TW202466B - - Google Patents
Download PDFInfo
- Publication number
- TW202466B TW202466B TW081103767A TW81103767A TW202466B TW 202466 B TW202466 B TW 202466B TW 081103767 A TW081103767 A TW 081103767A TW 81103767 A TW81103767 A TW 81103767A TW 202466 B TW202466 B TW 202466B
- Authority
- TW
- Taiwan
- Prior art keywords
- nvp
- implant material
- gamma radiation
- graft polymerization
- solution
- Prior art date
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/14—Macromolecular materials
- A61L27/16—Macromolecular materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/28—Materials for coating prostheses
- A61L27/34—Macromolecular materials
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/02—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber
-
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G02B1/041—Lenses
- G02B1/043—Contact lenses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/14—Eye parts, e.g. lenses, corneal implants; Implanting instruments specially adapted therefor; Artificial eyes
- A61F2/16—Intraocular lenses
- A61F2/1613—Intraocular lenses having special lens configurations, e.g. multipart lenses; having particular optical properties, e.g. pseudo-accommodative lenses, lenses having aberration corrections, diffractive lenses, lenses for variably absorbing electromagnetic radiation, lenses having variable focus
- A61F2/1648—Multipart lenses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/0077—Special surfaces of prostheses, e.g. for improving ingrowth
- A61F2002/0086—Special surfaces of prostheses, e.g. for improving ingrowth for preferentially controlling or promoting the growth of specific types of cells or tissues
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2400/00—Materials characterised by their function or physical properties
- A61L2400/18—Modification of implant surfaces in order to improve biocompatibility, cell growth, fixation of biomolecules, e.g. plasma treatment
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2430/00—Materials or treatment for tissue regeneration
- A61L2430/16—Materials or treatment for tissue regeneration for reconstruction of eye parts, e.g. intraocular lens, cornea
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/06—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation
- B05D3/068—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to radiation using ionising radiations (gamma, X, electrons)
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Ophthalmology & Optometry (AREA)
- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Medicinal Chemistry (AREA)
- Physics & Mathematics (AREA)
- Wood Science & Technology (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Graft Or Block Polymers (AREA)
- Materials For Medical Uses (AREA)
- Prostheses (AREA)
- Polymerisation Methods In General (AREA)
Description
202466 Λ 6 η 6 經濟部十央標準局Α工消许合作社印製 五、發明説明() 本發明你鼷於一種眼部植入物及其製迪方法·藉以改 進其材質表面的性質。 本發明是延鑛美國専利第304479號申請案的發明精 神,但内容不同;第304479號申謫案之申誚日為1989 年2月1日,該申請案又是延鑛美画專利的發明播神。 第037153號申讅案之申請日為 1987年4月10日, 其美國専利證耆第480638(號像於1989年2月21日 由美國專利局發予。 據研指出眼睛植入物如眼内逸鏡 (I0L)於手術時嵌 入眼瞒後,會將導致相當數量之眼角膜内皮組織之損倕, 只有當眼瞒植入物與眼角膜内皮組鐵之間没有任何接觸時 才不會造成眼角膜内皮組鐵之損傷。大部份的眼臃植入物 是由疏水性之聚甲基丙烯酸甲酯(PMHA)所製成。PMMA 聚合物具有極佳的光學性質,並且可以抗拒生物降解作用 。但是卽使在PMMA聚合物表面偁然接K内皮細胞的時候 ,PHHA聚合物表面都會黏附内皮組織並且在PMMA聚合 物表面與内皮組織分雄時都會使得部份内皮組織剝離並黏 附於PMMA聚合物表面上。间樣的道理,當PMMA聚合物 表面與其他眼部的組嫌如虹彩接嫌時,也會黏附其他眼躕 組雜而造成組織傷害。其他疏水性聚合物如聚丙烯(PP) ,聚氟亞乙烯 (PVDF),聚«酸_ (PC),聚硅«烷 (PSI)等雖然都可以作為眼晴植入物但是都會黏附眼部組 雜而迪成眼部組嫌的傷寄。 即使在PMMA製的眼睛透鏡與眼角膜内皮組鐵作短暫 而無創傷性之接«時,亦會造成眼角膜内皮組織之廣泛傷 (請先.閲讀背而之注意市項#项寫本ί 裝- 訂_ 線< 本紙5良尺度遑用中a B家橒準(CNS) T4規格(2丨0><297公沘) A 6 η 6 203466 五、發明説明() 害。此種猞點可見於下列文獻:Bourne et al, A·. J. Ophthalmol., Vol. 81, PP.482-485 (1976) 5 Forster et al, Trans. An. Acad. Ophthalaol. Otolaryngol., Vol. 83, OP- 195-OP-203 (1977) ; Katz et al,202466 Λ 6 η 6 Printed by the Shiyang Standardization Bureau of the Ministry of Economic Affairs, Cooperative Society V. Description of the invention () The present invention is based on an ocular implant and its method of preparation · thereby improving the properties of its material surface. The present invention is the spirit of invention of the Yanmin Mining Application No. 304479, but the content is different; the filing date of the No. 304479 application is February 1, 1989, and the application is the invention of the Yanmei Mining Painting Patent. Soothe. The application date of the No. 037153 application is April 10, 1987, and its US Patent No. 480638 (the image was issued by the US Patent Office on February 21, 1989. According to research, eye implants such as ocular After the endoscopic (I0L) is embedded in the eye concealment during surgery, it will cause a considerable amount of damage to the corneal endothelial tissue, only when there is no contact between the eye concealment implant and the corneal endothelial group iron Causes iron damage to the corneal endothelium. Most of the ocular implants are made of hydrophobic polymethyl methacrylate (PMHA). PMMA polymer has excellent optical properties and can resist biological Degradation. But when the PMMA polymer surface is connected to K endothelial cells, the PHHA polymer surface will adhere to the endothelial tissue and when the PMMA polymer surface is separated from the endothelial tissue, it will cause part of the endothelial tissue to peel off and adhere to the endothelial tissue. On the surface of the PMMA polymer. For the same reason, when the surface of the PMMA polymer is in iridescence with other eye groups, it will also adhere to other eye groups and cause tissue damage. Other hydrophobic polymers such as polypropylene (P P), Polyvinylidene fluoride (PVDF), poly «acid_ (PC), polysilicon« (PSI), etc. can be used as eye implants, but they will stick to the eye group and become the eye group. Even if the PMMA eye lens and the corneal endothelial group make a short and non-invasive connection, it will cause extensive damage to the corneal endothelial tissue (please read back and pay attention to the market item # Item write-up 記-資 _ 線 < 5 good scales of the original paper are used in a B home standard (CNS) T4 specification (2 丨 0> < 297 gong) A 6 η 6 203466 V. Invention description () Harm This kind of lynx can be found in the following documents: Bourne et al, A ·. J. Ophthalmol., Vol. 81, PP.482-485 (1976) 5 Forster et al, Trans. An. Acad. Ophthalaol. Otolaryngol., Vol. 83, OP- 195-OP-203 (1977); Katz et al,
Trans. Ad. Acad. Ophthalaol. Otolaryngol., Vol. 83, OP-204-OP-212 (1977) ί Kaufman et al.Trans. Ad. Acad. Ophthalaol. Otolaryngol., Vol. 83, OP-204-OP-212 (1977) ί Kaufman et al.
Science, Vol. 198, PP. '525-527 (1977) ; Sugar et al, Arch. Ophthaleol., Vol. 96,PP.449-450(1978) 〇 上述文獻都談論到植入物表面與内皮組嫌接觸時所産生問 題之諸種現象。 然而於手術過程中很難不讓植入物表面與眼角膜内皮 組織或其他敏戚的眼部組孅如虹彩與睫狀溝等有所接觸, 故有些研究者藉著修》PMMA眼睛植入物表面的方法來減 少植入物表面對眼角膜内皮組鍇之黏附與傷赛。 修飾眼臃植入物表面之方法不只一種,有些方法你以 不同種類的親水性聚合物溶液或以可溶性塗層塗於眼晴植 入物表面,以減少植入物表面對内皮組嫌細胞之黏附性。 逭些親水性聚合物溶液或塗靥包括甲基繼維素與聚乙烯基 咯烷酮(PVP)。 上述修飾眼睛植入物表面的方法可見於 下列文獻:Katz et al, supra, and Knight et al, Chen. Abs., Vol, 92 : 203547f (1980)。上逑方法固然 對内皮組餓細胞有暫時之保護作用,然而仍然不能令人滿 意。因為上述方法所製成之塗層並不能適當黏附於植入物 表面,當嵌入眼睛之時或之後,塗層會移動或變谢,在手 術後更會迅速溶解,甚至會發生手術後併發症等現象而使 本紙尺度边用中a Η家«毕(CNS) 規格(210X297公龙) (請先閲1?背而之注愈事項#構寫.^〆 裝- 經濟部屮央標準局只工消f合作杜印製 202466 A 6 η 6 經濟部中央標準局A工消伢合作杜印製 五、發明説明() 手術更為後雜。更進一步而言,上述方法均不能産生均勻 一致之塗層亦難以控制塗層之厚度。耶饞等人〔請參閲下 列文獻: Yalon et al, Acta: XXVI, International Congress of Ophthalaologyt ed. Paul Henkind (1983)〕IT試以伽瑪輻射激起乙烯基咯烷釅(NVP)聚 合於PMMA植入物表面以形成保護性塗層,但是因為控制 塗層之光學性質與組鏃保漱性質有相當大的問題,故此種 以單腰聚合於PMMA材質表面的方法並不成功。耶睡等人 的之方法無法指定反應遇程之條件舆參數(例如單鱷濃度 ,伽瑪輻射爾量舆劑量率等)。以耶皤等人所述之方法所 得之塗層品質極差,塗層棰不均匀及其機械性質極不穩定 等諸多缺失。 利用PTFE伽瑪一 PVP處理方式己見於報告,但在 嚴重情況下,需要伽瑪JHS約在1 Mrad上下,如此, PTFE的《稹和表面待性都發生變異,故不迪用 [Boffa et al, J.Biomed Mater, Res. Vol. 11, P317 (1977)] 。 單腥高濃度非親水性溶液(此匕啶中之50J: NVP )之採 用,亦痛要相當高劑《 (1-5 Mrad)之伽瑪射線造成高程 度的接枝現象,但PTFE之體積和表面待性變異更大,因 PTFE通常在約1 Mrad劑悬之伽瑪射線下,即鞋易質變 0 本發明之發明人層經完成一種表面聚合方法己獲得美 國專利,其美國專利證窨第480638 2號像於1989年2 月21曰由美國專利局發予。該專利僳以伽瑪輥射激起親 水性單腰在聚合物製成之眼睛植入物表面接枝聚合成塗層 (請先閲讀背而之注意事項孙填窍立 裝. 訂_ 線· 本紙張尺度逍用中a Η家標準(CHS)肀4規格(210X297公址) 202466 Λ 6 Η 6 經濟部屮央摇準局A工消货合作杜印製 五、發明説明() 之方法,可以成功的克服耶睡等人所述的方法之諸多困難 與缺失。 本發明人在第 4806382號美圔專利中發現採用某些 待定反應過程之條件舆參數中可以得到棰薄之表面塗層。 在上述専利中所使用的單醱為乙烯咯烷酮(NVP),羥 乙基丙烯酸甲酯 (HEMA)或NVP與HEMA共聚物上述單 醱也可以離子性單鱧混合並,以本發明所述的方法在材質表 面形成共聚物。可作為眼睛植入物之材質包括聚甲基丙烯 酸甲酯(PMMA),聚丙烯(PP)聚氟亞乙烯(PVDF), 聚 磺酸酯(PC),聚硅氣烷(PSi)。 上述専利係以伽瑪輻 射撖起單饑於植入物表面接枝聚合形成捶薄之塗層。此種 塗層可以增加植入物表面之親水性並減少嵌入物表面鲟敏 感眼部組織如虹彩與眼角膜内皮組餓之黏附作用,故可減 少植入物與組鐡接觸時對組織之傷害與手術後發生併發症 的機會。以第480632號美國専利所用之方法處理材質表 面後可形成一層薄而均勻之塗層。由於塗層偽以化學结合 之型式與眼睛植入物之表面结合,故塗層可以使用更久, 不易移除、不易降解亦不易變壊,此為習用技術所不及之 處0 本發明偽以伽瑪輻射激起 NVP , HEMA或NVP與 HEMA混合之單《於限两植入物表面形成 PVP , PHEMA 或P(NVP-HEHA)接枝聚合物之表面塗層,上述靑面接枝聚 合反應偽於水溶液中進行並符合下列各反鼴條件之姐合: (甲)單體濃度於0.5至50重董百分率之範園間; (乙)伽瑪輻射之结量於0.01至0.50Mrad之範圃間ί -先 *閲 ih 背 而 之 注 意 事 項 堝 寫 裝 訂Science, Vol. 198, PP. '525-527 (1977); Sugar et al, Arch. Ophthaleol., Vol. 96, PP.449-450 (1978). The above documents all talk about the implant surface and endothelial group. All kinds of phenomena caused by the problem of contact. However, it is difficult to prevent the surface of the implant from contacting the corneal endothelial tissue or other sensitive eye groups such as iridescent and ciliary sulcus during the operation, so some researchers implanted PMMA eye implants Method to reduce the adhesion and injury of the implant surface to the corneal endothelial group. There are more than one method to modify the surface of the ocular implant. Some methods apply different types of hydrophilic polymer solutions or soluble coatings to the surface of the ocular implant to reduce the surface of the implant to the endothelial group. Adhesion. Some hydrophilic polymer solutions or coatings include methyl methoxine and polyvinyl pyrrolidone (PVP). The above method of modifying the surface of the eye implant can be found in the following literature: Katz et al, supra, and Knight et al, Chen. Abs., Vol, 92: 203547f (1980). Although the above method has a temporary protective effect on endothelial cells, it is still not satisfactory. Because the coating made by the above method cannot be properly adhered to the surface of the implant, the coating will move or change when it is embedded in the eye, or it will dissolve quickly after the operation, and even post-operative complications may occur. Phenomena and other phenomena make this paper use the standard a Η home «Bi (CNS) specifications (210X297 male dragon) (please read 1? Back to the note more matters # 建 写. ^ 〆 装-Ministry of Economic Affairs Industry and Consumers f cooperation Du Printing 202466 A 6 η 6 Ministry of Economic Affairs Central Standards Bureau A Industry and Consumer Cooperation Du printing V. Description of the invention () The operation is more complicated. Furthermore, the above methods can not produce a uniform It is also difficult to control the thickness of the coating. Ye et al. [Please refer to the following documents: Yalon et al, Acta: XXVI, International Congress of Ophthalaologyt ed. Paul Henkind (1983)] IT tried to stimulate ethylene with gamma radiation NVP is polymerized on the surface of the PMMA implant to form a protective coating, but because of the considerable problems of controlling the optical properties of the coating and the protective properties of the component, this type of single waist polymerized PMMA material The superficial method is not successful. The human method cannot specify the conditions and parameters of the reaction process (such as single crocodile concentration, gamma radiation dose and dose rate, etc.). The quality of the coating obtained by the method described by Ye Zi et al. Is extremely poor, and the coating is not good. There are many defects such as unevenness and extremely unstable mechanical properties. The treatment method using PTFE gamma-PVP has been seen in the report, but in severe cases, the gamma JHS is required to be around 1 Mrad. Both sexes are mutated, so it is not recommended to use [Boffa et al, J. Biomed Mater, Res. Vol. 11, P317 (1977)]. The single high-concentration non-hydrophilic solution (50J in this dagger: NVP) The use of it also requires a fairly high dose of "(1-5 Mrad) gamma rays to cause a high degree of grafting, but the volume and surface waitability of PTFE vary more, because PTFE is usually suspended at about 1 Mrad. Under the Mar ray, the quality of shoes changes. The inventor of the present invention has obtained a US patent after completing a surface polymerization method. The US Patent No. 480638 No. 2 image was issued by the US Patent Office on February 21, 1989. The patent uses gamma roller to stimulate the hydrophilic waist to polymerize The surface of the prepared eye implant is grafted and polymerized into a coating (please read the precautions first. Sun fills the standing dress. Order _ line · This paper standard is used in a Η house standard (CHS) 4 specifications ( (210X297 public address) 202466 Λ 6 Η 6 The Ministry of Economic Affairs, the Central Bureau of Industry and Commerce, A Industry and Consumer Goods Cooperation, Du Printing 5. The method of invention (), can successfully overcome the many difficulties and deficiencies of the method described by Ye sleep and others . The inventor found in US Patent No. 4806382 that a thin surface coating can be obtained from certain conditions and parameters of the reaction process to be determined. The single compound used in the above-mentioned compound is vinylpyrrolidone (NVP), methyl hydroxyethyl acrylate (HEMA) or NVP and HEMA copolymer. The above single compound can also be mixed with ionic single snakes as described in the present invention. The method of forming a copolymer on the surface of the material. Materials that can be used as eye implants include polymethyl methacrylate (PMMA), polypropylene (PP), polyvinyl fluoride (PVDF), polysulfonate (PC), and polysilazane (PSi). The above mentioned method is to use gamma radiation to lift the single hungry graft on the surface of the implant to form a thin coating. This coating can increase the hydrophilicity of the implant surface and reduce the adhesion of sturgeon sensitive eye tissues such as iridescent and corneal endothelial group on the surface of the implant, so it can reduce the damage to the tissue when the implant is in contact with the group With the chance of complications after surgery. A thin and uniform coating can be formed by treating the surface of the material with the method used by U.S. Patent No. 480632. Because the coating is chemically bonded to the surface of the eye implant, the coating can be used for a longer period of time, and it is not easy to remove, degrade, and change. This is beyond the reach of conventional technology. Gamma radiation stimulates NVP, HEMA, or a mixture of NVP and HEMA to form a surface coating of PVP, PHEMA, or P (NVP-HEHA) graft polymer on the surface of the two implants. It is carried out in an aqueous solution and meets the following anti-molecular conditions: (A) The monomer concentration is between 0.5 and 50% of the weight of the standard garden; (B) The amount of gamma radiation is between 0.01 and 0.50Mrad Room ί-first * read ih back to the notes, writing and binding
MiUlL尺度边用中8«家猱準(0昍)肀4規格(2丨0><297公龙) A 6 Π6 202466 五、發明説明() (丙)伽瑪轘射之劑量率於毎分錶10至250Qrade之範圃 間; (丁)維持溶液中聚合物之分子置於250,000至5,000 ,0 00範園間。 本發明之目@在提供一種更為進步之方法以便在眼部 植入物材質之表面形成親水性之表1。 錁是,本發明旨在對依據美团專利第4806382號, 將溶液中聚合物分子量”維持”在 250, 000 至 5,0G0.G00之間,可在眼部植入物表面産生親水性表層的 方法予以艦定其非為應界狀況。 本發明更進步斷定為有效實行上述美國專利第 4806382號所掲示的方法,則伽瑪緦劑置将超越其最低值 0.001 Mrad 〇 不遇,本發明所掲改進方法最成功之《你斷定,若精 確地將上述美圃專利第 4806382號描述條件中之殘餘物 予以保持,可逹成在眼部植入物表面增加一種接枝聚合表 層。 圖式部份: 附圖1-3你依據本發明所描繪之眼部植入物之實例: 圃一你一片鼸形眼鏡之上視圓。 圈二你一種具有纖維觸威之皤形眼鏡之上視·,咳鏡 可以用光學以外的不同下層聚合物«迪者。 臞三你眼角膜彌補物之上視鼷。 詳細説明: 美國専利第4806382號所界定,在»界狀況下將聚 本紙張尺Λ遑用中B Η家標準(CNS) T4規格(210X297公龙) ........................f · !#· · · .^ (請-Λ閲讀背而之注意事項#堝寫矣 經濟部屮央標準局β工消t合作杜印製 -8-202466 Λ 6 η 6 經濟部屮央標準局访工消伢合作社印製 五、發明説明() 合溶液中克分子量維持在一定值之法並不實際。倒不如本 發明所掲示,依雄從事接枝聚合程序所得反應狀況所産生 的结果。因此,本發明不適於詳述聚合溶液中的克分子董 ,單體下層裂程狀況因其受不同伽瑪接枝影響産生廣泛的 變化。假定將一組如單醱、單臞濃度、伽瑪總劑量和伽琢 劑悬率置於固定狀況,則溶液中形成的聚合物分子量無法 獮自改變,但卻成為上逑單1龌濃度,伽瑪结劑置和伽瑪薄 量率定值的一種産物。例如,離子單鼸溶劑或基根抑制削 之出現,将被大量抑制,如果不播牲有效的表面接枝聚合 i 的話,同時,影《到溶液聚合物克分子量相對的降低(低 到 5,000-10,000 左右)。 雖然這項發明己速申請美國 4806382 K専利的程度 ,但其發明人於從事繼鑛研究中發現,雖然,其在發明中 認為0.01至0.20 Mrad是合成中相當低的_量,但在 合成作業中的伽瑪總劑量卻有低到0.001 Rrad的可能。 雖然,美國専利第4806382號所稱先前技術對伽瑪 聚合接枝有用的劑量一般高於0.5 Mrad ,同時,更驚人 地發現表面接枝可以用0.Q1 Mrad低剤量逹成,〃但本發 .明成功地鑛將有效接枝的伽瑪爾置降低到 0.01 Nrad實 為預想不到的結果。尤有進者,美國4806382號専利案 中雖將單賭壤縮接枝颳低為0.5重 X ,在同樣的實施 例中,本發明經過進一步研究發現,其單體濃度可降低為 0.1重置S;。 下列條件可有可無,若有下列條件則反應條件更為良 好: (請先閲讀背而之注意事項-l1)-项寫#. 裝· _ 線· 本紙張尺度逍用中a Η家樣毕(CNS) T4規格(210X297公徒) 202466 經濟部屮央榣準局员工消伢合作社印製MiUlL scale edge-use medium 8 «home standard (0 昍) Yu 4 specifications (2 丨 0> < 297 male dragon) A 6 Π6 202466 V. Description of invention () (C) The dose rate of gamma radiation Divide table 10 to 250 Qrade in the model nursery; (D) Maintain the polymer molecules in the solution in the 250,000 to 5,000, 00 model garden. The purpose of the present invention is to provide a more advanced method to form a hydrophilic table 1 on the surface of the eye implant material. It is the purpose of the present invention to "maintain" the molecular weight of the polymer in solution between 250, 000 and 5,0G0.G00 according to Meituan Patent No. 4806382, which can produce a hydrophilic surface layer on the surface of the ocular implant The method is to determine the status of the ship's non-compliance. The further improvement of the present invention concludes that the method shown in the above-mentioned US Patent No. 4806382 is effectively implemented, and the gamma setting will exceed its minimum value of 0.001 Mrad. The most successful improvement method of the present invention, "You conclude, if accurate The residue under the conditions described in the above-mentioned Meipu Patent No. 4806382 can be maintained to add a grafted polymer surface layer on the surface of the ocular implant. Figure part: Figures 1-3 Examples of eye implants that you describe according to the present invention: You see a circle of eyeglasses above a piece of man-shaped glasses. Circle two you look at the top of a pair of glasses with fiber touch power, cough mirror can use a different lower polymer other than optics. You see the eyebrows above your corneal prosthesis. Detailed description: As defined by the United States No. 4806382, the standard paper size Λ is used in the B Η home standard (CNS) T4 specification (210X297 male dragon) under the condition of »........ ............. f ·! # · · ·. ^ (please -ΛRead back to the notes) # 幣 写 矣 Ministry of Economics, Central Standards Bureau β 工 消 t cooperation du printing -8-202466 Λ 6 η 6 Printed by the Ministry of Economic Affairs, Bureau of Standards, Bureau of Industry and Commerce Co., Ltd. V. Description of the invention () The method of maintaining the gram molecular weight in the combined solution at a certain value is not practical. The results of the reaction conditions obtained by Xiong engaged in the graft polymerization procedure. Therefore, the present invention is not suitable for detailing the molecular weight of the polymerization solution. The cracking conditions of the monomer underlayer are widely changed due to the influence of different gamma grafts. Assuming that a group such as monosodium, monosodium concentration, total gamma dose, and gamma suspension are placed in a fixed state, the molecular weight of the polymer formed in the solution cannot be changed by itself, but it has become the concentration of the first single, A product of the setting of the gamma coagulant and the setting value of the gamma thinning rate. A large amount of inhibition, if the effective surface graft polymerization I is not broadcast, at the same time, the relative molecular weight of the solution polymer is reduced (as low as 5,000-10,000). Although this invention has been applied for US 4806382 K Degree, but the inventors found that in the mining research, although they believe that 0.01 to 0.20 Mrad is a relatively low amount in the synthesis, the total gamma dose in the synthesis operation is as low as 0.001 Rrad Although the dosage of the prior art mentioned in US No. 4806382 is useful for gamma polymerization grafting is generally higher than 0.5 Mrad, at the same time, it is more surprising to find that surface grafting can be achieved with a low amount of 0.Q1 Mrad, 〃However, the successful successful mining reduced the gamma of the effective grafting to 0.01 Nrad is an unexpected result. In particular, in the US case No. 4806382, the single-gambling soil shrinkage graft was scraped down. 0.5 X, in the same embodiment, the present invention found that after further research, its monomer concentration can be reduced to 0.1 to reset S ;. The following conditions are optional, if there are the following conditions, the reaction conditions are better : (Please read the notes on the back-l1) -item writing #. 装 · _ 线 · In this paper standard for easy use a Η 家 样 毕 (CNS) T4 specifications (210X297 public) 202466 Ministry of Economic Affairs Printed by the quasi-bureau employee consumer cooperative
It 6_ 五、發明説明() (戊)自接枝聚合反應之溶液中除去《氣ί (己)將接枝聚合於材質表面之PVP或P(NVP-HEMA)厚度 維持於100埃至150撖米之範園内; (庚)於接枝聚合反應之溶液中加入自由基清除劑; (辛)於接枝聚合之溶液中加入材質如PMMA或其他聚合 物之膨脹溶剤。 本發明係以伽瑪輻射激起NVP , HEMA ,或HVP或 HEMA混合之單鼸於PP , PVDF , PC或PSi所製成之 眼晴植入物表面形成PVP , PHEMA或P(HVP-HEMA)表 面接枝聚合物, 其反軀條件可與上述單釀接枝聚合於 PMMA之反應條件相同,若能從溶液中澝除氣氣則接枝聚 合反應之結果將會更好,且對植入物表面之修钸效果更佳 Ο 本發明在莆景部份鎗經提到耶« (Yalon)及奈特 (knight)嘗試以伽瑪輻射-敦起 NVP及HEKA聚合在 PMMA表面所形成的塗層性質不佳,所形成的塗層對内皮 組嫌有磨攢作用。奈特(Knight)以聚乙烯酵(PVA)塗 覆在眼晴透嫌表面,但是臨床試驗的结果證實其無法令人 谋意故不實用。耶皤(Yalon)及奈待(KnUht)對於單 體濃度、溶劑、伽瑪輻射劑量及劑ft率等反蠹條件無法確 認,而且其塗層的品質極差又會磨損組繊。耶陲(Yalon) ,奈特(Knight)或過去三十年以來的文獻都不能製造具 有實用性及W久性的 PVP或PHEMA塗層於PUMA材質所 製成的眼鏡透鏡表面上。在塑鏐材質表面欲製造有用的塗 層必須滿足下列複雜的要求: 本紙5艮尺度边用中a Η家樣準(CNS)肀4規格(210><297公龙) -10- -10- Λ 6 Β 6 202466 五、發明説明() (甲)接枝聚合反應所形成之塗層必須很薄,又耐 用,透明清澈且能永久塗覆於眼睛透嫌如隱形眼嫌表面。 文獻上常常使用高輻射劑量(大於IMrad)的伽瑪輻射 與非水溶劑,但所産生之塗層很厚而且有斑紋又不均匀。 髙劑量伽瑪輻射足以令材質變形或降解。此種現象亦記錄 於下述文獻中: Chapiro, Radiation Cheaistry of Polyneric Systens , John ^Wiley and Sons, Inc., New York ( 1 962)及 Henglein et al, Aiigeii. Che·., Vol. 15, P46K1958) 〇 (乙)由本發明所得的塗層在活鼸内應具有長期的 生物相容性。 (丙)由本發明所得的塗層上面放置氣泡時,氣泡 在水中的接《角必須小於30 ° (低接觸角表示具有高浸 潤作用)。 (丁)由本發明所得的塗層對組織無黏附性(對内 皮組鐡之黏附力小於150料/ca )。 (戊)由本發明所得的塗層對内皮组雄傷窨性很小 (活鼸外接》試驗對組嫌的傷害害率小於20% )。 (己)ESCA或FTIR分析可以測到接枝聚合的塗層。 (庚)在滑動摩擦試驗時,塗層的抗磨損性極高( 其接嫌角在滑動摩擦試驗前幾乎不會改變。 (辛)由本發明所得的塗層可快速水合。由本發明 所得的塗層浸入水中後由乾燥狀態轉為獮潤平》狀態,其 時間只痛5分鐘,水合速度相當快。 耶睡(Yalon) 掲示一種於活體外測Μ内皮組雄傷害 本紙尺度逍用中a Η家標準(CNS)Τ4規格(210X297公釐) (請先閲讀背而之注悉事項孙项寫 裝. 線- 經濟部屮央標準局Α工消t合作杜印奴 11- 11- A 6 It 6 202466 五、發明説明() ’’ (請先閲讀背而之注意亊項孙项窩本一 '丨 程度之技術。雖然耶陲(Yalon)指出在高單鼸濃度時, 接枝聚合的PVP塗層對細胞傷害程度較低,但是對於反 應條件如伽瑪輻射之两董及劑量率不能確認,且反應條件 與産物之間的朗像亦無法指明。 經濟部屮央標準局员Η消赀合作社印製 本發明所使用的反應遇程條件與#數必須在一定的範 圍内,才能利用伽瑪輻射瀲起有效的接枝聚合反應而形成 杜層以修飾的材質表面。本發明所得的塗層包括PVP , PHEMA或P (NVP-HEMA)。本發明所使用的反《條件與參 數包括單醱之重量百分率,伽瑪輻射剤量及劑量率,單》 對材質之滲透時間或膨脹時間,與去除氧氣等。本發明其 他較佳之反應條件包括催化剤,自由基清除劑,聚合物之 膨脹溶液與溫度等。然而溶液中聚合物之分子量與分子最 之分佈,單醱的轉換率輿剩餘未反應之單髓合物,接枝聚 合物塗層之厚度與表面性質等,皆為接枝聚合反應之结果 。上述反應之結果随着反應條件之改變而變化。例如,利 用O.IHrad 伽瑪輻射之削量照射材質表面會使得接枝聚 合反應的速度減慢而使得溶液中聚合物之分子置較高。如 果在上述的反應中去除氧氣也可使接枝聚合反應於較低伽 瑪輻射剤置下進行。於高單齷濃度之溶液中加入自由基澝 除剤,如銅鹽、雄鹽或有機邇原劑如抗壤血酸,可減低溶 液中之聚合物分子*並避免溶液凝膠化。 本發明所利用的反應過程條件與參數可在一定範函内 變動以産生待殊組合而有利於聚合物表面之表面修.銖。本 發明所利用的反«過程條件以及參數如下: (甲)單髓濃度:增加單體嬝度則接枝聚合反應溶 本紙張尺度边用中因Η家樣準(CNS) Τ4規格(210x297公釐) 202466 A 6 Π 6 - 12- 五、發明説明( 經濟部屮央標準局Α工消作合作杜印製 液之聚合物分子量會增加而接觸角會降低,故材質表面之 親水性會增加。。例如.使用 O.lMrad _量與 309rads/Bin.琍置率.之伽瑪輻射撖起 NVP接枝聚合於 PMMA表面以形成PVP塗層,當HVP之濃度由3 %增為 15 %時測得PVP之分子董(Mv)經黏度測置之結果將由 560,000增為2 , 700,000。 而且其接《I角由29。降為 21 °。 然而上述結果會受伽瑪輻射之劑量率與總_量之 \ 影響。例如伽瑪輻射之劑量率低至64rads/nin., NVP之 濃度由1 %增至10 %時, PVP之分子量由 400,000 增為4 , 590 , 000且接觸角由49 °降至18 °。 一般而言,本發明所用之單艚瀣度介於0.1至50%之 間,再配合其他反應條件。當單體之潰度低至0.1至0.5% ,並維持伽瑪輻射於低劑量率時,所産生之親水性接枝聚 合表面之接觸角可降至30°至40°之間。當單龌*度髙至 20%舆30%之範团内時必須使用自由基清除劑與低伽瑪劑 量才能産生有效之接枝聚合物並避免溶液板膠化。翥單》 濃度离於50%時,單體之轉換率將顯著降低。當HEMA之濃 度維持於在0.5至10%之範圍時,可産生良好之PHEMA塗層 塗層。 (乙)伽瑪轘射之劑量:一般而言,若增加伽瑪轘 射之總剤量可增加溶液中聚合物之分子量並滅小材質表面 接觸角。然而酋單釀之雄劑量太高,且維持低伽瑪轘射劑 量率以及离單K濃度,則溶液變得很黏稠或産生凝謬作用 ,故很難澝洗或移除(例如,伽瑪輥射剤董為Q.25Mrad 且劑量率為3 09 rads/Bin ,而NVP瀵度為10J!時)。 Τη 先 -W] 背 而 之 注 愈 項 Α 堝 % 本 本紙5艮尺度边用中a國家櫺毕(CNS) T4規格(210父297公龙) -13- 202466 五、發明説明() (請先閲讀背而之注意市項再项窍杰 本發明亦可利用霣子束輻射亦可瀲起接枝聚合反應。* 若電子束輻射之能量與伽瑪輻射之能量相同時,則可用電 子束輻射代替本發明所用之伽瑪輻射。電子束輻射之轚壓 維持於50Kev至10 Mev之範園内,其電流介於5·Α至 IOObA之間。本發明之霣子束輻射劑量率通常高於伽瑪輥 射劑量率,其劑麗率通常介於10至10 radS/ Bin之範 圔時。 (丙)伽瑪輻射或霣子束輻射之劑量率:減少伽瑪 輻射之劑量率將可增加溶液中PVP之分子置。若NVP之 單鼸灌度維持於 10%且伽瑪輥射劑量維持於 0.1 Mrad 時,而伽瑪輻射劑最率由由 1 2 35刺減至49 rads/Bin ,則材質表面之接觸角將由31 °降為15 ° ,若以霄子 束輻射代替伽瑪輻射,則其劑量率可离至if rads/*in. Ο (丁)反應溶液中聚合物之分子量:反應溶液中聚 合物之分小量會随著反應過程條件之改變,如單β濃度或 是否使用自由基淸除剤而改變。反應溶液中聚合物之分子 量低至5000或1000時,仍可産生有效的接枝聚合反* 經濟部屮央標準局A工消t合作社印¾. 。 當反匾溶液中聚合物之襄度大於5,000,000 ,}容液會 過於黏稠或産生凝謬作用而難以淸洗,所以並不實用。It 6_ V. Description of the invention () (E) Remove the gas from the solution of the graft polymerization reaction to maintain the thickness of PVP or P (NVP-HEMA) grafted on the surface of the material from 100 angstroms to 150 angstroms In the rice garden; (G) Add free radical scavenger to the solution of graft polymerization; (Sin) Add swellable material of PMMA or other polymers to the solution of graft polymerization. The invention uses gamma radiation to stimulate NVP, HEMA, or HVP or HEMA mixed single mole to form PVP, PHEMA or P (HVP-HEMA) on the surface of an eye implant made of PP, PVDF, PC or PSi The surface graft polymer, the reverse conditions can be the same as the reaction conditions of the above-mentioned single brewing graft polymerization on PMMA, if the gas can be degassed from the solution, the result of the graft polymerization reaction will be better, and the The effect of repairing plutonium on the surface of the object is better. In the invention, in the Pujing part, the gun is mentioned as "Yalon" and Knight (Knight) try to use gamma radiation-to lift the coating formed by NVP and HEKA polymerization on the surface of PMMA The properties of the layer are not good, and the coating formed may have a detrimental effect on the endothelial group. Knight coated the surface of the eyes with polyvinyl yeast (PVA), but the results of clinical trials confirmed that it was not conceivable and therefore not practical. Yalon and KnUht cannot confirm the anti-bite conditions such as monomer concentration, solvent, gamma radiation dose and agent ft rate, and the poor quality of their coatings will wear out. Yalon, Knight, or the literature over the past three decades cannot produce a practical and durable PVP or PHEMA coating on the lens surface of glasses made of PUMA. In order to make a useful coating on the surface of the plastic lutetium material, the following complex requirements must be met: The paper is used on the 5 gram scale side with a Η home sample standard (CNS) 4 specifications (210 > < 297 gong) -10- -10 -Λ 6 Β 6 202466 V. Description of the invention () (A) The coating formed by the graft polymerization reaction must be very thin, durable, transparent and transparent, and can be permanently applied to the surface of the eyes that looks like invisible eyes. The literature often uses high radiation doses (greater than IMrad) of gamma radiation and non-aqueous solvents, but the resulting coatings are thick and streaky and uneven. High dose gamma radiation is sufficient to deform or degrade the material. This phenomenon is also recorded in the following documents: Chapiro, Radiation Cheaistry of Polyneric Systens, John ^ Wiley and Sons, Inc., New York (1 962) and Henglein et al, Aiigeii. Che., Vol. 15, P46K1958 ) (B) The coating obtained by the present invention should have long-term biocompatibility in living mussels. (C) When air bubbles are placed on the coating obtained by the present invention, the connection angle of air bubbles in water must be less than 30 ° (low contact angle indicates high wetting effect). (D) The coating obtained by the present invention has no adhesion to tissues (adhesion to the inner skin group is less than 150 / ca). (E) The coating obtained by the present invention has little male injury to the endothelial group (the rate of injury to the group is less than 20%). (X) ESCA or FTIR analysis can detect the graft polymerized coating. (G) During the sliding friction test, the abrasion resistance of the coating is extremely high (its contact angle hardly changes before the sliding friction test. (Xin) The coating obtained by the present invention can be quickly hydrated. The coating obtained by the present invention After the layer was immersed in water, it changed from a dry state to a tarnished state. The time was only 5 minutes, and the hydration speed was quite fast. Yalon showed a kind of in vitro measurement of male injury in the endothelial group. Standard (CNS) Τ4 specification (210X297mm) (Please read the notes on the back of the book to read Sun Xiang. LINE-Ministry of Economic Affairs, Bureau of Standards, A Gongxiaot, Cooperative Duinu 11- 11- A 6 It 6 202466 V. Description of the invention () '' (Please read back to note the technology of the degree of Sun Xiangwo's first degree. Although Yalon pointed out that at a high concentration of monads, the PVP coating of the graft polymerization The level of damage to the cells is low, but the reaction conditions such as gamma radiation and the dose rate cannot be confirmed, and the image between the reaction conditions and the product cannot be specified. Member of the Bureau of Standards, Ministry of Economic Affairs H Xiaojun Cooperative Print the reaction bar used in the present invention And # number must be within a certain range, in order to use Gamma radiation to form an effective graft polymerization reaction to form a Du layer to modify the surface of the material. The coating obtained by the present invention includes PVP, PHEMA or P (NVP-HEMA) The conditions and parameters used in the present invention include the weight percentage of the single unit, the gamma radiation dose and the dose rate, single. The penetration time or expansion time of the material, and the removal of oxygen, etc. Other preferred reaction conditions of the present invention Including catalyst, free radical scavenger, polymer swelling solution and temperature, etc. However, the molecular weight and molecular distribution of the polymer in the solution, the conversion rate of the single compound and the remaining unreacted single myelin compound, grafted polymer The thickness and surface properties of the coating are the results of the graft polymerization reaction. The results of the above reaction vary with the change of the reaction conditions. For example, irradiating the surface of the material with the amount of O.IHrad gamma radiation will make the graft The speed of the polymerization reaction is slowed down so that the polymer molecules in the solution are set higher. If oxygen is removed in the above reaction, the graft polymerization reaction can be made at a lower gamma radiation Carry out under high temperature. Add a free radical scavenger to the solution with high single concentration, such as copper salt, male salt or organic progenitor such as ascorbic acid, which can reduce the polymer molecules in the solution * and avoid solution condensation Gelation. The reaction process conditions and parameters used in the present invention can be changed within a certain range to produce a special combination that is beneficial to the surface repair of the polymer surface. Baht. The reverse process conditions and parameters used in the present invention are as follows: (A) Concentration of single pith: increase the degree of monomer, then graft polymerization, dissolve the paper, and use it as a standard (CNS) Τ4 specification (210x297 mm) 202466 A 6 Π 6-12- 5. Invention Explanation (The molecular weight of the polymer of the Duo Printing Liquid of the Central Standards Bureau of the Ministry of Economic Affairs and Industry will increase and the contact angle will decrease, so the hydrophilicity of the surface of the material will increase. . For example, use 0.1Mrad_quantity and 309rads / Bin.Gamma radiation rate to lift NVP graft polymerization on PMMA surface to form a PVP coating, measured when the concentration of HVP increases from 3% to 15% The molecular weight (Pv) molecular weight (Mv) of PVP will be increased from 560,000 to 2,700,000. And it is connected to "I Angle by 29. Reduced to 21 °. However, the above results will be affected by the dose rate of gamma radiation and the total dose. For example, when the dose rate of gamma radiation is as low as 64rads / nin., And the concentration of NVP increases from 1% to 10%, the molecular weight of PVP increases from 400,000 to 4,590,000 and the contact angle decreases from 49 ° to 18 °. Generally speaking, the unit of the present invention is between 0.1 and 50%, and it is combined with other reaction conditions. When the degree of collapse of the monomer is as low as 0.1 to 0.5% and the gamma radiation is maintained at a low dose rate, the contact angle of the resulting hydrophilic graft polymerization surface can be reduced to between 30 ° and 40 °. When the temperature is within the range of 20% and 30%, free radical scavenger and low gamma dose must be used to produce effective graft polymer and avoid gelation of the solution plate. When the concentration of "Phu Shan" is close to 50%, the conversion rate of monomers will be significantly reduced. When the concentration of HEMA is maintained in the range of 0.5 to 10%, a good PHEMA coating can be produced. (B) The dose of gamma radiation: Generally speaking, if the total amount of gamma radiation is increased, the molecular weight of the polymer in the solution can be increased and the contact angle of the surface of small materials can be extinguished. However, if the dosage of the male single brewer is too high, and the low gamma radiation dose rate and the concentration of Li K are maintained, the solution becomes very viscous or has a condensing effect, so it is difficult to wash or remove it (eg, gamma roller When the shooting director is Q.25Mrad and the dose rate is 3 09 rads / Bin, and the NVP degree is 10J!). Τη 先 -W] Contrary to the note item Α %% of the original paper with 5 gram scale side in the use of a National Completion (CNS) T4 specifications (210 father 297 male dragon) -13-202466 V. Description of invention () (please Read first, pay attention to the market, and then know how to use the invention. The invention can also use the beam radiation and the graft polymerization reaction. * If the energy of the electron beam radiation and the energy of the gamma radiation are the same, the electron beam can be used. Radiation replaces the gamma radiation used in the present invention. The electron beam radiation is maintained at a pressure range of 50Kev to 10 Mev, and its current is between 5 · A and 100bA. The dose rate of the 霣 子 束 of the present invention is generally higher than The dose rate of the gamma roller is usually between 10 and 10 radS / Bin. (C) The dose rate of gamma radiation or beam radiation: reducing the dose rate of gamma radiation will increase The molecular weight of PVP is set in the solution. If the single-element irrigation of NVP is maintained at 10% and the dose of the gamma roller is maintained at 0.1 Mrad, the gamma radiation dose rate is reduced from 1 2 35 to 49 rads / Bin. Then the contact angle of the surface of the material will be reduced from 31 ° to 15 °. The dosage rate can be as low as if rads / * in. Ο (D) The molecular weight of the polymer in the reaction solution: the small amount of the polymer in the reaction solution will change with the reaction process conditions, such as single β concentration or whether to use free radicals It can be changed after being removed. When the molecular weight of the polymer in the reaction solution is as low as 5000 or 1000, it can still produce effective graft polymerization. If the polymer has a degree of greater than 5,000,000, the liquid will be too viscous or have a coagulation effect that is difficult to wash, so it is not practical.
