This disclosure generally relates to medical implants with improved roughness, including titanium and titanium alloy implants with such improved roughness.
Degenerative change and injury of bone and joints and partially and fully edentulous jaw are on a rapid increase in an aging society. Implants formed of titanium or titanium alloys are used to repair, immobilize, stabilize, restore, and reconstruct these unhealthy, diseased, and defective areas. Titanium implants include screws, pins, plates, cages, and braces for spine and other areas of bone, artificial joints and stems for knee and hip areas, and dental implants in jaw and maxillofacial areas. Implant treatment faces many challenges of protracted healing time to integrate implants with bone, failure and revision surgery of implants, surgical complications, contraindications in patients with poor quality and quantity of bone and with adverse systemic conditions, post-surgery morbidity like inflammation and infection, insufficient mechanical tolerance and anchorage of implants, and so forth. Many, if not all, of these challenges and problems are closely associated with the insufficient capability of a titanium implant to allow growth of bone around the implant or adhere to the surrounding bone, namely the insufficient capability of bone-implant integration.
It is against this background that a need arose to develop the embodiments described herein.
In some embodiments, a medical implant has a hierarchical surface roughness and includes an implant body, which includes a combination of meso-scale surface features, micro-scale surface features, and nano-scale surface features.
In some embodiments of the medical implant, the meso-scale surface features have sizes in a range of about 5 μm to about 1 mm.
In some embodiments of the medical implant, the meso-scale surface features have sizes in a range of about 5 μm to about 200 μm.
In some embodiments of the medical implant, the meso-scale surface features include protruding structures. In some embodiments, the protruding structures have lateral sizes in a range of about 5 μm to about 200 μm, and heights in a range of about 5 μm to about 200 μm. In some embodiments, the protruding structures include cone-shaped structures, nodule-shaped structures, pyramid-shaped structures, stud- or spike-like trapezoidal structures, hemispherical structures, or hemispheroidal structures.
In some embodiments of the medical implant, the micro-scale surface features have sizes in a range of about 1 μm to about 5 μm.
In some embodiments of the medical implant, the nano-scale surface features have sizes in a range up to about 1 μm.
In some embodiments of the medical implant, the nano-scale surface features have sizes in a range of about 10 nm to about 1 μm.
In some embodiments of the medical implant, the nano-scale surface features include protruding structures. In some embodiments, the protruding structures include ridge-shaped, pillar/needle-like, or nodular structures.
In some embodiments of the medical implant, the nano-scale surface features include compartmental structures.
In some embodiments of the medical implant, the nano-scale surface features and the micro-scale surface features are superimposed onto the meso-scale surface features.
In some embodiments, the medical implant is a metallic implant. In some embodiments, the metallic implant is a titanium or titanium alloy implant.
In additional embodiments, a medical implant includes an implant body including a surface characterized by an average roughness (Ra) of about 1.5 μm or greater. In some embodiments, Ra is about 2 μm or greater. In some embodiments, Ra is about 2.5 μm or greater.
In additional embodiments, a medical implant includes an implant body including a surface characterized by an average peak-to-valley roughness (Rz) of about 7 μm or greater. In some embodiments, Rz is about 8 μm or greater. In some embodiments, Rz is about 10 μm or greater.
In additional embodiments, a medical implant includes an implant body including a surface characterized by an average slope of roughness profile (Rδa) of about 0.21 or greater. In some embodiments, Rδa is about 0.23 or greater. In some embodiments, Rδa is about 0.25 or greater.
In additional embodiments, a medical implant includes an implant body including a surface characterized by: (a) an average roughness (Ra) of about 1.5 μm or greater; (b) an average peak-to-valley roughness (Rz) of about 7 μm or greater; and (c) an average slope of roughness profile (Rδa) of about 0.21 or greater. In some embodiments, Ra is about 2.5 μm or greater, Rz is about 10 μm or greater, and Rδa is about 0.25 or greater.
In additional embodiments, a method of forming a medical implant having a hierarchical surface roughness includes subjecting the medical implant to surface treatment by exposing the medical implant to an etching liquid while generating bubbles within the etching liquid.
In some embodiments of the method, the etching liquid includes an acid.
In some embodiments of the method, exposing the medical implant to the etching liquid includes disposing an auxiliary material within the etching liquid, and disposing the medical implant over the auxiliary material. In some embodiments, the auxiliary material is or includes a same material as that of the medical implant. In some embodiments, the auxiliary material is or includes a different material as that of the medical implant. In some embodiments, the auxiliary material is or includes substantially pure titanium (e.g., purity of about 98% or greater, or about 99% or greater). In some embodiments, the auxiliary material is or includes substantially pure titanium, and the medical implant is a titanium or titanium alloy implant.
