METHOD AND SYSTEM FOR FORMING A DOSAGE FORM WITHIN A PACKAGING
A method and system of forming a pharmaceutical dosage form within a portion of a blister packaging. The method includes the steps of providing a blister packaging for the dosage form with depressions. A predetermined amount of a drug-containing powder material comprising drug-containing particles is deposited into a substantially uniform powder layer within the depressions. A binding liquid is then deposited in a pattern on the powder layer within the depressions, to bind the particles of the powder layer and form an incremental wetted layer, Excess solvent in the binding material can be removed to form an incremental bound layer. These steps are repeated in sequence at least one or more times to form the pharmaceutical dosage form within the blister packaging.
The present application is a continuation of U.S. application Ser. No. 17/285,186, filed Apr. 14, 2021, which is a National Stage Entry of International Application Number PC/US2019/056323, filed Oct. 15, 2019, which claims the benefit of U.S. Provisional application Ser. No. 62/745,750, filed Oct. 15, 2018, the disclosures of which are hereby incorporated by reference in their entireties.
FIELD OF THE INVENTIONThis invention relates to the field of manufacturing of dosage or tablet forms for pharmaceuticals or other active ingredients.
BACKGROUND OF THE INVENTIONIn recent years, pharmaceutical producers have turned to the use of blister packs for use in both the forming and dispensing of pharmaceutical tablets. These blister packs generally consist of a blister sheet or blister film and a lidding sheet. The blister sheet contains spatial depressions for containing individual dosages, including tablets, capsule, pills, etc.
In a standard process for manufacturing freeze-dried tablets, a single dosage, in liquid form, is introduced into each depression of the blister sheet. The blister sheet, along with the liquid dosages, is then placed into a refrigerated environment where the dosages are subjected to low temperatures to freeze them. The blister sheets are then transferred to a freeze drier, where the ice is removed by sublimation. When freeze drying is completed, the sheets are removed from the drying chamber and covered with an adhesive lidding sheet, which seals the solid dosages into their individual depressions. International Publication WO/1994/012142 is incorporated herein by reference as teaching, inter alia, known processes for manufacturing freeze dried tablets in a blister package.
Notwithstanding, a freeze-drying or lyophilizing method may have significant, negative impacts on product activity, shelf stability, and batch consistency and repeatability. The process inherently is expensive in terms of energy and manpower resources, and quality control and regulatory requirements present additional challenges. In some cases, the freeze-drying or lyophilizing method is simply unsuitable for a particular drug or pharmaceutical.
Rapid prototyping describes various techniques for fabricating a three-dimensional prototype of an object from a computer model of the object. One technique is three-dimensional printing, whereby a printer is used to fabricate the 3-D prototype from a plurality of two-dimensional layers. In particular, a digital representation of a 3-D object is stored in a computer memory. Computer software sections the representation of the object into a plurality of distinct 2-D layers. Alternatively, a stream (sequential series) of instructions for each incremental layer may be entered directly, e.g. a series of images. A 3-D printer then fabricates a thin layer of bound material for each 2D image layer sectioned by the software. Together, the layers are printed one on top of the other and adhere to each other to form the desired prototype.
Powder-liquid three-dimensional printing technology has been used to prepare articles such as pharmaceutical dosage forms, mechanical prototypes and concept models, molds for casting mechanical parts, bone growth promoting implants, electronic circuit boards, scaffolds for tissue engineering, responsive biomedical composites, tissue growth promoting implants, dental restorations, jewelry, fluid filters and other such articles.
Three-dimensional printing can include a solid freeform fabrication technique/rapid-prototyping technique in which thin layers of powder are spread onto a surface and selected region of the powder are bound together by the controlled deposition (“printing”) of a liquid, This basic operation is repeated layer-by-layer, with each new layer formed on top of and adhered to the previously printed layer, to eventually make three-dimensional objects within a bed of unbound powder. When the printed objects have sufficient cohesion, they may be separated from the unbound powder.
Systems and equipment assemblies for three-dimensional printing of articles are commercially available or in use by others, for example Massachusetts Institute of Technology Three-Dimensional Printing Laboratory (Cambridge, Mass.), Z Corporation's (now part of 3D Systems) 3DP and HD3DP™ systems (Burlington, Mass.), The Ex One Company, LLC, (Irwin, Pa.), Soligen (Northridge, Calif.), Specific Surface Corporation (Franklin, Mass.), TDK Corporation (Chiba-ken, Japan), Therics L.L.C. (Akron, Ohio, now a part of Integra Lifesciences), Phoenix Analysis & Design Technologies (Tempe, Ariz.), Stratasys, Inc's Dimension™ system (Eden Prairie, Minn.), Objet Geometries (Billerica, Mass. or Rehovot, Israel), Xpress3D (Minneapolis, Minn.), and 3D Systems' Invision™ system (Valencia, Calif.).
Three-dimensional printing systems employing powder and binding liquid typically form articles by depositing binding liquid onto the individual, sequentially-applied layers of the powder. The binding liquid is applied in patterns to predetermined regions of the powder in each powder layer such that unbound powder material remains on the outer periphery of the patterns. The unbound powder typically surrounds the printed articles that are being formed. The printed articles, which comprise bound powder, are then separated from substantial amounts of unbound powder. Such processes undesirably require wasting or recycling the unbound powder. It would be a substantial improvement in the field to provide an equipment assembly, system and method for substantially reducing or eliminating the need to waste or recycle unbound powder.
US Patent Publication 2018/0141275, the disclosure of which is incorporated herein by reference, describes manufacturing systems, equipment assemblies, and use thereof for the preparation of articles by cavity three-dimensional printing. The cavities may be part of build modules on the machine within which articles are formed that approximate the periphery of the cavity. The articles are formed by a succession of plural incremental layers formed within the cavities. Following completion, a 3DP article is discharged from the cavity, The 3DP article is optionally dried, optionally dedusted, and/or optionally packaged.
A need therefore remains for improved and more convenient pharmaceutical dosage forms, and their method for making.
SUMMARY OF THE INVENTIONThe present invention provides a method and system for the forming of a bound-powder or bound-particulate article within a volume of a depression of a packaging material, and for an article of manufacture that is formed in situ within the depression of its packaging. In some embodiments, the article is a dosage form, which can be a medicament, drug, or pharmaceutical tablet or pill, including solid oral prescription drugs. The methods described herein are also referred to as depression three-dimensional printing, or depression 3DP. The packaging can comprise one or more, and in some embodiments a pattern of a plurality of depressions. The method and system can be used for high through-put continuous, semi-continuous, or batch manufacture with minimal product loss, high efficiency, and high product reproducibility.
The embodiments and features described herein provide a method for the formation of pharmaceutical- and drug-containing tablets directly within their packaging, such as a blister pack, and in a particular embodiment, a method for making rapidly-disintegrating pharmaceutical tablets in disposable single-dose blister packs.
