CN1160385C - 表面润滑医用高分子材料的光偶联制备方法 - Google Patents
表面润滑医用高分子材料的光偶联制备方法 Download PDFInfo
- Publication number
- CN1160385C CN1160385C CNB011072911A CN01107291A CN1160385C CN 1160385 C CN1160385 C CN 1160385C CN B011072911 A CNB011072911 A CN B011072911A CN 01107291 A CN01107291 A CN 01107291A CN 1160385 C CN1160385 C CN 1160385C
- Authority
- CN
- China
- Prior art keywords
- preparing
- molecular material
- coupling process
- optical coupling
- medical polymer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000002861 polymer material Substances 0.000 title abstract description 20
- 238000002360 preparation method Methods 0.000 title abstract description 4
- 239000000178 monomer Substances 0.000 claims abstract description 15
- 229920001577 copolymer Polymers 0.000 claims abstract description 12
- 238000010168 coupling process Methods 0.000 claims abstract description 11
- 239000007864 aqueous solution Substances 0.000 claims abstract description 8
- 239000003999 initiator Substances 0.000 claims abstract description 7
- 238000006243 chemical reaction Methods 0.000 claims abstract description 6
- 230000008878 coupling Effects 0.000 claims abstract description 5
- 238000005859 coupling reaction Methods 0.000 claims abstract description 5
- 230000009471 action Effects 0.000 claims abstract description 3
- 238000005406 washing Methods 0.000 claims abstract 2
- -1 distyryl compound Chemical class 0.000 claims description 16
- 239000000463 material Substances 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims description 12
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 8
- 230000001050 lubricating effect Effects 0.000 claims description 8
- 239000002904 solvent Substances 0.000 claims description 5
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000012299 nitrogen atmosphere Substances 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 4
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 4
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 4
- 239000004800 polyvinyl chloride Substances 0.000 claims description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 3
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical group C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 claims description 3
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 3
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 claims description 3
- 235000019400 benzoyl peroxide Nutrition 0.000 claims description 3
