Patent Grant
11051543
A variety of different ingestible compositions have been developed for nutritional, therapeutic and non-therapeutic uses. Examples of different types of ingestible compositions include orally ingestible tablets, capsules and liquids. A given orally ingestible formulation may include a variety of different components, such as active agents, carrier materials (including binders, bulking agents and other excipients), flavoring agents, coloring agents, etc. More recently, ingestible compositions which include a device component, such as an RFID tag or an ingestible event marker, have been developed.
As with many consumer products, ingestible compositions are not manufactured at the time of and location of use. Instead, they are generally manufactured at one or more fabrication facilities, stored for a period of time and then shipped to the end-user. Upon receipt, the end-user may further store them for a period of time before use.
During the multiple storage periods, and even manufacturing periods, such as mentioned above, the quality of the ingestible composition, e.g., in terms of effectiveness, may be degraded in some way. For example, exposure to humidity, elevated temperatures, microorganisms and oxidizing agents, as well other environmental hazards, can negatively impact the quality of the ingestible composition. Stability of ingestible compositions is therefore a significant consideration in their manufacture and use.
Components for providing stability to ingestible compositions are disclosed herein. In addition, aspects of the present disclosure include ingestible compositions that include layers that are configured to provide stability. Aspects further include methods of making and using the compositions.
Polymeric films that provide a barrier moisture vapor to protect an ingestible circuit and/or components thereof that may comprise a moisture sensitive material or combination of materials are disclosed herein. Adhesives, which may be edible and/or ingestible, are also disclosed. Aspects of the present disclosure also include ingestible compositions that include the adhesives, as well as polymeric films, such as, for example, a highly-swellable polymeric film. The adhesive and polymeric film may be combined with an ingestible component, such as, for example, an ingestible circuit component such as an ingestible event marker (IEM). Aspects further include methods of making and using such components and compositions.
Compositions
As mentioned above, aspects of the present disclosure are directed to polymeric films that provide a barrier moisture vapor to protect ingestible circuits and/or components thereof that may comprise a moisture sensitive material or combination of materials. Aspects of the present disclosure are also directed to compositions which include these in addition to other components, e.g., ingestible components such as ingestible devices, minimally dimensioned components, adhesives, etc.
In aspects of the present disclosure, ingestible compositions of interest include both an ingestible component and shelf-life stability component. As the compositions are ingestible, they are configured to be ingested or swallowed, i.e., taken into the stomach by drawing through the throat and esophagus with a voluntary muscular action. Accordingly, the compositions may be dimensioned so as to be capable of being ingested. In some instances, the compositions have a longest dimension of 30 mm or less, such as 20 mm or less, e.g., 10 mm or less. The volume of the ingestible composition may also vary so long as the composition is suitable for ingestion, where the volume in some instances may be 25 mm3 or less, such as 15 mm3 or less, including 10 mm3 or less.
Shelf-life stability components may elements of ingestible compositions that enhance shelf-life stability of the composition as compared to a suitable control, e.g., as described above. Shelf-life stability components may vary widely, and may or may not be integrated with one or more other components of the compositions, e.g., a pharmaceutically acceptable solid carrier, an ingestible event marker, a micro-battery, etc. Furthermore, a given composition may include a single shelf-life stability component or two or more distinct shelf-life stability components, as desired. Examples of different types of shelf-life stability components of interest include, but are not limited to: a water vapor desensitizer (e.g., a protective barrier, a desiccant, etc.), an electrochemical material variant that imparts shelf-life stability, an antioxidant, a stabilizer, or combination thereof, etc.
Of interest as shelf-life stability components are water vapor desensitizers. Water vapor desensitizers are components that reduce the sensitivity of the ingestible component or portions thereof to the deleterious effects of water vapor which may be present in the environment of the ingestible composition. Deleterious effects are harmful results of exposure to water vapor, where examples of such effects include loss or chemical change of material, color change, loss of performance, etc. The magnitude of deleterious effect reduction may vary, and may be 5% or greater, such as 10% or greater, including 25% or greater. The particular protocol for determining such magnitude may vary depending on the particular deleterious effect of interest. Water vapor desensitizers of interest include, but are not limited to: protective barriers, water vapor sequestering agents, etc.
In some instances, the water vapor desensitizer is a protective barrier. Protective barriers of interest include any structure or element that functions as an obstruction, hindrance, or impediment to the passage of water vapor from one portion of the ingestible composition to another, e.g., from the exterior of the ingestible composition to another region of the ingestible composition, e.g., an interior location that houses an IEM. Of interest as protective barriers are those barriers that rapidly disrupt upon contact with a liquid, such as an aqueous liquid, e.g., stomach acid. By “rapidly disrupt” is meant that, upon contact with the liquid, the barrier is compromised in some fashion, such that it ceases to function as a complete barrier in a limited period of time, e.g., 60 minutes or less, such as 15 minutes or less, including 2 minutes or less. The protective barrier may be disrupted according to a number of different mechanisms, such as physical disruption, dissolution, etc.
Protective barriers may enclose an entire ingestible composition or a component thereof (e.g., an IEM) or be present on just a portion (e.g., one or more surfaces) of an ingestible composition or component thereof, as desired. The dimensions of a given barrier may vary, and in some instances the barrier has a thickness of 10 μm or greater, such as 25 μm or greater, including 50 μm or greater. In some instances, the thickness ranges from 10 to 1000 μm, such as 25 to 500 μm including 50 to 200 μm. Protective barriers may have a variety of different configurations, ranging from homogenous layers of a single material to heterogeneous layers of two or more materials to multilayer structures of two or more materials. Examples of various types of protective barriers of interest are described in greater detail below.
According to aspects of the present invention, an ingestible composition may include a mono or multi-layer protective barrier made of a single material or multiple materials, and an IEM device. Protective barriers may be present on one side or both opposing sides of the IEM device and each in the form of a single homogenous layer. The thickness of each protective barrier may vary, where in some instances the thickness ranges from 25 to 500 μm including 50 to 200 μm. Each protective barrier may include a single material, or be a homogeneous mixture of two or more different materials, as reviewed in greater detail below.
A variety of different materials may be employed in protective barrier, where materials of interest are those that impart hydrophobicity to the layer such that the layer acts as a suitable water vapor desensitizer. In addition to acting as a water vapor barrier prior to contact with a liquid, the protective barrier will also be made up of a material that imparts the desired rapid disruptability to the protective barrier upon contact of the protective barrier with a liquid.
Materials of interest include, but are not limited to, lipids and functionally analogous materials which are solid at room temperature, are suitable for ingestion, are non-toxic and dissociate from each other (e.g., melt or dissolve) at internal body temperatures (i.e., core body temperatures, where such materials may be referred to as low-melting point materials). Lipids of interest include fatty acyls, glycerolipids, glycerophospholipids, etc. Lipid materials that find use in protective barriers include, but are not limited to: long chain organic materials, e.g., waxes, such as acrawax, bayberry wax, beeswax, candelilla wax, castor wax, carnauba wax, ceresin wax, coconut oil, cotton seed oil, esparto wax, glycowax, jojoba wax, Japan wax, lignite wax, linear polyethylene wax, microcrystalline petroleum wax, montan wax, olive oil, ouricouri wax, ozokerite wax, paraffin wax, rice bran wax, shellac wax, silicone waxes, synthetic waxes, sugarcane wax, cetyl palmitate, etc.; fatty alcohols, e.g., cetyl alcohol, lanolin alcohol, stearyl alcohol, etc.; fatty acids, such as lauric acid, myristic acid, palmitic acid, stearic acid, behenic acid, lignoceric acid, ceratic acid, montanoic acid, isostearic acid, isononanoic acid, 2-ethylhexanoic acid, oleic acid, ricinoleic acid, linoleic acid, linolenic acid, erucic acid, soybean fatty acid, linseed fatty acid, dehydrated castor fatty acid, tall oil fatty acid, tung oil fatty acid, sunflower fatty acid, safflower fatty acid, etc.; phospholipids; and triglycerides, etc.
Protective barriers of interest may further include pharmaceutically acceptable polymeric materials, including but not limited to, cellulosic materials, such as ethyl cellulose, cellulose acetate phthalate, cellulose acetate trimaletate, hydroxy propyl methylcellulose phthalate, polyvinyl acetate phthalate, polyvinyl alcohol phthalate, shellac; hydrogels and gel-forming materials, such as carboxyvinyl polymers, sodium alginate, sodium carmellose, calcium carmellose, sodium carboxymethyl starch, poly vinyl alcohol, hydroxyethyl cellulose, methyl cellulose, ethyl cellulose, gelatin, starch, and cellulose based cross-linked polymers in which the degree of crosslinking is low so as to facilitate adsorption of water and expansion of the polymer matrix, hydroxypropyl cellulose, hydroxypropyl methylcellulose, polyvinylpyrrolidone, crosslinked starch, microcrystalline cellulose, chitin, pullulan, collagen, casein, agar, gum arabic, sodium carboxymethyl cellulose, (swellable hydrophilic polymers) poly(hydroxyalkyl methacrylate) (molecular weight 5 k to 5000 k), polyvinylpyrrolidone (molecular weight 10 k to 360 k), anionic and cationic hydrogels, zein, polyvinyl alcohol having a low acetate residual, a swellable mixture of agar and carboxymethyl cellulose, copolymers of maleic anhydride and styrene, ethylene, propylene or isobutylene, pectin (molecular weight 30 k to 300 k), polysaccharides such as agar, acacia, karaya, tragacanth, algins and guar, polyethylene oxides (molecular weight 100 k to 5000 k), diesters of polyglucan, crosslinked polyvinyl alcohol and poly N-vinyl-2-pyrrolidone, hydrophilic polymers such as polysaccharides, methyl cellulose, sodium or calcium carboxymethyl cellulose, hydroxypropyl methyl cellulose, hydroxypropyl cellulose, hydroxyethyl cellulose, nitro cellulose, carboxymethyl cellulose, cellulose ethers, methyl ethyl cellulose, ethylhydroxy ethylcellulose, cellulose acetate, cellulose butyrate, cellulose propionate, gelatin, starch, maltodextrin, pullulan, polyvinyl pyrrolidone, polyvinyl alcohol, polyvinyl acetate, glycerol fatty acid esters, natural gums, lecithins, pectin, alginates, ammonia alginate, sodium, calcium, potassium alginates, propylene glycol alginate, agar, and gums such as arabic, karaya, locust bean, tragacanth, carrageens, guar, xanthan, scleroglucan and mixtures and blends thereof, pharmaceutically acceptable acrylic polymers, including but not limited to acrylic acid and methacrylic acid copolymers, methyl methacrylate copolymers, ethoxyethyl methacrylates, cyanoethyl methacrylate, poly(acrylic acid), poly(methacrylic acid), methacrylic acid alkylamide copolymer, poly(methyl methacrylate), polymethacrylate, poly(methyl methacrylate) copolymer, polyacrylamide, aminoalkyl methacrylate copolymer, poly(methacrylic acid anhydride), and glycidyl methacrylate copolymers, etc.