The embodiments described herein can provide a substantial reduction in or elimination of waste or recyclable unbound powder as compared to other three-dimensional printing (3DP) processes. Depression 3DP provides for most, substantially all, or all of the particulate material entering a depression to be incorporated into a corresponding single 3-D printed dosage form.
The embodiments described herein provide a method of forming a dosage form within a portion of a packaging for the dosage form. The method comprises the steps of: 1) providing a portion of a packaging for the dosage form, the portion of the packaging comprising at least one depression; 2) depositing a predetermined amount of a powder material comprising particles into a powder layer within the at least one depression; 3) depositing a binding liquid in a pattern on the powder layer within the at least one depression, to bind at least a portion of the particles of the powder layer to form an incremental bound layer; and 4) repeating steps 2) and 3) in sequence at least one or more times, thereby forming a dosage form within the portion of the packaging for the dosage form.
The embodiments described herein also provide a method of forming a dosage form within a portion of a packaging for the dosage form, comprising the steps of: 1) providing a portion of a packaging for the dosage form, comprising at least one spatial depression, depositing a predetermined amount of a powder material comprising particles into a powder layer within the at least one depression, 3) depositing a binding liquid in a pattern on the powder layer within the at least one depression, to bind at least a portion of the particles of the powder layer to form an incremental wetted layer, and 4) repeating steps 2) and 3) in sequence at least one or more times, thereby forming the dosage form within the portion of the packaging for the dosage form.
In some embodiments, the deposited layer of powder is a substantially uniform powder layer.
In either or both of the above methods, the powder material can be deposited into the at least one depression in a powder depositing region (or system) of an apparatus or system assembly, and the powder material can be layered, or formed into an incremental layer of powder material, in the powder depositing region (or system), or in a dedicated powder leveling region (or system) of an apparatus or system assembly. The binding liquid can be applied to the incremental powder layer when the receptacle is in the binding liquid application region (or system) of an apparatus or system assembly. The shaping or tamping of a powder material or a wetted material layer can be completed in the powder depositing region (or system) or the powder leveling region (or system) of an apparatus or system assembly, or in a dedicated shaping region (or system) of an apparatus or system assembly.
The dosage form packaging comprising the one or more depressions, can be movable between any two or more of the above-mentioned regions (or systems) in any order. In some non-limited embodiments, the receptacle( )moves: a) from the powder depositing region to the binding liquid application region, repeatedly and then optionally to the shaping region; b) from the powder layering region to the shaping region, and then to the binding liquid application region; c) from the powder layering region to the binding liquid application region then back to the powder layering region and then to the shaping region; or d) from the powder layering region to the leveling region, then to the binding liquid application region, then to a drying region. A discharge region can be placed after the powder layering region, the binding liquid application region, the shaping region, and/or the drying region.
The manufactured product package can comprise a film material having one or more depressions therein, the one or more depressions, containing a shaped, bound-powder dosage form, formed within the one or more depressions, and a peelable or removable covering sheet adhered to the film material, so as to enclose the dosage form within the one or more depressions.
In an embodiment, the dosage form is a bound-powder matrix is formed within the one or more depressions by binding a powder deposited within the one or more depressions with a binding liquid.
In an embodiment, a portion of the shaped, bound-powder matrix conforms to an inner surface of the one or more depressions.
An embodiment can also provide a package comprising a film material having one or more depressions therein, the one or more depressions containing a shaped, bound-powder matrix formed within the one or more depressions, and a peel able covering sheet adhered to the film material, so as to enclose the bound-powder matrix within the one or more depressions.
In an embodiment, the bound-powder matrix is formed within the one or more depressions by binding a powder deposited within the one or more depressions with a binding liquid. A portion of the shaped, bound-powder matrix can conform to an inner surface of the one or more depressions. A peripheral portion of the bound-powder matrix that confronts the inner surface of the one or more depressions can include an additional amount of a binding liquid.
In an embodiment, the bound-powder matrix comprises a 3D printed, rapidly-dispersible dosage, and can be formed within the one or more depressions by binding a powder deposited within the one or more depressions with a binding liquid.
In an embodiment, the bound-powder matrix comprises an active pharmaceutical ingredient (API).
In another embodiment, a peripheral portion of the bound-powder matrix that confronts the inner surface of the one or more depressions includes an additional amount of a binding liquid.
In an embodiment, the at least one depression has a fixed shape and volume, which does not change or vary under ordinary use and handling of the packaging.
In an embodiment, the packaging comprises one or more blisters, cups, pods, or other receptacles.
In an embodiment, the packaging is pre-formed and/or pre-cut ahead of the dosage-forming process.
In an embodiment, the packaging comprises a sheet including a plurality of the depressions formed into the sheet, and where the depression includes a sidewall that extends from the sheet to the closed end,
In an embodiment, the step 4) is repeated at least three times.
In an embodiment, a portion of the powder material comprises particles of a binder material, and the binding liquid binds the particles of the binder material.
In an embodiment, the method can include a step, preceding step 2), of depositing a binding liquid on at least the closed end of the depression.
In an embodiment, the at least one depression includes an inner surface that includes a release agent.
In an embodiment, the binding liquid comprises a volatile solvent, and the method can include a step of evaporatively removing a portion of the volatile solvent from the incremental bound layer.
In an embodiment, the sidewall has a depression depth, and each powder layer has a thickness of at least 5%, and up to about 100%, and in some embodiments, up to about 50%, of the depression depth.
In some embodiment, the number of powder layers that are deposited into a depression and formed into an incremental bound-powder layer can be one or a plurality of layers, including two or more layers, three or more layers, four or more layers, five or more layers, six or more layers, seven or more layers, or eight or more layers, and up to fifty or fewer layers, forty or fewer layers, thirty or fewer layers, twenty or fewer layers, eighteen or fewer layers, sixteen or fewer layers, fourteen or fewer layers, twelve or fewer layers, ten or fewer layers, eight or fewer layers, six or fewer layers, or four or fewer layers, in any combination.
An incremental powder layer can have a target or weight average thickness, of a predetermined thickness (vertical height). In sonic embodiments, the predetermined thickness can be varied from 0.005 to 0.015 inches, 0.008 to 0.012 inches, 0.009 to 0.011 inches, about 0.01 inches, 100-300 μm, 100-500 μm, about 200 μm, or about 250 μm. In some embodiments, the thickness of the incremental powder layers range from 100 - 400 microns, 150-300 microns, or 200-250 microns. In one embodiment, the powder layer thickness is 200 microns. In another embodiment, the powder layer thickness is 250 microns.
