生物成像用nir发射苯熔低聚体。

Gabriele Selvaggio, R. Nissler, P. Nietmann, A. Patra, Lukas J. Patalag, A. Janshoff, D. Werz, S. Kruss
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摘要

近红外(NIR)荧光团由于其减少散射,增加组织穿透和低光毒性而成为生物光子学的新兴工具。然而,近红外荧光团的文库仍然有限。本文报道了两种六聚体(H)和八聚体(O)形式的苯融合寡聚体(bodipys)的近红外荧光。这些染料发出明亮的近红外荧光(H:最大值943/1075 nm, O:最大值976/1115 nm),可以在近红外(H = 921 nm, O = 956 nm)中激发或在可见光区域的宽范围内非共振。随着染料浓度的增加,H的发射带呈现出色移和峰锐化。此外,在不同极性的溶剂中,氢和氧的最大发射位移都达到了20 nm。这些染料可以用作近红外油墨,并在20厘米的距离上远距离成像。我们进一步通过在生物聚合物(f -肌动蛋白)网络中涂覆微尺度珠和通过近红外视频粒子跟踪(NIR- vpt)进行微流变学,证明了它们在生物光子学方面的多功能性。不发生肌动蛋白丝的光损伤,这是典型的可见荧光团观察到的,突出了这些近红外染料的优点。
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NIR-emitting benzene-fused oligo-BODIPYs for bioimaging.
Near-infrared (NIR) fluorophores are emerging tools for biophotonics because of their reduced scattering, increased tissue penetration and low phototoxicity. However, the library of NIR fluorophores is still limited. Here, we report the NIR fluorescence of two benzene-fused oligo-BODIPYs in their hexameric (H) and octameric (O) forms. These dyes emit bright NIR fluorescence (H: maxima 943/1075 nm, O: maxima 976/1115 nm) that can be excited in the NIR (H = 921 nm, O = 956 nm) or non-resonantly over a broad range in the visible region. The emission bands of H show a bathochromic shift and peak sharpening with increasing dye concentration. Furthermore, the emission maxima of both H and O shift up to 20 nm in solvents of different polarity. These dyes can be used as NIR ink and imaged remotely on the macroscopic level with a stand-off distance of 20 cm. We furthermore demonstrate their versatility for biophotonics by coating microscale beads and performing microrheology via NIR video particle tracking (NIR-VPT) in biopolymer (F-actin) networks. No photodamaging of the actin filaments takes place, which is typically observed for visible fluorophores and highlights the advantages of these NIR dyes.
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