- 239000012153 distilled water Substances 0.000 claims description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000004677 Nylon Substances 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 239000008367 deionised water Substances 0.000 claims description 2
- 229910021641 deionized water Inorganic materials 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 2
- 229920001778 nylon Polymers 0.000 claims description 2
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 claims description 2
- 239000002994 raw material Substances 0.000 claims description 2
- 239000000376 reactant Substances 0.000 claims description 2
- 229920002379 silicone rubber Polymers 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims 10
- GNWBLLYJQXKPIP-ZOGIJGBBSA-N (1s,3as,3bs,5ar,9ar,9bs,11as)-n,n-diethyl-6,9a,11a-trimethyl-7-oxo-2,3,3a,3b,4,5,5a,8,9,9b,10,11-dodecahydro-1h-indeno[5,4-f]quinoline-1-carboxamide Chemical compound CN([C@@H]1CC2)C(=O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H](C(=O)N(CC)CC)[C@@]2(C)CC1 GNWBLLYJQXKPIP-ZOGIJGBBSA-N 0.000 claims 1
- ZMARGGQEAJXRFP-UHFFFAOYSA-N 1-hydroxypropan-2-yl 2-methylprop-2-enoate Chemical compound OCC(C)OC(=O)C(C)=C ZMARGGQEAJXRFP-UHFFFAOYSA-N 0.000 claims 1
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 claims 1
- 239000004160 Ammonium persulphate Substances 0.000 claims 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 claims 1
- 239000004159 Potassium persulphate Substances 0.000 claims 1
- 235000019395 ammonium persulphate Nutrition 0.000 claims 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N ferric oxide Chemical compound O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims 1
- VLCAYQIMSMPEBW-UHFFFAOYSA-N methyl 3-hydroxy-2-methylidenebutanoate Chemical group COC(=O)C(=C)C(C)O VLCAYQIMSMPEBW-UHFFFAOYSA-N 0.000 claims 1
- 150000004702 methyl esters Chemical class 0.000 claims 1
- 235000019394 potassium persulphate Nutrition 0.000 claims 1
- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 claims 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 claims 1
- 229920001480 hydrophilic copolymer Polymers 0.000 abstract description 11
- 229920000642 polymer Polymers 0.000 abstract description 5
- 239000000243 solution Substances 0.000 abstract description 2
- 238000001035 drying Methods 0.000 abstract 1
- 230000004048 modification Effects 0.000 description 8
- 238000012986 modification Methods 0.000 description 8
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- 229920001477 hydrophilic polymer Polymers 0.000 description 3
- 229920002635 polyurethane Polymers 0.000 description 3