In some embodiments, the predetermined thickness is at least 0.05 inches, at least 0.008 inches, at least 0.010 inches, at least 0.012 inches, at least 0.014 inches, or at least 0.016 inches, and up to 0.020 inches, up to 0.018 inches, up to 0.016 inches, up to 0.014 inches, up to 0.012 inches, or up to 0.010 inches. As thicker incremental layers are used, an increasing amount of printing fluid is deposited on that layer to ensure adequate binding both within the plane of the layer and layer-to-layer. Conversely, for a thinner incremental layer, a lesser amount of printing fluid is deposited to obtain the same extent of binding. For a given amount of printing liquid deposited per layer, using a larger layer thickness will reduce (worsen) dosage form handleability and reduce (improve) dispersion time. If too thick of a layer is used for a given amount of fluid, laminar defects may form that cause the dosage form to easily fracture along the plane of the layers (delamination), or the dosage form itself may not have adequate strength to handle at all.
Dosage forms produced by a 3DP process described herein can ranged in diameter (of equivalent diameter of a non-circular area) from about 13-14 mm to about 20-25 mm, and in height (total thickness) from about 5-6 mm to about 8-10 mm.
In an embodiment, the pattern of the binding liquid deposited on the powder layer has a periphery that is disposed against or in contact with the sidewall of the packaging.
In an embodiment, the pattern of the binding liquid deposited on the powder layer has a shape selected from the group consisting of an annular ring and a circle.
In an embodiment, the method can include a step of applying a lidding layer over the dosage form and the at least one depression to form a sealed packaging for the dosage form,
In an embodiment, the binding liquid is deposited by inkjet printing to form the wetted or bound powder layer,
In an embodiment, the step 2) of depositing the predetermined amount of the powder material comprising particles into the substantially uniform powder layer within the at least one depression, comprises: 1) depositing a predetermined amount of a powder material comprising particles into the at least one depression, and 2) forming the deposited, predetermined amount of the powder material into a substantially uniform powder layer within the at least one depression.
In an embodiment, the step of forming includes shaping and/or tamping the deposited, predetermined amount of the powder material into the formed powder layer having an upper surface. in another embodiment, the step of forming includes tamping a last deposited, predetermined amount of the powder material into a last formed powder layer having an upper surface.
In an embodiment, the method includes a step, following a step of depositing a binding liquid in a pattern on the powder layer within the at least one depression, comprising a step of shaping and/or tamping the incremental wetted layer into a shaped or tamped wetted layer. The formed wetted layer has an upper surface that in one embodiment is flat or planar, and in another embodiment is convex or concave.
In an embodiment, the method includes a step, following the formation of a plurality of incremental wetted layers into a wetter structure comprising multiple wetted layers, comprising a step of shaping and/or tamping the multiple wetted layer into a shaped or tamped wetted structure.
In an embodiment, the step of shaping and/or tamping employs a stamp or tamper. In some embodiments. the stamp has a lower concave surface,
In an embodiment, the powder material can comprise one or more types of drug-containing particles.
The present invention can also provide a 3DP equipment system and assembly for providing and positioning a depression or a pattern of depressions, for example, associated with dosage form packaging, and for the forming of 3DP dosage forms within the depressions. The equipment system and assembly can comprise, without limitation, a powder depositing system, disposed in a powder depositing region, a powder leveling system, disposed in a powder leveling region, a binding liquid application system, disposed in a binding liquid application region, a shaping system, disposed in shaping region, and a drying system, disposed in drying region.
In some embodiments, the 3DP equipment assembly can comprise a control system comprising one or more computerized controllers, one or more computers, and one or more user interfaces for one or more computers. In some embodiments, one or more components of the equipment assembly are computer controlled. In some embodiments, one or more components of the 3DP build system are computer controlled. In some embodiments, the powder depositing system, the powder leveling system, the binding liquid application system, the shaping system, disposed in shaping region, and the drying system, are computer controlled.
In some embodiments, a 3DP equipment assembly can also comprise one or more harvesting systems, one or more liquid removal systems, one or more powder recovery systems, one or more article transfer systems, one or more inspection systems. The 3DP equipment assembly, apparatus or system can comprise some or all of the above systems. For example, in certain embodiments of a. cavity 3DP equipment assembly, apparatus, or system, it is not necessary to have a harvesting system since substantially all of the powder material entering a depression is incorporated into a respective dosage form formed within the depression, with little or no excess powder for separation.
Definitions:
As used herein, the term “depression” refers to a spatial cavity formed into a portion of a packaging for a dosage form. Non-limiting examples of the depression portion of a packaging include a blister, cup, pod, or other packaging receptacle capable of receiving and containing flowable materials such as powder or liquid.
As used herein, “3DP” means three-dimensional printing, three- dimensionally printed or other such conjugation thereof.
As used herein, the term “tamping” pertains to an act of reducing the porosity or pore volume within a volume of a mass of powder under a force that reduces the volume of the mass of powder. Tamping can be effected with a tamper system, whereby a volume of one or more incremental formed layer of powder formed within a depression is shaped and/or reduced.
As used herein, “shaping” refers to the act of altering the shape of one or more surfaces of an incremental layer of a material, or the shape of a plurality of one or multiple layers. The altering of the shape can be of the entire surface or of only a portion of the surface, and typically the upper surface at the step of shaping.. The altered shape can be flat or planar, convex, concave, or any other shape as desired. The altered shape of the upper surface can be different from the shape of the lower surface.
A process of the invention can comprise one or more tamping steps, one or more shaping steps, and/or one or more marking steps.
As used herein, a “three-dimensional printing build system” or “3DP build system” generally comprises a powder layering system (region), where a powder material is deposited and/or layered into an incremental powder layer within a depression, and a printing system (region), wherein a binding liquid is applied to the incremental powder layer according to a predetermined pattern thereby forming a partially or fully bound powder layer (an incremental printed layer).
In one embodiment, the predetermined amount of powder 40 can be a predetermined volume of a powder material, the powder material having presumably a substantially uniform powder density such that the predetermined volume delivers a substantially fixed mass weight of the powder material. An accurate and reproducible mass weight of a deposited amount of powder material is important to ensure that the finished dosage form, consisting of two or more deposits of the powder material, has a consistent, accurate amount of the total powder material. In an embodiment where the powder material comprises an active ingredient in particulate form, such as a particulate pharmaceutical or drug, and the powder material comprises one or more other particulate materials, it is preferred that the particulate active ingredient does not segregate from the other particulate materials.
In another embodiment, the predetermined amount of powder can be a predetermined mass weight of a powder material. Again, presuming a substantially uniform powder density, the predetermined mass weight delivers a substantially fixed volume of the powder material. In the illustrated embodiment, the predetermined mass weight of a powder material provides a volume of powder material sufficient to form a substantially uniform powder layer of the fixed volume, within the bottom portion of the available space within the depression 4, Depending on the size and shape of the bottom portion of the available space within the depression 4, a first powder layer consisting of a substantially uniform powder layer of a predeterminable depth is formed.
