CA2175370C - Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles - Google Patents
Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles Download PDFInfo
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Abstract
A pharmaceutical composition comprising biodegradable and biocompatible microparticle containing a 1,2-benzazole of the formula (I), or a pharmaceutically acceptable acid addition salt thereof, wherein R is hydrogen or C1-6alkyl; R1 and R2 independently are hydrogen, halo, hydroxy, C1-6alkyloxy and C1-6alkyl; X is O or S; Alk is C1-4alkanediyl; and R3 is hydrogen or C1-6alkyl; Z is -S-, -CH2, or -CR4=CR5-; where R4 and R5 independently are hydrogen or C1-6alkyl; A is a bivalent radical -CH2-CH2-, -CH2-CH2-CH2- or -CR6=CR7-; wherein R6 and R7 are hydrogen, halo, amino or C1-6alkyl; and R8 is hydrogen or hydroxyl; within a polymeric matrix.
Description
W O 95113814 _ ~ t ~ ~ ~ ~ ~ PCTlEP94103754 Microencapsulated 3-Piperidinyl-Substituted 1,2-Benzisoxazoles and 1,2-Benzisothiazoles Background of the Invention The present invention relates to microencapsulared 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles, their preparation and their use in the treatment of mental illness.
ll0 U.S. Patent No. 4,804,663 discloses 3-piperidinyl-1,2-benzisothiazoles and 3-piperidinyl-1 ,2~benzisoxazoles that have antipsychotic properties.1n particular, 3-[2-[4-(6-fluoro-l,2-benzisoxazol-3-yl)-I -piperidinyl) ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a] pyrimidin-4 one ("risperidone") is disclosed.
U.S. Patent No. 5,158,952 describes 3-piperidinyl-1,2-benzisoxazoles having long-acting antipsychotic properties. In particular, 3-[2-[4-(6-fluorv-I,2-benzisoxazol 3 yl)-1-piperidinyl) ethyl]-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido[1,2-a]
pyrimidin-4-one ("9-hydroxy-risperidone")is disclosed.
A number of methods are known by wlrich compounds can be encapsulated in the form of microparticles. In many of these processes, the material to be encapsulated is dispersed in a solvent containing a wall foaming material. At a single stage of the process, solvent is removed from the microparticles and thereafter the microparticle product is obtained U. S. Patent No. 3,737,337 discloses the preparation of a wall or shell forming polymeric material in a solvent that is only partially miscible in water. A
solid or core material is dissolved or dispersed in the polymer-containing solution and, thereafter, the care material-containing solution is dispersed in an aqueous liquid that is immiscible in the organic solvent in order to remove solvent from the microparticles.
Another example of a process in which solvent is removed from microparticles containing a substance is disclosed in U. S. Patent No. 3,523,906. In this process a material to be encapsulated is emulsified in a solution of a polymeric material in a solvent that is immiscibIe in water and then the emulsion is emulsified in an aqueous solution containing a hydrophilic colloid. Solvent removal from the microparticles is then accomplished by evaporation and the product is obtained In U. S. Patent No. 3,691,090, organic solvent is evaporated from a dispersion of microparticles in an aqueous medium, preferably under reduced pressure.
Similarly, U. S. Patent No. 3,891,570 discloses a method in which solvent from a dispersion of microparticles in a polyhydric alcohol medium is evaporated from the ' WO 95113814 _ PCTlEP94103754 microparticles by the application of heat or by subjecting the microparticles to reduced pressure. Another example of a solvene removal process is shown in U. S.
Patent No.
ll0 U.S. Patent No. 4,804,663 discloses 3-piperidinyl-1,2-benzisothiazoles and 3-piperidinyl-1 ,2~benzisoxazoles that have antipsychotic properties.1n particular, 3-[2-[4-(6-fluoro-l,2-benzisoxazol-3-yl)-I -piperidinyl) ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a] pyrimidin-4 one ("risperidone") is disclosed.
U.S. Patent No. 5,158,952 describes 3-piperidinyl-1,2-benzisoxazoles having long-acting antipsychotic properties. In particular, 3-[2-[4-(6-fluorv-I,2-benzisoxazol 3 yl)-1-piperidinyl) ethyl]-6,7,8,9-tetrahydro-9-hydroxy-2-methyl-4H-pyrido[1,2-a]
pyrimidin-4-one ("9-hydroxy-risperidone")is disclosed.
A number of methods are known by wlrich compounds can be encapsulated in the form of microparticles. In many of these processes, the material to be encapsulated is dispersed in a solvent containing a wall foaming material. At a single stage of the process, solvent is removed from the microparticles and thereafter the microparticle product is obtained U. S. Patent No. 3,737,337 discloses the preparation of a wall or shell forming polymeric material in a solvent that is only partially miscible in water. A
solid or core material is dissolved or dispersed in the polymer-containing solution and, thereafter, the care material-containing solution is dispersed in an aqueous liquid that is immiscible in the organic solvent in order to remove solvent from the microparticles.
Another example of a process in which solvent is removed from microparticles containing a substance is disclosed in U. S. Patent No. 3,523,906. In this process a material to be encapsulated is emulsified in a solution of a polymeric material in a solvent that is immiscibIe in water and then the emulsion is emulsified in an aqueous solution containing a hydrophilic colloid. Solvent removal from the microparticles is then accomplished by evaporation and the product is obtained In U. S. Patent No. 3,691,090, organic solvent is evaporated from a dispersion of microparticles in an aqueous medium, preferably under reduced pressure.
Similarly, U. S. Patent No. 3,891,570 discloses a method in which solvent from a dispersion of microparticles in a polyhydric alcohol medium is evaporated from the ' WO 95113814 _ PCTlEP94103754 microparticles by the application of heat or by subjecting the microparticles to reduced pressure. Another example of a solvene removal process is shown in U. S.
Patent No.
3,960,757.
U. S. Patents No. 4,389,330 and 4,530,840 describe the preparation of microparticles containing an active agent by a method comprising: (a) dissolving or dispersing an active agent in a solvent and dissolving a wall forming material in that solvent; (b) dispersing the solvent containing the active agent and wall forming material in a continuous-phase processing medium; (c) evaporating a portion of the solvent from the dispersion of step (b), thereby forming microparticles containing the active agent in the suspension; and (d) extracting the remainder of the solvent from the microparticles.
Description of the Invention The invention relates to a pharntaceutical composition comprising biodegradable and biocompatible microparticles containing a 1,2-benzazole of formula (I) i R8 Z N R3 R ,X /R
N I ~~ cn, ~ N Alk-N
O
or a pharmaceutically acceptable acid addition salt thereof, wherein R is hydrogen or Cl.6alkyl;
RI and RZ independently are hydrogen, halo, hydroxy, Cl~atkyloxy and Cl_6alkyl;
XisOorS;
Alk is Ct.~alkanediYl; and R3 is hydrogen or Cl~alkyl;
Z is -S-, -CHZ-, or -CR4=CR5-; where R4 and RS independently are hydrogen or Cl~alkyl;
A is a bivalent radical -CHZ-CHZ-, -CH2-CHZ-CHZ- or -CR6°CR~-: wherein R6 and R~
are hydrogen, halo, amino or Cl-6alkyl; and R8 is hydrogen or hydroxyl.
In the foregoing definitions, the term "halo" is generic to fluoro, chloro, bromo, and iodo; "Ct_balkyl" is meant to include straight and branched chain saturated hydrocarbon radicals having from I to 6 carbon atoms, such as, for example, methyl, ethyl, propyl, ' w0 95113814 , PCT'IEP94103754 butyl, pentyl, hexyl, and isomers thereof; "Ci.~allcanediyl" is meant to include bivalent straight or branched chain alkanediyi radicals having from 1 to 4 carbon atoms, such as, for example, methylene, ethylene, propylene, butylene, and isomers thereof.
Preferred compounds within the invention are those wherein R3 is Cl.salkyl and in particular is methyl and A is a bivalent radical -CH2-CH2-, -CHZ-CH2-CH2-, or -CR6=CRS-, wherein R6 and R~ independently are hydrogen or Cl.6allryl.
Particularly preferred compounds are those preferred compounds wherein X is oxygen, R is hydrogen, Rt is halo or in particular is hydrogen, and R2 is hydrogen, halo, hydroxy, or Cl~alkyloxy.
More particularly preferred compounds are those particulary preferred compounds wherein -Z-A- is -CH2-CH2-CH2-CHZ-, -S-CH2-CH2-, -S-(CFi~3-, -S-CR6=CRS-, or -CH=CH-CR6=CRS-, wherein R6 and R~ independently are hydrogen or methyl and R$
is hydrogen or 9-hydroxy.
