WO2004043431A1 - Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally - Google Patents
Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally Download PDFInfo
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- WO2004043431A1 WO2004043431A1 PCT/US2003/035002 US0335002W WO2004043431A1 WO 2004043431 A1 WO2004043431 A1 WO 2004043431A1 US 0335002 W US0335002 W US 0335002W WO 2004043431 A1 WO2004043431 A1 WO 2004043431A1
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- Prior art keywords
- tizanidine
- pharmaceutical composition
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- dosage form
- acid
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- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229930195727 α-lactose Natural products 0.000 description 1
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4168—1,3-Diazoles having a nitrogen attached in position 2, e.g. clonidine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4164—1,3-Diazoles
- A61K31/4178—1,3-Diazoles not condensed 1,3-diazoles and containing further heterocyclic rings, e.g. pilocarpine, nitrofurantoin
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/433—Thidiazoles
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2013—Organic compounds, e.g. phospholipids, fats
- A61K9/2018—Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2072—Pills, tablets, discs, rods characterised by shape, structure or size; Tablets with holes, special break lines or identification marks; Partially coated tablets; Disintegrating flat shaped forms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/282—Organic compounds, e.g. fats
- A61K9/2826—Sugars or sugar alcohols, e.g. sucrose; Derivatives thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/2004—Excipients; Inactive ingredients
- A61K9/2022—Organic macromolecular compounds
- A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
- A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/20—Pills, tablets, discs, rods
- A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
- A61K9/2806—Coating materials
- A61K9/2833—Organic macromolecular compounds
- A61K9/286—Polysaccharides, e.g. gums; Cyclodextrin
- A61K9/2866—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
Definitions
- the present invention relates to anti-spasmodic agents and, more particularly, to improved methods of administration and dosage forms of tizanidine.
- Xa-adrenergic receptor agonist is a centrally acting (Xa-adrenergic receptor agonist. It is indicated for suppression of muscle spasms occurring with a wide range of etiologies: spasticity in general (refs. 2-5); muscle spasms caused by multiple sclerosis (refs. 6-8); spinal chord injury (refs. 9, 10); and brain injury (refs. 11, 12). Tizanidine also has been evaluated for treatment of chronic headache with positive results (refs. 13-16).
- Tizanidine hydrochloride is commercially available in an immediate release oral tablet formulation under the brand name ZanaflexTM-.
- ZanaflexTM is a conventional oral dosage form whose active ingredient is absorbed into the bloodstream through the mucosa lining the stomach and small intestine. This route of administration is referred to in this disclosure as enteric delivery.
- Pharmaceutical compositions and dosage forms that are taken through the mouth alternatively may be held there while the active ingredient is released. Depending upon the active ingredient, it may be absorbed through the mucosa lining the mouth.
- tizanidine The bioavailability of tizanidine is highly variable from patient to patient, necessitating titration of the dose level on an individual basis. Tizanidine can cause hepatic toxicity, which is another reason that the dosage and plasma level of tizanidine should be carefully controlled (refs. 1, 18). Tizanidine that is administered in ZanaflexTM is essentially completely absorbed by the intestinal mucosa but the bioavailability of tizanidine is only about 40% due to first-pass hepatic metabolism to metabolites, all of which appear to be pharmacologically inactive. Alternative routes of administration that do not involve gastric absorption will by-pass first-pass metabolism in the liver.
- FIG. 1 is a perspective view of a multicompression tablet having a core surrounded by an annular body in accordance with a preferred dosage form embodiment of the invention.
- the bioavailability of tizanidine is increased by sublingual or buccal administration relative to administration of a comparable dosage of tizanidine in a conventional enteral dosage form.
- the increase in bioavailability as measured by the area under the curve extrapolated to infinity of the blood stream concentration of tizanidine can be increased by as much as 10% or more.
- bioavailability of tizanidine when administered by conventional enteral dosage forms is highly variable from patient to patient.
- sublingual or buccal administration of tizanidine reduces the inter-patient variability of the bioavailability of tizanidine.
- Sublingual or buccal administration of tizanidine in accordance with this invention to a population of patients can reduce the relative standard deviation of the bloodstream concentration of tizanidine of the patient population by 10% or more.
- Dosage forms especially adapted for sublingual and buccal administration of tizanidine are provided by this invention as well.