- 239000004814 polyurethane Substances 0.000 description 3
- DBHYHAZBHLULCT-UHFFFAOYSA-N 1-azido-3-ethenylbenzene Chemical compound C=CC1=CC=CC(N=[N+]=[N-])=C1 DBHYHAZBHLULCT-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000007774 longterm Effects 0.000 description 2
- 229940127554 medical product Drugs 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 description 1
- WHNPOQXWAMXPTA-UHFFFAOYSA-N 3-methylbut-2-enamide Chemical compound CC(C)=CC(N)=O WHNPOQXWAMXPTA-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 125000003172 aldehyde group Chemical group 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 150000001540 azides Chemical class 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 239000004811 fluoropolymer Substances 0.000 description 1
- 229920002313 fluoropolymer Polymers 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- IQPQWNKOIGAROB-UHFFFAOYSA-N isocyanate group Chemical group [N-]=C=O IQPQWNKOIGAROB-UHFFFAOYSA-N 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004005 microsphere Substances 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000307 polymer substrate Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 1
- 239000004810 polytetrafluoroethylene Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000002910 solid waste Substances 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Materials For Medical Uses (AREA)
Abstract
表面润滑医用高分子材料的光偶联制备方法,其特点是将含光活性基团的不饱和单体与亲水性单体配成溶液,在引发剂存在下,加入带有搅拌器和温度计的反应釜中,于温度50~100℃反应4~24小时,获得亲水共聚物,将共聚物配成40~0.1%的水溶液,涂抹到医用高分子表面,置于功率为10~500瓦的紫外光下照射0.5~30分钟,照射距离5~100厘米,共聚物在紫外光作用下偶联到医用高分子材料表面上,经水洗、烘干,测得偶联密度为0.01~15mg/cm2。
Description
本发明涉及一种紫外光引发医用高分子材料表面偶联亲水性高分子共聚物的方法,属于医用高分子材料表面改性领域。
欧洲专利0521605A2公开了用紫外光在含氟聚合物中接枝亲水和疏水单体,共聚物组成的短链聚合物以提高聚合物粒子微球表面的亲水性和润滑性。美国专利4847324报道了用亲水性高分子共混后涂层到聚合物的表面以获得润滑性。美国专利4589873将亲水性高分子聚乙烯吡咯烷酮溶于二甲基甲酰胺涂层到聚氯乙烯表面,然后挥发掉溶剂,使亲水高分子聚乙烯吡咯烷酮吸附到聚氯乙烯表面以提高亲水性和润滑性,美国专利4729914通过异氰酸根将亲水性高分子联接到高分子材料表面以提高亲水性和润滑性。欧洲专利0693293A1在医用高分子材料表面通过活泼的官能团,如异氰酸根、环氧基团,醛基等将亲水性或可被水溶胀的高分子通过嵌段或接枝反应在医用高分子材料表面形成涂层,提高亲水性和润滑性。前面提到的各个专利都存在这样的问题:1.改性后的表面不具有长效润滑性;2.实施起来较麻烦,实验步骤多,改性后表面润滑性重复性差;3.对基材本体的物理机械性能有影响。
本发明的目的是针对现有技术的不足而提供一种表面润滑医用高分子材料的光偶联制备方法,其特点是在医用高分子基材表面涂覆一层含有光活性基团的亲水共聚物的溶液后,用紫外光照射表面,引发光活性基团的分解成双自由基,将共聚物插入到基材表面,以提高其表面润滑性能。
本发明的目的由以下技术措施实现,其中所述原料份数除特殊说明外,均为摩尔份数。
表面润滑医用高分子材料的光偶联制备方法
a.将含光活性基团的不饱和单体0.01~10份,亲水性单体0.50~50份,溶剂25~250毫升/1摩尔反应单体,引发剂0.1~1.5%,引发剂重量/反应物总重量,加入带有搅拌器、温度计和冷凝器的反应釜中,在氮气氛下,于温度50~100℃,反应4~24小时,获得带有光活性基团的亲水共聚物,亲水共聚物具有光活性基团单体占的摩尔含量为0.01~30%。
b.将亲水共聚物溶于水中,配成质量浓度40~0.1%的水溶液,再将该水溶液涂抹到医用高分子材料表面上,置于功率为10~500瓦的紫外光下照射0.5~30分钟,照射距离为5~100厘米,共聚物在紫外光作用下偶联到医用高分子材料表面上。
