New quasiperiodic structures in nematic liquid crystals.

Liquid crystal molecules tend to align with each other, often forming regions of opposite alignment that meet at a boundary-topological defects. These often offer information on configuration of the liquid crystal molecules with competing constraints on their order. Here, we experimentally demonstrate a mechanism to generate topological defects in the form of spatially oscillatory domain walls in nematic liquid crystals. We initially orient the molecules perpendicular to the substrate (i.e. homeotropic alignment) and when a horizontal electric field is applied, domain walls that change their shape with time emerge. These walls form at low frequencies of the applied electric field and remain stable as the frequency increases. If the initial biasing field is at larger frequencies (kHz regime), the domain walls still form, but are not oscillatory. We develop a general theory to predict the three-dimensional liquid crystal director evolution in any two-dimensional varying field. This theory gives the time dependence for the domain walls and confirms that both the oscillatory and straight walls are stable.

Mouse models and human islet transplantation sites for intravital imaging.

Human islet transplantations into rodent models are an essential tool to aid in the development and testing of islet and cellular-based therapies for diabetes prevention and treatment. Through the ability to evaluate human islets in an in vivo setting, these studies allow for experimental approaches to answer questions surrounding normal and disease pathophysiology that cannot be answered using other in vitro and in vivo techniques alone. Intravital microscopy enables imaging of tissues in living organisms with dynamic temporal resolution and can be employed to measure biological processes in transplanted human islets revealing how experimental variables can influence engraftment, and transplant survival and function. A key consideration in experimental design for transplant imaging is the surgical placement site, which is guided by the presence of vasculature to aid in functional engraftment of the islets and promote their survival. Here, we review transplantation sites and mouse models used to study beta cell biology in vivo using intravital microscopy and we highlight fundamental observations made possible using this methodology.

Fast Switching Dual-Frequency Nematic Liquid Crystal Tunable Filters.

We develop tunable optical filters with dual-frequency nematic liquid crystal optical retarders to enable fast switching between the passed wavelengths. The filters are composed of a series of two liquid crystal optical retarders. We select the specific thicknesses of the liquid crystal retarders and use individual biasing schemes to continuously tune the wavelength and bandwidth of the filter. This enables fine-tuned filter switching speeds of filter operation in the ms regime. We present theoretical predictions and experimental results for the electro-optical filter characterization as well as an example application for our filter in total internal reflection fluorescence microscopy. We find that our filter switching speeds can be as short as a few ms, an order of magnitude improvement over typical mechanical filter wheel switching speeds. The quality of our fluorescence images is similar to those obtained by conventional filters.