X-RAY DETECTABLE BIOABSORBABLE BONE SCREW

Abstract

A X-ray detectable bioabsorbable bone screw comprises a light-emitting element, a light-sensing element, a transparent inner encapsulant body, an outer covering body, and two conductive frames on which. An optically reflective surface is in contact and formed between the dome enclosing portion of the transparent inner encapsulant body and the outer encapsulant body. A portion of the light emitted by the light-emitting element is reflected to the light-sensing element through the optically reflective surface, and the other portion of the light emitted from the light-emitting element is directly emitting to the light-sensing element through the transparent inner encapsulant body. The present invention applies the optically reflective surface to minimize the overlapping area between the two conductive frames, and reduces the capacitance value, and increases the CMRR in a manner that the photo coupler of the present invention is able to meet the standard of electrical characteristics as required.

Claims

1. An X-ray detectable bioabsorbable bone screw, which is radiographable under X-ray exposure, comprising: a screw member having a cylindrical shape; and a cap member provided on an end of the screw member and being extended outwardly from the screw member, wherein the cap member and the screw member are formed integrally, and the cap member and the screw member are made of polylactice acid and iron oxide nanoparticles.

2. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein the cap member and the screw member contain 0.5 to 40 weight percent of iron oxide nanoparticles.

3. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein the cap member and the screw member are manufactured by an injection molding process or a 3D printing process.

4. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein a length extending in an axial direction of the x-ray detectable bioabsorbable bone screw is 16 mm and a diameter of the screw member is 3.1 mm.

5. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, further comprising a bioabsorbable material, which is selected from a group consisting of hydroxyapatite, β-tricalcium phosphate and calcium polyphosphate.

6. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein the X-ray detectable bioabsorbable bone screw is biocompatible with an animal cell and is biodegradable by the animal cell.

7. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein the X-ray detectable bioabsorbable bone screw is manufactured by an injection molding process.

8. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein the X-ray detectable bioabsorbable bone screw is manufactured by a die casting process.

9. The X-ray detectable bioabsorbable bone screw as claimed in claim 1, wherein the X-ray detectable bioabsorbable bone screw is manufactured by a 3D printing process.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0016] The structure and the technical means adopted by the present invention to achieve the above and other objects can be best understood by referring to the following detailed description of the preferred embodiments and the accompanying drawings.

[0017] FIG. 1 is a flow diagram illustrating a method of manufacturing an X-ray detectable bioabsorbable bone screw according to an embodiment of the present invention;

[0018] FIG. 2 is a schematic diagram illustrating the X-ray detectable bioabsorbable bone screw;

[0019] FIG. 3 is a radiograph illustrating the X-ray detectable bioabsorbable bone screw manufactured by an injection molding process;

[0020] FIG. 4 is a radiograph illustrating the X-ray detectable bioabsorbable bone screw manufactured by a 3D printing process;

[0021] FIG. 5 is a photomicrograph illustrating a degradation condition of the X-ray detectable bioabsorbable bone screw of the present invention implanted in a rabbit bone;

[0022] FIG. 6a is a radiograph illustrating that a position of a conventional bone screw made of pure PLA in a bone is unlocatable when being exposed to X-ray radiation;

[0023] FIG. 6b is a radiograph illustrating that the bone screw of the present invention in a bone is clearly identified when being exposed to X-ray radiation; and

[0024] FIG. 7 is a result of a Micro-CT based quantitative analysis, which shows a greater amount of new bone formation around implanted X-ray detectable bioabsorbable bone screw of the present invention compared to the amount of new bone formation around implanted conventional bone screws.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0025] As illustrated in FIG. 2, an X-ray detectable bioabsorbable bone screw 1 comprises a screw member 12 and a cap member 11. The screw member 12 has a cylindrical shape. The cap member 11 is provided on an end of the screw member 12 and extended outwardly from the screw member 12. The cap member 11 and the screw member 12 are formed integrally, and the cap member 11 and the screw member 12 are made of polylactice acid and iron oxide nanoparticles. A nanoparticle is defined as a microscopicparticle with at least one dimension less than 100 nm. Preferably, the sizes of the iron oxide nanoparticles are less than 50 nanometer in size.

[0026] As shown in the flow diagram of FIG. 1, the method of manufacturing the X-ray detectable bioabsorbable bone screw is described according to steps S1 to S8. The method of manufacturing the bone screw comprises steps of: providing an injection molding device, a die, polylactice acid and iron oxide nanoparticles, wherein the die is provided with a bone screw mold, and the injection molding device is connected to the die; mixing the polylactice acid and the iron oxide nanoparticles to form a raw material; granulating the raw material to form a raw granule; providing the injection molding device with the raw granule; pressurizing and heating the raw granule with the injection molding device until the raw granule reach a predetermined state; providing the die with the raw granule of in the predetermined state to form a bone screw shaped by the bone screw mold. The embodiment of the present invention will be described in detail with reference to the appended drawings hereinafter in order to make the objects, characteristics and advantages of the present invention more clear and comprehensible.

