Patent Application
20210046014
The present invention relates to a pharmaceutical abuse deterrent composition and method of making the same.
Abuse of prescription drug is a serious public health problem that affects almost every community and family in some way. Each year drug abuse causes millions of serious illnesses or injuries among the peoples. Drug abuse also plays a role in many major social problems, such as drugged driving, violence, stress, and child abuse. Drug abuse can lead to homelessness, crime, and missed work or problems with keeping a job. It also harms unborn babies and destroys families. There are different types of treatment for drug abuse. But the best is to reduce the drug abuse in the first place by making abuse deterrent pharmaceutical composition.
Some common techniques for intentionally abusing a drug begin with an abuser is obtaining a solid dosage form such as an orally administered tablet or capsule, and crushing the solid dosage form into a powder. The powder may be administered by an abuser by nasal insufflation (i.e., “snorting”) to introduce the drug to the abuser's bloodstream intranasally. Alternately, the crushed dosage form may be combined with a solvent that is capable of dissolving the drug substance, and the solvent with the dissolved drug substance may be injected directly into an abuser's bloodstream. This type of administration results in an even faster diffusion of the drug substance compared to the oral abuse, with the result desired by the abuser, namely the kick.
Alternatively, with immediate release or modified release oral dosage forms, an abuser might simply ingest multitude of the dosage form (e.g., tablets or capsule) together, e.g., simultaneously. Each one of the multiple dosage form units produce a short-term or a long-term concentration spike of the drug in the user's bloodstream.
Various concepts for the avoidance of drug abuse have been developed by making abuse deterrent dosage form. The requirements for abuse deterrent dosage forms that nowadays need to be satisfied are complex and sometimes are difficult to be combined and arranged with one another. While a certain measure may improve abuse deterrent in a certain aspect, the same measure may deteriorate abuse deterrent in another aspect or otherwise may have a detrimental effect on the properties of the dosage forms.
Although the pharmaceutical industry has identified a variety of abuse deterrent features useful with oral dosage forms, still there is continuing need to improve and identify new abuse deterrent features to inhibit or prevent abuse or overdosing of active ingredients.
It is therefore an object of the present invention is to construct a pharmaceutical abuse deterrent composition that has a unique overdose prevention feature and at least resistant to physical tampering and chemical tampering.
An object of the present invention is to construct a pharmaceutical abuse deterrent composition in one strength or more than one strength, wherein each strength in alone or in combination with another strength has a unique overdose prevention features.
In preferred embodiment, a pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
In preferred embodiment, each of the first strength and the second strength is administered individually to treat a disease condition of a subject in need thereof
Another object of the present invention is to construct a pharmaceutical abuse deterrent composition which is at least resistant to physical or chemical tampering.
In preferred embodiment, a pharmaceutical abuse deterrent composition comprising coated particulates, wherein each coated particulate comprising
The terms used in this specification generally have their ordinary meanings in the art, within the context of this invention and in the specific context where each term is used. Certain terms are discussed below, or elsewhere in the specification, to provide additional guidance to the practitioner in describing the compositions and methods of the invention and how to make and use them.
As used herein, the use of the word “a” or “an” when used in conjunction with the term “comprising” in the claims and/or the specification can mean “one,” but it is also consistent with the meaning of “one or more,” “at least one,” and “one or more than one.” Still further, the terms “having,” “including,” “containing”, “comprising” and “comprises” are interchangeable, and one of skill in the art is cognizant that these terms are open-ended terms.
The term “pharmaceutical abuse deterrent composition” or “abuse deterrent pharmaceutical composition” is used to refer to a composition that deter the potential for abuse but delivers a therapeutically effective amount of a drug substance when administered as directed. For example, these terms refer to a composition that can be at least resistant to physical or chemical tampering. The term physical tampering includes, with or without heat treatment or freezing, at least one of crushing, grinding, melting, cutting, and like. The term chemical tampering includes, extracting the drug substance from the composition, dose dumping (e.g., alcohol dose dumping), and solubilizing the composition for injection purposes. The abuse deterrent composition deters an improper administration of the composition or drug substance contained in the composition, wherein improper administration includes, without limitation, administering the drug substance or the composition with 40% w/w alcohol, administering the drug substance or the composition by any route other than that instructed after physical or chemical tampering with the composition. For example, without limitation, improper administration includes snorting after grinding, administration after heat treatment, oral administration after crushing, or parenteral administration after extraction of the drug substance from the composition with a solvent, and the like, and combinations thereof. The abuse deterrent composition diminishes the drug substance release after accidental or intentional simultaneous administration of a plurality of dosage units of the composition containing an overall supratherapeutic dose of the drug substance. The term “supratherapeutic dose” refer to the overall content of the drug substance originally contained in the plurality of dosage units of the composition is greater than two or more time of the highest strength or greater than maximum daily recommended dose of the drug substance. In other word, a pharmaceutical abuse deterrent composition has overdose protection feature. The term “overdose protection” refers to a feature of dosage form that reduces the potential for the detrimental consequences of overdose but delivers a therapeutically effective dose when administered as directed or prescribed by a physician.
The term “dosage form” or “dosage unit” or “strength” are used interchangeably to refer to oral drug delivery system of the pharmaceutical abuse deterrent composition comprising a predetermined quantity (therapeutically effective dose) of one or more active ingredient(s) and suitable as unitary dosages for administration to human patients to attain the desired therapeutic effect.
In preferred embodiment, a pharmaceutical abuse deterrent composition deliver a drug substance in at least one of immediate release form and modified release form.
The term “immediate release” refers to dosage form that are formulated to allow the drug to dissolve in the gastrointestinal contents or in dissolution media with no intention of delaying or prolonging the absorption when taken as prescribed or the dissolution of the drug substance when subjected to in vitro dissolution testing.
The term “modified release” refers to dosage forms that are formulated to allow the drug to dissolve at slower rate in the gastrointestinal contents or in dissolution media over a greater period of time, e.g. for period of 4 hours, 8 hours, 12 hours, 16 hours, 20 hours and like, as compared to a drug presented as a conventional dosage form (e.g., immediate release). The term “modified release” also include release of the drug substance at any rate after the predetermined lag time or in the predetermined location of gastrointestinal tract after administration.
As used herein, use of phrases such as “diminish” or “lower” is meant to include at least a 10% change in, e.g., the release rate of an active ingredient or amount of the drug substance. With respect to “the release rate of an active ingredient”, greater percentage changes being preferred for reduction in overdose potential. For example, but without limitation, the change may be greater than 25%, 35%, 45%, 55%, 65%, 75%, 85%, 95%, 96%, 97%, 98%, 99%, or increments therein.
