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Light-adjustable lens.光可调透镜。
Trans Am Ophthalmol Soc. 2003;101:417-36.

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Light-adjustable lens: customizing correction for multifocality and higher-order aberrations.可调节人工晶状体:针对多焦点和高阶像差定制矫正。
Trans Am Ophthalmol Soc. 2006;104:29-39.

本文引用的文献

1
Theory of transparency of the eye.眼的透明度理论
Appl Opt. 1971 Mar 1;10(3):459-73. doi: 10.1364/AO.10.000459.
2
Light-adjustable lens.光可调透镜。
Trans Am Ophthalmol Soc. 2003;101:417-36.
3
Difficult lens power calculations.
Curr Opin Ophthalmol. 2004 Feb;15(1):1-9. doi: 10.1097/00055735-200402000-00002.
4
Intraocular lens with reversibly adjustable optical power: pilot study of concept and safety.具有可逆可调光学功率的人工晶状体:概念与安全性的初步研究。
J Cataract Refract Surg. 2003 Sep;29(9):1795-9. doi: 10.1016/s0886-3350(03)00068-3.
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Complications of foldable intraocular lenses requiring explantation or secondary intervention--2001 survey update.需要取出或二次干预的可折叠人工晶状体并发症——2001年调查更新
J Cataract Refract Surg. 2002 Dec;28(12):2193-201. doi: 10.1016/s0886-3350(02)01612-7.
6
UV absorbance of the human cornea in the 240- to 400-nm range.人眼角膜在240至400纳米范围内的紫外线吸收率。
Invest Ophthalmol Vis Sci. 2002 Jul;43(7):2165-8.
7
Predicting the refractive outcome after cataract surgery: the comparison of different IOLs and SRK-II v SRK-T.预测白内障手术后的屈光结果:不同人工晶状体及SRK-II与SRK-T的比较
Br J Ophthalmol. 2002 Jun;86(6):620-2. doi: 10.1136/bjo.86.6.620.
8
Clinical and theoretical results of intraocular lens power calculation for cataract surgery after photorefractive keratectomy for myopia.近视性屈光性角膜切削术后白内障手术人工晶状体屈光力计算的临床及理论结果
Arch Ophthalmol. 2002 Apr;120(4):431-8. doi: 10.1001/archopht.120.4.431.
9
Multifocal intraocular lens implantation in prepresbyopic patients with unilateral cataract.
Ophthalmology. 2002 Apr;109(4):680-6. doi: 10.1016/s0161-6420(01)01029-6.
10
Accuracy and reproducibility of biometry using partial coherence interferometry.使用部分相干干涉测量法进行生物测量的准确性和可重复性。
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光可调透镜:体外列线图的开发

Light-adjustable lens: development of in vitro nomograms.

作者信息

Schwartz Daniel M, Sandstedt Christian A, Chang Shiao H, Kornfield Julie A, Grubbs Robert H

机构信息

Beckman Vision Center, Department of Ophthalmology, University of California, San Francisco, San Francisco, California, USA.

出版信息

Trans Am Ophthalmol Soc. 2004;102:67-72; discussion 72-4.

PMID:15747746
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1280088/
Abstract

PURPOSE

To determine whether digital spatial intensity patterns can be developed to effect precise in vitro correction of myopic, hyperopic, and astigmatic refractive errors in a silicone light-adjustable lens (LAL). Also, to determine whether a new spatial intensity pattern for "lock-in" is effective in vitro.

METHODS

A digital interferometer/irradiation system was developed to irradiate LALs and measure the power change following irradiation. Light-adjustable lenses were mounted into a wet cell maintained at 35.0 +/- 0.5 degrees C (simulated ocular temperature) and allowed to equilibrate for a minimum of 2 hours. Ultraviolet light was then applied with spatial light intensity patterns to correct hyperopia, myopia, and astigmatism. Light-adjustable lenses were also treated to effect lock-in with a separate spatial light intensity pattern. Treated lenses were characterized for power change and optical quality. In the case of lock-in, exhaustive chemical extraction was also performed to determine the percentage of remaining macromer.

RESULTS

Appropriate digital irradiation spatial intensity patterns were created to develop nomograms for in vitro correction of myopia, hyperopia, and astigmatism in approximate 0.25 D steps. Power changes were reproducible and did not alter optical quality of the LALs. Further, lock-in dosing of the LALs did not alter optical quality or significantly change LAL power.

CONCLUSIONS

In vitro nomograms have been developed for a silicone LAL that permit precise correction of myopia, hyperopia, and astigmatism. Furthermore, a spatial light intensity pattern has been devised that effects lock-in without significantly altering LAL power or optical quality.

摘要

目的

确定是否可以开发数字空间强度模式,以在硅酮光可调透镜(LAL)中实现对近视、远视和散光屈光不正的精确体外矫正。此外,确定一种用于“锁定”的新空间强度模式在体外是否有效。

方法

开发了一种数字干涉仪/辐照系统,用于辐照LAL并测量辐照后的屈光力变化。将光可调透镜安装到保持在35.0±0.5摄氏度(模拟眼内温度)的湿盒中,并使其平衡至少2小时。然后应用具有空间光强度模式的紫外光来矫正远视、近视和散光。还使用单独的空间光强度模式对光可调透镜进行处理以实现锁定。对处理后的透镜进行屈光力变化和光学质量表征。在锁定的情况下,还进行了彻底的化学提取以确定剩余大分子单体的百分比。

结果

创建了合适的数字辐照空间强度模式,以开发用于以约0.25 D步长在体外矫正近视、远视和散光的列线图。屈光力变化具有可重复性,并且未改变LAL的光学质量。此外,LAL的锁定剂量未改变光学质量或显著改变LAL屈光力。

结论

已为硅酮LAL开发了体外列线图,可精确矫正近视、远视和散光。此外,还设计了一种空间光强度模式,可实现锁定,而不会显著改变LAL屈光力或光学质量。