相关实验视频
Updated: Jul 1, 2025

05:51
A Bright NIR-II Fluorescence Probe for Vascular and Tumor Imaging
Published on: March 17, 2023
1.8K
激发近红外光激发的-碳素小分子作为两光子光核酸探测器
Yanqing Sun1, Bi Wu1, Xinyu Liu1
1College of Pharmacy, Jiamusi University, Jiamusi 154007, China.
Molecules (Basel, Switzerland)
|March 13, 2024
概括
三种新型的烯-碳醇衍生物表现出显著的两光子吸收和光特性,使它们成为核酸DNA成像的前景. 这些材料表现出极好的光稳定性和核定位,性能优于DAPI.
科学领域:
- 材料科学 材料科学 材料科学
- 有机化学 有机化学
- 生物光子学 生物光子学
背景情况:
- 两光子吸收 (TPA) 材料对于先进的成像技术至关重要,因为它们的透深度提高,光损伤减少.
- 开发具有高TPA截面和光稳定的新型光探针对于生物应用,特别是DNA染色至关重要.
研究的目的:
- 为了合成和描述三种新的烯-碳醇衍生物,以了解它们作为两光子光探针的潜力.
- 为了评估它们的TPA特性,光发射,DNA染色能力和光稳定性.
主要方法:
- 三种烯-碳醇衍生物的合成:M4,H2和H4.
- 测量两个光子吸收截面和光发射光谱.
- 与Hoechst 33342相比,核定位和DNA染色功效的评估.
- 在持续近红外激光照射下对光稳定性的评估.
主要成果:
- 合成的化合物 (M4,H2,H4) 分别表现出 491,515 和 512 GM 的 TPA 截面.
- 在近红外激发下,在650nm左右观察到光辐射.
- 这些化合物表现出有效的核酸DNA染色,其核定位与Hoechst 33342.2相比.
- 与DAPI相比,观察到更高的光稳定性,平均光衰变速率较低 (0.016%/s,0.020%/s,0.023%/s).
结论:
- 新型烯-碳醇衍生物显示出出色的两光子吸收和光特性.
- 这些化合物是核酸DNA的有效和光稳定的光探针.
- 他们的表现表明了先进的生物成像应用的潜力.
相关概念视频
Labeling DNA Probes
8.2K
DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
8.2K
Photoluminescence: Applications
393
Photoluminescence offers a wide range of applications due to its inherent sensitivity and selectivity. This technique allows for both direct and indirect analyses of the analyte. Direct quantitative analysis is possible when the analyte exhibits a favorable quantum yield for fluorescence or phosphorescence. However, an indirect analysis may be feasible if the analyte is not fluorescent or phosphorescent, or if the quantum yield is unfavorable. Indirect methods include reacting the analyte with...
393