- Tizanidine has lower solubility in saliva that in gastric fluid due to the difference in pH.
- One of the dosage form embodiments includes an acidulant that acidifies the pH in the local environment in the sublingual or buccal cavity to accelerate release of tizanidine into the bloodstream.
- Yet further dosage form embodiments of this invention enable timed release of the tizanidine that is slow enough to avoid accumulation of tizanidine in the mouth, yet rapid enough to be acceptable to a patient who holds the dosage form in the mouth while the tizanidine is being released.
- these dosage forms is a liquid that congeals in the mouth and conforms to the space under the tongue or between the cheek and gum to provide a large contact surface area and comfortable feel.
- tizanidine also "the drug” improve the drug's bioavailability and greatly diminish absorption variability between patients.
- one aspect of the present invention is a method of treating muscle spasms by buccal or sublingual administration of tizanidine.
- Tizanidine can be administered in any pharmaceutical composition or dosage form that can be held in the mouth for an extended period of time and permits diffusion or erosion of the drug into the mouth cavity where it can be absorbed through the mucosa lining of the mouth.
- dosage forms include tablets, lozenges, troches, pastilles, pills, viscous liquids, pastes, sprays, drops, gels, patches and the like.
- the invention provides pharmaceutical compositions and dosage forms especially adapted for buccal and sublingual administration of tizanidine, described below.
- tizanidine is 80% released or more within 20 minutes after administration of the drug, since most patients do not like to hold a tablet or lozenge under the tongue for longer periods. More preferably the composition or dosage form releases 80% or more tizanidine in 5 minutes or less.
- Bioavailability refers to the proportion of the drug administered that reaches the physiological site where the drug exerts its therapeutic effect, which is generally regarded as the blood stream for many drugs, and is so regarded in this disclosure for tizanidine.
- the bioavailability of a drug is most readily expressed as the concentration of the drug (or in some instances of active metabolites) in the blood plasma integrated over time. This quantity is commonly referred to as the "area under the curve" or "AUC".
- AUC area under the curve
- the bioavailability of a drug administered in different formulations and by different routes can be compared by comparing the AUCs from patients that have taken both formulations at different times.
- a population of test subjects is divided into two groups equal in number. Under controlled conditions, one group is administered the drug in one formulation while the other group is adrninistered the other formulation. Their blood plasma concentrations of the drug are monitored for a period of time and the data is collected and analyzed. A "wash out" period is then allowed to pass during which the drug is eliminated from their bodies so that a second phase of the study will begin with a zero blood plasma concentration of the drug. In the second phase, the group that received the first formulation of the drug is administered the drug in the second formulation, the group that received the second formulation is administered the first formulation, and monitoring, data collection and analysis are repeated. Administering both formulations to the same population minimizes error in comparison of bioavailability due to age, sex and individual physiological factors.
- the blood plasma concentration of test subjects is measured over a limited amount of time and with limited frequency to minimize discomfort to the test subjects. Integration of the blood plasma concentration of the drug over that limited time period affords the AUC for an individual.
- the blood plasma concentration of the drug in an individual will not necessarily have fallen to zero at the end of the monitoring period. Therefore, the AUC will underestimate the relative bioavailability of the drug for that individual.
- Data analysis software adapted for analyzing the results of clinical studies is commercially available. Such software is able to extrapolate the blood plasma concentration curve beyond the monitoring period based upon the shape of the curve during the monitoring period.
- the area under the extrapolated portion of the curve can be determined by integration and that area added to the area determined during the monitoring period to arrive at the area under the curve extrapolated to infinity or "AU nf: " AUC inf provides a more accurate measure of relative bioavailability than AUC when the monitoring is ceased before the drug has been substantially completely eliminated.
- Buccal or sublingual administration of tizanidine preferably increases the drug's bioavailability 10 % or more as determined by comparison of the AUC ⁇ f of the particular composition or dosage form used with the AUC in for patient(s) who swallow a conventional oral dosage form containing an equivalent dosage of tizanidine.
- the increase in bioavailability can be determined against a dosage form of different strength provided the difference is taken into account.
- sublingual or buccal administration according to the invention increases the drug's bioavailability by 20% or more.
- An equivalent dosage is one that contains approximately the same number of millimoles of tizanidine, regardless of whether differing weights of the active ingredient are added to the formulations to compensate for use of tizanidine in free base form, the use of a different salt anion or different states of solvation.
