mg.
In various embodiments, the pharmaceutical composition present in the unit dosage form is stable at room temperature (about 23° C. to 27° C., or about 25° C.) and about 60% relative humidity for a period of at least six months, at least one year, or at least two years. By “stable” is intended that the solubilized statin does not precipitate out of solution to any appreciable degree, for example, in amounts of less than 10%, preferably less than 5%, of the originally dissolved statin.
5.4. Dosage KitsIn another aspect, a plurality of unit dosage forms as above-described may usefully be packaged together in a dosage kit to increase ease of use and patient compliance.
In certain embodiments, the dosage kit is a bottle. In other embodiments, the plurality of dosage forms is packaged in blister packs, a plurality of which blister packs may optionally be packaged together in a box or other enclosure. Typically, whether in a bottle or one or more blister packs, the plurality of unit dosage forms is sufficient for 30 days, 60 days, or 90 days of dosing. Thus, in selected embodiments, in which the unit dosage form is a capsule that encapsulates approximately one gram of the pharmaceutical composition as described herein above, the dosage kit comprises 30, 60, 90, 120, 150, 180, 240, 270, or 300 such capsules.
In various embodiments, the plurality of unit dosage forms is packaged under an inert gas, such as nitrogen or a noble gas, or is packaged under vacuum.
5.5. Dosing and AdministrationIn typical embodiments, the pharmaceutical composition is administered from 1 to 4 times a day, e.g. twice a day, with each dose comprising from 1 to 10 unit doses, such as capsules, as described herein. In typical embodiments, the administration is oral administration, although other routes of administration may be used.
In certain embodiments, at least about 2 g of the pharmaceutical composition is administered per day. In some embodiments, at least about 3 g of the pharmaceutical composition is administered per day. In certain embodiments, at least about 4 g of the pharmaceutical composition is administered per day. Typically, the pharmaceutical is administered as a plurality of unit dosage forms, such as those described above. Thus, in certain embodiments, at least 2 unit dosage forms, each comprising 1 g of the pharmaceutical composition, are administered per day. In various embodiments, at least 3 unit dosage forms, each comprising 1 g of the pharmaceutical composition, are administered per day. In particular embodiments, at least 4 unit dosage forms, each comprising 1 g of the pharmaceutical composition, are administered per day.
5.6. Methods of TreatmentIn another aspect, methods of treating a blood lipid disorder are presented, comprising administering a pharmaceutical composition or compositions as described herein, typically in the form of unit dosage forms as described herein, in an amount and for a duration sufficient to treat the blood lipid disorder. Blood lipid disorders include, but are not limited to hypertriglyceridemia, dyslipidemias, hypercholesterolemia, coronary heart disease (CHD), heart failure, myocardial infarction, cardiac arrhythmias, ischemic dementia, hypertension, coagulation related disorders, nephropathy, retinopathy, vascular disease, atherosclerotic disease and related conditions. Methods of the disclosure are also directed to the treatment and/or prevention and/or reduction of cardiac events, cardiovascular events and symptoms.
The present combination of a statin and omega-3 fatty acids in a single composition may allow for a greater effect than any expected combined or additive effect of the two drugs alone. Moreover, the combined or additive effect of the two drugs may depend on the initial level of lipid parameter in the blood of a subject.