The most prefenrd compounds are 3-[2-[4-(6-fluoro-l,2-benzisaxawl-3-yl)-1-piperidinyl) ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[l,2-a] pyrimidin-4-one ("ltisperidone") and the pharmaceutically acceptable acid addition salts thereof.
The compounds of formula (1) can generally be prepared by the methods described in US-4,804,663 or US-5,158,952.
The compounds of formula (I) have basic properties and, consequently, can be converted to their therapeutically active non-toxic acid addition salt forms by treatment with appropriate acids, such as, for example, inorganic acids, such as hydrohalic acid, e.g., hydrochloric, hydrobromic, and the Like; sulfuric acid, nitric acid, phosphoric acid, and the like; or organic acids, such as, for example, acetic, propanoic, hydroacetic, 2-hydroxypropanoic, 2-oxopropanoic,ethanedioic,propanedioic, butanedioic, (Z)-2-butenedioic, (E)-2-butenedioic, 2-hydroxybutanedioic, 2,3-dihydroxybutanedioic, 2-hydroxy-1,2,3-propanetricarboxylic, methanesulfonic, ethanesulfonic, benzenesulfonic, toluenesulfonic, cyclohexanesulfamic, 2-hydroxybenwic, 4-amino-2-hydroxybenwic, and the like acids.
The compounds of formula (I) are potent antagonists of a series of neurotransmitters and, as a result, have useful pharmacological properties. In particular, the compounds of formula (I) are combined serotonin and dopamine antagonists. Consequently, they are useful as anti-psychotics and in the treatment of a variety of complaints in which serotonin release is of predominant importance such as, for example, in the blocking of 217 ~ 3 7 0 p~~,p94103754 ~'O 95113814 serotonin-induced contractions of bronchial tissues and of blood vessels, arteries as well as veins. Therapeutic indications for using the present compounds are mainly in the CNS
area, i.e. as antipsychotic agents and therefore they can be used in combatting psychoses, in particular schizophrenia, aggressive behaviour, anxiety, depression and migraine.
Additionally the compounds of form (I) are also useful as sedating, anxiolytic, anti-aggressive, anti-stress and muscular protectant agents.
The present invention further provides a method of treating warm-blooded animals suffering from psychotic disorders, said method comprising the systemic administration of a effective amount of a mictnencapsulated compound of formula (1) or a pharmaceutically acceptable acid addition salt thereof in admixture with a pharmaceutical carrier. Or alternatively, there is provided the use for the manufacture of a medicament of a microencapsulated compound of formula (1] for treating psychotic disorders.
Or still alternatively, there is provided the use of microencapsulated compound of formula ()7 or a pharmaceutically acceptable acid addition salt thereof in admixture with a pharmaceutical carrier for treating psychotic disorders. In general, it is contemplated that an effective amount of the active ingredient per se would be from 0.01 mg/kg to 4 mg/kg body weight, more preferably, from 0.04 mg/kg to 2 mg/kg body weight.
By the term "administered" as used herein, any method of delivering the 1,2-benzaaole-containing microparticles of the invention to a warn blooded animal is intended, such as, for example, parenteral (intravenous, intramuscular, or subcutaneous) administration.
By "microparticles" solid particles that contain an active agent, herein the 1,2-benzawle, either in solution or in crystalline form are meant. The active agent is dispersed or dissolved within the polymer that serves as the matrix of the particle.
In another aspect, the present invention relates to a method of inhibiting serotonergic or dopaminergic overstimulation in warm-blooded animals wherein said method comprises administration of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of formula (1) within a polymeric matrix. Or alternatively>
there is provided the use for the manufacture of a medicament, of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of formula (I) within a polymeric mattix, for inhibiting serotonergic or dopaminergic overstimulation in warm-blooded animals. Or the use of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzaaole of formula (1) within a polymeric matrix far inhibiting serotonergic or dopaminergic overstimulation in warm-blooded animals.
' WO 95/13814 . Pt°lYEP94103754 1n still another aspect, the invention relates to microparticles made of a biocompatible and biodegradable matrix containing a compound of formula (I) or a pharmaceutically acceptable acid addition salt thereof.
3 The compositions of this invention are useful for treating mental illness in warm-blooded anirttals, preferably mammals, more preferably humans, (hereinafter, collectively referred to as "patients") that comprises providing to such patients biodegradable micropatticles loaded with a 1,2-benzazole, as described above.
The compositions of the present invention comprise microparticles designed for the controlled release from a biocompatible, biodegradable matrix over an extended period of time of an effective amount of the 1,2-benzaaole of formula (I). They provide advantages over compositions lmown in the art, such advantages comprising, inter alla, the fact that it is a biodegradable system, an injectable system that prevents the loss of IS dose during treatment, the ability to mix microparticles containing different drugs, and the ability to program release (multiphasic release patterns) to give faster or slower rates of drug release as needed.
In a preferred embodiment, adminisaation of the 1,2-benzazoles to patients is achieved by a single administration of the drug loaded microparticles, releasing the drug in a constant or pulsed manner into the patient and eliminating the need for repetitive injections.
The product of the present invention offers the advantage of having a duration of action ranging from 7 to more than 200 days, depending upon the type of microparticle selected. In a preferred embodiment, the microparticles are designed to afford treatment to patienu over a period of 14 to 100 days, in particular 14 to 50 or to 60, or 30 to 60 days. The duration of action can be controlled by manipulation of the polymer composition, the polymer:drug ratio, and the micropatticle size.
Another important advantage of the present invention is that practically all of the active agent is delivered to the patient because the polymer used is biodegradable, thereby permitting all of the entrapped agent to be released into the patient.
The polymeric matrix material of the microparticles of the present invention is a biocompatible and biodegradable polymeric material. The term"biocompatible" is defined as a polymeric material that is not toxic to the human body, is not carcinogenic, and does ' ~JfO 95/13814 PCTIEP94103754 not significantly induce inflammation in body tissues. The matrix material should be biodegradable in the sense that the polymeric material should degrade by bodily processes to products readily disposable by the body and should not accumulate in the body. The products of the biodegradation should also be biocompatible with the body in the same sense that the polymeric matrix is biocompatible with the body.
Suitable examples of polymeric matrix materials include poly(glycoIic acid), poly-D,L-lactic acid, poly-Irlactic acid, copolymers of the foregoing, poly(aliphatic carboxylic acids), copolyoxalates, polycaprolactone, polydioxonone, poly(ortho carbonates), poly(acetals), poly(lactic acid-caprolactone), polyorthoesters, poly(glycolic acid caprolactone), polyanhydrides, and natural polymers including albumin, casein, and waxes such as, glycerol mono- and distearate, and the like. The preferred polymer for use in the practice of this invention is dl-(polylactide-co-glycolide) i.e. a copolymer of poly(glycolic acid) and poly-D,L-lactic acid. It is preferred that the molar ratio of lactide to glycolide in such a copolymer be in the range of from about 85:15 to about 35:65, more in particular from about 75:25 to about 50:50, e.g. 85:15, 75:25, b5:35 or 50:50.
The amount of active agent incorporated in the microparticles usually ranges from about 1 wt °Jo to about 90 wt. %, preferably 30 to 50 wt. 9b, more preferably 35 to 40 wt. % . By weight % is meant parts of agent per total weight of microparticle. For example, 10 wt.
96 agent would mean 10 parts agent and 90 parts polymer by weight.
The molecular weight of the polymeric matrix material is of some importance.
The molecular weight should be high enough to permit the formation of satisfactory polymer coatings, i.e., the polymer should be a good film former. Usually, a satisfactory molecular weight is in the range of 5,000 to 500,000 daltons, preferably from 50,000 to 400,000, more preferably from 100,000 to 300,000, in particular from 100,000 to 200,000 and especially about 150,000 daltons. However since the properties of the film are also partially dependent on the particular polymeric material being used, it is very difficult to specify an appropriate molecular weight range for all polymers.
The molecular weight of a polymer is also important from the point of view of its influence upon the biodegtadation rate of the polymer. For a diffusional mechanism of drug release, the polymer should remain intact until all of the drug is released form the microparticles and then degrade. The drug can also be released from the micropatticles as the polymeric excipient bioerodes. By an appropriaae selection of polymeric materials, a microparticle formulation can be made in which the resulting microparticles exhibit both diffusional release and biodegradation release properties. This is useful in affording multiphasic w0 J5113814 PCT1EP94/03754 release patnerns.
The microparticle produce of the present invention can be prepared by any method capable of producing micaoparticles in a size range acceptable for use in an injectable composition such as the methods described in U.S: 4,389,330 and U.S:
4,530,840.
One preferred method of preparation is that described in the former patent and comprises dissolving or dispersing the active agent in an appropriate solvent. To the agent containing medium is added the polymeric matrix material in an amount relative to the active ingredient that provides a product having the desired loading of active agent.