- the increase in bioavailability is referenced against an immediate release orally administered dosage form and in particular against ZanaflexTM, as described in ref. 1, above, since it is known that ZanaflexTM is essentially completely absorbed. Therefore, ZanaflexTM is the highest benchmark of which we are aware against which to reference improvement in bioavailability consistent with the knowledge of those in the art prior to this invention.
- commercially available ZanaflexTM contains colloidal silicon dioxide, stearic acid, microcrystalline cellulose and anhydrous lactose.
- tizanidine is preferably adrninistered in individual doses containing from about 2 mg to about 8 mg, more preferably from about 2 mg to about 4 mg, of tizanidine based on the weight of the free base regardless whether it is administered as the free base or in a salt form.
- the individual doses are preferably administered at 6 to 8 hour intervals during the day up to a daily cumulative dose of from about 4 mg to about 36 mg, more preferably from about 8 to about 24 mg.
- the invention provides a method of reducing variations in the blood plasma levels of tizanidine between individuals in a patient population by buccal or sublingual administration of tizanidine.
- a patient population includes any group of people who suffer from muscle spasms and are identifiable as a group because they share a common nexus.
- a population may refer to a group of patients who are under the care of the same doctor or healthcare provider or receive treatment for their muscle spasms at the same health care facility.
- Variation in the parameter can be quantified by calculation of the standard deviation (s.d.) or variance (s.d. 2 ) of the parameter over the population.
- Relative standard deviation (r.s.d.) is the standard deviation of a parameter divided by the average value of the parameter for the population. The r.s.d. allows meaningful comparison of the degree of variation in a parameter between populations.
- the improvement in consistency of absorption achieved by administering tizanidine buccally or sublingually is reflected in a lower relative standard deviation of AU nf for a population that has been administered tizanidine sublingually or buccally than the r.s.d. of a population that has been administered tizanidine in a conventional oral dosage form that was swallowed.
- the r.s.d. of the population that was adrninistered tizanidine buccally or sublingually is about 10% lower, more preferably about 20% lower and most preferably about 30% lower.
- the two populations being compared preferably comprise the same individuals who have received tizanidine via these routes at different times, with a washout period separating the administrations.
- Discrete dosage forms like tablets, capsules and the like preferably contain doses of from about 2 mg to about 8 mg, more preferably from about 2 mg to about 4 mg, of tizanidine based on the weight of the free base.
- compositions and dosage forms are prepared with nontoxic pharmaceutically acceptable excipients.
- the excipients are known to those skilled in the preparation of buccal and sublingual dosage forms. Ingredients and exemplary formulations may be found in Remington 's Pharmaceutical Sciences 16th ed. (Mack Publishing 1980).
- the patent literature also contains many disclosures of buccal and sublingual formulations, including U.S. Patents Nos. 4,020,558; 4,229,447; 3,972,995; 3,870,790; 3,444,858; 2,698,822; 3,632,743, all of which are incorporated herein by reference in their entirety.
- Excipients that are commonly formulated into buccal and sublingual dosage forms include, maltodextrin, colloidal silicon dioxide, starch, starch syrup, sugar and -lactose.
- Conventional methods of processing active ingredients and excipients into pharmaceutical compositions and dosage forms for buccal and sublingual administration are well known to the skilled formulation specialist.
- Preferred pharmaceutical compositions and dosage forms release at least about 80% of the tizanidine within about twenty minutes of administration, more preferably within about 5 minutes of administration.
- a further aspect of the invention provides compositions and dosage forms especially adapted for buccal and sublingual administration of tizanidine.
- Tizanidine is absorbed better in the acid environment of the stomach than in the neutral environment of the mouth. Acidifying the saliva, preferably to a pH between 2 and 7, improves the absorption of tizanidine.
- compositions and dosage forms of the present invention are able to acidify the local environment in the sublingual cavity or buccal cavity during the desired drug release period.
- dosage forms contain an effective acidifying amount of an acidulant.
- An acidulant is an excipient that acidifies the local environment around the dosage form or composition after it has been put in the patient's mouth. It need not acidify the saliva in all regions of the sublingual or buccal cavity to be effective, only the saliva that provides direct fluid communication between the surface of the dosage form from which the tizanidine is released and adjacent oral mucosa. Acidulants are approved or generally recognized as safe (GRAS) excipients for use in oral drug administration.