The term “about” or “approximately” means within an acceptable error range for the particular value as determined by one of ordinary skill in the art, which will depend in part on how the value is measured or determined, i.e., the limitations of the measurement system. For example, “about” can mean within 3 or more than 3 standard deviations, per the practice in the art. Alternatively, “about” can mean a range of up to 20%, up to 15%, up to 10%, up to 5%, or up to 1% of a given value. Alternatively, particularly with respect to biological systems or processes, the term can mean within an order of magnitude, preferably within five-fold, and more preferably within two-fold, of a value.
The term “in-vitro dissolution testing” refers to in-vitro test that measure the rate and extent of release of the drug substance from dosage unit(s) of the composition at 37°±1° C. in 900 ml 0.01N HCl in a USP Apparatus 2 (paddle) at 50 rpm and optionally with sinker.
The “wt. %” or “% wt.” refers to percentage by weight.
In preferred embodiment, a pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
In certain embodiment, the particulate of the drug substance further comprising a functional ingredient to attain modified release profile of the drug substance, wherein the functional ingredient is at least one of pH independent ingredient and water insoluble ingredient. In preferred embodiment, the functional ingredient is present in the each particulate of drug substance as
In preferred embodiment, a pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
A similarity factor F2 value can be used as indicative for evaluating a similarity of release profile of the drug substance from two different strengths, i.e. the first strength and the second strength. A f2 value of 50 or greater (50 to 100) ensures sameness or similarity of the two different release profile. The f2 value is calculated by the following equation:
f2=50×log{[1+(1/n)Σt=1n(FT+ST)2]−0.5×100}
For calculating f2 value,
In one embodiment, the first strength is highest strength or lower strength than the highest strength but higher strength than the lowest strength. In another embodiment, the second strength is lowest strength or higher strength than the lowest strength but lower strength than the highest strength.
The term “highest strength” refers to a dosage unit comprising highest amount of active ingredient compared to all other strengths comprising the same active ingredient. The term “lowest strength” refers to a dosage unit comprising lowest amount of active ingredient compared to all other strengths comprising the same active ingredient. For example, unit dosage form of different strength such as 10 mg, 15 mg, 20 mg, 30 mg, wherein 30 mg is highest strength (first strength), 10 mg is lowest strength (second strength), 15 mg and 20 mg can be considered either as a first strength with respect to the lowest strength (10 mg) or as a second strength with respect to the highest strength (30 mg). Furthermore, 15 mg can be considered either as a second strength with respect to 20 mg strength and 30 mg strength or as a first strength with respect to 10 mg strength. Similarly, 20 mg can be considered either as a second strength with respect to 30 mg strength or as a first strength with respect to 10 mg strength and 15 mg strength. In other word, 30 mg is first strength, 10 mg is lowest strength, 15 mg or 20 mg can be considered either as first strength or as second strength.
In preferred embodiment, a pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
In preferred embodiment, pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
In preferred embodiment, a pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
In preferred embodiment, a pharmaceutical abuse deterrent composition containing particulates in which a release of a drug substance is controlled,
The pharmacokinetic parameter, namely Cmax, considered dose proportional if increasing approximately proportionally with respect to increasing the amount of the drug substance. The term “approximately proportionally” means±20% of the reference value. The “less than the minimum level for dose proportionality” means less than 80% of reference value. In the present invention, value of single dose Cmax of the first strength is the reference value.
According to invention, the acid neutralisation capacity of the first strength and the second strength can be measure by following method (perform the following procedure at 37°±1° C. in USP apparatus II (Paddle) at 250 RPM and optionally with sinker):
Difference of the final pH(X)=the final pH(A)−the final pH(B)
Acid neutralisation capacity of the first strength is considered higher than acid neutralisation capacity of the second strength when the value of the final pH (X) is positive value (+).
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising more than one matrix particulates, wherein the each matrix particulate comprising
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising a more than one coated particulates, wherein the each coated particulate comprising
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising more than one coated particulates, wherein the each coated particulate comprising
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising more than one coated particulates, wherein the each coated particulate comprising
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising more than one coated particulates, wherein the each coated particulate comprising
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising more than one coated particulates, wherein the each coated particulate comprising
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength comprising more than one matrix particulates, wherein the each matrix particulate comprising a pharmaceutically acceptable derivative of the drug substance and a pH dependent ingredient, wherein the derivatives of drug substance is dispersed within matrix of the pH dependent ingredient, wherein the pH dependent ingredient is present in amount of not less than about 50% w/w of an amount of the drug substance and is at least one of
In preferred embodiment, the particulates of the drug substance in each of the first strength and the second strength further comprising at least one ingredient of pH independent ingredient, ion-exchange resin, water insoluble ingredient, gelling ingredient, anti-crushing ingredient, diluent, glidant, surfactant, stabilizer, binder, lubricant, disintegrant, plasticizer, anti-tacking agent, surfactant, and stabilizer.
In preferred embodiment, each of the first strength and the second strength individually further containing particulates of an aversion agent, wherein the aversion agent is not released in effective amount to produce its intended aversive effect unless the composition is administered after physical alteration but is released in effective amount to produce its intended aversive effect when the composition is administered after the physical alteration. Physical alteration includes crushing, grinding, cutting and like. Thus, the particulates of an aversion agent deter an abuse from physical tampering and chemical tampering. The aversion agent is present as coated particulates in each of the first strength and the second strength, wherein each coated particulate comprising
In certain embodiment, the particulates of the drug substance in each of the first strength and the second strength further comprising barrier coat before and/or after the outer coat of the pH dependent ingredient, wherein the barrier coat comprising at least one of pH independent ingredient, water insoluble ingredient, surfactant, stabilizer, plasticizer and anti-tacking ingredient.
In certain embodiment, the particulates of the first strength and/or the second strength further comprising functional coat before and/or after the outer coat of the pH dependent ingredient to attain modified release profile, wherein the functional coat comprising at least one of pH independent ingredient, water insoluble ingredient, surfactant, stabilizer, plasticizer and anti-tacking ingredient.
In preferred embodiment, acid neutralisation capacity of the first strength and/or the second strength is attained by the acid neutralising ingredient.
In preferred embodiment, the acid neutralising ingredient can be present as separate particulates in the dosage unit or coated on the particulates of the drug substance. In one embodiment, the acid neutralising ingredient is present as the separate particulates in the dosage unit, wherein each particulate comprising the acid neutralising ingredient, and optionally, at least one of diluent, glidant, binder, lubricant and disintegrant.
