The present invention relates to additive manufacturing processes for making implants, and more particularly to additive manufacturing processes that utilize projections of laser energy to create sequential layers of an implant.
Additive manufacturing by selective laser sintering or melting denotes a process whereby sequential fusion of powder layers is used to create a three-dimensional (3D) object. To begin, a thin powder layer is dispensed on a working table (frequently referred to as the “build platform”), so that at least one layer of powder forms a powder bed. Selected areas of the powder layer are then fused by exposure to a directed energy source, typically a laser beam. The exposure pattern of the laser beam thus forms a cross-section of the three-dimensional object. The part is built through consecutive fusion of so-formed cross-sections that are stacked in layer-by-layer fashion along a vertical direction, and between the fusion of each layer the build platform is incremented downward and a new layer of powder is deposited onto the build surface. The general process of laser powder-fusion additive manufacturing has become known by several terms including selective laser melting (SLM), selective laser sintering (SLS), and direct metal laser sintering (DMLS), which terms are encompassed by the term laser powder bed fusion (L-PBF). These processes have been applied to various metals, ceramics, polymers, alloys, and composites.
According to an embodiment of the present disclosure, a method of making an implantable device includes directing a projection of laser energy on a build surface atop a bed of powder, thereby forming a layer of the implantable device. The projection of laser energy comprises adjacent energy pixels that share common boundaries on the build surface. Each pixel has a respective power density that is substantially uniform on the build surface. The directing step is repeated a plurality of times, in a layer-by-layer manner, such that a totality of the formed layers define at least a portion of the implantable device.
According to another embodiment of the present disclosure, an implant has a body that defines dimensions along first, second, and third directions that are substantially perpendicular to each other. The body defines at least one edge having a stepped profile that includes segments that are observable in a reference plane at 50× magnification. The at least one edge is curved and/or oriented oblique with respect to at least one of the first, second, and third directions.
The foregoing summary, as well as the following detailed description of illustrative embodiments of the present application, will be better understood when read in conjunction with the appended drawings. For the purposes of illustrating the features of the present application, there is shown in the drawings illustrative embodiments. It should be understood, however, that the application is not limited to the precise arrangements and instrumentalities shown. In the drawings:
The present disclosure can be understood more readily by reference to the following detailed description taken in connection with the accompanying figures and examples, which form a part of this disclosure. It is to be understood that this disclosure is not limited to the specific devices, methods, applications, conditions or parameters described and/or shown herein, and that the terminology used herein is for the purpose of describing particular embodiments by way of example only and is not intended to be limiting of the scope of the present disclosure. Also, as used in the specification including the appended claims, the singular forms “a,” “an,” and “the” include the plural, and reference to a particular numerical value includes at least that particular value, unless the context clearly dictates otherwise.
The term “plurality”, as used herein, means more than one. When a range of values is expressed, another embodiment includes from the one particular value and/or to the other particular value. Similarly, when values are expressed as approximations, by use of the antecedent “about,” it will be understood that the particular value forms another embodiment. All ranges are inclusive and combinable.
The terms “approximately”, “about”, and “substantially”, as used herein with respect to dimensions, angles, ratios, and other geometries, takes into account manufacturing tolerances. Further, the terms “approximately”, “about”, and “substantially” can include 10% greater than or less than the stated dimension, ratio, or angle. Further, the terms “approximately”, “about”, and “substantially” can equally apply to the specific value stated.
It should be understood that, although the terms first, second, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are instead used to distinguish one element from another. For example, a first element could be termed a second element, and, similarly, a second element could be termed a first element without departing from the scope of the embodiments disclosed herein.
The embodiments disclosed herein pertain to techniques for additive manufacturing of implantable devices (also referred to herein as “implants”), particularly techniques using at least one projection of laser energy on a build surface atop a powder bed to melt, sinter, or otherwise transform select regions of the powder into one or more solid, monolithic, implantable constructs. These techniques, encompassed herein by the term “laser powder bed fusion” (L-PBF), can provide for the rapid manufacture of implants, including those with complex geometries, with less material waste than reductive manufacturing processes. These techniques can also provide fine control of material properties of a manufactured implant.