- GRAS safe
- Any approved or safe organic acid is suitable, such as ascorbic acid, benzoic acid, citric acid, fumaric acid, lactic acid, malic acid, sorbic acid and tartaric acid.
- a preferred acidulant is citric acid.
- the amount of acidulant that is effective in any particular composition or dosage form will depend upon many factors such as the intended rate of release of the drug, the choice of acidulant, the rate at which it is released into the mouth and even the profundity of the patient's salivation.
- One method is to sample the pH of the patient's saliva coating the dosage form or pharmaceutical composition and see whether it is within the 2-7 pH range, or, yet more preferred, within the range of 2-5. Such routine experimentation is not considered to be undue.
- a pharmaceutical composition of tizanidine is a liquid that congeals when placed under the tongue or between cheek and gum.
- the congealed liquid is a mucoadhesive solid or semi-solid that slowly releases tizanidine over time.
- This embodiment possesses the advantage that the gelled composition conforms to the surfaces of the mouth, giving it a more comfortable feel.
- the liquid composition comprises a hydrophilic polymer selected from the group consisting of proteins, polysaccharides, cellulosic polymers and polyacrylates. Proteins include gelatin, hydrolyzed gelatin, albumin and collagen.
- Polysaccharides include pectin, carrageenan and alginic acid and their salts, guar gum, and tragacanth gu Cellulosic polymers include hydroxyethylcellulose, hydroxypropylcellulose and hydroxypropylmethylcellulose.
- Preferred hydrophilic polymers are hydroxypropylcellulose and hydroxypropylmethylcellulose having a molecular weight range from 25000 to 2.5 million daltons.
- Such hydrophilic polymers are available under the trade names KlucelTM from the Hercules Corporation and MethocelTM from Dow Chemical Company.
- An alternative embodiment of this pharmaceutical composition comprises solutions of polymers having reverse thermal gellation (gel upon heating instead of upon cooling).
- polymers examples include methylcellulose, triblock poly(lactide-co-glycolide) polyethylene glycol copolymers described in U.S. Patents Nos. 6,004,573; 6,117,949 and 6,201,072, and thermosensitive biodegradable polymers based on poly(ether-ester)block copolymers as described in U.S. Patent No. 5,702,717.
- liquid pharmaceutical compositions for buccal administration of drugs containing a polymer and tannic acid are described in International Publication No. WO 99/04764, of which we are inventors, that publication does not teach or suggest the use of such ingredients in a pharmaceutical composition adapted to deliver tizanidine sublingually or buccally.
- Preferred liquid formulations that congeal in the mouth comprise about 0.1 wt.% to about 0.5 wt.% tizanidine, from about 0.1 wt % to about 5 wt. % of a hydrophilic polymer and from about 0.1 wt% to about 0.5 wt% of tannic acid with the remainder of the composition being made up of solvent, which is preferably water, ethanol and mixtures thereof, and other excipients such as colorants, flavorants, tonicity modifiers, viscosity modifiers, preservatives and the like.
- solvent which is preferably water, ethanol and mixtures thereof
- congealing liquid compositions that contain tannic acid within the preferred amounts generally do not require a separate acidulant since the tannic acid functions both as a hydrogen bonding cross-linking agent and an acidulant.
- An especially preferred dosage form of this invention is a tablet formed by multiple compression steps into an inner tablet core containing tizanidine surrounded by an annular body.
- the advantage of this tablet configuration is that the tizanidine-containing portion of the tablet is protected from disintegration by handling and, once in use, by mastication.
- the protected dosage form comprises a core tablet containing tizanidine sheathed in an annular body comprised of compressed powder or granular material.
- the core tablet has first and second opposed surfaces and a circumferential surface.
- “Sheathing” means that the annular body encircles the core tablet and is in contact with the core tablet about its circumferential surface, but leaves opposed surfaces of the core tablet substantially exposed.
- Core tablet 1 containing the tizanidine is recessed in the annular body 2.
- Core tablet 1 has opposed first and second surfaces 3 and 4 and an outer circumferential surface 5 extending between the opposed surfaces.
- Core tablet 1 is preferably cylindrical or disk shaped for ease of manufacture, but need not be so.