Adhesives
Aspects of the present disclosure include adhesive compositions, such as, for example, edible adhesive compositions. Aspects of adhesives for use in the present disclosure include examples disclosed in PCT Application Serial No. PCT/US2015/012252 published as WO2015112604, entitled “EDIBLE ADHESIVES AND INGESTIBLE COMPOSITIONS INCLUDING THE SAME”, which is incorporated by reference herein in its entirety. As the compositions are edible, they are suitable for ingestion by a living animal, e.g., a vertebrate, including a mammal, such as a human. Accordingly, the adhesive compositions are non-toxic to the living animal, at least in the amounts at which the adhesive is present in the ingestible composition of which it is a part. By non-toxic is meant not capable of causing harm, at least for a normal subject not having an allergy to an ingredient of the adhesive composition.
As the compositions are adhesive, when positioned between two materials, e.g., a film and an ingestible components, such as described below, the compositions cause the two objects to adhere to each other. Accordingly, when an adhesive composition is positioned between two objects, the two objects stay attached to each other, i.e., stick fast to, cleave to, or cling to, each other. The strength of the adhesive compositions may vary, and in some instances is sufficiently strong such that two objects adhered to each other with the adhesive stay adhered to each other under pharmaceutical storage conditions, e.g., in a sterile packaging at standard temperature/pressure. While the adhesive strength of the compositions may vary, in some instances the adhesives have a strength as measured by the T-Peel test that ranges from 1 mN to 100 mN. An example of a T-Peel test that may be employed to determine adhesive strength is ASTM D1876.
Adhesive compositions of interest include a cellulose ether, a tackifier and a plasticizer. Of interest as cellulose ethers are nonionic cellulose ethers. Examples of such cellulose ethers include, but are not limited to: methylcellulose, ethylcellulose, hydroxymethylcellulose, hydroxyethylcellulose, carboxymethylcellulose, carboxyethylcellulose and hydroxypropylcellulose, hydroxypropyl methyl cellulose; additional celluloses, such as carboxymethylcellulose sodium, carboxymethylcellulose calcium, carboxymethylstarch; etc. In certain embodiments, the cellulose ether is a hydroxypropyl cellulose. Hydroxypropyl cellulose is available from a variety of commercial sources, including but limited to, Nisso America Inc. In certain embodiments, the average molecular weight of the hdyroxypropyl cellulose is 10,000 daltons or higher, such as 25,000 daltons or higher, where the average molecular weight may be as high as 40,000 daltons or higher, e.g., 50,000 daltons or higher, 100,000 daltons or higher, and including 250,000 daltons or higher, 500,000 daltons or higher, 750,000 daltons or higher, such as 1,000,000 daltons or higher, where in some instances the molecular weight ranges from 10,000 to 1,000,000 daltons, such as 25,000 to 500,000 daltons, including 30,000 to 250,000 daltons. While the degree of substitution may also vary, in some instances the cellulose has a degree of substitution ranging from 50 to 80%. The proportion of the cellulose ether in the adhesive compositions may vary, ranging in some instances from 50 to 95%, (w/w), such as from 60 to 90% (w/w), including from 70 to 85% (w/w).
Adhesives of interest may further include a tackifying agent, i.e., a tackifier. Tackifying agents of interest include, but are not limited to: natural, semi-synthetic and synthetic water-soluble tackifiers. Examples of the natural tackifiers include xanthan gum, xanthane flow, pectin from vegetables, gum arabic and guar gum. Examples of the semi-synthetic tackifiers include methylated products of cellulose or starch derivatives, their carboxyalkylated products and hydroxyalkylated products and examples of the synthetic tackifiers include polyacrylates, polymaleates, polyvinylpyrrolidone, and the like. In some instances, the tackifying agent is a polyvinylpyrrolidone (i.e., povidone), which is synthetic polymer consisting mainly of linear 1-vinyl-2-pyrrolidone groups. Povidones (which may be cross-linked) are available from a variety of different commercial sources, including but not limited to: Sigma, BASF and the like. In some instances, the povidone has a molecular weight ranging from 35 kilodaltons to 45 kilodaltons. The proportion of the tackifying agent in the adhesive may vary, ranging in some instances from 1 to 25%, (w/w), such as from 3 to 20% (w/w), including from 5 to 15% (w/w), e.g., from 5 to 10% (w/w).
Also a plasticizer may be present in the adhesive compositions. Plasticizers of interest include glycerin, polyethylene glycol, triethylcitrate, and dibutyl sebacate. In some instances, the plasticizer is glycerin. The proportion of the plasticizer in the adhesive may vary, ranging in some instances from 5 to 30%, (w/w), such as from 7.5 to 25% (w/w), including from 10 to 20% (w/w).
While the adhesive compositions described herein may find use in a variety of applications, they may be used in adhering highly-swellable polymeric films to ingestible components. As such, each of these two classes of objects that can be adhered to each other with adhesives described herein are now reviewed in greater detail.
Polymeric Films
According to aspects of the present disclosure, the adhesive is present in a composition that also includes a polymeric film, such as, for example a highly-swellable polymeric film. As used herein, the term “film” means a thin sheet or layer. While the dimensions of the film may vary, in some instances the film has a thickness of 10 microns or greater, such as 50 microns or greater, including 100 microns or greater, and ranges in thickness in some instances from 10 to 1000, such as 20 to 200 and including 30 to 60 microns. The top and bottom surfaces of the film may have a variety of different configurations, including but not limited to rectangular, trapezoidal, triangular, etc.; curvilinear, such as circular, ovoid or other curvilinear shape, etc. Where the film has surface which may be defined by length and width, these dimensions may vary, where in some instances the length ranges from 1 to 20, such as 2 to 10 and including 3 to 6 mm and the width ranges from 1 to 20, such as 2 to 10 and including 3 to 6 mm.
Films of interest may be highly-swellable. By highly-swellable is meant that that the films are able to swell substantially upon contact with a liquid aqueous medium, such that they grow substantially in bulk (i.e., magnitude in three dimensions, e.g., which may be assessed in terms of a change in volume, etc.) by the absorption of water upon contact with an aqueous medium. Where the swelling results in a change in volume of the film, the volume may increase by a factor of 10 or greater, such as a factor of 15 or greater, including a factor of 20 or greater, e.g., a factor of 25 or greater, a factor of 30 or greater, a factor of 40 or greater, including a factor of 50 or greater, such as a factor of 100 or greater, for example a factor of 500 or greater, including a factor of 1000 or greater, as compared to the initial volume prior to contact with the liquid aqueous medium. Upon swelling, the mass of film may increase as well, where in some instances the mass increases by a factor of 10 or greater, such as a factor of 15 or greater, including a factor of 20 or greater, e.g., a factor of 25 or greater, a factor of 30 or greater, a factor of 40 or greater, including a factor of 50 or greater, such as a factor of 100 or greater, for example a factor of 500 or greater, including a factor of 1000 or greater, as compared to the initial mass prior to contact with the aqueous medium.
Highly-swellable polymeric films described herein rapidly swell upon contact with a liquid aqueous medium. By “rapidly swell” is meant that upon contact with a liquid aqueous medium, the films achieve substantially maximum swelling in a short period of time. As such, following contact with an aqueous medium, the films achieve 90% or more, such as 95% percent or more maximal swelling in a period of time of 10 minutes or less, such as 5 minutes or less, including 1 minute or less. In some instances, the films swell in volume by a factor of 10 or greater, such as a factor of 15 or greater, including a factor of 20 or greater, e.g., a factor of 25 or greater, a factor of 30 or greater, a factor of 40 or greater, including a factor of 50 or greater, such as a factor of 100 or greater, for example a factor of 500 or greater, including a factor of 1000 or greater, as compared to the initial volume prior to contact with the aqueous medium, in 10 minutes or less, such as 5 minutes or less, including 1 minute or less.
As mentioned above, films of interest may be configured to absorb water upon contact with an aqueous medium. While the amount of water that is absorbed by a given film may vary, in some instances the films absorb 10 or more grams of water per gram dry weight of film, such as 25 or more grams of water per gram of dry weight of film, including 50 or more grams of water per gram of dry weight film, upon contact with an aqueous medium.
Highly-swellable polymeric films of interest are those that swell substantially upon contact with a liquid aqueous medium, but do not swell substantially, if at all, upon contact with a gaseous medium that includes water vapor. As such, upon contact with a gaseous medium that includes water vapor (e.g., where the partial pressure of water ranges from 1.0 to 49.8, such as 2.7 to 21.4 mmHg), the films swell little, if at all. As such, any swelling that occurs upon contact with such a gaseous medium as determined by a change in volume is a factor of five or less, such as a factor of 2 or less as compared to the film prior to contact with the gaseous medium.
Highly swellable polymeric films of interest exhibit rapidly swelling behavior without disintegrating upon contact with a liquid aqueous medium. As such, the films swell upon contact with an aqueous medium but do not break up or separate into parts, such that they do not lose intactness or solidness, at least not for a prolonged period of time, such as 1 hour or longer, e.g., 2 hours or longer, including 3 hours or longer, such as 5 hours or longer, including 6, 12, 18, 24, 36, 48, 60, or 72 hours or longer, wherein in some instances the films may be fabricated not to disintegrate, e.g., dissolve, for a period of time ranging from 1 to 100, such as 5 to 75 hours following contact with an aqueous medium. As such, they do not dissolve upon contact with a liquid aqueous medium. Accordingly, a film that contacts a liquid aqueous medium will remain as a single entity following swelling, and will not go into solution. Therefore, following contact with a liquid aqueous medium, the film can still be manipulated, i.e., handled.