In one embodiment, the pH dependent ingredient has the pH dependent solubility, wherein it is soluble in stomach fluid or aqueous fluid at pH below about 5 but substantially insoluble in intestinal fluid or in stomach fluid or in aqueous fluid at pH above about 5.5. In another embodiment, the acid neutralisation capacity of the first strength and/or the second strength retard the solubilisation of the pH dependent ingredient in stomach fluid or in aqueous fluid by elevating the pH of stomach fluid or the aqueous fluid above about 5.5 as a function of the amount of the pharmaceutical composition ingested: when the first strength and/or the second strength is ingested in an appropriate amount, the acid neutralisation capacity of the first strength and/or the second strength not sufficiently raise the pH of stomach fluid or aqueous fluid above about pH 5.5, and the pH dependent ingredient dissolves and releases the drug substance; when the first strength and/or the second strength is ingested in an excess amount, the acid neutralisation capacity of the first strength and/or the second strength elevate the gastrointestinal pH above about 5.5, thereby preventing the pH dependent ingredient from dissolving and releasing the drug substance.
When the second strength or a multitude of the second strength subjected to the in-vitro dissolution testing, the content of the acid neutralising ingredient originally contained in the second strength or the overall content of the acid neutralising ingredient originally contained in the multitude of the second strength not elevate the pH of 0.01N HCl above about 5.5, wherein the content of the drug substance originally contained in the second strength or the overall content of the drug substance originally contained in the multitude of the second strength is lower than the supratherapeutic dose of the drug substance, respectively.
When a multitude of the second strength subjected to the in-vitro dissolution testing, the overall content of the acid neutralising ingredient originally contained in the multitude of the second strength elevate the pH of 0.01N HCl above about 5.5, wherein the overall content of the drug substance originally contained in the multitude of the second strength is equal or greater than the supratherapeutic dose of the drug substance.
When the combination dosage units of the second strength(s) and the first strength(s) subjected to the in-vitro dissolution testing, the overall content of the acid neutralising ingredient originally contained in the combination dosage units not elevate the pH of 0.01N HCl above about 5.5, wherein the overall content of the drug substance originally contained in the combination dosage units is lower than the supratherapeutic dose of the drug substance.
When the combination dosage units of the second strength(s) and the first strength(s) subjected to the in-vitro dissolution testing, the overall content of the acid neutralising ingredient originally contained in the combination dosage units elevate the pH of 0.01N HCl above about 5.5, wherein the overall content of the drug substance originally contained in the combination dosage units is equal or greater than the supratherapeutic dose of the drug sub stance.
In preferred embodiment, a pharmaceutical abuse deterrent composition manufactured by non-thermal process comprising coated particulates, wherein each coated particulate comprising
In preferred embodiment, a pharmaceutical abuse deterrent composition manufactured by non-thermal process comprising coated particulates, wherein each coated particulate comprising
In preferred embodiment, a pharmaceutical abuse deterrent composition manufactured by non-thermal process comprising coated particulates, wherein each coated particulate comprising
In preferred embodiment, a pharmaceutical abuse deterrent composition manufactured by non-thermal process comprising coated particulates, wherein each coated particulate comprising
In the present invention, the term “particulates” refers to a discrete, small, repetitive unit of particle, granule, pellet, sphere, bead, mini-tablet, or micro-tablet, that include at least one excipient and, optionally, an active ingredient.
In the present invention, the term “outer coat” refers to a coating, layer, membrane, film, etc. applied to a surface, and, in certain embodiments, can partially, substantially, or completely surround, envelop, cover, enclose, or encase the surface of a particulate to which it is applied. For example, a coat may cover portions of the surface to which it is applied, e.g., as a partial layer, partial coating, partial membrane, or partial film, or the coat may completely cover the surface to which it is applied.
In preferred embodiment, a pharmaceutical abuse deterrent composition is manufacture either by non-thermal process or thermal process. In thermal manufacturing process, heat is employed in at least one stage of manufacturing process of the pharmaceutical composition and temperature of the heat is at least about melting or softening temperature of the anti-crushing ingredient or the pH dependent ingredient used in the pharmaceutical composition. In non-thermal manufacturing process, heat is employed in at least one stage of manufacturing process of the pharmaceutical composition and temperature of the heat is at least about 10% lower than melting or softening temperature of the anti-crushing ingredient or the pH dependent ingredient used in the pharmaceutical composition. In thermal process, heat is employed to attain anticrushing property of the composition while in non-thermal process, heat is employed as per need of manufacturing process to evaporate binder or coating solvent during manufacturing process.
In pharmaceutical industry, thermal process is well known for making innovative pharmaceutical composition from last few decades. Examples of thermal process include hot melt extrusion (HME), melt granulation, curing of pharmaceutical composition at melting temperature, exposing of the composition to a heat during shaping into a dosage unit, etc.
In certain embodiment, a pharmaceutical abuse deterrent composition prepared by thermal process comprising step of exposing the pharmaceutical composition to the temperature which is at least melting or softening temperature of the anti-crushing ingredient or the pH dependent ingredient used in the pharmaceutical composition.
In certain embodiment, a pharmaceutical abuse deterrent composition prepared by thermal process comprising step of exposing mixture of the drug substance with at least one of the pH dependent ingredient and anti-crushing ingredient to the temperature which is at least melting or softening temperature of the anti-crushing ingredient or the pH dependent ingredient used in the pharmaceutical composition. The mixture further comprising at least one ingredient of pH independent ingredient, ion-exchange resin, water insoluble ingredient, gelling ingredient, diluent, glidant, surfactant, stabilizer, binder, lubricant, disintegrant, plasticizer, anti-tacking agent, surfactant, and stabilizer.
In certain embodiment, the pharmaceutical composition manufactured by thermal process exhibit breaking strength at least sufficient to resist pulverisation of the dosage form and thereby not more than about 35% pulverized particles of the pharmaceutical composition pass through #200 sieve (75 microns) when subjected to the coffee grinder for about 1 minutes.
In certain embodiment, each of the first strength and the second strength have resistance to alcohol dose dumping. Alcohol dose dumping resistance of the first strength and the second strength can be achieved by applying coat surrounding the particulates of the drug substance or the composition, wherein the coat comprising at least one ingredient which is insoluble in alcohol or 40% w/w alcohol in water but substantially a soluble in water.
