Patent Application
20180318226
The present invention relates to drug delivery system using orally dissolving capsules (ODC) to deliver medicines in the mouth cavity for local action or to gastro-intestinal tract for a systemic action. Formulation contains a pharmaceutical active ingredient(s), plasticizer, water-soluble flavor, sweetener, preservatives and other excipients. The ODCs will allow drug administration without water, and it may allow buccal absorption thereby helping to reduce hepatic first-pass effect.
Capsules are one of the most commonly pharmaceutical dosage forms, which are easy to manufacture. Capsules are made from aqueous solution of a gelling agent such as animal protein or plant polysaccharide or their derivatives. Capsules are generally of two types: hard and soft capsules. Hard capsules as name suggests are hard for feel and soft being soft.
Many specific constituents have been used to form the shell of capsule. One basic component is film forming material or matrix such as gelatin, hydroxylpropyl methylcellulose (HPMC), starch, cellulose or other polymer materials.
Capsules are readily soluble in water at 37° C. Types of materials for filling into hard gelatin capsules are dry solids such as powders, pellets, granules or semisolids such as suspensions, pastes or liquids such as non-aqueous liquids.
There are various sizes of hard capsule shells available ranging from sizes ‘000’ to ‘5’ (higher the number, smaller is the dose volume), the most commonly used are sizes ‘0’ and ‘1’.
A hard capsule size chart is shown in Table 1. These values may vary for each capsule manufacturer.
Currently orally disintegrating tablet or orally dissolving tablet (ODT) are available in the market. They were designed for people suffering for dysphagia who can take the drugs as ODT without water. Now ODT has been used as a new kind of drug delivery system and has been widely accepted. Currently, many drugs are administered as ODT as listed in Table 2. Some of examples of approved orally fast dissolving tablets are—Loratidine, Cetirizine, Cisapride monohydrate, Risperidone, Zolmitriptan, Hyoscyamine Sulfate, Famotidine, Tramadol HCL, Phloroglucinol Hydrate etc. It is evident from Table 2 that ODT's are useful to various age groups. The same drugs and many additional drugs can also be delivered using ODC technology.
U.S. Pat. No. 8,105,625 describes the formulation of fast dissolving capsules to enhance the therapeutic effect. The capsule comprises of pullulan, a plasticizer, and a dissolution enhancing agent. The capsules have a normalized breakthrough of less than 30 seconds in water at 37° C. EP20080745143 claims the formulation of fast orally dissolving capsules comprising pullulan, one or more plasticizer and a dissolution enhancing agent. The same inventors filed these two patents.
US 2008/0274187 A1 prepared hard capsule compositions comprising carrageenan, locust bean gum, xanthan gum, sorbitol, and pullulan. These capsules eliminated the problem of cracking, embrittlement, chipping and deformation due to water loss and mechanical stress.
Ronald Bodmeier et al. (Int. J. of Pharm., Vol. 303, 2005, Pages 62-71) prepared fast dissolving capsules for administration in the oral cavity. Their study suggested that the disintegrating time of films decreased with decreasing bloom strength and could be further decreased by addition of sugars or PEGs. Later, they prepared modified conventional hard gelatin capsules either by perforation or by vacuum-drying of conventional hard capsules (Eur. J. Pharma. & Biopharm., Vol. 62, 2006, Pages 178-184). The disintegration time of conventional hard gelatin capsules (HGC) was reduced from 91 to 39 seconds by introducing 6-10 small holes (diameter=25-50 μm) into the capsule shell.
The present patent application proposed slow-release orally dissolving capsules (ODC), which would release the drug over a long time (not a fast dissolving system but a sustained release) and one can administer a drug dosage form without need of water.
The present invention proposes a design of slow-release ODC as a drug delivery system. A capsule is one of the solid dosage forms, which is used as a delivery system for an active moiety or moieties. In general, capsules are prepared with a suitable material or matrix such as gelatin, HPMC or another polymer to form a capsule shell. They are administered with water via oral cavity.
The key objective of the invention is to enable patient to take a capsule—ODC, without water. It is not mandatory to administer ODC without water, but the patients obtain many advantages of release of drug in the mouth cavity over time. For elderly patients, it is customary to take medication in the evening or before going to bed. If the medications are taken with water, the water intake so late at night may make them use the restroom at night and thereby, disturbing their sleep. In such instances, taking medication without water can be very useful.