In some embodiments, upon treatment in accordance with the present invention, the subject exhibits an improvement in one or more parameters associated with a blood lipid disorder. Non-limiting examples of such improved parameters are reduced triglyceride levels compared to baseline or placebo control; reduced Apo B levels compared to baseline or placebo control; reduced Apo CIII levels compared to baseline or placebo control; increased HDL-C levels compared to baseline or placebo control; a reduction in LDL-C levels compared to baseline or placebo control; a reduction in non-HDL-C levels compared to baseline or placebo control; a reduction in vLDL levels compared to baseline or placebo control; an increase in Apo A-I levels compared to baseline or placebo control; an increase in Apo A-I/Apo B ratio compared to baseline or placebo control; a reduction in lipoprotein a levels compared to baseline or placebo control; a reduction in LDL particle number compared to baseline or placebo control; a reduction in LDL particle size compared to baseline or placebo control; a reduction in remnant-like particle cholesterol compared to baseline or placebo control; a reduction in oxidized LDL compared to baseline or placebo control; a reduction in fasting plasma glucose (FPG) compared to baseline or placebo control; a reduction in hemoglobin A (HbA) compared to baseline or placebo control; a reduction in homeostasis model insulin resistance compared to baseline or placebo control; a reduction in lipoprotein associated phospholipase A2 compared to baseline or placebo control; a reduction in intracellular adhesion molecule-1 compared to baseline or placebo control; a reduction in interleukin-2 compared to baseline or placebo control; a reduction in plasminogen activator inhibitor-1 compared to baseline or placebo control; a reduction in high sensitivity C-reactive protein (hsCRP) compared to baseline or placebo control; an increase in serum phospholipid EPA compared to baseline or placebo control; an increase in red blood cell membrane EPA compared to baseline or placebo control; a reduction in serum or plasma arachidonic acid (AA) level compared to baseline or placebo control; an increase in plasma or red blood cell membrane EPA/arachidonic acid (AA) ratio; and an increase in omega-3:omega-6 ratio.
Measurements of parameters associated with a blood lipid disorder can be made using methods known in the art. Measurements can be made to determine baseline levels of one or more parameters associated with a blood lipid disorder, prior to treatment, or during the course of treatment.
For example, triglycerides, total cholesterol, HDL-C and fasting blood sugar can be sampled from serum or plasma and analyzed using standard photometry techniques. VLDL-TG, LDL-C and VLDL-C can be calculated or determined using serum lipoprotein fractionation by preparative ultracentrifugation and subsequent quantitative analysis by refractometry or by analytic ultracentrifugal methodology. Apo A1, Apo B and hsCRP can be determined from serum using standard nephelometry techniques. Lipoprotein (a) can be determined from serum using standard turbidimetric immunoassay techniques. LDL particle number and particle size can be determined using nuclear magnetic resonance (NMR) spectrometry. Remnants lipoproteins and LDL-phospholipase A2 can be determined from EDTA plasma or serum and serum, respectively, using enzymatic immunoseparation techniques. Oxidized LDL, intercellular adhesion molecule-1 and interleukin-2 levels can be determined from serum using standard enzyme immunoassay techniques. These techniques are described in detail in standard textbooks, for example Tietz Fundamentals of Clinical Chemistry, 6th Ed. (Burtis, Ashwood and Borter Eds.), WB Saunders Company.
In some embodiments, a subject fasts for up to 12 hours prior to blood sample collection, for example about 10 hours.
5.6.1. Treatment of Severe Hypertriglyceridemia (≧500 mg/dL)
In various embodiments, the method is a method of treating severe (≧500 mg/dL) hypertriglyceridemia, the method comprising orally administering the pharmaceutical composition described herein to a patient having pre-treatment serum or plasma triglyceride levels≧500 mg/dL, in an amount and for a duration effective to reduce serum or plasma triglycerides below pre-treatment levels.
In certain embodiments, the method comprises administering the pharmaceutical composition in an amount and for a duration effective to reduce serum or plasma triglyceride levels by at least about 5%, 6%, 7%, 8%, or at least about 9% below pre-treatment levels. In certain embodiments, the composition is administered in an amount and for a duration effective to reduce serum or plasma triglyceride levels by at least 10%, 11%, 12%, 13%, 14%, 15%, 16%, 17%, 18% or 19% below pre-treatment levels. In particular embodiments, the composition is administered in an amount and for a duration effective to reduce serum or plasma triglyceride levels by at least about 20% below pre-treatment levels. In various embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce serum or plasma triglycerides by at least about 25%, 30%, 35%, 40%, 45%, even at least about 50% below pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce serum or plasma triglyceride levels by at least about 50 mg/dL, 60 mg/dL, 70 mg/dL, 80 mg/dL, 90 mg/dL, even at least about 100 mg/dL. In certain embodiments, the composition is administered in an amount and for a duration effective to reduce serum or plasma triglyceride levels by at least about 110 mg/dL, 120 mg/dL, 130 mg/dL, 140 mg/dL, even at least about 150 mg/dL. In specific embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce serum or plasma triglyceride levels by at least about 160 mg/dL, 170 mg/dL, 180 mg/dL, even at least about 190 mg/dL or 200 mg/dL.