(戊)去除氣醱:以真空或惟性氣鳢如氬氣從接枝 聚合之溶液中去除氣氣時,降低伽瑪輻射總劑董(實際上 其總劑量可低至 O.lMrad )亦能激起有效之接枝聚合反 應。去除氣氣對於PVP聚合物之分子量單黼轉換率與有 相當的彩響。例如,於伽瑪輻射劑量為0.05Mrad輿NVP 本紙張尺度边用中a s家標iMCNS) T4規格(210x297公*) 202466 A 6 It 6 14 經濟部中央櫺準局A工消价合作杜印製 五、發明説明() 單體灌度為10 %時,若去除氣氣,可將NVP接枝聚合 於PP上而形成良好之 PVP表面塗層,其接觸角為15 °。若不去除氧氣,則於上述條件中很難進行接枝聚合反 應。因此去除氣氣對産生良好的PVP表面塗層非常重要 。當材質為PP,PVDF或PSi時,於其表面接枝聚合須先 去除氣體,否則無法産生良好的PVP表面塗層。去除氣 氣亦有助於單醴在PMMA或、PC表面産生良好的表面塗層 ,即利用極低的伽瑪輻射剤置(0.01至0.15 Mrad)就 可以在PKMA或PC表面形成有效的接枝聚合物。在上述 反應條件之下,若不先去除氣氣,則接枝聚合之效果不良 0 (己)接枝聚合物之厚度:酋接枝聚合物所形成之 塗層厚度極薄時(100至200埃),固然具有親水性且 對組嫌沒有黏附性,但其機械性質太軟也可能産生類似凝 膠之塗層所以與組嫌接觸時容易引起創傷。當接枝聚合塗 層的層厚度為300 - 500埃至50撖米之間較適合於許 多不同的用途。較厚之表面塗層具有光》、均勻、光學清 澈及迅速水合等性質。 若不使用膨脹溶劑亦不延長單體與材質表面之接觭時 間,則接枝聚合塗層之厚度較薄,其厚度約為0.1至5 微米。若使用膨脹溶劑如乙酸乙酯,則PMMA表面接枝聚 合塗層之厚度約為100撤米以上。 在有些特殊的應用中須使表面塗層之厚度速到20至100 撤米,.以形成較厚的海棉狀塗層。 (庚)自由基清除劑:常用還原劑如Cu · Fe , (請先閲誚背而之注意事項#艰寫太| 本紙张尺度逍用中a Η家搮準(CNS) T4規格(210X297公:《:) 202466 五、發明説明() 抗痰血酸等捕獲自由基,可有效抑制溶液中自由基之聚合 反應。(待別在高單讎灌度•高伽瑪輻射劑置及劑量率時 ),因而可減缓溶液之謬凝作用。然而使用自由基淸除雨 亦有下述缺黏,即導致聚合物分子景較低,未反應單髓較 多與分子量分佈較寬。若使用金靥鹽類則對生物相容性較 為不利。 纗是於大部份之接枝反窿中,鼴儋量避免使用自由基 清除劑,然而於形成PVP , PHEMA或P(HVP-HEMA)塗 層時抗血酸有助於降低溶液&拥性與凝膠作用。在上述條 件下,於單醱溶液中加入乙酸乙酯(0.5至5 % )作溶 劑·即使單醱之濃度高至5〇χ亦可得到較厚之表面塗層 且能避免溶液之黏稠性與凝驊作用。 (辛)膨脹溶液:於單《溶液中加入材質之有效的 膨脹溶劑對材霣之膨脹有利並對單鼸在材霣表面之散有所 助益。於照射伽瑪輻射之前與之時均會發生上述現象。單 醱對材質作充分的滲透可增加表面塗層之厚度並提离表面 塗層於材質表面鍵結之程度。 乙酸乙酯可作為材質如 ΡΜΜΑ之有效的膨脹溶剤。 經濟部屮央標準局β工消t合作杜印3i 本發明利用(甲)至(辛)之方法可得良好之表 面接枝聚合物,此種方法為習用方法所不及。由於上述方 法之參數及條件的组合可作不同的遘擇,因此所得的结果 不同。 若 NVP 與 ΗΕΗΑ 單驩於材質表面共聚成 Ρ (NVP-HEMA)表面塗層,則ΗΕΜΑ於NVP及ΗΕΜΑ單鼸混 合物中之繼度可以高逹 50重麗百分率。然而ΗΕΜΑ及 本紙5艮尺度逍用中a S家標毕(CNS) >f 4規格(2】0X297公;«:) 202466 經濟部屮央標準局页工消价合作社印奴 五、發明説明() NVP及HEMA單醱混合物中之灌度若离連 20至30S;時 ,則單腰混合物中必須使用自由基淸除劑且須降低單朦路 應度才能避免溶液凝睡作用,因為HEMA會促主溶液凝謬 作用。 雖然上述方法代表了一種對先行技術的重大改進,而 每一傾案之最適合結果端視對執行參數镧數的組合以及現 場條件的遘擇而定。 本發明不但可以利用NVP , HEMA或NVP及HEMA單«以形 成?卩?,?〇>^或?(》^?-1^1(/0表面塗層,還可以在上述單酸 中加入不同的雔子性單醴。又非離子性單《與離子性單B 可以形成共聚物。本發明所用的離子性單鼸包括乙烯«酸 ,苯乙烯磺酸,硫乙基丙烯酸甲酯,硫丙基丙烯酸甲酯或 其他乙烯基磺酸,或乙烯羧酸甲酯,丁烯酸或異丁烯酸等 均可作為陰離子性單龌。本發明所用的離子性單*若含有 齡基或胺基等官能基的單醱如乙烯啶,親基苯乙烯.丙 烯酸氨酯,或氛基丙烯酸甲酯如二甲基氛乙基丙烯酸甲酯 或二甲基氨苯乙烯等均可作為限離子性單B。本發明也可 以混合離子性單腥之鹽類與非離子性單體以形成共聚物。 考嫌上述現象及反應過程,不同材質所裂成之物品須 應用不同的反應條件,將列舉於下述諸實施例將詳述本發 明所需之條件。在此先概述一些反匾條件之重點如下: 決定反應條件之範圍對於裂得應良産物非常有用。最 佳反應過程之S擇須視材質分子結構與接枝聚合塗層厚度 而定。本發明應避免使溶液黏稠或産生凝睡作用之條件, 同時應避免使材質龜裂或産生裂痕之反應條件。(例如离 (請先閲讀背而之注意事項#项寫吏 _丨 本紙張尺度逍用中a國家樣準(CNS) τ 4規格(210X297公;«:) 202466 Λ 6 Η 6 經濟部屮央榣準局Μ工消t合作社印Μ 五、發明説明() 於203!之乙酸乙酯作為PMMA之膨脹溶薄I)。以下四僱反鼴 過程的條件對於改進材質表面的性質非常實用: (1) 水溶液中單覼之濃度維持於5至20%之範鼷内(最 佳》度為10%)。伽瑪輻射之劑量維持於〇.〇5至0.20Mrad 之範圔内(最佳劑量為O.lOMrad)。伽瑪輻射之劑量率維持 於2 0至1500 0rads/nin之範圍内(最佳劑董率為50至2000 rads/atin)。接觸角小於30°。 (2) 除了多出清除氣氣之條件外,其他條件與(1)相 似。可用真空或氬氣等惰性氣醴清除氣氣,伽瑪輻射之劑 量維持於0.01至〇.15Mrad之範園内(最佳劑置為0.05Mrad) 。NVP單體之重量百分率維持於1至15%之範圍内(最佳重 量百分率為5至10%)。清除氣氣後之反應條件比(1)更佳。 (3) 除了多出膨脹溶劑之條件外,其他條件與(1)及 (2)相似。例如以乙酸乙酯作為PUMA材質之膨脹溶剤,可 使更多單體滲透至材質表面並增加接枝聚合塗層之厚度。 (4) 使用高單驩濃度(25至50%),小於5%之乙酸乙 酯膨脹溶液,及自由基淸除剤如抗壊血酸(濃度為0.1至 I.ObM)。又伽瑪輥射之劑量維持於0.10至0.20Mrad之範圃 内,劑量率維持於20至50 0 0 rads/Bin之範圔内。 上述百分比若無特別指示,均為重量百分率。 若無特別陳述,所有接《角及表面性質之測定皆先經 下列處理過程•·伽瑪輻射接枝聚合反應所得之塗層先於室 溫中或高於室溫之水或水與酒精混合之溶液中洗除剌餘之 單體與未接枝聚合之聚合物以增進材質表面之性質。接枝 聚合之塗層性質穩定可經常期使用而不會溶於水溶液中。 本紙張尺度边用中國困家榣準(CNS)肀4規格(210X297公釐) 202466 Λ 6 Η6 18· 經濟部中央榣準局Α工消费合作社印製 五、發明説明() 本發明可在下述材質包括ΡΗΜΑ, PP, PVDF, PC與 PSi表面製得接枝聚合塗層。本發明可在上述材質表面作 部份接枝聚合或全部接枝聚合以增進器材或器具之材質表 面的性質。 本發明所採用的親水性接枝聚合物表面修飾方法,對 於嵌入眼内各部(如前房、後房、晶狀《)的眼透嫌特別 有利。同時,對肌肉組餓的保護,以及對其他眼部植入物 ,如角膜鑲嵌物、角膜補缺物、外角膜手術器具、靑光眼 分流器、視網膜鎖琛與固膜扣等生物相容性的改進,皆具 重大價值。 *施例1 : 本實施例指出由於改變上述反應遇程之搽件與伽瑪賴 射激起PVP接枝聚合於PMMA表面之聚合參數將對反應之結 果産生重要之效醮。 先將PMMA板片之樣品用肥皂溶液澝洗兩次,再用蒸 胞水於超音波處理機中清洗。當PMMA板片完全乾燥後, 將樣品置於含有NVP溶液之玻瑰品中。再以不同條件之 伽瑪輻射照射搛品。於照射伽瑪輻射之後,再以淸水淸洗 PMMA表面數次。 以NVP接枝聚合於PHUA樣品表面後,再将樣品置於真 空中冷凍乾燥。溶液中之PVP搛品可用黏度計测定分子量 Oiv)或用凝睡滲透層析儀測定分子量(Mw)。拥定Mv時.可 將PVP溶於蒸躕水中,並於時用毛細黏度計測定其特 性黏度。 PVP接枝聚合於PMHA表面之塗層可用水滴或水中氣 (請先背而之注意事項#项舄木< 裝· 訂- 線. 本紙5艮尺度边用中a B家楳準(CNS)肀4規格(210X297公址) 202466 -19- Λ 6 Π 6 五、發明説明() 泡測量其接觸角。在極為親水性之塗層上,氣泡測量法比 水滴測量法更為正確。本發明測Λ氣泡接«角之方法如下 :先將接枝聚合後之ΡΜΚΑ水平放置於蒸皤水中,將《積 約為0.8微升之氣泡置於ΡΜΜΑ之底面。 ΡΜΜΑ相對之 兩面皆加以測量。每一樣品均作五次測量。表一至表九為 測量結果。 表1 :以伽瑪輻射誘起NVP接枝聚合於ΡΜΜΑ表面之伽瑪輻 射劑置率對特性黏度之影響: 濃度:10% NVP於水中 伽瑪輻射總劑置:O.lMrads 劑量率 時 間 度 2m 1235rads/nin 刺21 通 1.48 1.15X10‘ 麵 309rads/nin 5/J塒24纖 2.21 2.27X104 _ 137rads/nin 12/j姆0吩鐘 2.61 3.04X106 sm 77rads/ain 2_3吩鐘 2.85 3.49X10* 1麵 49rads/min 3.56 5.09X106 經濟部中央標準局Μ工消费合作社印製 表1以黏度测曼估計伽瑪輻射之劑量率對溶液中PVP 分子量及黏度之影響。酋伽瑪輻射劑董率降低且增加照 射時間時,即使樣品吸收之伽瑪輻射劑置一樣,溶液中 PVP之分子量會增加。在最低之劑董劑為49rads/Bin時, 本紙張尺度边用中81Η家樣準(CNS)T4規格(210X297公;《:) -20-202466 Λ 6 It 6 五、發明説明() 可得最高之PVP分子量.Mv = 5.09X 106 0 表2 :以伽瑪輻射撖起HVP接枝聚合於ΡΜΜΑ表面之伽瑪輻 射總_量對待性黏度之彩播: 獷度:10%NVP於水中 伽瑪輻射劑ft率:309rads/nin.(距伽瑪輻射源之 距離為4英吋) 伽瑪輻射總》置時 間特性鈷度分子量(Mv) 0. OSMrads 2小時42分鐘 0 . lONrads 5 小择.24 分鐘 0.25Mrads 13小時 30分鐮 0. 50Mrads 27 小時 6 1 8 2 1 2 ο ο 11 1* XX 9 7 6 2 (請先閲讀背而之注意节項孙填寫木/ 裝- *聚合物在溶篏中凝醪化。 -一未測定分子置(Mv)。 表2掲示利用黏度測量法估計伽瑪輻射總劑量對溶液 中PVP分子悬及黏度之影»。當表2之伽瑪輻射剤量率 維持於309 rads/nin時,若增加伽瑪輻射總劑JK可墙 加PVP之分子量。伽瑪輻射结劑量高於0.25Mrads時 ,聚合物於溶液中會産生凝膠作用。表2指出太高之伽瑪 輻射劑量會導致PVP溶液的凝謬作用與交脚聚合反應。 經濟部屮央榣準局A工消合作社印ft'14 本紙5良尺度边用中S國家標準(〇奶)肀4規格(210X297公龙) 五、發明説明() 表3 :以伽瑪輻射激起NVP接枝聚合於PKMA表面之ΝνΡ濃度 對溶液中PVP分子量之影ίΡ : 伽瑪輯射總劑量:〇.1Mrads 伽瑪輻射劑量率: 309 rads/aiin. 伽瑪輻射照射時間:5小時24分鐘 NVP濃度 待性黏度 分子量(Mv) 3% 0.97 0.5、6Χ 1〇‘ 6% 1.58 1 . 2 9 X 10* 1096 1,94 1.82Χ 1〇6 1596 2.45 2 . 7 0 X 1 〇4 表3顯示於固定之伽瑪輻射劑量及劑量率下, NVP 單體濃度與PVP分子量之間的鼸傜。當NVP濃度越高 時,溶液中PVP聚合物之分子董越高。又伽瑪轘射劑量 率對PVP分子量之影鬱亦可由下述事實得知。當濃 度維持於15 %時,劑量率309rads/ain之伽瑪輻射可 産生2,7 X 10分子量之PVP,而劑量率49rads/Bin 之伽瑪輻射可産生5.0 X 10分子量之PVP。 表4 :不同伽瑪輻射之爾量率對pvp接枝聚合於?}()^表面 之接觸角之影鬱: 經濟部屮央櫺準局只工消作合作社印製(E) Removal of gas: When the gas is removed from the solution of graft polymerization by vacuum or unique gas snake such as argon, the total dose of gamma radiation can be reduced (in fact, the total dose can be as low as 0.1Mrad) Can stimulate effective graft polymerization. The conversion rate of degassing gas is comparable to the molecular weight of single PVP polymer. For example, the gamma radiation dose is 0.05Mrad and NVP. The paper is used as the home standard iMCNS) T4 specification (210x297 g *) 202466 A 6 It 6 14 Central Printing and Quarantine Bureau of the Ministry of Economic Affairs. V. Description of the invention () When the monomer irrigation is 10%, if the gas is removed, NVP can be grafted and polymerized on PP to form a good PVP surface coating with a contact angle of 15 °. If oxygen is not removed, it is difficult to carry out graft polymerization under the above conditions. Therefore, the removal of gas is very important to produce a good PVP surface coating. When the material is PP, PVDF or PSi, the graft polymerization on the surface must first remove the gas, otherwise a good PVP surface coating cannot be produced. Degassing also helps to produce a good surface coating on the surface of PMMA or PC, that is, using very low gamma radiation (0.01 to 0.15 Mrad) can form an effective graft on the surface of PKMA or PC polymer. Under the above reaction conditions, if the gas is not removed first, the effect of graft polymerization is not good. 0 (H) Thickness of the graft polymer: when the thickness of the coating layer formed by the graft polymer is extremely thin (100 to 200 A) Although it is hydrophilic and has no adhesion to the group, but its mechanical properties are too soft, it may also produce a gel-like coating, so it is easy to cause trauma when it comes into contact with the group. When the thickness of the graft polymer coating is between 300-500 Angstroms to 50 nanometers, it is more suitable for many different applications. The thicker surface coating has the properties of light, uniformity, optical clarity and rapid hydration. If no swelling solvent is used and the bonding time between the monomer and the material surface is not prolonged, the thickness of the grafted polymer coating is relatively thin, with a thickness of about 0.1 to 5 microns. If a swelling solvent such as ethyl acetate is used, the thickness of the grafted polymer coating on the PMMA surface is about 100 meters or more. In some special applications, the thickness of the surface coating must be increased to 20 to 100 meters to form a thick sponge-like coating. (Geng) free radical scavengers: commonly used reducing agents such as Cu · Fe, (please read the notes on the back first # 难 写 太 | This paper is used in a standard ah family quasi (CNS) T4 specifications (210X297 : ":) 202466 V. Description of invention () Anti-phlegm blood acid and other trapped free radicals can effectively inhibit the polymerization reaction of free radicals in the solution. (To be distinguished in high single irradiance and high gamma radiation dose and dose rate Time), which can slow down the coagulation of the solution. However, the use of free radicals to remove rain also has the following lack of viscosity, which results in a lower polymer molecular scene, more unreacted single marrow and a wider molecular weight distribution. If used The gold salts are not good for biocompatibility. In most of the grafts, the amount of moles avoids the use of free radical scavengers. However, when forming PVP, PHEMA or P (HVP-HEMA) coatings Ascorbic acid helps to reduce the solution & supportability and gelation. Under the above conditions, add ethyl acetate (0.5 to 5%) as a solvent to the single-phase solution. Even if the concentration of the single-phase is as high as 5 〇χ can also get a thicker surface coating and can avoid the viscosity and coagulation of the solution. Liquid: Adding an effective swelling solvent of the material to the solution in the single sheet is beneficial to the expansion of the material eye and helps the dispersion of the single mole on the surface of the material eye. The above phenomenon will occur before and at the time of gamma radiation. Single full penetration of the material can increase the thickness of the surface coating and lift off the degree of bonding of the surface coating on the surface of the material. Ethyl acetate can be used as an effective swelling solution for materials such as PMMA. Gong Xiaot cooperation Du Yin 3i The method of (A) to (Xin) can be used to obtain a good surface graft polymer in this invention, this method is inferior to the conventional method. Because the combination of parameters and conditions of the above methods can be made different The results are different. If NVP and HEHΑ are copolymerized on the surface of the material to form a P (NVP-HEMA) surface coating, then the succession of HEMA in the mixture of NVP and HEMA can be as high as 50 Percentage. However, HEME and the original size of the 5G standard of the original paper are used in a S home standard (CNS) > f 4 specifications (2) 0X297 public; «:) 202466 Ministry of Economic Affairs, Bureau of Standards, the page work consumer price cooperative, Indian slaves. Description of the invention ) If the infusion of NVP and HEMA single-hybrid mixture is 20 to 30 seconds apart, then a free radical scavenger must be used in the single-waist mixture and the single haze stress must be lowered to avoid the solution's sleep effect, because HEMA will Promote the coagulation effect of the main solution. Although the above method represents a major improvement to the prior art, the most suitable result for each case depends on the combination of the execution parameter lanthanum number and the choice of on-site conditions. The present invention not only NVP, HEMA or NVP and HEMA single «can be used to form? 卩?,? 〇> ^ or? (》 ^?-1 ^ 1 (/ 0 surface coating, and different caries can be added to the above single acid Single sweet wine. And non-ionic single "and ionic single B can form a copolymer. The ionic monomers used in the present invention include ethylene «acid, styrene sulfonic acid, methyl thioethyl acrylate, methyl thiopropyl acrylate or other vinyl sulfonic acid, or ethylene methyl carboxylate, crotonic acid or isobutylene Acids, etc. can be used as anionic monochelic. If the ionic monomer used in the present invention contains a functional group such as a vinyl group or an amine group, such as vinylidine, a styrene-based urethane acrylate, or a methyl cyanoacrylate such as dimethyl ethyl methacrylate Or dimethylaminostyrene can be used as ion-limiting single B. In the present invention, ionic monosodium salts and nonionic monomers can also be mixed to form a copolymer. Considering the above phenomena and the reaction process, different reaction conditions must be applied to the articles split by different materials. The following examples will detail the conditions required by the present invention. Here are some highlights of the anti-plaque conditions: The determination of the range of reaction conditions is very useful for cracking good products. The choice of S for the best reaction process depends on the molecular structure of the material and the thickness of the graft polymer coating. The present invention should avoid the conditions that make the solution viscous or produce a sleeping effect, and at the same time avoid the reaction conditions that cause the material to crack or crack. (E.g. Li (please read the back and attention notes # 项 写 官 _ 丨 This paper is used in a national standard (CNS) τ 4 specifications (210X297; «:) 202466 Λ 6 Η 6 Ministry of Economic Affairs Printed by the Cooperative Society of the Provincial Bureau of Management. V. Description of the invention () Ethyl acetate at 203! Is used as the swelling solution of PMMA I). The following four conditions of the anti-mole process are very practical for improving the properties of the material surface: 1) The concentration of singe in aqueous solution is maintained within a range of 5 to 20% (the optimal degree is 10%). The dose of gamma radiation is maintained within a range of 0.05 to 0.20 Mrad (the optimal dose O.lOMrad). The dose rate of gamma radiation is maintained in the range of 20 to 1500 rads / nin (the optimal dose rate is 50 to 2000 rads / atin). The contact angle is less than 30 °. (2) Except for the conditions for purging the gas, other conditions are similar to (1). The gas can be purged with an inert gas such as vacuum or argon, and the dose of gamma radiation is maintained within the range of 0.01 to 0.15 Mrad (the optimal agent is 0.05Mrad). The weight percentage of NVP monomer is maintained in the range of 1 to 15% (the optimal weight percentage is 5 to 10%). The conditions should be better than (1). (3) Except for the condition with extra swelling solvent, the other conditions are similar to (1) and (2). For example, using ethyl acetate as the swelling solvent for PUMA material can make more The body penetrates to the surface of the material and increases the thickness of the grafted polymer coating. (4) Use a high concentration of ethyl acetate (25 to 50%), less than 5% of ethyl acetate swelling solution, and free radicals such as anti-blood Acid (concentration: 0.1 to 1.0 ObM). The dose of the gamma roller is maintained within the range of 0.10 to 0.20 Mrad, and the dose rate is maintained within the range of 20 to 50000 rads / Bin. Special instructions are weight percentages. Unless otherwise stated, all measurements of angles and surface properties are first subjected to the following treatment process • The coating obtained by the gamma radiation graft polymerization reaction is at room temperature or above the room temperature Wash the remaining monomers and ungrafted polymer in warm water or a solution mixed with water and alcohol to improve the properties of the surface of the material. The grafted polymer coating has stable properties and can be used regularly without being soluble In aqueous solution. The size of this paper is in accordance with China National Standard (CNS) 4 (210X297) PCT) 202466 Λ 6 Η6 18 · Printed by the Ministry of Economic Affairs, Central Bureau of Industry and Commerce, Co., Ltd. V. Description of the invention () The present invention can be prepared on the following materials including PHMA, PP, PVDF, PC and PSi surface graft polymer coating The present invention can perform partial graft polymerization or full graft polymerization on the surface of the above material to improve the properties of the material surface of the device or appliance. The surface modification method of the hydrophilic graft polymer used in the present invention is suitable for embedding into various parts of the eye (Such as anterior chamber, posterior chamber, crystalline ") is particularly advantageous for eye penetration. At the same time, the protection of the muscle group and the biocompatibility of other ocular implants, such as corneal inlays, corneal fillings, external corneal