A representative example of a dosing apparatus 24 is shown in
An example of an automated dosing apparatus for filling a plurality of depressions in a dosing package is a rotary dosing apparatus shown in
The bin 271 includes a plurality, illustrated as three, dispensing ports that feed powder material into the fill cavities 277.
The rotary dosing apparatus 224 also includes a shell 274 that has an arcuate inner surface that confronts the outer cylindrical surface 276 between the slide gate 279 and the discharge point 273 of the apparatus 224, covering the filled cavities 277f (fill cavities 277 filled with powder material 20) to prevent spillage of the powder material. The leading edge of the shell 274 provides a means for clearing excess powder dispensed into the fill cavity 277, and leveling off the surface of the powder within the filled cavity 277f.
In some embodiments of a rotary dosing apparatus, a vacuum system can be included that applies a vacuum upon the inside surface of the fill cavities 277 to assist in maintaining the powder material charged into the fill cavities 277.
In some embodiments, each fill cavity is sufficient in size and depth to hold and dispense a layer of powder material 20 into each depression 4 of a blister sheet 2, forming a powder layer 61.
In some embodiments, the volumetric rate of powder material into the fill cavities 377 can be throttled using a slide gate or other well-known means for restricting the flow of powder material from the bin 271. A non-limiting example of a restricting means is the dispensing gate 278.
After each of the filled cavities 277f (or 3771) deposits its powder material into an empty depression 4 of the blister sheet 2, the fill cavities 277 (or 377) of the rotary drum 275 and the blister sheet 2 advance in registry at the same linear speed. Once emptied, the fill cavities advance toward the fill point 272. In some embodiments, the rotation of the rotary drum 275 the advancement of the blister sheet 2 proceed constantly, and in some embodiments the rotation of the rotary drum 275 the advancement of the blister sheet 2 are temporarily halted when the fill cavities arrive at the fill point and/or the discharge point.
In
It should be understood that the registering and filling of depressions, and the movement of the pocket bores between the filled and dispensing positions, occurs simultaneously or contemporaneously in the other depressions and volumetric dispensing pocket 282 laterally along the elongated bin 271.
101571 In
Once the pocket bore 297 is emptied, the blister sheet 2 is advanced to move the next empty depression 4 into registry beneath the dispensing opening 294, as shown in
In some embodiments, a 3DP system and apparatus can include a second or more dosing apparatus for dispensing a second powder material, including a different second powder material, into the depressions, for forming a dosage form that contains two (or more) sources, types and compositions of powder material.
Other non-limiting examples of a mechanical dosing and/or metering apparatus is described in U.S. Pat. Nos. 9,409,699 and 9,828,119, and US Patent Publications 2017/0322068 and 2018/0031410, the disclosures of which are incorporated by reference in their entireties. Piezo-needle dispensing apparatuses dispense a powder actuated by passing the powder material down a stainless-steel tube using a piezoelectric actuator-driven standing wave. At the dispensing tip of the needle, the standing wave serves to eject the powder material. These devices are effective at delivering low and fixed levels of powder material, delivered with precision.
Other non-limiting examples of a mechanical dosing and/or metering apparatus can include a gravimetric powder dispensing /powder dosing apparatus available from ChemSpeed Technologies (https://www.chemspeed.com/flex-powderdose/), the disclosures of which are incorporated by reference in its entirety.
In some embodiments, the method and system include a means for leveling a pile of powder material within a depression.
In some embodiments, a layer of powder material that is prepared within a depression has a flat, planar surface, parallel with the base of the depression. In some embodiments, a layer of powder material that is prepared within a depression can have a uniform thickness with a tolerance. In such embodiments, the thickness of a layer of powder material that is slightly non-uniform in thickness but within the tolerance can be bound with a binding liquid into a bound-powder dosage form. In some embodiments, the non-uniformity in level of the powder material layer can be defined by the variance in thickness of the powder layer from a weight average or target thickness. A minimum thickness in the powder layer and a maximum thickness in the powder layer can have a variance relative to the weight average thickness, where the variance is up to about 25% variance. In some embodiments, the variance is up to about 20% variance, up to about 15%,variance, and in some embodiments, up to about 10% variance, and the variance can be at least 5%, at least 10%, at least 15%, or at least 20% variance. For example, a layer of powder material having a weight average (target) thickness of 0.50 mm can have a thickness with a tolerance of 20%, wherein the powder layer has a minimum and maximum thickness from 0.40 mm to 0.6 mm, while the binding of the powder material with a binding liquid is still effective. In another example, a layer of powder material having a weight average (target) thickness of 1.0 mm can have a thickness with a tolerance of 15%, wherein the powder layer has a minimum and maximum thickness from 0.85 mm to 1.15 mm, while the binding of the powder material with a binding liquid is still effective.
An alternative apparatus for leveling a pile of powder into a substantially uniform layer of powder within a depression is shown in
As shown in
The rotor shaft 82 can also be assembled integrally within a housing or shroud (not shown), that extends around the outer periphery of the circular disk 84, to create a dust barrier during the leveling of the powder material.
As shown in
In alternative embodiments, the powder level member can include a single horizontal member, including using a blade or a bar.
in another embodiment, the powder level member can have a curvature within the plane of rotation.
In another embodiment, the powder level member can have a lower edge that is curved and non-linear, for example, concave or convex, in order to sweep the surface of the pile of powder material into a layer of powder material with the same surface profile.
In some embodiments, the dosing apparatus 24 can comprise an apparatus that both dispenses a predetermined amount of the powder material and forms the powder into a substantially uniform layer of powder within the depression. An example of such an apparatus is shown in
The layer depositing apparatus 90 is shown in
The inlet-facing surface of the porous plate 95 is positioned axially at a distance or depth “h” from the inlet rim 96 to define a cylindrical powder take-up volume 97. In one embodiment, the axial position of the porous plate 95 can be moved toward or away from the inlet rim 96 to pre-determinably vary the cylindrical powder take-up volume 97, to achieve the predetermined amount of powder materials for forming a substantially uniform layer of powder.
As also shown in
The body 92 can be configured with a thin and/or tapered wall at the inlet end 94 to minimize the space that the wall occupies between the deposited amount 42 of powder and the inside of the wall 9 of the depression 4. Notwithstanding, an excessive thickness of the wall at the inlet end 94 can result in the lateral diameter (width) of the deposited powder layer 42 to be smaller than the diameter (width) of the inside walls 9 of the depression, which can cause the peripheral wall of the deposited layer 42 of powder to fall away into the gap therebetween as shown in
In an alternative embodiment, the interior diameter of the powder take-up volume 97 can be matched to the same diameter as the diameter of the inside walls 9 of the depression 4 at the bottom of the space 5. In this embodiment, though not shown, the inlet end 94 of the body 92 is position well above the last bound powder layer 61 within the depression 4. When the application of vacuum to the body 92 is removed, the amount 140 of the powder 20 within the powder take-up volume 97 will fall a short distance by gravity onto the upper surface of the last bound powder layer 61, with the powder area matching the top surface area of the last bound powder layer 61, While this embodiment avoids the gap of the aforementioned embodiment, the free-falling of the powder volume through an airspace can create turbulence that can affect the uniformity of resulting deposited layer of powder.
