阅读说明：本技术 一种种植体活化方法及活化种植体 (Implant activation method and activated implant ) 是由 常林 周俊 宾士友 于 2020-05-08 设计创作，主要内容包括：本发明公开了一种种植体活化方法及活化种植体,属于医疗产品领域。该方法包括：将待活化的种植体于准分子光源的照射下进行活化处理；其中,准分子光源向待活化的种植体提供148-196nm及具有6.3-8.4eV光子能量的真空紫外线。通过上述活化方法,不仅能够在种植手术前快速获得亲水效果保持时间较久的亲水性种植体,而且还能降低种植体表面有机碳化物的污染,提高氧含量,使其表面吸附更多的生物活性物质与成骨蛋白,促进种植体与骨结合。活化处理后的活化种植体,表面接触角低且能较长时间保持亲水性,其表面氧和钛的含量较高,污染元素含量较低。(The invention discloses an implant activation method and an activated implant, and belongs to the field of medical products. The method comprises the following steps: activating the implant to be activated under the irradiation of an excimer light source; wherein the excimer light source provides 148-196nm vacuum ultraviolet rays with photon energy of 6.3-8.4eV for the implant to be activated. By the activation method, the hydrophilic implant with longer hydrophilic effect retention time can be quickly obtained before an implant operation, the pollution of organic carbides on the surface of the implant can be reduced, the oxygen content is increased, more bioactive substances and osteogenic protein are adsorbed on the surface of the implant, and the combination of the implant and bone is promoted. The activated implant after the activation treatment has low surface contact angle, can keep hydrophilic for a long time, and has high surface oxygen and titanium content and low content of pollution elements.)

1. An implant activation method, comprising the steps of: activating the implant to be activated under the irradiation of an excimer light source;

wherein the excimer light source provides 148-196nm and vacuum ultraviolet rays with photon energy of 6.3-8.4eV for the implant to be activated;

preferably, the implant is a dental implant;

preferably, the implant comprises a titanium implant.

2. The implant activation method according to claim 1, wherein the excimer light source provides the implant to be activated with vacuum ultraviolet light of 160-184nm and with photon energy of 6.7-7.8eV, preferably with vacuum ultraviolet light of 172nm and with photon energy of 7.2 eV.

3. The implant activation method according to claim 1, wherein the distance between the excimer light source and the implant to be activated is 10-100mm, and the activation time is 0.5-30 min;

preferably, the distance between the excimer light source and the implant to be activated is 10-50mm, more preferably 30 mm;

preferably, the activation time is 0.5-5min, more preferably 1 min.

4. The implant activation method according to any one of claims 1 to 3, further comprising, before the activation treatment, pre-treating the implant to be activated to form holes in the surface of the implant.

5. The implant activation method according to claim 4, wherein the pre-treatment comprises sand blasting the surface of the implant to be activated to form primary holes in the surface;

preferably, the diameter of the primary pores is 20-200 μm.

6. The implant activation method according to claim 5, wherein the blasting material used for the blasting treatment comprises rutile sand or corundum sand;

preferably, the blasting distance is 5-15mm, more preferably 8-12mm during the blasting treatment;

preferably, the blasting angle is 30-60 °, more preferably 40-50 ° during the blasting process;

preferably, the blasting time is 10 to 20s, more preferably 13 to 17s, during the blasting process.

7. The implant activation method according to claim 5 or 6, wherein the pre-treatment further comprises subjecting the surface of the implant after the sand blasting treatment to an acid etching treatment to form secondary pores on the surface;

preferably, the secondary pores have a diameter of less than 5 μm.

8. The implant activation method according to claim 7, wherein the acid used for the acid etching treatment comprises sulfuric acid or hydrochloric acid;

preferably, the acid etching treatment is carried out at 50-100 ℃, more preferably at 60 ℃;

preferably, the acid etching treatment time is 3-120min, more preferably 60 min.