Preparation Example 1

[0027] Injection molding method, a conventional plastic processing method, is employed to manufacture a bone screw model. Pure PLA granules and iron oxide nanoparticles are mixed to form a raw material, and the raw material is granulated to obtain a PLA raw granule containing 20 wt % iron oxide nanoparticles as a raw granule. The raw granule is pressurized and heated by the injection molding device until the raw granule reaches a predetermined state. The die is filled with the raw granule in the predetermined state rapidly, and the pressure is kept constant until the raw material is cooled. After the raw material is cooled, the raw material is demolded to form a bone screw model which is shaped by the bone screw mold. The bone screw model is manufactured by an injection molding process. The bone screw model can be used to make bone screws of specific size. More specifically, the bone screw model can be used to manufacture, by injection molding process, a bone screw with a length of 11-20 mm in an axial direction, and a diameter of 2.5-3.6 mm. In this preparation example, as shown in FIG. 3, the bone screw model is used to manufacture bone screws with a length of 2.5 mm in the axial direction, and a diameter of 3.1 mm. However, the present invention is not limited to this. Furthermore, in order to make the present invention applicable to various parts of the body to be treated and various bone diseases, other bioabsorbable material, such as hydroxyapatite, β-tricalcium phosphate and calcium polyphosphate, is selectively added into the PLA raw material. In addition, PLA can be substituted by materials as follows: polyglycolic acid (PGA), polycaprolactone (PCL), polyethylene glycol (PEG), lactic acid-glycol copolymer, polydioxanone (PDO) and/or chitin. The iron oxide nanoparticles include Fe.sub.2O.sub.3, Fe.sub.3O.sub.4 and FeO. Iron oxide nanoparticles can be substituted by materials as follows: nano-sized oxides of iron, cobalt, nickel and/or chromium, such as Fe.sub.2CoO.sub.4, NiO and CrO.sub.2.

Preparation Example 2

[0028] Besides the injection molding process, the bone screw can be manufactured by a 3D printing process. The bone screw model is rod-shaped and can be applied to a 3D printing process, in which the bone screw model is used to manufacture a bone screw by a 3D printing process. As mentioned above, pure PLA raw material and iron oxide nanoparticles are mixed to form a raw material, and the raw material is granulated to obtain a PLA raw granule containing 20 wt % iron oxide nanoparticles as a raw granule. The raw granule is pressurized and heated by the injection molding device until the raw granule reaches a predetermined state. The die is filled with the raw granule in the predetermined state rapidly, and the pressure is kept constant until the raw material is cooled. After the raw material is cooled, the raw material is demolded to form a bone screw model with a length in an axial direction of is 20 mm and a diameter of 1.65 mm. The bone screw model, which is rod-shaped, can be applied to an additive manufacturing device. A bone screw of 16 mm in length and 3.1 mm is formed by utilizing 3D printing process (as shown in FIG. 4) with the bone screw model being used as a 3D printing model. Furthermore, in order to make the present invention applicable to various parts of the body to be treated and various bone diseases, other bioabsorbable material, such as hydroxyapatite, β-tricalcium phosphate and calcium polyphosphate, is selectively added into the PLA raw material. In addition, PLA can be substituted by materials as follows: polyglycolic acid (PGA), polycaprolactone (PCL), polyethylene glycol (PEG), lactic acid-glycol copolymer, polydioxanone (PDO) and/or chitin. The iron oxide nanoparticles include Fe.sub.2O.sub.3, Fe.sub.3O.sub.4 and FeO. Iron oxide nanoparticles can be substituted by materials as follows: nano-sized oxides of iron, cobalt, nickel and/or chromium, such as Fe.sub.2CoO.sub.4, NiO and CrO.sub.2.

Preparation Example 3

[0029] In order to prove that the cap member 11 and the screw member 12 containing 0.5 to 40 weight percent of iron oxide nanoparticles is able to be manufactured and is radiographable under X-ray exposure, polylactice acid and iron oxide nanoparticles are mixed in different mix proportions by weight, producing Fe.sub.3O.sub.4/PLA samples at different weight ratios: 0 wt %, 20 wt %, 30 wt % and 40 wt %. A plurality of I-shaped specimens for tensile strength testing are manufactured with the Fe.sub.3O.sub.4/PLA samples by an injection molding process according to the ASTM (American Society for Testing and Materials) D638 Type V testing standard. The I-shaped specimens have the following specifications: a width of 2.6 mm, a thickness of 4.2 mm and a parallel length of 20 mm During the tensile strength testing, the I-shaped specimens manufactured by the injection molding process are provided on a clamping member of the tensile strength testing device, and a set the strain rate to be 2 mm/min to measure and record the yield strength of the I-shaped specimens. The yield strength of the I-shaped specimens is shown in Table I.