The terms “resistance to alcohol dose dumping” are used to refer to two or more dosage units (e.g., any form(s) of tablets or capsules) that at least fulfil the condition that in vitro dissolution, characterized by the percentage of drug substance released at, e.g., 30 minutes or 60 minutes or 120 minutes of dissolution, when measured at 37°±1° C. in 900 ml 0.01N HCl comprising 40% ethanol in a USP Apparatus 2 (paddle) or USP apparatus 1 at 50 rpm and optionally with sinker, deviates no more than 35% from the corresponding in vitro dissolution measured at the same time point in the same apparatus at the same speed in 900 ml 0.01N HCl without ethanol at 37°±1° C. Such resistance to alcohol dose dumping deters the abuse of the dosage form.
In present invention, the terms “drug”, “active substance”, “active ingredient”, “active agent”, “drug substance”, “pharmacologically active agent”, “physiologically active agent”, “drug substance in physiologically active form” or “pharmaceutically acceptable derivatives of the drug substance” are used interchangeably herein to refer to a chemical compound that induces a desired pharmacological or physiological effect or biological activity. The terms pharmaceutically acceptable derivatives of the drug substance mentioned herein, include, but not limited to, salts, ether, stereo-isomer solvates, polymorphs, hydrates, complexes with one or more molecules, complexes with one or more cationic or anionic ingredient, drug-ion exchange resin complex, prodrug, active metabolites, analogs, homologue, and the like. In some embodiment, a drug substance is present in base form. The term drug substance is also meant to encompass the use of all such possible forms as well as their racemic and resolved forms thereof, and all tautomers as well. The term “racemic” refers to a mixture of equal parts of enantiomers.
In preferred embodiment, the drug substance is present in form of a pharmaceutically acceptable derivatives, wherein the pharmaceutically acceptable derivatives is drug-ion exchange resin, or complexes with one or more cationic or anionic ingredient.
In some embodiment, the drug substance is present in powder form, in amorphous form, in crystalline form, in micronized form, in complexes with one or more molecules, in combination of two or more active substance or any combination of thereof.
In some embodiments, the active ingredient include, but are not limited to, analgesics, anti-inflammatory agents, anti-helminthics, anti-arrhythmic agents, anti-asthma agents, anti-bacterial agents, anti-viral agents, anti-coagulants, anti-dementia agents, anti-depressants, anti-diabetics, anti-epileptics, anti-fungal agents, anti-gout agents, anti-hypertensive agents, anti-malarials, anti-migraine agents, anti-muscarinic agents, anti-neoplastic agents, immunosuppressants, antiprotozoal agents, anti-thyroid agents, anti-tussives, anxiolytics, sedatives, hypnotics, neuroleptics, neuroprotective agents, β-blockers, cardie inotropic agents, cell adhesion inhibitors, corticosteroids, cytokine receptor activity modulators, diuretics, anti-Parkinson's agents, gastro-intestinal agents, histamine H-receptor antagonists, keratolyses, lipid regulating agents, muscle relaxants, nitrates and other anti-anginal agents, non-steroid anti-asthma agents, nutritional agents, opioid analgesics, sex hormones, stimulants and anti-erectile dysfunction agents; and salts, esters, and mixtures thereof.
In preferred embodiments, a drug substance is associated with abuse syndromes and the drug substance may, thus for example, be selected from opioids, opiates, CNS depressants or sedative, anxiolytics, narcotic, tranquilizers, barbiturates, hormones, CNS stimulants, cannabinoids, nicotine-like compounds, glutamate antagonists, N-methyl-D-aspartate (NMDA) antagonists or drugs that can cause psychological and/or physical dependence. Drugs that are preferred include those classified as Schedule I, II, III, IV and V drugs based upon the substance's medicinal value, harmfulness, and potential for abuse or addiction under the control substance act of United State.
The present invention is very particularly suitable for preventing overdose of active drug substances includes, but not limited to, are:
1-(1-Phenylcyclohexyl)pyrrolidine, 1-(2-Phenylethyl)-4-phenyl-4-acetoxypiperidine, 1-[1-(2-Thienyl)-cyclohexyl]piperidine, 1-[1-(2-Thienyl)cyclohexyl]pyrrolidine, 1-Methyl-4-phenyl-4-propionoxy-piperidine, 1-Phenylcyclohexylamine, 1-Piperidinocyclohexanecarbonitrile, 2,5-Dimethoxy-4-ethyl amphetamine, 2,5-Dimethoxyamphetamine, 2C-B-(4-bromo-2,5-dimethoxylpenethylamine), 2C-D (2,5-dimethoxy-4-methylphenethylamine), 2C-I (4-iodo-2,5-dimethoxy-phenethylamine), 2C-T-2 (2,5-dimethoxy-4-ethylthiophenethylamine), 2C-T-4 (2,5-dimethoxy-4-isopropyl thiophenethylamine), 2C-T-7 (2,5-dimethoxy-4-(n)-propylthiopenethylamine), 3,4-Methylene-dioxymethamphetamine, 3,4,5-Trimethoxyamphetamine, 3,4-Methylenedioxy amphetamine, 3,4-Methylenedioxy-N-ethylamphetamine, 3-Methylfentanyl, 3-Methylthiofentanyl, 4-Bromo-2,5-dimethoxyamphetamine, 4-Bromo-2,5-dimethoxyphenethylamine, 4-Methoxyamphetamine, 4-Methyl-2,5-dimethoxyamphetamine, 4-Methylaminorex (cis isomer), 5-MeO-DMT (5-Methoxy-N,N-diisopropyltryptamine), 5-MeO-DMT (5-Methoxy-N,N-dimethyltryptamine), 5-Methoxy-3,4-methylenedioxyamphetamine, Acetorphin, Acetorphine, Acetyl-alpha-methylfentanyl, Acetyl-alpha-methylfentanyl, Acetyldihydrocodeine, Acetylmethadol, Acetylmethadol, aniloridine, Alfentanil, Allobarbital, Allylprodin, Allylprodine, Alphacetylmethadol