9. The implant activation method according to claim 1, wherein the excimer light source is provided by an excimer lamp;

preferably, the excimer lamp comprises an inner quartz tube and an outer quartz tube which are coaxially arranged, a closed annular cavity is formed between the inner quartz tube and the outer quartz tube, the cavity is used for filling inert gas or halogen, an inner electrode is arranged on the inner wall of the inner quartz tube, an outer electrode is arranged on the outer wall of the outer quartz tube, and the outer electrode and the inner electrode are both electrically connected with a power supply;

preferably, the length of the outer layer quartz tube is 100-500mm, the width is 30-120mm, and the height is 1-5mm, and more preferably, the length of the outer layer quartz tube is 140mm, the width is 40mm, and the height is 1.5 mm;

preferably, the length of the inner-layer quartz tube is 150-700mm, the width is 20-90mm, and the height is 0.8-2.5mm, more preferably, the length of the inner-layer quartz tube is 200mm, the width is 25mm, and the height is 1 mm;

preferably, the discharge gap of the excimer lamp is 5-7mm, more preferably 6 mm;

preferably, the inert gas comprises xenon;

preferably, the material of the inner electrode comprises stainless steel;

preferably, the inner electrode is in a sheet shape;

preferably, the inner electrode is a stainless steel sheet;

preferably, the thickness of the inner electrode is 0.02-0.10mm, more preferably 0.05 mm;

preferably, the material of the outer electrode comprises stainless steel;

preferably, the outer electrode is in a mesh shape;

more preferably, the outer electrode is a stainless steel mesh;

preferably, the excimer lamp has a transmittance of > 80% for ultraviolet light of 200nm wavelength.

10. An activated implant, wherein the activated implant is activated by the implant activation method according to any one of claims 1 to 9;

preferably, the contact angle of the activated implant is 0-0.5 °, more preferably 0 °;

preferably, the activated implant has a surface C content of 9.1-16% in atomic percentage;

preferably, the surface N content of the activated implant is 0.5-0.7% in atomic percentage;

preferably, the surface O content of the activated implant is 57-64% in atomic percentage;

preferably, the surface Mg content of the activated implant is 0.3-0.9% in atomic percentage;

preferably, the surface Si content of the activated implant is lower than 1%, more preferably 0.6%, in atomic percentage;

preferably, the S content of the surface of the activated implant is 0.2-0.4% in atomic percentage;

preferably, the surface Ca content of the implant is 0.4-0.7% in atomic percentage;

preferably, the surface Ti content of the activated implant is 20-23% in atomic percentage;

preferably, the surface Zn content of the activated implant is 0.1-0.4% in atomic percentage;

preferably, the surface I content of the activated implant is lower than 0.3%, more preferably lower than 0.1%, in atomic percentage.

Technical Field

The invention relates to the technical field of medical products, in particular to an implant activation method and an activated implant.

Background

The dental implant is implanted into the upper and lower jawbone of the edentulous part of human body by means of surgical operation, and after the operation wound is healed, a device for repairing the abutment and the crown is arranged on the upper part of the dental implant. For modern oral cavity, the implant is widely used for tooth loss and restoration due to its features of beauty, comfort and long life, and is called the third pair of human teeth.

The hydrophilic dental implant often has more excellent bioactivity, and a series of researches show that the hydrophilic dental implant has a promotion effect on the differentiation of osteocytes and is particularly effective on early osseointegration. However, the contact angle of the existing implant is generally higher (more than 90 degrees), and the hydrophilicity of part of hydrophilic implant is obviously reduced after the part of hydrophilic implant is placed for a period of time.

The ultraviolet irradiation is a process which can activate the surface of an implant before a dental implant operation to obtain a hydrophilic surface again, and although a corresponding implant activation instrument can enable the implant to reach the hydrophilic level to a certain extent, the ultraviolet irradiation has not been widely popularized in the market, and the main reasons are that the activation power of common UVC ultraviolet rays (with the wavelength of 253.7nm) is low, the energy is not concentrated, and the activation time is long (generally more than 4 hours). In the clinical use process, doctors need to prepare the activation of the implant 4 hours in advance, and the actual operation process is complicated and time-consuming. And the implant can not be sterilized for the second time after being taken out, and once the operation time needs to be changed due to the reasons of patients or doctors, the implant can not be used continuously, thereby causing waste.

