CN103655002A - 一种水凝胶人工晶体及其制备方法 - Google Patents

一种水凝胶人工晶体及其制备方法 Download PDF

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CN103655002A
CN103655002A CN201310677907.7A CN201310677907A CN103655002A CN 103655002 A CN103655002 A CN 103655002A CN 201310677907 A CN201310677907 A CN 201310677907A CN 103655002 A CN103655002 A CN 103655002A
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intraocular lens
hydrogel
gelatin
preparing method
crystal
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王香兵
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WUXI HEZHONG INFORMATION TECHNOLOGY Co Ltd
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WUXI HEZHONG INFORMATION TECHNOLOGY Co Ltd
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Abstract

本发明公开一种水凝胶人工晶体及其制备方法。包括人工晶体光学部主体和D型支撑袢,其中人工晶体光学部1主体为中间厚,周围薄的圆形薄片。由胶原蛋白和明胶组成。制备方法是将胶原蛋白1-5g和明胶5-10g放入100ml生理盐水中,于4℃中溶胀,待完全溶解后,倒入D型晶体模具中,置于37℃,1hr。待凝固后,即得。本发明的有益效益在于制备具有稳定的惰性、可折叠,光学透明性,其弹性较小,手术操作安全的人工晶体。

Description

一种水凝胶人工晶体及其制备方法
 
技术领域:
本发明涉及一种人工晶体的设计和制备领域,尤其涉及一种水凝胶人工晶体设计和制备领域。
技术背景:
    人工晶体植入术是治疗白内障等最有效的手段,也是矫正视力最彻底的方法。
现在的硬质人工晶体,这种晶体不能折叠,手术时需要一个与晶体光学部大小相同的切口(6 mm左右),才能将晶体植入眼内。随着白内障超声乳化手术技术迅速发展,白内障超声乳化是以超声的能量将晶体核粉碎并乳化吸出,并通过该切口植入人工晶体。手术医生已经可以仅仅使用 3.2 mm 甚至更小的切口就已经可以清除白内障,但在安放人工晶体的时候却还需要扩大切口,才能植入。为了适应手术的进步,改进人工晶体的材料,使直径为6 mm 的人工晶体可以对折,甚至卷曲起来,通过植入镊或植入器将其植入,待进入眼内后,折叠的人工晶体会自动展开,支撑在指定的位置。因此,软质可折叠人工晶体,受到关注。
人工晶体材料是植入生物体内的材料,需要理化性质稳定,能够与机体组织和谐共处,对机体无毒副作用,无刺激性,不引起机体的免疫反应(生物相容性), 且折光率与正常晶体的折光率相同。现阶段,缺少生物相容性小,理化性质稳定的软质可折叠人工晶体,开发新型软质可折叠人工晶体显得尤为重要。
水凝胶作为一种新型的植入生物体内的材料已被应用于人工晶体填充物,但未见用于人工晶体的制备。
发明内容:
发明目的:设计一种水凝胶人工晶体,具有生物相容性小,理化性质稳定,软质可折叠的特点。
技术方案:
本发明提供一种水凝胶人工晶体及其制备方法。技术方案是包括人工晶体光学部1主体,D型支撑袢2,其中人工晶体光学部1主体为中间厚,周围薄的圆形薄片。制备方法是将胶原蛋白1-5g和明胶5-10g放入100ml生理盐水中,于4℃中溶胀,待完全溶解后,倒入D型晶体模具中,置于37℃,1hr。待凝固后,即得。
  
 附图说明
附图1  人工晶体模型图。1. 人工晶体光学部;2. D型支撑袢。
 
有益效益:
本发明制备的人工晶体,具有稳定的惰性、可折叠,光学透明性,其弹性较小,手术操作安全。 
具体实施方式:
实施例1:将胶原蛋白1g和明胶10g放入100ml生理盐水中,于4℃中溶胀,待完全溶解后,倒入D型晶体模具中,置于37℃,1hr。待凝固后,即得。
实施例2:将胶原蛋白2g和明胶5g放入100ml生理盐水中,于4℃中溶胀,待完全溶解后,倒入D型晶体模具中,置于37℃,1hr。待凝固后,即得。

Claims (3)

1.一种水凝胶人工晶体,其特征在于:包括人工晶体光学部主体,D型支撑袢,其中人工晶体光学部主体为中间厚,周围薄的圆形薄片。
2.一种水凝胶人工晶体,其特征在于:由胶原蛋白和明胶组成。
3.水凝胶人工晶体制备方法:其特征在于:将胶原蛋白1-5g和明胶5-10g放入100ml生理盐水中,于4℃中溶胀,待完全溶解后,倒入D型晶体模具中,置于37℃,1hr,待凝固后,即得。
CN201310677907.7A 2013-12-13 2013-12-13 一种水凝胶人工晶体及其制备方法 Pending CN103655002A (zh)

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EP0579528A1 (fr) * 1992-07-16 1994-01-19 Corneal Implant intra-oculaire souple
WO1997017915A1 (fr) * 1995-11-13 1997-05-22 Corneal Laboratoires Implant intraoculaire souple
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US6200344B1 (en) * 1999-04-29 2001-03-13 Bausch & Lomb Surgical, Inc. Inraocular lenses
US6241777B1 (en) * 1999-09-01 2001-06-05 Robert E. Kellan Phakic intraocular lenses
WO2007028258A2 (en) * 2005-09-09 2007-03-15 Ottawa Health Research Institute Interpenetrating networks, and related methods and compositions
CN102573944A (zh) * 2009-07-02 2012-07-11 亚洲大学校产学协力团 原位成型水凝胶及其生物医学用途
CN102940583A (zh) * 2012-11-26 2013-02-27 中国工程物理研究院核物理与化学研究所 一种可作为营养面膜的温敏水凝胶及其制备方法

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* Cited by examiner, † Cited by third party
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EP0579528A1 (fr) * 1992-07-16 1994-01-19 Corneal Implant intra-oculaire souple
WO1997017915A1 (fr) * 1995-11-13 1997-05-22 Corneal Laboratoires Implant intraoculaire souple
US6200344B1 (en) * 1999-04-29 2001-03-13 Bausch & Lomb Surgical, Inc. Inraocular lenses
US6241777B1 (en) * 1999-09-01 2001-06-05 Robert E. Kellan Phakic intraocular lenses
CN1280856A (zh) * 2000-07-12 2001-01-24 曾群 一组稳定生物活性物质组合物及其制备方法
WO2007028258A2 (en) * 2005-09-09 2007-03-15 Ottawa Health Research Institute Interpenetrating networks, and related methods and compositions
CN102573944A (zh) * 2009-07-02 2012-07-11 亚洲大学校产学协力团 原位成型水凝胶及其生物医学用途
CN102940583A (zh) * 2012-11-26 2013-02-27 中国工程物理研究院核物理与化学研究所 一种可作为营养面膜的温敏水凝胶及其制备方法

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