Page 48 - 《精细化工》2023年第3期

·504· 精细化工 FINE CHEMICALS 第 40 卷

图 11 TBP 和 CB[8]化学结构式（a）；向 1 mol/L TBP-CB[8]水溶液中加入不同物质的量 Me-Ad 的光致发光发射光谱（b）；
TBP-CB[8]（左）、明亮环境（中）和合并（右）用 TBP 与 CB[8]混合物培养的 Hela 细胞的共聚焦显微图像（c） [11]
Fig. 11 Chemical structural formula of TBP and CB[8] (a); Photoluminescence emission spectra of 1 mol/L TBP-CB[8]
adding different substance amount of Me-Ad (b); TBP-CB[8] (left), bright field (middle), and merge (right) confocal
microscopic images of Hela cells cultured with a mixture of TBP with CB[8] (c) [11]

图 12 HA-BrBP（黑）、HA-BrBP/N 2 （红）、CB[7]/HA-BrBP（浅蓝）、CB[7]/HA-BrBP/N 2 （粉红）、CB[8]/HA-BrBP（绿）
和 CB[8]/HA-BrBP/N 2 （紫红）在 25 ℃水溶液中的光致发光光谱（a）；HA-BrBP、CB[8]/HA-BrBP 和 CB[8]/HA-BrBP/N 2
在 298 K 水溶液中的磷光光谱（b）；A549、HeLa、KYSE-150 和 293T 细胞与 CB[8]/HA-BrBP 一起培育的共聚焦显微
镜图像（c）；A549 细胞与 HA-BrBP 一起培育的共聚焦显微镜图像（d）；A549 细胞与 CB[8]/HA-BrBP 一起培育的共
聚焦显微镜图像（e），4',6-二脒基-2-苯基吲哚（DAPI）（蓝色）用于染色细胞核、MitoTracker（线粒体红色荧光探针）
用于染色线粒体 [39]
Fig. 12 Photoluminescence spectra of HA-BrBP (black), HA-BrBP/N 2 (red), CB[7]/HA-BrBP (light blue), CB[7]/HA-
BrBP/N 2 (pink), CB[8]/HA-BrBP (green), and CB[8]/HA-BrBP/N 2 (wine) in aqueous solution at 25 ℃ (a);
Phosphorescence spectra of HA-BrBP, CB[8]/HA-BrBP, and CB[8]/HA-BrBP/N 2 at 298 K in aqueous solution (b);
Confocal microscope images of A549, HeLa, KYSE-150 and 293T cells incubated with CB[8]/HA-BrBP (c); Confocal
microscope images of A549 cells incubated with HA-BrBP (d); Confocal microscope images of A549 cells incubated with
CB[8]/HA-BrBP (e), 4',6-diamidino-2-phenylindole (DAPI) (blue) was used to stain the nuclei, and MitoTracker
(Mitochondria red probe) was used to stain the mitochondria [39]