In view of this, the invention is particularly proposed.

Disclosure of Invention

One of the objects of the present invention includes to provide an implant activation method which is simple and easy to operate, and can rapidly obtain a hydrophilic implant having a long retention time of hydrophilic effect before an implant operation.

The second object of the present invention is to provide an activated implant activated by the above-mentioned implant activation method, which has a low surface contact angle and can maintain hydrophilicity for a long time, and which has a high content of oxygen and titanium on the surface and a low content of contaminating elements.

The invention is realized by the following steps:

in a first aspect, the present application provides an implant activation method comprising the steps of: and (3) carrying out activation treatment on the implant to be activated under the irradiation of the excimer light source.

Wherein the excimer light source provides 148-196nm and vacuum ultraviolet rays with photon energy of 6.3-8.4eV to the implant to be activated.

In an alternative embodiment, the implant is a dental implant.

In an alternative embodiment, the implant comprises a titanium implant.

In an alternative embodiment, the excimer light source provides the implant to be activated with vacuum UV light at 184nm and with photon energy of 6.7-7.8 eV. Preferably, vacuum ultraviolet light of 172nm and having a photon energy of 7.2eV is provided.

In an alternative embodiment, the distance between the excimer light source and the implant to be activated is 10-100mm and the activation time is 0.5-30 min.

In an alternative embodiment, the distance between the excimer light source and the implant to be activated is 10-50mm, preferably 30 mm.

In an alternative embodiment, the activation time is 0.5-5min, preferably 1 min.

In an alternative embodiment, the method further comprises, before the activation treatment, pre-treating the implant to be activated to form holes in the surface of the implant.

In an alternative embodiment, the pre-treatment comprises grit blasting the surface of the implant to be treated to form primary holes in the surface.

In an alternative embodiment, the primary pores have a diameter of 20-200 μm.

In an alternative embodiment, the blasting material used for the blasting process comprises rutile or corundum sand.

In an alternative embodiment, the blasting distance is 5-15mm, preferably 8-12mm, during the blasting process.

In an alternative embodiment, the blasting angle during the blasting process is 30-60 °, preferably 40-50 °.

In an alternative embodiment, the blasting time is 10-20s, preferably 13-17s, during the blasting process.

In an alternative embodiment, the pre-treatment further comprises acid etching the surface of the implant after the sand blasting to form secondary holes on the surface.

In an alternative embodiment, the secondary pores are less than 5 μm in diameter.

In an alternative embodiment, the acid used in the acid etching process comprises sulfuric acid or hydrochloric acid.

In an alternative embodiment, the acid etching treatment is carried out at 50-100 ℃, preferably at 60 ℃.

In an alternative embodiment, the acid etching treatment time is 3-120min, preferably 60 min.

In an alternative embodiment, the excimer light source is provided by an excimer lamp.

In an alternative embodiment, the excimer lamp comprises an inner quartz tube and an outer quartz tube which are coaxially arranged, a closed annular cavity is formed between the inner quartz tube and the outer quartz tube, the cavity is filled with inert gas or halogen, an inner electrode is arranged on the inner wall of the inner quartz tube, an outer electrode is arranged on the outer wall of the outer quartz tube, and the outer electrode and the inner electrode are both electrically connected with a power supply.

In an alternative embodiment, the outer quartz tube has a length of 100-500mm, a width of 30-120mm and a height of 1-5 mm. Preferably, the outer quartz tube has a length of 140mm, a width of 40mm and a height of 1.5 mm.

In an alternative embodiment, the inner quartz tube has a length of 150-700mm, a width of 20-90mm and a height of 0.8-2.5 mm. Preferably, the inner quartz tube has a length of 200mm, a width of 25mm and a height of 1 mm.

In an alternative embodiment, the discharge gap of the excimer lamp is 5-7mm, preferably 6 mm.

