Foulad Allen, Ghasri Pedram, Garg Rohit, Wong Brian
Beckman Laser Institute and Medical Clinic, 1002 Health Sciences Rd E, University of California, Irvine, CA 92612, USA.
Arch Facial Plast Surg. 2010 Nov-Dec;12(6):405-11. doi: 10.1001/archfacial.2010.93.
To develop a method to rapidly stabilize the shape change process in peripheral slices of costal cartilage by using infrared laser irradiation in a porcine model.
Forty peripheral porcine costal cartilage specimens (40 × 10 × 2 mm) were harvested. Thirty of these specimens were immediately irradiated with an Nd:YAG laser (λ = 1.32 μm; spot size, 2-mm diameter) using 1 of 3 exposure treatments: 6 W, 2 seconds, and 4 spots; 8 W, 3 seconds, and 4 spots; or 6 W, 2 seconds, and 8 spots. Ten control specimens were only immersed in 0.9% saline solution. Angle of curvature was measured from photographs taken at 0 minutes, immediately after irradiation, and at 30 minutes, 1 hour, 5 hours, and 24 hours. Infrared imaging was used to measure surface temperatures during irradiation. Cell viability after irradiation was determined using a live/dead assay in conjunction with fluorescent confocal microscopy.
Compared with the untreated controls, the irradiated grafts underwent accelerated shape change within the first 30 minutes to reach a stable geometry. Thereafter, irradiated grafts underwent little or no shape change, whereas the control group exhibited significant change in curvature from 30 minutes to 24 hours (P < .001). The average peak irradiated spot temperatures ranged from 76°C to 82°C. Cell viability measurements at the laser spot sites demonstrated a hemispherically shaped region of dead cells with a depth of 0.8 to 1.2 mm and a surface diameter of 1.9 to 2.7 mm.
Laser irradiation of peripheral costal cartilage slices provides an effective method for rapidly stabilizing acute shape change by accelerating the warping process. The temperature elevations necessary to achieve this are spatially limited and well within the limits of tolerable tissue injury.
在猪模型中,通过红外激光照射开发一种快速稳定肋软骨周边切片形状变化过程的方法。
获取40个猪肋软骨周边标本(40×10×2毫米)。其中30个标本立即用Nd:YAG激光(波长=1.32μm;光斑尺寸,直径2毫米)进行照射,采用以下3种暴露处理中的1种:6瓦,2秒,4个光斑;8瓦,3秒,4个光斑;或6瓦,2秒,8个光斑。10个对照标本仅浸入0.9%盐溶液中。在照射后立即、0分钟、30分钟、1小时、5小时和24小时拍摄照片,测量曲率角度。在照射期间使用红外成像测量表面温度。照射后细胞活力通过活/死检测结合荧光共聚焦显微镜进行测定。
与未处理的对照组相比,照射后的移植物在最初30分钟内形状变化加速,以达到稳定的几何形状。此后,照射后的移植物形状变化很小或没有变化,而对照组在30分钟至24小时内曲率有显著变化(P<.001)。照射光斑的平均峰值温度范围为76°C至82°C。激光光斑部位的细胞活力测量显示,有一个半球形的死细胞区域,深度为0.8至1.2毫米,表面直径为1.9至2.7毫米。
对肋软骨周边切片进行激光照射,通过加速翘曲过程,为快速稳定急性形状变化提供了一种有效方法。实现这一目的所需的温度升高在空间上是有限的,且完全在可耐受的组织损伤范围内。