- the maximum distance across either of the opposed surfaces 3 or 4 is preferably from about 2 mm to about 12 mm, more preferably from about 4 mm to about 7 mm, most preferably about 5 mm.
- Opposed surfaces 3 and 4 can be flat, concave or convex and are preferably flat.
- annular body 2 is preferably cylindrically shaped, but it can have any cross section, such as oval, elliptical or oblong.
- the outer diameter is preferably of from about 5 mm to about 15 mm, more preferably of from about 7 mm to about 12 mm, most preferably about 9 mm.
- the inner diameter can be any size up to about 2 mm less than the outer diameter. Preferably, the inner diameter is 3 mm or greater.
- the solid dosage forms with a drug-containing core tablet sheathed in a compressed annular body of excipients can be produced using a novel set of tooling that is described in U.S. Patent Application Serial No. 10/419536, filed on April 21, 2003 and PCT Application No. PCT/US02/36081, filed on November 12, 2003 and published on July 17, 2003 as International Patent Publication No. WO 03/057136, which are hereby incorporated by reference in their entirety, or by other multicompression techniques known in the art.
- the core tablet can be formulated for any desired release profile, such as immediate release, delayed release, burst or pulsed release, sustained or zero order release, but most preferably immediate release.
- the core preferably contains a disintegrant like crospovidone to accelerate release.
- Other preferred excipients for an immediate release core tablet are ⁇ -lactose monohydrate, microcrystalline cellulose, sodium saccharine , and magnesium stearate.
- a preferred composition for the core tablet contains about 1-10 parts tizanidine hydrochloride, 50-70 parts ⁇ -lactose, 10-20 parts microcrystalline cellulose, about 0.1 to 1 part sodium saccharine and 15-25 parts crospovidone, exclusive of other excipients that may be present.
- the core tablet also may contain the acidulant.
- the annular body can be formulated with any desired purpose in mind, such as taste masking. It also can contain the acidulant.
- the annular body can be formed of any pharmaceutically acceptable excipients. In particular, it may be mentioned that diluents, binders, disintegrants, glidants, lubricants, flavorants, colorants and the like can be included in the annular body. Blending and granulation with conventional excipients is well within the knowledge of those skilled in the art of tableting.
- Preferred excipients for forming the annular body include hydroxypropyl cellulose (e.g., Klucel ® ), hydroxypropylmethylcellulose (e.g. Methocel ® ), microcrystalline cellulose (e.g., Avicel ® ), starch, lactose, sugars, compressible sugar, crospovidone (e.g. KollidonTM), polyvinylpyrrolidone (e.g. Plasdone ® ) and calcium phosphate.
- hydroxypropyl cellulose e.g., Klucel ®
- hydroxypropylmethylcellulose e.g. Methocel ®
- microcrystalline cellulose e.g., Avicel ®
- starch e.g., lactose, sugars, compressible sugar, crospovidone (e.g. KollidonTM)
- polyvinylpyrrolidone e.g. Plasdone ®
- calcium phosphate e.g., calcium
- excipients for forming the annular body are ⁇ -lactose monohydrate, microcrystalline cellulose and compressible sugar
- An especially preferred ring excipient is a spray dried mixture of about 75% ⁇ -lactose monohydrate and 25% microcrystalline cellulose with a particle size distribution of d(15) ⁇ 32 ⁇ m and d(90) ⁇ 250 ⁇ m.
- Such a mixture is commercially available from Meggle AG, Wasserburg, Germany, under the tradename MicrocellacTM.
- Compressible sugar is available under the tradename Nu-TabTM from CHR. Hansen, H ⁇ rsholm, Denmark.
- a preferred composition of the annular body is about 45-50 parts compressible sugar, about 30-40 parts ⁇ -lactose monohydrate, 1-10 parts microcrystalline cellulose, and 1-10 parts crospovidone.
- the sublingual tablets used in this study were formed into an inner core of a fast disintegrating formulation containing 2 mg tizanidine and an outer annular body of protective excipients.