In some embodiments, the pharmaceutical composition described herein is administered in an amount and for a duration sufficient to reduce non-HDL-cholesterol by at least about 1%, at least about 2%, at least about 3%, 4%, 5%, even at least about 7%, 8%, 9%, or at least about 10% below pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce non-HDL-cholesterol by at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40% below pre-treatment levels.
In various embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase HDL-c levels by at least about 1% above pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to increase HDL-c by at least about 2%, 3%, 4%, even at least about 5%, 6%, 7%, 8%, 9%, or 10% above pre-treatment levels.
In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce the total cholesterol:HDL-c (“TC/HDL”) ratio by at least about 1% below pre-treatment levels. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce the TC/HDL ratio by at least about 2%, 3%, 4%, 5%, 6%, 7%, 8%, even at least about 9% or at least about 10% below pre-treatment levels.
In some embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to decrease VLDL-c levels by at least about 5%, 6%, 7%, 8%, 9%, or at least about 10% below pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to decrease VLDL-c levels by at least about 11%, 12%, 13%, 14%, 15%, 16%, 17%, even at least about 18%, 19%, or 20% below pre-treatment levels. In particular embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to decrease VLDL-c levels by at least about 21%, 22%, 23%, 24%, even at least about 25% below pre-treatment levels.
In a variety of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to decrease ApoCIII levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to decrease ApoCIII levels by at least about 1%, 2%, 3%, 4%, 5%, 6%, 7%, even at least about 8%, 9% or 10% below pre-treatment levels.
In some embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma EPA levels by at least 100% above pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma EPA levels by at least about 200%, 250%, 300%, even at least about 350%, 400%, 450% or at least about 500% above pre-treatment levels. In selected embodiments, the pharmaceutical composition is administered for a time and in an amount effective to increase plasma EPA levels by at least about 550%, 600%, 650%, even at least about 700% above pre-treatment levels.
In various embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DHA levels by at least about 50% above pre-treatment levels. In particular embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DHA levels by at least about 55%, 60%, 65%, 70%, even at least about 75%, 80%, 85%, or 90% above pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DPA levels by at least about 50% above pre-treatment levels. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DPA levels by at least about 55%, 60%, 65%, 70%, 75%, even at least about 80%, 85%, 90%, 95%, or 100% above pre-treatment levels. In selected embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DPA levels by at least about 110%, 120%, even at least about 125% above pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce arachidonic acid (AA) concentration in plasma by at least about 5% below pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce arachidonic (AA) concentration in plasma by at least about 6%, 7%, 8%, 9%, 10%, even at least about 11%, 12%, 13%, 14%, even at least about 15%, 16%, 17%, 18%, 19%, 20%, or 21%, 22%, 23%, 24% even at least about 25% below pre-treatment levels.
In certain embodiments, the pharmaceutical composition is administered in an amount, and for a duration, effect to reduce plasma arachidonic acid concentration by at least about 25 μg/mL. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce plasma AA levels by at least about 50 μg/mL, 55 μg/mL, 60 μg/mL, 65 μg/mL, even at least about 70 μg/mL, 75 μg/mL, 80 μg/mL, 85 μg/mL, 90 μg/mL, even at least about 95 μg/mL or 100 μg/mL.
In certain embodiments, the effective amount is at least about 2 g per day. In various embodiments, the effective amount is at least about 3 g per day. In particular embodiments, the effective amount is at least about 4 g per day. In typical embodiments, the effective amount is about 2 g per day. In certain embodiments, the effective amount is about 4 g per day.
In typical embodiments, the pharmaceutical composition is administered for at least 30 days. In certain embodiments, the pharmaceutical composition is administered for at least 60 days. In particular embodiments, the pharmaceutical composition is administered for at least 90 days, 120 days, 180 days, 240 days, or at least 360 days. In certain embodiments, the pharmaceutical composition is administered indefinitely.
In some embodiments, the pharmaceutical composition is administered daily. In other embodiments, the pharmaceutical composition is administered every other day.
In particular embodiments, the daily dosage of pharmaceutical composition is administered in a single daily dose. In other embodiments, the pharmaceutical composition is administered in divided doses, with the daily dose divided into two administrations, three administrations, or even four administrations, over the course of the day.
