Ultraviolet (UV) spectroscopy reveals electronic transitions in matter that underpin atmospheric photochemistry and molecular dynamics. While dual-comb spectroscopy (DCS) has revolutionized precision measurements in the infrared region and expanded to the THz to the visible regions, its extension into the UV has been accomplished only very recently with demanding experimental efforts. Here we introduce free-running ultraviolet dual-comb spectroscopy (UV-DCS), a straightforward, high-fidelity method for absolute absorption cross sections and rapid molecular fingerprinting in the atmospheric UV window. The approach delivers high spectral resolution (1 GHz), broad bandwidth (12 THz), and fast acquisition (500 ms) without active stabilization, resulting in a UV-DCS quality factor that exceeds previously reported values.. Applied to formaldehyde (HCHO), a key atmospheric pollutant and photochemical driver, the technique yields an unprecedented count of rovibrational transitions in this window, enriching the molecular line list used for atmospheric chemistry and remote sensing. The measurements produce refined rotational constants, enabling high-accuracy quantum simulations of molecular eigenstates and informing ab initio models. Beyond robust absolute cross sections, UV-DCS provides a universal, rapid fingerprinting tool for transmissive species, offering fast atmospheric sensing and a rigorous benchmark for quantum theory without stabilization requirements. Coupled with advanced formaldehyde synthesis, these results support improved atmospheric monitoring, more reliable retrievals of HCHO abundances, and enhanced validation of fundamental molecular physics. Overall, this work realizes a free-running UV-DCS platform combining GHz resolution, multi-terahertz bandwidth, and sub-second acquisition, and applies it to refine formaldehyde ultraviolet spectroscopic parameters relevant to atmospheric and molecular science. The online version contains supplementary material available at 10.1186/s43074-026-00250-6.
Comprehensive understanding of brain functions necessitates high-speed imaging of neuronal and vascular dynamics across extensive volumes. Functional neuroimaging investigations with two-photon microscopy are commonly hindered by its limited depth of field which restricts imaging rates across multiple planes. We introduce needle-shaped beam two-photon microscopy (NB-2PM), a versatile platform for high-throughput neurovascular imaging at sub-cellular resolution across multiple depths. It employs customized diffractive optical elements to generate single- or multi-plane needle beams with up to 10 times elongated depth of field relative to Rayleigh lengths and engineered axial energy distribution to effectively offset light attenuation with depth. The proposed method was applied to snapshot volumetric vascular imaging and multi-plane neurovascular dynamic recordings of resting state and stimulus-evoked activity in mice. NB-2PM can seamlessly be integrated into existing microscopy systems, thus providing a scalable platform for gaining comprehensive insights into the functional architecture of murine brain. The online version contains supplementary material available at 10.1186/s43074-026-00237-3.
Real-time dynamic imaging of microbubbles is crucial for understanding their microscale biophysical interactions and advancing ultrasound therapy. Despite progress in time-resolved optical imaging, existing techniques still face trade-offs between acquisition speed, spatial resolution, affordability, and system complexity. Here, we introduce compressed optical-streaking dark-field ultrahigh-speed microscopy (COSDUM), a compact imaging platform that synergistically combines compressed sensing, streak imaging, dark-field microscopy, and deep learning. COSDUM compressively records megahertz acoustic microbubble dynamics over a wide field of view in a snapshot and reconstructs spatially resolved dynamics using a convolutional neural network-based algorithm. Using COSDUM, we captured stable cavitation, nonlinear oscillations, post-excitation free oscillations, and inertial collapse across microbubbles whose radii range from 0.5 to 2.1 μm. Applying COSDUM to microbubble-cell interaction in whole blood, we observed, for the first time, interplay between vibrating microbubbles and blood cells, including microbubble-driven platelet dynamics and highly asymmetric microbubble deformation and conformation around an adjacent red blood cell. The online version contains supplementary material available at 10.1186/s43074-026-00232-8.