Another objective of the invention is to provide a delivery system, which will enable a delivery of large quantity of doses. Many patients such as children, women, old people can't gulp large capsules and tablets. One can administer big capsules such as 00 or 000 as ODC. Based on Table 1, one will be able to deliver 1 to 2 grams of granules with the ODC.
Another objective of the invention is to release of active ingredient(s) in oral cavity to allow buccal absorption and thereby, reduce hepatic first pass effect at least for a portion of the drug which is absorbed through the buccal cavity.
Another objective of the invention is to release the active ingredient(s) over a long time allowing a sustained release in those instances where a local action in the mouth cavity is intended. It will also help buccal absorption of drug over loner period.
The present invention is directed to a novel drug delivery system for ODC, comprising a hard capsule shell a sweetener, a sequestering agent, suitable salts, a gelling agent and a flavoring agent or combination thereof. The capsule shell dissolves slowly in the mouth cavity allowing the release of drug composition filled inside the capsule. The sweeteners and flavoring agents will provide an acceptable taste or mask the taste of the drug, if necessary. The sequestering agent or other salts may induce salivation. It will help to swallow the drug particles. Many people suffer from dry mouth. It will alleviate the dry mouth condition.
In another embodiment, the sweetener and/or the flavoring agent are coated on the capsules.
The capsules are prepared by a pin-dip method.
In other embodiment of the invention, ODCs further comprising a drug or combination of drugs as microspheres, beads, powder, granules, pellets, mini-tablets, paste, combination thereof as core fill.
In another embodiment of the invention, ODCs comprising an inner hard or soft-shell capsule as core fill. The inner soft-shell capsules may be filled with suspension or non-aqueous formulation.
In another embodiment of the invention, capsule shell matrix contains a drug but the core of the capsule shell contains no drug. This is useful mainly for small capsules in sizes 2, 3, 4 and 5. The capsule shell matrix is the composition from which empty capsule shells are prepared. Drug(s) is dispersed throughout the body and cap of the capsule. The drug may be physically dispersed, molecularly dissolved or covalently bound to the polymer backbone of the composition.
In another embodiment of the invention, two different capsule shell matrices are prepared—one for the body of capsule and another for the cap of the capsule. Drug A is dispersed throughout the body of the capsule and drug B is dispersed throughout the cap of the capsule. The drug may be physically dispersed, molecularly dissolved or covalently bound to the polymer backbone of the composition.
In another embodiment of the invention, capsule filling material such as microspheres, granules, beads, pellets, and mini-tablets, can be coated with flavoring agent and/or a sweetener.
In another embodiment of the invention, capsule filling material such as microspheres, granules, beads, pellets, mini-tablets can be coated with polymer or coating material for slow release, sustained release, time-release, controlled release or modified release action or as an enteric coat.
In another embodiment, the drug composition is filled in a capsule which is placed in the ODC. The inner capsule may be place all by itself or along with additional drug composition.
The term “orally dissolving capsule” (ODC) refers to a capsule that dissolves in the oral cavity of a patient after getting wet with saliva without need of drinking liquids/water. The term “orally” means the dosage form is administered by mouth. The term dissolving capsules means the capsule material is incorporated into a liquid or dissolves so as to form a solution. The term “Orally Dissolving Capsule” means the orally administered capsule dissolving in the mouth cavity. When the capsule shell dissolves in the mouth, the material filled inside the capsule gets released in the mouth cavity. The ODCs can be administered orally without aid of water or any other liquid. However, the ODCs can behave like a typical capsule and can also be swallowed with water. As the name suggest, the slow-release ODC releases the drug incorporated in the capsule at a slower rate. Typically, the drug will be released from this ODC from 30 seconds to 60 minutes.
The “empty, hard capsule shell”—as name suggests, it is the capsule shell, which is empty, hard, durable and smooth. It retains its shape and it is dry in nature. As evident from the word “empty”, there is nothing inside core portion of the capsule shell. The capsule shell is prepared using a film-forming composition/matrix. The hard capsule shell comprises of two parts—a body and a cap. The shorter piece is called the “cap”, which fits over the open end of the longer piece, called the “body”. The body and the cap cooperatively define a hollow capsule. A manufacturer of empty capsule shells sells these to a manufacturer of a drug product who fills up the active drug along with excipients in the capsule shell core.