In some instances, the polymeric films are ingestible. As such films are ingestible, they are configured to be ingested or swallowed, i.e., taken into the stomach by drawing through the throat and esophagus with a voluntary muscular action. As such, the films themselves, as well as the components thereof, e.g., polymeric components, binders, plasticizers, porogens (such as described in greater detail below), do not exhibit an unacceptable level of toxicity when employed as intended. In other words, when the films are employed for their intended use, the toxicity level of the films, if present all, is acceptable.
Prior to contact with an aqueous medium, the freestanding films are mechanically stable. Films are flexible, able to easily wrap around rollers and rods and relatively strong under tension, but show little elongation under strain.
Films of interest may include an ionic polymer and may therefore be referred to as polymeric films. The phrase “ionic polymer” refers to a polymer comprising monomeric units having an acidic functional group, such as a carboxyl, sulfate, sulfonate, phosphate or phosphonate group, or a basic functional group, such as an amino, substituted amino or guanidyl group. When in aqueous solution at a suitable pH range, e.g., 7 to 14 pH, an ionic polymer comprising acidic functional groups will be a polyanion, and such a polymer is referred to herein as an “anionic polymer”. Likewise, in aqueous solution at a suitable pH range, e.g., 1 to 7 pH, an ionic polymer comprising basic functional groups will be a polycation. Such a polymer is referred to herein as a “cationic polymer”. As used herein, the terms ionic polymer, anionic polymer and cationic polymer refer to hydrophilic polymers in which the acidic or basic functional groups are not charged, as well as polymers in which some or all of the acidic or basic functional groups are charged, in combination with a suitable counterion. Suitable anionic polymers include alginates, e.g., alginic acid and salts thereof, polyacrylic acid, dextran sulfate, carboxymethylcellulose, hyaluronic acid, polyglucuronic acid, polymanuronic acid, polygalacturonic acid, polyarabinic acid; chrondroitin sulfate and dextran phosphate. Suitable cationic polymers include chitosan, polyethylenimine, poly-L-lysine, and dimethylaminodextran. Of interest in some instances are polysaccharide anionic polymers. Polysaccharide anionic polymers of interest include alginates, e.g., alginic acid and salts thereof. Alginic acid (i.e., alginate) is a linear copolymer with homopolymeric blocks of (1-4)-linked β-D-mannuronate (M) residues and α-L-guluronate (G) residues. The residues are covalently linked together in different sequences or blocks. The residues can appear in homopolymeric blocks of consecutive G-residues (G-blocks), consecutive M-residues (M-blocks) or alternating M and G-residues (MG-blocks). Also of interest are salts of alginic acid, e.g., sodium alginate, calcium alginate, potassium alginate, etc. The molecular weight of the alginate (e.g., alginic acid or alginate salt thereof) may vary, ranging in some instances from 10,000 to 600,000 Daltons, such as 50,000 to 100,000 Daltons. Alginates of interest will include a percentage of acidic groups sufficient to impart the above described swellability characteristic to the film. As such, where an alginate is employed that does not initially include the desired acidic groups; it may be modified as necessary to provide for the desired acidic groups. For example, where sodium alginate is employed, some of the sodium groups of the sodium alginate may be converted to acidic groups, e.g., by contacting the film with a suitable acid (such as HCl). To impart the desired mechanical properties to the film, the alginates may be cross-linked. For example, where sodium alginate is employed, the alginate may be cross-linked with a divalent cation salt, e.g., calcium chloride, magnesium chloride, etc.
Where desired, the film may include an additional component that provides for acidic, e.g., carboxyl, functional groups. For example, films of interest may include one or more additional polymers that provide for acidic functional groups, e.g., one or more additional anionic polymers that are present in addition to an alginate. Examples of additional anionic polymers of interest that may be present include, but are not limited to both natural and synthetic polymers.
In some instances, the film is a blend of both an alginate and a polyacrylic acid. Polyacrylic acids of interest include both homopolymeric polyacrylic acid as well as copolymers, including both random and block copolymers, of acrylic acid residues and one or more non-acrylic acid residues, e.g., acrylate residues, etc. Where desired, the polyacrylic acid may be cross-linked. When the film includes a blend of alginate to polyacrylic acid polymers, the dry weight ratio of the two types of polymers in the film may vary, and in some instances ranges from 25 to 95%, such as 50 to 80% and including 70 to 80% alginate.
In addition to the polymeric components, the films may further include one or more additional types of components. For example, films may include one or more agents that enhance conductivity of the film upon contact with an aqueous medium. Examples of such components include pore forming agents (i.e., porogens). The term “porogen” as used herein, refers to a chemical compound that is included in the film and, upon contact with an aqueous medium, is removed from the film, e.g., via diffusion, dissolution, and/or degradation, to leave a pore in the resultant film. The diameter of the pores produced by the porogen may vary, ranging in some instances from 1 to 1000 μm, such as 1 to 500 μm and including 1 to 250 μm. Porogens of interest include both inorganic and organic porogens. Inorganic porogens of interest include, but are not limited to: inorganic salts, e.g., NaCl, MgCl2, CaCl2, NH4Cl, NH4PO4, NH4CO3−; soluble biocompatible salts; sugars (e.g., sugar alcohols), polysaccharides (e.g., dextran (poly(dextrose)), water soluble small molecules, natural or synthetic polymers, oligomers, or monomers that are water soluble or degrade quickly under physiological conditions, including but not limited to: polyethylene glycol, polyvinyl alcohol, poly(vinylpyrollidone), pullulan, poly(glycolide), poly(lactide), poly(lactide-co-glycolide), other polyesters, and starches. When present, the total amount of porogen component made up of one or more porogens may vary. In some instances, the amount of porogen component ranges from 1 to 40, including from 5 to 10 dry weight percent of the film.
Where desired, films may include one or more binding agents or binders. Binders of interest include, but are not limited to: celluloses, e.g., methyl cellulose, hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose, hydroxypropyl methylcellulose, etc.; polyvinyl pyrrolidone; polyethylene oxides; gums, acrylate polymers; methacrylate polymers; copovidone; etc. When present, the total amount of binder component made up of one or more binding agents may vary. While the total amount of one or more binding agents in the film may vary, in some instances the amount ranges from 1 to 50, such as 5 to 10 dry weight percent of the film.
Where desired, films may include one or more plasticizing agents. Plasticizing agents of interest include, but are not limited to: fatty acids, e.g., oleic acid, palmitic acid, etc.; dioctylphtalate; phospholipid; phosphatidic acid; polyethylene glycol; glycerine; butylhydroxytoluene; salts; saccharides, e.g., sucrose; etc. When present, the total amount of plasticizer component made up of one or more plasticizing agents may vary. In some instances, the amount of plasticizer component ranges from 0.01 to 10, including from 2 to 5 dry weight percent of the film.
Highly-swellable polymeric films of interest are further described in U.S. Provisional Application Ser. No. 61/758,030 filed on Jan. 29, 2013 and U.S. application Ser. No. 14/763,217 published as U.S. Patent Application Pub. No. 2015/0361234; the disclosures of which are herein incorporated by reference in their entirety.
Ingestible Compositions
Aspects of the present disclosure include ingestible compositions. In these instances, ingestible compositions of interest include both an ingestible component and a film component which is associated therewith by an adhesive, e.g., as described above. As the compositions are ingestible, they are configured to be ingested or swallowed, i.e., taken into the stomach by drawing through the throat and esophagus with a voluntary muscular action. Accordingly, the compositions are dimensioned so as to be capable of being ingested. In some instances, the compositions have a longest dimension of 30 mm or less, such as 20 mm or less, e.g., 10 mm or less. The volume of the ingestible composition may also vary so long as the composition is suitable for ingestion, where the volume in some instances may be 25 mm3 or less, such as 15 mm3 or less, including 10 mm3 or less.
In the ingestible compositions, the ingestible component is a portion or part of the ingestible composition that is configured for ingestion. The ingestible component may vary widely and may include one or more subcomponents, e.g., a pharmaceutically acceptable solid carrier (which may or may not include an active agent), a device (which may or may not include electronic circuitry), etc. In the ingestible composition, the highly-swellable polymeric film may be associated with an ingestible composition in a number of different ways, e.g., depending on the nature of the ingestible composition, depending on the purpose of the film, etc.
In some instances, the ingestible component includes a pharmaceutically acceptable solid carrier. Pharmaceutically acceptable solid carrier configurations include tablet and capsule configurations. While the pharmaceutically acceptable solid carrier may have a solid configuration, the solid configuration may include a liquid component, such as is found in a liquid capsule, which includes a liquid component present in a solid capsule. In some instances, the pharmaceutically acceptable solid carrier is configured to impart a controlled release profile to an active agent that is associated with the pharmaceutically acceptable solid carrier. Examples of pharmaceutically acceptable solid carriers of interest can be found in Remington's Pharmaceutical Sciences, Mace Publishing Company, Philadelphia, Pa., 17th ed. (1985). In such instances, among other non-mutually exclusive functions, e.g., as described below, the highly-swellable polymeric films may serve to separate the ingestible component from the carrier. For instance, upon contact with an aqueous medium, the resultant swelling of the film may result in the component to which the film is associated being pushed away and separated from the carrier, e.g., tablet or capsule. Such functionality of the film may be desirable, e.g., where association of the carrier material impedes functionality of the ingestible component (such as by blocking access of electrode material to an aqueous environment).