Neural activity unfolds across three-dimensional circuits on millisecond-to-microsecond timescales, yet most optical microscopes still acquire volumes sequentially, limiting their ability to capture fast, distributed dynamics. Light-field microscopy (LFM) addresses this unmet need by encoding spatial and angular information into a single camera exposure, enabling snapshot volumetric imaging with low latency and strong robustness to motion. Here we review emerging advances in light-field neuroimaging, from brain-wide calcium recordings in freely moving animals to recent progress that brings kilohertz-class volumetric voltage imaging within reach. We argue that LFM should be evaluated based on information throughput, latency, photon efficiency, and motion robustness at the speed frontier, but not as a direct resolution or contrast competitor to confocal, multiphoton, or light-sheet microscopy. We conclude by highlighting future directions that preserve the LFM's snapshot advantage, including speed-preserving improvements in image quality, extreme temporal-bandwidth architectures that prioritize quantitative inference over visual appearance, and multimodal light-field sensing that adds spectral, lifetime, and polarization contrast.
Stimulated Raman scattering (SRS) microscopy is a highly sensitive chemical imaging technique. However, the SRS imaging performance hinges on two key factors: the reliance on low-noise but bulky solid-state laser sources and stringent sample requirements necessitated by high numerical aperture (NA) optics. Here, we present a fiber laser based stimulated Raman photothermal (SRP) microscope that addresses these limitations. While appreciating the portability and compactness of a noisy source, fiber laser SRP enables a two-order-of-magnitude improvement in signal to noise ratio over fiber laser SRS without balance detection. Furthermore, with the use of low NA, long working distance optics for signal collection, SRP expands the allowed sample space from millimeters to centimeters, which diversifies the sample formats to multi-well plates and thick tissues. The sensitivity and imaging depth are further amplified by using urea for both thermal enhancement and tissue clearance. Together, fiber laser SRP microscopy provides a robust, user-friendly platform for diverse applications. The online version contains supplementary material available at 10.1186/s43074-025-00196-1.
Thermal logic aims to create thermal counterparts to electronic circuits. In this work, we investigate experimentally the response of an analog memory device based on a thin film of an antiferromagnetic metal CuMnAs to bursts of heat pulses generated by the absorption of femtosecond laser pulses at room ambient temperature. When a threshold temperature in the heat-based short-term memory of the device is exceeded, the output of the in-memory logic operations is transferred within the same device to a long-term memory, where it can be retrieved at macroscopic times. The long-term memory is based on magnetoresistive switching from a reference low-resistive uniform magnetic state to high-resistive metastable nanofragmented magnetic states. The in-memory heat-based logic operations and the conversion of the outputs into the electrically-readable long-term magnetoresistive memory were performed at sub-nanosecond time scales, making them compatible with the GHz frequencies of standard electronics. Finally, we demonstrate the possibility of rapidly resetting the long-term memory to the reference low-resistive state by heat pulses. The online version contains supplementary material available at 10.1186/s43074-025-00207-1.
Fluorescence lifetime imaging (FLI) is a powerful tool for investigating molecular processes, microenvironmental parameters, and molecular interactions across tissue to (sub-)cellular levels. Despite its established value in biomedical applications, conventional FLI techniques suffer from long acquisition times, limiting their utility in real-time scenarios like fast biological processes and rapid clinical image-guided interventions. Here, we introduce a novel FLI approach that achieves real-time capability through single-snapshot acquisitions by combining a large-format time-gated SPAD array with dual-gate acquisition capability and a rapid lifetime determination algorithm, thus eliminating time-consuming temporal data collection. We demonstrate this method's scalability and versatility across challenging biomedical applications, such as fast neural dynamics (microscale), multimodal 3D volumetric FLI of tumor organoids (mesoscale), and FLI-guided surgical procedures using tissue-mimicking phantoms (macroscale). Overall, this new methodology significantly enhances FLI's temporal and spatial capabilities, enabling rapid dynamic biomedical signal acquisition and seamless integration into clinical workflows, particularly fluorescence-guided surgery. The online version contains supplementary material available at 10.1186/s43074-025-00216-0.