Optionally, all of the ingredients of the micropatticle product can be blended together in the solvent medium.
Solvents for the agent and the polymeric matrix material that can be employed in the practice of the present invention include organic solvents, such as acetone;
halogenated hydrocarbons, such as chloroform, methylene chloride, and the Iike; aromatic hydrocarbon compounds; halogenated aromatic hydrocarbon compounds; cyclic ethers;
alcohols, such as, benzyl alcohol; ethyl acetate; and the like. A preferred solvent is a mixture of benzyl alcohol and ethyl acetate.
The mixture of ingredienes in the solvent is emulsifed in a continuous-phase processing medium; the continuous-phase medium being such that a dispersion of microdroplets containing the indicated ingredients is formed in the continuous-phase medium.
Naturally, the continuous-phase processing medium and the ~ganic phase must be largely immiscible. The continuous-phase processing medium most commonly employed is water, although nonaqueous media, such as, xylene, toluene, and synthetic and natural oils can be used.
Usually, a surfactant is added to the continuous phase processing medium to prevent the microparticles from agglomerating and to control the size of the solvent microdroplets in the emulsion. A preferred surfactant-dispersing medium combination is a 0.1 to 10 wt.
96, more preferably 0.5 to 2 wt. % solution of polyvinyl alcohol) in water.
The dispersion is formed by mechanical agitation of the mixed materials. An emulsion can also be formed by adding small drops of the active agent-wall forming material solution to the continuous phase processing medium.
The temperature during the formation of the emulsion is not especially critical, but can influence the size and quality of the microparticles and the solubility of the agent in the ' WO 95/13814 ~_ ~ ~ 5 3 7 ~ PCT/EP94103754 _g_ continuous phase. Of course, it is desirable to have as little of the agent in the continuous phase as possible. Moreover, depending on the solvent and continuous-phase processing medium employed, the temperature must not be too low or the solvent and processing medium will solidify or become too viscous for practical purposes. On the other hand, it must not be so high that the processing medium will evaporate or that the liquid processing medium will not be maintained. Moreover, the temperature of the medium cannot be so high that the stability of the particular active agent being incorporated in the microparticles is adversely affected. Accordingly,the dispersion process can be conducted at any temperature that maintains stable operating conditions, preferably about 20°C to about 60°C, depending upon the agent and excipient selected.
The dispersion formed is stable and from this dispersion the organic phase fluid can be partially removed in the first step of the solvent removal process. The solvent can easily be removed by common techniques, such as heating, the application of a reduced pressure, or a combination of both. The temperature employed to evaporate solvent from the microdroplets is not critical, but should not be so high as to degrade the agent employed in the preparation of a given microparticle or to evaporate solvent at a rate rapid enough to cause defects in the wall forming material. Generally, from 10 to 90 ~Yo, preferably 40 to 60 R6 of the solvent is removed in the first solvent removal step.
After the first stage, the dispersed micrtaparticles in the solvent immiscible fluid medium are isolated from the fluid medium by any convenient means of separation.
Thus, for example, the fluid can be decanted from the microparticles or the micropaaticle suspension can be faltered. Various other combinations of separation techniques can be used, if desired.
Following the isolation of the microparticles ianm the continuous phase processing medium, the remainder of the solvent in the microparticles is removed by extraction. In this step, the microparticles can be suspended in the same continuous-phase processing medium used in step one, with or without surfactant, or in another liquid. The extraction medium removes the solvent from the microparticles, but does not dissolve them. During the exaaction, the extraction medium containing dissolved solvent must be removed and replaced with fresh extraction medium. This is best done on a continual or continuous basis where tha rate of exriaction medium replenishment is critical. If the rate is too slow, agent crystals may protrude from the microparticles or grow in the extraction medium.
Obviously, the rate of extraction medium replenishment for a given process is a variable that can easily be determined at the time the process is performed and, therefoae, no precise limits for the rate may be predetermined After the remainder of the solvent has t ' WO 95113814 _ PG17EP94103754 been removed, the microparticles are dried by exposure to air or by other conventional drying techniques, such as, vacuum drying, drying over a desiccant, or the like. This process is very efficient in encapsulating the agent since core loadings of up to 80 wt. 3'0, preferably up to 50 wt. % can be obtained.
A more preferred method of encapsulating the active agent to form the controlled release microparticles of the present invention involves the use of static mixers.
Static or motionless mixers consist of a conduit or tube in which is received a number of static mixing elements. Static mixers provide homogeneous mixing in a relatively short length of conduit, and in a relatively short period of time. With static mixers, the fluid moves through the mixer, rather than some part of the mixer, such as a blade, moving through the fluid. A static mixer is more fully described in U.S. Patent No.
4,511,258.
When using a static mixer to form an emulsion, a variety of factors determine emulsion particle size. These factors include the density and viscosity of the various solutions or phases to be mixed, volume ratio of the phases, interfacial tension between the phases, static mixer parameters (conduit diameter, length of mixing. element; number of mixing elements), and linear veloaty through the static mixer. Tcmperotttre is a variable because it affects density, viscosity, and interfacial tension. The controlling variables are linear velocity, shear rate, and pressure drop per unit length of static mixer.
Particularly, droplet size decreases as linear velocity increases and droplet size increases as pressure drop decreases. Droplets will reach an equilibrium size after a fixed number of elements for a given flow rate. The higher the flow rate, the fewer elements needed Because of these relationships, scaling from laboratory batch sizes to commercial batch sizes is reliable and accrsate, and the same equipment can be used for laboratory and commercial batch sizes.
In order to create microparticles containing an active agent, an organic phase and an aqueous phase are combined The organic and aqueous phases are largely or substantially immiscible, with the aqueous phase constituting the continuous phase of the emulsion.
The organic phase includes an active agent as well as a wall forming polymer or polymeric matrix material. The organic phase can be prepared by dissolving an active agent in an organic or other suitable soivent, or by forming a dispersion or an emulsion containing the active agent Preferably, the organic phase and the aqueous phase are pumped so that the two phases are simultaneously flowing through a static mixer, thereby fomting an emulsion, which comprises micropatticIes containing the active agent encapsulated in the polymeric matrix material. The organic and aqueous phases are ' w0 95/13814 , PCTlEP94103754 pumped through the static mixer into a large volume of quench liquid The quench liquid may be plain water, a water solution, or other suitable liquid Organic solvent may be removed from the microparticles while they are being washed or being stirred in the quench liquid. After the microparticles are washed in a quench to extract or remove the organic solvent, they are isolated, as through a sieve, and dried A laboratory set up for carrying out a static mixer process is illustrated in Figure 1. An organic ar oil phase 30 is prepared by dissolving and, optionally, heating an active agent and a polymeric matrix material or polymer in a stored pot 32 on a hot plate.
However, the process of the present invention is not limited to preparing organic phase 30 by dissolving an active agent. Alternatively, organic phase 30 may be prepared by dispersing an active agent in a solution containing a polymeric matrix material. In such a dispersion, the active agent is only slightly soluble in organic phase 3U.
Alternatively, organic phase 30 may be prepared by preparing an emulsion crontairung an active agent and a polymeric matrix material (double emulsion process). In the double emulsion process, a primary emulsion is prepared which contains an active agent and a polymeric matrix material (organic phase 30). The primary emulsion may be a water-in-oil emulsion, an oil-in-water emulsion, ar any suitable emulsion. The primary emulsion (organic phase 30) and an aqueous phase are then pumped through a static mixer to form a second emulsion which comprises microparticles containing the active agent encapsulated in the polymeric matrix material.
Organic phase 30 is pumped out of stirred pot 32 by a magnetically driven gear pump 34.
The discharge of pump 34 feeds a "Y" connection 36. One branch 361 of "Y"
connection 36 returns to pot 32 for recirculation flow. The other branch 362 feeds into an in-Iine static mixer 10. Aqueous or water phase 40 is prepared in like manner, with a stirred pot 42, a magnetically driven gear pump 44, and a "Y" connection 46.
One branch 461 of "Y" connection 46 returns to pot 42 for recirculation flow. The other branch 462 feeds into in-line static mixer 10. Organic phase 3~ and aqueous phase 40 are substantially immiscible.
Branches 362 and 462 from each solution which feed in-line static mixer 10 are joined by another "Y" connection 50 and feed through mixer inlet line 51 into static mixer 10. Static mixer 10 discharges through mixer outlet line 52 into wash tank 60. Silicone tubing and polypropylene fittings are used in the system illustrated in Figure I.
Silicone tubing having 9.53 mm ll~ is used for all Iines except mixer outlet line 52. Smaller diameter tubing (4.76 mm 1D) is used for mixer outlet line 52 to prevent collapse of the emulsion R'O 95113814 , PCTYEP94I03754 -I I-both in mixer outlet line 52 and upon entering wash tank 60.