except levo-alphacetylmethadol, Alpha-ethyltryptamine, Alphameprodine, Alphamethadol, Alphamethadol, Alpha-Methylfentanyl, Alpha-Methylthiofentanyl, Alphaprodine, Alprazolam, Amfepramon, Amfetaminil, Amineptin, Aminorex, Amobarbital, amfepramone, Amphetamine, amphetaminil, Amylnitrit (all isomers of the amyl group), Anabolic steroids, Anileridine, apocodeine, Aprobarbital, Barbital, Barbituric acid derivative, BDB (3,4-methylenedioxyphenyl)-2-butanamine), Benzethidin, Benzethidine, Benzoylecgonine, Benzphetamine, Benzphetamine, Benzylmethylketon, Benzylmorphine, Betacetylmethadol, Beta-Hydroxy-3-methylfentanyl, Beta-Hydroxyfentanyl, Betameprodine, Betameprodine, Betamethadol, Betaprodine, Bezitramide, Boldenone, Brolamfetamin, Bromazepam, Brotizolam, Bufotenine, Buprenorphine, Butabarbital, Butalbital, Butobarbital, Butorphanol, BZP (A 2)(1-benzylpiperazin), Camazepam, Cannabis, Carfentanil, carfentanyl, Catha edulis, Cathine, Cathinone, Chloral betaine, Chloral hydrate, Chlordiazepoxide, Chlorhexadol, Chlorotestosterone (same as clostebol), Chlorphentermine, Clobazam, Clonazepam, Clonitazene, Clorazepate, Clortermine, Clostebol, Clotiazepam, Cloxazolam, Coca Leaves, Cocaine, Codeine, Codeine &isoquinoline alkaloid, Codeine methylbromide, Codeine-N-oxide, Codoxim, cyclorphan, Cyclobarbital (Hexemal NFN), cyclazocine, Cyprenorphine, Dehydrochlormethyltestosterone, Delorazepam, Desomorphine, Dexamfetamine, dexamphetamine, dexmethylphenidate, Dexfenfluramine, Dextromoramide, dextromethorphan, Dextropropoxyphene, dezocine, Diacetylmorphine, diamorphone, Diampromide, diapromide, Diazepam, Dichloralphenazone, Diethylpropion, Diethylthiambutene, Diethyltryptamine, Difenoxin, Dihydrocodeine, Dihydroetorphine, Dihydromorphine, Dihydrotestosterone, dimephetanol, Dimenoxadol, Dimepheptanol, Dimethylthiambutene, Dimethyltryptamine, Dioxaphetyl butyrate, Diphenoxylate, Dipipanone, Diprenorphine, Dronabinol, Drostanolone, Drotebanol, Ecgonine, eptazocine, Estazolam, Ethchlorvynol, Ethinamate, ethoheptazine, Ethyl loflazepate, Ethylestrenol, Ethylmethylthiambutene, Ethylmorphine, Eticyclidin, Etilamfetamine, Etonitazene, Etorphine, Etoxeridine, Etryptamine, Fencamfamin, Fenethylline, Fenetylline, Fenfluramine, Fenproporex, Fentanyl, Fludiazepam, Flunitrazepam, Fluoxymesterone, Flurazepam, Formebolone, Fungi and Spores of the species PsilocypeSemilanceata, Furethidine, Gammahydroxybutanic acid, Glutethimide, Halazepam, Hallucinogens, Haloxazolam, Heroine, Hydrocodone, Hydrocodone &isoquinoline alkaloid, Hydromorphinol, Hydromorphone, Hydroxypethidine, Ibogaine, Isobutylnitrit, Isomethadone, Ketamine, Ketazolam, Ketobemidone, lefetamine, Levamfetamine, levallorphan, Levo-alphacetylmethadol, Levo-methamphetamine, Levomethorphan, Levomoramide, Levophenacylmorphan, Levorphanol, lisdexamphetamine, lofentanil, loperamide, Loprazolam, Lorazepam, Lormetazepam, Lysergic acid, Lysergic acid amide, Lysergic acid diethylamide, Marijuana, Mazindol, MBDN(N-methyl-1-(3,4-methylenedioxyphenyl)-2-butanamine), mCPP (1-(3-chlorphenyl)piperazine), Mebutamate, Mecloqualone, Medazepam, Mefenorex, MeOPP (1-(4-methoxyphenyl)piperazine), Meperidine intermediate, Meprobamate, meptazinol, Mescaline, Mesocarb, Mesterolone, Metamfetamine, Metazocine, Methadone, Methadone intermediate, Methamphetamine, Methandienone, Methandranone, Methandriol, Methandrostenolone, Methaqualone, Methcathinone, Methenolone, Methohexital, Methyldesorphine, Methyl dihydromorphine, Methylphenidate, Methylphenobarbital (mephobarbital), Methyltestosterone, Methyprylone, Metopone, Mibolerone, Midazolam, Modafinil, Moramide-intermediate, Morpheridine, Morphine, morphine 3-glucuronide, morphine 6-glucuronide, Morphine methylbromide, Morphine methyl sulfonate, Morphine-N-oxide, Myrophine, N,N-Dimethylamphetamine, Nabilone, nalbuphine, Nalorphine, Nandrolone, narccine, N-Ethyl-1-phenylcyclohexylamine, N-Ethyl-3-piperidyl benzilate, N-Ethylamphetamine, N-Hydroxy-3,4-methylenedioxyamphetamine, Nicocodeine, Nicocodine, Nicodicodine, Nicomorphine, Nimetazepam, Nitrazepam, N-Methyl-3-piperidyl benzilate, Noracymethadol, Norcodeine, Nordiazepam, Norethandrolone, Norlevorphanol, Normethadone, Normorphine, Norpipanone, ohmefentanyl, Opium, Oxandrolone, Oxazepam, Oxazolam, oxycodeine, Oxycodone, Oxymesterone, Oxymetholone, Oxymorphone, papavereturn, Para-Fluorofentanyl, Parahexyl, Paraldehyde, pethidine, Pemoline, Pentazocine, Pentobarbital, Petrichloral, Peyote, Phenadoxone, Phenampromide, Phenazocine, Phencyclidine, Phendimetrazine, Phenmetrazine, Phenobarbital, Phenomorphan, Phenoperidine, Phentermine, Phenylacetone, Pholcodine, Piminodine, Pinazepam, Pipradrole, Piritramide, PMMA (paramethyxymethyl amphetamine), Prazepam, prodine, Proheptazine, promedol, Properidine, Propiram, propheptazine, propoxyphene, Psilocybine, Psilocyn, Pyrovalerone, Quazepam, Racemethorphane, Racemoramide, Racemorphane, Remifentanil, Salvia divinorum, Salvinorin A, Secobarbital, Secobarbital, Sibutramine, SPA, Stanolone, Stanozolol, Sufentanil, Sulfondiethylmethane, Sulfonethylmethane, Sulfonmethane, Talbutal, Tapentadol, Temazepam, Tenamfetamin, Testolactone, Testosterone, Tetrahydrocannabinols, Tetrazepam, TFMPP (1-(3-triflourmethylphenyl)piperazine), Thebacon, Thebaine, Thiamylal, Thiofentanyl, Thiopental, Tiletamine, Tramadol, Zolazepam, Zolazepam, Tilidine, Trenbolone, Triazolam, Trimeperidine, Vinbarbital, Zaleplon, Zipeprol, Zolpidem, Zopiclon.
