Mordon S, Desmettre T, Devoisselle J M, Soulie S
Inserm U279, Pavillon Vancostenobel, CHU, Lille, France.
Lasers Surg Med. 1997;20(2):131-41. doi: 10.1002/(sici)1096-9101(1997)20:2<131::aid-lsm3>3.0.co;2-r.
The present study was undertaken to evaluate the feasibility of thermal damage assessment of blood vessels by using laser-induced release of liposome-encapsulated dye.
STUDY DESIGN/MATERIALS AND METHODS: Experiments were performed in a hamster skin flap model. Laser irradiation was achieved with a 300 microm fiber connected to a 805 nm diode laser (power = 0.8W, spot diameter = 1.3 mm and pulse exposure time lasting from 1 to 6 s) after potentiation using a specific indocyanine green (ICG) formulation (water and oil emulsion). Liposomes-encapsulated carboxyfluorescein were prepared by the sonication procedure. Carboxyfluorescein (5,6-CF) was loaded at high concentration (100 mM) in order to quench its fluorescence. The measurements were performed after i.v. injection of DSPC liposomes (1.5 ml) and lasted 40 min. Fluorescence emission was measured with an ultra high sensitivity intensified camera.
Three different shapes of fluorescent spots were identified depending on target (blood vessel or skin) and energy deposition in tissue: (i) intravascular fluorescence, (ii) transient low fluorescence circular spot, and (iii) persistent high intense fluorescence spot. These images are correlated with histological data.
Real-time fluorescence imaging seems to be a good tool to estimate in a non-invasive manner the thermal damage induced by a diode laser combined with ICG potentiation.
本研究旨在评估利用激光诱导脂质体包裹染料释放来评估血管热损伤的可行性。
研究设计/材料与方法:在仓鼠皮瓣模型上进行实验。使用连接到805nm二极管激光器(功率 = 0.8W,光斑直径 = 1.3mm,脉冲暴露时间为1至6秒)的300微米光纤进行激光照射,照射前使用特定的吲哚菁绿(ICG)制剂(水油乳液)进行增强处理。通过超声处理制备脂质体包裹的羧基荧光素。将羧基荧光素(5,6-CF)以高浓度(100mM)加载以淬灭其荧光。在静脉注射DSPC脂质体(1.5ml)后进行测量,持续40分钟。使用超高灵敏度增强相机测量荧光发射。
根据目标(血管或皮肤)和组织中的能量沉积,识别出三种不同形状的荧光斑点:(i)血管内荧光,(ii)短暂的低荧光圆形斑点,以及(iii)持续的高强度荧光斑点。这些图像与组织学数据相关。
实时荧光成像似乎是一种以非侵入性方式估计二极管激光联合ICG增强诱导的热损伤的良好工具。