In one embodiment of the process, pumps 34 and 44 are started in recirculation mode and desired flow rates are set for organic phase 30 and water phase 40. The flow rate of water phase 40 is preferably greater than the flow rate of organic phase 30.
However, the two flow rates may be substantially the same. The ratio of the flow rate of water phase 40 to the flow rate of organic phase 30 is preferably in the range of 1:1 to i0:1. "Y"
connection 46 is then switched so that water phase 40 flows through branch 462 to static mixer 10. Once water phase 40 fills mixer inlet line 51, static mixer 10, and mixer outlet line 52, "Y" connection 36 is switched so that organic phase 30 flows through branch 362 to static mixer 10. Organic phase 30 and aqueous phase 40 are now flowing simultaneously through static mixer 10. When the desired volume of organic phase has been pumped to static mixer 10, "Y" connection 36 is switched to recirculation through branch 361. Water phase 40 continues to flow for a short time to clean out any organic phase remaining in mixer inlet line SI, static mixer I0, and mixer outlet line 52. "Y"
connection 46 is then switched to recirculation through branch 461.
Organic phase 30 and aqueous phase 40 are mixed in static mixer 10 to form an emulsion. The emulsion formed comprises microparticles containing the active agent encapsulated in the polymeric matrix material.
The microparticles praluced by the method of the present invention are usually of a spherical shape, although they may be irregularly shaped. The microparticles produced by the method of the present invention can vary in size, ranging from submicron to millimeter diameters.1n a preferted embodiment of the present invention, static mixing elements 14 of static mixer 10 are selected so that the resulting microparticles range in size from i to 500 microns (pro), preferably 25 to 180 microns in particularly 60 to 120 microns, e.g. 90 microns, whereby administration of the microparticles can be carried out with a standard gauge needle. The microparticles may be stirred in wash tank 60 which contains a quench liquid. The microparricles may be isolated from the quench liquid, such as by using a sieve column. The microparticles may be dried using conventional drying techniques, and further size isolation may be done.
The active agent bearing microparticles are obtained and stored as a dry material. Prior to administration to a patient, the dry microparticles can be suspended in an acceptable pharmaceutical liquid vehicle, preferably a 2.5 wt. °.6 solution of carboxymethyl cellulose, whereupon the suspension is injected into the desired portion of the body.
The microparticles can be mixed by size or by type so as to provide for the delivery of *rB
WO 95/13814 , . PCT/EP94/03754 active agent to the patient in a multiphasic manner and/or in a manner that provides different agents to the patient at different times, or a mixture of agents at the same time.
In vitro dissolution studies measuring the release of risperidone from microparticles of the invention showed an almost constant release of risperidone during a sustained period of time. Similarly, in vivo studies in dogs being dosed intramuscularly with microparticle formulations of the invention, in particular with the formulations described thereinafter in the examples; showed almost constant and long-lasting plasma concentrations of active agent.
The following examples further describe the materials and methods used in carrying out the invention. The examples are not intended to limit the invention in any manner.
Example 1: Preparation of 35% Theoretically Loaded Risperidone Microparticles (Batch ProdeX 2) First, the aqueous phase (solution A) is prepared by weighing and mixing 906.1 g 1%
polyvinyl alcohol), (Vinyl 205"'', Air Products and Chemical Inc.), 29.7 g benzyl alcohol end 65.3 g ethyl acetate. Then the organic phase (solution B) is prepared by dissolving 29.3 g of high viscosity 75 :25 dl (polylactide-co-glycolide), in 108.7 g ethyl acetate and 108:4 g benzyl alcohol. Once the polymer is completely dissolved, 15.7 g risperidone base is added and dissolved in the polymer solution. The exposure time of the dissolved risperidone with the polymer is kept to a minimum ( < 10 minutes).
Solutions A and B are then pumped through a 6.35 mm diameter static mixer (Cole Parmer L04667-14) via a gear drive pump and head (Cole Parmer L07149-04, L07002-16) at flow rates of 198 and 24 ml/minute, respectively, into a quench composed of 55 liters of water for injection containing 1276.0 g of ethyl acetate, 92.3 g (0.02 Molar) of anhydrous sodium bicarbonate, and 116.2 g (0.02 Molar) of anhydrous sodium carbonate at 11 °C. The rnicroparticles are allowed to stir in the first wash for 1.75 hours, then isolated by sieving with a 25 micron sieve. The product retained by the sieve is transferred to a 20-liter wash at 13°C. After stirring in the sieved wash for 2.25 hours, the microparticles are isolated and size fractionated by sieving through a stainless steel sieve colurnn composed of 25- and 180-micron mesh sizes. The microparticles are dried overnight, then collected and weighed.
Example 2: Preparation of 40% Theoretically Loaded Risperidone Microparticles (Batch Prodex 3) First, the aqueous phase {solution A) is prepared by weighing and mixing 904.4 g 1 %
* trademark ' W095/13814 . PC1YEP94/03754 poly (vinyl alcohol), (Vinyl 205'2', Air Products and Chemical Inc.), 30.1 g benzyl alcohol and 65.8 g ethyl acetate. Then the organic phase (solution B) is prepared by dissolving 27.1 g of high viscosity 75 :25 dl (polylactide-co-glycolide), in 99.3 g ethyl, acetate and 99.1 g benzyl alcohol. Once the polymer is completely dissolved, 18.1 g tisperidone base is added and dissolved in the polymer solution. The exposure time of the dissolved risperidone with the polymer is kept to a minimum (c 10 minutes).
Solutions A and B are then pumped through a 6.35 mm diameter static mixer (Cole Parmer L04667-14) via a gear drive pump and head (Cole Parmer L07149-04, L07002-16) at flow rates of 198 and 24 ml/minute, respectively, and into a quench composed of 55 liters of water for injection containing 1375.6 g of ethyl acetate, 92.4 g (0.02 Molar) of anhydrous sodium bicarbonate, and 116.6 g (0.02 Molar) of anhydrous sodium carbonate at 12'C. The microparticIes are allowed to stir in the first wash for 2 hours, then isolated by sieving with a 25-micron sieve. The product retained by the sieve is transferred to a 20 liter wash at 12'C. After stirring in the sieved wash for 3 hours, the microparticles are isolated and size fractionated by sieving through a stainless-steel sieve column composed of 25- and 180 micron mesh sizes. The microparticles are dried overnight, then collected and weighed.
B~am~l : Lyophilisation and Gamma Irradiation of Microparticles from Batches Prodex 2 and Prodex 3 (Samples Prodex 4A, Prodex 4B, and Prodex 4C) Microparticles from batches Prodex 2 and Prodex 3 were lyophilized. The microparticles were weighed into 5 cc serum vials. Then an aqueous vehicle composed of 0.759!o CMC, 596 Mannitol, and 0.196 Tween 80~"'' was added to the vials. The microparticles were suspended in the vehicle by agitation, then quickly frozen in a dry ice/acetone bath. The vials were then lyophilized in a pilot-scale lyophilizer employing a camped 30'C
maximum temperature cycle for 50 hours. Samples Prodex 4A and Prodex 4C were lyophilized samples from Prodex 2 and Prodex 3, respectively. Sample Prodex 4B
was lyophilized from Prodex 2 that had bean subsequently sterilized by 2.2 MRad gamma irradiation from a 60Co source.
x le 4 : In vivo study The duration of action of the micropatticle-based risperidone formulations in the apomorphine-induced emesis test in dogs were studied. Neuroleptics are known to antagonize apomorphine-induced emesis by blocking dopamine D2 receptors in the area postrema of the fourth ventricle. The test is generally used to predict the onset and WO 95113814 ~ PGTIEP94103754 duration of antipsychotic action of neuroIeptics in man (Janssen et al., Arzneim. Forsch.IDrug Res. I5: 1 I96-1206 (1965); Niemegeers et al., Life Sci.
24:2201-2216 (1979)).
9-OH-risperidone has a pharmacological profile that is virtually identical to that of risperidone. Both constitute together the "active moiety" that determines the biological activity of risperidone.
Apomorphine was administered subcutaneously at 0.31 mg/kg to the dogs twice a week, during the whole course of the experianent. The dogs were observed for vomiting durang a I-hour period after the administration of apomorphine. Complete absence of emesis for 1 hour after apomorphine challenge was considered to reflect significant anti-emetic activity. The duration of the anti-emetic action was defined as the time interval during which 2 out of 3 dogs were protected from emesis.
The formulations were injected in a volume of OS ml into the biceps femoralis of one of the hind limbs at the level of the thigh. At several time intervals after the intramuscular injection, blood samples were taken and, immediately thereafter, the dogs were challenged with a dose of apomorphine. Complete absence of emesis within 1 h after apomorphine challenge (which is never observed in control animals; n> 1000) was considered to reflect significant antiemetic activity.