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The control mechanism of the laser source 1 can employ one or more various control devices to adjust or otherwise modulate the intensity profile of the linear projection 22. By way of non-limiting examples, such control devices can include light valves, such as a grating light valve (GLV) to modulate the intensity along the line or a planar light valve (PLV) to modulate the intensity both along and across the line. Other means of spatial light modulation can be employed, such as intersecting the laser with a medium having locally tunable optical transmission, so only a portion of the laser energy, in a desired spatial pattern, is transmitted through the medium and incident upon the build surface.
Examples of projections of laser energy for fusing powder bed particles will now be described with reference to
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The power density across any single pixel can be substantially uniform such that the pixel has a square shaped or “top hat” shaped energy profile when that pixel is turned on. The laser energy pixels 31-38 can have their respective power levels individually controlled and can each be turned on or turned off (i.e., iterated between an ON state and an OFF state) independently. In other embodiments, the power density across any single pixel can optionally vary according to various other energy profiles when that pixel is turned on. It should be appreciated that various means and instrumentalities for providing the laser energy pixels 31-38 and modulating their intensities can be provided, such as those more fully described in the '094 Reference, by way of a non-limiting example.
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It should be appreciated that yet other means for directing, and/or modulating the intensity of, a linear projection of laser energy onto a build surface are within the scope of the present disclosure.
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Example methods of making an implantable device (also referred to herein as an “implant”) will now be described. It should be appreciated that the following example methods are provided as non-limiting example methods. Accordingly, other methods not specifically set forth below can be within the scope of the present disclosure.
A method of making an implant, according to one example, includes a step of directing a liner projection of laser energy and/or an areal projection of laser energy to a build surface atop a bed of powder, thereby fusing particles of the powder together in a manner forming a layer of an implant. The linear and/or areal projection can optionally be an array of energy pixels that are configured such that adjacent energy pixels therein share common boundaries on the build surface, and each pixel has a respective power density that is substantially uniform on the build surface. This example method includes steps of repeating the directing step a plurality of times, in a layer-by-layer manner, such that a totality of the formed layers define at least a portion of the implant. The repeating steps can be performed until, upon conclusion of a final one of the repeating steps, an entirety of the implant is formed.
Each repeating step includes lowering the powder bed 4 and spreading a new build layer of powder over the previously formed layer, such as with the spreader mechanism 8. At the conclusion of the repeating steps, unfused powder particles can be removed, such as via one or more vacuum nozzles.
As described above, the implant formed at the conclusion of the repeating steps has edges that define irregular/stepped profiles that are observable in a horizontal reference plane and/or a vertical reference plane when viewed under 50× magnification of greater. The magnification can be performed using light optical microscopy, by way of a non-limiting example.
The implant formed according to these example methods and steps can be an orthopedic implant, such as an intervertebral implant (e.g., an expandable spinal fusion cage), a vertebral body replacement (VBR) implant, or a bone plate fixation device (e.g., a cervical spinal implant), by way of non-limiting examples. It should be appreciated that numerous other types of orthopedic implants can be manufactured according to the additive manufacturing processes described herein, including, but not limited to, bone plates (e.g., rigid plates and articulable, interconnected link-type plates), bone anchors (e.g., bone screws), anchor heads, spinal rods, guide wires (e.g., K-wires), rigid suture anchors, suture hubs, reconstructed joints, platforms, intramedullary nails, synthetic bone graft, and the like. It should further be appreciated that the additive manufacturing processes described herein can be employed to manufacture instrumentation for assistance during an implantation procedure, such as insertion instruments, retractors, guide channels, trial spacers, tissue-cutting members, and bone graft delivery devices, by way of non-limiting examples. The implants herein can be configured for use in bone tissues (including cortical and/or cancellous tissue) and soft tissues (e.g., muscle, tendon, ligament, organs). Virtually any type of rigid implant or implant having rigid components can be manufactured according to the additive manufacturing processes described herein.
Based on, for example, implant type, one or more of the build layers can include separate components of the implant, which components can be interconnected within the build layer and/or across multiple layers. When separate components are interconnected within a build layer, the respective repeating step can be characterized as effectively interconnecting the components, or at least a layer-wise portion thereof, as described in more detail below.