surgical instruments, shunts for tarsal eyes, retinal locks and solid buckles The improvements are of great value. * Example 1: This example indicates that the polymerization parameters of the PVP graft polymerization on the surface of PMMA due to the change of the above-mentioned reaction process and gamma-ray irradiation will have an important effect on the results of the reaction. First wash the sample of PMMA plate with soap solution twice, and then wash it with ultrasonic water in the ultrasonic processor. When the PMMA plate is completely dry, place the sample in the glassware containing NVP solution. Then irradiate the product with gamma radiation of different conditions. After irradiating with gamma radiation, the surface of PMMA was washed several times with rubbing water. After being grafted and polymerized with NVP on the surface of the PHUA sample, the sample was freeze-dried in the air. The PVP product in the solution can be measured with a viscometer for molecular weight (Oiv) or with a gel permeation chromatograph for molecular weight (Mw). When you have Mv, you can dissolve PVP in distilled water, and then use a capillary viscometer to measure its characteristic viscosity. The coating of PVP graft polymerization on the surface of PMHA can be used for water droplets or water vapor (please pay attention to the matter first # 项 舄 木 < Binding · Binding-line. This paper is used in 5 gram size side a B Jiayu standard (CNS)肀 4 specifications (210X297 public address) 202466 -19- Λ 6 Π 6 V. Description of the invention () Bubble measuring its contact angle. On extremely hydrophilic coatings, the bubble measurement method is more accurate than the water drop measurement method. The invention The method for measuring the angle of the bubble joint is as follows: first place the PMMA after graft polymerization horizontally in distilled water, and place bubbles with a volume of about 0.8 μl on the bottom surface of PMMA. Both opposite sides of PMMA are measured. A sample is measured five times. Tables 1 to 9 are the measurement results. Table 1: The effect of gamma radiation on the intrinsic viscosity of gamma radiation induced by NVP graft polymerization on the surface of PMMA: Concentration: 10% NVP The total dose of gamma radiation in water: O.lMrads dose rate time 2m 1235rads / nin thorn 21 pass 1.48 1.15X10 'surface 309rads / nin 5 / J t 24 fiber 2.21 2.27X104 _ 137rads / nin 12 / j 0m 0 2.61 3.04X106 sm 77rads / ain 2_3 phen 2.85 3.49X10 * 1 side 49rads / min 3.56 5.09X106 Printed in Table 1 of the Central Standards Bureau of the Ministry of Economic Affairs, Mgong Consumer Cooperatives 1. Estimate the effect of the dose rate of gamma radiation on the molecular weight and viscosity of PVP in the solution by viscometry. When the rate of the gamma radiation agent decreases and the exposure time is increased Even if the gamma radiation agent absorbed by the sample is the same, the molecular weight of PVP in the solution will increase. When the lowest agent is 49rads / Bin, this paper is used in the 81HS home standard (CNS) T4 specification (210X297 ; ":) -20-202466 Λ 6 It 6 V. Description of the invention () The highest molecular weight of PVP available. Mv = 5.09X 106 0 Table 2: Gamma radiation is used to lift the HVP graft polymerized on the surface of the gamma gamma Total Radiation_Measurement of the color viscosity of the color broadcast: R: 10% NVP in water gamma radiation agent ft rate: 309rads / nin. (Distance from the gamma radiation source is 4 inches) Gamma radiation total "set time Characteristics Cobalt molecular weight (Mv) 0. OSMrads 2 hours 42 minutes 0. lONrads 5 small selection. 24 minutes 0.25Mrads 13 hours 30 minutes sickle 0.50Mrads 27 hours 6 1 8 2 1 2 ο ο 11 1 * XX 9 7 6 2 (please read the note section first, fill in the wood / install-* polymer condensed in the mash . -An undetermined molecular home (Mv). Table 2 shows the effect of using the viscosity measurement method to estimate the total dose of gamma radiation on the suspension and viscosity of PVP molecules in solution ». When the gamma radiation rate in Table 2 is maintained at 309 rads / nin, the molecular weight of PVP can be increased if the total gamma radiation agent JK is increased. When the gamma radiation junction dose is higher than 0.25Mrads, the polymer will gel in solution. Table 2 indicates that too high a gamma radiation dose will cause the condensation effect of PVP solution and the polymerization reaction. Printed by the Ministry of Economic Affairs, the Central Bureau of Industry and Commerce, A Industrial and Consumer Cooperatives, ft'14 paper, 5 good-size side-use Chinese S national standards (〇 奶), 4 specifications (210X297 male dragons) 5. Description of invention () Table 3: Gamma radiation The effect of NVP concentration on the surface of PKMA induced by NVP graft polymerization on the molecular weight of PVP in the solution ί Ρ: Total gamma dose: 0.1Mrads Gamma radiation dose rate: 309 rads / aiin. Gamma radiation exposure time: 5 hours 24 minutes NVP concentration to be determined viscosity molecular weight (Mv) 3% 0.97 0.5, 6Χ 1〇 '6% 1.58 1.2 9 X 10 * 1096 1,94 1.82Χ 1〇6 1596 2.45 2 .7 0 X 1 〇4 Table 3 Shown at a fixed gamma radiation dose and dose rate, between the concentration of NVP monomer and the molecular weight of PVP. The higher the NVP concentration, the higher the molecular weight of the PVP polymer in the solution. The influence of the gamma radiation dose rate on the molecular weight of PVP can also be known from the following facts. When the concentration is maintained at 15%, gamma radiation at a dose rate of 309rads / ain can produce PVP of 2,7 X 10 molecular weight, while gamma radiation at a dose rate of 49rads / Bin can produce PVP of 5.0 X 10 molecular weight. Table 4: What is the ratio of gamma radiation to pvp graft polymerization? } () ^ The shadow of the contact angle on the surface: Printed by the Ministry of Economic Affairs
A 6 Π 6 五、發明説明() 濃度:10% NVP 伽瑪輻射總劑ft : O.lMrad 時 間 mn — — 65。 1 2斯 1235rads/nin 刺21颁 31。 綱 309rads/oin 5/J僻24分鐘 24。 麵 137rads/niin 12<J僻。粉鍾 21。 麵 77rads/nin 2觸36健 19。 1麵 49rads/min 33/jM^45^« 15。 經濟部屮央梂準局员工消费合作杜印製 表4顯示伽瑪輻射之劑量率降低時,接觸角之角度亦 降低。此乃親水性PVP接枝聚合於PMMA表面之程度愈 高所致。 表5 :不同伽瑪輻射之總劑量對PVP接枝聚合於PUMA表面 之接觸角之影W: 鼸度:10% NVP於水中 劑量率:3 0 9 rads/nin. 本紙張尺度边用中國國家標準(CNS)ΤΜ規格(210X297公;《:) -23*202466 Λ 6 It 6 五、發明説明() 總劑量 接《角 未照射伽瑪輻射之對照組 65° PVP接枝聚合於PMMA ♦· 0.05Mrads 27° 0.lOHrads 、 25° 0.05»Mrads 24。 0.50*Mrads 24。 »含聚合物之溶液凝膠化。 表5顯示伽瑪輻射之總劑量對PVP接枝聚合於PMMA 表面之接觸角之影雄。由表5可知,當伽瑪輻射劑量率 為 309rads/nin時,其總剤纛在0.05Mrads以上之變 化對接觸角之費化影響很小。 表6 :不同單睡濃度對PVP接枝聚合於PMMA表面之接觸角 影繼: 伽瑪輻射總劑悬:Q.lMrad 伽瑪輻射劑量率:309rads/Bin NVP»度 接觸角 (請先閲讀背而之注意事項孙项寫—/ 經濟部中央標準局A工消"合作杜印製 未經伽瑪輻射照射之PMMA 65。 3% (NVP接枝聚合於PMMA) 29。 6% (NVP接枝聚合於PMMA) 27。 10% (NVP接枝聚合於PMMA) 25。 15% (NVP接枝聚合於PMJiA) 21。 本紙汝尺度边用中BB家揉1MCNS)T4規格(210><297公龙) 202466 Λ 6 Π6 -24- 五、發明説明() 表6顯示不同 NVP 單《濃度對 PVP 接枝聚合於 PMMA表面之接觸角之彩響。當NVP之單驪濃度小至3 %時,伽瑪輻射劑量維持於O.lMrad ,亦可産生很小之 接觸角,而使親水性大為提高。當NVP單體濃度大於3 %時,接觸角之受化很小。 表7 :不同單體潰度對PVP接枝聚合於PMMA表面之溶液中 PVP分子量之影« : 伽瑪輻射總劑ft : O.lMrad 伽瑪輻射薄!量率:64rads/nin NVPift度 持性黏度分子量(Hv) %¾¾% 13 5 0 9 5 3 5 7 6 2 3 • · · · 0 12 3 1* 1X 1* X X X X 0 8 0 9 4 3 3 5 請 .先 間 背 而 之 注 t- 事 項 再 % 木 經濟部屮央榣準局貝工消伢合作杜印製 表7顯示UVP單釅之濃度與溶液中PVP分子量之两 你。當伽瑪轘射劑Λ率維持於64rads/Bin時,且增加 NVP單腥漉度則溶液中PVP之分子量亦會增加。 表8 :不同單體灌度對PVP接枝聚合於PHMA表面之接觸角 影锻: 伽瑪輻射總劑Ji : O.IHrad 伽瑪輻射劑置率:64rads/Bin 本紙张尺度边用.中圉S家標準(CNS) T4規格(2丨0X297公;«:) -25-202466 Λ 6 Ii6 五、發明説明() NVP«度 未經伽瑪輻射照射之PMMA 0% (NVP接枝聚合於PMMA) 1% (NVP接枝聚合於PMMA) 3% (HVP接枝聚合於PMHA) 5% (NVP接枝聚合於PHKA) 15% (NVP接枝聚合於PKMA) 接觸角 65° 62° 49° 43° 31° 18° 經濟部中央標準局A工消赀合作社印製 表8顯示當伽瑪輻射劑《率維持於64rads/iin時, 不同NVP單膿濃度對PVP接枝聚合於 PMMA表面之接 觸角之影»。當HVP濃度增加時,接觸角之角度會滅小 。表8之結果與表6相似。其不同之處在於表8之伽瑪 輻射劑量率為 64rads/nin而表6之伽瑪輻射劑S率為 3 0 9 rads/Bin。 比較表8與表6可知,當 NVP »度為 10 %時,較低之伽瑪輻射劑量率將使接枝聚合塗層之親 水性略為增加(將表8之18 °與表6之25 °接梅角作 比較)。 極性有機溶剤或其舆水溶液之混合液對於親水性軍《 之接枝聚合反應頗為有利。典型之極性有機溶劑包括酵類 與醚類如甲酵、乙二醇、聚乙二酵、二《雜琛己烷等皆可 使用。當上述有機溶兩作為自由基鏈轉移劑時,其濃度 必須小於50 %,而單鼸之«度可以很高(例如大於25 % )。例如甲酵有清除自由基之性質,且甲醇於水中之 濃度可高逹50至60 % ,若NVP單«之濃度為ία % 先 'W1 讀 背 而 之 注 項 /Η m % 木 裝 π 線 Κ紙5良尺度返用中a困家榣iMCHS) Τ4規格(210X297公;Jt) 202466 Λ 6 It 6 -26- 五、發明説明() ,則可利用O.lMrad劑量之伽瑪輻射將PVP接枝聚合 於PMMA表面。上述條件請參閲表9 。甲酵溶_可促進 自由基鏈轉移,但須將反應條件局限於低伽瑪輻射爾麗 率及10% NVP單鳗中。一般而言,上述反應之溶液鲇 度很低,表示在自由基抑制劑存在的溶液中聚合物之分 子置會很低。 表9 :不同之伽瑪輻射劑量率對溶於甲酵之PVP接枝聚合 於PMMA表面之接觸角影播: 灌度:10%NVP於50%甲酵中 伽瑪輻射總劑麗:O.lMrad 伽瑪輻射劑置率 接觸角 未經伽瑪輻射照射之PMMA 65° 1065rads/oin 36° 326rads/nin 28° 157rads/nin 27。 64 rads/n in 20° 實施例2 : (請先間^背而之注念亊項#项艿木^ 經濟部中央槛準局只工消扑合作社印51 本實施例說明膨脹溶劑對於表面修飾過程之彩響。 在伽瑰輻射激起之單體接枝聚合於PMMA表面之反匾 溶液中·若加入膨脹溶液如乙酸乙酯於單醴溶液,可使 本紙张尺度边用中國困家搮準(CNS)肀4規格(210X297公龙) 27.202466 經濟部屮央榀準乃貝工消仲合作社印製 五、發明説明() 單體更有效擴散至PKMA表面。雖然乙酸乙酯於水中之 溶解度不高,但溶液中若有NVP單醴仍可製成均勻之反 應溶液。當乙酸乙酯之濃度增高及單體擴散之時間延長 時,可得較厚之接枝聚合表面。上述步《所經遇的時間 可稱為預浸時間。一般而言,若不去除氧氣而維持伽瑪 輻射劑量於0.10至0.15 Mrad之範圍内可得相酋良好 之接枝聚合物。 、 HVP·乙酸乙酯-水之溶劑糸統亦為PVP之良好溶劑 ,並使溶液中之聚合物保持均勻狀態。 本發明亦可將PVP埋置接枝聚合於PMHA表面。先 將PMMA浸於單醱-膨脹溶劑-水之混合液中,再以伽瑪 輻射激起接枝聚合反醮,即可将 PVP 埋置接枝聚合於 PMMA表面。 於實驗時可使用下述技術以含10 %肥皂水之超音波 處理機淸洗樣品,然後再以蒸餾水淸洗樣品。在作表面 處理之前,先在真空乾燥器中將樣品乾燥18小時後再 稱重。在4 1C真空蒸蹓中淨化NVP單讎。 於伽瑪輻射瀲起之接枝聚合反醮中,先将ΡΚΜΑ材霣 浸入單腥溶液中,再利用伽瑪輻射照射之。典型之方法 係將 ΡΜΜΑ材質浸入NVP-乙酸乙酯一水混合液中,再 以600居里的鈷六十伽瑪輻射源誘起接枝聚合反應。將 樣品曝露於單體溶液中之時間不同,可得到不同厚度之 接枝聚合塗層。伽瑪輻射劑量雒持於0.01至Q.lSMrad 之間,並以法里克氏 (Fricke)劑*拥定器拥|定之。伽 瑪輻射的薄I量率也可以在一定範圍内作變化。樣品於照 (請先閲讀背而之注意事項#项寫务 裝- 訂_ 線· 本紙張尺度边用中國Η家標準(CNS)T4規格(210X297公*) -28-202466 Λ 6 It 6A 6 Π 6 V. Description of the invention () Concentration: 10% NVP total gamma radiation ft: O.lMrad Time mn — — 65. 1 2 Si 1235 rads / nin Thorn 21 award 31. Outline 309rads / oin 5 / J secluded 24 minutes 24. Face 137rads / niin 12 < J secluded. Pink Clock 21. Face 77rads / nin 2 touch 36 Jian 19. 1 side 49rads / min 33 / jM ^ 45 ^ «15. The Ministry of Economic Affairs, Ministry of Economic Affairs, Bureau of Employee Consumption, Du Yin, Table 4 shows that when the dose rate of gamma radiation decreases, the angle of contact angle also decreases. This is due to the higher degree of hydrophilic PVP graft polymerization on the surface of PMMA. Table 5: The shadow of the total dose of different gamma radiation on the contact angle of PVP graft polymerization on the surface of PUMA W: 鼸 度: 10% NVP in water Dose rate: 3 0 9 rads / nin. The paper scale uses the country of China Standard (CNS) TM specifications (210X297 g; ":") -23 * 202466 Λ 6 It 6 V. Description of the invention () Total dose is connected to the control group 65 ° PVP grafted and polymerized in PMMA at the angle not exposed to gamma radiation ♦ · 0.05Mrads 27 ° 0.lOHrads, 25 ° 0.05 »Mrads 24. 0.50 * Mrads 24. »Gelation of polymer-containing solutions. Table 5 shows the total dose of gamma radiation on the contact angle of PVP graft polymerization on the surface of PMMA. It can be seen from Table 5 that when the gamma radiation dose rate is 309 rads / nin, the change of its total value above 0.05 Mrads has little effect on the contact angle fee. Table 6: Effect of different single-sleep concentrations on the contact angle of PVP graft polymerization on the surface of PMMA: Gamma radiation total agent suspension: Q.lMrad Gamma radiation dose rate: 309rads / Bin NVP »degree contact angle (please read the back And the matters needing attention written by Sun Xiang— / Cooperative Du Printing of PMMA 65. 3% (NVP graft polymerization on PMMA) 29. 6% (NVP connection) Branch polymerization in PMMA) 27. 10% (NVP graft polymerization in PMMA) 25. 15% (NVP graft polymerization in PMJiA) 21. The size of this paper is used in the BB home kneading 1MCNS) T4 specification (210 > < 297 Gonglong) 202466 Λ 6 Π6 -24- V. Description of the invention () Table 6 shows the colorful sound of different NVP single concentrations on the contact angle of PVP graft polymerization on the surface of PMMA. When the concentration of NVP is as low as 3%, the gamma radiation dose is maintained at 0.1Mrad, which can also produce a small contact angle, which greatly improves the hydrophilicity. When the concentration of NVP monomer is greater than 3%, the influence of the contact angle is very small. Table 7: The effect of different monomers on the molecular weight of PVP in the solution of PVP graft polymerization on the surface of PMMA «: Gamma radiation total agent ft: O.lMrad Gamma radiation is thin! Quantity rate: 64rads / nin NVPift Viscosity molecular weight (Hv)% ¾¾% 13 5 0 9 5 3 5 7 6 2 3 • · · 0 12 3 1 * 1X 1 * XXXX 0 8 0 9 4 3 3 5 Please. Note t- The matter is again%. The Ministry of Economic Affairs, Ministry of Economic Affairs, Bureau of Industry and Fisheries cooperates with Du Yin, and Table 7 shows the concentration of the UVP unit and the molecular weight of the PVP in the solution. When the gamma rate of the gamma propellant is maintained at 64 rads / Bin, and increasing the single NVP degree, the molecular weight of PVP in the solution will also increase. Table 8: Contact angle shadow forging of PVP graft polymerization on the surface of PHMA with different monomer intensities: Gamma radiation total agent Ji: O.IHrad Gamma radiation agent setting rate: 64rads / Bin This paper is for standard use. Zhongwei S home standard (CNS) T4 specification (2 丨 0X297 male; «:) -25-202466 Λ 6 Ii6 V. Description of invention () NVP« degree PMMA 0% without gamma radiation exposure (NVP graft polymerized in PMMA ) 1% (NVP graft polymerization on PMMA) 3% (HVP graft polymerization on PMHA) 5% (NVP graft polymerization on PHKA) 15% (NVP graft polymerization on PKMA) Contact angle 65 ° 62 ° 49 ° 43 ° 31 ° 18 ° The Ministry of Economic Affairs, Central Bureau of Standards, A Industrial Consumer Affairs Cooperative Printed Table 8 shows the contact angle of different NVP single pus concentrations for PVP graft polymerization on the surface of PMMA when the rate of gamma radiation is maintained at 64rads / iin Shadow ». When the HVP concentration increases, the angle of the contact angle will decrease. The results in Table 8 are similar to Table 6. The difference is that the gamma radiation dose rate in Table 8 is 64 rads / nin and the gamma radiation dose rate in Table 6 is 3 0 9 rads / Bin. Comparing Table 8 and Table 6, it can be seen that when the NVP degree is 10%, the lower gamma radiation dose rate will slightly increase the hydrophilicity of the grafted polymer coating (combine 18 ° in Table 8 and 25 ° in Table 6). Take Meijiao for comparison). The mixture of polar organic solvent or its aqueous solution is quite beneficial to the graft polymerization of hydrophilic armour. Typical polar organic solvents include enzymes and ethers such as formazan, ethylene glycol, glyphosate, and dioxane, etc. can be used. When the above organic solvent is used as a free radical chain transfer agent, its concentration must be less than 50%, and the degree of single mollusc can be very high (for example, greater than 25%). For example, formazan has the property of scavenging free radicals, and the concentration of methanol in water can be as high as 50% to 60%. If the concentration of NVP is «α1, please read the note on the first W1 / H m% wooden π line Κpaper 5 good-scale reuse iMCHS) Τ4 specifications (210X297 g; Jt) 202466 Λ 6 It 6 -26- V. Description of invention (), then use 0.1Mrad dose of gamma radiation to convert PVP Graft polymerization on the surface of PMMA. Refer to Table 9 for the above conditions. Formazan can promote free radical chain transfer, but the reaction conditions must be limited to low gamma radiation rate and 10% NVP single eel. In general, the above-mentioned reaction solution has a very low degree of catfish, which means that the molecular weight of the polymer in the solution where the free radical inhibitor is present will be very low. Table 9: Effect of different gamma radiation dose rates on the contact angle of PVP grafted and dissolved in formazan on the surface of PMMA: Irrigation: 10% NVP in 50% of the total gamma radiation in formazan: O. lMrad Gamma radiation agent contact angle PMMA without gamma radiation 65 ° 1065rads / oin 36 ° 326rads / nin 28 ° 157rads / nin 27. 64 rads / n in 20 ° Example 2: (Please ^ ^ 而 而 之 念 亊 项 # 项 艿 木 ^ The Ministry of Economic Affairs, Central Bureau of Standards and Quarantine only printed by the cooperative cooperative 51 This example illustrates the expansion of the solvent for surface modification The sound of the process. The monomers stimulated by gamma radiation are grafted and polymerized on the anti-plaque solution on the surface of PMMA. If a swelling solution such as ethyl acetate is added to the solution of single alcohol, the paper scale can be used as a trapped house in China. Standard (CNS) 4 specifications (210X297 male dragon) 27.202466 Printed by the Ministry of Economic Affairs of the People's Republic of China, the standard is printed by the Beigong Xiaozhong Cooperative Society. 