In certain embodiments, the pharmaceutical composition is administered with food. In certain embodiments, the pharmaceutical composition is administered with a low fat meal. In other embodiments, the pharmaceutical composition is administered without food. In certain embodiments, the pharmaceutical composition is administered in the fasting state.
5.6.2. Treatment of Hypertriglyceridemia (200-500 Mg/dL)
In another series of treatment embodiments, methods are provided for treating patients who have pre-treatment serum or plasma triglyceride levels of about 200 mg/dL to about 500 mg/dL. In certain embodiments, the patients are already on statin therapy; in these patients, the pre-treatment serum or plasma triglyceride levels are those measured during statin treatment, prior to administration of the pharmaceutical compositions described herein.
The method comprises orally administering the pharmaceutical composition described herein to a patient having pre-treatment serum or plasma triglyceride levels of about 200 mg/dL to about 500 mg/dL, in an amount and for a duration effective to reduce serum or plasma triglycerides below pre-treatment levels.
In certain embodiments, the pharmaceutical composition described herein is administered in an amount and for a duration sufficient to reduce serum or plasma triglyceride levels by at least about 5% below pre-treatment levels. In various embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce serum or plasma triglyceride levels by at least about 6%, 7%, 8%, 9%, 10%, 11%, 12%, 13%, 14%, 15%, even at least about 16%, 17%, 18%, 19%, or at least about 20% below pre-treatment levels.
In some embodiments, the pharmaceutical composition described herein is administered in an amount and for a duration sufficient to reduce non-HDL-cholesterol by at least about 1%, at least about 2%, at least about 3%, 4%, 5%, even at least about 7%, 8%, 9%, or at least about 10% below pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce non-HDL-cholesterol by at least about 15%, at least about 20%, at least about 25%, at least about 30%, at least about 35%, at least about 40% below pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to raise HDL-c levels by at least about 1%, 2%, 3%, 4%, 5%, 6%, 7%, even at least about 8%, 9%, or 10% or more above pre-treatment levels.
In some embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma EPA levels by at least 100% above pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma EPA levels by at least about 200%, 250%, 300%, even at least about 350%, 400%, 450% or at least about 500% above pre-treatment levels. In selected embodiments, the pharmaceutical composition is administered for a time and in an amount effective to increase plasma EPA levels by at least about 550%, 600%, 650%, even at least about 700% above pre-treatment levels.
In various embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DHA levels by at least about 50% above pre-treatment levels. In particular embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DHA levels by at least about 55%, 60%, 65%, 70%, even at least about 75%, 80%, 85%, or 90% above pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DPA levels by at least about 50% above pre-treatment levels. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DPA levels by at least about 55%, 60%, 65%, 70%, 75%, even at least about 80%, 85%, 90%, 95%, or 100% above pre-treatment levels. In selected embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DPA levels by at least about 110%, 120%, even at least about 125% above pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce arachidonic acid (AA) concentration in plasma by at least about 5% below pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce arachidonic (AA) concentration in plasma by at least about 6%, 7%, 8%, 9%, 10%, even at least about 11%, 12%, 13%, 14%, even at least about 15%, 16%, 17%, 18%, 19%, 20%, or 21%, 22%, 23%, 24% even at least about 25% below pre-treatment levels.
In certain embodiments, the pharmaceutical composition is administered in an amount, and for a duration, effect to reduce plasma arachidonic acid concentration by at least about 25 μg/mL. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce plasma AA levels by at least about 50 μg/mL, 55 μg/mL, 60 μg/mL, 65 μg/mL, even at least about 70 μg/mL, 75 μg/mL, 80 μg/mL, 85 μg/mL, 90 μg/mL, even at least about 95 μg/mL or 100 μg/mL.
In various embodiments, the pharmaceutical composition described in Section 5.2 herein is administered in unit dosage forms as described in Section 5.3 above.
In various embodiments, the pharmaceutical composition is administered in an amount of at least about 1 g per day. In some embodiments, the pharmaceutical composition is administered in an amount of at least about 2 g/day. In certain embodiments, the pharmaceutical composition is administered in an amount of at least about 3 g/day. In particular embodiments, the pharmaceutical composition is administered in an amount of at least about 4 g/day. In typical embodiments, the pharmaceutical composition is administered in an amount of about 2 g/day. In certain embodiments, the pharmaceutical composition is administered in an amount of about 3 g/day or about 4 g per day.
