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MXPA01012225A - Novel formulations comprising lipid-regulating agents. - Google Patents

Novel formulations comprising lipid-regulating agents.

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Publication number
MXPA01012225A
MXPA01012225AMXPA01012225AMXPA01012225AMXPA01012225AMX PA01012225 AMXPA01012225 AMX PA01012225AMX PA01012225 AMXPA01012225 AMX PA01012225AMX PA01012225 AMXPA01012225 AMX PA01012225AMX PA01012225 AMXPA01012225 AMX PA01012225A
Authority
MX
Mexico
Prior art keywords
composition
further characterized
composition according
excipient
lipid regulating
Prior art date
Application number
MXPA01012225A
Other languages
Spanish (es)
Inventor
Devalina Law
Original Assignee
Abbott Lab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Abbott LabfiledCriticalAbbott Lab
Publication of MXPA01012225ApublicationCriticalpatent/MXPA01012225A/en

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Abstract

The present invention is directed to a solid formulation comprising the mixture of a lipid-regulating agent and an excipient, in which said agent and said excipient form a eutectic mixture.

Description

FORM ULACION IS NOVEDOSAS WHAT THEY BUY D IN AGENTS REGÍADORES DE LÍPI DOCAM PO OF THE INVENTIONThe present invention relates to novel formulations comprising lipid regulating agents.
BACKGROUND OF THE INVENTIONThe 2- [4- (4-chlorobenzoyl) phenoxy] -2-methylpropanoic acid methyl ester, also known as fenofibrate, is representative of a broad class of compounds which have pharmaceutical utility as lipid regulating agents. More specifically, this compound is part of a class of compounds lipid regulating agents, commonly known as fibrates, and is described in US Patent No. 4,058,552. Fenofibrate has been prepared in several different formulations; see U.S. Patent No. 4,800,079 and U.S. Patent No. 4,895,726. U.S. Patent 4,895,726 describes a co-micronized formulation of fenofibrate and a solid surfactant. U.S. Patent No. 4,961,890 describes a process for preparing a controlled release formulation,. a.tj containing fenofibrate in an intermediate layer, in the form of crystalline microparticles included within the pores of an inert matrix. The formulation is prepared by a process comprising the sequential steps of wetting the inert core with a solution based on the binder; then project the fenofibrate microparticles in a single layer, over the moistened core, and then dry before the binder-based solution dissolves the fenofibrate particles, and repeat these three steps in sequence until the intermediate layer is formed. European Patent Application No. EPO 793958 A2 describes a process for producing a solid dosage form of fenofibrate, which uses fenofibrate, a surfactant and polyvinylpyrrolidone, where the fenofibrate particles are mixed with a solution of polyvinylpyrrolidone. The mixture thus obtained is granulated with an aqueous solution of one or more surfactants, and the granules thus produced are dried. The publication of TCP No. WO 82/01649 describes a fenofibrate formulation having granules consisting of a neutral core which is a mixture of sucrose and starch. The neutral core is covered with a first layer of fenofibrate, mixed with an excipient, and with a second microporous outer layer of an edible polymer. U.S. Patent No. 5,645,856 describes the use of a carrier for hydrophobic drugs, which includesJ iiU fenofibrate; and pharmaceutical compositions based thereon. The carrier comprises a digestible oil and a pharmaceutically acceptable surfactant component to disperse the oil in vivo when the carrier is administered; comprising a hydrophobic surfactant agent; the surfactant component being such that it does not substantially inhibit the in vivo lipolysis of the digestible oil. Sheu, M. T. and co-authors, Int. J. Pharma. , 103 (1994) 1 37-146, reported that it is possible that the increase in the rate of dissolution, obtained by PEG 6000, could be due to the10 Reduction in particle size and / or increase in wetting capacity. Palmieri, G. F., Pharma Sciences 6 (1966), 188-194, reported that solid drug solutions are formed when the amount of fenofibrate present in the powder is less than 15%.15 percent, and the solubility of the drug is increased by the formation of a solid dispersion, particularly for the carrier: drug ratio of 90: 1. Gemfibrozi is another member of the fibrate class of lipid regulating agents. U.S. Patent No.