5. Description of the invention () The monomer diffuses more effectively to the surface of PKMA. Although the solubility of ethyl acetate in water It is not high, but if there is NVP monomer in the solution, it can still be made into a uniform reaction solution. When the concentration of ethyl acetate increases and the time of monomer diffusion increases, a thicker grafted polymerization surface can be obtained. The time of encounter can be called the prepreg time. Generally speaking, if the oxygen radiation is not removed and the gamma radiation dose is maintained in the range of 0.10 to 0.15 Mrad, a good graft polymer can be obtained. 、 HVP · ethyl acetate -The solvent system of water is also a good solvent for PVP, and The polymer in the solution remains in a uniform state. The invention can also embed PVP grafting polymerization on the surface of PMHA. PMMA is immersed in the mixture of single-expansion solvent-water first, and then the grafting is stimulated by gamma radiation After polymerization, PVP can be buried and grafted on the surface of PMMA. In the experiment, the following technique can be used to wash the sample with an ultrasonic processor containing 10% soapy water, and then wash the sample with distilled water. Before surface treatment, dry the sample in a vacuum dryer for 18 hours and then weigh it. Purify the NVP monocylinder in 4 1C vacuum distillation. In the graft polymerization reaction of gamma radiation, the PKMA material is first Dip into a single fishy solution, and then irradiate it with gamma radiation. The typical method is to immerse the PMMA material in NVP-ethyl acetate-water mixture, and then induce the grafting with a 600 Curie cobalt sixty gamma radiation source Polymerization. Exposure of the sample to the monomer solution at different times can result in grafted polymer coatings of different thicknesses. The gamma radiation dose is between 0.01 and Q.1SMrad, and Fricke is used. Agent * Holder Hold | Give it. Gamma The rate of the thin I can also be changed within a certain range. The sample is in the photo (please read the back-end notes first) # 项 写 务 装-order_ line · This paper scale uses the Chinese standard (CNS) T4 Specification (210X297g *) -28-202466 Λ 6 It 6
五、發明説明() 射伽瑪輻射之後,可從溶液中移出並以蒸®水淸洗數次 ,再置於除去離子之水中並攪動去離子水。有些樣品會 與水結合,故以濾紙吸取並移出材質表面之水份並將樣 品置於真空乾燥器中乾燥24小時。可聚合之溶液狀態由 澄清之黏稠溶液至凝睡化溶液不等。下列參數可被拥量 出來。 接枝聚合之程度可由材質重置之增加测出,並以下列 公式計算之: W -W 接枝聚合之百分率 -X 100 W0為ΡΗΜΑ原始之重量。 W1為經單«接枝聚合於表面之ΡΜΚΑ重量。 同理,水合之百分率可根據下列公式計算之: Ww-Wd 水合之百分率 -X 100 .先 閱 in 背 而 之 注 意 事 項 % 木5. Description of the invention () After emitting gamma radiation, it can be removed from the solution and washed several times with distilled water, then placed in deionized water and agitated in deionized water. Some samples will combine with water, so use filter paper to absorb and remove the water on the surface of the material and place the sample in a vacuum dryer to dry for 24 hours. The state of the polymerizable solution varies from a clear viscous solution to a solidified solution. The following parameters can be obtained from the volume. The degree of graft polymerization can be measured by the increase in material reset and calculated by the following formula: W -W Percentage of graft polymerization -X 100 W0 is the original weight of PHMA. W1 is the weight of PMKA polymerized on the surface by single graft grafting. In the same way, the percentage of hydration can be calculated according to the following formula: Ww-Wd The percentage of hydration -X 100. Read first in the back and pay attention to the item% wood
Wd 經濟部中央標準局A工消费合作社印5iWd, Ministry of Economic Affairs, Central Standards Bureau, A Industrial and Consumer Cooperative, printed 5i
Wd為PMHA經乾燥後所得之重量。 h為PMMA用濾紙吸乾後所得之重董。 以伽瑪輻射瀲起單《I接枝聚合於PMMA表面後,再以 氣泡接鱅角或辛烷接》角测置法評估材質表面經修飾後 之親水性程 度如何。 靜態接》角可由藍明一哈特氏 (Ra«e-Hart)接庙角測角器加以澜置。每一樣品至少採 取5處不同表面以測量其接梅角。 IR/ATR光嫌之表面分析可用桕金一耶其氏(perkin- 私紙张尺度边用中國S家標毕(CNS)甲4規格(210X297公龙) 202466 五、發明説明() 先 間 讀 背 而 之 注 意 事 項 %Wd is the weight of PMHA after drying. h is the weight of PMMA obtained after the filter paper is dried with PMMA. Gamma radiation was used to evaluate the degree of hydrophilicity of the modified surface of the material after the "I graft polymerization on the PMMA surface, and then the bubble connection angle or octane connection" angle measurement method. The angle of "Static Connection" can be set by Lan Ming-Hart (Ra «e-Hart) connecting temple angle protractor. Take at least 5 different surfaces for each sample to measure the joint angle. The IR / ATR surface analysis can be used in the form of perkin-yeschi (perkin-private paper scale side using the Chinese S home standard (CNS) A 4 specifications (210X297 male dragon) 202466 V. Invention description () Read in advance Contrary considerations%
Elmer)283B 型红外線光进儀以漸弱之總反射比測定未接 枝聚合之材質表面與接枝聚合之材質表面。 未接枝聚合與接枝聚合之PMMA檬品,各取lc·置 於克拉托氏(Kraros)ES3 00型ESCA光嫌儀中分析其表 面。該光譜儀使用鎂為X射線之來源。接枝聚合結果之 分析可由氮/碩之比值加以判定。 溶液中 PVP聚合物之分子置由待性黏度加以測定。 其待性黏度偽由優比福地氏(Ubbelhode)黏度計測定之 在本實施例中伽瑪伽瑪鞴射之劑置維持於 0.01至 0.15Mrad之範圃内,而單鳢濃度之範圔維持於5至15 %。 經濟部屮央標準局只工消伢合作社印製 表10顯示PVP接枝聚合於PMMA表面之结果,並 以乙酸乙酯為膨脹溶麵。雖然於照射伽瑪轘射之前将 PMMA預浸於膨脹溶液之效果較佳,但表10為於照射伽 瑪輻射之前並未將PMMA預浸於膨腥溶液,而係於PMMA 浸入膨脹溶液之時即以伽瑪輻射照射之。表1〇可作為 控制單體擴散之反應条統所呈現之典型行為。含有乙酸 乙酯之膨脹溶剤對於NVP單體擴散至疏水性之PMHA表 面很有幫助。Elmer) Model 283B Infrared Light Entry Meter measures the surface of ungrafted polymer material and the surface of grafted polymer material with a diminishing total reflectance. The PMMA lemon products of ungrafted polymerization and grafted polymerization, each lc · was placed in Kraros ES3 00 type ESCA optical detector to analyze its surface. The spectrometer uses magnesium as the source of X-rays. The analysis of the graft polymerization results can be judged by the ratio of nitrogen / master. The molecular placement of the PVP polymer in the solution is determined by the intrinsic viscosity. The pseudo-viscosity is determined by the Ubbelhode viscometer. In this embodiment, the dose of gamma gamma is maintained within the range of 0.01 to 0.15Mrad, while the range of the concentration of single snake is maintained at 5 to 15%. Printed by the Co-operative Society of the Ministry of Economic Affairs, Central Standards Bureau. Table 10 shows the results of PVP graft polymerization on the surface of PMMA, using ethyl acetate as the swelling surface. Although the effect of pre-immersing PMMA in the swelling solution before gamma irradiation is better, Table 10 shows that PMMA was not pre-immersed in the swelling solution before gamma irradiation, but when PMMA was immersed in the swelling solution It is irradiated with gamma radiation. Table 10 can be used as a typical behavior of the reaction system to control the monomer diffusion. The swelling solvent containing ethyl acetate is very helpful for the diffusion of NVP monomer to the hydrophobic PMHA surface.
若使用材質之膨脹溶劑如乙酸乙酯,則NVP-乙酸乙 酯-水之溶液糸統將膨脹 PMMA 之表面層,使得鄰近 PMMA表面層之NVP擊體很快接枝聚合於 PMMA表面。 在上述條件下, 接枝聚合之效果極為良好,一方面可用 較低之伽瑪輻射劑量另一方面HVP可接枝聚合於PMMA 本紙张尺度逍用中B Η家樣毕(CNS)甲4規格(210X297公龙) 202466If a swelling solvent of material such as ethyl acetate is used, the NVP-ethyl acetate-water solution system will swell the surface layer of PMMA, so that the NVP striker adjacent to the surface layer of PMMA will quickly graft and polymerize on the surface of PMMA. Under the above conditions, the effect of graft polymerization is very good. On the one hand, it can use a lower gamma radiation dose. On the other hand, HVP can be grafted and polymerized in PMMA. (210X297 male dragon) 202466
經济部屮央榣準历β工消伢合作杜印fr,A 五、發明説明() 表面層下較深之數層。 本發明以NVP-乙酸乙酯一水(1:1:8)之膨脹浓液 觀察膨脹時間長短對PMA樣品之膨脹百分率之彩響。 將PMMA浸入上述膨脹溶液中12小時,則PMMA可陈 脹6 %。 若控制單髏擴散時間之長短,則可控制NVP 接枝聚合於PMMA表面之厚度。表11顧示将PMMA預 浸於含15% NVP之1:9乙酸乙酯:水之膨脹溶液中 之結果。表10於照射伽輻射之前未將PMHA預浸於膨 脹溶液,而傜將 PHMA置於膨脹溶液後立即以伽瑪輻射 激起接枝聚合反應,比較表11與表10可知,將PMMA 預浸於膨脹溶液中之結果較好。當乙酸乙酯之濰度固定時 .PMMA是否預浸於膨脹溶液對低NVP單饈濃度(例如 5% )比對高單《濃度(例如15% )之差異更為顯箸 Ο 在膨脹溶液中加入NVP很重要,因為NVP既是單饉 亦是膨脹溶液之一份子。若無NVP存在,則膨脹溶液如 乙酸乙酯與水將形成可溶混之溶劑。故HVP可維持膨脹 溶液於均匀相中。當NVP單《之濃度固定時(例如維持 於10%),必須使乙酸乙酯之濃度維持於10¾以下 以避免相分離而産生撖乳液。又乙酸乙酯之濃度改變時, 將影響接枝聚合之産量。表12顯示當其他因素不變時, 若乙酸乙酯之濃度增加則接枝聚合物之産置百分率亦增加 。於低劑量之伽瑪輻射下,膨脹i容液對接枝聚合物之效率 影堪可由接枝聚合物之産量百分率增加與接《角之減小看 出來。例如,當伽瑪輻射劑量為0.05Mrad時,於單體之 (請先閲讀背而之注意事項#填寫木苁 裝· 訂- 線 本紙尺度逍用中B國家標準(CNS)T4規格(210X297公釐) -31-202466 Λ 6 Π 6 五、發明説明() 先 閲 in 背 而 之 注 意 項 /卜 堝 % Λ 單純水溶液中産生之接枝聚合物很少。 然而即使低至 O.OlMrad劑量之伽瑪輻射,於9·.1之水:乙酸乙酯膨脹 溶液中可使接觸角減小至35 ° , 而於9:1之水:乙酸 乙酯膨脹溶液中使用0.03Mrad劑量之伽瑪輻射,可使接 觸角減小至23 ° (謫參閲表11所示,其預浸膨脹時間 為24小時)。 有些化學分析技術可使用於整«聚合物之分析但不適 用於聚合物表面之分析。因為聚合物表面匾域之構迪與化 學性質和聚合物其他部份之性質有黷箸不同。聚合物表面 匾域僅佔整鼸聚合物之一小部份。故傅統之化學分析技術 k聚合物表面區域之分析並不恰當。故必須使用待殊之表 面分析技術分析聚合物表面區域及接枝聚合於聚合物表面 區域之塗層係颶必需。因為聚合物表齒區域偽由材質、接 枝聚合物、交腰之基園與鍵轉移産物所形成之禊雜混合物 ,故本發明採用兩種非常有用之表面#析技術邸ATR-IR 光譜分析及ESCA光譜分析以钂定接枝聚合後之材質表面 經濟部中央#準局只工消t合作杜印製 表13掲示ATR-IR光进分析之結果· PVP接枝聚 合於ΡΜΜΑ表面後,醯胺類之C = 0基臞之比值在ATR-IR 光譜分析中随著伽瑪輻射劑量之增加而減少。當伽瑪輻射 劑量由O.OlMrad增為O.lOMrad時,其比值由7.67減 為1.68。 酋伽瑪輻射劑麗高於O.lMrad時,其比值幾 乎不變。 ( 表14掲示ESCA光譜分析之结果。當伽瑪輻射薄量 增加時,則氮/磺(N/C)之比值增加,而氘之增加與 本紙張尺度边用中a Η家樣準(CNS) T4規格(210x297公;《:) 32202466 Λ 6 Π6 五、發明説明( PVP接枝聚合於PMHA表面之效應相間。 掃瞄式電子顯撖鏡可用於觀察PVP接枝聚合於PMMA 表面之表面形態。所有接枝聚合之塗層於放大一萬倍觀察 時仍很平滑,故接枝聚合之塗《非常均勻的塗覆於PMHA 表面。上述特性對於保有最佳之光學性質非常重要,待別 是 PMMA及其塗層作為光學植入物如眼睛透鏡時應保有 最佳之光學性質。 t 由本實施例可得下列結論: NVP- 乙酸乙酯一水之溶劑条統不但可以産生均勻之 親水性聚合物塗層,亦可控制NVP在PMA表面之滲透 及接枝聚合程度。若改變膨眼溶劑之《度與預浸膨脹時間 ,則可控制溶於單餵一乙酸乙酯-水溶劑之單臞對材質表 面的滲透程度。 由重ft分析,接觸角之變化, ATR-IR光譜分析及 ESCA光譜分析之結果可測知PVP接枝聚合於材質表面之 事實。 極低伽瑪輻射劑Λ對於有效之接枝聚合反瀛為必備之 條件。而極低之伽瑪輻射劑ft可滅少對材質表面之輻射破 壊。 先 閱 背 vfTj 之 注 意 項 lTh 项 % 本 經濟部中央櫺準局β工消讣合作杜印51 表10 : NVP接枝聚合於PMMA表面 膨腥時間:0小時 膨脹溶劑:乙酸乙酯:水(1:9) 本紙5良尺度边用中《困家樣1MCNS)<IM規格(2丨0X297公址) -33-202466 Λ 6 η 6 五、發明説明( 1111$ KfPlIt fe««10.01Xra<i Q.05Kraij O.lOIrad O.lSKrad m &m% ira μϊη m m nm 309rads/iin 77r8ds/iia ην Αν r5 rhv Λν Γο οο AD Λυ Λν CV οο 14· n 4· —4 MJ ΛίυThe Ministry of Economic Affairs has approved the cooperation of the β-worker and the consumer in Duin fr, A V. Description of invention () Deeper layers under the surface layer. In the present invention, the swelling concentrate of NVP-ethyl acetate monohydrate (1: 1: 8) was used to observe the colorful response of the swelling percentage of the PMA sample to the length of swelling time. PMMA can be swollen by 6% when immersed in PMMA for 12 hours. If the length of the single skull diffusion time is controlled, the thickness of NVP graft polymerization on the surface of PMMA can be controlled. Table 11 shows the results of pre-immersing PMMA in a 1: 9 ethyl acetate: water swelling solution containing 15% NVP. Table 10 The PMHA was not pre-immersed in the swelling solution before the irradiation of gamma radiation, but the graft polymerization was stimulated by gamma radiation immediately after the PHMA was placed in the swelling solution. Comparing Table 11 and Table 10, it can be seen that the PMMA was pre-immersed in The results in the swelling solution are better. When the degree of ethyl acetate is fixed. Is the difference between PMMA pre-immersed in the swelling solution and the low NVP single concentration (eg 5%) more pronounced than the higher single concentration (eg 15%)? In the swelling solution The addition of NVP is important because NVP is both a simple ingredient and a part of the swelling solution. If no NVP is present, the swelling solution such as ethyl acetate and water will form a miscible solvent. Therefore, HVP can maintain the swelling solution in a homogeneous phase. When the concentration of the NVP sheet is fixed (for example, maintained at 10%), the concentration of ethyl acetate must be maintained below 10¾ to avoid phase separation and generation of emulsion. When the concentration of ethyl acetate changes, it will affect the yield of graft polymerization. Table 12 shows that when other factors remain unchanged, if the concentration of ethyl acetate increases, the production percentage of graft polymer also increases. Under the low dose of gamma radiation, the effect of the expansion of the volume of the liquid on the graft polymer can be seen from the increase in the yield of the graft polymer and the decrease in the graft angle. For example, when the gamma radiation dose is 0.05Mrad, please use the single one (please read the back-end precautions #fill in the Cistanche · order-the Chinese standard B (CNS) T4 specification (210X297 %) -31-202466 Λ 6 Π 6 V. Description of the invention () First read in Contrary to note / Bu pot% Λ There are very few graft polymers produced in a simple aqueous solution. However, even as low as O.OlMrad dose Gamma radiation, in 9 · .1 water: ethyl acetate expansion solution can reduce the contact angle to 35 °, and in 9: 1 water: ethyl acetate expansion solution using 0.03Mrad dose of gamma radiation , The contact angle can be reduced to 23 ° (see table 11 for the postmortem, the prepreg expansion time is 24 hours). Some chemical analysis techniques can be used for polymer analysis but not for polymer surface Analysis. Because the structure of the plaque domain on the polymer surface is different from the chemical properties and the properties of other parts of the polymer. The plaque domain on the polymer surface only occupies a small part of the polymer. Therefore, Fu Tong ’s chemical analysis technology k The analysis of the polymer surface area is not appropriate, so it must be used Special surface analysis technology is necessary to analyze the polymer surface area and the coating polymer grafted on the polymer surface area. Because the polymer surface tooth area is pseudo-generated by the material, graft polymer, base garden and bond transfer products The formed heterogeneous mixture, so the present invention uses two very useful surface # analysis technology Di ATR-IR spectroscopic analysis and ESCA spectroscopic analysis to determine the material after graft polymerization of the surface of the Ministry of Economic Affairs #quasi bureau only work elimination t Cooperative Duprinting Table 13 shows the results of ATR-IR light analysis. After the PVP graft polymerization on the surface of PMMA, the ratio of C = 0 radicals of amides in the ATR-IR spectroscopic analysis with the gamma radiation dose Increase and decrease. When the gamma radiation dose is increased from 0.01Mrad to 0.1OMrad, the ratio is reduced from 7.67 to 1.68. When the ratio of emirates gamma radiation agent Li is higher than 0.1Mrad, the ratio is almost unchanged. (Table 14 The results of ESCA spectroscopic analysis are shown. When the amount of gamma radiation is increased, the nitrogen / sulfur (N / C) ratio is increased, and the increase in deuterium is equivalent to the standard of the paper standard (CNS) T4 specification. (210x297 male; ":) 32202466 Λ 6 Π6 V. Description of the invention ( The effect of PVP graft polymerization on the surface of PMHA is alternated. Scanning electronic display mirror can be used to observe the surface morphology of PVP graft polymerization on the surface of PMMA. All the graft polymerization coatings are still very smooth when viewed at 10,000 times magnification. Therefore, the coating of graft polymerization is very uniformly coated on the surface of PMHA. The above characteristics are very important for maintaining the best optical properties. When PMMA and its coating are used as optical implants such as eye lenses, the best Optical properties. T The following conclusions can be drawn from this example: The solvent system of NVP-ethyl acetate monohydrate can not only produce a uniform hydrophilic polymer coating, but also control the penetration of NVP on the surface of PMA and the degree of graft polymerization. If you change the "degree" and prepreg expansion time of the bulging solvent, you can control the degree of penetration of the single lysate dissolved in a single feed of ethyl acetate-water solvent on the surface of the material. From the results of heavy ft analysis, contact angle change, ATR-IR spectroscopy analysis and ESCA spectroscopy analysis, the fact that PVP grafted on the surface of the material can be determined. The extremely low gamma radiation agent Λ is a necessary condition for effective graft polymerization. The extremely low gamma radiation agent ft can destroy the radiation on the surface of the material. Read the notes of vfTj first lTh Item% The Ministry of Economic Affairs Central Bureau of Precision Industry β-Work Digest Cooperation Du Yin 51 Table 10: NVP graft polymerization on the surface of PMMA Swell time: 0 hours Swell solvent: ethyl acetate: water ( 1: 9) This paper is good for 5 good-size edges. "Sleepy home-like 1MCNS" < IM specifications (2 丨 0X297 public address) -33-202466 Λ 6 η 6 V. Description of the invention (1111 $ KfPlIt fe «« 10.01Xra < i Q.05Kraij O.lOIrad O.lSKrad m & m% ira μϊη mm nm 309rads / iin 77r8ds / iia ην Αν r5 rhv Λν Γο οο AD Λυ Λν CV οο 14 · n 4 — —4 MJ Λίυ