Table 1 indicates whether the dogs were protected (+) or not protected (-) from apomorphine-induced emesis at the various time intervals after intramuscular injection of the depot formulations. All formulations showed an immediate onset of anti-emetic action.
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U. S. Patents No. 4,389,330 and 4,530,840 describe the preparation of microparticles containing an active agent by a method comprising: (a) dissolving or dispersing an active agent in a solvent and dissolving a wall forming material in that solvent; (b) dispersing the solvent containing the active agent and wall forming material in a continuous-phase processing medium; (c) evaporating a portion of the solvent from the dispersion of step (b), thereby forming microparticles containing the active agent in the suspension; and (d) extracting the remainder of the solvent from the microparticles.
Description of the Invention The invention relates to a pharntaceutical composition comprising biodegradable and biocompatible microparticles containing a 1,2-benzazole of formula (I) i R8 Z N R3 R ,X /R
N I ~~ cn, ~ N Alk-N
O
or a pharmaceutically acceptable acid addition salt thereof, wherein R is hydrogen or Cl.6alkyl;
RI and RZ independently are hydrogen, halo, hydroxy, Cl~atkyloxy and Cl_6alkyl;
XisOorS;
Alk is Ct.~alkanediYl; and R3 is hydrogen or Cl~alkyl;
Z is -S-, -CHZ-, or -CR4=CR5-; where R4 and RS independently are hydrogen or Cl~alkyl;
A is a bivalent radical -CHZ-CHZ-, -CH2-CHZ-CHZ- or -CR6°CR~-: wherein R6 and R~
are hydrogen, halo, amino or Cl-6alkyl; and R8 is hydrogen or hydroxyl.
In the foregoing definitions, the term "halo" is generic to fluoro, chloro, bromo, and iodo; "Ct_balkyl" is meant to include straight and branched chain saturated hydrocarbon radicals having from I to 6 carbon atoms, such as, for example, methyl, ethyl, propyl, ' w0 95113814 , PCT'IEP94103754 butyl, pentyl, hexyl, and isomers thereof; "Ci.~allcanediyl" is meant to include bivalent straight or branched chain alkanediyi radicals having from 1 to 4 carbon atoms, such as, for example, methylene, ethylene, propylene, butylene, and isomers thereof.
Preferred compounds within the invention are those wherein R3 is Cl.salkyl and in particular is methyl and A is a bivalent radical -CH2-CH2-, -CHZ-CH2-CH2-, or -CR6=CRS-, wherein R6 and R~ independently are hydrogen or Cl.6allryl.
Particularly preferred compounds are those preferred compounds wherein X is oxygen, R is hydrogen, Rt is halo or in particular is hydrogen, and R2 is hydrogen, halo, hydroxy, or Cl~alkyloxy.
More particularly preferred compounds are those particulary preferred compounds wherein -Z-A- is -CH2-CH2-CH2-CHZ-, -S-CH2-CH2-, -S-(CFi~3-, -S-CR6=CRS-, or -CH=CH-CR6=CRS-, wherein R6 and R~ independently are hydrogen or methyl and R$
is hydrogen or 9-hydroxy.
The most prefenrd compounds are 3-[2-[4-(6-fluoro-l,2-benzisaxawl-3-yl)-1-piperidinyl) ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[l,2-a] pyrimidin-4-one ("ltisperidone") and the pharmaceutically acceptable acid addition salts thereof.
The compounds of formula (1) can generally be prepared by the methods described in US-4,804,663 or US-5,158,952.
The compounds of formula (I) have basic properties and, consequently, can be converted to their therapeutically active non-toxic acid addition salt forms by treatment with appropriate acids, such as, for example, inorganic acids, such as hydrohalic acid, e.g., hydrochloric, hydrobromic, and the Like; sulfuric acid, nitric acid, phosphoric acid, and the like; or organic acids, such as, for example, acetic, propanoic, hydroacetic, 2-hydroxypropanoic, 2-oxopropanoic,ethanedioic,propanedioic, butanedioic, (Z)-2-butenedioic, (E)-2-butenedioic, 2-hydroxybutanedioic, 2,3-dihydroxybutanedioic, 2-hydroxy-1,2,3-propanetricarboxylic, methanesulfonic, ethanesulfonic, benzenesulfonic, toluenesulfonic, cyclohexanesulfamic, 2-hydroxybenwic, 4-amino-2-hydroxybenwic, and the like acids.
The compounds of formula (I) are potent antagonists of a series of neurotransmitters and, as a result, have useful pharmacological properties. In particular, the compounds of formula (I) are combined serotonin and dopamine antagonists. Consequently, they are useful as anti-psychotics and in the treatment of a variety of complaints in which serotonin release is of predominant importance such as, for example, in the blocking of 217 ~ 3 7 0 p~~,p94103754 ~'O 95113814 serotonin-induced contractions of bronchial tissues and of blood vessels, arteries as well as veins. Therapeutic indications for using the present compounds are mainly in the CNS
area, i.e. as antipsychotic agents and therefore they can be used in combatting psychoses, in particular schizophrenia, aggressive behaviour, anxiety, depression and migraine.
Additionally the compounds of form (I) are also useful as sedating, anxiolytic, anti-aggressive, anti-stress and muscular protectant agents.
The present invention further provides a method of treating warm-blooded animals suffering from psychotic disorders, said method comprising the systemic administration of a effective amount of a mictnencapsulated compound of formula (1) or a pharmaceutically acceptable acid addition salt thereof in admixture with a pharmaceutical carrier. Or alternatively, there is provided the use for the manufacture of a medicament of a microencapsulated compound of formula (1] for treating psychotic disorders.
Or still alternatively, there is provided the use of microencapsulated compound of formula ()7 or a pharmaceutically acceptable acid addition salt thereof in admixture with a pharmaceutical carrier for treating psychotic disorders. In general, it is contemplated that an effective amount of the active ingredient per se would be from 0.01 mg/kg to 4 mg/kg body weight, more preferably, from 0.04 mg/kg to 2 mg/kg body weight.
By the term "administered" as used herein, any method of delivering the 1,2-benzaaole-containing microparticles of the invention to a warn blooded animal is intended, such as, for example, parenteral (intravenous, intramuscular, or subcutaneous) administration.
By "microparticles" solid particles that contain an active agent, herein the 1,2-benzawle, either in solution or in crystalline form are meant. The active agent is dispersed or dissolved within the polymer that serves as the matrix of the particle.
In another aspect, the present invention relates to a method of inhibiting serotonergic or dopaminergic overstimulation in warm-blooded animals wherein said method comprises administration of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of formula (1) within a polymeric matrix. Or alternatively>
there is provided the use for the manufacture of a medicament, of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of formula (I) within a polymeric mattix, for inhibiting serotonergic or dopaminergic overstimulation in warm-blooded animals. Or the use of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzaaole of formula (1) within a polymeric matrix far inhibiting serotonergic or dopaminergic overstimulation in warm-blooded animals.
' WO 95/13814 . Pt°lYEP94103754 1n still another aspect, the invention relates to microparticles made of a biocompatible and biodegradable matrix containing a compound of formula (I) or a pharmaceutically acceptable acid addition salt thereof.
3 The compositions of this invention are useful for treating mental illness in warm-blooded anirttals, preferably mammals, more preferably humans, (hereinafter, collectively referred to as "patients") that comprises providing to such patients biodegradable micropatticles loaded with a 1,2-benzazole, as described above.
The compositions of the present invention comprise microparticles designed for the controlled release from a biocompatible, biodegradable matrix over an extended period of time of an effective amount of the 1,2-benzaaole of formula (I). They provide advantages over compositions lmown in the art, such advantages comprising, inter alla, the fact that it is a biodegradable system, an injectable system that prevents the loss of IS dose during treatment, the ability to mix microparticles containing different drugs, and the ability to program release (multiphasic release patterns) to give faster or slower rates of drug release as needed.
In a preferred embodiment, adminisaation of the 1,2-benzazoles to patients is achieved by a single administration of the drug loaded microparticles, releasing the drug in a constant or pulsed manner into the patient and eliminating the need for repetitive injections.
The product of the present invention offers the advantage of having a duration of action ranging from 7 to more than 200 days, depending upon the type of microparticle selected. In a preferred embodiment, the microparticles are designed to afford treatment to patienu over a period of 14 to 100 days, in particular 14 to 50 or to 60, or 30 to 60 days. The duration of action can be controlled by manipulation of the polymer composition, the polymer:drug ratio, and the micropatticle size.
