Weerheim J A, Sivak J G
School of Optometry, University of Waterloo, Ontario, Canada.
Ophthalmic Physiol Opt. 1992 Jan;12(1):72-9.
An apparatus has been designed to automate the laser measuring technique and make it possible to monitor lens refractive function (spherical aberration) as well as change in lens transmittance during lens culture. A scanning laser beam (helium-neon) is used so that a number of beams pass through different spots on the lens to determine lens spherical aberration compared over time. Each refracted beam, received by two video cameras (X and Y directions), is digitized. The system first locates the optical centre of the lens by determining the beam position providing the least deflection for both the X and Y directions. The beam is then moved in predetermined steps on either side of the centre, and focal lengths are determined relative to the optic axis for each position. A measure of beam scatter is noted from post-refraction pixel excitation for each beam position. Improvements to the scanning laser system have led to greater accuracy and speed as well as to improved culture cells. Accuracy was increased by using high resolution (1 micron) stepping motors to move the scanning helium-neon laser. A new alignment process involving the superposition of the incident beam reflected on itself ensures that the incident beam is perpendicular to the lens equatorial axis. Scanning speed has been improved through a variety of hardware and software changes. Scanning time for a lens, including locating the optical centre and measuring focal length for 20 lens positions along the X and Y directions, takes about 60 seconds. Long-term studies on the degradation of lens optical performance frequency yield diffuse beams of very low intensity.(ABSTRACT TRUNCATED AT 250 WORDS)
已设计出一种装置,用于使激光测量技术自动化,并能够在晶状体培养过程中监测晶状体屈光功能(球差)以及晶状体透光率的变化。使用扫描激光束(氦氖激光),以便多束光线穿过晶状体上的不同点,从而随时间比较确定晶状体球差。由两个摄像机(X和Y方向)接收的每束折射光线都进行数字化处理。该系统首先通过确定在X和Y方向上偏转最小的光束位置来定位晶状体的光学中心。然后光束在中心两侧以预定步长移动,并针对每个位置相对于光轴确定焦距。从每个光束位置的折射后像素激发情况记录光束散射的测量值。对扫描激光系统的改进提高了准确性和速度,同时也改善了培养细胞。通过使用高分辨率(1微米)步进电机来移动扫描氦氖激光提高了准确性。一种涉及使入射光束自身反射叠加的新对准过程确保入射光束垂直于晶状体赤道轴。通过各种硬件和软件更改提高了扫描速度。对一个晶状体进行扫描的时间,包括定位光学中心以及测量沿X和Y方向20个晶状体位置的焦距,大约需要60秒。对晶状体光学性能退化频率的长期研究产生了强度非常低的漫射光束。(摘要截短于250字)