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A Novel Orbital Tissue Expander (OTE): Design, In-vitro and In-vivo Studies

机译:一种新型的轨道组织扩展器(OTE):设计,体外和体内研究

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Purpose: To assess the efficacy of a novel orbital tissue expander (OTE) in treating congenital anophthalmic and microphthalmic infants. Methods: The OTE implant is an inflatable (0.5 to > 6cc) silicone rubber globe sliding on a titanium T-shaped bone plate secured to the temporal bone with 1mm titanium screws. In vitro testing was performed to assess injection volume versus diameter measurements to determine consistency between devices, flex fatigue for durability of the implants when compressed, weight change in isotonic saline at 37°C to mimic human body temperature, seal durability by puncturing the globe numerous times while inflating, capacity before rupture to determine the maximum amount of saline it is able to contain, and effective sterilization. Ex-vivo testing was performed for adjustments prior to in vivo study. An OTE was then implanted in five 2-week old kittens (OS only) and inflated in 0.5cc increments. Three control animals received enucleation alone. All 8 animals were followed for 18 weeks and underwent euthanasia for morphological and histopathological analysis. Results: In vitro testing confirmed a < 5% diameter variance between different OTEs inflated in 0.5cc increments up to 5.0cc, < 5% weight change in isotonic saline at 37°C over 7 weeks, < 3% weight change over 14 months in the fatigue tester, and no quantifiable leakage ( < 1mg) after 65 consecutive 30ga needle punctures. The OTEs were successfully sterilized by autoclave and easily secured in the orbit of postmortem kittens. The in vivo study demonstrated biocompatibility of the implant which stimulates orbital bone growth resulting in almost no difference between the implanted socket and the control eye of the cat. There were no adverse effects in the normal maturation, weight gain, and food intake of the cats. Light microscopy showed no signs of foreign body reaction. Pictures of the implants were obtained by using a shadow-photogrammetry system to compare the explanted OTE with the OD control eye. Conclusion: In vitro and in vivo studies show the implant's potential to safely treat anophthalmic and microphthalmic infants.
机译:目的:为了在治疗先天性anophthalmic和microphthalmic婴儿评估的新颖轨道组织扩张器(OTE)的功效。方法:OTE植入物是可充气的(0.5至> 6CC)硅橡胶球体滑动在固定于1mm厚的钛螺丝的颞骨钛T形接骨板。在体外进行测试,以评估注射体积对直径测量来确定所述植入物的耐久性挠曲疲劳设备之间的一致性,当压缩时,在37℃下在等渗盐水中的重量变化,以模拟人的体温,密封的耐用性通过刺穿地球众多次而破裂前膨胀,容量,以确定它是能够包含盐水的最大量,和有效的消毒。为调整前的体内研究进行离体试验。一个OTE然后在5个2周龄小猫植入(仅OS)和在0.5cc增量膨胀。接受眼球摘除三个控制动物孤单。所有8只动物随访18周和形态和组织病理学分析后行安乐死。结果:在体外试验证实了在0.5cc增量膨胀至5.0cc,<5%重量在等渗盐水中在37改变不同OTES之间℃的<5%直径超过方差7周,<在超过14个月的3%的重量变化疲劳测试仪,和之后65个连续30ga针穿刺没有量化的泄漏(<1mg的)。该OTES成功通过高压灭菌和死后小猫的轨道易于保证。体内研究表明其刺激导致植入的插座和猫的对照眼之间几乎没有差别眼眶骨生长植入物的生物相容性。有正常成熟,体重增加,和猫的食物摄入量无不良影响。光镜下可见无异物反应的迹象。植入物的照片,通过使用阴影-摄影测量系统来比较与OD对照眼的外植OTE获得。结论:在体外和体内研究表明植入的潜在安全处理anophthalmic和microphthalmic婴儿。

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