PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
3D cell models that are induced to interact and grow in a 3D environment are formed up to several hundred micrometers. Since cells grow in all directions, an imaging system that can show molecular images using fluorescence as well as morphological structures without damaging the structure of the cell model is needed. We have developed a multimodal optical microscopy imaging system that combines extended depth of focus-optical coherence microscopy (EDOF-OCM) and two-photon fluorescence microscopy (TPFM) for more accurate measurement of 3D cells. This imaging system was able to acquire merged images without moving the spheroids, and the efficiency of the imaging systems was compared using optical coherence tomography (OCT), OCM, and confocal fluorescence microscopy(CFM).
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.
The alert did not successfully save. Please try again later.
Hyunji Lee, Jae-Won Choi, Min-Beom Heo, Sang-Won Lee, "3D Cell Model monitoring using multimodal optical microscopy imaging system ," Proc. SPIE PC12370, Design and Quality for Biomedical Technologies XVI, PC123700A (6 March 2023); https://doi.org/10.1117/12.2667037