Where desired, the pharmaceutically acceptable solid carrier may include an active agent. Active agents of interest include pharmaceutically active agents as well as non-pharmaceutical active agents, such as diagnostic agents. The phrase “pharmaceutically active agent” (also referred to herein as drugs) refers to a compound or mixture of compounds which produces a physiological result, e.g., a beneficial or useful result, upon contact with a living organism, e.g., a mammal, such as a human. Pharmaceutically active agents are distinguishable from such components as excipients, carriers, diluents, lubricants, binders and other formulating aids, and encapsulating or otherwise protective components. The pharmaceutically active agent may be any molecule, as well as binding portion or fragment thereof, that is capable of modulating a biological process in a living subject. In certain aspects, the pharmaceutically active agent may be a substance used in the diagnosis, treatment, or prevention of a disease or as a component of a medication. The pharmaceutically active agent is capable of interacting with a target in a living subject. The target may be a number of different types of naturally occurring structures, where targets of interest include both intracellular and extracellular targets. Such targets may be proteins, phospholipids, nucleic acids and the like, where proteins are of particular interest. Specific proteinaceous targets of interest include, without limitation, enzymes, e.g., kinases, phosphatases, reductases, cyclooxygenases, proteases and the like, targets comprising domains involved in protein-protein interactions, such as the SH2, SH3, PTB and PDZ domains, structural proteins, e.g., actin, tubulin, etc., membrane receptors, immunoglobulins, e.g., IgE, cell adhesion receptors, such as integrins, etc., ion channels, transmembrane pumps, transcription factors, signaling proteins, and the like. Broad categories of active agents of interest include, but are not limited to: cardiovascular agents; pain-relief agents, e.g., analgesics, anesthetics, anti-inflammatory agents, etc.; nerve-acting agents; chemotherapeutic (e.g., anti-neoplastic) agents; neurological agents, e.g., anti-convulsants, etc. The amount of active agent that is present in the solid carrier may vary. In some instances, the amount of active agent that is present may range from 0.01 to 100% by weight.
Further examples of pharmaceutically acceptable solid carriers and active agents which may or may not be included therein are described in PCT Application Serial No. PCT/US2006/016370 published as WO/2006/116718; PCT Application Serial No. PCT/US2007/082563 published as WO/2008/052136; PCT Application Serial No. PCT/US2007/024225 published as WO/2008/063626; PCT Application Serial No. PCT/US2007/022257 published as WO/2008/066617; PCT Application Serial No. PCT/US2008/052845 published as WO/2008/095183; PCT Application Serial No. PCT/US2008/053999 published as WO/2008/101107; PCT Application Serial No. PCT/US2008/056296 published as WO/2008/112577; PCT Application Serial No. PCT/US2008/056299 published as WO/2008/112578; PCT Application Serial No. PCT/US2008/077753 published as WO2009/042812; PCT Application Serial No. PCT/US2008/085048 published as WO2009/070773; PCT Application Serial No. PCT/US2009/36231 published as WO2009/111664; PCT Application Serial No. PCT/US2009/049618 published as WO2010/005877; PCT Application Serial No. PCT/US2009/053721 published as WO2010/019778; PCT Application Serial No. PCT/US2009/060713 published as WO2010/045385; PCT Application Serial No. PCT/US2009/064472 published as WO2010/057049; PCT Application Serial No. PCT/US2009/067584 published as WO2010/068818; PCT Application Serial No. PCT/US2009/068128 published as WO2010/075115; PCT Application Serial No. PCT/US2010/020142 published as WO2010/080765; PCT Application Serial No. PCT/US2010/020140 published as WO2010/080764; PCT Application Serial No. PCT/US2010/020269 published as WO2010/080843; PCT Application Serial No. PCT/US2010/028518 published as WO2010/111403; PCT Application Serial No. PCT/US2010/032590 published as WO2010/129288; PCT Application Serial No. PCT/US2010/034186 published as WO2010/132331; PCT Application Serial No. PCT/US2010/055522 published as WO2011/057024; the disclosures of which are herein incorporated by reference.
With such ingestible compositions, the polymeric film may be associated with the ingestible component in a number of different ways. For example, the polymeric film may form a coating or layer that substantially if not completely encloses the ingestible component. Such a configuration may be employed where it is desired to impart shelf-life stability to the ingestible composition. In such instances, the film imparts shelf-life stability to the composition, in that the film enhances the storage stability of the composition by a quantifiable measure as compared to a control or reference composition (i.e., a composition that lacks the shelf-life stability component). Polymeric films of interest may enhance the shelf-life stability of the composition as compared to a suitable control by a magnitude of 2-fold or greater, such as 5-fold or greater including 10-fold or greater, e.g., 25-fold or greater. The presence of the film may allow the composition to be stable for extended periods of time during or following manufacture, where the ingestible composition may be stable for one year or longer, such as two years or longer, including five years or longer, following manufacture when the composition is maintained under conditions in which the temperature ranges from 10 to 40° C., the pressure ranges from 0.5 to 2.0 ATM and the relative humidity ranges from 10 to 100%. By “stable” is meant that the functionality of the composition does not degrade to a point that the composition is no longer suitable for use in its intended purpose. For example, if the composition includes an active pharmaceutical agent, the amount of active agent following the storage time period may be 85% or more, such as 90% or more, including 95% or more of the original amount present in the composition following manufacture, e.g., as determined using an HPLC protocol or other suitable analytical technique which can distinguish the amount of active agent from any degradation byproducts, such as oxidation byproducts. Aspects and examples of shelf-life stability components are described in U.S. application Ser. No. 13/304,260, published as U.S. Patent Application Pub. No. US2013/0129869, which is incorporated by reference herein in its entirety.
In one aspect, a polymeric film for extending the shelf-life of an ingestible composition comprises a first layer comprising a polymer material, a second layer comprising an adhesive material, the second layer associated with the first layer and configured to adhere to the first layer and the first layer is configured to provide a moisture vapor barrier for an ingestible circuit component comprising a moisture sensitive material or combination of materials. The polymer material of the first layer may comprise an anionic polymer and/or an alginate material. The first layer and the second layer may be configured to be laminated to an ingestible circuit component, such as, for example, an ingestible event marker (IEM).
In another aspect, the polymeric film also comprises a third layer associated with the first layer and a fourth layer associated with the second layer. The first layer and the second layer may be disposed between the third layer and the fourth layer, such that the third layer and the fourth layer form the outermost layers of a multilayer film. The third layer may also be releasable from the first layer and/or the fourth layer may be releasable from the second layer. In addition, the third layer and/or the fourth layer may comprise Polyethylene terephthalate (PET). In one aspect, the fourth layer comprises a PET film with a silicone coating adjacent the adhesive material of the second layer. The third layer may also comprise an uncoated PET film adjacent the polymer material of the first layer.
In addition to or instead of a pharmaceutically acceptable solid carrier, ingestible compositions may include a device. The term “device” is used broadly to refer to a mechanical and/or electrical component configured for a particular purpose, where the device may or may not include a circuitry component.
Of interest as devices are ingestible devices, e.g., RFID-enabled devices; ingestible event indicators (also known as ingestible event markers or IEMS), etc. An ingestible event indicator is a device that is dimensioned to be ingestible and includes an identifier circuitry component and, optionally, a current path extender, e.g., a membrane, sometimes referred to herein as a “skirt”. Various aspects of an event indicator may include a control device for altering conductance; and a partial power source. The partial power source may include a first material electrically coupled to the control device; and a second material electrically coupled to the control device and electrically isolated from the first material, where the first and second materials are dissimilar.
Upon ingestion, the event indicator contacts a conducting fluid, e.g., stomach fluid. When the event indicator is in contact with the conducting liquid, a current path is formed through the conducting liquid between the first and second materials. The voltage potential created between the materials provides the power for operating the event indicator as well as produces the current flow through the conducting fluid and the system. In one aspect, the event indicator operates in direct current mode. In an alternative aspect, the event indicator controls the direction of the current so that the direction of current is reversed in a cyclic manner, similar to alternating current. The current path through the system is controlled by the control device. Completion of the current path allows for the current to flow and in turn a receiver, not shown, can detect the presence of the current and recognize that the system has been activated and the desired event is occurring or has occurred.
In one aspect, the two materials are similar in function to the two electrodes needed for a direct current power source, such as a battery. The conducting liquid acts as the electrolyte needed to complete the power source. The completed power source is defined by the electrochemical reaction between the dissimilar materials of the event indicator and the completion of the power source is enabled by the fluids of the body. The completed power source may be viewed as a power source that exploits electrochemical conduction in an ionic or a conducting solution such as gastric fluid, blood, or other bodily fluids and some tissues.
In certain aspects, the complete power source or supply is one that is made up of active electrode materials, electrolytes, and inactive materials, such as current collectors and packaging. The active materials are any pair of materials with different electrochemical potentials. Suitable materials are not restricted to metals, and in certain aspects the paired materials are chosen from metals and non-metals, e.g., a pair made up of a metal (such as Mg) and a salt (such as CuI). With respect to the active electrode materials, any pairing of substances—metals, salts, or intercalation compounds—with suitably different electrochemical potentials (voltage) and low interfacial resistance are suitable. Where desired, the voltage provided by the two dissimilar electrochemical materials upon contact of the materials of the power source with the target physiological site is 0.001 V or higher, including 0.01 V or higher, such as 0.1 V or higher, e.g., 0.3 V or higher, including 0.5 volts or higher, and including 1.0 volts or higher, where in certain aspects, the voltage ranges from about 0.001 to about 10 volts, such as from about 0.01 to about 10 V.
Anode materials of interest include, but are not limited to: magnesium, zinc, sodium, lithium, iron and alloys thereof, e.g., Al and Zn alloys of Mg, which may or may not be intercalated with a variety of materials such, as graphite with Li, K, Ca, Na, Mg, and the like. Cathode materials of interest include, but are not limited to, copper salts, such as copper salts of iodide, chloride, bromide, sulfate, formate, Fe3+ salts, e.g., orthophosphate, pyrophosphate, silver salts, etc. One or both of the metals may be doped with a non-metal, for example to enhance the voltage output of the battery. Non-metals that may be used as doping agents in certain aspects include, but are not limited to: sulfur, iodine and the like. In certain aspects, the electrode materials are cuprous iodine (CuI) or cuprous chloride (CuCl) as the anode and magnesium (Mg) metal or magnesium alloy as the cathode. Aspects of the present disclosure use electrode materials that are not harmful to the human body.
In such ingestible compositions, the film may be associated with the event indicator in a number of different ways, where the different ways are not mutually exclusive such that films may be associated with an event indicator in more than one way. For example, a highly-swellable polymer film may cover a portion of at least one of the first or second dissimilar materials. As such, the film may cover a portion or all of the cathode material. Alternatively or in addition, the film may cover a portion or all of the anode material. In such instances, the film may cover 10% or more, 20% or more, 25% or more, 50% or more, including 75% or more, e.g., 90% or more, etc., of the cathode and/or anode materials, including all of the cathode or anode materials.
With respect to current signatures produced by such event indicators, the current signatures may distinguish one class of event indicator from other types or may be universally unique, such as where the current signature is analogous to a human fingerprint which is distinct from any other fingerprint of any other individual and therefore uniquely identifies an individual on a universal level. In various aspects, the control circuit may generate a variety of different types of communications, including but not limited to: RF signals, magnetic signals, conductive (near-field) signals, acoustic signals, etc.
