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Noninvasive intratissue refractive index shaping (IRIS) of the cornea with blue femtosecond laser light

机译:蓝色飞秒激光对角膜的无创组织内折射率整形(IRIS)

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Purpose. To test the feasibility of intratissue refractive index shaping (IRIS) in living corneas by using 400-nm femtosecond (fs) laser pulses (blue-IRIS). To test the hypothesis that the intrinsic two-photon absorption of the cornea allows blue-IRIS to be performed with greater efficacy than when using 800-nm femtosecond laser pulses. Methods. Fresh cat corneas were obtained postmortem and cut into six wedges. Blue laser pulses at 400 nm, with 100-fs pulse duration at 80 MHz were used to micromachine phase gratings into each corneal wedge at scanning speeds from 1 to 15 mm/s. Grating lines were 1 μm wide, 5 μm apart, and 150 μm below the anterior corneal surface. Refractive index (RI) changes in micromachined regions were measured immediately by recording the diffraction efficiency of inscribed gratings. Six hours later, the corneas were processed for histology, and TUNEL staining was performed to assess whether blue-IRIS causes cell death. Results. Scanning at 1 and 2 mm/s caused overt corneal damage in the form of bubbles and burns. At faster scanning speeds (5, 10, and 15 mm/s), phase gratings were created in the corneal stroma, which were shown to be pure RI changes ranging from 0.037 to 0.021 in magnitude. The magnitude of RI change was inversely related to scanning speed. TUNEL staining showed cell death only around bubbles and burns. Conclusions. Blue-IRIS can be performed safely and effectively in living cornea. Compared with near-infrared laser pulses, blue-IRIS enhances both achievable RI change and scanning speed without the need to dope the tissue with two-photon sensitizers, increasing the clinical applicability of this technique.
机译:目的。通过使用400 nm飞秒(fs)激光脉冲(蓝色IRIS)测试活体角膜中组织内折射率整形(IRIS)的可行性。为了检验这一假设,即与使用800 nm飞秒激光脉冲时相比,角膜固有的两个光子吸收可使蓝色IRIS的执行效率更高。方法。死后获得新鲜的猫角膜并切成六个楔形。使用400 nm的蓝色激光脉冲,在80 MHz处具有100 fs的脉冲持续时间,以1至15 mm / s的扫描速度将相位光栅微加工到每个角膜楔形物中。光栅线宽1μm,相距5μm,在角膜前表面以下150μm。通过记录内接光栅的衍射效率,可以立即测量微加工区域的折射率(RI)变化。六个小时后,对角膜进行组织学处理,并进行TUNEL染色以评估blue-IRIS是否导致细胞死亡。结果。以1和2 mm / s的速度扫描会以气泡和灼伤的形式造成明显的角膜损伤。在更快的扫描速度(5、10和15 mm / s)下,在角膜基质中形成了相位光栅,显示为纯RI变化,幅度范围为0.037至0.021。 RI变化的幅度与扫描速度成反比。 TUNEL染色仅在气泡和灼伤周围显示细胞死亡。结论Blue-IRIS可在活的角膜中安全有效地进行。与近红外激光脉冲相比,blue-IRIS可以提高可实现的RI变化和扫描速度,而无需使用双光子敏化剂对组织进行掺杂,从而提高了该技术的临床适用性。

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