An alternative embodiment shown in
In a typical embodiment, the binding liquid includes an amount of a solvent that remains in excess in the resulting wetted powder layer 51, and is preferably removed to form a finished bound powder layer.
A liquid removal system is provided and is adapted to receive one or more blister sheets having one or more layers of wetted powder, or completed 3DP dosage forms, contained within depressions, to remove a liquid there from. A liquid removal system can be a process area through which one or more of the blister sheets are conducted. For example, the liquid removal system can remove or reduce liquid from the incremented printed layers of an in-process 3DP form. Alternatively, the liquid removal system can be another process area not directly associated with the three-dimensional printing system, such as a temporary retaining or storage area wherein three-dimensionally printed blister sheets are placed and dried under ambient conditions. In some embodiments, a liquid removal system is one or more dryers.
In some embodiments, a drying apparatus includes a multiplicity of infrared light emitting sources arranged in a pattern, for emitting infrared energy toward an upper surface of a blister sheet 1. The blister sheet 1 including wetted powder material disposed within depressions is passed into a housing and positioned at determined coordinates. In some embodiments, the pattern and coordinates of the upper surface of the wetted powder material is detected and mapped to form a drying profile. The infrared (IR) light sources are illuminated and controlled to emit the IR light exclusively at the upper surfaces of the wetted powder material. The time and intensity of the IR light emitted is maintained to heat and evaporate the upper surfaces and to evaporate moisture and other solvents from the volume for the wetted powder material. In some embodiments, the IR light emitted onto the wetted powder is controlled using a mask that has a pattern of shaped openings to permit passage of the IR energy. In some embodiments, the light emitted through the mask is focused using refractive material, for example, a lens. In some embodiments, IR light source includes a high-resolution IR light emitter, controlled to emit a pattern of IR light.
After each successive wetted powder layer is formed within the depression, any excess solvent from the binding liquid can be removed from the wetted powder layer or layers, as described above.
In some embodiments, some or all of the wetted powder layers can be formed in sequence, and a single drying step can be performed upon the some or all wetted powder layers for solvent removal. In certain embodiments, the removal of excess solvent may be performed continuously or concurrently during materials deposition.
In
In an embodiment of the invention, the inner surface of the packaging sheet 6 forming the depression 4 can include a release agent. The release agent provides a means for the outer wall 11 and the bottom surface 12 of the dosage form 10 (see
In certain embodiments, the release agent may be characterized by low surface energy when compared to the surface tension of the depositing liquid, thereby limiting or mediating the extent of wetting on the inner surface of the depression, and inhibiting migration of the binding liquid along the periphery of the dosage form.
In some embodiments, for depositing a binding liquid having a surface tension in the range of 40 to 50 mN/m, the interior surface of the depression desirably has a surface energy less than 40 mN/m, and more particularly less than 35 mN/m. In some embodiments, for depositing a binding liquid haying a surface tension in the range of 30 to 40mNm, the interior surface of the depression desirably has a surface energy 29 mN/rn or less, and more particularly less than 25 mNm. lf a multilaminate cavity material is used, for example a polyvinyl chloride/polychlorotrifluoroethylene (PVC/PCTrFE) is chosen, the PCTrFE lamina (30.9 mN/m) is desirably placed on the interior surface of the depression, and the PVC lamina. (41.5 mN/m) on the exterior of the depression.
In general, the surface energy of the release agent (or plastic) is desirably lower than the surface tension of the depositing fluid by 1 mN/m to 5 mN/m, or 5 mN/m to 10 mN/m, or 10 mN/m or more. Table 1 shows provides a listing of common polymers and data on their solid surface energy (source: http://surface-tension.de/solid-surface-energy.htm).
If the release agent is a further material applied to the packaging sheet that forms the depression, when employing a water-based binding liquid, the release agent is suitable for consumption and can be selected from the group consisting of an oil, wax, or fatty acid, metallic salt of fatty acid, or fatty acid ester, A suitable release agent can be selected from the materials listed in relevant compendia such as USP/NF, in excipient guides, in listings of materials that are GRAS (Generally Recognized As Safe), or in food additive regulations. Example release agents may include, without limitation, magnesium stearate, stearic acid, glyceryl di palmitostearate, glyceryl distearate, glycerol palmitostearate, glyceryl dibehenate, mono and diglyceride mixture, glycerol monostearate, beeswax, carrnuba. wax, cetyl esters wax, or combinations thereof.
While the forming of a single dosage form 10 within a single depression 4 has been illustrated, the methods and devices described herein can be used to form a plurality of dosage forms within respective depressions of a packaging material, such as a blister sheet as shown in
In another embodiment, as illustrated in
In one embodiment, the droplets 34 are applied using an inkjet printing system 33 in which a multiplicity of printing nozzles 132 are aligned in an array, typically one or more linear rows of nozzles 132. The depression 4 containing the powder layer 41 and the array of nozzles 132 are moved with respect to one another, the depression 4 passing horizontally beneath the array of nozzles 132 while the droplets 34 are deposited in a timed, predetermined pattern so that the droplets 34 of the binding liquid are only applied at the peripheral portions of the powder layer 41. In one embodiment, the array of nozzles 132 are stationary, and the depression or depressions 4 are moved horizontally and below the nozzles 132. In an alternative embodiment, the depression 4 is stationary, and the array of nozzles 132 are passed horizontally over the depression 4. As the depression 4 is passing below the array of nozzles 132, selected ones of the nozzles along the array 33 are activated to express droplets 34 only as the corresponding portions of the powder layer 41 pass below, the resulting expression of droplets 34 forming an annular pattern of liquid binder 151 over the peripheral portions of the powder layer 41.
In another embodiment, not shown, the droplets 34 are applied from a liquid spray nozzle in a fixed and uniform pattern while the depression 4 containing the powder layer 41 is disposed beneath the nozzle. The depression(s) 4 and the nozzle(s) are typically both stationary, although in an alternative embodiment they can both be moving simultaneously and synchronously. In a typical embodiment, the nozzle emits an annular pattern of droplets as a hollow cone.
In another embodiment, the droplets 34 are applied using a liquid streaming nozzle, which is configured to deposit a volume of the second binding liquid without the precise droplet size control of an inkjet nozzle. Typically, the spray velocity of the droplets of such liquid streaming nozzles are significantly slower than that of the inkjet spraying system. A non-limiting example of a liquid streaming nozzle is an ultrasonic deposition nozzle, available as the AccuN;Iist™ System from Sonotek Corporation, Milton N.Y. These spray nozzles result in low velocity droplets, which causes less disturbance to powder materials, with minimal overspray and a wide range of volumetric rates and median droplet size (diameter). The spray patterns are available in a variety of patterns, including both wide and narrow conical patterns, and focused linear streams.