In an alternative embodiment, the inert gas comprises xenon.

In an alternative embodiment, the material of the inner electrode comprises stainless steel.

In an alternative embodiment, the inner electrode is in the form of a sheet.

In an alternative embodiment, the inner electrode is a stainless steel sheet.

In an alternative embodiment, the thickness of the inner electrode is 0.02-0.1mm, preferably 0.05 mm.

In an alternative embodiment, the material of the outer electrode comprises stainless steel.

In an alternative embodiment, the outer electrode is mesh-shaped.

In an alternative embodiment, the outer electrode is a stainless steel mesh.

In an alternative embodiment, the excimer lamp has a transmittance of > 80% for ultraviolet light at a wavelength of 200 nm.

In a second aspect, the present application also provides an activated implant activated by the implant activation method according to any one of the preceding embodiments.

In an alternative embodiment, the contact angle of the activated implant is 0-0.5 °, preferably 0 °;

in an alternative embodiment, the activated implant has a surface C content of 9.1-16% in atomic percentage.

In an alternative embodiment, the surface N content of the activated implant is 0.5-0.7% in atomic percentage.

In an alternative embodiment, the surface O content of the activated implant is 57-64% in atomic percentage.

In an alternative embodiment, the activated implant has a surface Mg content of 0.3-0.9% in atomic percentage.

In an alternative embodiment, the surface Si content of the activated implant is lower than 1%, preferably 0.6%, in atomic percentage.

In an alternative embodiment, the surface S content of the activated implant is 0.2-0.4% in atomic percentage.

In an alternative embodiment, the surface Ca content of the implant is 0.4-0.7% in atomic percentage.

In an alternative embodiment, the surface Ti content of the activated implant is 20-23% in atomic percentage.

In an alternative embodiment, the surface Zn content of the activated implant is 0.1-0.4% in atomic percentage.

In an alternative embodiment, the surface I content of the activated implant is lower than 0.3%, preferably lower than 0.1%, in atomic percentage.

The application has the following beneficial effects:

the implant activation method provided by the application adopts an excimer light source ultraviolet activation technology, utilizes the characteristic that an excimer light source emits single and energy-concentrated 148-196nm Vacuum Ultraviolet (VUV) to emit vacuum ultraviolet photon energy as high as 6.3-8.4eV, and is enough to open most molecular bonds, so that the rapid removal of organic carbides on the surface of an implant (such as a dental implant) is realized, and therefore, a hydrophilic implant with a longer hydrophilic effect retention time can be rapidly obtained before an implant operation, on one hand, the problem of low efficiency of the existing ultraviolet lamp can be improved, the clinical use requirement is met, and on the other hand, more operation preparation time can be provided for doctors. In addition, ozone can be formed in the activation device in the excimer light source ultraviolet activation process, the ozone is decomposed to generate active oxygen, and the active oxygen can be attached to the surface of the implant, so that direct interaction can be better generated between the active oxygen and the osteogenic protein and osteoblasts in body fluid, and the excimer light source ultraviolet activation device has higher hydrophilicity and bioactivity.

Drawings

In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the drawings needed to be used in the embodiments will be briefly described below, it should be understood that the following drawings only illustrate some embodiments of the present invention and therefore should not be considered as limiting the scope, and for those skilled in the art, other related drawings can be obtained according to the drawings without inventive efforts.

FIG. 1 is a diagram of the binding energy of a common chemical bond;

FIG. 2 is a schematic view of the wavelength distribution range of the excimer lamp of the present application;

FIG. 3 is a schematic structural view of an excimer lamp in example 1 of the present application;

FIG. 4 is a graph showing the results of a contact angle test of the activated implant in example 1 of the present application;

FIG. 5 is a graph showing the results of the surface element content of the activated implant according to application example 1;

FIG. 6 is a graph showing the results of a contact angle test of an activated implant in example 2 of the present application;

FIG. 7 is a graph showing the results of the surface element content of the activated implant according to application example 2;

FIG. 8 is a graph showing the results of a contact angle test of an activated implant in comparative example 1 of the present application;

FIG. 9 is a graph showing the results of a contact angle test of an activated implant in comparative example 2 of the present application;

FIG. 10 is a graph showing the results of a contact angle test of an activated implant in comparative example 3 of the present application;

FIG. 11 is a graph showing the results of a contact angle test of an activated implant in comparative example 4 of the present application;

fig. 12 is a graph showing the results of the contact angle test of the activated implant in comparative example 5 of the present application.