It should be appreciated that the methods described herein allow in-layer interconnection of components that have macrostructure (e.g., dimensions from 1 mm to 200 mm or greater), microstructure (e.g., dimensions from 1 micrometer (μm) to 1000 micrometers (μm)), and nanostructure (e.g., dimensions under 100 μm). For example, in some embodiments, the interconnected components have spatial resolution and accuracy at scales less than about 10 μm. In further embodiments, nanostructures can be added to the powder bed, such as within one or more respective build layers. In such embodiments, the build layer can contain a powder base material and a second material comprising or consisting of nanostructures, such as carbon nanotube (CNT's) or nanoparticles, with at least one dimension in the range of 1-100 nm. It should be appreciated that such nanostructures need not differ in material composition from the base material of the powder, though the nanoparticles can have a suppressed melting/sintering temperature due to their size.
In some embodiments of the example structures and methods, an in-layer construct or a multi-layer construct can include a first interconnected component of the construct defines a guide surface that is sufficiently smooth to provide a sliding contact interface with a complimentary movement surface, such as a sliding surface, defined by at least a second interconnected component of the construct. The sliding contact interface can facilitate an actuation process of the implant during an implantation procedure, such as an expansion process of an expandable fusion cage, by way of a non-limiting example. In this manner, such complimentary guide/movement surfaces can be defined on various movable components of the implant, such as actuators, expansion members, securing and/or retention members (e.g., deployable spikes and/or barbs for engaging adjacent tissue, such as vertebrae), and/or locking members, by way of non-limiting examples. In some such embodiments, such as those involving an expandable fusion cage, the interconnected movable components can include expansion wedges having portions configured to slide along guide grooves or channels defined in one or both of the endplates. In further such embodiments, the interconnected movable components can include mating threads, such as external threads on an actuator configured to intermesh with internal threads within respective bores of the expansion wedges, by way of non-limiting examples. In yet additional such embodiments, the interconnected movable components can include locking members, such as locking pins that are deployable to affix a position of an actuator and/or an expansion member (e.g., expansion wedge), thereby affixing an expanded height of a fusion cage, by way of non-limiting examples. It should be appreciated that, in some embodiments of the structures and methods herein, the interconnected movable components can be functional or at least pseudo-functional at the conclusion of the build and removal of unfused powder, including without need of supplemental surface finishing processes.
Additionally or alternatively, portions of an in-layer construct or multi-layer constructs can define interior spaces such as voids and/or conduits through the implant or portions thereof. Such spaces, voids, and/or conduits can be configured for delivering, transmitting, receiving, and/or retaining bio-materials, such as bone graft, bone ingrowth inducing material, and the like, by way of non-limiting examples. Additionally or alternatively, such spaces, voids, and/or conduits can be configured for selective reception of movable components of the implant, such as those described above.
Additionally or alternatively, such spaces, voids, and/or conduits can be configured to receive electronic circuitry, such as printed circuit boards (PCBs), processors, microprocessors, computer memory, communication devices, sensors, and the like, by way of non-limiting examples. Such electronic circuitry can include “smart” electronic components, such as types configured to autonomously or semi-autonomously execute one or more algorithms, such as software or other computer programs. Such smart electronics can include one or more of an accelerometer, a strain gauge, a proximity sensor, a PH sensor, a thermal sensor, and a thermal conductor, by way of non-limiting examples. In such embodiments, the methods herein can include disposing preconstructed electronics within receptacles defined within a build-layer or across multiple build layers. Additionally or alternatively, the methods herein can include steps of making electrical components in a build-layer or in multiple build-layers. For example, such steps can include depositing, such as via printing, such as 3D printing, electronic circuitry on a build layer. The circuitry can be 3D printed by one or more deposition 3D print heads 18, such as that described above with reference to
The powder bed 4 can have various material compositions depending on the desired composition of the implant. The powder materials can include metals, ceramics, polymers, alloys, and composites. The materials can include medical-grade or otherwise biocompatible materials, and can optionally include non-biocompatible materials, such as in embodiments where such latter materials are encased or otherwise sealed within a biocompatible material in the built implant. By way of non-limiting examples, the metals can include stainless steels, construction steels, light metals and alloys (titanium, aluminum and aluminum-lithium alloys), additional alloys (titanium-aluminum-vanadium allows (e.g., TAV, such as Ti64Al4V, also referred to as Ti64), titanium-molybdenum alloys (e.g., TiMo), cobalt-chromium alloys (e.g., CoCr)), superalloys (e.g. nickel base alloys such as Inconel and Hastelloy), hard and refractory metals (e.g. tungsten and molybdenum), precious metals (e.g. gold), heat and electrically conductive metals (e.g., copper and silver). Ceramics may herein refer to, but are not limited to inorganic, non-metallic solids comprised of metallic, metalloid or non-metallic atoms. Examples are carbides, nitrides and borides (e.g. tungsten and titanium carbide, silicon nitride and carbide and boron nitride) as well as oxides such as aluminum oxide, zinc oxide and zirconia. Polymer may herein refer to, but are not limited to photopolymers, thermoplastics and thermosetting polymers.