5.6.3. Treatment of Primary Hyperlipidemia or Mixed Dyslipidemia
In a series of treatment embodiments, methods are provided for treating patients who have primary hyperlipidemia or mixed dyslipidemia. The method comprises orally administering the pharmaceutical composition described herein to a patient having primary hyperlipidemia or mixed dyslipidemia, in an amount and for a duration effective to reduce one or more of elevated total-cholesterol, elevated LDL-C, elevated ApoB, non-HDL-C, and elevated triglyceride levels, and/or to increase HDL-C.
In various embodiments, the pharmaceutical composition is administered in an amount of at least about 1 g per day. In some embodiments, the pharmaceutical composition is administered in an amount of at least about 2 g/day. In certain embodiments, the pharmaceutical composition is administered in an amount of at least about 3 g/day. In particular embodiments, the pharmaceutical composition is administered in an amount of at least about 4 g/day. In typical embodiments, the pharmaceutical composition is administered in an amount of about 2 g/day. In certain embodiments, the pharmaceutical composition is administered in an amount of about 3 g/day or about 4 g per day.
5.6.4. Treatment to Increase Plasma EPA:AA Ratios
Methods are also provided for increasing the EPA:AA ratio. The methods comprise administering the pharmaceutical composition described in Section 5.2 herein to a patient having an EPA:AA ratio below about 0.25, in an amount and for duration sufficient to increase the patient's EPA:AA ratio to at least about 0.25. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to increase the patient's EPA:AA ratio to at least about 0.3, at least about 0.35, at least about 0.40, at least about 0.45, at least about 0.50, even to a level of at least about 0.55, 0.60, 0.61, 0.62, 0.63, 0.64, or 0.65.
In certain embodiments, the method comprises administering the pharmaceutical composition in an amount and for a duration effective to increase plasma EPA levels by at least 100% above pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma EPA levels by at least about 200%, 250%, 300%, even at least about 350%, 400%, 450% or at least about 500% above pre-treatment levels. In selected embodiments, the pharmaceutical composition is administered for a time and in an amount effective to increase plasma EPA levels by at least about 550%, 600%, 650%, even at least about 700% above pre-treatment levels.
In various embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DHA levels by at least about 50% above pre-treatment levels. In particular embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to increase plasma DHA levels by at least about 55%, 60%, 65%, 70%, even at least about 75%, 80%, 85%, or 90% above pre-treatment levels.
In a series of embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce arachidonic acid (AA) concentration in plasma by at least about 5% below pre-treatment levels. In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration effective to reduce arachidonic (AA) concentration in plasma by at least about 6%, 7%, 8%, 9%, 10%, even at least about 11%, 12%, 13%, 14%, even at least about 15%, 16%, 17%, 18%, 19%, 20%, or 21%, 22%, 23%, 24% even at least about 25% below pre-treatment levels.
In certain embodiments, the pharmaceutical composition is administered in an amount, and for a duration, effect to reduce plasma arachidonic acid concentration by at least about 25 μg/mL. In some embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to reduce plasma AA levels by at least about 50 μg/mL, 55 μg/mL, 60 μg/mL, 65 μg/mL, even at least about 70 μg/mL, 75 μg/mL, 80 μg/mL, 85 μg/mL, 90 μg/mL, even at least about 95 μg/mL or 100 μg/mL.
In various embodiments, the pharmaceutical composition described in Section 5.2 herein is administered in unit dosage forms as described in Section 5.3 above.
In various embodiments, the pharmaceutical composition is administered in an amount of at least about 1 g per day. In some embodiments, the pharmaceutical composition is administered in an amount of at least about 2 g/day. In certain embodiments, the pharmaceutical composition is administered in an amount of at least about 3 g/day. In particular embodiments, the pharmaceutical composition is administered in an amount of at least about 4 g/day. In typical embodiments, the pharmaceutical composition is administered in an amount of about 2 g/day. In certain embodiments, the pharmaceutical composition is administered in an amount of about 3 g/day or about 4 g per day.
