Abstract

Light scattering limits the quality of optical imaging of unlabeled specimens: too little scattering and the sample is transparent, exhibiting low contrast and too much scattering washes the structure information altogether. As a result, current instruments, target specifically either the thin (low-scattering) specimens or the optically thick (multiply scattering) samples. We developed gradient light interference microcopy (GLIM) to extract 3D information from both thin and thick unlabeled specimens. GLIM exploits the principle of low-coherence interferometry to extract phase information, which in turn yields strong, intrinsic contrast of transparent samples, such as single cells. Because it combines multiple intensity images that correspond to controlled phase shifts between two interfering waves, GLIM is capable of suppressing the incoherent background due to multiple scattering. Due to the specific, common path interferometric geometry used, the two interfering fields are affected identically by multiple scattering and remain comparable in power even in deep tissue, thus, allowing them to interfere with great contrast. Thus, GLIM yields real-time tomography of optically thick samples via full field imaging. These results indicate that GLIM can become a valuable label-free analysis tool for in-vitro fertilization, where contrast agents and fluorophores may impact the viability of the embryo. We demonstrate the use of GLIM to image various samples, including standard micron size beads, single cells, cell populations, and thick bovine embryos. GLIM operates as an add-on to a conventional microscope and overlays seamlessly with the existing channels (e.g., epi-fluorescence).

© 2017 Optical Society of Japan