Description of the main reference numerals: 1-an outer electrode; 2-a cavity; 3-an inner electrode; 4-outer wall; 5-inner wall; 6-high voltage power supply; a-an inner layer quartz tube; b-outer quartz tube.

Detailed Description

In order to make the objects, technical solutions and advantages of the embodiments of the present invention clearer, the technical solutions in the embodiments of the present invention will be clearly and completely described below. The examples, in which specific conditions are not specified, were conducted under conventional conditions or conditions recommended by the manufacturer. The reagents or instruments used are not indicated by the manufacturer, and are all conventional products available commercially.

The method for activating an implant and the activated implant provided by the present application will be described in detail below.

The inventors have long studied that the reason why the hydrophilicity of the previously activated implant is difficult to maintain for a long period of time is mainly contamination of surface carbides. In the production and processing process, the existence of carbon dioxide in the environment enables the hydrophilic surface of the implant to easily form molecular bonds with carbon molecules, the hydrophilic surface of the implant is adhered to the surface of the implant, so that the hydrophilic surface of the implant cannot be combined with water molecules and becomes hydrophobic, and the process makes the storage of the hydrophilic implant quite difficult.

The application provides an implant activation method, which comprises the following steps: and (3) carrying out activation treatment on the implant to be activated under the irradiation of the excimer light source.

Wherein the excimer light source provides 148-196nm and vacuum ultraviolet rays with photon energy of 6.3-8.4eV to the implant to be activated.

In an alternative embodiment, the excimer light source provides the implant to be activated with vacuum UV light at 184nm and with photon energy of 6.7-7.8 eV. Preferably, vacuum ultraviolet light of 172nm and having a photon energy of 7.2eV is provided.

In an alternative embodiment, the distance between the excimer light source and the implant to be activated is 10-100mm and the activation time is 0.5-30 min.

In an alternative embodiment, the distance between the excimer light source and the implant to be activated is 10-50mm, preferably 30 mm.

In an alternative embodiment, the activation time is 0.5-5min, preferably 1 min.

In an alternative embodiment, the implant may be a dental implant.

In an alternative embodiment, the implant comprises a titanium implant.

The excimer light source is a non-coherent light source, and the special light source is not a molecule or an atom, but an excited state molecule which cannot exist stably. The excimer exists as an excited molecule in an unstable state for a very short time, and then it is decomposed by transition to a ground state by spontaneous radiation, while emitting photons and energy.

The excimer molecules can be divided into four types: noble gas diatomic excimer (R)_g2X), halogen excimer (X)₂Rare gas-halogen excimer (R)_gX), and mercury-halogen excimer (H)_gX*)。

The formation of the excimer molecules is mainly divided into three processes: respectively, ionization excitation, excimer formation and irradiation of photon energy. Take rare gas-halogen excimer as an example: firstly, rare gas molecules collide with electrons to be excited and ionized; then, generating rare gas-halogen excimer through Harponing reaction or three-body collision reaction; finally, the excimer decomposes into atoms and releases energy.

It follows that energy and gas pressure are two requirements for the formation of the excimer. Firstly, electrons have certain energy and can collide with each other to generate excited atoms, molecules or ions; secondly, the system has certain air pressure, so that the atom molecules in the excited state undergo a three-body collision composite reaction before attenuation or quenching.

The generation of the excimer molecules mainly comprises the following steps: dielectric Barrier Discharge (DBD), alpha particles, high energy electron beams, microwave discharge, pulse discharge, and the like.