- the inner cores were made by mixing 4.5 parts tizanidine hydrochloride and 20 parts crospovidone for 2 minutes. One half part sodium saccharin, 73.6 parts of MicrocellaclOOTM, and 0.4 parts menthol were added and the mixing was continued for 3 more minutes. One part magnesium stearate was added and the mixing was continued for a half a minute. This mixture was compressed on a Manesty f3 tablet press fitted with a five mm flat beveled punch. The tablets formed were of 5 mm diameter, weighed 45 mg each, were about 2 mm thick and had a hardness of 1 - 3.5 Kp.
- the outer annular body was made by mixing 48.5 parts Nu-TabTM, 45 parts of MicrocellaclOOTM, 0.5 parts of sodium saccharin and 5 parts of crospovidone for 5 minutes, adding one part magnesium stearate, mixing for another half of a minute, and then compressing on a Manesty f3 tablet press fitted with a set of tooling like that described in U.S. Patent Application Serial No. 10/419536, filed on April 21, 2003 and International Patent Publication No. WO 03/057136.
- the entire tablet weight was 290 mg.
- the outer diameter was 9 mm.
- the tablet height about 4.5 mm and the hardness was 5-9 Kp.
- Table 1 collects the results of analyses of tizanidine in plasma for twelve test subjects who were administered 2 mg tizanidine in a sublingual formulation. Table 1: Plasma Tizanidine Levels (ng/g) after Sublingual Delivery of 2 mg Tizanidine
- Table 2 collects the data for 11 of the same twelve test subjects (test subject 6 did not participate in this arm of the trial) who were administered 4 mg tizanidine in a standard commercial oral formulation.
- Table 3 collects the calculated pharmacokinetic parameters for both groups. Table 3: Summary of Pharmacokinetic Data for 2mg Sublingual (test) vs. 4 mg Oral (ref)
- the average total amount absorbed (the area under the plasma concentration vs. time curve extrapolated to infinity (AUC ⁇ f )) was 6560 for the 4 mg oral tablet while the result was 3960 for the 2 mg sublingual tablet . Normalizing for dose gives 1640/mg for the oral delivery and 1980/mg for the sublingual delivery, reflecting a 20% increase in bioavailability.
- the average C max for the 2 mg sublingual delivery was 1462 (731/mg) while for the 4 mg oral dose it was 2519 (630/mg) or about 16% higher.
- the standard deviation of the AUC for the oral formulation was 4353 (relative standard deviation of 66%) while the standard deviation of the data for the 2 mg sublingual formulation was 1871 (relative standard deviation of 47%) reflecting a decrease in variation of 28.8%. Therefore, we have shown by this study that sublingual and buccal delivery gives less variable results and improved bioavailability compared to conventional oral delivery in which the drug is absorbed in the intestine.
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- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Neurology (AREA)
- Medicinal Preparation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Description
Claims
Priority Applications (8)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NZ540106A NZ540106A (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally |
EA200500764A EA200500764A1 (en) | 2002-11-12 | 2003-11-03 | PHARMACEUTICAL COMPOSITIONS AND MEDICAL FORMS FOR TRANSBUCCAL AND SUBLINGUAL DELIVERY TIZANIDINE AND METHODS OF INTRODUCTION TIZANIDINE SUBLINGUAL OR TRANSBUCKAL |
JP2004551688A JP2006508122A (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or buccal |
AU2003287488A AU2003287488B8 (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally |
EP03781729A EP1567124A1 (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally |
CA002505861A CA2505861A1 (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally |
MXPA05005038A MXPA05005038A (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally. |