The term “slow-release ODC” is different from rapid or fast-release ODC. “Rapid/Fast disintegration/dissolution” as used herein should be understood to encompass disintegration/dissolution of at least 80% of the core composition of the ODC, typically 90% and more typically 100% of the core composition in an aqueous medium or in saliva (in the oral cavity) within 10 seconds and at times, even within 5 to 9 second. Rapid/fast ODC is meant to release the drug very fast in 10 seconds to 20 seconds. The term “slow release” refers as dissolution of at least 80% of the composition of the invention, typically 90% and more typically 100% of the composition in an aqueous medium or in saliva (in the oral cavity) in more than 30 seconds and within 60 minutes. In this case, the dissolution test of ODC is conducted in the mouth cavity and not in the USP dissolution apparatus, which uses 900 mL volume per vessel. The volume of 900 mL in the USP is not representative of volume in the mouth cavity. Specifically, the ODC, in this case, is placed in the buccal cavity. Buccal cavity is that part of the mouth bounded anteriorly and laterally by the lips and the cheeks, posteriorly and medially by the teeth and/or gums, and above and below by the reflections of the mucosa from the lips and cheeks to the gums. It can be also called the vestibule of mouth.
The term “immediate release” refers to an immediate release of medicament from a dosage form. When administered to the gastrointestinal tract, it allows the drug to dissolve in the gastrointestinal contents, with no intention of delaying or prolonging the dissolution or absorption of the drug.
The term “modified release” refers as the dosage form, which is designed to modify the release of the drug over a given time or after the dosage form reaches the required location. Modified release solid oral dosage forms include both delayed- and extended-release drug products. The term “delayed release” refers as the release of a drug (or drugs) at a time other than immediate following oral administration. The term “extended release” refers as systems which allow for the drug to be released over prolonged time periods. The term “sustained-release” refers to a system, which slows the rate of release of the active ingredient dissolved or dispersed in the system.
The term “empty shell capsule matrix” refers the material with which the empty capsule shell is prepared. The empty shell capsule matrix is generally a solution of gelatin or polymer with other excipients from which capsule shell cap or body are made by pin-dip method following by drying. The capsule shell includes both parts of the capsule—cap and the body. The material is filled in the capsule body and then the cap is placed on the body of the capsule.
The term “capsule core” refers to the inside empty portion or the cavity within the capsule where other materials such as powders, granules, beads, mini-tablets etc. are filled in.
The term “non-aqueous” refers to a system in which the dispersing or dissolving solvent is something other than water. For this patent, the definition is broader encompassing cosolvents similar to water including glycerin, propylene glycol, and polyethylene glycol in pure form or a mixture of water to one or more of these cosolvents.
The term “controlled release” refers to systems which offer a sustained-release profile but controlled-release systems are actually controlling the drug concentration in the body, not just the release of the drug from the dosage form, as is the case in a sustained-release system.
The term “coating” is defined as a layer of a substance spread over a surface for the protection or decoration and it might be flavored or sweetened.
A “medicament” is an agent that promotes recovery from an ailment or an injury. Similar words to medicament are medicines, drugs, therapeutic agent, biologically active molecule/agent, active component, and an active moiety. These agents affect physical and/or biochemical properties of a biological system. The classes of medicament applicable in this invention include, but not limited to, anti-tumor agents, cardiovascular drugs, hormones, growth factors, steroidal agents, anti-viral agents, antibiotics and the like. The medicament when mixed with suitable excipients forms a drug composition, which is then converted to dosage forms such as microspheres, granules, pellets, mini-tablets, etc. It is assumed or it is imperative that the drug composition in this patent contains a “therapeutically effective amount” of drug(s).
A “sweetener” is a substance that provides a sweetening effect. Sweetener is one especially other than sugar.
The term “sequestering agent” or “chelating agent” refers to a substance that is able to bond with metal ions to form chelate complex. The sequestering agent can promote salivation by eliminating water hardness. Salt, buffer acids, lemons, cinnamon etc. can also help salivation.
The term “flavoring agent” is defined as the substance that added to give a taste.