Compared with the traditional light source, the excimer light source has the following advantages: narrow radiation spectrum, strong plasticity, high photoelectric conversion efficiency, no radiation self-absorption, large radiation area, long service life and the like.

In summary, the method for activating the implant provided by the present application uses the excimer light source ultraviolet activation technology, and utilizes the characteristic that the excimer light source emits single 148-196nm (especially 172nm) Vacuum Ultraviolet (VUV) with concentrated energy, and emits vacuum ultraviolet photon energy as high as 6.3-8.4eV (especially 7.2eV), which is enough to open most molecular bonds, to achieve the rapid removal of organic carbide on the surface of the implant (such as a dental implant), so as to rapidly obtain a hydrophilic implant with a longer hydrophilic effect retention time before the implant operation. In addition, ozone can be formed in the activation device in the excimer light source ultraviolet activation process, the ozone is decomposed to generate active oxygen, and the active oxygen can be attached to the surface of the implant, so that direct interaction can be better generated between the active oxygen and the osteogenic protein and osteoblasts in body fluid, and the excimer light source ultraviolet activation device has higher hydrophilicity and bioactivity.

Further, the implant activation method may further include, before the activation treatment, pre-treating the implant to be activated to form holes on the surface of the implant.

In an alternative embodiment, the pre-treatment comprises grit blasting the surface of the implant to be treated to form primary holes in the surface. The primary pores may, by reference, have a diameter of 20-200 μm. The primary pores formed by sand blasting can promote the adhesion of osteoblasts.

As a reference, the blasting material used for the blasting treatment may include, for example, rutile sand or corundum sand. The preferred rutile sand that adopts carries out sand blasting to the implant surface, and the rutile sand not only makes pure titanium implant surface not have the interference of other foreign element, and the large granule sandblast can also effectively form one-level hole, reaches the purpose that promotes the osseointegration.

In an alternative embodiment, the blasting distance during the blasting process is 5-15mm, such as 5mm, 6mm, 8mm, 10mm, 12mm or 15mm, etc., preferably 8-12 mm. The sand blasting distance is controlled to be 5-15mm, the sand blasting efficiency can be improved, and a primary hole structure can be formed quickly.

In an alternative embodiment, the blasting angle during the blasting process is 30-60 °, such as 30 °, 35 °, 40 °, 45 °, 50 °, 55 °, or 60 °, etc., preferably 40-50 °. In the application, the sand blasting angle is controlled to be 30-60 degrees, so that the depth of the hole is deeper, and osteoblast attachment is facilitated.

In an alternative embodiment, the blasting time is 10-20s, such as 10s, 12s, 15s, 18s or 20s, etc., preferably 13-17s during the blasting process. The sand blasting time is controlled to be 10-20s in the application, so that a uniform hole structure can be formed, and the change of the size of the implant can not be caused.

Further, the pre-treatment may further include performing an acid etching treatment on the surface of the implant subjected to the sand blasting treatment to form secondary holes on the surface. For reference, the secondary pores may be less than 5 μm in diameter. The secondary holes are formed through acid etching treatment, so that the adhesion of protein can be promoted, the osteogenesis efficiency is improved, and the size and distribution of the holes on the surface of the implant can be regulated and controlled, so that the implant can be combined with cells more easily.

By reference, the acid used for the acid etching treatment may include, for example, sulfuric acid or hydrochloric acid.

In an alternative embodiment, the acid etching treatment may be performed at 50 to 100 ℃, preferably 50 to 70 ℃, more preferably 60 ℃. In the application, the acid etching treatment temperature is controlled to be 50-70 ℃, so that a hole structure can be formed in a relatively mild way, and the acid liquor is prevented from volatilizing.

In an alternative embodiment, the acid etching treatment time is 3-120min, preferably 50-70min, more preferably 60 min. In the application, the acid etching treatment time is controlled to be 50-70min, so that a uniform hole structure can be formed, and the surface is not excessively corroded.

In an alternative embodiment, the excimer light source in the present application is provided by an excimer lamp.