5.6.5. Treatment to Lower Serum or Plasma ApoCIII Levels
Methods are also provided for increasing a patient's serum or plasma ApoCIII levels, without regard to the patient's pre-treatment plasma triglyceride levels. The methods comprise administering the pharmaceutical composition described in Section 5.2 herein to a patient in need of lower ApoCIII levels, in an amount and for duration sufficient to decrease the patient's serum or plasma ApoCIII levels. In typical embodiments, the patient is at risk for cardiovascular heart disease.
In certain embodiments, the pharmaceutical composition is administered in an amount and for a duration sufficient to decrease ApoCIII levels by at least about 1%, 2%, 3%, 4%, 5%, 6%, 7%, even at least about 8%, 9% or 10% below pre-treatment levels.
5.6.6. Other Methods of Treatment
In another aspect, the pharmaceutical compositions described herein is used to treat other disorders, including one or more of nonalcoholic steatohepatitis (NASH), hyperlipoproteinemia, including type III hyperlipoproteinemia, and metabolic syndrome.
In certain embodiments, the pharmaceutical composition is used to reduce resistance to platelet aggregation inhibitors, such as Plavix, including use in the methods described in U.S. patent application Ser. No. 13/620,312, the disclosure of which is incorporated herein by reference in its entirety.
6. EXAMPLES Example 1 Solubility of Statins in Various pH Buffers50 mg of atorvastatin was added to 5 mL of water, 0.1N NaCl, 0.1N NaOH, 0.1N HCl (pH 1.2), acid phthalate buffer (pH 2.2), acid phthalate buffer (pH 4.0), neutralized phthalate buffer (pH 5.0), phosphate buffer (pH 7.0), or alkaline borate buffer (pH 9.0). The solutions were sonicated for 10 minutes and allowed to sit overnight. Aliquots of the sample solutions were centrifuged and an aliquot of the supernatant from each sample was assayed for atorvastatin solubility. Samples were then allowed to sit for 1 week when they were again assayed to determine atorvastatin solubility. The results of solubility measurements are displayed in Table 3.
50 mg of rosuvastatin was added to 5 mL of water, 0.1N NaCl, 0.1N NaOH, 0.1N HCl (pH 1.2), acid phthalate buffer (pH 2.2), acid phthalate buffer (pH 4.0), neutralized phthalate buffer (pH 5.0), phosphate buffer (pH 7.0), or alkaline borate buffer (pH 9.0). The solutions were sonicated for 10 minutes and allowed to sit overnight. Aliquots of the sample solutions were centrifuged and an aliquot of the supernatant from each sample was assayed for rosuvastatin solubility. Samples were then allowed to sit for 1 week when they were again assayed to determine rosuvastatin solubility. The results of solubility measurements are displayed in Table 3.
The results showed that Rosuvastatin displayed significant aqueous solubility at time zero, with the maximal solubility at about pH 7.0. Atorvastatin showed a lower overall aqueous solubility than rosuvastatin, but the solubility also displayed a maximum at pH 7.0.
Example 2 Solubility of Statins in PUFA Free Acid Solvent SystemSamples of 20-30 mg of atorvastatin and 20-30 mg of rosuvastatin were each dissolved in 2 g of a PUFA free acid solvent system. The composition of the solvent system is given in Table 4, below (batch #37225).
Initial solubility was measured, and results of solubility measurement are displayed in Table 5.
20 mg of atorvastatin and 20 mg of rosuvastatin were each added to 2 g of fill extracted from capsules of Lovaza, in which the PUFA species are present substantially in the ethyl ester form. The samples were then sonicated for 1 hour and incubated overnight, after which they displayed excess un-dissolved solids. The samples were centrifuged and the supernatant assayed by HPLC for the respective statin. The results of the solubility measurement are displayed in Table 6. As is apparent from comparing Tables 5 and Table 6, atorvastatin and rosuvastatin were solubilized to a significantly greater extent in a PUFA free acid solvent system than in a PUFA ethyl ester solvent system.
Solubility of atorvastatin calcium, rosuvastatin calcium, simvastatin, pitavastatin calcium, and pravastatin sodium was evaluated in both a PUFA free acid solvent system (see Table 4) and a PUFA ethyl ester solvent system (Lovaza).