n nyw ot AO 11 t Λν Λπν Λν Αυ. H 7— —4 Λί ΛΛν 9W Γ5 4J 7U Λ/m Ρ3 J7 Γ3 9« »4 CJ Λν *Μν Λν Λν ΛΜν Λν f · οβ Αο 7— οο ην - Λην Λν Λν Απν Λο 71 οο οο eD < 3 1-1 11 ΛίιΜ 3- 71» ΓΊν r9 u cv «ο Αν Λν ΛΜν Λν ο 表11 : NVP接枝聚合於ΡΜΜΑ表面 • 膨脹時間:24小時 膨腥溶劑:9:1之水與乙酸乙酯及15% NVP ^M^!iAfi309rads/iDin M^Phl^ft77rads/nin '麵率-- 合百分率 O.OlMrads 38 1.0 35 1.3 0.03Mrads 27 2.3 23 2.8 0.05Mrads 17 2.5 17 2.4 O.lOMrads 16 3.0 16 3.2 0.15Mrads 10 3.0 16 3.4 請• iL 閲讀 背 而 之 注 意事 項 % 本 經濟部屮央榣準局员工消费合作社印製 表12 : NVI接枝聚合於ΡΗΜΑ表面 : 12/J 塒 賴黻:10» 率:309rads/ain 本紙張尺度边用中®國家標毕(CNS) ΊΜ規格(210X29/公龙) 202466 Λ 6 156 -34- 五、發明説明 mmmmm mzmzm 百分率 ϊ O.OlMrads 43 0.2 44 0.4 48 0.6 0.03Mrads 38 0.3 26 0.5 25 1.7 0.05Mrads 23 0.3 21 0.5 22 1.9 O.lOHrads 18 O.S 17 0.5 18 2.2 0.15Mrads 15 0.5 17 0.6 18 2.2 mzrnm :l 餓ae^·百分·Ι 背 而 之 /i 事 項 m .杰 表13 :以ATR-IR光箝分析PVP接枝聚合於PMMA表面之樣品《: 伽瑪輻射總劑量 Vc = 0(酯類) 經濟部屮央櫺準局只工消费合作社印ft,l4 O.OlMrad Vc = C(酵胺類) 7.67 0.03Mrad 6.51 0.07Mrad 4.61 0.lOMrad 1,68 0.15Mrad 1. 66 >:<混合5% NVP於9:1之水:乙酸乙酯之溶劑中 膨脹時間:17小時 伽瑪輻射劑量奉:lQ65rads/min 表14:以ESCA分析PVP接枝聚合於PMMA表面之樣品 伽瑪輻射總劑ft Ot:時 N/C之比值 0.03Mrad 2 . 2 X 1 〇'Z 0·05Mrad 3 . 1 X 1 〇'2 0 . 07Mrad 4.5X 10'4 0 . lOMrad 4 . 7 x 1 *混合5% NVP於9:1之水:乙酸乙酯之溶劑中 膨脹時間:17小時 伽瑪輻Ihi劑量率:l〇65rads/nin 本紙張尺度边用中國Η家榣毕(CNS)T4規格(210x297公;¢) ο 2 經濟部屮央標準局只工消设合作杜印ft'14 -35" Λ 6 Η 6466 五、發明説明() 實施例3 : 下列實驗證明氧氣對伽珊《射輥起接枝聚合反應之影 鬱極為顯著,故缺氣狀態對伽瑪輻射激起接枝聚合反應非 常重要。 伽瑪輻射激起 1〇 % HVP水溶液接枝聚合反應之狀 況如下: (甲)於氣氣存在之狀況下瀲起接枝聚合反慝。 (乙)於缺氣之狀況下瀲起接枝聚合反應,而且加入氬 氣以便於清除氧氣。 (丙)於缺氧之狀況下激起接枝聚合反應,而且抽出氣 氣至真空狀態。 於狀況(甲)中,若維持伽瑪轘射之剤量率於 213rads/nin,並以不同劑量如 0.01 , 0.05 , 0.20 與0.25Mrad之伽瑪輻射誘起 10 % HVP産生接枝聚合 作用。於狀況(乙)中,加入氬氣1Q分鐘以去除氣氣 。於狀況(丙)中,以真空冷凍融解法抽出氣《。先將 單體溶液置於液態氮中冷凍,再抽氣至真空狀態(0.3BB 汞柱)以去除氣體。於照射伽瑪輻射之前先將上述冷凍 溶液融解至室溫為止。有些搛品須經三次真空冷凍融解。 每一實驗均重覆兩次以確保其再現性。 為確定去氣效應對伽瑪輻射激起接枝聚合反應之影播 . 本發明於伽瑪輻射劑量率為2 13rads/nin及削量分別 為O.OlMrad及0.25Mrad時分別測定不同濃度單觴之轉 換率及分子量。 為了確定未參與反應之NVP單雔之量,本發明所用 (請先-wift背而之注意事項孙项寫木ar. -線· 本紙張尺度边用中國B家搮iMCNS)肀4規格(210X297公没) 202466 Λ 6 II 6 -36** 經濟部屮央標準局Μ工消赀合作社印51 五、發明説明() 之方法如下:先以伽瑪輻射照射 5«1NVP溶掖,再以 50ml乙睛荦取NVP溶液。未反應之NVP可溶於乙晴,但 NVP聚合成PVP以後就不溶於乙睛。以離心機分離PVP 沈殺與上層液,該上層液含有NVP。本發明探用10 % NVP溶液,其NVP之分析結果如下:以乙晡稀釋1〇 % NVP水溶液至 0.5g/Bl到5.0撖克/ml之範围内。以 3 2 3nni波長之紫外光測量其吸收率,並以NVP濃度對吸收 率作圖,可得一樣準曲線,該曲線之迴歸係數為0.99。 其分子量及分子量分佈可由凝謬滲透分析儀加以測定。 NVP轉換率(參與反應之 NVP單體之數量)深受 注入氬氣以去除氧氣或真空冷凍融解以去除氣觴等方法之 影響。若未去除氣體.則低至lHrad劑量之伽瑪輻射 不能瀲起任何接枝聚合反應。然而以氬氣去除氧*以後, NVP轉換成PVP之轉換率為46 %,以真空冷凍融解法淸 除氣體一次與三次,各得NVP轉換成 PVP之轉換率為 61 %與63 %。 卽使伽瑪輻射劑量高至O.lOMrad ,於 空氣中激起接枝聚合之轉換率只有 90 % (即有10炻 NVP單體未參與反應);然而去除氧氣之接枝聚合之轉 換率卻高至99 %。 因為未參與反應之 NVP單髓會在植入物表面與生物 鼸接觸時産生嚴重之中毒反應,故上述接近完金反應(99 % )之結果對生物體植入物非常重要。 本發明已證明去除氧氣之後可用低劑量之伽瑪輻射激 起PVP接枝聚合於PMMA表面,本發明以0.05Mrad劑 量及 157 rads/nin 劑最率之伽瑪輻射激起去除氡氣之 (請先間讀背而之注意事項孙填寫本一! 本紙張尺度边用中SB家楳準(CNS)T4規格(210X297公;《:) -37-202466 Λ 6 Η 6 經濟部屮央標準灼Η工消伢合作杜印製 五、發明説明() 10 % NVP接枝聚合於PMMA搛品。親水性之接枝聚合物 表面之接觸角為20° .且對機械摩損作用有穩定性(即 接》角不變)。如上所述,對機械摩損作用有穩定性之 親水性PVP係接枝聚合於ΡΜΜΑ表面,其KVP單體之轉 換率頗高(98 % )且溶液中聚合物之分子蛋頗高(分 子置為1.65 X 106)。若溶液中有氣氣存在,則痛用高 伽瑪輻射劑置(大於〇.11^3(1)或高單醚濃度(15%以 上)才能得到低接《角,高單體轉換率與高分子量之結 果。當親水性單體被伽瑪輻射激起聚合於其他聚合物材質 如聚丙烯、氟硪聚合物(例如PTFE或PVDF)或硅氧烷 表面時時,去除氣氣所産生之效應更為顯著。去除氣氣可 結合膨脹溶劑與自由基清除劑之使用以增進伽瑪輻射撖起 接枝聚合反醞之效果。本發明所用之自由基淸除劑包括可 氣化之金屬邇類或有機化合物如抗壞血酸。利用自由基淸 除劑的好處在於能産生有效之接枝聚合反應並使溶液中聚 合物之分子蛋降低。 去除氧氣對pvp分子量之影響相當大。以思;氣去除 氣氣或以真空冷凍融解去除氣匾後, 再使用低至 O.OlMrad劑量之伽瑪輻射可産生 1.6X 1〇6分子量之 PVP。反之,未去除氣氣之PVP分子量極低。笛伽瑪輻 射之劑量為〇.〇5Krad時,未清除氛氣之PVP分子置僅 為0.35 X 106, 而去除氣氣之PVP分子《在1.65 X 106至1.8 X 106之間。酋伽瑪輻射之劑量為〇.l〇Mrad 時,所有樣品無論是否去除氣氣皆可得到介於1.8 X 1〇* 至2.0 X 104之間之PVP分子量。 先 • W 讀 背 而 之 >主 意 項 η- m 寫 裝 η 線 Κ紙5艮尺度边用中a Β家樣iMWS) Ψ 4規格(210><297公址) 202466 五、發明説明() 實施例4 : 以下實驗傜用以證明自由基清除剤可抑制溶液聚合反 應與溶液凝謬之産生,持別在高單醞濃度之接枝聚合過程 中。 如實施例1所述之條件,以伽瑪輻射撖起PVP接枝聚 合於PMMA樣品之表面。本實施例使用抗祺血酸作為自由基 清除劑。伽瑪輻射激起之接枝聚合反醞條件列於表15。 (甲)30!I!NVP/0.5bM抗壊血酸/2.53;乙酸乙酯/0.21^8(1 伽瑪輻射《 (乙)3(^1^?/0.51111<抗壊血酸/2.5*乙酸乙酯/0.151^3(1 伽瑪輻射《 (丙)4 0%NVP/1. OmM抗壊血酸/0· IMrad伽瑪輻射 (丁)50!KNVP/1. ObM抗壊血酸/0. IMrad伽瑪輻射 (戊)5 0!£HVP/1.0iiiM抗谢血酸/0.2Mrad伽瑪輻射* *起始劑量為O.IHrad,將溶液中未參與反應之單腰與溶 液聚合物從樣品表面洗除外再以O.lMrad劑量之伽瑪輻 射照射樣品。 經濟部+央標準局员工消奸合作杜印製 (請先閲讀背而之注意亊項#项寫木一 表15中所有PMMA樣品的接觸角介於 18 °至24 °之間,故接枝聚合物之親水性很高。在(甲)(乙)( 丙)(丁)(戊)中伽瑪輻射之劑*率為 33 rads/iin , 僅在(乙)中使用667rads/Bin之伽瑪輻射之琍量 率。當單體濃度為30 %至50 %時,若不利用自由基清 除劑會導致溶液聚合物的凝醪作用。若在溶液中使用自由 基淸除劑如抗壞血酸時會抑制溶液聚合物的凝謬作用。而 使溶液聚合物的分子量降低但不會影鬱接枝聚合物之産量 本紙張尺度边用中8 Η家標準(CNS) «Ρ4規格(210乂297公龙) -39-20:466 Λ 6 It 6 經濟部屮央栉準局只工消#合作杜印^. 五、發明説明() 。PVP接枝聚合於PMMA表面的證明除了可用接觸角測董 之方法以外,亦可用ESCA與FTIR-ATR分析證明材質表 面有氮的存在,氮的來源為PVP接枝聚合之醯亞胺基圃 。良好之機械性質可由磨損試驗後接觸角的改變很小或材 質表面氮的存在加以證明。 實驗例5 : 本實施例以經本發明表面修飾後之材質對内皮組嫌之 組織黏附作用降低與對繼維'組嫌母細胞之細胞黏附作用降 低證明親水性接枝聚合物可改菩材質表面之效益。此種效 應對於改善材質之生物相容性,減少材質表面對組嫌之剌 激性或傷害作用相當重要。 一種用來測量材質與組嫌表面接觸時之黏附力(單位 為mg/cin )之儀器可以測定兔子眼角膜内皮組继與材質 表面接觸時之鈷附力。PMA,硅氣烷,聚丙烯等材質與 兔子眼角膜内皮組織接觸時之黏附力介於 250 至 4 00BU/CIB之間。上述材質表面經接枝聚合後呈現較小之 黏附力, 其黏附力皆低於 15〇Bg/cn 且通常低於 lOOmg/cm。 黏附力之減少亦伴随着材質對組餓傷害率之 降低。以電子顯微鏡觀察内皮組鏃之傷害率時,未經本發 明處理之PKMA或聚硅氣烷之傷害率為50至80 %,但 經本發明處理之PHMA或硅氣烷之傷害率降至20 %以下 〇 材質對活體細胞之傷害率亦可由材質對難胚胎之繼維 組織母細胞(CEF)或兔眼晶狀艟之内皮細胞(LE)之黏附作 用得知。實驗證明未經本發明處理之材質比經本發明處理n nyw ot AO 11 t Λν Λπν Λν Αυ. H 7— —4 Λί ΛΛν 9W Γ5 4J 7U Λ / m Ρ3 J7 Γ3 9 «» 4 CJ Λν * Μν Λν Λν ΛΜν Λν f · οβ Αο 7- οη ν Λν Λν Απν Λο 71 οο οο eD < 3 1-1 11 ΛίιΜ 3-71 »ΓΊν r9 u cv« ο Αν Λν ΛΜν Λν ο Table 11: NVP graft polymerization on PMMA surface • Expansion time: 24 hours swelling solvent : 9: 1 water with ethyl acetate and 15% NVP ^ M ^! IAfi309rads / iDin M ^ Phl ^ ft77rads / nin 'Area-to-Percentage O.OlMrads 38 1.0 35 1.3 0.03Mrads 27 2.3 23 2.8 0.05Mrads 17 2.5 17 2.4 O. OMrads 16 3.0 16 3.2 0.15Mrads 10 3.0 16 3.4 Please • iL Read the contrary notes% This table is printed by the Employee Consumer Cooperative of the Ministry of Economic Affairs of the Ministry of Economic Affairs 12: NVI graft polymerization on the surface of PHMA : 12 / J Sai Laifu: 10 »Rate: 309rads / ain The standard size of this paper is used in the national standard (CNS) ΊΜ specification (210X29 / male dragon) 202466 Λ 6 156 -34- V. Description of the invention mmmmm mzmzm Percentage ϊ O. OlMrads 43 0.2 44 0.4 48 0.6 0.03Mrads 38 0.3 26 0.5 25 1.7 0.05Mrads 23 0.3 21 0.5 22 1.9 O.lOHrads 18 OS 17 0.5 18 2.2 0.15Mrads 15 0.5 17 0.6 18 2.2 mzrnm: l starve ae ^ · percentage · I Contrary / i matter m. Jie Table 13: ATR-IR light Clamp analysis of samples of PVP graft polymerized on the surface of PMMA ": Gamma radiation total dose Vc = 0 (esters) The Ministry of Economic Affairs, Ministry of Economic Affairs, Central Bureau of Labor and Welfare Cooperative Printing Co., Ltd. ft, l4 O. OlMrad Vc = C (enzymes ) 7.67 0.03Mrad 6.51 0.07Mrad 4.61 0.lOMrad 1,68 0.15Mrad 1.66 >: < Mix 5% NVP in 9: 1 water: ethyl acetate solvent expansion time: 17 hours gamma radiation dose Feng: lQ65rads / min Table 14: Analysis of the sample gamma-radiation total agent ft Ot of PVP graft polymerized on the surface of PMMA by ESCA: N / C ratio 0.03Mrad 2 .2 X 1 〇'Z 0 · 05Mrad 3.1 X 1 〇'2 0 .07Mrad 4.5X 10'4 0 .lOMrad 4.7 x 1 * Mixing 5% NVP in 9: 1 water: ethyl acetate solvent Expansion time: 17 hours Gamma Ihi dose rate : L〇65rads / nin This paper scale is used in China 漣 戣 Bi (CNS) T4 specification (210x297 g; ¢) ο 2 The Ministry of Economic Affairs ’Bureau of Standards only works with the Consumers and Consumers to set up a cooperation du ft'14 -35 " Λ 6 Η 6466 five DESCRIPTION OF THE INVENTION () Example 3: The following experiments show that the oxygen of gamma Shan "Movies exit roller from the graft polymerization of the reaction is extremely significant depression, run flat state so that graft polymerization is very important to excite gamma radiation. The state of gamma-radiation-induced graft polymerization of 10% HVP aqueous solution is as follows: (A) In the presence of gas, the graft polymerization is reversed. (B) In the absence of gas, the graft polymerization reaction is initiated, and argon is added to facilitate the removal of oxygen. (C) Initiate graft polymerization under anoxic conditions, and evacuate the gas to a vacuum state. In condition (A), if the rate of gamma radiation is maintained at 213rads / nin, and different doses such as 0.01, 0.05, 0.20 and 0.25Mrad of gamma radiation induce 10% HVP to produce graft polymerization. In condition (B), add argon for 1Q minutes to remove the gas. In condition (C), extract the gas by vacuum freezing and thawing method. The monomer solution was first frozen in liquid nitrogen, and then evacuated to a vacuum (0.3BB Hg) to remove the gas. Before irradiating gamma radiation, the above-mentioned frozen solution is melted to room temperature. Some products must be frozen and thawed three times in vacuum. Each experiment was repeated twice to ensure its reproducibility. In order to determine the effect of the degassing effect on the gamma-radiation-induced graft polymerization reaction. The present invention measures different concentrations of the single dose when the gamma radiation dose rate is 2 13rads / nin and the cut amount is 0.01Mrad and 0.25Mrad respectively Conversion rate and molecular weight. In order to determine the amount of NVP single carbohydrates that did not participate in the reaction, the present invention is used (please note first -wift Sun Xiang writes wood ar. (Public) 202466 Λ 6 II 6 -36 ** Printed by the Mongong Consumer Cooperative of the Central Standards Bureau of the Ministry of Economic Affairs 51 V. Description of invention () The method is as follows: firstly irradiate 5 «1NVP with gamma radiation, then 50ml Take NVP solution. Unreacted NVP is soluble in acetonitrile, but NVP is insoluble in acetonitrile after it is polymerized into PVP. Separate PVP sludge and supernatant with a centrifuge. The supernatant contains NVP. The invention uses 10% NVP solution, and the NVP analysis result is as follows: 10% NVP aqueous solution is diluted with ethyl acetate to the range of 0.5g / Bl to 5.0mg / ml. The absorption rate is measured with ultraviolet light of 3 2 3nni wavelength, and the NVP concentration is plotted against the absorption rate to obtain the same quasi-curve. The regression coefficient of this curve is 0.99. Its molecular weight and molecular weight distribution can be determined by a condensate permeation analyzer. The NVP conversion rate (the number of NVP monomers participating in the reaction) is strongly influenced by methods such as injecting argon to remove oxygen or vacuum freezing and thawing to remove gas. If the gas is not removed, gamma radiation with a dose as low as 1Hrad cannot initiate any graft polymerization reaction. However, after removing oxygen * with argon, the conversion rate of NVP to PVP was 46%, and the gas was removed by vacuum freezing and thawing once and three times. The conversion rates of NVP to PVP were 61% and 63%. The gamma radiation dose is as high as 0.1 OMrad, and the conversion rate of the graft polymerization induced in the air is only 90% (that is, there are 10 nm NVP monomers not participating in the reaction); however, the conversion rate of the oxygen removal graft polymerization is As high as 99%. Because the NVP single marrow that is not involved in the reaction will produce a serious poisoning reaction when the surface of the implant comes into contact with the biological mule, the result of the near-finish metal reaction (99%) is very important for the biological implant. The present invention has proved that after removing oxygen, low dose of gamma radiation can be used to stimulate PVP graft polymerization on the surface of PMMA. The present invention uses 0.05Mrad dose and 157 rads / nin dose of gamma radiation to stimulate radon removal (please Read the notes beforehand. Sun fills in this one! This paper is used in the standard SB Family Standard (CNS) T4 specification (210X297 ;;: :) -37-202466 Λ 6 Η 6 The Ministry of Economic Affairs Standard Standard Η Cooperated with the Consumers and Consumers Co., Ltd. Du Printed 5. Description of the invention () 10% NVP graft polymerized on PMMA coatings. The contact angle of the surface of the hydrophilic graft polymer is 20 °. And it is stable against mechanical friction (ie. 》 The angle remains unchanged. As mentioned above, the hydrophilic PVP that is stable to mechanical abrasion is grafted and polymerized on the surface of PMMA, the conversion rate of KVP monomer is quite high (98%) and the molecular egg of the polymer in solution Very high (the molecule is set to 1.65 X 106). If there is gas in the solution, you can use high gamma radiation agent (greater than 0.11 ^ 3 (1) or high monoether concentration (more than 15%) to get Low connection angle, high monomer conversion rate and high molecular weight results. When the hydrophilic monomer is stimulated by gamma radiation When polymerized on the surface of other polymer materials such as polypropylene, fluoropolymer (such as PTFE or PVDF) or siloxane, the effect of degassing is more significant. Degassing can be combined with swelling solvent and free radical scavenging The use of the agent enhances the effect of gamma radiation on grafting polymerization. The free radical scavengers used in the present invention include vaporizable metal compounds or organic compounds such as ascorbic acid. The advantage of using free radical scavengers is that It can produce effective graft polymerization and reduce the molecular egg of the polymer in the solution. The effect of removing oxygen on the molecular weight of pvp is quite large. Isi; after removing the gas or removing the gas plaque by vacuum freezing and thawing, use it as low as O. OlMrad dose of gamma radiation can produce PVP with a molecular weight of 1.6 × 106. Conversely, the molecular weight of PVP without degassing gas is extremely low. When the dose of flute gamma radiation is 0.05Krad, the PVP of atmosphere is not cleared The molecular setting is only 0.35 X 106, and the PVP molecule for degassing is between 1.65 X 106 and 1.8 X 106. When the dose of Emirates gamma radiation is 0.1 Mrad, all samples can be degassed or not Get The molecular weight of PVP is between 1.8 X 10 * and 2.0 X 104. First • W read back and forth> idea term η-m writing η line κ paper 5 Gen scale side use a Β 家 样 iMWS) Ψ 4 Specifications (210 > < 297 public address) 202466 V. Description of the invention () Example 4: The following experimental examples are used to prove that free radical scavengers can inhibit the solution polymerization reaction and the solution condensation, which is a high order. The concentration of the graft polymerization process. According to the conditions described in Example 1, the PVP graft was polymerized on the surface of the PMMA sample by gamma radiation. In this example, ascorbic acid was used as a free radical scavenger. Gamma radiation-induced graft polymerization anti-incubation conditions are listed in Table 15. (A) 30! I! NVP / 0.5bM ascorbic acid / 2.53; ethyl acetate / 0.21 ^ 8 (1 gamma radiation <(B) 3 (^ 1 ^? / 0.51111 < ascorbic acid / 2.5 * Ethyl acetate / 0.151 ^ 3 (1 Gamma Radiation ((C) 4 0% NVP / 1. OmM Ascorbic Acid / 0 · IMrad Gamma Radiation (D) 50! KNVP / 1. ObM Ascorbic Acid / 0. IMrad gamma radiation (E) 5 0! £ HVP / 1.0iiiM ascorbic acid / 0.2Mrad gamma radiation * * The starting dose is O.IHrad, the single waist in the solution that does not participate in the reaction is polymerized with the solution The objects are washed from the surface of the sample, and then the sample is irradiated with gamma radiation at a dose of 0.1 Mrad. The Ministry of Economic Affairs + Central Standards Bureau staff eliminates crimes and cooperates with Du printed (please read the back and pay attention to the item # item write wood in Table 15 The contact angle of all PMMA samples is between 18 ° and 24 °, so the graft polymer is very hydrophilic. Gamma radiation agent in (A) (B) (C) (D) (E) * The rate is 33 rads / iin, and the gamma radiation rate of 667rads / Bin is used only in (B). When the monomer concentration is 30% to 50%, the use of free radical scavenger will cause solution