In various aspects, the event indicator may further include a current path extender, such as a membrane, which produces a virtual dipole length between the pair of dissimilar materials (functioning as transmission elements) that is longer than the actual dipole length. In addition to controlling the magnitude of the current path between the materials, such a membrane (sometimes referred to herein as “amplifier” or “skirt”) is used to increase the “length” of the current path and, hence, act to boost the conductance path, as disclosed in the PCT application no. PCT/US2008/077753 published as WO2009/042812 and in U.S. Pat. No. 7,978,064, the entire contents of which are incorporated herein by reference. Throughout the disclosure herein, the terms “membrane”, “skirt” and “amplifier” are used interchangeably with the term “current path extender” without impacting the scope or the present aspects and the claims herein.
Where desired, an ingestible event indicator may be stably associated in some manner to another ingestible component, e.g., pharmaceutically acceptable carrier component (e.g., as described above). By “stably associated” is meant that the event indicator and second ingestible component, e.g., a pharmaceutically acceptable carrier component, do not separate from each other, at least until administered to the subject in need thereof, e.g., by ingestion. As the event indicators are dimensioned to be ingestible, they are sized so that they can be placed in a mammalian, e.g., human or animal, mouth and swallowed. In some instances, event indicators have a longest dimension that is 30 mm or less, such as 20 mm or less, including 5 mm or less.
Various aspects of ingestible event indicators of interest (including protocols for the fabrication thereof) are described in PCT Application Serial No. PCT/US2006/016370 published as WO/2006/116718; PCT Application Serial No. PCT/US2007/082563 published as WO/2008/052136; PCT Application Serial No. PCT/US2007/024225 published as WO/2008/063626; PCT Application Serial No. PCT/US2007/022257 published as WO/2008/066617; PCT Application Serial No. PCT/US2008/052845 published as WO/2008/095183; PCT Application Serial No. PCT/US2008/053999 published as WO/2008/101107; PCT Application Serial No. PCT/US2008/056296 published as WO/2008/112577; PCT Application Serial No. PCT/US2008/056299 published as WO/2008/112578; PCT Application Serial No. PCT/US2008/077753 published as WO2009/042812; PCT Application Serial No. PCT/US2008/085048 published as WO2009/070773; PCT Application Serial No. PCT/US2009/36231 published as WO2009/111664; PCT Application Serial No. PCT/US2009/049618 published as WO2010/005877; PCT Application Serial No. PCT/US2009/053721 published as WO2010/019778; PCT Application Serial No. PCT/US2009/060713 published as WO2010/045385; PCT Application Serial No. PCT/US2009/064472 published as WO2010/057049; PCT Application Serial No. PCT/US2009/067584 published as WO2010/068818; PCT Application Serial No. PCT/US2009/068128 published as WO2010/075115; PCT Application Serial No. PCT/US2010/020142 published as WO2010/080765; PCT Application Serial No. PCT/US2010/020140 published as WO2010/080764; PCT Application Serial No. PCT/US2010/020269 published as WO2010/080843; PCT Application Serial No. PCT/US2010/028518 published as WO2010/111403; PCT Application Serial No. PCT/US2010/032590 published as WO2010/129288; PCT Application Serial No. PCT/US2010/034186 published as WO2010/132331; PCT Application Serial No. PCT/US2010/055522 published as WO2011/057024; the disclosures of which are herein incorporated by reference.
In certain aspects, the ingestible event indicators are disrupted upon administration to a subject. As such, in certain aspects, the compositions are physically broken, e.g., dissolved, degraded, eroded, etc., following delivery to a body, e.g., via ingestion, injection, etc. The compositions of these aspects are distinguished from devices that are configured to be ingested and survive transit through the gastrointestinal tract substantially, if not completely, intact.
Where desired, an active agent (e.g., as described above) may be present in one or more of the event indicator components, e.g., in the electrochemical materials, the support, the membrane, etc. Examples of such configurations are described in PCT Application Serial No. PCT/US2010/032590 published as WO2010/129288; the disclosures of which are herein incorporated by reference.
In some instances the membrane may be made up partially or completely of a highly-swellable polymeric film. For example, the entire membrane may be fabricated from a highly-swellable polymeric film. Alternatively, a portion of the membrane, such as the outer-periphery of the membrane, may be made up of the highly-swellable polymeric film, with the remainder of the membrane being made up of one or more other suitable materials.
With reference to
In the specific example of the system 30 combined with the pharmaceutical product, as the product or pill is ingested, the system 30 is activated. The system 30 controls conductance to produce a unique current signature that is detected, thereby signifying that the pharmaceutical product has been taken. In other aspects, the current signature may contain information on the ingredients of the ingested pharmaceutical product which may include their chemical composition, date of manufacture, batch number, etc., among other desired information related to the pharmaceutical product which may be a placebo as well. The system 30 includes a framework 32. The framework 32 is a chassis for the system 30 and multiple components are attached to, deposited upon, or secured to the framework 32. In this aspect of the system 30, a digestible material 34 is physically associated with the framework 32. The material 34 may be chemically deposited on, evaporated onto, secured to, or built-up on the framework all of which may be referred to herein as “deposit” with respect to the framework 32. The material 34 is deposited on one side of the framework 32. The materials of interest that can be used as material 34 include, but are not limited to those described above. The material 34 is deposited by using any convenience protocol, including but not limited to physical vapor deposition, electro-deposition, or plasma deposition, liquid deposition, among other protocols. The material 34 may be from about 0.05 to about 500 μm thick, such as from about 5 to about 100 μm thick. The shape may be controlled by shadow mask deposition, or photolithography and etching. Additionally, even though only one region is shown for depositing the material, each system 30 may contain two or more electrically unique regions where the material 34 may be deposited, as desired. It should be noted that while the electrode materials described in connection with
At a different side, which may be the opposite side as shown in
Thus, when the system 30 is in contact with the conducting fluid, e.g., a liquid, a current path, an example is shown in
The voltage potential created between the materials 34 and 36 provides the power for operating the system as well as produces the current flow through the conducting fluid and the system. In one aspect, the system operates in direct current mode. In an alternative aspect, the system controls the direction of the current so that the direction of current is reversed in a cyclic manner, similar to alternating current. As the system reaches the conducting fluid or the electrolyte, where the fluid or electrolyte component is provided by a physiological fluid, e.g., stomach acid, the path for current flow between the materials 34 and 36 is completed external to the system 230; the current path through the system 30 is controlled by the control device 38. Completion of the current path allows for the current to flow, through conductive communication through the stomach, and in turn to a receiver, not shown, the receiver capable of detecting the presence of the current signature containing information and further recognize that the system 30 has been activated and the desired event is occurring or has occurred.
In one aspect, the two materials 34 and 36 are similar in function to the two electrodes needed for a direct current power source, such as a battery. The conducting liquid acts as the electrolyte needed to complete the power source. The completed power source described is defined by the physical chemical reaction between the materials 34 and 36 of the system 30 and the surrounding fluids of the body. The completed power source may be viewed as a power source that exploits reverse electrolysis in an ionic or a conductive solution such as gastric fluid, blood, or other bodily fluids and some tissues. Additionally, the environment may be something other than a body and the liquid may be any conducting liquid. For example, the conducting fluid may be salt water or a metallic based paint.
Referring again to
As described above, in various aspects, the event indicator may further include a current path extender such as a membrane which, for example, produces a virtual dipole length between the pair of transmission elements that is larger than the actual dipole length. As illustrated in
As can be seen in the aspect depicted in
Referring now to
Referring now to
The control device 38 can vary the duration of a fixed ionic exchange rate or current flow magnitude while keeping the rate or magnitude near constant, similar to when the frequency is modulated and the amplitude is constant. Also, the control device 38 can vary the level of the ionic exchange rate or the magnitude of the current flow while keeping the duration near constant. Thus, using various combinations of changes in duration and altering the rate or magnitude, the control device 38 encodes information in the current flow or the ionic exchange. For example, the control device 38 may use, but is not limited to any of the following techniques namely, Binary Phase-Shift Keying (PSK), Frequency modulation, Amplitude modulation, on-off keying, and PSK with on-off keying.
As indicated above, the various aspects disclosed herein, such as systems 30 and 440 of
As indicated above, the system, such as system 30 and 440, control the conductance between the dissimilar materials and, hence, the rate of ionic exchange or the current flow. Through altering the conductance in a specific manner the system is capable of encoding information in the ionic exchange and the current signature. The ionic exchange or the current signature is used to uniquely identify the specific system. Additionally, the systems 30 and 440 are capable of producing various different unique exchanges or signatures and, thus, provide additional information. For example, a second current signature based on a second conductance alteration pattern may be used to provide additional information, which information may be related to the physical environment. To further illustrate, a first current signature may be a very low current state that maintains an oscillator on the chip and a second current signature may be a current state at least a factor of ten higher than the current state associated with the first current signature.
Referring now to
The control module 662 is also electrically coupled to and in communication with the sensor modules 672 and 274. In the aspect shown, the sensor module 672 is part of the control device 38 and the sensor module 74 is a separate component. In alternative aspects, either of the sensor modules, 672 and 74, can be used without the other and the scope of the present disclosure is not limited by the structural or functional location of the sensor modules 672 or 74. Additionally, any component of the system 30 may be functionally or structurally moved, combined, or repositioned without limiting the scope of the present disclosure as claimed. Thus, it is possible to have one single structure, for example a processor, which is designed to perform the functions of all of the following modules: the control module 662, the clock 664, the memory 666, and the sensor module 672 or 274. On the other hand, it is also within the scope of the present disclosure to have each of these functional components located in independent structures that are linked electrically and able to communicate.
Referring again to
Referring now to
As indicated above, the control device 38 can be programmed in advance to output a pre-defined current signature. In another aspect, the system can include a receiver system that can receive programming information when the system is activated. In another aspect, not shown, the clock 664 and the memory 666 can be combined into one device.
In addition to the above components, the system 30 may also include one or other electronic components. Electrical components of interest include, but are not limited to: additional logic and/or memory elements, e.g., in the form of an integrated circuit; a power regulation device, e.g., battery, fuel cell or capacitor; a sensor, a stimulator, etc.; a signal transmission element, e.g., in the form of an antenna, electrode, coil, etc.; a passive element, e.g., an inductor, resistor, etc.