For this study, ten vials were prepared such that 5 vials contained 2 mL of Lovaza oil and 5 vials contained 2 mL of PUFA free acid solvent system. About 20 mg of each statin were added to one Lovaza oil vial and to one PUFA free acid solvent system vial. Vials containing the samples were blanketed with nitrogen, then sealed. The vials were then sonicated for 1 hour or until contents appeared clear. After sonication, vials which remained clear received additional 20 mg aliquots of their respective statin and were again blanketed with nitrogen. The process was repeated until all vials contained un-dissolved statin, with the exception of the pravastatin sodium in PUFA free acid solvent, which, after the addition of about 313 mg of pravastatin sodium, still remained clear. The samples were allowed to sit overnight, after which all samples were observed to contain un-dissolved statins. The samples were centrifuged and the supernatant was assayed for the respective statin by HPLC. Assay results are shown in Table 7 below.
All of the tested statins displayed markedly higher solubility in the PUFA free fatty solvent system as compared to the PUFA ethyl ester solvent system.
Example 5 Stability Testing of Statins Dissolved in Omega-3 Free Fatty AcidsThe stability of atorvastatin calcium and rosuvastatin calcium solubilized in a PUFA free acid solvent system was evaluated over the course of four weeks under 25° C., 60% relative humidity (RH) storage conditions.
Three batch formulations were prepared in parallel, by adding a sufficient amount of PUFA free acid solvent system to (i) 2.0 g of atorvastatin calcium, (ii) 2.0 g of rosuvastatin calcium, and (iii) no statin (control), to fill a 200 mL vessel, followed by blanketing of the solution with nitrogen and capping of the vessel. The compositions were then mixed until full dissolution was observed, using a magnetic stir bar and sonication for 30-60 second intervals, taking care to maintain a nitrogen headspace over the solution throughout processing.
Each statin-solvent system solution and the control solvent system were each respectively aliquoted into nine separate 20 mL Type I borosilicate vials, which were then blanketed with nitrogen, capped with a Teflon-coated serum stopper, and crimp sealed. Vials were covered with foil to protect from light and stored at 25° C., 60% RH.
One vial of each of the three compositions was retrieved at each timepoint for testing. Procedures as listed in the USP Monograph for Omega-3-Acid Ethyl Ester Capsules were followed for measuring quantities of acid value, peroxide value, and absorbance for fats and fixed oils. The results are shown in Tables 8 and 9, below.
After pH adjustment, the two peaks were shown to reduce to a single peak of intact statin. No significant degradation was observed.
All publications, patents, patent applications and other documents cited in this application are hereby incorporated by reference in their entireties for all purposes to the same extent as if each individual publication, patent, patent application or other document were individually indicated to be incorporated by reference for all purposes.
While various specific embodiments have been illustrated and described, it will be appreciated that various changes can be made without departing from the spirit and scope of the invention(s).
Claims
1. A pharmaceutical composition comprising a statin dissolved in a PUFA free acid solvent system.
2. The pharmaceutical composition according to claim 1, wherein no more than about 10% by weight of the statin is undissolved in the solvent system.
3. The pharmaceutical composition according to claim 1, wherein the statin is dissolved in the PUFA free acid solvent system at a concentration of at least about 5 mg statin per gram solvent system.
4. The pharmaceutical composition according to claim 3, wherein the statin is dissolved in the PUFA free acid solvent system at a concentration of at least about 7.5 mg/g.
5. The pharmaceutical composition according to claim 4, wherein the statin is dissolved in the PUFA free acid solvent system at a concentration of at least about 10 mg/g.
6. The pharmaceutical composition according to claim 5, wherein the statin is dissolved in the PUFA free acid solvent system at a concentration of at least about 20 mg/g.
7. The pharmaceutical composition according to claim 1, wherein the statin is selected from the group consisting of pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, rosuvastatin, and pitavastatin.
8. The pharmaceutical composition according to claim 7, wherein the statin is rosuvastatin.
9. The pharmaceutical composition according to claim 7, wherein the statin is atorvastatin.
10. The pharmaceutical composition according to claim 7, wherein the statin is simvastatin.
11. The pharmaceutical composition according to claim 1, wherein the PUFA free acid solvent system comprises EPA.
12. The pharmaceutical composition according to claim 11, wherein EPA is present in the PUFA free acid solvent system in an amount of at least about 40% (a/a).