The excimer lamp comprises an inner quartz tube and an outer quartz tube which are coaxially arranged, a closed annular cavity is formed between the inner quartz tube and the outer quartz tube and is used for filling inert gas or halogen, an inner electrode is arranged on the inner wall of the inner quartz tube, an outer electrode is arranged on the outer wall of the outer quartz tube, and the outer electrode and the inner electrode are both electrically connected with a power supply.

The operation principle and the using method of the excimer lamp can be referred to the prior art, and will not be described in detail herein.

In an alternative embodiment, the outer quartz tube has a length of 100-500mm, a width of 30-120mm and a height of 1-5 mm. Preferably, the outer quartz tube has a length of 140mm, a width of 40mm and a height of 1.5 mm.

In an alternative embodiment, the inner quartz tube has a length of 150-700mm, a width of 20-90mm and a height of 0.8-2.5 mm. Preferably, the inner quartz tube has a length of 200mm, a width of 25mm and a height of 1 mm.

In an alternative embodiment, the discharge gap of the excimer lamp is 5-7mm, preferably 6 mm.

In an alternative embodiment, the inert gas may include xenon, for example. Compared with other inert gases, the inert gas used as the inert gas has higher color temperature, more aggregation and lower energy consumption.

In an alternative embodiment, the material of the inner electrode may comprise stainless steel.

In an alternative embodiment, the inner electrode is in the form of a sheet.

In an alternative embodiment, the inner electrode is a stainless steel sheet.

In an alternative embodiment, the thickness of the inner electrode may be 0.02-0.1mm, preferably 0.05 mm.

In an alternative embodiment, the material of the outer electrode may comprise stainless steel.

In an alternative embodiment, the outer electrode is mesh-shaped.

In an alternative embodiment, the outer electrode is a stainless steel mesh.

In an alternative embodiment, the excimer lamp has a transmittance of > 80% for ultraviolet light with a wavelength of 200nm, and the whole lamp body can be made of synthetic quartz of GE corporation.

On the basis, the common chemical bond binding energy is shown in fig. 1, and vacuum ultraviolet rays with the wavelength of 172nm can be generated by using an excimer lamp technology (the wavelength distribution range schematic diagram of an excimer lamp is shown in fig. 2), so that the photon energy of 7.2eV (166Kcal/mol) is excited, and is greater than that of common ultraviolet rays by 4.9eV (113Kcal/mol), thereby rapidly cutting off the molecular chemical bonds of most organic matters, and achieving the effects of surface modification and hydrophilic activation. And the ultraviolet ray with the wavelength of 172nm is easily absorbed by oxygen to generate active oxygen and ozone, and the ozone can be decomposed to form the active oxygen: o is₂+ hv → active oxygen, O₃+hv→O₂+ an active oxygen.

After the chemical bond of the surface carbide is cut off, the atoms on the surface of the titanium metal can be rapidly combined with active oxygen, and after a series of reactions, a hydrophilic oxidation film is generated, the wetting angle of the material is reduced, and thus the purpose of activating the surface of the implant is achieved.

In addition, the application also provides an activated implant which is activated by the implant activation method.

In an alternative embodiment, the contact angle of the activated implant after activation is 0-0.5 °, preferably 0 °. It is worth noting that the contact angle of the activated implant after being activated is close to 0 degrees after being placed in the air for 15 min.

In an alternative embodiment, the activated implant after activation has a surface C content of 9.1-16%, a N content of 0.5-0.7%, an O content of 57-64%, a Mg content of 0.3-0.9%, a Si content of less than 1, preferably 0.6%, a S content of 0.2-0.4%, a Ca content of 0.4-0.7%, a Ti content of 20-23%, a Zn content of 0.1-0.4%, and an I content of less than 0.3%, preferably less than 0.1%, in atomic percentage.

Namely, the contact angle of the surface of the activated implant irradiated by the excimer lamp is lower, the hydrophilicity can be kept for a longer time, the content of oxygen and titanium on the surface is higher, and the content of pollution elements is lower.

The features and properties of the present invention are described in further detail below with reference to examples.