The “drug composition” for this patent application means a mixture in which the therapeutically effective amount of drug(s) is mixed with suitable excipients and the mixture is used as a powder, or converted to granules, pellets, suspension, paste or non-aqueous liquids. An excipient is a substance formulated alongside the active ingredient of a medication included for the purpose of long-term stabilization, bulking up solid formulations that contain potent active ingredients (thus often referred to as “bulking agents”, “fillers”, or “diluents”), or to confer a therapeutic enhancement on the active ingredient in the final dosage form, such as facilitating drug absorption, reducing viscosity, or enhancing solubility. Excipients can also be useful in the manufacturing process, to aid in the handling of the active substance concerned such as by facilitating powder flowability or non-stick properties, in addition to aiding in vitro stability such as prevention of denaturation or aggregation over the expected shelf life. The “therapeutically effective amount” is the amount of pharmaceutical or nutraceutical medicament needed to treat, totally or partially, a disease state or alleviates one or more symptoms of the condition.
The term “Ayurvedic” medicine refers to one of the world's oldest holistic (“whole-body”) healing systems. It was developed more than 3,000 years ago in India. It's based on the belief that health and wellness depend on a delicate balance between the mind, body, and spirit. Many herbal medicines are being used in the Ayurvedic medical system. The other commonly used system contains—“allopathic” medicines. The allopathic medicine refers to mainstream medical use of pharmacologically active agents or physical interventions to treat or suppress symptoms or pathophysiologic processes of diseases or conditions.
The advantages of slow-release ODCs are—it reduces hepatic first pass effect by allowing absorption of drug from the mouth cavity, dose accuracy in comparison to oral liquids, no need of water or a spoon for administration and lowering of T-max, which is time to achieve the maximum drug concentration in the blood. The hepatic first pass effect or the first pass metabolism is a phenomenon of drug metabolism in the liver whereby the concentration of a drug is greatly reduced before it reaches the systemic circulation.
Gelatin and hydroxypropyl methylcellulose (HPMC) are the widely used to prepare capsule shells. HPMC capsule shells demonstrate lack of brittleness even at moisture levels below 2%, no cross-linking and improved chemical stability as compared to the gelatin capsule shells. The polymers that can be used in making the present empty, hard capsule shells can be divided into the following groups: 1) Cellulose or cellulose compounds, which include, but are not limited to, cellulose, cellulose ether, methyl cellulose (MC), HPMC, hydroxypropyl cellulose (HPC), hydroxyethyl cellulose, carboxymethyl cellulose (CMC), cellulose acetate phthalate (CAP), 2) starch-based compounds, which include, but not limited to hydroxyethyl starch, hydroxypropyl starch, hydroxyethyl methyl starch, 3) carrageenans—kappa and iota, 4) Acrylate compounds, which include, but not limited to, polyacrylate, polymethylacrylate, poly(acrylate-methylacrylate), poly(methylacrylate-methyl methacrylate), 5) polyolefins, which include, but limited to, polyvinyl chloride, polyvinyl alcohol, and polyvinyl acetate and 6) pullulan (a polysaccharide polymer consisting of maltotriose units). A hard capsule dosage form is manufactured by filling the core of the hard capsule shell with powders, microspheres, granules, beads, pellets, a tablet, suspension, paste or another capsule (also termed as “inner capsule”). In the recent times, scientists have started filling the hard capsule core with non-aqueous liquids too such oily and/or waxy substances. Currently, the hard capsule shells are mostly prepared with either gelatin or HPMC. The hard capsule shells are purchased from the capsule suppliers like Capsugel, Shionogi and Universal capsules. The process of manufacturing of HPMC or gelatin capsules has been fully established. After drying, the capsule shell contains mainly HPMC or gelatin, small percent of water, colors, plasticizers/gelling agent and other excipients. In this patent application, we propose to add other excipients such as a sweetener, flavoring agent etc. to provide a pleasant taste to the capsule shell.
Each capsule has two parts—a body and the cap. As mentioned in the background section, several new types of polymeric substances have been used to manufacture empty, hard capsule shells. These are—cellulosic compounds, acrylates, starch ethers, polyolefins, pullulans, and carrageenans. Apart from the main constituent of the capsule shell being gelatin or polymeric in nature, the shell also contains other excipients such as plasticizers (e.g., polyethylene glycol, sorbitol, glycerol), stabilizers (antimicrobial and antioxidants), colorants (FD&C colors, titanium dioxide, natural dyes including riboflavin, carotenes, turmeric and caramel) and sequestering agents (citric acid, sodium citrate, and ethylenediaminetetraacetic acid (EDTA)).
