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RGD-conjugated Two-photon Absorbing Near-IR Emitting Fluorescent Probes for Tumor Vasculature Imaging

机译:RGD共轭双光子吸收近红外发射荧光探针用于肿瘤血管成像。

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摘要

Observation of the activation and inhibition of angiogenesis processes is important in the progression of cancer. Application of targeting peptides, such as a small peptide that contains adjacent L-arginine (R), glycine (G) and L-aspartic acid (D) residues can afford high selectivity and deep penetration in vessel imaging. To facilitate deep tissue vasculature imaging, probes that can be excited via two-photon absorption (2PA) in the near-infrared (NIR) and subsequently emit in the NIR are essential. In this study, the enhancement of tissue image quality with RGD conjugates was investigated with new NIR-emitting pyranyl fluorophore derivatives in two-photon fluorescence microscopy. Linear and nonlinear photophysical properties of the new probes were comprehensively characterized; significantly the probes exhibited good 2PA over a broad spectral range from 700–1100 nm. Cell and tissue images were then acquired and examined, revealing deep penetration and high contrast with the new pyranyl RGD-conjugates up to 350 μm in tumor tissue.
机译:观察到血管生成过程的激活和抑制在癌症的进展中很重要。靶向肽(例如包含相邻L-精氨酸(R),甘氨酸(G)和L-天冬氨酸(D)残基的小肽)的应用可以在血管成像中提供高选择性和深层渗透。为了促进深部组织脉管成像,可以通过近红外(NIR)中的双光子吸收(2PA)激发并随后在NIR中发射的探针是必不可少的。在这项研究中,在双光子荧光显微镜中,使用新型近红外发射吡喃基荧光团衍生物研究了RGD缀合物对组织图像质量的增强作用。全面表征了新型探针的线性和非线性光物理性质;显然,这些探针在700-1100 nm的宽光谱范围内均显示出良好的2PA。然后获取并检查细胞和组织图像,揭示了新的吡喃基RGD缀合物在肿瘤组织中的最大穿透力和高达350μm的高对比度。

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