In case of the material being applied to the build surface as powder, such powder particles can be of various sizes, size (and average size) distributions as well as different geometrical shapes. Powder size (and average size) distributions may range from 1-1000 nm, 1-100 μm, and/or 10 μm to 1 mm. The powder particle sizes can be selected based on sizes and material compositions conducive for favorable fusing and fused grain structure of the built implant.
Various build layers can contain multiple materials and powders, such as a combination of at least one metallic powder and at least one ceramic powder. In such embodiments, the laser energy (e.g., the linear and/or areal projections 22, 23, such as those comprising arrays of energy pixels) can be applied to a build layer to form at least one metallic component of the implantable device and concurrently form at least one ceramic component of the implantable device. For example, such use of metallic powders and ceramic powders can be employed with the laser energy in layer-by-layer fashion to produce an implant that includes at least one metallic component and at least one ceramic component or feature. For example, the built implant can include at least one metallic component that has a ceramic coating that coats at least a portion of the at least one metallic component. In such embodiments, the ceramic coating can be resorbable, such as a ceramic coating comprising hydroxyapatite (HA).
At least one of the in-layer constructs can have a fused microstructure that is substantially devoid of surface defects. In further embodiments, the build implant can include one or more microstructures each substantially devoid of surface defects or defects adjacent the surfaces. Moreover, such microstructures can have alpha martensitic grain structures at the conclusion of the build (e.g., before any post-build heat treatment), such as those of stainless steel, TAV, cobalt-chromium, and TiMo, by way of non-limiting examples. The methods herein can further include performing one or more surface finishing steps on one or more of the implant surfaces, such as to provide a surface finish roughness configured to promote osteogenesis.
The methods herein can further include performing one or more heat treating processes, such as vacuum thermal processes. Such thermal processes can facilitate and/or enhance dynamic properties of the built implant, such as its fatigue performance over the life of the implant. For example, post-build heat treatment processes can facilitate alpha martensitic grain structures in the implant or can enhance existing alpha martensitic grain structures of the implant. Vacuum thermal processes can be a preferred post-build thermal process because it can enhance dynamic properties without the need for hot isostatic pressing. It should be appreciated, however, that various other heat treating processes can be employed as needed, including hot isostatic pressing. The methods herein can yet also include optional post-build finishing processes, such as applying one or more various coatings or supplemental exterior layers to the implant.
Various aspects of the foregoing steps can be adapted as needed so that the built implant or at least a respective portion thereof has a targeted modulus of elasticity. In one such non-limiting example, select aspects of the foregoing steps can be adapted such that a first discrete region of a portion of the built implant has a first modulus of elasticity, and a second discrete region of the portion of the built implant has a second modulus of elasticity that differs from the first discrete region.
According to embodiments of the methods described above, after conclusion of the repeated steps (i.e., at the conclusion of the “build”), the implant (i.e., the “built implant”) or select portions thereof can have a printed infill density in a range of about 35 percent to 100 percent, which can vary as-desired at different regions of the implant. The solid portions of the built implant can also have a volume density in a range of about 99.5 percent to about 100 percent, and more particularly about 99.8 percent. The build implant can have a hardness in a range from about 32 HRC to about 40 HRC, as measured according to the Hardness Rockwell C (HRC) scale. It should be appreciated that the implant's printed density and/or hardness can be adapted, such as by adjusting the material composition, powder size, and infill volume, by way of non-limiting examples.