No. 4,927,639 discloses a disintegrable gemfibrozil formulation, which provides both immediate and sustained release, comprising a tablet compressed from a mixture of a first and a second granulation, and a disintegrating excipient operable to effect partial or complete disintegration in the25 stomach. The first granulation comprises particles finely^ ^. ^ aa. .i »-. divided from pure gemfibrozil, granulated with at least one cellulose derivative; and the second granulation comprises finely divided particles of pure gemfibrozil, granulated with a pharmaceutically acceptable, water soluble or insoluble polymer, which is then uniformly coated with a pharmaceutically acceptable (meth) acrylate copolymer, before being mixed with the first granulation. The first and second granulations are present in the final composition in an approximate ratio of 10: 1 to 1:10. U.S. Patent No. 4,925,676 discloses a disintegrable gemfibrozil tablet that provides immediate and enteric release, which is compressed from a mixture of a first granulation of gemfibrozil with at least one binder disintegrable with acid, and a second granulation formed from the first granulation, but again granulated or coated with an alkali-disintegrable formulation, of at least one polymer substantially soluble in alkali and substantially insoluble in acid. Another class of lipid regulating agents is commonly known as statins, of which pravastatin and atorvastatin are members. U.S. Patents 5,030,447 and 5,180,589 describe stable pharmaceutical compositions which, when dispersed in water, have a pH of at least 9, and include a medicament that is sensitive to a low pH environment, such as pravastatin; one or more fillers, such as lactose and / or microcrystalline cellulose; one or more binders, such as microcrystalline cellulose (dry binder) or polyvinylpyrrolidone (wet binder); one or more disintegrating agents, such as croscarmellose sodium; one or more lubricants, such as magnesium stearate, and one or more basifying agents, such as magnesium oxide. It is an object of the present invention to provide formulations of lipid regulating agents having increased bioavailability, as compared to commercially available formulations.
BRIEF DESCRIPTION OF THE INVENTIONThe present invention is directed to a solid formulation comprising the mixture of a lipid regulating agent and an excipient, such as polyethylene glycol, in which the agent and excipient form a eutectic mixture. The reduction in size obtained during the preparation of a dispersion is usually difficult to obtain. However, using a melting technique or a solvent evaporation technique, a dispersion of the crystalline lipid regulating agent is prepared in the excipient; so that the agent and the excipient form a eutectic mixture.
The resulting formulation results in an increase in the solubility of the drug and oral bioavailability, and an improved dissolution rate.
"- • - • - '^ -» "- The formulation can be administered directly, diluted in a suitable vehicle for administration, encapsulated in hard gelatin capsules or capsules, or compressed to tablets for administration; or it can be administered by other means, obvious to those who are experts in the field.
BRIEF DESCRIPTION OF THE DRAWINGSFigure 1 is a graph showing plasma concentration in dogs fed the formulation of Example 1 and with a reference compound.
DETAILED DESCRIPTION OF THE INVENTIONThe bulk lipid regulating agent can be prepared by any available means, such as, for example, the fenofibrate compound can be prepared by the process described in US Patent No. 4,058,552, or by the process described in U.S. Patent No. 4,739,101, both incorporated here by means of this reference. The composition comprising the lipid regulating agent and the excipient is first determined, in such a ratio, that the melting point of the lipid regulating agent and the excipient are reduced to a single value, below the melting point1 j.of any of the components. This composition, that is, the composition in which