One of the features of the present invention is to incorporate medicaments in the empty, hard capsule shell matrix. The medicament in the hard capsules matrix is either physically or molecularly dispersed and/or chemically bound to the polymeric material of the capsule matrix. In another embodiment, drug A is incorporated in the Cap and drug B is incorporated in the Body of the capsules. When put together, this capsule contains two drugs A and B in the capsule shell matrix. This capsule is administered as is without filling another drug composition in the core of the capsule shell. Else, one can fill a drug composition inside this capsule shell containing drugs A and B. This can be a good way to produce combination dosage forms.
In one embodiment citric acid as sequestering agent have been added in the capsule shell matrix. In yet another embodiment, a sweetener is added in hard capsule shell matrix. In yet another embodiment, a colorant is added in hard capsule shell matrix. It yet another embodiment, a flavoring agent is added in the hard capsule shell matrix.
In one embodiment, different medicaments are incorporated in the hard capsule core. In another embodiment, a combination of medicaments is incorporated in the hard capsule core.
Capsule Fill Formulations
The drug composition is defined as the composition containing active drug substances along with suitable excipients. It is then converted to a suitable dosage form such as—powder, granules, pellets, microspheres, mini-tablets, a non-aqueous suspension, a paste, non-aqueous solution or a combination of two or more. For the purpose of this patent, the drug composition is filled in the ODC shell, which is prepared by putting together a cap and a body.
The capsule fill formulation comprises one or more pharmaceutical agents and one or more excipients. Exemplary pharmaceutical agents used in the capsule fill formulation are selected from one or more of, but not limited to:
Selective serotonin reuptake inhibitors such as Fluoxetine, sertraline, paroxetine, fluvoxamine, citalopram, alaproclate and the like
Anti-emetics such as Ondansetron, granisetron, palonosetron, dronabinol, aprepitant, ramosetron, metopimazine, nabilone, tropisetron, metoclopramide, prochlorperazine, trimethobenzamide, dimenhydrinate, prochlorperazine, dolasetron and the like
5HT3 antagonists such as alosetron, ondansetron, granisetron, palonosetron, ramosetron, tropisetron and the like
Anti-epileptics such as carbamazepine, clonazepam, diazepam, divalproex sodium, fosphenyloin, gabapentin, lamotrigine, levetiracetam, oxcarbazepine, phenyloin, pregabalin, primidone, tiagabine, topiramate, valproate sodium, vigabatrin, zonisamide and like
Anti-migraines such as Almotriptan, dihydroergotamine mesylate, eletriptan, frovatriptan, naratriptan, rizatriptan, sumatriptan, zolmitriptan and the like.
Antihistamines, such as diphenhydramine, dirnenhydrinate, perphenazine, triprolidine, pyrilamine, chlorcyclizine, promethazine, carbinoxamine, tripelennamine, brompheniramine, hydroxyzine, cyclizine, meclizitle, clorprenaline, terfenadine, and chlorpheniramine, and the like. Other antihistamines are represented by, but are not limited to, cimetidine, ranitidine, diphenydramine, prylamine, promethazine, chlorpheniramine, chlorcyclizine, terfenadine, carbinoxamine maleate, clemastine fumarate, diphenhydramine hydrochloride, dimenhydrinate, prilamine maleate, tripelennamine hydrochloride, tripelennamine citrate, chlorpheniramine maleate, brompheniramine maleate, hydroxyzine pamoate, hydroxyzine hydrochloride, cyclizine lactate, cyclizine hydrochloride, meclizine hydrochloride, acrivastine, cetirizine hydrochloride, astemizole, levocabastine hydrochloride, and loratadine;
Antacids, such as cimetidine, ranitidine, nizatidine, famotidine, omeprazole, bismuth antacids, metronidazole antacids, tetracycline antacids, clarithromycin antacids, hydroxides of aluminum, magnesium, sodium bicarbonates, calcium bicarbonate and other carbonates, silicates, and phosphates;
Dopamine D1 and D2 antagonists such as Amisulpride, bromperidol, cabergoline, domperidone, fenoldopam, haloperidol, metoclopramide, metopimazine, pergolide mesylate, prochlorperazine, quetiapine, ropinirole hydrochloride, sulpiride, tiapride and zotepine. Nootropics Almitrine dimesylate and raubasine, cevimeline hydrochloride, codergocrine mesylate, donepezil, galantamine, ginkgo biloba extract (EGb 761), memantine, nicergoline, piracetam, rivastigmine, sulbutiamine, tacrine, vinpocetine and the like