According to one such non-limiting example, the implant can be constructed by exposing a TAV powder (specifically, Ti64Al4V) to a linear and/or areal projection of laser energy in a layer-by-layer 3D-printing process utilizing a 100 percent infill volume. In one study of such 3D-printed TAV constructs, the inventors tested various 3D-printed samples of solid bodies having different shapes, each of these solid constructs printed from Ti64Al4V constituent powder. For comparison, the inventors also tested additional samples of similar shaped objects that were 3D-printed from the same constituent powder type (Ti64Al4V) but having a reduced infill volume (i.e., having open spaces therein). The 3D-printed and tested samples can be characterized as representing various components of an implant. The printed samples were imaged with a Keyence Light Optical System (Model VHX-5000) and a Zeiss EV060 XVP scanning electron microscope (SEM) for inspection of, among other things, sample porosity and microstructure. Various images of one of the samples are shown in
The inventors made several surprising observations during these tests. For example, by analyzing cross-sections of the samples it was observed that the microstructures of the solid portions of the samples possessed a volume density (i.e., inverse of porosity) of about 99.8 percent. It was also observed that the last printed layers in all of the above-referenced samples exhibited non-melted spheres around the outer surfaces. No microcracks, burrs or any deformed material was observed in any of the samples. The samples each demonstrated a hardness in a range from 35-38 HRC and a 0% area porosity within the confines of the measurement systems. One advantage of the additive manufacturing processes described herein, as demonstrated by these test results, is that because the as-built porosity of the solid portions of the implant/components is near 0% porosity, the need for post-build processing to resolve defects can be avoided or at least reduced.
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It should be appreciated that the methods and instrumentalities described above can advantageously be employed for rapid implant manufacture. It should also be appreciated that the rapidity of the manufacturing processes described herein can allow for rapid, on-demand production of an implant having a patient-specific geometry (i.e., an implant geometry tailored to correspond to the patient-specific anatomy in which the implant is configured to reside), which geometry can be based on part on scan data of patient anatomy. For example, in the case of a VBR implant, the implant geometry can be created in 3D virtual space with the assistance of patient scan data of the vertebral body to be replaced (such as a 3D model constructed with the assistance of a series of CT-scan slices of the vertebral body), which 3D virtual implant geometry can be tailored as needed to provide a treatment objective. In the case of an expandable spinal fusion cage, the implant geometry can be created in 3D virtual space with the assistance of scan data of the adjacent vertebral bodies. In particular, the opposed outer surfaces of the endplates can be tailored in 3D virtual space to have contours that correspond to those of the respective superior and inferior surface of the adjacent vertebral bodies. The cage geometry can be further tailored, for example, based on the desired post-operative intervertebral height. The rapid additive manufacturing methods described herein can be employed to create an implant possessing the tailored 3D virtual geometry based on patient-specific data.
It should be appreciated that the various parameters, properties, and characteristics of the materials, energy, and processes described above are provided as exemplary features for adapting the manufacturing processes and instrumentalities to 3D print or otherwise additively manufacture implants. These parameters can be adjusted as needed without departing from the scope of the present disclosure.
It should further be appreciated when a numerical preposition (e.g., “first”, “second”, “third”) is used herein with reference to an element, component, dimension, step, or a feature thereof (e.g., “first” portion, “second” portion, “first” step, “second” step), such numerical preposition is used to distinguish said element, component, dimension, step, and/or feature from another such element, component, dimension, step, and/or feature, and is not to be limited to the specific numerical preposition used in that instance. For example, a “first” portion, component, or step can also be referred to as a “second” portion, component, or step in a different context without departing from the scope of the present disclosure, so long as said portions, components, and/or steps remain properly distinguished in the context in which their numerical prepositions are used.
Although the disclosure has been described in detail, it should be understood that various changes, substitutions, and alterations can be made herein without departing from the spirit and scope of the invention as defined by the appended claims. Moreover, the scope of the present disclosure is not intended to be limited to the particular embodiments described in the specification. In particular, one or more of the features from the foregoing embodiments can be employed in other embodiments herein. As one of ordinary skill in the art will readily appreciate from that processes, machines, manufacture, composition of matter, means, methods, or steps, presently existing or later to be developed that perform substantially the same function or achieve substantially the same result as the corresponding embodiments described herein may be utilized according to the present disclosure.
The present application claims the benefit of U.S. Provisional Application No. 63/226,212, filed Jul. 28, 2021, the entire contents of which are incorporated herein by this reference.
Number | Date | Country | |
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63226212 | Jul 2021 | US |