c.经紫外光照射的医用高分子材料用蒸馏水或者去离子水洗去表面没有发生偶联的共聚物,将水洗后的医用高分子材料置于温度30~100℃烘1~48小时,用重量法测得偶联密度为0.01~15mg/cm2。
含光活性基团的不饱和单体为含有叠氮基的苯乙烯化合物及其衍生物,其结构表示为:
R=H,-NO2,卤素或C1~C3的烷基。
亲水性单体为甲基丙烯酸羟乙酯,甲基丙烯酸羟丙酯,丙烯酸,丙烯酸甲酯,丙烯酸乙酯,马来酸、马来酸酐,乙烯基吡咯烷酮,丁烯基吡咯烷酮,二甲基丙烯酰胺和/或丙烯酰胺至少一种。
引发剂为过氧化二苯甲酰,过硫酸钾,过硫酸铵,偶氮二异丁腈和/或偶氮二异庚腈至少一种。
溶剂为二甲基甲酰胺,二甲基乙酰胺,四氢呋喃和/或二氧六环至少一种。
医用高分子材料为聚乙烯,聚丙烯,聚氯乙烯,聚四氟乙烯,聚甲基丙烯酸甲酸,聚对苯二甲酸乙二醇酯,尼龙、硅橡胶和/或聚氨酯至少一种。
本发明制备的表面润滑医用高分子材料,其表面偶联亲水共聚物,经测试结果表明,其饱和吸水率,水接触角和摩擦系数的变化详见表1所示。
本发明具有如下优点:
1.本发明制备的表面润滑医用高分子材料制成的医疗器械,在润湿的环境下使用有良好的润滑性和长效润滑性,
2.本发明可使医用高分子材料表面摩擦系数最低达到0.05,能满足医疗制品的临床使用要求。对同一制品,重复使用多次后仍具有相当好的润滑性,可使某些医疗制品由一次性使用转化为重复使用,节省大量的资源,并减少固体废弃物的产生,大大降低了制造成本的使用价格。
3.本发明采用紫外光照射时间短,对医用高分子材料本体性能影响小。
4.操作简单、效果好。
实施例
下面通过实施例对本发明进行具体描述,有必要在此指出的是以下实施例只用于对本发明进行进一步说明,不能理解为对本发明保护范围的限制,本领域的技术熟练人员可以根据上述本发明内容对本发明作出一些非本质的改进和调整。
1.将间叠氮苯乙烯0.1mol,丙烯酰胺0.9mol,二甲基乙酰胺100ml,偶氮二异丁腈0.3%加入带有搅拌器和温度计的反应釜中,在氮气氛下,于温度60℃反应5小时,形成带有光活性基团的亲水共聚物。将亲水共聚物配成质量浓度10%的水溶液,涂抹到清洗后的聚乙烯样品表面上,置于250瓦的紫外光下照射5分钟,距离50厘米,照射后的样品用50℃的去离子水浸泡24小时,每2小时换水一次,充分洗去表面粘附的共聚物,再将样品置于60℃烘箱内烘24小时。
2.将间甲基间叠氮苯乙烯0.2mol,N-乙烯基吡咯烷酮0.8mol,四氢呋喃100ml,偶氮二异庚腈0.2%,加入带有搅拌器和温度计的反应釜中,在氮气氛下,于温度50℃反应8小时,形成带有光活性的亲水共聚物。将亲水共聚物配成质量浓度8%的水溶液,涂抹到清洗后的聚氨酯样品表面上,置于500瓦紫外光下照射8分钟,距离为60厘米,照射后的样品用50℃的蒸馏水浸泡24小时,每2小时换水一次,充分洗去表面粘附的共聚物,再将样品置于60℃烘箱内烘24小时。
3.将间叠氮苯乙烯0.05mol,N,N-二甲基丙烯酰胺0.95mol,二甲基甲酰胺100ml,过氧化苯甲酰0.1%,加入带有搅拌器和温度计的反应釜中,在氮气氛下,于温度70℃反应6小时,形成带有光活性基因的亲水共聚物,将亲水共聚物配成质量浓度12%的水溶液、涂抹到清洗后的聚对苯二甲酸乙二醇酯表面上,置于250瓦的紫外光下照射10分钟,距离为40厘米,照射完毕后的后处理同实施例1的工艺。
表1偶联前后医用高分子材料的相关物理性能比较
材料 | 饱和吸水率(%) | 水接触角θ(°) | 摩擦系数(μ) | |
聚乙烯 | 改性前 | 0.001 | 100 | 0.25 |
改性后 | 0.60 | 40 | 0.054 | |
聚氨酯 | 改性前 | 0.42 | 80 | 0.65 |
改性后 | 0.82 | 36 | 0.05 | |
聚对苯二甲酸乙二醇酯 | 改性前 | 0.60 | 74 | 0.60 |
改性后 | 0.85 | 41 | 0.053 |
Claims (6)
1.表面润滑医用高分子材料的光偶联制备方法,其特征在于:
a.将含光活性基团的不饱和单体(其中原料份数除特殊说明外,均为摩尔份数)0.01~10份,亲水性单体0.50~50份,溶剂25~250毫升/1摩尔反应单体,引发剂0.1~1.5%,引发剂重量/反应物总重量,加入带有搅拌器、温度计和冷凝器的反应釜中,在氮气氛下,于温度50~100℃反应4~24小时,获得带有光活性基团的亲水共聚物,亲水共聚物具有光活性基团单体占的摩尔含量为0.01~30%,
b.将亲水共聚物溶于水中,配成质量浓度40~0.1%的水溶液,再将该水溶液涂抹到医用高分子材料表面上,置于功率为10~500瓦的紫外光下照射0.5~30分钟,照射距离为5~100厘米,共聚物在紫外光作用下偶联到医用高分子材料表面上,
c.经紫外光照射的医用高分子材料用蒸馏水或者去离子水洗去表面没有发生偶联的共聚物,将水洗后的医用高分子材料置于温度30~100℃烘1~48小时,用重量法测得偶联密度为0.01~15mg/cm2。
3.按照权利要求1所述表面润滑医用高分子材料的光偶联制备方法,其特征在于亲水性单体为甲基丙烯酸羟乙酯,甲基丙烯酸羟丙酯,丙烯酸,丙烯酸甲酯,丙烯酸乙酯,马来酸,马来酸酐,乙烯基吡咯烷酮,丁烯基吡咯烷酮,二甲基丙烯酰胺和/或丙烯酰胺至少一种。
4.按照权利要求1所述表面润滑医用高分子材料的光偶联制备方法,其特征在于引发剂为过氧化二苯甲酰,过硫酸钾,过硫酸铵,偶氮二异丁腈和/或偶氮二异庚腈至少一种。
5.按照权利要求1所述表面润滑医用高分子材料的光偶联制备方法,其特征在于溶剂为二甲基甲酰胺、二甲基乙酰胺、四氢呋喃和/或二氧六环至少一种。