Another important advantage of the present invention is that practically all of the active agent is delivered to the patient because the polymer used is biodegradable, thereby permitting all of the entrapped agent to be released into the patient.
The polymeric matrix material of the microparticles of the present invention is a biocompatible and biodegradable polymeric material. The term"biocompatible" is defined as a polymeric material that is not toxic to the human body, is not carcinogenic, and does ' ~JfO 95/13814 PCTIEP94103754 not significantly induce inflammation in body tissues. The matrix material should be biodegradable in the sense that the polymeric material should degrade by bodily processes to products readily disposable by the body and should not accumulate in the body. The products of the biodegradation should also be biocompatible with the body in the same sense that the polymeric matrix is biocompatible with the body.
Suitable examples of polymeric matrix materials include poly(glycoIic acid), poly-D,L-lactic acid, poly-Irlactic acid, copolymers of the foregoing, poly(aliphatic carboxylic acids), copolyoxalates, polycaprolactone, polydioxonone, poly(ortho carbonates), poly(acetals), poly(lactic acid-caprolactone), polyorthoesters, poly(glycolic acid caprolactone), polyanhydrides, and natural polymers including albumin, casein, and waxes such as, glycerol mono- and distearate, and the like. The preferred polymer for use in the practice of this invention is dl-(polylactide-co-glycolide) i.e. a copolymer of poly(glycolic acid) and poly-D,L-lactic acid. It is preferred that the molar ratio of lactide to glycolide in such a copolymer be in the range of from about 85:15 to about 35:65, more in particular from about 75:25 to about 50:50, e.g. 85:15, 75:25, b5:35 or 50:50.
The amount of active agent incorporated in the microparticles usually ranges from about 1 wt °Jo to about 90 wt. %, preferably 30 to 50 wt. 9b, more preferably 35 to 40 wt. % . By weight % is meant parts of agent per total weight of microparticle. For example, 10 wt.
96 agent would mean 10 parts agent and 90 parts polymer by weight.
The molecular weight of the polymeric matrix material is of some importance.
The molecular weight should be high enough to permit the formation of satisfactory polymer coatings, i.e., the polymer should be a good film former. Usually, a satisfactory molecular weight is in the range of 5,000 to 500,000 daltons, preferably from 50,000 to 400,000, more preferably from 100,000 to 300,000, in particular from 100,000 to 200,000 and especially about 150,000 daltons. However since the properties of the film are also partially dependent on the particular polymeric material being used, it is very difficult to specify an appropriate molecular weight range for all polymers.
The molecular weight of a polymer is also important from the point of view of its influence upon the biodegtadation rate of the polymer. For a diffusional mechanism of drug release, the polymer should remain intact until all of the drug is released form the microparticles and then degrade. The drug can also be released from the micropatticles as the polymeric excipient bioerodes. By an appropriaae selection of polymeric materials, a microparticle formulation can be made in which the resulting microparticles exhibit both diffusional release and biodegradation release properties. This is useful in affording multiphasic w0 J5113814 PCT1EP94/03754 release patnerns.
The microparticle produce of the present invention can be prepared by any method capable of producing micaoparticles in a size range acceptable for use in an injectable composition such as the methods described in U.S: 4,389,330 and U.S:
4,530,840.
One preferred method of preparation is that described in the former patent and comprises dissolving or dispersing the active agent in an appropriate solvent. To the agent containing medium is added the polymeric matrix material in an amount relative to the active ingredient that provides a product having the desired loading of active agent.
Optionally, all of the ingredients of the micropatticle product can be blended together in the solvent medium.
Solvents for the agent and the polymeric matrix material that can be employed in the practice of the present invention include organic solvents, such as acetone;
halogenated hydrocarbons, such as chloroform, methylene chloride, and the Iike; aromatic hydrocarbon compounds; halogenated aromatic hydrocarbon compounds; cyclic ethers;
alcohols, such as, benzyl alcohol; ethyl acetate; and the like. A preferred solvent is a mixture of benzyl alcohol and ethyl acetate.
The mixture of ingredienes in the solvent is emulsifed in a continuous-phase processing medium; the continuous-phase medium being such that a dispersion of microdroplets containing the indicated ingredients is formed in the continuous-phase medium.
Naturally, the continuous-phase processing medium and the ~ganic phase must be largely immiscible. The continuous-phase processing medium most commonly employed is water, although nonaqueous media, such as, xylene, toluene, and synthetic and natural oils can be used.
Usually, a surfactant is added to the continuous phase processing medium to prevent the microparticles from agglomerating and to control the size of the solvent microdroplets in the emulsion. A preferred surfactant-dispersing medium combination is a 0.1 to 10 wt.
96, more preferably 0.5 to 2 wt. % solution of polyvinyl alcohol) in water.
The dispersion is formed by mechanical agitation of the mixed materials. An emulsion can also be formed by adding small drops of the active agent-wall forming material solution to the continuous phase processing medium.
The temperature during the formation of the emulsion is not especially critical, but can influence the size and quality of the microparticles and the solubility of the agent in the ' WO 95/13814 ~_ ~ ~ 5 3 7 ~ PCT/EP94103754 _g_ continuous phase. Of course, it is desirable to have as little of the agent in the continuous phase as possible. Moreover, depending on the solvent and continuous-phase processing medium employed, the temperature must not be too low or the solvent and processing medium will solidify or become too viscous for practical purposes. On the other hand, it must not be so high that the processing medium will evaporate or that the liquid processing medium will not be maintained. Moreover, the temperature of the medium cannot be so high that the stability of the particular active agent being incorporated in the microparticles is adversely affected. Accordingly,the dispersion process can be conducted at any temperature that maintains stable operating conditions, preferably about 20°C to about 60°C, depending upon the agent and excipient selected.
The dispersion formed is stable and from this dispersion the organic phase fluid can be partially removed in the first step of the solvent removal process. The solvent can easily be removed by common techniques, such as heating, the application of a reduced pressure, or a combination of both. The temperature employed to evaporate solvent from the microdroplets is not critical, but should not be so high as to degrade the agent employed in the preparation of a given microparticle or to evaporate solvent at a rate rapid enough to cause defects in the wall forming material. Generally, from 10 to 90 ~Yo, preferably 40 to 60 R6 of the solvent is removed in the first solvent removal step.
After the first stage, the dispersed micrtaparticles in the solvent immiscible fluid medium are isolated from the fluid medium by any convenient means of separation.
Thus, for example, the fluid can be decanted from the microparticles or the micropaaticle suspension can be faltered. Various other combinations of separation techniques can be used, if desired.
Following the isolation of the microparticles ianm the continuous phase processing medium, the remainder of the solvent in the microparticles is removed by extraction. In this step, the microparticles can be suspended in the same continuous-phase processing medium used in step one, with or without surfactant, or in another liquid. The extraction medium removes the solvent from the microparticles, but does not dissolve them. During the exaaction, the extraction medium containing dissolved solvent must be removed and replaced with fresh extraction medium. This is best done on a continual or continuous basis where tha rate of exriaction medium replenishment is critical. If the rate is too slow, agent crystals may protrude from the microparticles or grow in the extraction medium.
Obviously, the rate of extraction medium replenishment for a given process is a variable that can easily be determined at the time the process is performed and, therefoae, no precise limits for the rate may be predetermined After the remainder of the solvent has t ' WO 95113814 _ PG17EP94103754 been removed, the microparticles are dried by exposure to air or by other conventional drying techniques, such as, vacuum drying, drying over a desiccant, or the like. This process is very efficient in encapsulating the agent since core loadings of up to 80 wt. 3'0, preferably up to 50 wt. % can be obtained.
A more preferred method of encapsulating the active agent to form the controlled release microparticles of the present invention involves the use of static mixers.
Static or motionless mixers consist of a conduit or tube in which is received a number of static mixing elements. Static mixers provide homogeneous mixing in a relatively short length of conduit, and in a relatively short period of time. With static mixers, the fluid moves through the mixer, rather than some part of the mixer, such as a blade, moving through the fluid. A static mixer is more fully described in U.S. Patent No.
4,511,258.
When using a static mixer to form an emulsion, a variety of factors determine emulsion particle size. These factors include the density and viscosity of the various solutions or phases to be mixed, volume ratio of the phases, interfacial tension between the phases, static mixer parameters (conduit diameter, length of mixing. element; number of mixing elements), and linear veloaty through the static mixer. Tcmperotttre is a variable because it affects density, viscosity, and interfacial tension. The controlling variables are linear velocity, shear rate, and pressure drop per unit length of static mixer.
Particularly, droplet size decreases as linear velocity increases and droplet size increases as pressure drop decreases. Droplets will reach an equilibrium size after a fixed number of elements for a given flow rate. The higher the flow rate, the fewer elements needed Because of these relationships, scaling from laboratory batch sizes to commercial batch sizes is reliable and accrsate, and the same equipment can be used for laboratory and commercial batch sizes.