In one embodiment of present invention, the drug substance may also include a new chemical entity for which the amount of information is limited. In such cases, the dosage form regimen needs to evaluate based on preclinical and clinical trials.
The above-mentioned drug substance may also be in the form of pharmaceutically acceptable salts, uncharged or charged molecules, molecular complexes, solvates or anhydrates thereof, and, if relevant, isomers, enantiomers, racemic mixtures, and mixture thereof.
In some embodiments, a dosage unit of the pharmaceutical composition contains an effective dose of drug to provide a therapeutic effect.
In the present invention, the term “acid neutralising ingredient” may be used to refer to an excipient that acts to increase the pH of, e.g., the stomach fluid (e.g., roughly pH 1.2-4.5) or the aqueous fluid (e.g., 0.01N HCl with pH about 2.0) to a pH greater than about 5.5. For example, acid neutralising ingredient may refer to substances that are capable of increasing the pH to greater than 4.5, greater than 5.5, greater than 6.5, etc. It also refers to basic substances and substances that can convert an acidic environment to a less acidic or a basic environment. Typically, these agents, when present in a sufficient amount, are able to elevate the pH of the stomach fluid or the aqueous fluid to greater than about 4.5 or 5.5 and thereby prevent, reduce, or inhibit solubilisation of pH dependent ingredient.
In some embodiment, antacid may be used as acid neutralising ingredient.
In some embodiments, the acid neutralising ingredient is present in an amount of about 5 wt % to about 95 wt %; about 15 wt % to about 85 wt %; about 20 wt % to about 80 wt % or about 25 wt % to about 75 wt % of total weight of dosage form.
Suitable acid neutralising ingredient includes, but are not to be limited, magnesium oxide, meglumine, sodium oxide, sodium hydroxide, sodium bicarbonate, sodium potassium tartrate, bismuth aluminate, bismuth carbonate, bismuth subcarbonate, bismuth subgallate, bismuth subnitrate, potassium citrate, sodium citrate, sodium carbonate, potassium bicarbonate, potassium carbonate, calcium carbonate, calcium phosphate, dibasic calcium phosphate, dihydroxyaluminumaminoacetate, dihydroxyaluminum sodium carbonate, glycine, magnesium glycinate, magnesium hydroxide, magnesium carbonate, sodium borate, aluminum oxide, aluminum hydroxide, ammonium carbonate, monoethanolamine, diethanolamine, triethanolamine, potassium hydroxide, calcium hydroxide, sodium phosphate dibasic, trolamine, sodium potassium tartrate, tribasic sodium phosphate, tricalcium phosphate and like. The acid neutralising ingredient also include agents that inhibit acid secretion in stomach such as, but not to be limited, histamines receptor antagonists and proton pump inhibitors.
In the present invention, the term “pH dependent ingredient” is used to refer an ingredient whose solubility vary according to the pH of the surrounding environment. The surrounding environment may comprise any type of liquid medium, such as gastrointestinal fluid, water, acid solution, alkaline solution, dissolution media, and like.
In some embodiments, pH dependent ingredient is present in an amount of about 0.5 wt % to about 75 wt %; about 1 wt % to about 55 wt %; about 2 wt % to about 35 wt % or about 3 wt % to about 25 wt % of total weight of dosage form.
In some embodiment, pH dependent ingredient include, but are not to be limited, calcium carbonate, chitin, chitosan, di and tribasic calcium phosphate, magnesium hydroxide, casein, polyvinylacetal diethylamino acetate (AEA), polymethacrylate or methacrylic acid and its derivative such as copolymer of dimethylaminoethyl methacrylate, butyl methacrylate, methyl methacrylate, copolymer of diethylaminoethyl methacrylate and methyl methacrylate, for example, Eudragit EPO, Eudragit E100, Eudragit 12.5, Kollicoat smartseal and like.
According to the present invention, pH dependent ingredient also includes those ingredient, other than mentioned in the present invention, whose characteristic and particularly solubility vary according to the pH of the physiological condition of the gastrointestinal fluid or the aqueous fluid.
The term “aversion agent” is used herein to refer agent or ingredient that discourages the intention of incorrect administration of dosage form by producing aversive effect. Aversive effect means effect produced by the aversion agent that discourages incorrect administration of dosage form for obtaining intoxication. Aversive effect produced by the aversion agent include decrease or block the action of drug substance or produce feeling of dislike, feeling of uncomfortable or any unpleasant effect.
According to invention, the aversion agent suitable according to present invention include, but not to be limited, antagonist agent, emetic agent, flushing agent, irritating agent, burning agent and like. However, the aversion agent as describe here are for information, which not limit the scope of invention, i.e. agent other than described here may also be used as the aversion agent, for instance, agent which act according to definition of the aversion agent as described above.
In some embodiment, the aversion agent like antagonist agent, emetic agent or flushing agent are added in physiologically active form or in pharmacologically active form and in pharmaceutically acceptable form in dosage form including, but not limited to, free base, free acid, salts, solvates, hydrates, complexes with one or more molecules, prodrugs, active metabolites, and analogs. Free base or free acid forms of the aversion agent have pH dependent solubility in aqueous environment.
In preferred embodiment, dosage form may comprise at least one aversion agent or combination of two or more aversion agent of same category or of different category.
In some embodiment, antagonist agent can be used as the aversion agent to antagonize the effect of drug substance upon incorrect administration of dosage form. Selection of the antagonist agent is based on drug substance used in dosage form and it may vary according to therapeutic classes of drug substance. Antagonists useful in the present invention include, but not limited to, antagonists for opioids, non-opioid, central nervous system (CNS) depressants, stimulants, tranquilizers, barbiturates, hormones, cannabinoids, nicotine-like compounds, cold and cough drugs such as pseudoephedrine, glutamate antagonists, N-methyl-D-aspartate (NMDA) antagonists, etc. Suitable antagonist agents include, but are not limited to, naloxone, naltrexone, nalmefene, nalide, nalmexone, nalorphine, naluphine, haloperidol, promethazine, fluphenazine, perphenazine, levomepromazine, cyclazocine, thioridazine, perazine, chlorpromazine, chlorprothixine, zuclopentixol, flupentixol, prothipendyl, zotepine, benperidol, pipamperone, melperone, bromperidol and like.
