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This work reports the realization of Gd 3+ persistent luminescence in the narrowband ultraviolet-B (NB-UVB; 310–313 nm) through persistent energy transfer from a sensitizer of Pr 3+ , Pb 2+ or Bi 3+ . We propose a general design concept to develop Gd 3+ -activated NB-UVB persistent phosphors from Pr 3+ -, Pb 2+ - or Bi 3+ -activated ultraviolet-C (200–280 nm) or ultraviolet-B (280–315 nm) persistent phosphors, leading to the discovery of ten Gd 3+ NB-UVB persistent phosphors such as Sr 3 Gd 2 Si 6 O 18 :Pr 3+ , Sr 3 Gd 2 Si 6 O 18 :Pb 2+ and Y 2 GdAl 2 Ga 3 O 12 :Bi 3+ as well as five ultraviolet-B persistent phosphors such as Y 3 Al 2 Ga 3 O 12 :Pr 3+ , Sr 3 Y 2 Si 6 O 18 :Pb 2+ and Y 3 Al 2 Ga 3 O 12 :Bi 3+ . The persistent energy transfer from the sensitizers to Gd 3+ is very efficient and the Gd 3+ NB-UVB afterglow can last for more than 10 hours. This study expands the persistent luminescence research to the NB-UVB as well as the broader ultraviolet-B spectral regions. The NB-UVB persistent phosphors may act as self-sustained glowing NB-UVB radiation sources for dermatological therapy. 

Abstract Structured Illumination Microscopy enables live imaging with sub-diffraction resolution. Unfortunately, optical aberrations can lead to loss of resolution and artifacts in Structured Illumination Microscopy rendering the technique unusable in samples thicker than a single cell. Here we report on the combination of Adaptive Optics and Structured Illumination Microscopy enabling imaging with 150 nm lateral and 570 nm axial resolution at a depth of 80 µm throughCaenorhabditis elegans. We demonstrate that Adaptive Optics improves the three-dimensional resolution, especially along the axial direction, and reduces artifacts, successfully realizing 3D-Structured Illumination Microscopy in a variety of biological samples. 

We propose localizing point-like fluorescent emitters in three dimensions with nanometer precision throughout large volumes using self-interference digital holography (SIDH). SIDH enables imaging of incoherently emitting objects over large axial ranges without refocusing, and single molecule localization techniques allow sub-50 nm resolution in the lateral and axial dimensions. We demonstrate three-dimensional localization with SIDH by imaging 100 and 40 nm fluorescent nanospheres. With 49,000 photons detected, SIDH achieves a localization precision of 5 nm laterally and 40 nm axially. We are able to detect the nanospheres from as few as 13,000 detected photons. 

Diffraction limited imaging of structures in a highly scattering heterogeneous tissue like bone is a non-trivial task. Here we show binary wavefront optimization using a genetic algorithm, for 2-photon imaging of bone endogenous cells. 

Near infrared and infrared multi-photon imaging through or inside bone is an emerging field that promises to help answer many biological questions that require minimally invasive intravital imaging. Neuroscience researchers especially have begun to take advantage of long wavelength imaging to overcome multiple scattering and image deep inside the brain through intact or partially intact bone. Since the murine model is used in many biological experiments, here we investigate the optical aberrations caused by mouse cranial bone, and their effects on light propagation. We previously developed a ray tracing model that uses second harmonic generation in collagen fibers of bone to estimate the refractive index structure of the sample. This technique is able to rapidly provide initial information for a closed loop adaptive optics system. However, the ray tracing method does not account for refraction or scattering. Here, we extend our work to investigate the wavefront aberrations in bone using a full electromagnetic model. We used Finite-Difference Time-Domain modeling of light propagation in refractive index bone datasets acquired with second harmonic generation imaging. In this paper we show modeled wavefront phase from different originating points across the field of view.