Once dried, the wetted peripheral portion 151 is formed into a stable solidified or resilient peripheral coating portion 161, with a bound powdered layer portion 61 within, as shown in
In an alternative embodiment, the wetted peripheral coating 155 can first be processed to remove excess binder solvent from the wetted peripheral coating 155 and form a solidified or resilient peripheral coating portions 165, prior to wetting the remaining unwetted portion of the fifth uniform powder layer 45 with binding liquid.
As shown in
In another embodiment,
The level or extent of tamping can effect an increase in the areal density of the powder material or wetted powder material. In some embodiments, the density of a powder material can be increased by tamping the powder material, by up to about 33%. In some embodiments, the increase in density effected by tamping of the powder material is up to about 30%, or up to about 25%, or up to about 20%, and can be at least about 5%, or at least about 10%, or at least about 15%, or at least about 20%. The desired or actual increase in density can be varied, or selected, based on the composition of the powder material, and/or the portion of the dosage form which the tampered powder material forms. In some embodiments, tamping can increase the density of a deposited layer of powder material of at least 0.05 grams per cubic centimeter (g/cc), including at least 1.0 g/cc, and up to about 1.5g./cc, including up to about 1.0 g./cc. In some embodiments, tamping can increase the density of a wetted powder material of at least 0.03 grams per cubic centimeter (g/cc), including at least 0.05 g/cc, of at least 1.0 g/cc, and up to about 1.5 g/cc, including up to about 1.0 g/cc.
In some embodiments, the tamper can be lowered into contact with the powder and advanced based on a detected or measured linear force or pressure on the tamper, the extent of linear force or pressure effecting the degree of tamping and/or leveling of the deposited powder layer. In some embodiments, the tamper 88 is rotated, as illustrated in
Though the under surface of the tampers 88 that contacts the in-process 3DP article is depicted as being a concave, circular shape, the under surface of a tamper can be a flat or other non-flat shape, meaning shaped (or contoured) as desired.
In an alternative embodiment, illustrated in
In some embodiments, the tamper and tamper system can be used to form a one or more, such as a series, tamped powder layers, or tamped wetted powder layers, within a depression. The one or more tamped powder layers can be uniformly or non-uniform tamped, resulting in one or more uniformly or non-uniform densified powder layers, or in one or more uniformly or non-uniform densified wetted powder layers.
In some embodiments, a tamper of one type or shape can be used on one or more powder layers or wetted powder layers, and a second tamper of a different type or shape can be used on a different one or more powder layer or wetted powder layer, to provide different aesthetic or performance effects or properties to the resulting dosage form.
In some embodiments, a rotary tamping device can comprise a laterally-extending cylindrical outer surface with a pattern of tampers extending radially outwardly from the cylindrical surface. The positioning of the tampers can be moved axially to adjust the distance that each tamper extends from the outer surface, to allow the tamper to extend different distance down into the depression.
An automated tamping apparatus can be provided for tamping a plurality of dispensed powder layers within depressions. An example is a rotary tamping apparatus shown in
Other tamper faces of various sizes, shapes and contours are contemplated. A tamper face may comprise raised (or potentially recessed) lettering, numbering, or other symbols in order to provide an imprint into an exterior or interior incremental layer of a 3DP article that reflects the contour of the tamper face in reverse (i.e., a raised feature on the tamper face creating a lowered feature on the incremental layer, and vice versa). The tamper face may include specific patterns or textures with a similar goal of creating and imprint into an interior or exterior incremental layer of a 3DP article. In certain embodiments, the pattern or texture of features on the tamper face allows the powder from more than one incremental layer to mingle within the same horizontal slice of a 3DP article. For example, in a case for which there are two sequential incremental layers with different respective powders, instead of each powder substantially remaining within its own respective layer, one or both powders may shift upward or downward into a neighboring incremental layer when displaced by the action of a non-smooth tamper face having raised or recessed features. In certain embodiments, this may include depressions that are created in an instant incremental layer comprised of a first powder that is subsequently filled with a second powder on the next powder spreading step, or this may include raised areas in an instant incremental layer comprised of a first powder and extending into the space allocated for the next incremental layer having a second respective powder, or combinations of both.
In some embodiments, a. tamper system consists of a pattern of tampers, positioned in registry over a corresponding pattern of depressions. In some embodiments, the pattern of tampers moves in a vertical direction, orthogonally to the base of the depressions. In some embodiments, the pattern of tampers moves in unison, as an assembly, though in some embodiments each tamper moves independent of other tampers. In some embodiments, the pattern of tampers is fixed in lateral position, and registration with the pattern of depressions is provided by maneuvering the pattern of depressions (for example, a blister-type packaging sheet having a pattern of depressions 4). In some embodiments, the pattern of depressions is fixed in lateral position, and registration with the pattern of tampers is provided by maneuvering the pattern of tampers. In some embodiments, both the pattern of tampers and the pattern of depressions can be maneuvered independently into registry with the other.
Generally, a 3DP equipment assembly and/or apparatus can comprise various subsystems including one or more three-dimensional printing build systems, and optionally one or more liquid removal systems. The system can comprise one or more three-dimensional printing build systems, one or more liquid removal (drying) systems and optionally one or more other systems. In some embodiments, the equipment assembly can comprise one or more (sub)systems selected from the group consisting of one or more upper tamper systems, one or more control systems, and one or more inspection systems. For example, in certain embodiments of a depression 3DP system, it is not necessary to have a harvesting system since substantially all of the powder material entering a depression is incorporated into a respective dosage form within the depression. Similarly, in certain embodiments of a depression 3DP system, it is not necessary to eject the formed tablets, transport them, and/or feed them into separate packaging, since the tablets are forming in situ in the packaging.
The equipment assembly 501 includes a powder bin 521 and rotary dosing apparatus 531, as described herein, or other embodiment disclosed herein for dispensing powder material into the depressions. The equipment assembly 501 includes a leveling device or apparatus 541, illustrated as vibratory plate, or other embodiment of a powder leveling means, device or apparatus described herein. The equipment assembly 501 includes a printing device or apparatus 551, such as an inkjet printing system as described herein. The equipment assembly 501 includes a drying apparatus 561, illustrate as an irradiative heating apparatus, or other embodiment of a drying apparatus as described herein.