In order to create microparticles containing an active agent, an organic phase and an aqueous phase are combined The organic and aqueous phases are largely or substantially immiscible, with the aqueous phase constituting the continuous phase of the emulsion.
The organic phase includes an active agent as well as a wall forming polymer or polymeric matrix material. The organic phase can be prepared by dissolving an active agent in an organic or other suitable soivent, or by forming a dispersion or an emulsion containing the active agent Preferably, the organic phase and the aqueous phase are pumped so that the two phases are simultaneously flowing through a static mixer, thereby fomting an emulsion, which comprises micropatticIes containing the active agent encapsulated in the polymeric matrix material. The organic and aqueous phases are ' w0 95/13814 , PCTlEP94103754 pumped through the static mixer into a large volume of quench liquid The quench liquid may be plain water, a water solution, or other suitable liquid Organic solvent may be removed from the microparticles while they are being washed or being stirred in the quench liquid. After the microparticles are washed in a quench to extract or remove the organic solvent, they are isolated, as through a sieve, and dried A laboratory set up for carrying out a static mixer process is illustrated in Figure 1. An organic ar oil phase 30 is prepared by dissolving and, optionally, heating an active agent and a polymeric matrix material or polymer in a stored pot 32 on a hot plate.
However, the process of the present invention is not limited to preparing organic phase 30 by dissolving an active agent. Alternatively, organic phase 30 may be prepared by dispersing an active agent in a solution containing a polymeric matrix material. In such a dispersion, the active agent is only slightly soluble in organic phase 3U.
Alternatively, organic phase 30 may be prepared by preparing an emulsion crontairung an active agent and a polymeric matrix material (double emulsion process). In the double emulsion process, a primary emulsion is prepared which contains an active agent and a polymeric matrix material (organic phase 30). The primary emulsion may be a water-in-oil emulsion, an oil-in-water emulsion, ar any suitable emulsion. The primary emulsion (organic phase 30) and an aqueous phase are then pumped through a static mixer to form a second emulsion which comprises microparticles containing the active agent encapsulated in the polymeric matrix material.
Organic phase 30 is pumped out of stirred pot 32 by a magnetically driven gear pump 34.
The discharge of pump 34 feeds a "Y" connection 36. One branch 361 of "Y"
connection 36 returns to pot 32 for recirculation flow. The other branch 362 feeds into an in-Iine static mixer 10. Aqueous or water phase 40 is prepared in like manner, with a stirred pot 42, a magnetically driven gear pump 44, and a "Y" connection 46.
One branch 461 of "Y" connection 46 returns to pot 42 for recirculation flow. The other branch 462 feeds into in-line static mixer 10. Organic phase 3~ and aqueous phase 40 are substantially immiscible.
Branches 362 and 462 from each solution which feed in-line static mixer 10 are joined by another "Y" connection 50 and feed through mixer inlet line 51 into static mixer 10. Static mixer 10 discharges through mixer outlet line 52 into wash tank 60. Silicone tubing and polypropylene fittings are used in the system illustrated in Figure I.
Silicone tubing having 9.53 mm ll~ is used for all Iines except mixer outlet line 52. Smaller diameter tubing (4.76 mm 1D) is used for mixer outlet line 52 to prevent collapse of the emulsion R'O 95113814 , PCTYEP94I03754 -I I-both in mixer outlet line 52 and upon entering wash tank 60.
In one embodiment of the process, pumps 34 and 44 are started in recirculation mode and desired flow rates are set for organic phase 30 and water phase 40. The flow rate of water phase 40 is preferably greater than the flow rate of organic phase 30.
However, the two flow rates may be substantially the same. The ratio of the flow rate of water phase 40 to the flow rate of organic phase 30 is preferably in the range of 1:1 to i0:1. "Y"
connection 46 is then switched so that water phase 40 flows through branch 462 to static mixer 10. Once water phase 40 fills mixer inlet line 51, static mixer 10, and mixer outlet line 52, "Y" connection 36 is switched so that organic phase 30 flows through branch 362 to static mixer 10. Organic phase 30 and aqueous phase 40 are now flowing simultaneously through static mixer 10. When the desired volume of organic phase has been pumped to static mixer 10, "Y" connection 36 is switched to recirculation through branch 361. Water phase 40 continues to flow for a short time to clean out any organic phase remaining in mixer inlet line SI, static mixer I0, and mixer outlet line 52. "Y"
connection 46 is then switched to recirculation through branch 461.
Organic phase 30 and aqueous phase 40 are mixed in static mixer 10 to form an emulsion. The emulsion formed comprises microparticles containing the active agent encapsulated in the polymeric matrix material.
The microparticles praluced by the method of the present invention are usually of a spherical shape, although they may be irregularly shaped. The microparticles produced by the method of the present invention can vary in size, ranging from submicron to millimeter diameters.1n a preferted embodiment of the present invention, static mixing elements 14 of static mixer 10 are selected so that the resulting microparticles range in size from i to 500 microns (pro), preferably 25 to 180 microns in particularly 60 to 120 microns, e.g. 90 microns, whereby administration of the microparticles can be carried out with a standard gauge needle. The microparticles may be stirred in wash tank 60 which contains a quench liquid. The microparricles may be isolated from the quench liquid, such as by using a sieve column. The microparticles may be dried using conventional drying techniques, and further size isolation may be done.
The active agent bearing microparticles are obtained and stored as a dry material. Prior to administration to a patient, the dry microparticles can be suspended in an acceptable pharmaceutical liquid vehicle, preferably a 2.5 wt. °.6 solution of carboxymethyl cellulose, whereupon the suspension is injected into the desired portion of the body.
The microparticles can be mixed by size or by type so as to provide for the delivery of *rB
WO 95/13814 , . PCT/EP94/03754 active agent to the patient in a multiphasic manner and/or in a manner that provides different agents to the patient at different times, or a mixture of agents at the same time.
In vitro dissolution studies measuring the release of risperidone from microparticles of the invention showed an almost constant release of risperidone during a sustained period of time. Similarly, in vivo studies in dogs being dosed intramuscularly with microparticle formulations of the invention, in particular with the formulations described thereinafter in the examples; showed almost constant and long-lasting plasma concentrations of active agent.
The following examples further describe the materials and methods used in carrying out the invention. The examples are not intended to limit the invention in any manner.
Example 1: Preparation of 35% Theoretically Loaded Risperidone Microparticles (Batch ProdeX 2) First, the aqueous phase (solution A) is prepared by weighing and mixing 906.1 g 1%
polyvinyl alcohol), (Vinyl 205"'', Air Products and Chemical Inc.), 29.7 g benzyl alcohol end 65.3 g ethyl acetate. Then the organic phase (solution B) is prepared by dissolving 29.3 g of high viscosity 75 :25 dl (polylactide-co-glycolide), in 108.7 g ethyl acetate and 108:4 g benzyl alcohol. Once the polymer is completely dissolved, 15.7 g risperidone base is added and dissolved in the polymer solution. The exposure time of the dissolved risperidone with the polymer is kept to a minimum ( < 10 minutes).
Solutions A and B are then pumped through a 6.35 mm diameter static mixer (Cole Parmer L04667-14) via a gear drive pump and head (Cole Parmer L07149-04, L07002-16) at flow rates of 198 and 24 ml/minute, respectively, into a quench composed of 55 liters of water for injection containing 1276.0 g of ethyl acetate, 92.3 g (0.02 Molar) of anhydrous sodium bicarbonate, and 116.2 g (0.02 Molar) of anhydrous sodium carbonate at 11 °C. The rnicroparticles are allowed to stir in the first wash for 1.75 hours, then isolated by sieving with a 25 micron sieve. The product retained by the sieve is transferred to a 20-liter wash at 13°C. After stirring in the sieved wash for 2.25 hours, the microparticles are isolated and size fractionated by sieving through a stainless steel sieve colurnn composed of 25- and 180-micron mesh sizes. The microparticles are dried overnight, then collected and weighed.
Example 2: Preparation of 40% Theoretically Loaded Risperidone Microparticles (Batch Prodex 3) First, the aqueous phase {solution A) is prepared by weighing and mixing 904.4 g 1 %
* trademark ' W095/13814 . PC1YEP94/03754 poly (vinyl alcohol), (Vinyl 205'2', Air Products and Chemical Inc.), 30.1 g benzyl alcohol and 65.8 g ethyl acetate. Then the organic phase (solution B) is prepared by dissolving 27.1 g of high viscosity 75 :25 dl (polylactide-co-glycolide), in 99.3 g ethyl, acetate and 99.1 g benzyl alcohol. Once the polymer is completely dissolved, 18.1 g tisperidone base is added and dissolved in the polymer solution. The exposure time of the dissolved risperidone with the polymer is kept to a minimum (c 10 minutes).
