According to the International agency for Research on Cancer, cadmium (Cd) is considered as a human carcinogen. Cadmium may induce cell death by apoptosis in various cell types, although the underlying mechanisms are still unclear. Nowadays, the cytotoxic potential of heavy metals is commonly evaluated by different cellular endpoints as reactive oxygen species formation, cell viability or cell death. Heavy metals cytotoxicity testing is based on in-vitro methods such as MTT assay, for the colorimetric detection of mitochondrial activity, propidium iodide-staining of DNA, as cell death marker, fluorometric detection of ROS generation to evaluate the stress response and colorimetric detection of cytokine secretion for the inflammatory reaction by ELISA method. In this work, we present a label-free digital holography (DH) based technique as an in-vitro cytotoxicity assay, which overcomes the limitations of conventional in vitro test based on color or fluorescence read outs. In particular, we show how DH is able to quantify the evolution of key biophysical parameters of cells during the exposure to cadmium. Murine embryonic fibroblasts NIH 3T3 are chosen here as cellular model for studying the cadmium effects. The results demonstrate that DH is able to retrieve the temporal evolution of different key parameters such as cell volume, projected area, cell thickness and dry mass, thus providing a full quantitative characterization of the cell physical behaviour during cadmium exposure. This demonstrates DH as an elegant label-free tool for heavy metals toxicity analysis.
We designed a LoC with embedded optofluidic holographic microscopy capabilities.
Object flow allows unlimited FoV microscopy of samples in a liquid volume. High-throughput
counting and 3D tracking of RBCs is demonstrated.
Here we introduce a compact holographic microscope embedded onboard a Lab-on-a-Chip (LoC) platform. A wavefront division interferometer is realized by writing a polymer grating onto the channel to extract a reference wave from the object wave impinging the LoC. A portion of the beam reaches the samples flowing along the channel path, carrying their information content to the recording device, while one of the diffraction orders from the grating acts as an off-axis reference wave. Polymeric micro-lenses are delivered forward the chip by Pyro-ElectroHydroDynamic (Pyro-EHD) inkjet printing techniques. Thus, all the required optical components are embedded onboard a pocket device, and fast, non-iterative, reconstruction algorithms can be used. We use our device in combination with a novel high-throughput technique, named Space-Time Digital Holography (STDH). STDH exploits the samples motion inside microfluidic channels to obtain a synthetic hologram, mapped in a hybrid space-time domain, and with intrinsic useful features. Indeed, a single Linear Sensor Array (LSA) is sufficient to build up a synthetic representation of the entire experiment (i.e. the STDH) with unlimited Field of View (FoV) along the scanning direction, independently from the magnification factor. The throughput of the imaging system is dramatically increased as STDH provides unlimited FoV, refocusable imaging of samples inside the liquid volume with no need for hologram stitching. To test our embedded STDH microscopy module, we counted, imaged and tracked in 3D with high-throughput red blood cells moving inside the channel volume under non ideal flow conditions.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
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.