In some embodiment, emetic agent can be used as the aversion agent. Emetics agent are agents which produce vomiting or emesis, which may be used in accordance with the invention as the aversion agent. Local or gastric emetics are the more rapid in their action, producing emesis in from two to five minutes. The systemic emetics must be absorbed and pass to the medulla before they produce vomiting, consequently requiring more time to exert their influence. Suitable emetic agents include, but not limited to, ipecacuanha, apomorphine, tartar emetic, zinc sulphate, copper sulphate, sodium chloride, mustard, ammonium carbonate and like.
In some embodiment, flushing agent can be used as the aversion agent in dosage form. For example, niacin, if taken in excessive dose, it produces warmth, flushing, and other uncomfortable symptoms.
In some embodiment, capsaicin can be used as irritating or burning agent in dosage form as the aversion agent. Capsaicin, if taken in excessive amount, it produces burning like feeling inside the stomach.
In preferred embodiment, each of the first strength and the second strength individually further comprising at least one ingredient of pH independent ingredient, water insoluble ingredient, gelling ingredient, anti-crushing ingredient, diluent, glidant, surfactant, stabilizer, binder, lubricant, disintegrant, plasticizer and anti-tacking agent, in amount of not less than about 0.25% w/w and not more than about 90% w/w of the dosage unit.
The “pH independent ingredient” refers to a component whose characteristics do not generally vary according to the pH of the physiological condition of the gastrointestinal fluid. The pH independent ingredient is water soluble ingredient. Suitable water-soluble ingredient includes, but are not limited to, polymer, sugar, salts, salts of organic acid, acid and polysaccharide. Water soluble polymer include, but are not to be limited, cellulose derivatives include, but are not limited to be, methyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxyethyl methylcellulose, ethylhydroxyethylcellulose, ethylmethylcellulose, hydroxymethylcellulose, hydroxymethylpropylcellulose, sodium carboxymethylcellulose, polyacrylamide derivatives, methacrylic acid derivatives, vinyl pyrrolidone polymers such as polyvinylpyrrolidone, starch derivative, polyalkylene oxide and copolymer thereof, alkylene oxide homopolymers, gums of plant, animal, mineral or synthetic origin, polyacrylic acid and copolymer thereof, polyvinyl alcohols, polyethylene glycol, poloxamer; and mixtures thereof. Preferred sugars include dextrose, glucose, arabinose, ribose, arabinose, xylose, lyxose, xylol, allose, altrose, inositol, glucose, sorbitol, mannose, gulose, glycerol, idose, galactose, talose, trehalose, mannitol, erythritol, ribitol, xylitol, maltitol, isomalt, lactitol, sucrose, raffinose, maltose, fructose, lactose, dextrin, dextran, amylase and xylan. Water soluble salts include sodium chloride, potassium chloride, calcium chloride or magnesium chloride, lithium chloride, lithium, sodium or potassium hydrogen phosphate, lithium, sodium or potassium dihydrogen phosphate, salts of organic acids such as sodium or potassium acetate, magnesium succinate, sodium benzoate, sodium citrate or sodium ascorbate. Preferred acids include ascorbic acid, 2-benzene carboxylic acid, benzoic acid, fumaric acid, citric acid, maleic acid, serbacic acid, sorbic acid, edipic acid, edetic acid, glutamic acid, toluene sulfonic acid, water-soluble amino acids such as glycine, leucine, alanine, or methionine and tartaric acid; and like. Polysaccharides are polymeric carbohydrate molecules composed of long chains of monosaccharide units bound together by glycosidic linkages and on hydrolysis give the constituent monosaccharides or oligosaccharides. They range in structure from linear to highly branched. Examples include storage polysaccharides such as starch and glycogen, and structural polysaccharides such as cellulose and chitin.
The term “water insoluble ingredient” refers to a component which is insoluble in water. Suitable water insoluble ingredient includes natural, synthetic or semi synthetic ingredient. Natural, synthetic or semi synthetic water insoluble ingredient include, but are not to be limited, cellulose derivatives include cellulose acetate, cellulose acetate butyrate, cellulose triacetate, microcrystalline cellulose, ethyl cellulose, glycerol palmitostearate, wax include microcrystalline wax, beeswax, glycowax, castor wax, carnauba wax, glycerol monostearate, oil include hydrogenated vegetable oil, hydrogenated castor oil, vegetable oil, stearyl alcohol, acetylated hydrogenated soybean oil glycerides, castor oil, glycerol behenic acid ester, glyceryl monooleate, glyceryl monostearate, propylene glycol monostearate, cetyl alcohol, natural and synthetic glycerides, fatty acids, fatty alcohol, lipid, methacrylic acid derivatives such polymethaacrylate and its copolymer (such as eudragit polymer); polyvinyl acetate, copolymers of vinyl pyrrolidone and vinyl acetate; vinyl acetate and copolymer thereof, ethyl vinyl acetate, modified starch like pregelatinised starch, polylactic acid or polyglycolic acid and copolymers thereof, methacrylates, cocoa butter, macrogol Stearate, diethylene glycol monostearate, polyoxyethylene 50 stearate, and mixtures thereof.
The term “gelling ingredient” as used herein refers to an ingredient that increase the viscosity of aqueous or non-aqueous media. Suitable gelling ingredient is at least one of natural, semi-synthetic or synthetic ingredient which includes at least one of gum, polysaccharide, water soluble polymer, water soluble protein, and starch. Suitable gelling ingredient includes, but not limited to, xanthan gum, acacia gum, diutan gum, tragacanth, gellan gum, guar gum, fenugreek gum, locust bean gum, pullulan, welan gum, starch or its derivative, celluloseor its derivative (such as hydroxyethyl cellulose, hydroxypropylmethyl cellulose), polyalkylene oxide and its co-polymer such as polyethylene oxide and copolymer of ethylene oxide—propylene oxide, ploycarboxylic acid such as polyacrylic acid, polypeptide such as gelatin, albumin, polylysine, soy protein, polyolefinic alcohol (such as polyvinyl alcohol), or a polyvinyl lactam such as, e.g., polyvinylpyrrolidone, polyvinyl caprolactam, alginic acid and its derivative, methacrylic acid and its copolymer, polyacrylic acid and copolymer thereof, and like. According to invention, more preferable gelling ingredient has cloud point greater than about 85° C. Gelling ingredient having cloud point greater than about 85° C. resist separation of the drug substance from a dosage unit by hot water having temperature greater than about 90° C. and thereby create a complexity in efforts of getting pure drug substance from the dosage unit.
The anti-crushing ingredient include thermoplastic material such as polyalkylene oxide or its copolymer, polyvinyl acetate, polysaccharide such as starch or its derivative, cellulose or its derivatives or glycogen, or mixture thereof.