BR0315482-3A BR0315482A (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for oral and sublingual tizanidine release and methods of sublingual or buccal administration of tizanidine |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US42532602P | 2002-11-12 | 2002-11-12 | |
US60/425,326 | 2002-11-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2004043431A1 true WO2004043431A1 (en) | 2004-05-27 |
Family
ID=32312969
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2003/035002 WO2004043431A1 (en) | 2002-11-12 | 2003-11-03 | Pharmaceutical compositions and dosage forms for buccal and sublingual delivery of tizanidine and methods of administering tizanidine sublingually or bucally |
Country Status (12)
Country | Link |
---|---|
US (1) | US20040122065A1 (en) |
EP (1) | EP1567124A1 (en) |
JP (1) | JP2006508122A (en) |
KR (1) | KR100801946B1 (en) |
CN (1) | CN1738600A (en) |
AU (1) | AU2003287488B8 (en) |
BR (1) | BR0315482A (en) |
CA (1) | CA2505861A1 (en) |
EA (1) | EA200500764A1 (en) |
MX (1) | MXPA05005038A (en) |
NZ (1) | NZ540106A (en) |
WO (1) | WO2004043431A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006012634A1 (en) * | 2004-07-26 | 2006-02-02 | Teva Pharmaceutical Indudstries, Ltd. | Dosage forms with an enterically coated core tablet |
JP2008540688A (en) * | 2005-08-01 | 2008-11-20 | テバ ファーマシューティカル インダストリーズ リミティド | Tizanidine composition and method of treatment using said composition |
WO2009151394A1 (en) * | 2008-06-11 | 2009-12-17 | Astrazeneca Ab | Sublingual compositions comprising (2s) - (4e) -n-methyl-5- (3- (5-isopropoxypyridin) yl) -4-penten-2-amine |
CN101045051B (en) * | 2006-04-12 | 2010-05-26 | 四川科瑞德制药有限公司 | Novel use of tizanidine or its derivatives in preparing medicine for prolonging fast wave sleep |
EP2338473A1 (en) | 2009-12-18 | 2011-06-29 | MDM S.p.A. | Pharmaceutical dosage forms of tizanidine and administration routes thereof |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9066847B2 (en) * | 2007-01-05 | 2015-06-30 | Aceirx Pharmaceuticals, Inc. | Storage and dispensing devices for administration of oral transmucosal dosage forms |
BRPI1010639A2 (en) * | 2009-05-13 | 2016-03-15 | Protein Delivery Solutions Llc | pharmaceutical system for transmembrane distribution |
EP2952191B1 (en) | 2009-06-12 | 2018-08-22 | Sunovion Pharmaceuticals Inc. | Sublingual apomorphine |
CA3115378A1 (en) | 2010-12-16 | 2012-06-21 | Sunovion Pharmaceuticals Inc. | Sublingual films comprising apomorphine and an organic base |
JP2021515038A (en) * | 2018-02-27 | 2021-06-17 | デルポー・インコーポレイテッドDelpor, Inc. | Compositions for Small Molecular Therapeutic Compounds |
US20220193043A1 (en) | 2019-03-29 | 2022-06-23 | Cipla Limited | Pharmaceutical Combination Formulations Comprising Tizanidine, Resveratrol and Piperine |
CN113081997A (en) * | 2021-04-01 | 2021-07-09 | 杭州泓友医药科技有限公司 | Tizanidine hydrochloride capsule and preparation method thereof |
Citations (3)
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GB2197198A (en) * | 1986-11-03 | 1988-05-18 | Sandoz Ltd | Analgesic preparations |
US5576014A (en) * | 1994-01-31 | 1996-11-19 | Yamanouchi Pharmaceutical Co., Ltd | Intrabuccally dissolving compressed moldings and production process thereof |
WO2003075893A1 (en) * | 2002-03-04 | 2003-09-18 | Teva Pharmaceutical Industries Ltd. | Controlled release dosage forms |
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GB1142325A (en) * | 1965-05-14 | 1969-02-05 | Higham Stanley Russell | Means for administering drugs |
GB1230472A (en) * | 1967-07-10 | 1971-05-05 | ||
US4150113A (en) * | 1969-06-03 | 1979-04-17 | Telec S.A. | Enzymatic dentifrices |
US3870790A (en) * | 1970-01-22 | 1975-03-11 | Forest Laboratories | Solid pharmaceutical formulations containing hydroxypropyl methyl cellulose |
FR2278317A1 (en) * | 1974-07-19 | 1976-02-13 | Commissariat Energie Atomique | ORAL IMPLANT FOR ADMINISTERING SOLUBILIZABLE PRODUCTS |
US3972995A (en) * | 1975-04-14 | 1976-08-03 | American Home Products Corporation | Dosage form |