13. The pharmaceutical composition according to claim 12, wherein DHA is present in the PUFA free acid solvent system in an amount of at least about 13% (a/a).
14. The pharmaceutical composition according to claim 13, wherein DPA (C22:5 n-3) is present in the PUFA free acid solvent system in an amount of at least about 1% (a/a).
15. The pharmaceutical composition according to claim 14, wherein the PUFA free acid solvent system comprises about 45% (a/a) to about 65% (a/a) EPA, about 15% (a/a) to about 25% (a/a) DHA, and about 1% (a/a) to about 8% (a/a) DPA (C22:5 n-3).
16. The pharmaceutical composition according to claim 1, wherein the PUFA free acid solvent system comprises no more than about 10% (a/a) omega-6 fatty acids in free acid form.
17. An oral unit dosage form, wherein the dosage form comprises a capsule, the capsule containing a pharmaceutical composition according to claim 1.
18. The oral unit dosage form according to claim 17, wherein the capsule comprises gelatin.
19. The oral unit dosage form according to claim 18, wherein the capsule is a soft gelatin capsule.
20. The oral unit dosage form of claim 19, wherein the soft gelatin capsule comprises Type A gelatin.
21. The oral unit dosage form of claim 20, wherein at least about 1% (w/w) of the gelatin is Type A gelatin.
22. The oral unit dosage form of claim 21, wherein the type A gelatin is porcine type A gelatin.
23. The oral unit dosage form of claim 17, further comprising a coating on the exterior of the capsule.
24. The oral unit dosage form according to claim 23, wherein the coating is a pH-sensitive enteric coating.
25. The oral unit dosage form according to claim 23, wherein the coating is a pH-insensitive coating.
26. The oral unit dosage form according to claim 25, wherein the coating is a poly(ethylacrylate-methylacrylate) copolymer.
27. The oral unit dosage form according to claim 26, wherein the coating is Eudragit NE-30 D.
28. The oral unit dosage form according to claim 17, wherein the capsule contains about 1 to about 100 mg of a statin dissolved in about 500 mg to about 1 g of a PUFA free acid solvent system.
29. The oral unit dosage form according to claim 28, wherein the capsule contains about 2.5 mg to about 40 mg of a statin dissolved in about 1 g of a PUFA free acid solvent system.
30. The oral unit dosage form of claim 17, wherein the statin is rosuvastatin.
31. The oral unit dosage form of claim 17, wherein the statin is atorvastatin.
32. The oral unit dosage form of claim 17, wherein the statin is simvastatin.
33. A method of treating a blood lipid disorder, comprising administering a pharmaceutical composition according to claim 1 to a subject with a blood lipid disorder in an amount and for a duration sufficient to treat the blood lipid disorder.
34. The method according to claim 33, wherein the blood lipid disorder is selected from the group consisting of: hypertriglyceridemia, hyperlipidemia, hypercholesterolemia, mixed dyslipidemia, and atherosclerosis.
35. The method according to claim 33, wherein the method comprises administering at least 2 g of the pharmaceutical composition daily.
36. The method according to claim 35, wherein the method comprises administering at least about 10 mg of statin daily.
37. The method according to claim 33, wherein the PUFA free acid solvent system of the pharmaceutical composition comprises at least about 45% (a/a) EPA.
38. The method according to claim 37, wherein the statin in the pharmaceutical composition is rosuvastatin.
39. The method according to claim 37, wherein the statin in the pharmaceutical composition is atorvastatin.
40. The method according to claim 37, wherein the statin in the pharmaceutical composition is simvastatin.
Type: Application
Filed: May 7, 2013
Publication Date: Nov 7, 2013
Inventors: Bernardus N M MACHIELSE (North Potomac, MD), Timothy J. Maines (Potomac, MD), Bharat M. Mehta (Mendham, NJ), Michael H. Davidson (Highland Park, IL)
Application Number: 13/889,202
International Classification: A61K 31/505 (20060101); A61K 31/22 (20060101); A61K 31/366 (20060101); A61K 31/47 (20060101); A61K 31/202 (20060101); A61K 31/40 (20060101);