Suitable disintegrant includes, but are not limited to, cellulose derivatives, including microcrystalline cellulose, low-substituted hydroxypropyl cellulose, ion-exchange resin, starch and its derivative, croscarmellose sodium, alginic acid, insoluble polyvinylpyrrolidone, and like.
Suitable plasticizers includes, but are not limited to, triacetin, triethyl acetate, acetylated monoglyceride, olive oil, acetyl tributyl citrate, acetyl triethyl citrate, glycerin, sorbitol, polyethylene glycol, polypropyleneglycol and like.
Suitable diluents includes, but are not limited to, sucrose, sorbitol, mannitol, various grades of lactose, various grades of microcrystalline cellulose, dextrins, maltodextrins, starches or modified starches, sodium phosphate, calcium phosphate, calcium carbonate, and like.
Suitable glidants and lubricants may be incorporated such as stearic acid, metallic stearates, talc, waxes, and glycerides with high melting temperatures, colloidal silica, sodium stearyl fumarate, polyethyleneglycols, and alkyl sulphates.
Suitable surfactants include, but are not limited to, non-ionic surfactants, anionic surfactants, and cationic surfactants. Example of surfactant include, but are not limited to, ammonium lauryl sulfate, sodium lauryl sulfate, docusate (dioctyl sodium sulfosuccinate), perfluorooctanesulfonate, perfluorobutanesulfonate, alkyl-aryl ether phosphates, alkyl ether phosphates, sodium stearate, sodium lauroylsarcosinate, perfluorononanoate, perfluorooctanoate, cetrimonium bromide, cetylpyridinium chloride, benzalkonium chloride, benzethonium chloride, dimethyldioctadecyl ammonium chloride, dioctadecyldimethylammonium bromide, phospholipids, phosphatidyl serine, phosphatidylethanolamine, phosphatidylcholine, sphingomyelins, poloxamer, fatty acid ester of glycerol, fatty acid ester of sorbitol such as tween and sorbitan, and like.
Suitable anti-tacking agent is selected from the group consisting of, but are not limited to, stearates, stearic acid, vegetable oil, waxes, a blend of magnesium stearate and sodium lauryl sulfate, boric acid, surfactants, sodium benzoate, sodium acetate, sodium chloride, DL-Leucine, polyethylene glycol, sodium oleate, sodium lauryl sulfate, magnesium lauryl sulfate, talc, corn starch, amorphous silicon dioxide, syloid, metallic stearates, Vitamin E, Vitamin E TPGS, silica and combinations thereof.
Suitable binder include, but are not to be limited, cellulose derivatives include, but are not limited to be, methyl cellulose, hydroxypropyl methylcellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxyethyl methylcellulose, ethylhydroxyethylcellulose, ethylmethylcellulose, hydroxymethylcellulose, hydroxymethylpropylcellulose, sodium carboxymethylcellulose, polyacrylamide derivatives, methacrylic acid derivatives, vinyl pyrrolidone polymers such as polyvinylpyrrolidone, starch derivative, polyalkylene oxide and copolymer thereof, alkylene oxide homopolymers, gums of plant, animal, mineral or synthetic origin, polyacrylic acid and copolymer thereof, polyvinyl alcohols, polyethylene glycol, poloxamer, and mixtures thereof.
In certain embodiment, some ingredient has more than one functionality in the composition. For example, polyethylene oxide can be used as anti-crushing ingredient as well as gelling ingredient having cloud point greater than about 80° C.
In preferred embodiment, the pharmaceutical composition further comprising any functional ingredient mentioned in the Handbook of Pharmaceutical excipients, 7th edition. The term “functional ingredient” refer to an ingredient that add some functional characteristic, as mentioned in application part (use of ingredient) of each ingredient in the Handbook of Pharmaceutical excipients, in to the composition.
In certain embodiment, a pharmaceutical abuse deterrent composition can be formulated in the form of a sprinkle formulation. Sprinkle formulation is useful for children and other patients, who have difficulty swallowing the conventional solid dosage forms. The sprinkle formulation may be administered without the need to take it with water. The term “sprinkle formulation” includes any formulation that is suitable for oral administration, wherein the formulation is sprinkled upon any consumable item. According to invention, “Sprinkle formulation” is coated particulates of the pharmaceutical abuse deterrent composition and is < about 2.8 mm in size and can be administered orally with food with or without chewing.
Certain aspects of the present invention may be better understood as illustrated by the following examples, which are meant by way of illustration and not limitation.
Manufacturing Procedure:
In-vitro dissolution testing of the first strength, the second strength and multitude of the second strength manufactured as per example 2 was performed at 37°±1° C. in 900 ml 0.01N HCl in a USP Apparatus 2 (paddle) at 50 rpm for 30 minutes time point in the following sequence:
In-vitro dissolution testing of the first strength, the second strength and multitude of the second strength manufactured as per example 2 was performed at 37°±1° C. in 900 ml 0.01N HCl in a USP Apparatus 2 (paddle) at 50 rpm for 30 minutes time point in the following sequence:
In-vitro dissolution testing of the first strength, the second strength and multitude of the second strength manufactured as per example 2 was performed at 37°±1° C. in 900 ml 0.01N HCl in a USP Apparatus 2 (paddle) at 50 rpm for 30 minutes time point in the following sequence:
5 grams of the drug substance particulates of example 2 were subjected to pulverisation using a coffee grinder for 1 minute and the resultant crushed drug substance particulates were sifted through #200 mesh sieve. The crushed drug substance particulates passed through #200 mesh sieve was less than 35% of initial weight of the drug substance particulate, i.e. 5 grams.
0.5 gram of the drug substance particulates of example 2 were subjected to pulverisation using a coffee grinder for 5 minutes. When the resultant crushed drug substance mixed with 5 ml purified water, it form high viscous mixture which is unsuitable for injection.
Less than 10% w/w particulates were collected when 1 gram particulates of example 8 were sifted through #200mesh sieve.
5 grams of the drug substance particulates of example 8 were subjected to pulverisation using a coffee grinder for 1 minute and the resultant crushed drug substance particulates were sifted through #400 mesh sieve. The crushed drug substance particulates passed through #400 mesh sieve was less than 40% of initial weight of the drug substance particulate, i.e. 5 grams.
0.5 gram of the drug substance particulates of example 8 were subjected to pulverisation using a coffee grinder for 5 minutes. When the resultant crushed drug substance mixed with 5 ml purified water, it form highly viscous mixture which is unsuitable for injection.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201727034838 | Oct 2017 | IN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2018/054443 | 6/16/2018 | WO | 00 |