As mentioned above, highly-swellable polymeric films may be associated with an ingestible event marker in a number of different, non-mutually exclusive ways. For example, the film may cover a portion of at least one of the first or second dissimilar materials. As such, the film may cover a portion or all of the cathode material. Alternatively or in addition, the film may cover a portion or all of the anode material. In such instances, the film may cover 10% or more, 20% or more, 25% percent or more, 50% or more, including 75% percent or more, e.g., 90% or more, of the cathode and/or anode material, including all of the cathode material or anode material.
An edible adhesive composition, e.g., as described herein, is associated with the highly-swellable polymeric film and the ingestible component in a manner that mediates adherence of the film and the ingestible component to each other. The adhesive may cover a portion of all of one or both of the surfaces of the film and ingestible component that are facing each other when adhered to each other by the adhesive. As such, the adhesive may cover a portion of or the entire surface of the film that faces the ingestible component in the adhered state. Accordingly, the adhesive may 10% or more, 20% or more, 30% or more, 40% or more, 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, including 95% or more of the entire surface of the film that faces the ingestible component in the adhered state. Similarly, the adhesive may cover a portion of or the entire surface of the ingestible component that faces the film in the adhered state. Accordingly, the adhesive may 10% or more, 20% or more, 30% or more, 40% or more, 50% or more, 60% or more, 70% or more, 80% or more, 90% or more, including 95% or more of the entire surface of the ingestible component that faces the film in the adhered state.
Highly-swellable polymeric films such as 740 illustrated in
Another function that the film may serve is to provide for conduction between at least one of the first and second materials and an aqueous medium when the ingestible composition is placed in the aqueous medium. As the films are conductive upon swelling, when compositions containing such films are placed into an aqueous medium and the film swells, the films provide for conduction between the first and/or second materials and the aqueous medium. As such, the films can serve to improve the functionality of the ingestible indicator, by providing for conductive communication between the marker and the aqueous environment into which it is placed during use. In some instances, the films provide for a region of conductivity which is known to provide for a signal that is sufficient for the intended purpose of the event marker. In other words, the films may provide a region of consistent conductivity that is known to provide for adequate functionality of the event marker, despite variations in the local environment. For example, the presence of food particles in the local environment, proximity to the gastric mucosa, or variations in the pH and composition of stomach contents may alter the local aqueous environment in which the event marker may be present. The conductivity of the film in the swollen state may be selected to provide for a consistent local environment over a broad range of differing stomach conditions.
In some instances, improvement of functionality results because the presence of the swollen conductive film impedes the blockage of the first and/or second materials by non-conductive entities that may be present in the environment of the ingestible event marker. Examples of such non-conductive potentially interfering entities that may be present in the environment of the ingestible composition include, but are not limited to: food particles, tissue such as gastrointestinal lining, non-conductive components of the ingestible event marker, and the like. By forming a conductive film over the first and second materials upon swelling, the film serves to prevent contact of non-conductive entities to the materials and thereby improves the function of the composition.
In some instances, event indicators include a highly-swellable film associated with the first and/or second materials and a distinct protective barrier made up of different components and in turn associated with the film, such that the film is between the protective barrier and the first and/or second dissimilar material. Protective barriers which may be employed in such compositions may vary. Examples of such barriers include, but are not limited to, layers that may include one or more of: lipids and functionally analogous materials; pharmaceutically acceptable polymeric materials, etc., e.g., as described in U.S. application Ser. No. 13/304,260, the disclosure of which application is herein incorporated by reference.
An example of such a composition is depicted in
In an event indicator as illustrated in
Other Minimally Dimensioned Components
Aspects of the present disclosure further include compositions that are not necessarily ingestible, wherein such compositions may include a polymeric film adhered to a minimally dimensioned component by an adhesive, e.g., as described herein. Such compositions may include a polymeric film (e.g., as described herein) physically associated with a minimally dimensioned component. While the minimally dimensioned component may vary, e.g., as described above, in some instances the minimally dimensioned component is a micro-battery. Micro-batteries of interest may include “all-solid” batteries, and may include components of a battery, such as current collectors, positive and negative electrodes, an electrolyte, in a minimally dimensioned structure, e.g., as described above. In some instances, micro-batteries of interest are thin films, which may be obtained by deposition, such as by physical vapor deposition (PVD) or chemical vapor deposition (CVD). The micro-battery may take a variety of different configurations, such as but not limited to: a chip configuration, a cylinder configuration, a spherical configuration, a disc configuration, etc., where a particular configuration may be selected based on intended application, method of manufacture, etc. In some instances, the micro-battery is dimensioned to have a width ranging from about 0.05 mm to about 1 mm, such as from about 0.1 mm to about 0.2 mm; a length ranging from about 0.05 mm to about 1 mm, such as from about 0.1 mm to about 0.2 mm and a height ranging from about 0.1 mm to about 1 mm, such as from about 0.05 mm to about 0.3 mm, including from about 0.1 mm to about 0.2 mm. In certain instances, the micro-battery is 1 mm3 or smaller, such as 0.1 mm3 or smaller, including 0.2 mm3 or smaller. In such instances the film may serve to enhance stability of the component, e.g., by improving shelf-life, etc., such as described above.
Manufacturing Methods
Also provided are methods of manufacturing adhesive compositions, including edible adhesive compositions, as well as ingestible compositions that include the same. The adhesive compositions may be prepared or applied as films, which may be free-standing or present on a support. For example, solvent casting fabrication methods may be employed in which a liquid composition of the adhesive components is prepared by combining the components and a suitable solvent(s). Solvents of interest include, but are not limited to: water and aqueous solvents which include one or more solutes (e.g., salts); organic solvents, e.g., alcohols, such as ethanol, propanol, isopropanol, methanol, butanol, etc.; polyols, e.g., propylene glycol, glycerin, butylene glycol, ethoxydiglycol, polyethylene glycol, methyl or ethyl ethers of diglycols, cyclic polyols, ethoxylated or propoxylated glycols; and other organic solvents, e.g., Heptane, Isobutyl acetate, Butyl acetate, Methylethylketone, tert-Butylmethyl ether, Methylisobutyl ketone, Dimethyl sulfoxide, Pentane, Toluene, Trichloroethylene, and Xylene; etc. The liquid composition may be prepared at any convenient temperature, e.g., 15 to 45° C., using any convenient protocol, e.g., stirring, etc. Following preparation of the liquid composition, the liquid composition may be cast on a suitable support, such as a release liner, etc., following which the solvent may be separated from the remainder of the liquid composition to produce the adhesive composition which is ready for use. Solvent separation may be achieved a number of different ways, e.g., via evaporation, which may occur at room temperature or elevated temperatures, such that the temperature may range in some instances from 25 to 100° C., such as 45 to 75° C.
A protocol, in which a pre-fabricated adhesive film, e.g., prepared as described above, may be employed. An example of an IEM which includes an adhesive as described above is depicted in
For ingestible compositions that include a polymeric film, such as a highly-swellable polymeric film, and an ingestible component which are adhered to each other by an edible adhesive, e.g., as described herein, aspects of the methods include combining an ingestible component (which may or may not include a device, such as an IEM) and a highly-swellable polymeric film, e.g., as described above, with an edible adhesive composition in a manner sufficient to produce a desired ingestible composition in which the film is adhered to the ingestible component by the adhesive. Any convenient manufacturing protocol may be employed, where protocols of interest include both manual and automated protocols, as well as protocols that include both manual and automated steps. Protocols of interest that find use in various aspects of the fabrication methods described herein include lamination, molding, pressing, extrusion, stamping, coating (such as spray coating and dipping), gluing, etc. In some instances, fabrication protocols as described in PCT application serial nos. PCT/US2010/020142 published as WO 2010/080765; PCT/US2006/016370 published as WO 2006/116718 and PCT/US2008/077753 published as WO2009/042812 (the disclosures of which applications are herein incorporated by reference); are employed.
Aspects of the fabrication protocols include stably associating the ingestible component with a polymeric film component using an edible adhesive composition, e.g., as described above. By “stably associating” is meant that the ingestible component and polymeric film component do not separate from each other, at least until desired during intended use, e.g., upon administration to a subject in need thereof, such as by ingestion. Any convenient approach for stably associating the ingestible component and the polymeric film component using an adhesive may be employed.
Where an ingestible event marker having one of its dissimilar materials covered by a highly-swellable polymeric film is desired, e.g., as illustrated in
In yet another fabrication protocol of interest, a coating process may be employed. For example, a premade ingestible component in the form of a tablet may be provided, e.g., as described in in PCT application serial nos. PCT/US2010/020142 published as WO 2010/080765; PCT/US2006/016370 published as WO 2006/116718 and PCT/US2008/077753 published as WO2009/042812; the disclosures of which applications are herein incorporated by reference. This premade ingestible component may then be spray coated with a liquid precursor composition of the adhesive (e.g., as described above). Following spray coating, a polymeric film as described herein, such as a highly swellable polymeric film, may be adhered to the ingestible component via the adhesive to produce the desired product.
According to aspects of the present disclosure, a polymeric film may be applied to an ingestible component, such as, for example, an ingestible event marker (IEM) according to an appropriate protocol. The polymeric film may be a multilayer film, for example a bilayer film, which comprises an alginate layer and an adhesive layer that may be applied to an IEM. In one aspect, the polymeric film may be applied via lamination.
The requirements for the manufacture and release according to one aspect of a polymeric film, such as an alginate/adhesive bilayer film, used in the manufacturing of ingestible compositions are described below. The material properties and inspection requirements for a supplier and manufacturing are described. In one aspect, the polymeric film may be made from the materials listed in Table 1 at the specified thicknesses. The formulation of each layer may be made from the percentages of material as listed Table 2 and 3. In one aspect, the polymeric film material is off-white to light brown transparent film.
