自体荧光
光漂白
材料科学
双光子激发显微术
荧光寿命成像显微镜
荧光
显微镜
荧光显微镜
光漂白后的荧光恢复
量子产额
吸收(声学)
多光子荧光显微镜
生物物理学
纳米技术
光电子学
生物医学工程
光学
生物
物理
复合材料
医学
作者
Peuli Nath,Adrian Ross Liversage,Luke J. Mortensen,Aniruddha Ray
标识
DOI:10.1021/acsami.4c08672
摘要
Multiphoton fluorescence microscopy is a powerful tool for imaging and exploring biological tissue at subcellular spatial resolution while minimizing photobleaching and autofluorescence. For optimal performance in multiphoton microscopy, materials exhibiting a large multiphoton absorption cross section (σn) and fluorescence quantum yield are desired. Notably, perovskite nanocrystals (CsPbX3, PNCs) exhibit exceptionally large two-, three-, up to five photon absorption cross section (σ2 ∼ 106 GM, σ3 ∼ 10-73 cm6s2 photon-2, σ5 ∼ 10-136 cm10s4 photon-4), along with near unity fluorescence quantum yield, making them desirable for deep tissue applications. Here, we employed PNCs as contrast agents to image mesenchymal stromal cells in a living mouse. The PNCs were stabilized by encapsulating them in a SiO2 matrix (∼60-70 nm in diameter), offering versatility for subsequent surface modification to target specific biological entities for both diagnostic and therapeutic applications. Multiphoton imaging of PNCs offers substantial benefits for dynamic tracking of cells in deep tissue, such as in understanding immune cell migration and other biological processes in both healthy and diseased tissues.
科研通智能强力驱动
Strongly Powered by AbleSci AI