Measurements and imaging of the mechanical response of biological cells are critical for understanding the mechanisms of many diseases, and for fundamental studies of energy, signal and force transduction. The recent emergence of Brillouin microscopy as a powerful non-contact, label-free way to non-invasively and non-destructively assess local viscoelastic properties provides an opportunity to expand the scope of biomechanical research to the sub-cellular level. Brillouin spectroscopy has recently been validated through static measurements of cell viscoelastic properties, however, fast (sub-second) measurements of sub-cellular cytomechanical changes have yet to be reported. In this report, we utilize a custom multimodal spectroscopy system to monitor for the very first time the rapid viscoelastic response of cells and subcellular structures to a short-duration electrical impulse. The cytomechanical response of three subcellular structures - cytoplasm, nucleoplasm, and nucleoli - were monitored, showing distinct mechanical changes despite an identical stimulus. Through this pioneering transformative study, we demonstrate the capability of Brillouin spectroscopy to measure rapid, real-time biomechanical changes within distinct subcellular compartments. Our results support the promising future of Brillouin spectroscopy within the broad scope of cellular biomechanics.
Far-UVC light in the wavelength range of 200-230 nm has attracted renewed interest because of its safety for human exposure and effectiveness in inactivating pathogens. Here we present a compact solid-state far-UVC laser source based on second-harmonic generation (SHG) using a low-cost commercially-available blue laser diode pump. Leveraging the high intensity of light in a nanophotonic waveguide and heterogeneous integration, our approach achieves Cherenkov phase-matching across a bonded interface consisting of a silicon nitride (SiN) waveguide and a beta barium borate (BBO) nonlinear crystal. Through systematic investigations of waveguide dimensions and pump power, we analyze the dependencies of Cherenkov emission angle, conversion efficiency, and output power. Experimental results confirm the feasibility of generating far-UVC, paving the way for mass production in a compact form factor. This solid-state far-UVC laser source shows significant potential for applications in human-safe disinfection, non-line-of-sight free-space communication, and deep-UV Raman spectroscopy.
Holography is an essential technique of generating three-dimensional images. Recently, quantum holography with undetected photons (QHUP) has emerged as a groundbreaking method capable of capturing complex amplitude images. Despite its potential, the practical application of QHUP has been limited by susceptibility to phase disturbances, low interference visibility, and limited spatial resolution. Deep learning, recognized for its ability in processing complex data, holds significant promise in addressing these challenges. In this report, we present an ample advancement in QHUP achieved by harnessing the power of deep learning to extract images from single-shot holograms, resulting in vastly reduced noise and distortion, alongside a notable enhancement in spatial resolution. The proposed and demonstrated deep learning QHUP (DL-QHUP) methodology offers a transformative solution by delivering high-speed imaging, improved spatial resolution, and superior noise resilience, making it suitable for diverse applications across an array of research fields stretching from biomedical imaging to remote sensing. DL-QHUP signifies a crucial leap forward in the realm of holography, demonstrating its immense potential to revolutionize imaging capabilities and pave the way for advancements in various scientific disciplines. The integration of DL-QHUP promises to unlock new possibilities in imaging applications, transcending existing limitations and offering unparalleled performance in challenging environments. The online version contains supplementary material available at 10.1186/s43074-024-00155-2.