In some embodiments of the method, exposing the medical implant to the etching liquid is carried out at a temperature of about 140° C. or higher. In some embodiments, exposing the medical implant to the etching liquid also includes disposing an auxiliary material within the etching liquid, and disposing the medical implant over the auxiliary material.
In some embodiments of the method, exposing the medical implant to the etching liquid is carried out while agitating the etching liquid using an agitator. In some embodiments, the agitator is an ultrasonic device.
Other aspects and embodiments of this disclosure are also contemplated. The foregoing summary and the following detailed description are not meant to restrict this disclosure to any particular embodiment but are merely meant to describe some embodiments of this disclosure.
For a better understanding of the nature and objects of some embodiments of this disclosure, reference should be made to the following detailed description taken in conjunction with the accompanying drawings.
Besides various macroscopic designs, other titanium implants have micro-scale (scale between about 1 μm and about 5 μm) topography to promote bone-implant integration. To further improve titanium implants, adding meso-scale (scale between about 5 μm to about 200 μm) surface roughness can enhance a mechanical interlocking between titanium and bone, while adding nano-scale (scale up to about 1 μm or less) surface roughness can further promote the function of bone-forming cells. Here some embodiments are directed to the formation of an improved titanium surface with hierarchical morphology of meso-, micro- and nano-scale structures. Titanium implants with this hierarchical surface roughness have been demonstrated to show greater strength of bone-implant integration than titanium implants with micro-scale topography alone.
Provided herein are medical implants for enhancing bone-implant integration capabilities.
In some embodiments, the medical implant 100 having the hierarchical surface roughness is characterized by, according to surface profiling using a profilometer, one or a combination of two or more of the following: (1) an average roughness (Ra) (arithmetic average of absolute values of vertical deviations of a surface profile about a mean line within a sampling length) in a range of about 1.2 μm or greater, such as about 1.3 μm or greater, about 1.5 μm or greater, about 1.8 μm or greater, about 2 μm or greater, about 2.3 μm or greater, or about 2.5 μm or greater, and up to about 8 μm or greater, or up to about 10 μm or greater; (2) an average peak-to-valley roughness (Rz or Rp-v) (arithmetic average of vertical distances between peaks and valleys of a surface profile within a sampling length) in a range of about 6.5 μm or greater, such as about 7 μm or greater, about 7.5 μm or greater, about 8 μm or greater, about 8.5 μm or greater, about 9 μm or greater, about 9.5 μm or greater, or about 10 μm or greater, and up to about 15 μm or greater, or up to about 20 μm or greater; and (3) an average slope of roughness profile (Rδa) (arithmetic average of absolute values of a slope of a surface profile within a sampling length) in a range of about 0.2 or greater, such as about 0.21 or greater, about 0.22 or greater, about 0.23 or greater, about 0.24 or greater, or about 0.25 or greater, and up to about 0.5 or greater, or up to about 0.8 or greater.
In some embodiments, the medical implant 100 is a metallic implant including one or more metals, such as a titanium implant. Other examples of metallic implants include titanium alloy implants, chromium-cobalt alloy implants, platinum and platinum alloy implants, nickel and nickel alloy implants, stainless steel implants, zirconium implants, zirconia implants, titanium-zirconia alloy implants, gold or gold alloy implants, and aluminum or aluminum alloy implants. In other embodiments, the medical implant 100 is a non-metallic implant. Examples of non-metallic implants include ceramic implants, calcium phosphate implants, and polymeric implants.
Also provided herein are methods of forming medical implants having a hierarchical surface roughness. In some embodiments, a method includes subjecting a medical implant to surface treatment by exposing the medical implant to an etching liquid while generating bubbles within the etching liquid. In some embodiments, the etching liquid includes an acid, such as sulfuric acid (H2SO4) or another strong acid. In some embodiments, exposing the medical implant to the etching liquid is carried out for a time period in a range of 5 seconds to about 10 minutes, such as about 5 seconds to about 5 minutes, about 10 seconds to about 5 minutes, about 10 seconds to about 3 minutes, or about 10 seconds to about 2 minutes. In some embodiments, exposing the medical implant to the etching liquid is carried out at a temperature in a range of about 100° C. to about 140° C., such as about 110° C. to about 130° C., or about 120° C. Other manners of surface treatment are contemplated in place of, or in combination with, acid treatment, such as alkaline treatment, oxidation, light irradiation, material deposition (e.g., sputtering, plasma spraying, or vapor deposition), and physical treatments like laser-etching, machining, or sandblasting. For example, laser-etching can be performed to yield meso-scale surface features, along with acid treatment to yield micro- and nano-scale surface features.