Statins such as Atorvastatin, cerivastatin, fluvastatin, lovastatin, pitavastatin, pravastatin, rosuvastatin, simvastatin and the like
Oral contraceptives such as ethinyl estradiol, norgestrel, norethindrone, ethinodiol, levonorgestrel, mestranol, desogestrel, norgestimate and the like
In one aspect, the hard capsule shell fill formulation optionally further comprises one or more flavoring agents. The flavoring agents that may be used include those flavors known to the skilled artisan, such as natural and artificial flavors. Several flavoring agents are described in U.S. patent Ser. No. 12/062,727, which are incorporated herein by reference. These flavoring agents may be chosen from synthetic flavor oils and flavoring aromatics and/or oils, oleoresins and extracts derived from plants, leaves, flowers, fruits, and so forth, and combinations thereof. Non-limiting representative flavor oils include spearmint oil, cinnamon oil, oil of wintergreen (methyl salicylate), peppermint oil, clove oil, bay oil, anise oil, eucalyptus oil, thyme oil, cedar leaf oil, oil of nutmeg, allspice, oil of sage, mace, oil of bitter almonds, and cassia oil. Also useful flavorings are artificial, natural and synthetic fruit flavors such as vanilla, and citrus oils including, without limitation, lemon, orange, lime, grapefruit, and fruit essences including apple, pear, peach, grape, strawberry, raspberry, cherry, plum, pineapple, apricot and so forth. These flavoring agents may be used in liquid or solid form and may be used individually or in admixture. Commonly used flavors include mints such as peppermint, menthol, artificial vanilla, cinnamon derivatives, and various fruit flavors, whether employed individually or in admixture. Other useful flavorings include aldehydes and esters such as cinnamyl acetate, cinnamaldehyde, citral diethylacetal, dihydrocarvyl acetate, eugenyl formate, p-methylamisol, and so forth may be used. The flavor is present from about 0 to about 5% by weight of the capsule shell fill formulation.
In one aspect, the hard capsule shell fill formulation optionally further comprises one or more saliva stimulating agents. One or more salivary stimulants can be optionally added to the capsule shell fill formulation. Several salivary stimulants are described in U.S. patent Ser. No. 12/062,727, which are incorporated herein by reference. Salivary stimulants include, but are not limited to, certain organic acids, and sweeteners. Organic acid salivary stimulants include adipic, ascorbic, citric, fumaric, lactic, malic and tartaric acids. Preferred organic acids are citric, malic and ascorbic acids. The most common sweeteners for use as saliva stimulating agents are sugars such as glucose, dextrose, fructose, lactose, maltose, xylose, sucrose, corn sugar syrup, and other sweet mono- or di-saccharides, as well as artificial sweeteners such as acesulfame, aspartame, saccharin, as well as xylitol and other polyols. Preferred sweeteners that are known to be used as salivary stimulants include maltose, acesulfame, aspartame and saccharin.
In one aspect, the hard capsule shell fill formulation optionally further comprises one or more colorants and opacifiers. Colorants include such compounds as, by way of example and without limitation, titanium dioxide, talc, FD&C Red No. 3, FD&C Red No. 20, FD&C Yellow No. 6, FD&C Blue No. 2, FD&C Green No. 5, FD&C Orange No. 5, FD&C Red No. 8, caramel, ferric oxide, other FD&C dyes, lakes, and natural coloring agents such as grape skin extract, beet red powder, beta-carotene, annatto, carmine, turmeric, paprika, and other materials known in the art. The amount of coloring agent used will vary as desired.
The medicament(s) with suitable excipients are converted to various types of filling materials. Filling material of the capsule such as granules, pellets, powder, suspension, semisolids, can be coated for controlled release or modified release of active ingredient. Several coating agents are described in U.S. Pat. No. 7,713,550 B2, which are incorporated herein by reference.