The powder can comprise one or more materials suitable for pharmaceutical or non-pharmaceutical use. In some embodiments, the powder comprises one or more pharmaceutical excipients, one or more pharmaceutically active agents, or a combination thereof. In some embodiments, the three-dimensionally printed article is a pharmaceutical dosage form, medical device, medical implant, or other such article as described. Exemplary types of pharmaceutical excipients that can be included in a three-dimensionally printed article include, by way of example and without limitation, chelating agent, preservative, adsorbent, acidifying agent, alkalizing agent, antifoaming agent, buffering agent, colorant, electrolyte, flavorant, polishing agent, salt, stabilizer, sweetening agent, tonicity modifier, anti-adherent, binder, diluent, disintegrant, glidant, lubricant, opaquant, polishing agent, plasticizer, other pharmaceutical excipient, or a combination thereof.
One or more binders can be included in the bound-powder matrix. The binder can be included in either the powder material or in the binding liquid. The binder is independently selected upon each occurrence. Adhesion of the particles to and/or by the binder occurs either when the binder is contacted by the binding liquid from the printhead or when it is present (i.e., soluble) in the binding liquid. The binder is preferably water soluble, aqueous fluid soluble, partially water soluble or partially aqueous fluid soluble. In some embodiments, the printing fluid comprises 1-20% wt, 5-15% wt or 8-12% wt of binder. In some embodiments, the bulk powder comprises more than 0.1% to 10% wt, 5 to 15% wt, 0 to 15% wt, 8-14% wt or 9-11% wt of binder. In sonic embodiments, the printed matrix comprises 1-20% wt, 5-14% wt or 8-12% wt of binder. In some embodiments, binder is absent from the printing fluid or absent from the bulk material. Suitable binders include water-soluble synthetic polymer, polyvinlypyrrolidone (povidone), sorbitol, mannitiol, xylitol, lactitol, erythritol, pregelatinized starch, modified starch, hydroxypropylmethylcellulose and others. The preferred binder is polyvinylpyrrolidone, e.g. PVP K30, modified starch (e.g,, starch sodium octenylsuccinate), mannitol or a combination thereof. PVP with a K value different from 30 may be used, including without limitation PVP K25 and PVP K90.
In some embodiments, the powder material comprised in each of the one or more powder layers is the same powder material compositionally. In some embodiments, the powder material in one or more powder layers is different from the powder material in another powder layer. In such embodiments, the different compositional powder materials can comprise different active pharmaceutical ingredients (APIs) or API placebos, or no API content.
Pharmaceutically active agents generally include physiologically or pharmacologically active substances that produce a systemic or localized effect or effects in animals, cells, tissue, organs, non-humans and humans.
Whenever mentioned and unless otherwise specified, the term “wive agent” includes all forms of the active agent including neutral, ionic, salt, basic, acidic, natural, synthetic, diastereomeric, isomeric, enantiomerically pure, racemic, hydrate, solvate, chelate derivative, analog, optically active, optically enriched, free base, free acid, regioisomeric, amorphous, anhydrous and/or crystalline forms.
In some embodiments, the powder material composition in a powder layer can be the same. In some embodiments, one region of a powder layer can comprise a powder material that differs compositionally from a powder comprises in another region of the powder layer.
A three-dimensionally printed dosage form can comprise one, two or more different active agents. Particular combinations of active agents can be provided. Some combinations of active agents include: 1) a first drug from a first therapeutic class and a different second drug from the same therapeutic class; 2) a first drug from a first therapeutic class and a different second drug from a different therapeutic class; 3) a first drug having a first type of biological activity and a different second drug having about the same biological activity; 4) a first drug having a first type of biological activity and a different second drug having a different second type of biological activity. Exemplary combinations of active agents are described herein.
The active agent can be independently selected at each occurrence from active agents such as an antibiotic agent, antihistamine agent, decongestant, anti-inflammatory agent, antiparasitic agent, antiviral agent, local anesthetic, antifungal agent, amoebicidal agent, trichomonocidal agent, analgesic agent, anti-arthritic agent, anti-asthmatic agent, anticoagulant agent, anticonvulsant agent, antidepressant agent, antidiabetic agent, antineoplastic agent, anti-psychotic agent, neuroleptic agent, antihypertensive agent, hypnotic agent, sedative agent, anxiolytic energizer agent, anti parkinson agent, muscle relaxant agent, antimalarial agent, hormonal agent, contraceptive agent, sympathomimetic agent, hypoglycemic agent, antilipemic agent, ophthalmic agent, electrolytic agent, diagnostic agent, prokinetic agent, gastric acid secretion inhibitor agent, anti-ulcerant agent, anti-flatulent agent, anti-incontinence agent, cardiovascular agent or a combination thereof. A description of these and other classes of useful drugs and a listing of species within each class can be found in Martindale 37th Edition (2017), The Extra Pharmacopoeia, 31ST Ed. (The Pharmaceutical Press, London 1996), the disclosure of which is incorporated herein by reference in its entirety.
Exemplary types of non-pharmaceutical excipients that can be included in the powder material can include, by way of example and without limitation, ash, clay, ceramic, metal, polymer, biological material, plastic, inorganic material, salt, other such materials or a combination thereof.
In some embodiments, the powder comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more or plural components, each component being independently selected at each occurrence. In some embodiments, the equipment assembly comprises one or more, two or more, three or more, four or more, five or more, six or more, seven or more, eight or more, nine or more, ten or more or plural powder (or solid component) supply reservoirs.
The binding liquid applied to the powder can be a solution or suspension. The liquid can comprise an aqueous carrier, nonaqueous carrier, organic carrier or a combination thereof. The aqueous carrier can be water or an aqueous buffer, or combinations of water with one or more alcohols. The nonaqueous carrier can be an organic solvent, low molecular weight polymer, oil, silicone, other suitable material, alcohol, ethanol, methanol, propanol, isopropanol, polyethylene glycol), glycol, other such materials or a combination thereof. The terms liquid, binding liquid, printing fluid, binding fluid, and liquid may be used interchangeably to refer to a liquid delivered as part of 3DP.
In some embodiments, the equipment assembly comprises one or more, two or more, three or more, four or more or plural liquid reservoirs, The liquid can be colored or non-colored. The liquid can comprise pigment, paint, dye, tint, ink or a combination thereof. The liquid can comprise one or more solutes dissolved therein, The powder and/or liquid can comprise one or more binders. In one embodiment, the binding liquid can also include a binding agent. In some embodiments, the liquid may comprise an active ingredient.
In some embodiments, the binding liquid can be deposited on the upper surface of the powder layer in a pattern or over the entire surface. In some embodiments, the pattern of has a shape selected from the group consisting of an annular ring, a circle, a polygon, or any other desired shape. In some embodiments, the concentration (mass per unit area) of binding liquid applied to the upper surface of the powder layer in the pattern is uniform, while in other embodiments, a concentration of binding liquid applied in one or more portions of the pattern is more or less than a concentration of binding liquid applied in other portions. In some embodiments, wherein the layer of powder has a variance in thickness across the surface area, a higher concentration of binding liquid can be applied on a portion of the powder layer with a positive variance in thickness (thicker than the weight average thickness), and a lower concentration of binding liquid can be applied on a portion of the powder layer with a negative variance in thickness (thinner than the weight average thickness). Any one of the embodiments of this paragraph can be combined with any other embodiment described herein.