TABLE-US-00001 TABLE I Content of iron oxide nanoparticles 0 wt % 20 wt % 30 wt % 40 wt % Yield strength 51.1 49.2 42.7 41.5 (MPa)

Embodiment 1

[0030] Biocompatibility Testing

[0031] The bone screw is immersed in sterile water and oscillated by an ultrasonic oscillator for 10 minutes, and then immersed in 75% alcohol as a cleaning step. The bone screw is sterilized by γ-ray, after which the preoperative preparation for an animal experiment is completed. A New Zealand white rabbit is anesthetized by receiving a subcutaneous cervical injection; an implantation area at the front hind leg of the New Zealand white rabbit was shaved; a position in the implantation area to be cut is locally anesthetized with Lidocaine; subcutaneous layer and muscular layer are cut open with surgical scalpel blades No. 15 from a marked point in the middle of the two joints at both ends of the femur along a front side of the femur in a long axial direction; and the periosteum above the femur is lifted to expose femur. A proximal portion of the femoral diaphysis that is away from the articular pan is determined to be implanted. The bone tissue of the part to be implanted is drilled by a drilling machine and is rinsed with physiological saline, and the physiological saline is extracted. After the drilling is completed, the bone screw is implanted, and the subcutaneous layer and the muscular layer are sutured with 5-0 absorbable suture, and then epidermis is sutured with suture.

[0032] The rabbit is sacrificed 4 weeks after the surgery. The femur containing the bone screw is resected and immersed in a fixative solution containing 10% formalin. Then, the femur sample containing the bone screw is dehydrated through multiple processes, and then is wrapped with paraffin and sliced to form a paraffin section. The paraffin section is stained by Hematoxylin-Eosin Staining method and then a section slide of the paraffin section is prepared using mounting media. Then, the femur sample containing the bone screw is scanned by a slice-scanner, and an image file of the section slide obtained therefrom is observed.

[0033] After the bone screw of the present invention is degraded, the substance released from degradation is shown as the black parts in FIG. 5. The substance does not initiate an inflammatory response within body and can be covered by bone tissue, on which bone cells can grow. It is thus indicated that the bone screw of the present invention is biocompatible.

Embodiment 2

[0034] Examination of X-Ray Detectability

[0035] The bone screw is immersed in sterile water and oscillated by an ultrasonic oscillator for 10 minutes, and then immersed in 75% alcohol as a cleaning step. The bone screw is sterilized by γ-ray, after which the preoperative preparation for an animal experiment is completed. A New Zealand white rabbit is anesthetized by receiving a subcutaneous cervical injection; an implantation area at the front hind leg of the New Zealand white rabbit was shaved; a position in the implantation area to be cut is locally anesthetized with Lidocaine; subcutaneous layer and muscular layer are cut open with surgical scalpel blades No. 15 from a marked point in the middle of the two joints at both ends of the femur along a front side of the femur in a long axial direction; and the periosteum above the femur is lifted to expose femur. A proximal portion of the femoral diaphysis that is away from the articular pan is determined to be implanted. The bone tissue of the part to be implanted is drilled by a drilling machine and is rinsed with physiological saline, and the physiological saline is extracted. After the drilling is completed, the bone screw is implanted, and the subcutaneous layer and the muscular layer are sutured with 5-0 absorbable suture, and then epidermis is sutured with suture.

[0036] The rabbit is sacrificed 4 weeks after the surgery. The femur containing the bone screw is resected and immersed in a fixative solution containing 10% formalin. The femur section is scanned by a micro computed tomography (Micro CT) scanner for observation. The parts of the femur sample to be observed, including the bone screw and the bone tissue around the bone screw, are circled using a built-in instructional tool of the micro computed tomography to calculate the volume of new bone.

[0037] As shown in FIG. 6a, the bone screw made of pure PLA in bone is radiopaque when being exposed to X-ray radiation. As shown in FIG. 6b, the bone screw of the present invention is clearly shown in the bone when being exposed to X-ray radiation. It is thus indicated that the bone screw of the present invention is radiographable under X-ray exposure. As shown in FIG. 7, a result of a Micro-CT based quantitative analysis shows a greater amount of new bone around the implanted X-ray detectable and bioabsorbable bone screw prepared according to the above-mentioned preparation examples compared with the amount of new bone around an implanted conventional bone screw.

[0038] According to the above examination result, the bioabsorbable bone screw containing PLA and iron oxide nanoparticles of the present invention is radiographable, and thus can be used for radiographic inspection. Therefore, the bioabsorbable bone screw containing PLA and iron oxide nanoparticles of the present invention can be applied to orthopedics, neurosurgery and plastic surgery to improve the positioning of the implanted bone screw and to achieve the effect of accelerating bone healing. However, the present invention is not limited to the above mentioned advantages.

[0039] The above description should be considered as only the preferred embodiments of the present invention, and the scope of the embodiment of present invention is not limited thereto. Various equivalents and modifications without departing from the appended claims and the description of present invention are included in the scope of the present invention.