In some embodiments, generation of bubbles is promoted by disposing an auxiliary material within the etching liquid, such as within a container, and disposing the medical implant over the auxiliary material. In some embodiments, the auxiliary material is or includes a same or similar material as that of the medical implant, such as titanium or another metal or combination of metals. In some embodiments, the auxiliary material is or includes a different material as that of the medical implant. The auxiliary material can be in the form of fibers, a rod, a wire, an array, coil, or stack of the foregoing, or a disk or a cylinder. In some embodiments, the inclusion of the auxiliary material promotes vigorous, accelerated, and enhanced flow of the etching liquid and promotes generation of bubbles. In some embodiments, the bubbles are generated via a chemical reaction between the auxiliary material and the etching liquid, and at least some of the bubbles impinge upon or bombard a surface of the medical implant to impart a hierarchical surface roughness.
In some embodiments, generation of bubbles is promoted by exposing the medical implant to the etching liquid at an elevated temperature in a range of about 140° C. or higher, such as about 140° C. to about 160° C., or about 140° C. In some embodiments, the elevated temperature promotes vigorous, accelerated, and enhanced flow of the etching liquid and promotes generation of bubbles. In some embodiments, the bubbles are generated via a chemical reaction between the medical implant and the etching liquid, and at least some of the bubbles impinge upon or bombard the surface of the medical implant to impart the hierarchical surface roughness. In some embodiments, generation of the bubbles is promoted by exposing the medical implant to the etching liquid at an elevated temperature, along with disposing an auxiliary material within the etching liquid.
Other manners of promoting the flow of the etching liquid and generation of bubbles are contemplated, such as by agitating the etching liquid using a mechanical agitator, such as an ultrasonic device or a mechanical vibrator. Also, combinations of two or more of the foregoing surface treatments are contemplated, such as using two or more of an auxiliary material, an elevated temperature, material deposition, laser-etching, and agitation.
In some embodiments, the medical implant (or another reference medical implant) prior to surface treatment has, according to a large scale (λ=250 μm) surface profiling, a reference average roughness (Ra), a reference maximum peak-to-valley roughness (Rmax), a reference average width of roughness profile elements (Rsm), a reference skewness of roughness profile (Rsk), and a reference kurtosis of roughness profile (Rku), and the medical implant subsequent to surface treatment has, according to the large scale (λ=250 μm) surface profiling, an average roughness (Ra) greater than the corresponding reference value, a maximum peak-to-valley roughness (Rmax) greater than the corresponding reference value, an average width of roughness profile elements (Rsm) greater than the corresponding reference value, a skewness of roughness profile (Rsk) smaller than the corresponding reference value, and a kurtosis of roughness profile (Rku) smaller than the corresponding reference value.
In some embodiments, the medical implant (or another reference medical implant) prior to surface treatment has, according to a small scale (λ=0.25 μm) surface profiling, a reference average roughness (Ra), a reference maximum peak-to-valley roughness (Rmax), a reference average width of roughness profile elements (Rsm), a reference skewness of roughness profile (Rsk), and a reference kurtosis of roughness profile (Rh), and the medical implant subsequent to surface treatment has, according to the small scale (λ=0.25 μm) surface profiling, an average roughness (Ra) smaller than the corresponding reference value, a maximum peak-to-valley roughness (Rmax) smaller than the corresponding reference value, an average width of roughness profile elements (Rsm) smaller than the corresponding reference value, a skewness of roughness profile (Rsk) smaller than the corresponding reference value, and a kurtosis of roughness profile (Rku) smaller than the corresponding reference value.
The medical implant provided herein can be used for treating, preventing, ameliorating, correcting, or reducing one or more symptoms of a medical condition by implanting the medical implant in a mammalian subject. The mammalian subject can be a human or a veterinary animal such as a dog, a cat, a horse, a cow, a bull, or a monkey. Examples of medical conditions that can be treated or prevented include missing teeth or bone related medical conditions such as femoral neck fracture, orthodontic anchorage, wrist fracture, spine fracture/disorder, spinal disk displacement, edentulous jaw, fracture or degenerative changes of joints such as knee joint arthritis, bone and other tissue defect or recession caused by a disorder or a body condition such as cancer, injury, systemic metabolism, infection or aging, and combinations thereof.
The following examples describe specific aspects of some embodiments of this disclosure to illustrate and provide a description for those of ordinary skill in the art. The examples should not be construed as limiting this disclosure, as the examples merely provide specific methodology useful in understanding and practicing some embodiments of this disclosure.