Solutions A and B are then pumped through a 6.35 mm diameter static mixer (Cole Parmer L04667-14) via a gear drive pump and head (Cole Parmer L07149-04, L07002-16) at flow rates of 198 and 24 ml/minute, respectively, and into a quench composed of 55 liters of water for injection containing 1375.6 g of ethyl acetate, 92.4 g (0.02 Molar) of anhydrous sodium bicarbonate, and 116.6 g (0.02 Molar) of anhydrous sodium carbonate at 12'C. The microparticIes are allowed to stir in the first wash for 2 hours, then isolated by sieving with a 25-micron sieve. The product retained by the sieve is transferred to a 20 liter wash at 12'C. After stirring in the sieved wash for 3 hours, the microparticles are isolated and size fractionated by sieving through a stainless-steel sieve column composed of 25- and 180 micron mesh sizes. The microparticles are dried overnight, then collected and weighed.
B~am~l : Lyophilisation and Gamma Irradiation of Microparticles from Batches Prodex 2 and Prodex 3 (Samples Prodex 4A, Prodex 4B, and Prodex 4C) Microparticles from batches Prodex 2 and Prodex 3 were lyophilized. The microparticles were weighed into 5 cc serum vials. Then an aqueous vehicle composed of 0.759!o CMC, 596 Mannitol, and 0.196 Tween 80~"'' was added to the vials. The microparticles were suspended in the vehicle by agitation, then quickly frozen in a dry ice/acetone bath. The vials were then lyophilized in a pilot-scale lyophilizer employing a camped 30'C
maximum temperature cycle for 50 hours. Samples Prodex 4A and Prodex 4C were lyophilized samples from Prodex 2 and Prodex 3, respectively. Sample Prodex 4B
was lyophilized from Prodex 2 that had bean subsequently sterilized by 2.2 MRad gamma irradiation from a 60Co source.
x le 4 : In vivo study The duration of action of the micropatticle-based risperidone formulations in the apomorphine-induced emesis test in dogs were studied. Neuroleptics are known to antagonize apomorphine-induced emesis by blocking dopamine D2 receptors in the area postrema of the fourth ventricle. The test is generally used to predict the onset and WO 95113814 ~ PGTIEP94103754 duration of antipsychotic action of neuroIeptics in man (Janssen et al., Arzneim. Forsch.IDrug Res. I5: 1 I96-1206 (1965); Niemegeers et al., Life Sci.
24:2201-2216 (1979)).
9-OH-risperidone has a pharmacological profile that is virtually identical to that of risperidone. Both constitute together the "active moiety" that determines the biological activity of risperidone.
Apomorphine was administered subcutaneously at 0.31 mg/kg to the dogs twice a week, during the whole course of the experianent. The dogs were observed for vomiting durang a I-hour period after the administration of apomorphine. Complete absence of emesis for 1 hour after apomorphine challenge was considered to reflect significant anti-emetic activity. The duration of the anti-emetic action was defined as the time interval during which 2 out of 3 dogs were protected from emesis.
The formulations were injected in a volume of OS ml into the biceps femoralis of one of the hind limbs at the level of the thigh. At several time intervals after the intramuscular injection, blood samples were taken and, immediately thereafter, the dogs were challenged with a dose of apomorphine. Complete absence of emesis within 1 h after apomorphine challenge (which is never observed in control animals; n> 1000) was considered to reflect significant antiemetic activity.
Table 1 indicates whether the dogs were protected (+) or not protected (-) from apomorphine-induced emesis at the various time intervals after intramuscular injection of the depot formulations. All formulations showed an immediate onset of anti-emetic action.
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Claims (18)
1. A pharmaceutical controlled-release composition comprising a suitable pharmaceutical carrier and further comprising biodegradable and biocompatible microparticles containing a 1,2-benzazole of the formula or a pharmaceutically acceptable acid addition salt thereof, wherein R is hydrogen or C1-6alkyl;
R1 and R2 independently are hydrogen, halo, hydroxy, C1-6alkyloxy and C1-6alkyl;
X is O or S;
Alk is C1-4alkanediyl; and R3 is hydrogen or C1-6alkyl;
Z is -S-, -CH2-, or -CR4=CR5-; where R4 and R5 independently are hydrogen or C1-6alkyl;
A is a bivalent radical =CH2-CH2-, -CH2-CH2-CH2- or CR6=CR7-; wherein R6 and R7 are hydrogen, halo, amino or C1-6alkyl; and R8 is hydrogen or hydroxyl, said microparticles being made of a polymeric matrix material having a molecular weight in the range of 100,000 to 300,000.
R1 and R2 independently are hydrogen, halo, hydroxy, C1-6alkyloxy and C1-6alkyl;
X is O or S;
Alk is C1-4alkanediyl; and R3 is hydrogen or C1-6alkyl;
Z is -S-, -CH2-, or -CR4=CR5-; where R4 and R5 independently are hydrogen or C1-6alkyl;
A is a bivalent radical =CH2-CH2-, -CH2-CH2-CH2- or CR6=CR7-; wherein R6 and R7 are hydrogen, halo, amino or C1-6alkyl; and R8 is hydrogen or hydroxyl, said microparticles being made of a polymeric matrix material having a molecular weight in the range of 100,000 to 300,000.
2. The composition of claim 1, wherein the polymeric matrix material of said microparticle is selected from poly(glycolic acid), poly-D,L-lactic acid, poly-L-lactic acid, copolymers of the foregoing, poly(aliphatic carboxylic acids), copolyoxalates, polycaprolactone, polydioxonone, poly(ortho carbonates), poly(acetals), poly(lactic acid-caprolactone), polyorthoesters, poly(glycolic acidcaprolactone), polyanhydrides, albumin, casein, and waxes.
3. The composition of claim 2, wherein the polymeric matrix material of said microparticle is a copolymer of poly(glycolic acid) and poly-D,L-lactic acid.
4. The composition of claim 3 wherein the molar ratio of lactide to glycolide is in the range of 85:15 to 50:50.
5. The composition of claim 1, wherein said microparticles comprise 1 to 90 wt. % of said 1,2-benzazole.
6. The composition of claim 1, wherein said microparticles comprise about 35 to 40 wt.
of said 1,2-benzazole.
of said 1,2-benzazole.
7. The composition of claim 1, wherein said microparticles range in size from 1 to 500 microns.
8. The composition of claim 1 wherein said microparticles range in size from 25 to 180 microns.
9. The composition of claim 1, wherein said microparticles are formulated in a liquid injection vehicle.
10. The composition of claim 9, wherein said liquid vehicle is physiological saline solution or an aqueous solution of carboxymethyl cellulose with a surfactant.
11. Biodegradable and biocompatible microparticles containing a 1,2-benzazole as defined in any of claims 1-10.
12. The use for the manufacture of a medicament for treating psychotic disorders, of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of the formula (1) as defined in any of claims 1-10.
13. A process for preparing microparticles as claimed in claim 11, characterized by dissolving or dispersing the 1,2-benzazole of the formula (I), as defined in claim 1, in an appropriate solvent and adding thereto a polymeric matrix material.
14. A process for preparing a pharmaceutical composition as claimed in any of claims 1-10, characterized in that the microparticles are mixed with the pharmaceutical carrier.
15. A use of a biodegradable and biocompatible microparticle composition comprising a 1,2-benzazole of the formula (I) as defined in any of claims 1 to 10 for treating psychotic disorders.
16. A pharmaceutical controlled-release composition comprising a suitable pharmaceutical carrier and further comprising biodegradable and biocompatible microparticles containing 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl) ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2-a] pyrimidin-4-one or a pharmaceutically acceptable acid addition salt thereof, said microparticles being made of a polymeric matrix material having a molecular weight in the range of 100,000 to 300,000.
17. A use of the composition as defined in claim 16 for the manufacture of a medicament for treating psychotic disorders.
18. A use of the composition as defined in claim 16 for treating psychotic disorders.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US15440393A | 1993-11-19 | 1993-11-19 | |
| US08/154,403 | 1993-11-19 | ||
| PCT/EP1994/003754 WO1995013814A1 (en) | 1993-11-19 | 1994-11-11 | Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2175370A1 CA2175370A1 (en) | 1995-05-26 |
| CA2175370C true CA2175370C (en) | 2006-06-27 |
Family
ID=36644825
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002175370A Expired - Lifetime CA2175370C (en) | 1993-11-19 | 1994-11-11 | Microencapsulated 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2175370C (en) |
-
1994
- 1994-11-11 CA CA002175370A patent/CA2175370C/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| CA2175370A1 (en) | 1995-05-26 |
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