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分束激光微切割、多模态成像和光学透明化在体定位和揭示上转换发光微球和量子点的定位。

Delivery and reveal of localization of upconversion luminescent microparticles and quantum dots in the skin in vivo by fractional laser microablation, multimodal imaging, and optical clearing.

机构信息

Saratov State University (National Research University), Optics and Biophotonics Department, Saratov, Russia.

University of Oulu, Optoelectronics and Measurement Techniques Research Unit, Oulu, Finland.

出版信息

J Biomed Opt. 2018 Feb;23(2):1-11. doi: 10.1117/1.JBO.23.2.026001.

Abstract

Delivery and spatial localization of upconversion luminescent microparticles [Y2O3:Yb, Er] (mean size ∼1.6  μm) and quantum dots (QDs) (CuInS2/ZnS nanoparticles coated with polyethylene glycol-based amphiphilic polymer, mean size ∼20  nm) inside rat skin was studied in vivo using a multimodal optical imaging approach. The particles were embedded into the skin dermis to the depth from 300 to 500  μm through microchannels performed by fractional laser microablation. Low-frequency ultrasound was applied to enhance penetration of the particles into the skin. Visualization of the particles was revealed using a combination of luminescent spectroscopy, optical coherence tomography, confocal microscopy, and histochemical analysis. Optical clearing was used to enhance the image contrast of the luminescent signal from the particles. It was demonstrated that the penetration depth of particles depends on their size, resulting in a different detection time interval (days) of the luminescent signal from microparticles and QDs inside the rat skin in vivo. We show that luminescent signal from the upconversion microparticles and QDs was detected after the particle delivery into the rat skin in vivo during eighth and fourth days, respectively. We hypothesize that the upconversion microparticles have created a long-time depot localized in the laser-created channels, as the QDs spread over the surrounding tissues.

摘要

体内实验中,我们采用多模态光学成像方法研究了上转换发光微球 [Y2O3:Yb, Er](平均粒径约 1.6μm)和量子点(CuInS2/ZnS 纳米颗粒,表面涂有基于聚乙二醇的两亲聚合物,平均粒径约 20nm)在大鼠皮肤中的传递和空间定位。通过分数激光微切割在皮肤真皮层中形成 300-500μm 深的微通道,将颗粒嵌入其中。低频超声用于增强颗粒向皮肤的渗透。通过荧光光谱、光学相干断层扫描、共聚焦显微镜和组织化学分析相结合来显示颗粒。光学透明化用于增强颗粒发光信号的图像对比度。结果表明,颗粒的穿透深度取决于其尺寸,导致微球和量子点在体内大鼠皮肤中的发光信号的检测时间间隔(天)不同。我们证明,上转换微球和量子点的发光信号分别在体内将颗粒递送至大鼠皮肤后的第八天和第四天被检测到。我们假设上转换微球在激光创建的通道中形成了一个长时间的储库,而量子点则在周围组织中扩散。

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