Results
Surface Morphology of Micro-Scale Rough Titanium and Hierarchically Rough Titanium Surfaces
Surface Profiles of Micro-Scale Rough Titanium and Hierarchically Rough Titanium Surfaces
Roughness and Profile Parameters of Micro-Scale Rough Titanium and Hierarchically Rough Titanium Surfaces
Strength of Bone-Implant Integration for Micro-Scale Rough Titanium and Hierarchically Rough Titanium
Methods to Form Hierarchically Rough Titanium Surface
Method 1: Using Auxiliary Titanium
About 30 ml of H2SO4 (about 66% concentration) is heated to about 120° C. Commercially pure titanium wire (about 1 mm diameter, about 90 cm in length) in a coil form is submerged in the heated H2SO4. After confirming a chemical reaction is started and bubbles are vigorously generated, titanium implants or other titanium samples of interest are soaked into H2SO4 for about 75 seconds. Titanium implants are removed and rinsed with double-distilled H2O.
Method 2: Using High-Temperature Acid
About 30 ml of H2SO4 (about 66% concentration) was heated to about 140° C. or higher. Titanium implants or other titanium samples of interest are soaked into H2SO4 for about 75 seconds. Titanium implants are removed and rinsed with double-distilled H2O.
Surface profiling was performed for a hierarchically rough titanium surface and comparative titanium surfaces (under a condition with a sampling length of interest being 4 mm and a threshold of 0.8).
The hierarchically rough titanium showed a remarkably greater average roughness (Ra) of 2.8468±0.090 μm, in comparison with Ra of 0.3814±0.0233 μm for a comparative acid-etched surface, Ra of 0.8508±0.060 μm for a comparative sand-blasted surface, and Ra of 1.056±0.094 μm for a comparative sand-blasted and acid-etched surface.
The hierarchically rough titanium showed a remarkably greater average peak-to-valley roughness (Rz or Rp-v) of 13.985±0.259 μm, in comparison with Rz of 1.933±0.147 μm for the comparative acid-etched surface, Rz of 4.790±0.392 μm for the comparative sand-blasted surface, and Rz of 5.931±0.543 μm for the comparative sand-blasted and acid-etched surface.
The hierarchically rough titanium showed a remarkably greater average slope of roughness profile (Rδa) of 0.3692±0.0088, in comparison with Rδa of 0.0656±0.0035 for the comparative acid-etched surface, Rδa of 0.1504±0.0097 for the comparative sand-blasted surface, and Rδa of 0.1854±0.0139 for the comparative sand-blasted and acid-etched surface.
A hierarchically rough surface was formed on titanium alloy (Ti-6Al-4V). Specifically, a titanium alloy rod was treated with acid using titanium as an auxiliary material.
As used herein, the singular terms “a,” “an,” and “the” may include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to an object may include multiple objects unless the context clearly dictates otherwise.
As used herein, the term “set” refers to a collection of one or more objects. Thus, for example, a set of objects can include a single object or multiple objects.
As used herein, the terms “substantially” and “about” are used to describe and account for small variations. When used in conjunction with an event or circumstance, the terms can refer to instances in which the event or circumstance occurs precisely as well as instances in which the event or circumstance occurs to a close approximation. For example, when used in conjunction with a numerical value, the terms can refer to a range of variation of less than or equal to ±10% of that numerical value, such as less than or equal to ±5%, less than or equal to ±4%, less than or equal to ±3%, less than or equal to ±2%, less than or equal to ±1%, less than or equal to ±0.5%, less than or equal to ±0.1%, or less than or equal to ±0.05%.
Additionally, concentrations, amounts, ratios, and other numerical values are sometimes presented herein in a range format. It is to be understood that such range format is used for convenience and brevity and should be understood flexibly to include numerical values explicitly specified as limits of a range, but also to include all individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly specified. For example, a range of about 1 to about 200 should be understood to include the explicitly recited limits of about 1 and about 200, but also to include individual values such as about 2, about 3, and about 4, and sub-ranges such as about 10 to about 50, about 20 to about 100, and so forth.
While the disclosure has been described with reference to the specific embodiments thereof, it should be understood by those skilled in the art that various changes may be made and equivalents may be substituted without departing from the true spirit and scope of the disclosure as defined by the appended claims. In addition, many modifications may be made to adapt a particular situation, material, composition of matter, method, operation or operations, to the objective, spirit and scope of the disclosure. All such modifications are intended to be within the scope of the claims appended hereto. In particular, while certain methods may have been described with reference to particular operations performed in a particular order, it will be understood that these operations may be combined, sub-divided, or re-ordered to form an equivalent method without departing from the teachings of the disclosure. Accordingly, unless specifically indicated herein, the order and grouping of the operations are not a limitation of the disclosure.
This application claims the benefit of U.S. Provisional Application No. 62/526,202, filed Jun. 28, 2017, the contents of which are incorporated herein by reference in their entirety.
Filing Document | Filing Date | Country | Kind |
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PCT/US2018/039832 | 6/27/2018 | WO | 00 |
Number | Date | Country | |
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62526202 | Jun 2017 | US |