the two components exhibit a single melting point, is called a eutectic mixture. A composition of the lipid regulating agent and excipient, ranging from about 0.5% (w / w) to 10% above the eutectic mixture, is then heated to a temperature sufficient to obtain a clear solution. Then the solution is cooled until a solid mass is formed. As an alternative method, these components in the composition scale10 mentioned above can be dissolved in a suitable solvent to obtain a clear solution. In this last case it is necessary to separate the solvent to obtain the solid mass. The solid mass is then ground, brought to the desired size and, optionally, formulated into an appropriate delivery system. The delivery system of the present invention results in an increased dissolution rate and greater bioavailability, and an improved dissolution rate of the lipid regulating agent. The term "eutectic mixture" refers to a system20 biphasic crystalline having a melting point that is lower than that of any of the pure components of the mixture. The presence of a eutectic mixture can be determined by thermal analysis and X-ray powder diffractometry. Suitable excipients include, for example:25 polyethylene glycol (PEG), pentaerythritol, pentaerythritol tetraacetate,S &R-S succinic acid, urea, polyoxyethylene stearates and poly-e-caprolactone or, more preferably, PEG. If a solvent evaporation technique is used, suitable solvents include, for example: methanol-water, ethanol-water or other water-miscible organic solvent, in which the lipid-regulating agent and the polymers have appreciable solubility. Other pharmaceutically acceptable excipients may be added to the formulation before forming the desired final product. Suitable excipients include, for example, lactose, starch, magnesium stearate or other fillers, other diluents, lubricants or pharmaceutically acceptable disintegrants, which may be necessary to prepare a capsule or tablet. The resulting composition comprising the lipid regulating agent can be dosed directly for oral administration, can be diluted in a vehicle suitable for oral administration, can be introduced into capsules or formed into tablets for oral administration, or can be supplied by other obvious means for those who are experts in the field. Said composition can be used to improve oral bioavailability and solubility of the lipid regulating agent. The invention will be understood more clearly from the following representative, non-limiting examples:EXAMPLE 1Fenofibrate and PEG were heated at a ratio of 15:85, at about 85 ° C until a clear solution was obtained. The solution was then cooled on an ice bath, which resulted in the formation of a solid mass. The resulting dry, solid mass was then ground and milled to a size passing through a 60-100 mesh screen. 446.7 mg of the granulated formulation (containing 67 mg fenofibrate) was introduced into10 individual capsulesEXAMPLE 2Mixtures of a statin and PEG are prepared and the melting point of each of these mixtures is determined to locate the eutectic composition. The statin and PEG are then melted in a ratio which, preferably, is approximately 10 percent greater than the eutectic composition, to obtain a clear solution; The solution is then cooled in an ice bath to form a solid mass. This solid mass is milled and sieved between 60 and 100 mesh, and filled into capsules containing the appropriate desired dose.
EXAMPLE 3 25* -wr i _J Capsules prepared by the process described in Example 1 were administered, and from a commercial composition of fenofibrate, Lipanthyl 67M (Groupe Fournier) (as a reference), to a group of dogs, at a dose of 67 mg fenofibrate / dog. The concentrations of fenofibric acid in the plasma were determined by means of HPLC. The concentrations were normalized at a dose of 6.7 mg / kg in each dog. Figure 1 presents the resulting data in the form of a graph. The results provided as the mean ± standard deviation were the following: 10 Lipanthyl 67M (reference): Cmax = 2.83 ± 1.40 mcg / ml Tmax = 1.7 ± 0.6 hr t1 / 2 = 14.5 hr AUC (0-24) = 16.36 ± 6.93 mcg.hr/ml 15 Capsule of example 1: Cmax = 5.20 ± 1.15 mcg / ml Tmax = 1.3 ± 0.6 hr t1 / 2 = 10.8 hr AUC in relation to the reference = 149.08%& "R -" "-f ?? - k