Toroidal electrodynamics is now massively influencing research in toroidal (Marinov et al. New J. Phys. 2007, 9, 234; Basharin et al. Phys. Rev. X 2015, 5, 011036; Jeong et al. ACS Photonics 2020, 7, 1699) and anapole metamaterials (Basharin et al. Phys. Rev. B 2017, 95, 035104; Wu et al. ACS Nano 2018, 12, 1920), optical properties of nanoparticles (Miroshnichenko et al. Nature Commun. 2015, 6, 8069; Gurvitz et al. Laser Photonics Rev. 2019, 13, 1800266), plasmonics (Ogut et al. Nano Lett. 2012, 12, 5239; Yezekyan et al. Nano Lett. 2022, 22, 6098), sensors (Gupta et al. Appl. Phys. Lett. 2017, 110, 121108; Ahmadivand et al. Mater. Today 2020, 32, 108; Wang et al. Nanophotonics 2021, 10, 1295; Yao et al. Photonix 2022, 3, 23), and lasers (Huang et al. Sci. Rep. 2013, 3, 1237; Hwang et al. Nanophotonics 2021, 10, 3599), while a recent publication on toroidal optical transitions in hydrogen-like atoms (Kuprov et al. Sci. Adv. 2022, 8, eabq7651) promises to launch a new chapter in spectroscopy. In this Viewpoint, we review these progresses.
The Sensmart Model X-100 (Nonin Medical Inc, Plymouth, MN, USA) is a relatively new device that possesses two sets of emitters and detectors and uses near infrared spectroscopy (NIRS) to measure regional cerebral oxygen saturation (rSO2). The value of rSO2 obtained by other NIRS devices is affected by physiological and anatomical variables such as hemoglobin concentration, area of cerebrospinal fluid (CSF) layer and skull thickness. The effects of these variables have not yet been determined in measurement of rSO2 by Sensmart Model X-100. We examined the effects of area of CSF, hemoglobin concentration, and skull thickness on the values of rSO2 measured by Sensmart Model X-100 and tissue oxygen index (TOI) measured by NIRO-200NX (Hamamatsu Photonix, Hamamatsu, Japan). Forty neurosurgical, cardiac and vascular surgical patients who underwent preoperative computed tomographic (CT) scan of the brain were enrolled in this study. Regional cerebral oxygen saturation (rSO2) at the forehead was measured sequentially by NIRO-200NX and by Sensmart Model X-100. Simultaneously, mean arterial pressure, hemoglobin concentration, and partial pressure of carbon dioxide in arterial blood (PaCO2) were measured. To evaluate the effects of anatomical factors on rSO2, we measured skull thickness and area of CSF layer using CT images of the brain. Multiple regression analysis was used to examine the relationships between the rSO2 values and anatomical and physiological factors. The area of the CSF layer and hemoglobin concentration had significant associations with rSO2 measured by the Sensmart Model X-100, whereas none of the studied variables was significantly associated with TOI. The measurement of rSO2 by Sensmart Model X-100 is not affected by the skull thickness of patients. Area of the CSF layer and hemoglobin concentration may be the main biases in measurement of rSO2 by Sensmart Model X-100.
cAMP and IP3 act as secondary messengers in olfactory signal transduction and when activated, stimulate calcium levels in olfactory receptor cells. Little is known however, about the causal mechanism. We studied calcium kinetics in mouse olfactory receptor cells after odorant stimuli. Olfactory receptor cells were isolated from female BALB/c mice, treted with trypsin, and stained with Fura-2/AM. Changes in intracellular Ca2+ concentrations in stained cells were measured with a fluorescent microscopic image-processing device (ARGUS-50; Hamamatsu Photonix, Japan). We found that intracellular Ca2+ concentrations rose after exposure to a set of odorants, including 3-ethoxy-4-hydroxy-benzaldehyde, caprylic acid, heptanoic acid, nonanoic acid, eugenol, phenethyl alcohol, and n-amyl acetate. Adding 2', 5'-dideoxyadenosine, a cAMP inhibitor, beforehand suppressed olfactory receptor cell response to odorants. Intracellular Ca2+ concentrations increased substantially in response to stimulation by odorants in calcium-free Ringer's solution, but only a slight increase was seen in intracellular calcium concentration in response stimulation by a high concentration of K+ (145.6 mM) in calcium-free Ringer's solution. The increase in intracellular Ca2+ concentration after odorant stimuli was suppressed when olfactory receptor cells were pretreated with ryanodine, which releases Ca2+ from intracellular stores. These findings suggest that elevated Ca2+ concentrations may be involved in releasing Ca2+ from intracellular calcium stores in mouse olfactory receptor cells, in which cAMP functions as a secondary messenger in olfactory signal transduction.