As shown in
As indicated in Table 1, the first polymer layer 2102 may be a layer of PET with a silicone coating that has a thickness of about 0.002 inches. The second polymer layer 2108 may be a layer of PET that acts as a carrier for the alginate layer 2106 and has a thickness of about 0.003 inches. The adhesive layer 2104 may comprise an adhesive material, such as those described herein and the adhesive layer 2104 may be configured to releasably adhere to the first polymer layer 2102. As shown in Table 3, in one aspect the adhesive layer 2104 comprises hydropropyl-cellulose, povidone, glycerine, and dehydrated ethanol. The hydropropyl-cellulose may have a formulation weight of about 22.1% and a dry weight of about 83.33%, the povidone may have a formulation weight of about 2.2% and a dry weight of about 8.33%, the glycerine may have a formulation weight of about 2.2% and dry weight of about 8.33%, and the dehydrated ethanol may have a formulation weight of about 73.5%. Further, the adhesive layer 2104 may have a thickness of about 0.00079 inches.
As shown in Table 2, in one aspect, the alginate layer 2106 comprises sodium alginate, sorbitol, glycerine, and purified water. The sodium alginate may have a formulation weight of about 3.4% and a dry weight of about 81.3% or a formulation weight of about 0.38% and a dry weight of about 10.6%, the sorbitol may have a formulation weight of about 0.08% and a dry weight of about 2.3%, the glycerine may have a formulation weight of 0.20% and a dry weight of about 5.7%, and the purified water may have a formulation weight of about 95.92%. The alginate layer 2106 may have a thickness of about 0.0012 inches. All thicknesses and measurement mentioned herein may account for variations due to manufacturing tolerances. The two internal layers 2104, 2106 (i.e. the adhesive and alginate) provide a functional material that may be laminated to a final, manufactured ingestible component, such as an IEM as described herein. The ingestible circuit component may include a moisture sensitive material or combination of materials and the alginate layer is configured to provide a moisture vapor barrier to extend a shelf life of the ingestible circuit component.
As shown in
The film 2100 may be manufactured using two independent casting processes to create each of the adhesive layer 2104 and the alginate layer 2106. To make the alginate layer 2106, alginate(s), glycerine, and sorbitol may be premixed in purified water prior to casting. The alginate layer 2106 may be formed by casting the mixture onto the uncoated Polyethylene terephthalate (PET) carrier film 2108. To make the adhesive layer 2104, the Hydropropylcellulose (HPC), glycerine, and povidone will be premixed in ethanol prior to casting. The adhesive layer 2104 may be formed by casting the mixture onto the silicone coated PET release cover. In one embodiment, the alginate layer 2106 may be cast on the carrier film 2108 first, and then held on a roll. This alginate layer 2106 will then be used in the last step of the adhesive process below (i.e. lamination). The adhesive layer 2104 may be cast on the release cover layer 2102 second, and upon exit of a drying oven, the adhesive/release cover film may be laminated to the alginate/carrier film roll to create an alginate bilayer film stack as described in be used as commercial materials. In one aspect, the resulting bilayer film stack may be slit to about 5.6 mm width and wound onto individual spools.
As shown in
When shipping the film material, all packaging may be required to conform to FDA and/or USDA requirements. Spools of film 2100 may be individually bagged and heat sealed, for example in a film-foil pouch. The pouch may be heat sealed in 65% or less relative humidity.
Labeling for the material may contain the following information: batch number, spool number (e.g. where the spools may be numbered in order from left to right, as the operator faces the exit of the oven), part numbers (e.g. supplier numbers, manufacturer numbers, etc.), manufacture date of material blend (e.g. in the format of DD/MM/YYYY), expiration date (e.g. in the format of DD/MM/YYYY), and the length of spool. Material may also be labeled as required above on each spool and on the outside of the individual spool bags. Inspection and testing requirements for the material to determine whether the material meets predetermined criteria may include the following:
Staphylococcus
aureus
Pseudomonas
aeruginosa
Salmonella
Escherichia coli
As shown in
At least one of the first polymer layer or the second polymer layer may comprise Polyethylene terephthalate (PET) and the first polymer layer may be uncoated and the second layer may comprise a coating, such as, for example, silicon. In one aspect, forming the bilayer stack comprises contacting the adhesive to the alginate layer. In another aspect, contacting the adhesive layer to the alginate layer comprises laminating the adhesive layer to the alginate layer. Furthermore, casting the alginate mixture onto the first polymer layer may be performed prior to casting the adhesive mixture onto the second polymer layer.
In another aspect, the method 2300 further comprises cutting the bilayer stack and winding the cut bilayer stack onto a spool or a reel. Cutting the bilayer stack may comprise cutting the bilayer stack to a width of approximately 5.6 mm. Winding the cut bilayer stack onto the spool may comprise winding the cut bilayer stack such that the first polymer layer is an outermost layer on the spool.
As shown in
As shown in
As shown in
Referring back to
Systems
Also provided are systems that include an ingestible device, e.g., an IEM, and a detection component, e.g., in the form of a receiver. Receivers of interest are those configured to detect, e.g., receive, a communication from an ingestible device, such as an IEM as described herein. The signal detection component may vary significantly depending on the nature of the communication that is generated by the ingestible device. As such, the receiver may be configured to receive a variety of different types of signals, including but not limited to: RF signals, magnetic signals, conductive (near field) signals, acoustic signals, etc. In certain aspects, the receiver is configured to receive a signal conductively from an IEM, such that the two components use the body of the patient as a communication medium. As such, communication that is transferred between event indicator and the receiver travels through the body, and requires the body as the conduction medium. The IEM communication may be transmitted through and received from the skin and other body tissues of the subject body in the form of electrical alternating current (AC) voltage signals that are conducted through the body tissues. This communication protocol has the advantage that the receivers may be adaptably arranged at any desired location on the body of the subject, whereby the receivers are automatically connected to the required electrical conductor for achieving the signal transmission, i.e., the signal transmission is carried out through the electrical conductor provided by the skin and other body tissues of the subject.
The receivers of interest include external, semi-implantable, and implantable receivers. In external aspects, the receiver is ex vivo, by which is meant that the receiver is present outside of the body during use. Examples include wearable patches, e.g., adhesive patches, torso bands, wrist(s) or arm bands, jewelry, apparel, mobile devices such as phones, attachments to mobile devices, etc. Where the receiver is implanted, the receiver is in vivo. Examples include cardiac can and leads, under-the-skin implants, etc. Semi-implantable devices include those designed to be partially implanted under the skin.
In certain aspects, the receiver may be configured to provide data associated with a received signal to a location external to said subject. For example, the receiver may be configured to provide data to an external data receiver, e.g., which may be in the form of a monitor (such as a bedside monitor), a computer, a personal digital assistant (PDA), phone, messaging device, smart phone, etc. The receiver may be configured to retransmit data of a received communication to the location external to said subject. Alternatively, the receiver may be configured to be interrogated by an external interrogation device to provide data of a received signal to an external location.
Receivers may be configured variously, e.g., with various signal receiving elements, such as electrodes, various integrated circuit components, one or more power components (such as power receivers or batteries), signal transmission components, housing components, etc.
In one aspect, for example, the receiver includes one or more of: a high power-low power module; an intermediary module; a power supply module configured to activate and deactivate one or more power supplies to a high power processing block; a serial peripheral interface bus connecting master and slave blocks; and a multi-purpose connector, as further described in PCT Application Serial No. PCT/US2009/068128 published as WO2010/075115, infra.
Receivers of interest include, but are not limited to, those receivers disclosed in: PCT Application Serial No. PCT/US2006/016370 published as WO 2006/116718; PCT Application Serial No. PCT/US2008/52845 published as WO 2008/095183; PCT Application Serial No. PCT/US2007/024225 published as WO 2008/063626; PCT Application Serial No. PCT/US2008/085048 published as WO 2009/070773; PCT Application Serial No. PCT/US2009/068128 published as WO2010/075115; and PCT Application Serial No. PCT/US2012/047076 filed on Jul. 21, 2012; the disclosures of which applications (and particularly receiver components thereof) are herein incorporated by reference.
In certain embodiments, the signal receiver includes a set of two or more, such as two or three, electrodes that provide for dual functions of signal receiving and sensing. For example, in addition to receiving signal, the electrodes can also serve additional sensing functions. In certain embodiments, the electrodes are used to generate electrocardiogram data. From that data, there are many kinds of processing that can be done, e.g., to detect various cardiac events, such as tachycardia, fibrillations, heart rate, etc. The obtained electrocardiogram data can be used to titrate medications, or be used for alerts when an important change or significant abnormality in the heart rate or rhythm is detected. This data is also helpful in certain embodiments for monitoring heart rate in patients who do not have pacemakers or as an alternative to patients who might normally require a Holter monitor or a Cardiac Event Monitor, portable devices for continuously monitoring the electrical activity of the heart for twenty-four hours or other devices. An extended recording period is useful for observing occasional cardiac arrthymias that are difficult to identify in shorter time periods.
In some instances, two or more different demodulation protocols may be employed to decode a given received signal. In some instances, both a coherent demodulation protocol and a differential coherent demodulation protocol may be employed.
In addition to demodulation, the trans-body communication module may include a forward error correction module, which module provides additional gain to combat interference from other unwanted signals and noise. Forward error correction functional modules of interest include those described in PCT Application Serial No. PCT/US2007/024225 published as WO 2008/063626; the disclosure of which application is herein incorporated by reference. In some instances, the forward error correction module may employ any convenient protocol, such as Reed-Solomon, Golay, Hamming, BCH, and Turbo protocols to identify and correct (within bounds) decoding errors.
Receivers of the present disclosure may further employ a beacon functionality module. In various aspects, a beacon switching module may employ one or more of the following: a beacon wakeup module, a beacon signal module, a wave/frequency module, a multiple frequency module, and a modulated signal module.
A view of a beacon module is provided in the functional block diagram shown in 11. The scheme outlined in
Multiplexer 1320 is electrically coupled to both high band pass filter 1330 and low band pass filter 1340. The high and low frequency signal chains provide for programmable gain to cover the desired level or range. In this specific aspect, high band pass filter 1330 passes frequencies in the 10 KHz to 34 KHz band while filtering out noise from out-of-band frequencies. This high frequency band may vary, and may include, for example, a range of 3 KHz to 300 KHz. The passing frequencies are then amplified by amplifier 1332 before being converted into a digital signal by converter 1334 for input into high power processor 1380 (shown as a DSP) which is electrically coupled to the high frequency signal chain.