Claims (11)

MXPA01012225A1999-05-282000-05-23Novel formulations comprising lipid-regulating agents.MXPA01012225A (en)

Applications Claiming Priority (2)

Application NumberPriority DateFiling DateTitle
US32318399A1999-05-281999-05-28
PCT/US2000/014109WO2000072829A1 (en)1999-05-282000-05-23Novel formulations comprising lipid-regulating agents

Publications (1)

Publication NumberPublication Date
MXPA01012225Atrue MXPA01012225A (en)2002-08-12

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Family Applications (1)

Application NumberTitlePriority DateFiling Date
MXPA01012225AMXPA01012225A (en)1999-05-282000-05-23Novel formulations comprising lipid-regulating agents.

Country Status (5)

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EP (1)EP1183017A1 (en)
JP (1)JP2003500439A (en)
CA (1)CA2374117A1 (en)
MX (1)MXPA01012225A (en)
WO (1)WO2000072829A1 (en)

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US7276249B2 (en)2002-05-242007-10-02Elan Pharma International, Ltd.Nanoparticulate fibrate formulations
US6982251B2 (en)2000-12-202006-01-03Schering CorporationSubstituted 2-azetidinones useful as hypocholesterolemic agents
MY138301A (en)2001-01-262009-05-29Schering CorpThe use of substituted azetidinone compounds for the treatment of sitosterolemia
US7071181B2 (en)2001-01-262006-07-04Schering CorporationMethods and therapeutic combinations for the treatment of diabetes using sterol absorption inhibitors
CA2434682C (en)2001-01-262008-11-18Schering CorporationCombinations of peroxisome proliferator-activated receptor (ppar) activator(s) and sterol absorption inhibitor(s) and treatments for vascular indications
US7053080B2 (en)2001-09-212006-05-30Schering CorporationMethods and therapeutic combinations for the treatment of obesity using sterol absorption inhibitors
US7056906B2 (en)2001-09-212006-06-06Schering CorporationCombinations of hormone replacement therapy composition(s) and sterol absorption inhibitor(s) and treatments for vascular conditions in post-menopausal women
JP2005504091A (en)2001-09-212005-02-10シェーリング コーポレイション Treatment of xanthomas with azetidinone as a sterol absorption inhibitor
US20040092499A1 (en)2002-11-062004-05-13Schering CorporationMethods and therapeutic combinations for the treatment of autoimmune disorders
DE602004016123D1 (en)2003-03-072008-10-09Schering Corp SUBSTITUTED AZETIDINONE DERIVATIVES, THEIR PHARMACEUTICAL FORMULATIONS AND THEIR USE FOR THE TREATMENT OF HYPERCHOLESTEROLMIA
ATE418551T1 (en)2003-03-072009-01-15Schering Corp SUBSTITUTED AZETIDINONE DERIVATIVES, THEIR PHARMACEUTICAL FORMULATIONS AND THEIR USE IN THE TREATMENT OF HYPERCHOLESTEROLEMIA
CN1756755A (en)2003-03-072006-04-05先灵公司Substituted azetidinone compounds, formulations and uses thereof for the treatment of hypercholesterolemia
US7459442B2 (en)2003-03-072008-12-02Schering CorporationSubstituted azetidinone compounds, processes for preparing the same, formulations and uses thereof
MXPA06013252A (en)*2004-05-142007-02-28Emisphere Tech IncCompounds and compositions for delivering active agents.
GB2441499B (en)*2006-09-082011-09-14Jasin El SammadoniSlimming Spray
AU2008303129B2 (en)2007-09-252013-08-01Formulex Pharma Innovations Ltd.Compositions comprising lipophilic active compounds and method for their preparation
JP5437232B2 (en)2008-03-112014-03-12あすか製薬株式会社 Solid dispersion, pharmaceutical composition thereof, and production method thereof

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication numberPriority datePublication dateAssigneeTitle
DE2157201C3 (en)*1970-11-131974-12-12Boehringer Mannheim Gmbh, 6800 Mannheim Improved solid oral administration form of Raubasin
IT1180507B (en)*1984-06-291987-09-23Roberto Valducci PROCEDURE FOR THE PREPARATION OF ETOFIBRATE OR SUBSTANCES OF EQUAL OR SIMILAR CHARACTERISTICS, IN MICROGUNULI-DELAY AND PRODUCT OBTAINED WITH SUCH PROCEDURE
FR2627696B1 (en)*1988-02-261991-09-13Fournier Innovation Synergie NEW GALENIC FORM OF FENOFIBRATE
DK0617612T3 (en)*1991-12-181998-04-14Warner Lambert Co Process for preparing a solid dispersion

Also Published As

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WO2000072829A1 (en)2000-12-07
CA2374117A1 (en)2000-12-07
EP1183017A1 (en)2002-03-06
JP2003500439A (en)2003-01-07

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