Non-limiting examples of powder materials and binding liquids are described in U.S. Pat. Nos. 9,339,489, 9,492,380, and 9,314,429, the disclosure of which is incorporated herein by reference. Any embodiment described herein can employ a binding liquid comprising water (which can include distilled and/or deionized water), an alcohol that can be selected from any lower linear or branched alcohol having from 1 to 3 carbon atoms, a soluble binder agent, an antioxidant, glycerin, and a. surfactant or emulsifier. The printing fluid can comprise 1-25% weight, 5-20% weight, or 10-15% weight of at least one organic solvent, suitably an alcohol. A suitable alcohol can include ethanol, methanol, n-propanol, and isopropanol, or a combination thereof.
In some embodiments, the content of glycerin in the binding liquid ranges from at least about 0.1% by eight, up to about 20% by weight, including at least 0.5%, at least 1.0% and at least 1.5%, and up to about 10%, including up to about 5%, by weight. In some embodiments, the content of glycerin in the dosage form, based upon the final weight of the dosage form, ranges from at least about 0.05% by weight, including at least 0.1%, and at least 0.5%, and up to about 5%, including up to about 3%, up to about 2%, and up to about 1.0%, by weight.
The above is a detailed description of particular embodiments of the invention. It will be appreciated that, although specific embodiments of the invention have been described herein for purposes of illustration, various modifications may be made without departing from the spirit and scope of the invention. Accordingly, the invention is not limited except as by the appended claims, and any amendments to the claims that incorporate any elements or features of embodiments described herein are recognized by persons skilled in the art as being directly and unambiguously derived from the description herein, as of the date of filing. All of the embodiments disclosed and claimed herein can be made and executed without undue experimentation in light of the present disclosure.
Because the instant application is a continuation application, to the extent any amendments, characterizations, or other assertions previously made (in any related patent applications or patents, including any parent, sibling, or child) with respect to any art, prior or otherwise, could be construed as a disclaimer of any subject matter supported by the present disclosure of this application, Applicant hereby rescinds and retracts such disclaimer. Applicant also respectfully submits that any prior art previously considered in any related patent applications or patents, including any parent, sibling, or child, may need to be re-visited.
Claims
1. A method of forming a dosage form within a portion of a packaging for the dosage form, comprising the steps of:
- 1) providing a portion of a packaging for the dosage form, the portion of the packaging comprising at least one depression,
- 2) depositing an amount of a powder material comprising particles into powder layer within the at least one depression,
- 3) depositing a binding liquid in a pattern on the powder layer within the at least one depression, to hind at least a portion of the particles of the powder layer to form an incremental wetted layer, and
- 4) optionally repeating steps 2) and 3) in sequence one or more times, thereby forming the dosage form within the portion of the packaging for the dosage form.
2. The method according to claim 1, wherein the at least one depression has a. fixed shape and volume.
3. The method according to claim 1, wherein the packaging comprises a sheet including a plurality of the depressions formed into the sheet, and where the depression includes a sidewall that extends from the sheet to a closed end.
4. (canceled)
5. The method according to claim 1, wherein the powder material comprises particles of a binder material, and the binding liquid binds the particles of the binder material.
6. The method according to claim 1, further including a step, preceding step 2), of depositing an amount of a binding liquid on at least the closed end of the depression.
7. The method according to claim 1, wherein the at least one depression includes an inner surface that includes a release agent.
8. The method according to claim 1, wherein the binding liquid comprises a volatile solvent.
9.-11. (canceled)
12. The method according to claim 1, wherein the pattern of the deposited binding liquid includes a peripheral pattern of binding liquid, applied to the powder layer at the inner surface of the depression.
13. The method according to claim 1, further including a step of applying a lidding layer over the dosage form and the at least one depression to form a sealed packaging for the dosage form.
14. The method according to claim 1. wherein the binding liquid is deposited by inkjet printing to form the dosage form.
15. The method according to claim 1, wherein the step 2) of depositing the predetermined amount of the powder material comprising particles into the substantially uniform powder layer within the at least one depression, comprises:
- 1) depositing a predetermined amount of a powder material comprising particles into the at least one depression, and
- 2) forming the deposited, predetermined amount of the powder material into a substantially uniform powder layer within the at least one depression.
16. The method according to claim 1, wherein the step of forming includes tamping a last deposited, predetermined amount of the powder material into a last formed powder layer having an upper surface.
17. (canceled)
18. A method of forming a dosage form within a portion of a packaging for the dosage form, comprising the steps of:
- 1) providing a portion of a packaging for the dosage form, comprising at least one spatial depression;)
- 2) depositing a predetermined amount of a powder material comprising particles into a substantially uniform powder layer within the at least one depression,
- 3) depositing a binding liquid in a pattern on the powder layer within the at least one depression, to bind at least a portion of the particles of the powder layer to form an incremental wetted layer, and
- 4) repeating steps 2) and 3) in sequence at least one or more times, thereby forming the dosage form within the portion of the packaging for the dosage form.
19. A package comprising a film material having one or more depressions therein, the one or more depressions containing a shaped, bound-powder article, formed within the one or more depressions, and a peelable or removable covering sheet adhered to the film material, so as to enclose the bound-powder article within the one or more depressions.
20. The package according to claim 19, wherein the bound-powder article is formed within the one or more depressions by binding a powder deposited within the one or more depressions with a binding liquid.
21. The package according to claim 19, wherein a portion of the shaped, bound-powder article conforms to an inner surface of the one or more depressions.
22. (canceled)
23. The package according to claim 19, wherein the bound- powder article comprises a 3D printed, rapidly-dispersible dosage form.
24. The package according to claim 19, wherein the bound- powder article is formed within the one or more depressions by binding a powder deposited within the one or more depressions with a binding liquid.
25. The package according to claim 19, wherein the bound-powder article is formed within the one or more depressions by binding a powder deposited within the one or more depressions with a binding liquid.
26. The package according to claim 19, wherein the bound-powder article contains an API.
Type: Application
Filed: Mar 2, 2022
Publication Date: Jun 16, 2022
Inventors: Lauren E. Beach-Herrera (East Brunswick, NJ), Matthew F. Boldt (Santa Fe, NM), Thomas J. Bradbury (Yardley, PA), Henry Cabral (Hillsborough, NJ), Kelly E. Caputo (Langhorne, PA), William R. Gross (Lambertville, NJ), Munhee Lee (Princeton, NJ), Mahendra R. Patel (Delray Beach, FL), Aleece M. Phillips (Yardley, PA), Timothy S. Tracy (Huntsville, AL), Thomas G. West (Lawrenceville, NJ), Jaedeok Yoo (Princeton, NJ)
Application Number: 17/685,185