polymer Coagulation effect. If free radical scavenger is used in the solution such as anti-corruption Blood acid will inhibit the coagulation effect of the solution polymer. It will reduce the molecular weight of the solution polymer but will not affect the yield of the graft polymer. This paper is used in the middle of the 8 standard (CNS) «P4 specification (210侂 297 公 龙) -39-20: 466 Λ 6 It 6 The Ministry of Economic Affairs, Jiyang, Bureau of Industry and Engineering only Gongxiao # Cooperation Du Yin ^. V. Description of the invention (). Proof of PVP graft polymerization on the surface of PMMA except for available contacts In addition to the angle measurement method, ESCA and FTIR-ATR analysis can also be used to prove the presence of nitrogen on the surface of the material. The source of nitrogen is PVP grafted polymerized imide-based garden. Good mechanical properties can be changed by contact angle after the wear test It is proved by the presence of very small or nitrogen on the surface of the material. Experimental Example 5: This example demonstrates that the surface-modified material of the present invention has a reduced tissue adhesion effect on the endothelial group and a reduced cell adhesion effect on the susceptible mother cells of the Jiwei group. Hydrophilic graft polymers can improve the effectiveness of the surface of the material. This effect is very important for improving the biocompatibility of the material and reducing the irritability or damage of the surface of the material. table The adhesion force (unit is mg / cin) during surface contact can measure the cobalt adhesion force of the corneal endothelial group of rabbit eyes after contact with the surface of the material. Materials such as PMA, silicon, polypropylene and polypropylene come into contact with the corneal endothelial tissue of rabbit eyes The adhesion force is between 250 and 400 BU / CIB. The surface of the above materials exhibits a small adhesion force after graft polymerization, and the adhesion force is less than 15〇Bg / cn and usually less than 100mg / cm. The reduction in adhesion is also accompanied by a reduction in the damage rate of the material to the group. When observing the injury rate of endothelial group with electron microscope, the injury rate of PKMA or polysilazane without treatment of the present invention is 50 to 80%, but the injury rate of PHMA or silazane treated by the present invention is reduced to less than 20% 〇The damage rate of the material to living cells can also be known from the adhesion effect of the material to the difficult-to-embryo follow-up tissue mother cells (CEF) or rabbit eye lens endothelial cells (LE). The experiment proves that the material that is not treated by the present invention is more processed by the present invention
先 閲 $ 背 而 之 注 意 Ψ 項 % 木JI 裝 玎 線 本紙張尺度逍用中BI8家標準(CNS)T4規格(210X297公Λ) 202466 Λ 6 Μ 6 -40- 經濟部+央標準局Α工消价合作杜印51 五、發明説明() 之材質對活體細胞之傷害率髙2至4倍。以O.IHrad劑量與 15%NVP接枝聚合於PMMA表面對CEF細胞之黏附力僅為原 來PMMA黏附力之35%。PHEMA接枝聚合於PMMA表面對CEF 細胞之鈷附力僅為原來PMMA黏附力之38%。15:1之NVP: HEMA接枝聚合於PMMA表面對CEF細胞之黏附力僅為原來 PMMA黏附力之20%。於較佳條件下,經本發明處理之PVP 接枝聚合於PMMA, PC或PSi表面對LE之黏附作用僅為毎平 方毫米1至2個LE,而未經本發明處理之PMMA, PC或PSi表 面對LE之黏附作用為每平方毫米1(3個LE以上。 實施例6 : 本實施例說明將HEMA或NVP與HEMA混合物接枝聚合於 PMMA表面之結果。 本實施例除了用16%NVP/HEMA(15:1)單髓混合物, O.lOMrad劑置及1 300rads/oin劑量率之伽瑪轘射外,其他 條件與實施例1相同。以PVP-PHEMA修飾PMMA表面之接觸 角為17°。於相似條件下,7%NVP/HEMA(5:2)接枝聚合 於PMMA表面之接«角為23° ,而2.5%HEMA接枝聚合於PM HA表面之接觸角為18°。 實施例7 : 本實施例說明陰離子性單髏或陽離子性單鱧與親水性 單醱混合之效應。於本發明中可將離子性單龌或NVP單睡 混合使用。 甲、15%NVP加入1至5重Μ百分率之全啉二羧酸(AA) 或丁烯酸(CA)作混合單體,並如實施例1之方法以0. IMrad 劑量及1235rads/min剤量率之伽瑪輻射誘起接枝聚合反應 本紙5良尺度逍用中a Η家楳毕(CNS)>F4規格(210X297公址) -41-2〇24aa Λ 6 Π 6 五、發明説明() ,所得塗層之接觸角介於18°至22°之間,其對内皮組嫌 之黏附力僅為原來PMMA之一半以下,故可涅明接枝聚合之 塗層具有極佳之親水性。類似效果可由陽離子性單觸二甲 基氨乙基丙烯酸甲曲接枝聚合之塗層得到。苯乙烯磺酸 (SSA)可作為陰離子性單匾與NVP作為混合單龌接枝聚合於 PMMA表面。使用1:2 SSA:HVP(含33%SSA)之混合單齷《度 為30%,伽瑪輻射剤量為0. 15Mrad及劑量率為70 0rads/Bin ,可得親水性聚合之塗層且k接觸角為30°至40°。 乙、苯乙烯磺酸之納鹽(NaSSA)可作為具髙度親水 性之陰離子性單腥,並與 NVP 共聚於聚二甲基硅氧烷 (PDMS)表面。 本實施例以含乙酵之超音波處理機淸洗 PDMS樣品,再以真空乾燥之,然後置於含單體之水溶液 中並以伽瑪輻射照射之。表16列出接枝聚合之條件, 如單髏灌度,伽瑪輻射劑董,並保持伽瑪輻射劑量率於 70 0rads/Bin,並列出接枝聚合表面之接觸角。 表16 : 伽璁輻射劑量 NaSSA百分率 NVP百分率 接觸角 (請先閲請背而之注意事項孙项寫木j 訂_ 線- 0 . 05Mrad Ο .lOMrad 0.15Mrad ο ο ο 2 2 2 ο ο ο 2 2 2Read the first $ and pay attention to Ψ items% Wood JI Threading paper size in the use of BI8 standard (CNS) T4 specifications (210X297 public) 202466 Λ 6 Μ 6 -40-Ministry of Economic Affairs + Central Standards Bureau Price-cutting cooperation Du Yin 51 V. Invention description () The damage rate of the material to living cells is 2 to 4 times higher. The adhesion of O.IHrad and 15% NVP graft polymerization on the surface of PMMA to CEF cells is only 35% of the original PMMA adhesion. The cobalt adhesion of PHEMA grafted on the surface of PMMA to CEF cells is only 38% of the original adhesion of PMMA. 15: 1 NVP: The adhesion of HEMA grafted polymerized on the surface of PMMA to CEF cells is only 20% of the original adhesion of PMMA. Under preferred conditions, the adhesion of the PVP treated by the present invention to the surface of PMMA, PC or PSi to LE is only 1 to 2 LE per square millimeter, and the surface of PMMA, PC or PSi not treated by the present invention is The adhesion of LE is 1 per square millimeter (more than 3 LEs. Example 6: This example illustrates the results of graft polymerization of HEMA or NVP and HEMA mixture on the surface of PMMA. In this example, 16% NVP / HEMA ( 15: 1) Single-medullary mixture, O.lOMrad agent and 1 300 rads / oin dose rate gamma radiation, other conditions are the same as Example 1. The contact angle of PMMA surface modified with PVP-PHEMA is 17 °. Under similar conditions, the contact angle of 7% NVP / HEMA (5: 2) graft polymerization on the surface of PMMA is 23 °, and the contact angle of 2.5% HEMA graft polymerization on the surface of PM HA is 18 °. Example 7: This example illustrates the effect of mixing anionic mono-cary or cationic mono-lep and hydrophilic mono-hybrid. In the present invention, ionic mono-cary or NVP single-sleep can be used in combination. A, 15% NVP is added to 1 to 5 weight M Percentage of full-line dicarboxylic acid (AA) or crotonic acid (CA) as a mixed monomer, and as in the method of Example 1 with 0. IMrad dose and 12 35rads / min rate of gamma radiation induces graft polymerization reaction paper 5 good scales for easy use a Η Family tree (CNS) > F4 specifications (210X297 public address) -41-2〇24aa Λ 6 Π 6 5 Description of the invention (), the contact angle of the resulting coating is between 18 ° and 22 °, and its adhesion to the endothelial group is only less than one-half of the original PMMA. Good hydrophilicity. A similar effect can be obtained by a coating of cationic one-touch dimethylaminoethyl acrylic acid methylester graft polymerization. Styrene sulfonic acid (SSA) can be used as an anionic single plaque and NVP as a mixed single-dye graft It is polymerized on the surface of PMMA. Use 1: 2 SSA: HVP (containing 33% SSA) to mix the mixture, the degree is 30%, the gamma radiation dose is 0.15Mrad and the dose rate is 70 0rads / Bin, can get hydrophilic Polymerized coating with a k contact angle of 30 ° to 40 °. Na, sodium salt of styrene sulfonic acid (NaSSA) can be used as a highly hydrophilic anionic monosodium, and copolymerized with NVP in polydimethylsilicone Oxidane (PDMS) surface. In this example, the PDMS sample was washed with an ultrasonic treatment machine containing ethyl yeast, then dried in vacuum, and then placed in the monomer-containing The aqueous solution was irradiated with gamma radiation. Table 16 lists the conditions of graft polymerization, such as single-bone irrigation, gamma radiation agent, and keep the gamma radiation dose rate at 70 0rads / Bin, and list the graft The contact angle of the polymerized surface. Table 16: Gamma radiation dose NaSSA percentage NVP percentage contact angle (please read the notes beforehand Sun Xiangshu Mumu j _ line-0.05Mrad Ο.lOMrad 0.15Mrad ο ο 2 2 2 ο ο ο 2 2 2
7 5 3 1A 1X 經濟部屮央櫺準而只工消费合作杜印則4 如表 16 所示, 即使所用之伽瑪輻射翔1量低至 〇.〇5Mrad , 潺合單體之缌濃度為 40 %其中NaSSA與 NVP各佔一半,可得極具親水性之陰饑子性表面接枝聚 合物(其接觸角為17 ° ) 本紙张尺度逍用中S困家樣毕(CNS)T4規格(210X297公;it) -42-202466 Λ 6 Η6 經濟部屮央榣準局A工消价合作杜印51 五、發明説明() 實施例8 : 本實施例說明去除氧氣對於親水性單《接枝聚合於聚 丙烯(PP)表面之效應之重要性。 當氣氣存在時,以伽瑪輻射激起親水性單體接枝聚合 於PP表面之效果不佳。在如同實施例1之條件下,即使 伽瑪輻射之劑量高於Q.lMrad而單《之濃度髙於10 % . 若有«氣存在,則材質赛面之親水性棰差且接觸角之 減小並不顯箸。然而於去除氧氣之條件下,伽瑪輻射之劑 量低至 0.C1至0.05Mrad 之間,且保持其劑量率為 157rads/min ,單醱濃度為10 % MP ,所得塗層之接 觸角約為15 °。 PP表面性質之改變,亦可由機械磨 損試驗之接觸角改變很小測出,且可看出NVP接枝聚合 於 PP之塗層具有極佳之親水性。此種親水性對於以 PMMA裂成之眼睛透鏡與PP製成之觸黷之表面修眛非常 重要。 實施例9 : 聚碩酸乙酯(PC)是一種很有用之工程用塑®,可作 為眼睛植入物。於去氣狀況下,以伽瑪輻射激起NVP接 枝聚合於PC表面,可對PC表面作極佳之表面修飾。 例如,以0.05 Hrad劑量及93rads/Bin劑量率之伽瑪 輻射激起澝除氣氣之 1〇 % NVP接枝聚合於PC表面, 所得産物之接觴角為19 °。 實施例10 : 以伽瑪輻射撖起NVP接枝聚合於聚桂氧烷(PSi)表 面之速率雖然不如NVP接枝聚合於PMMA之速率,但其 (請先侧讀背而之注总事項#碼艿木亙 裝- 訂* 線_ 本紙張尺度4用中BH家樣準(CNS)T4規格(210x297公;«:) -43- 202466 Μ 五、發明説明() 産物之 接觸角亦會降低。 以 0.05Mrad 劑量及 93rads/min 劑Μ率之伽瑪輻射激起去除氣氣之 10 96 NVP接枝聚合於PSi表面,其産物之接觸角約為45 ° ,由此可知接枝聚合後之PSi表面具有相當程度之親水 性。若提高伽瑪輻射之劑量,並使用膨眼溶劑及較离之 、 單睡濃度,可增進其産物之親水性。例如,以.OlOMrad 劑量及 lSTrads/mUi 劑置率之伽瑪輻射撖起 NVP/HEMA(10:1)混合單體接枝聚合於PSi表面,邸使 於氣氣存在之情況下,其産物之接觸角降低為30 °。 實施例11 : 經沭部中央楳準杓员工消费合作社印ft,l4 (請先閲讀背而之注总市項洱项寫木頁-· 本實施例以聚氟亞乙烯(PVDF)作為氟磺聚合物材質 之實例。接枝聚合之溶液可用NVP水溶液,含KVP之 水與甲 醇溶液, 或含 NVP 之乙酸乙酯溶液,再以 0.20Hrad及3 2 6 rads/min之伽瑪轜射瀲起 NVP接枝 聚合於PVDF表面,其産物之接觸角約為30 °。 若去 除氣氣,則接枝聚合於PVDF表面之效果極佳。於去氣 之後,以0.05Mrad及157rads/篇in之伽瑪輻射激起 NVP接枝聚合於PVDF表面所形成之PVP塗層,其接觸 角僅為17 °。 HVP單醱對於PVDP亦為良好之膨脹溶 劑,故相當長之膨脹時間對於 NVP單《接枝聚合於 PVDF表面之效率有很大的幫助。例如,以7¾ HVP單 體預浸 PVDF 5小時後,再以O.lOMrad及94rads/^in 之伽瑪輻射照射之,所得産物之接«角僅為14 °。 實施例12:組合物之接枝條件:不同聚合物之觸《透嫌 本發明發現於特殊之接枝進行條件下,有將組合物修 本紙張尺度边用中Η B家樣爭(CNS) T4規格(210X297公;a:) 202466 Λ 6 Η 6 _ 4 4 五、發明説明() 飾之表面用作為眼部植入物内透鏡««群之可行性。 由 不同材質組合之眼睛透鏡可一次接枝聚合於其表面以産 生具有生物相容性之塗層。眼瞭透鏡之材質如 PMMA , PC與 PSi及觸鑕繼維之材質如 PVDF或PP可用本發 明之恃殊條件得到良好之接枝聚合産物。表16列出迪 當之相互接枝條件使 PVP接枝聚合於透鏡與钿鬚組合物 表面。 t7 5 3 1A 1X The Ministry of Economic Affairs is approved by the Ministry of Economic Affairs and the only consumer cooperation is Du Yin. 4 As shown in Table 16, even if the amount of gamma radiation used is as low as 0.05 Mrad, the concentration of the monomers is 40% of which NaSSA and NVP account for half of each, can get extremely hydrophilic surface graft polymer (the contact angle is 17 °) The paper size is easy to use in the middle of the S sleepy home sample (CNS) T4 specifications (210X297 public; it) -42-202466 Λ 6 Η6 Ministry of Economic Affairs, Bureau of Economics and Trade, A industrial price-cutting cooperation Du Yin 51 V. Description of invention () Example 8: This example illustrates the removal of oxygen for hydrophilic The importance of the effect of branch polymerization on the surface of polypropylene (PP). In the presence of gas, the effect of grafting polymerization of hydrophilic monomers on the surface of PP with gamma radiation is not good. Under the same conditions as in Example 1, even if the dose of gamma radiation is higher than Q.lMrad and the concentration of single radiation is higher than 10%. If there is «qi, the hydrophilicity of the material surface is poor and the contact angle is reduced. Small is not obvious. However, under the condition of removing oxygen, the dose of gamma radiation is as low as 0.C1 to 0.05Mrad, and the dose rate is maintained at 157rads / min, the single concentration is 10% MP, the contact angle of the resulting coating is about 15 °. The change in the surface properties of PP can also be measured by a small change in the contact angle of the mechanical abrasion test, and it can be seen that the coating of NVP graft polymerized on PP has excellent hydrophilicity. This hydrophilicity is very important for the repair of the surface of the eye lens split with PMMA and the contact surface made of PP. Example 9: Polyethylesterate (PC) is a useful engineering plastic® that can be used as an eye implant. Under degassing conditions, the NVP grafting is induced by gamma radiation to polymerize on the PC surface, which can make excellent surface modification on the PC surface. For example, gamma radiation with a dose of 0.05 Hrad and a dose rate of 93 rads / Bin stimulates 10% NVP of the degassed gas to be grafted and polymerized on the surface of the PC. The joint angle of the resulting product is 19 °. Example 10: The rate of NVP graft polymerization on the surface of polyoxyalkylene (PSi) by gamma radiation is not as good as the rate of NVP graft polymerization on PMMA, but its (please read the back side and note the general matters # Code 艿 木 亘 装-Order * Line _ This paper size 4 is used in the BH home sample standard (CNS) T4 specifications (210x297 public; «:) -43- 202466 Μ 5. Invention description () The contact angle of the product will also be reduced Gamma radiation at a dose of 0.05 Mrad and a rate of 93 rads / min M stimulates the degassed 10 96 NVP graft polymerization on the surface of the PSi, the contact angle of the product is about 45 °, which shows that the graft polymerization The surface of PSi has a considerable degree of hydrophilicity. If the dose of gamma radiation is increased, and the use of eye-expansion solvent and a relatively single, single-sleep concentration, the hydrophilicity of the product can be improved. The gamma radiation of the setting rate lifts the NVP / HEMA (10: 1) mixed monomer graft polymerization on the surface of PSi. In the presence of gas, the contact angle of the product is reduced to 30 °. Example 11: Printed ft, l4 by the Ministry of the People ’s Republic of China Central People ’s Government Staff Cooperative Association (please read the back-to-back notes of the general city item Wood sheet- · In this embodiment, polyvinyl fluoride (PVDF) is used as an example of fluorosulfon polymer material. The solution for graft polymerization can be NVP aqueous solution, KVP-containing water and methanol solution, or NVP-containing ethyl acetate solution. Then, the NVP graft polymerized with 0.20Hrad and 3 2 6 rads / min of GPR on the PVDF surface, the contact angle of the product is about 30 °. If the gas is removed, the effect of the graft polymerization on the PVDF surface Very good. After degassing, the PVP coating formed by NVP graft polymerization on the PVDF surface with 0.05Mrad and 157rads / in. Gamma radiation is excited, and its contact angle is only 17 °. HVP is also applicable to PVDP. It is a good swelling solvent, so a relatively long swelling time is of great help to the efficiency of NVP single graft polymerization on the surface of PVDF. For example, after pre-soaking PVDF with 7¾ HVP monomer for 5 hours, O.lOMrad and Radiated by 94rads / ^ in of gamma radiation, the joint angle of the resulting product is only 14 °. Example 12: Grafting conditions of the composition: the contact of different polymers Under the conditions, there is a medium-scale B (CNS) T4 specification (210X297; a :) 202466 Λ 6 Η 6 _ 4 4 V. Description of invention () The feasibility of using the decorated surface as a lens «« group in an eye implant. Composed of different materials The eye lens can be grafted and polymerized on its surface at one time to produce a biocompatible coating. It can be seen that the lens materials such as PMMA, PC and PSi and the contact materials such as PVDF or PP can obtain good graft polymerization products under the special conditions of the present invention. Table 16 lists the conditions for mutual grafting of PVP to polymerize PVP onto the surface of the lens and whisker composition. t
PMM/PP與 PMMA/PVDF 於去氧狀況下,以0.05Mrad及157rads/ain伽瑪 輻射撖起10 % NVP接枝聚合於PMHA及’PP組合物表 面,所製得産物之接觸角分別為 20 ° (PMMA)與15 0 (PP), 並具有機械穗定性。若不去除氣氣,則PP 表面之接枝聚合效果比 PMMA表面之接枝聚合效果差。 去除氧氣對PVDF表面之接枝聚合效果非常重要。於去 除氣氣之狀況下,以〇.〇5Mrad及157rads/nin 伽瑪輻 射激起10 % NVP接枝聚合於 PMHA及PVDF組合物表 面之效果極佳。請參閲表16。PMM / PP and PMMA / PVDF were deoxygenated at 0.05 Mrad and 157 rads / ain gamma radiation and 10% NVP was grafted and polymerized on the surface of PMHA and PP compositions. The contact angles of the products were 20 ° (PMMA) and 15 0 (PP), and has mechanical ear qualitative. If the gas is not removed, the effect of graft polymerization on the surface of PP is worse than that on the surface of PMMA. The removal of oxygen is very important for the effect of graft polymerization on the PVDF surface. Under the condition of degassing gas, the effect of stimulating 10% NVP graft polymerization on the surface of PMHA and PVDF compositions with 0.05 Mrad and 157 rads / nin gamma radiation is excellent. See Table 16.