In certain embodiments of the present invention, wherein the dosage form contains a pharmaceutically acceptable polymer, the pharmaceutically acceptable polymer is for example and without limitation, HPC, HPMC. MC, CMC, vinyl acetate/crotonic acid copolymers, maleic anhydride/methyl vinyl ether copolymers, polyalkylene oxide including but not limited to poly(ethylene) oxide, poly(methylene oxide), poly(butylene oxide); poly(hydroxy alkyl methacrylate); poly(vinyl) alcohol, having a low acetal residue, which is cross-linked with glyoxal, formaldehyde or glutaraldehyde and having a degree of polymerization of from 200 to 30,000; a mixture of methyl cellulose, cross-linked agar and carboxymethyl cellulose; a hydrogel forming copolymer produced by forming a dispersion of a finely divided copolymer of maleic anhydride with styrene, ethylene, propylene, butylene or isobutylene cross-linked with from 0.001 to 0.5 moles of saturated cross-linking agent per mole of maleic anyhydride in the copolymer; Carbopol® acidic carboxy polymers having a molecular weight of 450,000 to 4,000,000; Cyanamer polyacrylamides; cross-linked water swellable indenemaleic anhydride polymers; Goodrite® polyacrylic acid having a molecular weight of 80,000 to 200,000; starch graft copolymers; Aqua-Keeps® acrylate polymer polysaccharides composed of condensed glucose units such as diester cross-linked polyglucan and the like. Other polymers which form hydrogels are described in U.S. Pat. Nos. 3,865,108; 4,002,173 and 4,207,893 all of which are incorporated by reference. Mixtures of the aforementioned pharmaceutically acceptable polymers may also be used. In certain preferred embodiments the pharmaceutically acceptable polymer in combination with the drug is capable of forming a drug matrix for the controlled delivery of the drug.
Other excipients or inactive ingredients such as calcium carbonate, Croscarmellose sodium. Cellulose, Carboxymethylcellulose calcium, Calcium stearate, Castor oil hydrogenated, calcium phosphate di or tri basic, Glyceryl behenate, Glyceryl monostearate, Lactose hydrous or anhydrous or monohydrate or spray dried, Magnesium stearate, Magnesium carbonate, Magnesium oxide, PEG, Polyoxy 140 stearate, Starch pregelatinized, Sodium lauryl sulfate, starch, Sodium benzoate, stearic acid, saccharin sodium, Sodium stearyl fumarate, sodium chloride, talc and the like.
With the following examples, one skilled in the art, can understand and use the present invention.
Loratidine 5 mg Capsule for Allergy Symptoms
A capsule composition containing HPMC is prepared by incorporating a sweetener, Acesulfame-K and citric acid as sequestering agent. The capsules are prepared using the pin-dip method. Capsules are also prepared with HPMC only or HPMC and sweetener optionally or HPMC and sequestering agent or combination of thereof:
Capsule fill formulation containing Loratidine equivalent to 5 mg dose is filled in size ‘5’ hard capsule core. Powder containing Loratidine is prepared by trituration to produce the same particle size and then mixed with excipients by geometric dilution method. Formula for Loratidine powder is given below:
Simvastatin 40 mg Capsules for Cholesterol
Granules containing Simvastatin are prepared by using a conventional technique. Simvastatin equivalent to 40 mg dose are filled in size ‘0’ HPMC hard capsule core. Formula for granule preparation of simvastatin is given below. A similar composition can also be used for different strengths of simvastatin or other statins.
Ibuprofen 200 mg Capsule for Pain Relief and to Reduce Fever
Granules of Ibuprofen are prepared by using a conventional technique. Granules containing Ibuprofen equivalent to 200 mg dose are filled in size ‘0’ HPMC hard capsule core. Similar composition can be used to prepare different strengths too. Formula for granules of Ibuprofen is given below:
Tenofovir 300 mg Capsule for Hepatitis B Treatment
Tenofovir equivalent to 300 mg dose are filled in size ‘00’ hard capsule core. Tenofovir pellets are prepared by using a conventional technique. Pellets are coated with a sweetener. Additionally, capsule may be coated with a flavoring agent. Tenofovir is often administered in combination with other anti-viral agents. The other antiviral agent is either mixed with tenofovir in the same pellet or can be made as an independent pellet or it is filled in the capsule as granules along with tenofovir pellets. One such combination drug can be—Tenofovir/emtricitabine. Formula for preparation of tenofovir pellets is given below:
Inner Capsule in a Capsule Formulation: Ibuprofen 200 mg/Pseudoephedrine HCL 30 mg Capsule for Cold and Sinus
Preparation of an inner capsule: Pseudoephedrine equivalent to 30 mg dose are filled in size ‘5’ hard capsule core. Powder containing Pseudoephedrine is prepared by trituration method to produce the same particle size and then mixed by geometric dilution method. Formula for Pseudoephedrine powder is given below. The inner capsules of pseudoephedrine are filled in the orally dissolving capsule along with ibuprofen granules.