Distributed time-domain Brillouin scattering fiber sensors have been widely used to measure the changes of the temperature and strain. The linear dependence of the temperature and strain on the Brillouin frequency shift enabled the distributed temperature and strain sensing based on mapping of the Brillouin gain spectrum. In addition, an acoustic wave can be detected by the four wave mixing (FWM) associated SBS process, in which phase matching condition is satisfied via up-down conversion of SBS process through birefringence matching before and after the conversion process. Brillouin scattering can be considered as the scattering of a pump wave from a moving grating (acoustic phonon) which induces a Doppler frequency shift in the resulting Stokes wave. The frequency shift is dependent on many factors including the velocity of sound in the scattering medium as well as the index of refraction. Such a process can be used to monitor the gain of random fiber laser based on SBS, the distributed acoustic wave reflect the distributed SBS gain for random lasing radiation, as well as the relative intensity noise inside the laser gain medium. In this review paper, the distributed time-domain sensing system based on Brillouin scattering including Brillouin optical time-domain reflectometry (BOTDR), Brillouin optical time-domain analysis (BOTDA), and FWM enhanced SBS for acoustic wave detection are introduced for their working principles and recent progress. The distributed Brillouin sensors based on specialty fibers for simultaneous temperature and strain measurement are summarized. Applications for the Brillouin scattering time-domain sensors are briefly discussed.
To investigate the efficacy of conventional root canal treatment (cRCT) with adjunctive photodynamic therapy (aPDT) against microbial biofilms within infected c-shaped root canals. In this in vitro report, the inoculation of 20 freshly extracted human mandibular molar teeth having c-shaped root canal configuration was performed with E. faecalis and P. aeruginosa to produce three-day biofilms in prepared canal system. PDT used a combination of chlorin (ce6) and polyethylenimine (PEI) as the photosensitizer (PS). A 200 μ-fiber was employed to deliver a 660 nm diode laser light into the root canal, and this was compared and conjugated with conventional endodontic treatment utilizing antiseptic irrigation and mechanical debridement. The utilization of aPDT (group-2) resulted in a considerable decrease in the count of E. faecalis and P. aeruginosa from 12.84 ± 2.18 CFU/mL to 5.13 ± 0.67 CFU/mL, and from 14.06 ± 3.98 CFU/mL to 4.82 ± 1.05 CFU/mL pre-and post-treatment, respectively. A statistically significant reduction in the bacterial counts of both microbes was observed after treatment among the samples of the both study groups (p < 0.05). Specimens in group-2 (8.42 ± 1.14 MPa) demonstrated the highest mean push-out bond strength, whereas the lowest was shown by samples in group-1 (7.08 ± 1.09 MPa). ANOVA showed no statistical difference between the research groups (p = 0.676). The independent t-test revealed that the mean push-out bond strength scores of the cervical segments were higher than the apical and middle segments of roots in research groups (p < 0.05). In c-shaped root canals, the application of photodynamic therapy as an adjuvant to conventional root canal treatment contributes to a statistically significant decrease in the microbial count of E. faecalis and P. aeruginosa along with an improved push-out bond strength of the root canal filling material with root.
Information encryption with optical technologies has become increasingly important due to remarkable multidimensional capabilities of light fields. However, the optical encryption protocols proposed to date have been primarily based on the first-order field characteristics, which are strongly affected by interference effects and make the systems become quite unstable during light-matter interaction. Here, we introduce an alternative optical encryption protocol whereby the information is encoded into the second-order spatial coherence distribution of a structured random light beam via a generalized van Cittert-Zernike theorem. We show that the proposed approach has two key advantages over its conventional counterparts. First, the complexity of measuring the spatial coherence distribution of light enhances the encryption protocol security. Second, the relative insensitivity of the second-order statistical characteristics of light to environmental noise makes the protocol robust against the environmental fluctuations, e.g, the atmospheric turbulence. We carry out experiments to demonstrate the feasibility of the coherence-based encryption method with the aid of a fractional Fourier transform. Our results open up a promising avenue for further research into optical encryption in complex environments.