Low band pass filter 1340 is shown passing lower frequencies in the range of 0.5 Hz to 150 Hz while filtering out out-of-band frequencies. The frequency band may vary, and may include, for example, frequencies less than 300 Hz, such as less than 200 Hz, including less than 150 Hz. The passing frequency signals are amplified by amplifier 1342. Also shown is accelerometer 1350 electrically coupled to second multiplexer 1360. Multiplexer 1360 multiplexes the signals from the accelerometer with the amplified signals from amplifier 1342. The multiplexed signals are then converted to digital signals by converter 1364 which is also electrically coupled to low power processor 1370.
In one aspect, a digital accelerometer (such as one manufactured by Analog Devices), may be implemented in place of accelerometer 1350. Various advantages may be achieved by using a digital accelerometer. For example, because the signals the digital accelerometer would produce signals already in digital format, the digital accelerometer could bypass converter 1364 and electrically couple to the low power microcontroller 1370—in which case multiplexer 1360 would no longer be required. Also, the digital signal may be configured to turn itself on when detecting motion, further conserving power. In addition, continuous step counting may be implemented. The digital accelerometer may include a FIFO buffer to help control the flow of data sent to the low power processor 1370. For instance, data may be buffered in the FIFO until full, at which time the processor may be triggered to turn awaken from an idle state and receive the data.
Low power processor 1370 may be, for example, an MSP430 microcontroller from Texas Instruments. Low power processor 1370 of receiver 1300 maintains the idle state, which as stated earlier, requires minimal current draw—e.g., 10 μA or less, or 1 μA or less. High power processor 1380 may be, for example, a VC5509 digital signal process from Texas Instruments. The high power processor 1380 performs the signal processing actions during the active state. These actions, as stated earlier, require larger amounts of current than the idle state—e.g., currents of 30 μA or more, such as 50 μA or more—and may include, for example, actions such as scanning for conductively transmitted signals, processing conductively transmitted signals when received, obtaining and/or processing physiological data, etc.
The receiver may include a hardware accelerator module to process data signals. The hardware accelerator module may be implemented instead of, for example, a DSP. Being a more specialized computation unit, it performs aspects of the signal processing algorithm with fewer transistors (less cost and power) compared to the more general purpose DSP. The blocks of hardware may be used to “accelerate” the performance of important specific function(s). Some architectures for hardware accelerators may be “programmable” via microcode or VLIW assembly. In the course of use, their functions may be accessed by calls to function libraries.
The hardware accelerator (HWA) module comprises an HWA input block to receive an input signal that is to be processed and instructions for processing the input signal; and, an HWA processing block to process the input signal according to the received instructions and to generate a resulting output signal. The resulting output signal may be transmitted as needed by an HWA output block.
An example of a system of the present disclosure is shown in
Systems of the present disclosure may include an external device which is distinct from the receiver (which may be implanted or topically applied in certain aspects), where this external device provides a number of functionalities. Such an apparatus can include the capacity to provide feedback and appropriate clinical regulation to the patient. Such a device can take any of a number of forms. By example, the device can be configured to sit on the bed next to the patient, e.g., a bedside monitor. Other formats include, but are not limited to, PDAs, phones, such as smart phones, computers, etc. The device can read out the information described in more detail in other sections of the subject patent application, both from pharmaceutical ingestion reporting and from physiological sensing devices, such as is produced internally by a pacemaker device or a dedicated implant for detection of the pill. The purpose of the external apparatus is to get the data out of the patient and into an external device. One feature of the external apparatus is its ability to provide pharmacologic and physiologic information in a form that can be transmitted through a transmission medium, such as a telephone line, to a remote location such as a clinician or to a central monitoring agency.
Methods of Use
Aspects of the present disclosure further include methods of using the compositions, such as those described above. Aspects of such methods include administering an ingestible composition to a subject, e.g., by self-administration or via the assistance of another, such as a health care practitioner. Such methods may include placing the ingestible composition in the mouth of a subject such that the subject swallows the ingestible composition. In this manner, the subject ingests the ingestible composition. Ingestible compositions may be employed with a variety of subjects. Subjects of interest include “mammals” including animals classified in the orders carnivore (e.g., dogs and cats), rodentia (e.g., mice, guinea pigs, and rats), and primates (e.g., humans, chimpanzees, and monkeys). In certain aspects, the subjects will be humans.
Following ingestion, the methods may include receiving a signal emitted from an ingestible composition, such as an IEM comprising ingestible composition, e.g., at a receiver, such as described above. In some instances, the received signal is a conductively transmitted signal.
Ingestible compositions may be employed in a variety of different applications. Applications of interest in which the ingestible composition comprises an IEM include, but are not limited to: monitoring patient compliance with prescribed therapeutic regimens; tailoring therapeutic regimens based on patient compliance; monitoring patient compliance in clinical trials; monitoring usage of controlled substances; monitoring the occurrence of a personal event of interest, such as the onset of symptoms, etc., and the like. Applications of interest are further described in PCT Application Serial No. PCT/US2006/016370 published as WO/2006/116718; PCT Application Serial No. PCT/US2007/082563 published as WO/2008/052136; PCT Application Serial No. PCT/US2007/024225 published as WO/2008/063626; PCT Application Serial No. PCT/US2007/022257 published as WO/2008/066617; PCT Application Serial No. PCT/US2008/052845 published as WO/2008/095183; PCT Application Serial No. PCT/US2008/053999 published as WO/2008/101107; PCT Application Serial No. PCT/US2008/056296 published as WO/2008/112577; PCT Application Serial No. PCT/US2008/056299 published as WO/2008/112578; and PCT Application Serial No. PCT/US2008/077753 published as WO2009/042812; the disclosures of which applications is herein incorporated by reference.
Kits
Also provided are kits that include one or more ingestible compositions, such as described above. In those aspects having a plurality of ingestible compositions, the ingestible compositions may be packaged in a single container, e.g., a single tube, bottle, vial, and the like, or one or more dosage amounts may be individually packaged such that certain kits may have more than one container of ingestible compositions. In certain aspects the kits may also include a receiver, such as reviewed above. In certain aspects, the kits may also include an external monitor device, e.g., as described above, which may provide for communication with a remote location, e.g., a doctor's office, a central facility etc., which obtains and processes data obtained about the usage of the composition.
The subject kits may also include instructions for how to practice the subject methods using the components of the kit. The instructions may be recorded on a suitable recording medium or substrate. For example, the instructions may be printed on a substrate, such as paper or plastic, etc. As such, the instructions may be present in the kits as a package insert, in the labeling of the container of the kit or components thereof (i.e., associated with the packaging or sub-packaging) etc. In other aspects, the instructions are present as an electronic storage data file present on a suitable computer readable storage medium, e.g. CD-ROM, diskette, etc. In yet other aspects, the actual instructions are not present in the kit, but means for obtaining the instructions from a remote source, e.g. via the internet, are provided. An example of this aspect is a kit that includes a web address where the instructions can be viewed and/or from which the instructions can be downloaded. As with the instructions, this means for obtaining the instructions is recorded on a suitable substrate.
Some or all components of the subject kits may be packaged in suitable packaging to maintain sterility. In many aspects of the subject kits, the components of the kit are packaged in a kit containment element to make a single, easily handled unit, where the kit containment element, e.g., box or analogous structure, may or may not be an airtight container, e.g., to further preserve the sterility of some or all of the components of the kit.
It is to be understood that this present disclosure is not limited to particular aspects described, as such may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular aspects only, and is not intended to be limiting, since the scope of the present disclosure will be limited only by the appended claims.
Where a range of values is provided, it is understood that each intervening value, to the tenth of the unit of the lower limit unless the context clearly dictates otherwise, between the upper and lower limit of that range and any other stated or intervening value in that stated range, is encompassed within the present disclosure. The upper and lower limits of these smaller ranges may independently be included in the smaller ranges and are also encompassed within the present disclosure, subject to any specifically excluded limit in the stated range. Where the stated range includes one or both of the limits, ranges excluding either or both of those included limits are also included in the present disclosure.
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this present disclosure belongs. Although any methods and materials similar or equivalent to those described herein can also be used in the practice or testing of the present disclosure, representative illustrative methods and materials are now described.
All publications and patents cited in this specification are herein incorporated by reference as if each individual publication or patent were specifically and individually indicated to be incorporated by reference and are incorporated herein by reference to disclose and describe the methods and/or materials in connection with which the publications are cited. The citation of any publication is for its disclosure prior to the filing date and should not be construed as an admission that the present disclosure is not entitled to antedate such publication by virtue of prior present disclosure. Further, the dates of publication provided may be different from the actual publication dates which may need to be independently confirmed.
It is noted that, as used herein and in the appended claims, the singular forms “a”, “an”, and “the” include plural referents unless the context clearly dictates otherwise. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as “solely,” “only” and the like in connection with the recitation of claim elements, or use of a “negative” limitation.
As will be apparent to those of skill in the art upon reading this disclosure, each of the individual aspects described and illustrated herein has discrete components and features which may be readily separated from or combined with the features of any of the other several aspects without departing from the scope or spirit of the present disclosure. Any recited method can be carried out in the order of events recited or in any other order which is logically possible.
Although the foregoing present disclosure has been described in some detail by way of illustration and example for purposes of clarity of understanding, it is readily apparent to those of ordinary skill in the art in light of the teachings of this present disclosure that certain changes and modifications may be made thereto without departing from the spirit or scope of the appended claims.
Accordingly, the preceding merely illustrates the principles of the present disclosure. It will be appreciated that those skilled in the art will be able to devise various arrangements which, although not explicitly described or shown herein, embody the principles of the present disclosure and are included within its spirit and scope. Furthermore, all examples and conditional language recited herein are principally intended to aid the reader in understanding the principles of the present disclosure and the concepts contributed by the inventors to furthering the art, and are to be construed as being without limitation to such specifically recited examples and conditions. Moreover, all statements herein reciting principles, aspects, and aspects of the present disclosure as well as specific examples thereof, are intended to encompass both structural and functional equivalents thereof. Additionally, it is intended that such equivalents include both currently known equivalents and equivalents developed in the future, i.e., any elements developed that perform the same function, regardless of structure. The scope of the present disclosure, therefore, is not intended to be limited to the exemplary aspects shown and described herein. Rather, the scope and spirit of present disclosure is embodied by the appended claims.
This application claims priority to U.S. Provisional Application No. 62/195,228, filed Jul. 21, 2015, entitled ALGINATE ON ADHESIVE BI LAYER LAMINATE FILM, the disclosure of which is incorporated in its entirety by this reference.
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