Sub‐picosecond light pulses are used to launch high‐frequency ultrasound in cells. The dual detection of acoustic echoes and of the time‐domain Brillouin scattering allows mapping remotely and in a single run experiment the cell adhesion, thickness, storage modulus and mass density, all with micron resolution. The dual picosecond opto‐acoustic microscope is demonstrated with the multiple imaging of a mitotic macrophage‐like cell. This novel modality is compatible with simultaneous fluorescence imaging. Further details can be found in the article by Liwang Liu, Laurent Plawinski, Marie‐Christine Durrieu, Bertrand Audoin ( e201900045 ).
A new quantitative phase imaging (QPI) modality, coined multi‐ATOM, can now capture and process enormous amount of quantitative phase single‐cell images (>700,000 cells) at a ultrahigh throughput without compromising sub‐cellular resolution. It could empower label‐free single‐cell analysis where large‐scale and cost‐effective screening is necessary. Further details can be found in the article by Kelvin C. M. Lee, Andy K. S. Lau, Anson H. L. Tang, et al. ( e201800479 ).
Spectra from microscopic tissue sections are strongly distorted by Mie‐type scattering and require correction by the ME‐EMSC algorithm. In the upper right, Mie extinction curves, which are simulated by the ME‐EMSC algorithm, are shown. Two measured spectra are shown in the foreground, a raw spectrum which contains Mie scattering, and the spectrum corrected by the ME‐EMSC algorithm. The cover figure was designed by Dr. Boris Zimmermann. Further details can be found in the article by Johanne H. Solheim, Evgeniy Gunko, Dennis Petersen, et al. ( e201800415 ).
This schematic depicts the classification of multiphoton images with different degrees of HCC differentiation using the VGG‐16 neural network. The convolution layer is further trained based on the original weights. The weights of the fully connected layers are initialized as a random number and the training is restarted to improve its classification accuracy. Further details can be found in the article by Hongxin Lin, Chao Wei, Guangxing Wang, et al. ( e201800435 ).
Label‐free optical projection tomography technique makes it possible for quantitative whole mouse embryo imaging without any exogenous contrast agent. Further details can be found in the article by Sungbea Ban, Nam Hyun Cho, Eunjung Min, et al. ( e201800481 ).
Nuclear pore complex imaged at three different resolutions by confocal, expansion, and Ex‐STED microscopy, respectively. NUP become a ruler to measure the expansion process. Further details can be found in the article by Luca Pesce, Marco Cozzolino, Luca Lanzanò, Alberto Diaspro, and Paolo Bianchini ( e201900018 ).
How does the ischemic tissue re‐vascularize? Now we can visualize the reperfusion process at high spatial resolution by using a dual‐wavelength MEMS scanning based optical resolution photoacoustic microscopy (OR‐PAM) system. The fast imaging capability enables continuous monitoring of skin reperfusion in a mouse model. It's also found that the ischemic tissue has a significantly higher oxygen consumption rate in the reperfusion stage comparing to the normal tissue. Further details can be found in the article by Renzhe Bi, U.S. Dinish, Chi Ching Goh, et al. ( e201800454 ).
A wearable device based on fiber optic biosensor for high‐precision radial pulse wave monitoring and diagnosis is proposed and demonstrated in this article. Owing to the high sensitivity of the tiny fiber tip with aluminum diaphragm assembled in the sportswristband, weak acoustic signal induced by arterial pulse can be high‐fidelity recovered and then quantitatively analyzed for clinical diagnosis, which is promising in early cardiovascular diseases indicating. Further details can be found in the article by Jingyi Wang, Kewei Liu, Qizhen Sun, et al. ( e201900084 ).
This review is aimed at interpreting development and advantages of intravital imaging as an emerging invaluable methodology and summarizing related representative discoveries in bone physiologies and pathologies. It also indicates current limitations, further refinement, and extended application of intravital imaging in bone research. Further details can be found in the article by Yuhao Liu, Quan Yuan, and Shiwen Zhanget ( e201960075 ).
Cationic gold nanorods stabilized by quaternary ammonium salts (QAS) are a promising tool for photothermal destruction of cancer cells. However, cytotoxicity of the alkanethiol‐QAS limits their medical applications. A novel design of cationic surfactant composed of the quaternary ammonium group and ethylene glycol chain significantly reduces the compound cytotoxicity in the free state while allowing the preparation of stable nanorods with high cellular uptake and lysosomal localization. Further details can be found in the article by Sarka Salajkova, Michal Sramek, David Malinak, et al. ( e201900024 ).
A low‐cost, automated microscope is combined with machine learning to bring veterinary parasite diagnosis to the point of need. The authors present an inexpensive robotic microscope that automatically focuses, scans, and images a large area McMaster chamber. A deep learning image segmentation pipeline identifies and counts eggs of parasitic worms and single‐celled parasites in goats, dogs, and monkeys, yielding >96% diagnostic accuracy without the need for a trained user. Further details can be found in the article by Yaning Li, Rui Zheng, Yizhen Wu, et al. ( e201800410 ).
Optical tissue clearing is a method allowing post‐mortem deep imaging of organs in three dimensions. By optimizing the CUBIC clearing protocol, the authors provide rapid and simple approach to clear the entire adult rat organism within as little as four days, which is accompanied by the variety of its staining and imaging techniques. The image was captured with polarizers and demonstrates transparent rodent heart with thread‐like crystals of clearing reagent. Further details can be found in the article by Pawe? Matryba et al. ( e201700248 ).
Intraoperative margin assessment is clinically important, especially for tissue conserving surgery like Mohs micrographic surgery in which minimization of the surgical area is crucial. Instead of the complex frozen pathology protocol, slide‐free histopathological imaging of hematoxylin‐eosin stained whole‐mount skin tissues is demonstrated by using nonlinear microscopy, thus facilitating rapid intraoperative assessment of surgical tissues for future applications. Further details can be found in the article by Chi‐Kuang Sun, Chien‐Ting Kao, Ming‐Liang Wei, et al. ( e201800341 ).
This paper presents a novel compact fiberoptic based singlet oxygen near‐infrared luminescence probe coupled to an InGaAs/InP single photon avalanche diode (SPAD) detector. Patterned time gating of the single‐photon detector is used to limit unwanted dark counts and eliminate the strong photosensitizer luminescence background. Singlet oxygen luminescence detection at 1270 nm is confirmed through spectral filtering and lifetime fitting for Rose Bengal in water, and Photofrin in methanol as model photosensitizers. The overall performance, measured by the signal‐to‐noise ratio, improves by a factor of 50 over a previous system that used a fiberoptic‐coupled superconducting nanowire single‐photon detector. The effect of adding light scattering to the photosensitizer is also examined as a first step towards applications in tissue in vivo.
A large‐depth‐of‐field full‐field optical angiography (LD‐FFOA) method is developed to expand the depth‐of‐field (DOF). The contrast pyramid fusion algorithm is used to fuse 10 FFOA images at different focus depth. Cover images of mouse ear shows LD‐FFOA image has higher contrast and more detailed features. The LD‐FFOA method solves the defocused problem caused by the limited DOF of lens, the curved surface and uneven thickness of the sample. Further details can be found in the article by Mingyi Wang, Nanshou Wu, Hongheng Huang, et al. ( e201800329 ).
CARS microscopy was employed to monitor the reorganization of intracellular lipids and proteins, as well as cellular transformations, after irradiation with near infrared (NIR) light. NIR light was shown to induce apoptosis in HeLa cells in vitro in a dose‐dependent manner. The progression of apoptosis assessed with CARS microscopy is apparently associated with the generation of reactive oxygen species followed by an excessive formation of lipid droplets and their peroxidation. Further details can be found in the article by Svitlana M. Levchenko, Andrey N. Kuzmin, Artem Pliss, et al. ( e201900179 )
STED microscopy is a tool that enables superresolution fluorescence imaging by overcoming the diffraction limitation, and has become more useful in various fields such as biology and material science. STED resolution enhancement can be useful in resolving and visualizing sophisticated details of structures of a sample. For this, the excitation focal spot reduction of CW STED microscopy is achieved by PSF engineering using radial polarization and annular aperture, and improved lateral resolution is obtained by STED effect. This leads to a performance improvement that can lower the depletion beam power required to achieve the same superresolution Further details can be found in the article by Geon Lim, Wan‐Chin Kim, Seunghee Oh, Hyungsuk Lee, No‐Cheol Parket ( e201900060 ).
Monitoring the blood‐brain barrier (BBB) permeability plays a key role in assessing drug release with high resolution. In this work, with the help of optical clearing skull window, we not only realized non‐invasive BBB opening by photodynamic therapy, but also developed a method based on spectral‐imaging to in vivo dynamically monitor the changes in BBB permeability. Further details can be found in the article by Wei Feng, Chao Zhang, Tingting Yu, et al. ( e201800330 ).
A novel, camera phone‐based laser speckle imager creates new possibilities for quantitative and noninvasive investigations into diagnosis and pathogenesis of cerebral malaria through the eye. In a longitudinal study, a camera‐phone imager detected decreased retinal blood flow speed as experimental cerebral malaria developed in a murine model. The device may ultimately permit recognition of the syndrome prior to the onset of clinical symptoms which is not currently possible. Further details can be found in the article by Itay Remer, Lorraine F. Pierre‐Destine, David Tay, Linnie M. Golightly, and Alberto Bilenca ( e201800098 ).
To optimize the resection of gliomas during neurosurgery we present an imaging system capable of wide field fluorescence lifetime mapping with 11 mm field of view and 250 mm working distance. Based on a time of flight dual‐tap CMOS camera and a modulated laser at 405 nm we show unobserved quenching effects in tissue phantoms and demonstrate life‐time imaging on 5‐ALA labeled human ex vivo brain tumor samples. Further details can be found in the article by Mikael T. Erkkilä, Bianca Bauer, Nancy Hecker‐Denschlag, et al. ( e201800378 ).
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