GB1559811A (en) * | 1975-07-28 | 1980-01-30 | Sandoz Ltd | Pharmaceutically active benzothiadiazole derivatives |
US4229447A (en) * | 1979-06-04 | 1980-10-21 | American Home Products Corporation | Intraoral methods of using benzodiazepines |
JP2807346B2 (en) * | 1991-12-24 | 1998-10-08 | 山之内製薬株式会社 | Orally disintegrating preparation and production method thereof |
WO1993015724A1 (en) | 1992-02-18 | 1993-08-19 | Nippon Shinyaku Co., Ltd. | Fast soluble tablet |
US5702717A (en) * | 1995-10-25 | 1997-12-30 | Macromed, Inc. | Thermosensitive biodegradable polymers based on poly(ether-ester)block copolymers |
BR9710289A (en) * | 1996-07-11 | 1999-08-17 | Farmarc Nederland Bv | Pharmaceutical composition containing acid salt with basic medicine addition |
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US6455557B1 (en) * | 2001-11-28 | 2002-09-24 | Elan Pharmaceuticals, Inc. | Method of reducing somnolence in patients treated with tizanidine |
NZ552513A (en) * | 2001-12-24 | 2008-08-29 | Teva Pharma | Dosage form with a core tablet of active ingredient sheathed in a compressed annular body of powder or granular material, and process and tooling for producing it |
-
2003
- 2003-11-03 BR BR0315482-3A patent/BR0315482A/en not_active IP Right Cessation
- 2003-11-03 AU AU2003287488A patent/AU2003287488B8/en not_active Ceased
- 2003-11-03 EP EP03781729A patent/EP1567124A1/en not_active Withdrawn
- 2003-11-03 CA CA002505861A patent/CA2505861A1/en not_active Abandoned
- 2003-11-03 KR KR1020057008527A patent/KR100801946B1/en not_active IP Right Cessation
- 2003-11-03 CN CNA2003801086495A patent/CN1738600A/en active Pending
- 2003-11-03 MX MXPA05005038A patent/MXPA05005038A/en unknown
- 2003-11-03 EA EA200500764A patent/EA200500764A1/en unknown
- 2003-11-03 NZ NZ540106A patent/NZ540106A/en unknown
- 2003-11-03 JP JP2004551688A patent/JP2006508122A/en active Pending
- 2003-11-03 WO PCT/US2003/035002 patent/WO2004043431A1/en active IP Right Grant
- 2003-11-03 US US10/699,991 patent/US20040122065A1/en not_active Abandoned
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
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GB2197198A (en) * | 1986-11-03 | 1988-05-18 | Sandoz Ltd | Analgesic preparations |
US5576014A (en) * | 1994-01-31 | 1996-11-19 | Yamanouchi Pharmaceutical Co., Ltd | Intrabuccally dissolving compressed moldings and production process thereof |
WO2003075893A1 (en) * | 2002-03-04 | 2003-09-18 | Teva Pharmaceutical Industries Ltd. | Controlled release dosage forms |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006012634A1 (en) * | 2004-07-26 | 2006-02-02 | Teva Pharmaceutical Indudstries, Ltd. | Dosage forms with an enterically coated core tablet |
JP2008540688A (en) * | 2005-08-01 | 2008-11-20 | テバ ファーマシューティカル インダストリーズ リミティド | Tizanidine composition and method of treatment using said composition |
CN101045051B (en) * | 2006-04-12 | 2010-05-26 | 四川科瑞德制药有限公司 | Novel use of tizanidine or its derivatives in preparing medicine for prolonging fast wave sleep |
WO2009151394A1 (en) * | 2008-06-11 | 2009-12-17 | Astrazeneca Ab | Sublingual compositions comprising (2s) - (4e) -n-methyl-5- (3- (5-isopropoxypyridin) yl) -4-penten-2-amine |
EP2338473A1 (en) | 2009-12-18 | 2011-06-29 | MDM S.p.A. | Pharmaceutical dosage forms of tizanidine and administration routes thereof |
Also Published As
Publication number | Publication date |
---|---|
AU2003287488B8 (en) | 2007-05-17 |
US20040122065A1 (en) | 2004-06-24 |
EA200500764A1 (en) | 2005-12-29 |
KR20050075398A (en) | 2005-07-20 |
NZ540106A (en) | 2008-03-28 |
BR0315482A (en) | 2005-08-23 |
AU2003287488B2 (en) | 2007-04-05 |
JP2006508122A (en) | 2006-03-09 |
CN1738600A (en) | 2006-02-22 |
CA2505861A1 (en) | 2004-05-27 |
AU2003287488A1 (en) | 2004-06-03 |
KR100801946B1 (en) | 2008-02-12 |
MXPA05005038A (en) | 2005-07-01 |
EP1567124A1 (en) | 2005-08-31 |
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