6.按照权利要求1所述表面润滑医用高分子材料的光偶联制备方法,其特征在于医用高分子材料为聚乙烯、聚丙烯、聚氯乙烯、聚四氟乙烯,聚甲基丙烯甲酯,聚对苯二甲酸乙二醇酯,尼龙、硅橡胶和/或聚氨酯至少一种。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB011072911A CN1160385C (zh) | 2001-03-28 | 2001-03-28 | 表面润滑医用高分子材料的光偶联制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB011072911A CN1160385C (zh) | 2001-03-28 | 2001-03-28 | 表面润滑医用高分子材料的光偶联制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1376723A CN1376723A (zh) | 2002-10-30 |
CN1160385C true CN1160385C (zh) | 2004-08-04 |
Family
ID=4656235
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB011072911A Expired - Fee Related CN1160385C (zh) | 2001-03-28 | 2001-03-28 | 表面润滑医用高分子材料的光偶联制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1160385C (zh) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108563038A (zh) * | 2018-04-23 | 2018-09-21 | 青岛高新区尚达医药研究所 | 一种润滑抗菌型隐形眼镜及其制备方法 |
CN109078503B (zh) * | 2018-08-17 | 2021-01-12 | 东华大学 | Pet精密输液过滤核孔膜亲水化处理工艺 |
CN109651562A (zh) * | 2018-12-10 | 2019-04-19 | 苏州维泰生物技术有限公司 | 一种含有活性酯基团的光活性聚合物及其合成方法 |
-
2001
- 2001-03-28 CN CNB011072911A patent/CN1160385C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
CN1376723A (zh) | 2002-10-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5231240B2 (ja) | 柔軟高吸収性バインダーポリマー組成物 | |
CN106967191B (zh) | 一种超双疏含氟聚合物纳米材料的绿色制备方法 | |
Bai et al. | Preparation and characterizations of poly (2-methyl-2-oxazoline) based antifouling coating by thermally induced immobilization | |
CN1916040A (zh) | 仿细胞膜结构共聚物及其制备方法和应用 | |
GB2081725A (en) | A Process for the Production of a Hydrogel | |
CN101092471A (zh) | 一种超分子结构温度敏感性水凝胶的制备方法 | |
CN106540336B (zh) | 一种医用介入导管表面的亲水改性涂料 | |
CN113292671A (zh) | 一种含有苯硼酸基团的高分子交联剂、其制备的生物粘合剂及制备方法和应用 | |
CN107629379B (zh) | 一种可逆光控疏水性的复合膜及其制备方法 | |
CN111393942B (zh) | 一种超疏水涂层剂、透明超疏水涂层及其制备方法和应用 | |
EP2238452A1 (en) | Surface functionalisation of plastic optical fibre | |
CN103059215A (zh) | 结构相对可控的甜菜碱酯类智能水凝胶及制备方法和应用 | |
CN1160385C (zh) | 表面润滑医用高分子材料的光偶联制备方法 | |
CN111825798B (zh) | 一种高分子化紫外光吸收剂的制备方法 | |
CN1321164C (zh) | 亲水性高分子防雾涂料及其制备方法 | |
CN108117830B (zh) | 一种水性亲水润滑涂层 | |
WO2023125100A1 (zh) | 一种材料表面改性的方法和基于该方法得到的表面改性的材料 | |
JP6560560B2 (ja) | 耐汚染性表面修飾剤、及び表面処理方法 | |
CN114106361A (zh) | 加载两性离子聚合物涂层的聚丙烯材料及其制备方法 | |
Gupta et al. | Synthesis and characterization of poly (AAm-co-BMA-co-AAc) hydrogels: Effect of acrylamide content on swelling behaviour | |
JP2547431B2 (ja) | 防曇化方法 | |
JPH0632844A (ja) | 水溶性重合体の製造方法および水溶性重合体 | |
CN102161738A (zh) | 异球分别负载光引发剂和raft试剂以制备多重环境响应型毛发状聚合物微球的方法 | |
CN1318579A (zh) | 医用高分子材料表面润滑改性方法 | |
JPH02115238A (ja) | プラスチック塗料用樹脂組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |