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 ).
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 ).
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 ).
Photodynamic inactivation of prions by disulfonated hydroxyaluminum phthalocyanine. Further details can be found in the article by Marie Kostelanska, Jaroslav Freisleben, Zdenka Backovska Hanusova, et al. ( e201800430 ).
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 ).
The nuclei of epithelial cells in stratified squamous epithelia have been reported to be either low scattering or high scattering. Using micro‐optical coherence tomography, we demonstrate that the nuclei are ‘low scattering’ in the core; those previously reported ‘high‐scattering’ signals are likely from the nucleocytoplasmic boundary. Further details can be found in the article by Si Chen, Xinyu Liu, Nanshuo Wang, et al. ( e201900073 ).
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 ).
This study provides a simple method to detect human distal radius bone density based on near infrared (NIR) imaging. The information of bone mineral density can be measured by transluminational optical bone densitometric system. Compared to dual‐energy x‐ray absorptiometry (DXA) results in clinical trial, NIR images show a strong correlation to DXA. Further details can be found in the article by Chun Chung, Yu‐Pin Chen, Tsai‐Hsueh Leu, and Chia‐Wei Sun ( e201700342 ).
We report the development of a depth‐sensitive Raman spectroscopy system using the configuration of cone–shell excitation and cone detection. The system uses a 785 nm diode laser and three identical axicons for Raman excitation of the target sample in the form of a hollow conic section. The Raman scattered light from the sample, passed through the same (but solid) conic section, is collected for detection. Apart from its ability of probing larger depths (? few mm), an important attraction of the system is that the probing depths can be varied by simply varying the separation between axicons in the excitation arm. Furthermore, no adjustment is required in the sample arm, which is a significant advantage for noncontact, depth‐sensitive measurement. Evaluation of the performance of the developed setup on nonbiological phantom and biological tissue sample demonstrated its ability to recover Raman spectra of layers located at depths of ?2–3 mm beneath the surface.
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 novel design of an SRS microscope exploiting spectral pulse shaping allows measurement of fingerprint to CH‐stretch SRS spectra without any modification of the optical setup. High spectral resolution over a broad vibrational range allows label‐free quantitative imaging of biological samples. An exemplary SRS broadband spectrum of lipid droplets in a liver cancer cell is shown in the picture. Further details can be found in the article by Sergey P. Laptenok, Vijayakumar P. Rajamanickam, Luca Genchi, et al. ( e201900028 ).
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 ).
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 ).
In this work, intravital multiphoton microscopy was used to image and quantify hepatobiliary metabolism of 6‐carboxyfluorescein diacetate in the recovery of acetaminophen‐overdose mice. It was found that the excretion of the probe molecule was time‐dependent and hepatobiliary metabolism is higher in recovered mice, suggesting that newly regenerated hepatocytes have higher metabolic capabilities. This approach may be further developed applied to studying drug‐induced hepatotoxicity in vivo. Further details can be found in the article by Feng‐Chieh Li, Sheng‐Lin Lee, Hung‐Ming Lin, et al. ( e201800296 ).
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 ).
A novel urine analysis technique combining affinity chromatography with Au nanoparticle‐based SERS spectroscopy for potential applications in noninvasive gastric cancer and breast cancer screening. Both the gastric cancer and the breast cancer group can be discriminated from the normal group using SERS spectroscopy combined multivariate diagnostic algorithm, leading to high diagnostic accuracy. These results demonstrate that the urine analysis method has great potential for cancer detection in liquid biopsies. Further details can be found in the article by Xueliang Lin, Lingna Wang, Huijing Lin, et al. ( e201800327 ).
We experimentally demonstrate an ultra‐sensitive immunoassay biosensor using diatom biosilica with self‐assembled plasmonic nanoparticles. As the nature‐created photonic crystal structures, diatoms have been adopted to enhance surface plasmon resonances of metal nanoparticles on the surfaces of diatom frustules and to increase the sensitivity of surface‐enhanced Raman scattering (SERS). In this study, a sandwich SERS immunoassay is developed based on the hybrid plasmonic‐biosilica nanostructured materials that are functionalized with goat anti‐mouse IgG. Our experimental results show that diatom frustules improve the detection limit of mouse IgG to 10 pg/mL, which is ?100× better than conventional colloidal SERS sensors on flat glass.
Ultra‐sensitive immunoassay biosensor using diatom biosilica with self‐assembled plasmonic nanoparticles. 相似文献
Germanium vs Silicon: All‐dielectric nanoparticles provides the heat resistance for proteins under light‐induced heating. Further details can be found in the article by Andrei A. Krasilin et al. ( e201700322 )
The tremendous enhancement factors possessed by surfaceenhanced Raman scattering (SERS), coupled with the flexibility of photonic crystal fibers (PCFs), pave the way to a new generation of ultrasensitive biosensors. This review article aims to provide the latest advancement in SERS‐based PCF sensors for various biochemical applications. Such a sensitive biosensor could be translated for the detection of biomarkers in body fluids for early diagnosis of diseases. Further details can be found in the article by U. S Dinish, Flavien Beffara, Georges Humbert, Jean‐Louis Auguste, and Malini Olivo ( e201900027 ).
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 ).
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