PC/PP與 PC/PVDF 經濟部中央櫺準,^工消"合作社印製 (請先閲讀背而之注意事項#構寫木1 於去氣狀況下,以0.05Mrad及157rads/Bin伽瑪 輻射激起10 % NVP接枝聚合於 PC及PP組合物表面 ,其産物之接觸角分別為19 ° (PC)與15 ° (PP)。 於去氣狀況下,以〇.〇5Mrad及157rads/Bin伽瑪 輻射激起10炻NVP接枝聚合於PVDF及PC組合物表 面,其結果與 PC/PP或PMMA/PP組合物相似。因為 PVDF於NVP中會膨脹,故預先膨脹時間有助於PVP與 本紙張尺度边用中a Η家榣iMCNS) Τ4規格(210X297公;it) -45-203466 Λ 6 Η 6 經濟部屮央樑準杓A工消赀合作社印製PC / PP and PC / PVDF Central Ministry of Economic Development, Printed by ^ Work Consumers' Cooperative (please read the back-to-back notes first # 建 写 木 1 under degassing conditions, with 0.05Mrad and 157rads / Bin gamma Radiation induced 10% NVP graft polymerization on the surface of PC and PP compositions, the contact angles of the products were 19 ° (PC) and 15 ° (PP). Under degassing conditions, with 0.05Mrad and 157rads / Bin gamma radiation inspires 10 nm NVP graft polymerization on the surface of PVDF and PC composition, the result is similar to PC / PP or PMMA / PP composition. Because PVDF will expand in NVP, the pre-expansion time helps PVP Printed on the side of this paper for standard a Η 家 榣 iMCNS) Τ4 specifications (210X297 g; it) -45-203466 Λ 6 Η 6 Ministry of Economic Affairs, Biyang Liangzhunpao A industrial consumer cooperation cooperative
五、發明説明() PVDF之結合。其他由兩種以上聚合物組成之組合物所裂 成之眼睛植入物表面亦可得良好之親水性接枝聚合物。 請參閲表16。 實施例13 : 眼球内部嵌入透鏡(IOLs)之表面修飾之數種條件己 在前述實施例中敘明,並經依據本發明所定之裂程條件將 其植入兔眼約一年時間,以證明經過親水性伽瑪聚合表面 修飾後的眼睛植入物(I0LS)的良好生物接納性。例如, 將辛斯剴(Sinskey) 型- 03 7 丁琛狀透鏡 (PMMA光學 /PP觸類)以PVP表面修飾及乙烯氣化殺菌後,植入紐 西蘭白兔眼部前房,再以一 Η彈性觸纊之PMMA IOLs植 入其眼部後房。而其IOLs表面修飾之條件如下: (甲)15%NVP, O.lOMrad, 30與 12rads/ain,接«角 C.A. 20° - 25° (乙)依實施例4及表15中a、b、c、d條件,以開缝燈 對眼睛作定期檢査,一年後的病歴以及對植入透鏡作顯撖 鏡檢視(與未作接枝PMMA控制IOLs比較),顯示了良好的生 物相容性及本發明親水性聚合表面接枝修飾之正常行為。 表17:以PVP修飾透鏡/觸親之表面 透鏡/觸饌 典型的伽瑪輻射接枝聚合條件X PMMA/PP 甲、去氣之10%NVP,低劑量率*※,0.05 Mrad 乙、2.5%乙酸乙酯,6小時膨脹時間,去氧 之10%NVP,低剤量率*※.0.05Mrad PMHA/PVDF 甲、去«之10%NVP,低劑量率※※,0.05 Mrad 乙、去氧之10% NVP, 5小時膨脹時間,低劑 量率米米,0 .15Mrad 丙、2.5%乙酸乙酯,S小時膨脹時間,去氣 之10%HVP,低劑量率※来,0.05Mrad 本紙張尺度边用中國國家標準(CNS)f 4規格(210x297公;ft) * 4 6 A 6 It 6 五、發明説明() PC/PP 甲、去氧之10% NVP,低劑量率米※,0.05 Mrad 請 .先 閱 "ift 背 而 之 注 节 項 再 m % 木 乙、2.5%乙酸乙酯,6小時膨脹時間,去氧 之10%NVP,低劑量率※※,0.05Mrad PC/PVDF 甲、去氧之10% NVP,低劑量率*来,0 . 05 Hrad 乙、去《之10% NVP, 5小時膨膜·時間,低劑 量率来来,0 . 05Mrad 丙、2.5%乙酸乙酯,6小時膨脹時間,去氣 之10%NVP,低劑量率※※,0.05Mrad *其産物之接觸角少於25°。 米※低剤量率為30至300rads/nino 實施例14 : 本實施例説明在極低濃度 (0.5重置百分率以下 ) 的單體,可用極低劑量(〇.Q〇5Mrad以下)之伽瑪轘射 激起有效之接枝聚合反應。5. Description of the invention () The combination of PVDF. Good hydrophilic graft polymers can also be obtained on the surface of ocular implants split by other compositions composed of two or more polymers. See Table 16. Example 13: Several conditions for surface modification of embedded lenses (IOLs) inside the eyeball have been described in the previous examples, and they were implanted into the rabbit eye for about one year under the cracking conditions determined according to the present invention, to prove Good bio-acceptance of eye implants (IOLS) modified with hydrophilic gamma polymerized surface. For example, the Sinskey-03 7 Ding Chen-shaped lens (PMMA optics / PP contact type) was surface-modified with PVP and sterilized by ethylene vaporization, and then implanted into the anterior chamber of the New Zealand white rabbit eye. PM elastic IOLs with Η elasticity are implanted in the posterior chamber of the eye. The conditions for the surface modification of IOLs are as follows: (A) 15% NVP, O. l OMrad, 30 and 12 rads / ain, connection angle CA 20 °-25 ° (B) According to Example 4 and Table 15, a, b, c and d conditions, regular inspection of eyes with slit lamp, one year later, and visual inspection of implanted lens (compared with non-grafted PMMA control IOLs), showing good biocompatibility And the normal behavior of the hydrophilic polymer surface graft modification of the present invention. Table 17: Modified Gamma Radiation Grafting Polymerization Conditions with PVP Modified Lens / Touch Surface Lens / Thumb X PMMA / PP A, degassed 10% NVP, low dose rate * ※, 0.05 Mrad B, 2.5% Ethyl acetate, 6 hours swelling time, deoxygenated 10% NVP, low volume rate * ※ .0.05Mrad PMHA / PVDF A, dehydrated 10% NVP, low dose rate ※※, 0.05 Mrad B, deoxygenated 10% NVP, 5 hours swelling time, low dose rate Mimi, 0.15Mrad C, 2.5% ethyl acetate, S hour swelling time, degassing 10% HVP, low dose rate ※ Come, 0.05Mrad the paper size side Use Chinese National Standard (CNS) f 4 specifications (210x297 g; ft) * 4 6 A 6 It 6 V. Description of invention () PC / PP A, deoxygenated 10% NVP, low dose rate meter ※, 0.05 Mrad please .First read " ift back to the note section and then m% wood B, 2.5% ethyl acetate, 6 hours expansion time, deoxygenated 10% NVP, low dose rate ※ ※, 0.05Mrad PC / PVDF A, go Oxygen 10% NVP, low dose rate *, 0. 05 Hrad B, go to "10% NVP, 5 hours film expansion time, low dose rate come, 0.05 Mrad C, 2.5% ethyl acetate, 6 Expansion time in hours 10% NVP, low dose rate ※※, 0.05Mrad * The contact angle of the product is less than 25 °. Rice ※ The low volume rate is 30 to 300 rads / nino. Example 14: This example illustrates that at very low concentration (below 0.5 reset percentage) monomers, very low dose (below 〇.Q〇5Mrad) gamma can be used The shot stimulates effective graft polymerization.
經濟部屮央榀準局员工消炸合作社印M 本資施例以極低劑董 (0.01與0.0 05Mrad)之伽瑪 輻射激起低澳度 (0.5至2.0 % )之羥乙基丙烯酸甲 酯(HEMA)接枝聚合於乾淨之PVDF表面,而其他反應 條件與上述諸實施例相似時,其結果列於表18。 首先 將PVDF樣品擦乾淨,再浸於HEMA水溶液中,再以伽 瑪輻射激起HEMA接枝聚合於PVDF表面,然後以實施例 1之方法淸洗之。由表18所示之低接觸角,可知接枝 聚合之表面具有很高之親水性。表19之XP S分析结 果,顯示接枝聚合之表面含有極少量之氟但有大量之硪 ,其成份為PHEMA。可知PHEMA接枝聚合於PVDF表面 (PHEMA-g-PVDF).並且極低劑量之伽瑪輻射與單龌濃度 可將PHEHA有效接枝聚合於PVDF表面。 本紙張尺度边用中B明家樣準(CNS) 規格(210x297公;¢) 202466 Λ 6 li 6 -47- 五、發明説明() 表18:以88rads/nin伽瑪輻射誘起HEMA接枝聚合於PVDF 表面,並以氬氣清除其他氣龌 伽瑪輻射綰剤量 HEKA百分率 接觸角 0.005Nrad 0.5 24° 1.0 24。 2.0 12。 0.01 Nrad 0.5 21。 1.0 19° 2.0 16。 即使在極低的伽瑪輻射_量如0.005Mrad以下,並 在 〇.5重量百分率的棰低單《濃度的條件下,親水性的 PHEMA仍可有效的接枝聚合於PVDF表面。反之,未經本 發明處理之PVDF本身具有疏水性,其接觸角大於85°。 即使在極低的伽瑪輻射劑量如0 . 005Mrad以下,並在 0.5重置百分率的極低單體灌度的條件下,親水性的PHEMA 仍可有效的接枝聚合於PVDF表面。反之,未經本發明處理 之PVDF本身具有疏水性,其接觸角大於85°。 表 19:以 XPS分析 PVDF與 PHEKA-g-PVDF m 氟 未經本發明處理之PVDF 50.5 45.3 PHEHA-g-PVDF 69.0 0.9 (雒持於2% HEMA及0 . 0 05Mrad之條件) PVDF(理論值) 50.0 50.0 PHEMA(理論值) 66.7 一 ,(請先閲讀背而之注意苹項#项寫木&;- 裝- 訂- 經汫部屮央榣準局月工消设合作杜印奴 XPS對表面之分析顯示〇.〇〇5Mi:ad之伽瑪輻射可誘起 PHEMA有效接枝聚合於PVDF表面。表19分析材質表面之碩 濃度與PHEMA接枝聚合於PVDF表面之结果相同,只有極少 量之氟可被測出。表示只有少量之PVDF於PHEMA-g-PVDF表 面上。 本紙张尺度边用中《Β家標毕(CNS)T4規格(2丨0x297公;«:)The Ministry of Economic Affairs, Ministry of Economic Affairs, Bureau of Employee's Explosive Cooperation Cooperative M. This example stimulates low-degree (0.5 to 2.0%) methyl hydroxyethyl acrylate with gamma radiation from very low dose Dong (0.01 and 0.0 05Mrad) (HEMA) graft polymerization on a clean PVDF surface, and other reaction conditions are similar to the above examples, the results are shown in Table 18. First, wipe the PVDF sample clean, then immerse it in the HEMA aqueous solution, and then use gamma radiation to stimulate the HEMA graft polymerization on the PVDF surface, and then wash it by the method of Example 1. From the low contact angle shown in Table 18, it can be seen that the surface of the graft polymerization has high hydrophilicity. The results of XPS analysis in Table 19 show that the surface of the graft polymerization contains a very small amount of fluorine but a large amount of aluminum. Its composition is PHEMA. It can be seen that PHEMA is grafted and polymerized on the surface of PVDF (PHEMA-g-PVDF). Gamma radiation with a very low dose and a single concentration can effectively graft and polymerize PHEHA on the surface of PVDF. The size of the paper is used in the standard B Mingjia sample standard (CNS) (210x297mm; ¢) 202466 Λ 6 li 6 -47- V. Description of the invention () Table 18: HEMA graft polymerization induced by 88rads / nin gamma radiation On the surface of PVDF, use argon gas to remove other gas anions. Gamma radiant radiation volume HEKA percentage Contact angle 0.005Nrad 0.5 24 ° 1.0 24. 2.0 12. 0.01 Nrad 0.5 21. 1.0 19 ° 2.0 16. Even at very low gamma radiation levels below 0.005 Mrad, and at a concentration of 0.5 weight percent, the hydrophilic PHEMA can still be effectively graft polymerized on the PVDF surface. Conversely, PVDF that has not been treated by the present invention is inherently hydrophobic, and its contact angle is greater than 85 °. Even at very low gamma radiation doses, such as 0.005 Mrad or less, and at 0.5 reset percentage of very low monomer irrigation, the hydrophilic PHEMA can still be effectively graft polymerized on the PVDF surface. Conversely, PVDF that has not been treated by the present invention is inherently hydrophobic, and its contact angle is greater than 85 °. Table 19: Analysis of PVDF and PHEKA-g-PVDF by XPS. Fluoride PVDF not treated by the present invention 50.5 45.3 PHEHA-g-PVDF 69.0 0.9 (Conditions for Luo held at 2% HEMA and 0.005 Mrad) PVDF (theoretical value) 50.0 50.0 PHEMA (theoretical value) 66.7 One, (please read the back first and note the item # 项 写 木 &;-outfit-order-by the quasi-bureau of the quasi-bureau, the quasi-bureau of the monthly work, the cooperation, the Duinu XPS pair Analysis of the surface shows that the gamma radiation of 〇.〇〇5Mi: ad can induce PHEMA to effectively graft and polymerize on the PVDF surface. Table 19 The analysis of the material surface concentration and PHEMA graft polymerization on the PVDF surface is the same, only a very small amount of Fluorine can be detected. It means that there is only a small amount of PVDF on the surface of PHEMA-g-PVDF. The paper is used in the "B Jia Biao Bi (CNS) T4 specification (2 丨 0x297 public;« :)
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/592,483 US5130160A (en) | 1987-04-10 | 1990-10-05 | Ocular implants and methods for their manufacture |
Publications (1)
Publication Number | Publication Date |
---|---|
TW202466B true TW202466B (en) | 1993-03-21 |
Family
ID=24370835
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
TW081103767A TW202466B (en) | 1990-10-05 | 1992-05-15 |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0551383A4 (en) |
JP (1) | JPH06502782A (en) |
CA (1) | CA2052836C (en) |
TW (1) | TW202466B (en) |
WO (1) | WO1992005694A1 (en) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5603774A (en) * | 1993-09-27 | 1997-02-18 | Alcon Laboratories, Inc. | Method for reducing tackiness of soft acrylic polymers |
KR100487016B1 (en) * | 1996-07-29 | 2005-05-03 | 가부시끼가이샤 바유 | Modified polymers containing poly (2-hydroxyethyl(meth) acrylate) segment in the molecule |
AU765705B2 (en) * | 1999-09-02 | 2003-09-25 | Alcon Inc. | Covalently-bound, hydrophilic coating compositions for implants |
WO2001015627A1 (en) * | 1999-09-02 | 2001-03-08 | Alcon Universal Ltd. | Hydrophobically-bound, hydrophilic coating compositions for surgical implants |
US7628810B2 (en) | 2003-05-28 | 2009-12-08 | Acufocus, Inc. | Mask configured to maintain nutrient transport without producing visible diffraction patterns |
US20050046794A1 (en) | 2003-06-17 | 2005-03-03 | Silvestrini Thomas A. | Method and apparatus for aligning a mask with the visual axis of an eye |
US7976577B2 (en) * | 2005-04-14 | 2011-07-12 | Acufocus, Inc. | Corneal optic formed of degradation resistant polymer |
US10004593B2 (en) | 2009-08-13 | 2018-06-26 | Acufocus, Inc. | Intraocular lens with elastic mask |
WO2011020078A1 (en) | 2009-08-13 | 2011-02-17 | Acufocus, Inc. | Masked intraocular implants and lenses |
IN2012DN02153A (en) | 2009-08-13 | 2015-08-07 | Acufocus Inc | |
EP2785296B1 (en) | 2011-12-02 | 2018-06-20 | AcuFocus, Inc. | Ocular mask having selective spectral transmission |
US9204962B2 (en) | 2013-03-13 | 2015-12-08 | Acufocus, Inc. | In situ adjustable optical mask |
US9427922B2 (en) | 2013-03-14 | 2016-08-30 | Acufocus, Inc. | Process for manufacturing an intraocular lens with an embedded mask |
JP2017534404A (en) | 2014-11-19 | 2017-11-24 | アキュフォーカス・インコーポレーテッド | Cleavage mask for treating presbyopia |
WO2017062316A1 (en) | 2015-10-05 | 2017-04-13 | Acufocus, Inc. | Methods of molding intraocular lenses |
EP3384342B1 (en) | 2015-11-24 | 2021-08-25 | AcuFocus, Inc. | Toric small aperture intraocular lens with extended depth of focus |
US11364110B2 (en) | 2018-05-09 | 2022-06-21 | Acufocus, Inc. | Intraocular implant with removable optic |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4459318A (en) * | 1981-11-09 | 1984-07-10 | American Hospital Supply Corporation | Method for forming a self-lubricating fill tube |
US4707380A (en) * | 1985-02-04 | 1987-11-17 | Fuji Photo Film Co., Ltd. | Process for preparing a magnetic recording medium |
US4897433A (en) * | 1986-12-08 | 1990-01-30 | Japan Atomic Energy Research Inst. | Process for producing an anti-thrombogenic material by graft polymerization |
US4806382A (en) * | 1987-04-10 | 1989-02-21 | University Of Florida | Ocular implants and methods for their manufacture |
JPH01300959A (en) * | 1988-05-31 | 1989-12-05 | Canon Inc | Intraocular lens having surface functional film |
JPH01300958A (en) * | 1988-05-31 | 1989-12-05 | Canon Inc | Intraocular lens having surface functional film |
-
1991
- 1991-09-20 EP EP19910918249 patent/EP0551383A4/en not_active Withdrawn
- 1991-09-20 WO PCT/US1991/006729 patent/WO1992005694A1/en not_active Application Discontinuation
- 1991-09-20 JP JP3516980A patent/JPH06502782A/en active Pending
- 1991-10-04 CA CA002052836A patent/CA2052836C/en not_active Expired - Fee Related
-
1992
- 1992-05-15 TW TW081103767A patent/TW202466B/zh active
Also Published As
Publication number | Publication date |
---|---|
WO1992005694A1 (en) | 1992-04-16 |
CA2052836C (en) | 1998-02-03 |
CA2052836A1 (en) | 1992-04-06 |
EP0551383A4 (en) | 1993-11-03 |
JPH06502782A (en) | 1994-03-31 |
EP0551383A1 (en) | 1993-07-21 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TW202466B (en) | ||
TW203621B (en) | ||
TWI292410B (en) | ||
US4806382A (en) | Ocular implants and methods for their manufacture | |
TW208709B (en) | ||
TW581783B (en) | Surface-treatment of silicone medical devices comprising an intermediate carbon coating and graft polymerization | |
TWI226348B (en) | Surface treatment for silicone hydrogel contact lenses comprising hydrophilic polymer chains attached to an intermediate carbon coating | |
US5130160A (en) | Ocular implants and methods for their manufacture | |
TW201900225A (en) | medical equipment | |
JP2707497B2 (en) | Ophthalmic implant and manufacturing method thereof | |
EP1036102A1 (en) | Method for making a transparent polymer material resistant to protein deposit, material obtained by said method, contact lenses and intraocular implants made of said material | |
WO1987005124A1 (en) | Soft contact lens and process for its production | |
JPH08505295A (en) | Biocompatible surface modified material and method of making the same | |
JP2000122005A (en) | Coating for bio-medical device | |
WO1992005697A1 (en) | Surface modified surgical instruments, devices, implants, contact lenses and the like | |
JP2002513947A (en) | Plasma surface treatment of silicone hydrogel contact lenses | |
JPH012644A (en) | Ophthalmic implants and their manufacturing methods | |
Zhang et al. | Synthesis of pH-responsive hydrogel thin films grafted on PCL substrates for protein delivery | |
JP5697654B2 (en) | Formation of copolymers from bicontinuous microemulsions containing monomers of different hydrophilicity | |
JP2002513948A (en) | Plasma surface treatment of silicone hydrogel contact lenses | |
EP3569623B1 (en) | Vinyl-lactam-based hydrogel coatings | |
TW201722486A (en) | Intraocular lens and method of manufacturing the same | |
US5698192A (en) | Ocular implants and methods for their manufacture | |
EP1337594B1 (en) | Titanium dioxide aqueous dispersion, substrate obtained from said dispersion and self-cleaning method for said substrate | |
JP2006238914A (en) | Intraocular lens and its manufacturing method |