Abstract
AbstractThere is a significant gap in cost-effective quantitative phase microscopy (QPM) systems for studying dynamic cellular processes while maintaining accuracy for long-term cellular monitoring. Current QPM systems often rely on complex and expensive voltage-controllable components like Spatial Light Modulators or two-beam interferometry. To address this, we introduce a QPM system optimized for time-varying phase samples using azobenzene liquid crystal as a Zernike filter with a polarization-sensing camera. This system operates without input voltage or moving components, reducing complexity and cost. Optimized for gentle illumination to minimize phototoxicity, it achieves a 1 Hz frame rate for prolonged monitoring. The system demonstrated accuracy with a maximum standard deviation of ±42 nm and low noise fluctuations of ±2.5 nm. Designed for simplicity and single-shot operations, our QPM system is efficient, robust, and precisely calibrated for reliable measurements. Using inexpensive optical components, it offers an economical solution for long-term, noninvasive biological monitoring and research applications.
Funder
National Science Foundation
Research Corporation for Science Advancement
Publisher
Springer Science and Business Media LLC
Reference54 articles.
1. Popescu, G. Quantitative Phase Imaging of Cells and Tissues. (McGraw-Hill Education, New York, 2011).
2. Wang, Z. et al. Spatial light interference microscopy (SLIM). Opt. Express 19, 1016–1026 (2011).
3. Kumar, P. & Nishchal, N. K. Phase response optimization of a liquid crystal spatial light modulator with partially coherent light. Appl Opt. 60, 10795 (2021).
4. Balasubramani, V. et al. Roadmap on digital holography-based quantitative phase imaging. J. Imaging 7, 252 (2021).
5. Creath, K. V. Phase-measurement interferometry techniques. Prog. Optics 26, 351–391 (1988).