The present clinical trial assessed the effectiveness of photodynamic therapy in association with topical acyclovir in the treatment of herpes labialis in adolescent patients. 45 individuals with herpes labialis were divided into three groups on the basis of provision of treatment. (a) Group I: Topical acyclovir therapy (AVT) (n = 15, mean age: 17.5 years) (b) Group 2: photodynamic therapy (PDT) (n = 15, mean age:16.8 years) and (c) Group III: AVT + adjunctive PDT (n = 15, mean age: 17.0 years) respectively. HSV-1 quantification and pain scales [visual analogue scale (VAS) and McGill Pain Questionnaire (MPQ)] were calculated. Pro-inflammatory biomarkers including interleukin (IL-6) and tumor necrosis factor-alpha (TNF-α) were quantified using enzyme linked immunosorbent assay (ELISA). Shapiro-Wilk test was used to assess the normality. The Friedman test was employed to compute the comparison for changes recorded in pain scores, proinflammatory cytokines and HSV-1 quantification, whereas Mann-Whitney test was used to analyze the mean values and establish inter-group comparisons. All assessments were performed at baseline, immediate post op, 2-weeks, 4-weeks, 3-months, and 6-months. A total of 44 individuals completed the clinical trial. According to the data obtained from the clinical assessment, all the study groups reported a decrease in the parameters being observed. However, Group III (anti-viral (acyclovir) therapy + adjunctive PDT) showed a statistically significant decrease, in comparison to Group II (PDT) and Group I [AVT] respectively. The quantified HSV-1 among all groups showed significant reduction among all groups at each successive follow-up. However, Group-III (AVT + PDT) showed statistically significant reduction as compared to Groups I and II, respectively (p < 0.05). Topical anti-viral therapy with adjunctive PDT significantly helped in reducing the pain and pro-inflammatory biomarkers in adolescent herpes labialis patients.
Protein assays show great importance in medical research and disease diagnoses. Liquid crystals (LCs), as a branch of sensitive materials, offer promising applicability in the field of biosensing. Herein, we developed an ultrasensitive biosensor for the detection of low-concentration protein molecules, employing LC-amplified optofluidic resonators. In this design, the orientation of LCs was disturbed by immobilized protein molecules through the reduction of the vertical anchoring force from the alignment layer. A biosensing platform based on the whispering-gallery mode (WGM) from the LC-amplified optofluidic resonator was developed and explored, in which the spectral wavelength shift was monitored as the sensing parameter. The microbubble structure provided a stable and reliable WGM resonator with a high Q factor for LCs. It is demonstrated that the wall thickness of the microbubble played a key role in enhancing the sensitivity of the LC-amplified WGM microcavity. It is also found that protein molecules coated on the internal surface of microbubble led to their interactions with laser beams and the orientation transition of LCs. Both effects amplified the target information and triggered a sensitive wavelength shift in WGM spectra. A detection limit of 1 fM for bovine serum albumin (BSA) was achieved to demonstrate the high-sensitivity of our sensing platform in protein assays. Compared to the detection using a conventional polarized optical microscope (POM), the sensitivity was improved by seven orders of magnitude. Furthermore, multiple types of proteins and specific biosensing were also investigated to verify the potential of LC-amplified optofluidic resonators in the biomolecular detection. Our studies indicate that LC-amplified optofluidic resonators offer a new solution for the ultrasensitive real-time biosensing and the characterization of biomolecular interactions. The online version contains supplementary material available at 10.1186/s43074-021-00041-1.