Preparation of Ibuprofen Granules:
Granules of Ibuprofen are prepared by using a conventional technique. Ibuprofen granules containing equivalent to 200 mg dose are filled in size ‘00’ HPMC hard capsule core with pseudoephedrine capsule. Formula for granules of Ibuprofen is given below:
Ayurvedic Capsules for Mouth Ailments
The oil components are first mixed as a solution and loaded on the mixture of solid components to provide a free flowing powder, which is filled in the capsules.
Eucalyptus oil
The Ayurvedic drug composition is defined as the composition containing active Ayurvedic substances along with suitable excipients. It is then converted to a suitable dosage form such as—powder, granules, microspheres, pellets, mini-tablets, a non-aqueous suspension, a paste, non-aqueous solution or a combination of two or more.
Cetrizine 10 mg Extended Release Capsule for Allergy Symptoms
Cetrizine beads are filled in size ‘2’ HPMC hard capsule core. Cetrizine beads are prepared by using a conventional technique and coated with HPMC solution. Formula for the cetirizine beads is given below:
ODC with Ethinyl Estrdiol in the Cap and Norgestrel in the Body and No Drug Composition in the Capsule Core for Oral Contraceptives.
The base composition of cap and body of the ODC contained HPMC, water, carrageenan, potassium ions, a sweetener, and a flavoring agent. The composition from which caps for the capsules are made contains ethinyl-estradiol. The amount added in the solution from which the caps are made is chosen in such a way that after drying each cap contains 50 micrograms of ethinyl estradiol. The composition from which body for the capsules are made contains norgestrel. The amount added in the solution from the body are made is chosen in such a way that after drying each body contains 500 micrograms of norgestrel. Then the cap and the body are put together, the empty capsule shell contains 50 micrograms of ethinyl estradiol and 500 micrograms of norgestrel. The empty capsule shells are not filled with any other drug and are administered as ODC. One can also have ODCs with 30 micrograms of ethinyl estradiol and 300 micrograms of norgestrel. There are various combinations of contraceptive products already available in the market. This concept can be applied to any combination. For example, in another ODC, the cap contains 0.02 mg ethinyl estradiol and the body contains 3 mg of drospirenone. It is not just the contraceptives, but other drug combinations can be delivered as ODC. The key is—the dose of each drug should be very small, less than 6 mg per capsule. In another example, single drug is dissolved in the capsule composition from which Cap and Body of the capsule are made. In another ODC, 3 mg of melatonin, a commonly used sleep-aid agent is incorporated in the ODC shell matrix.
From the foregoing, it will be seen that this invention opens up several possibilities using the polymeric hard capsules containing different medicaments along with a combination of drugs in the core. As described in the patent application, these capsules are to be placed in the mouth. The capsule shell will dissolve over 60 minutes releasing the drug filled in the capsule slowly in the mouth cavity. One of the advantages of this delivery system is—the dosage form is administered without the aid of water. A portion of drug may get absorbed through the mucosa of mouth cavity and the remaining portion proceeds to stomach. The portion absorbed from the mouth cavity enters the blood stream and does not undergo first-pass metabolism in the liver. Many drugs may have local action such as the Ayurvedic formulation described in this patent specification. As ODCs dissolve in the mouth cavity, large capsules can also be administered, such as size ‘000’ which are not used in the pharmaceutical drug delivery system. In another embodiment, drug is incorporated in the capsule shell matrix of ODC and no drug is filled in the capsule core. Polymeric ODC are suitable ionizing radiation sterilization. When the ODCs are prepared under aseptic conditions, ODCs filled with suitable drug can also be placed in the intraperitoneal cavity or under the skin, in the interior wounds etc. where the shell will dissolve over time releasing the medicament.
While specific examples have been presented here, various modifications can be made and the invention is not limited to the examples shown in this patent application.
