通过阻断非生产性的形交叉点,有效吸收远红/近红外光的BODIPY光
Pradeep Shrestha1, Komadhie C Dissanayake1, Elizabeth J Gehrmann1
1Department of Chemistry, Iowa State University, 1608 Gilman Hall, Ames, Iowa 50010, United States.
Journal of the American Chemical Society
|August 14, 2020
概括
研究人员开发了新的BODIPY光,可以吸收近红外光,用于深层组织. 这些改进的光具有显著更高的光释放效率,克服了生物分子激活和光疗法的先前限制.
科学领域:
- 摄影化学
- 有机化学
- 生物分子工程
背景情况:
- 光可以通过光控制生物分子的激活.
- 远红/近红外吸收光对于深层组织应用至关重要.
- 现有的近IR BODIPY光具有较低的光释放效率.
研究的目的:
- 为了提高近IR吸收BODIPY光的光释放效率.
- 开发适合深层组织生物分子激活和光疗的光.
- 研究改善光量子产量的策略.
主要方法:
- 合成的甲基化BODIPY光.
- 使用激发状态的动态模拟来识别衰变通道.
- 研究了1,7-二替代物对光释放的作用.
- 使用试剂蓝色排除评估细胞毒性.
- 在HeLa细胞中显示光激活.
主要成果:
- 在700 nm左右强烈吸收的BODIPY光.
- 在 680 nm 获得 4650 M-1 cm-1 的量子效率.
- 与以前的长波Bodipy相比,新型光的量子效率提高了50倍.
- 1,7-diaryl替代改善了量子产量和减少了离子对重组.
- 在20μM度下没有观察到细胞毒性.
结论:
- 抑制非生产性的激发状态衰变通道有效提高光效率.
- 符合限制的甲基化BODIPY结构对近IR光具有前景.
- 开发的光为深层组织应用提供了更高的性能.
- 这种策略为设计更高效的光反应提供了途径.
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