Biomedical Optical Imaging Research Articles

Imaging light fluence in blood vessels by combining photoacoustic fluctuation imaging and ultrasound power Doppler

Objectives. Numerous optical biomedical imaging or therapeutic modalities suffer from unknown light fluence distribution at depths. Photoacoustic (PA) imaging, which enables imaging blood vessels at the acoustic resolution, probes the product between the fluence and effective optical absorption that depends on the size or density of blood vessels. In the case of unresolved vessels, fluence and absorption can not be decoupled using PA imaging alone without the use of inverse problems. Thus, we propose combining two modalities that are sensitive to blood vessels to directly image fluence maps within vascularized areas, including in unresolved vessels. Approach. To achieve fluence imaging, the combination of photoacoustic fluctuation (PAFI) and Ultrasound Power Doppler (UPD) images is considered. After exposing a new theoretical expression of the UPD image, we establish a fluence imaging method giving quantitative fluence in blood vessels. Fluence imaging involves resolution compensation with a PSF filter that is compared to alternative simpler corrections. Main results. This method universally applies to arbitrary hematocrit and multi-scale vessel imaging. Using a spherical sparse array, we demonstrate 3D fluence imaging within blood vessels in simulation and experiments which is not possible with PAFI alone. Significance. Overall, we show that combining PAFI and UPD has the potential for real-time light dosimetry or could enhance quantitative inverse problems in PA imaging.

Complex transmission matrix retrieval for a highly scattering medium via regional phase differentiation

Accurately measuring the complex transmission matrix (CTM) of the scattering medium (SM) holds critical significance for applications in anti-scattering optical imaging, phototherapy, and optical neural networks. Non-interferometric approaches, utilizing phase retrieval algorithms, can robustly extract the CTM from the speckle patterns formed by multiple probing fields traversing the SM. However, in cases where an amplitude-type spatial light modulator is employed for probing field modulation, the absence of phase control frequently results in the convergence towards a local optimum, undermining the measurement accuracy. Here, we propose a high-accuracy CTM retrieval (CTMR) approach based on regional phase differentiation (RPD). It incorporates a sequence of additional phase masks into the probing fields, imposing a priori constraints on the phase retrieval algorithms. By distinguishing the variance of speckle patterns produced by different phase masks, the RPD-CTMR can effectively direct the algorithm towards a solution that closely approximates the CTM of the SM. We built a prototype of a digital micromirror device modulated RPD-CTMR. By accurately measuring the CTM of diffusers, we achieved an enhancement in the peak-to-background ratio of anti-scattering focusing by a factor of 3.6, alongside a reduction in the bit error rate of anti-scattering image transmission by a factor of 24. Our proposed approach aims to facilitate precise modulation of scattered optical fields, thereby fostering advancements in diverse fields including high-resolution microscopy, biomedical optical imaging, and optical communications.

Fabrication of agar-based tissue-mimicking phantom for the technical evaluation of biomedical optical imaging systems

The development process of the optical systems for various biomedical applications typically involve evaluations of technical performance. One popular evaluation method is to use a reference object such as a phantom that exhibits similar optical properties of tissue. Fabrication of a consistent phantom with known optical properties, such as scattering and absorption, is essential for accurate technical evaluation of the optical system. This paper presents a protocol for fabricating an agar-based tissue-mimicking phantom, offering practical guidance to ensure consistent and reproducible phantom creation. In addition, optical setups that measure light information required for quantifying the optical properties via an inverse adding-doubling (IAD) method are discussed. We demonstrated the fabrication of phantoms with diverse scattering and absorption properties, and the IAD method successfully quantified the optical properties. Moreover, we employed the phantom to assess the imaging depth limitation of a hyperspectral imaging system, demonstrating potential usage of phantoms for performing technical evaluation.

CylinGCN: Cylindrical structures segmentation in 3D biomedical optical imaging by a contour-based graph convolutional network

Cylindrical organs, e.g., blood vessels, airways, and intestines, are ubiquitous structures in biomedical optical imaging analysis. Image segmentation of these structures serves as a vital step in tissue physiology analysis. Traditional model-driven segmentation methods seek to fit the structure by constructing a corresponding topological geometry based on domain knowledge. Classification-based deep learning methods neglect the geometric features of the cylindrical structure and therefore cannot ensure the continuity of the segmentation surface. In this paper, by treating the cylindrical structures as a 3D graph, we introduce a novel contour-based graph neural network for 3D cylindrical structure segmentation in biomedical optical imaging. Our proposed method, which we named CylinGCN, adopts a novel learnable framework that extracts semantic features and complex topological relationships in the 3D volumetric data to achieve continuous and effective 3D segmentation. Our CylinGCN consists of a multiscale 3D semantic feature extractor for extracting inter-frame multiscale semantic features, and a residual graph convolutional network (GCN) contour generator that combines the semantic features and cylindrical topological priors to generate segmentation contours. We tested the CylinGCN framework on two types of optical tomographic imaging data, small animal whole body photoacoustic tomography (PAT) and endoscopic airway optical coherence tomography (OCT), and the results show that CylinGCN achieves state-of-the-art performance. Code will be released at https://github.com/lzc-smu/CylinGCN.git.

A priori free spectral unmixing with periodic absorbance changes: application for auto-calibrated intraoperative functional brain mapping.

Spectral unmixing designates techniques that allow to decompose measured spectra into linear or non-linear combination of spectra of all targets (endmembers). This technique was initially developed for satellite applications, but it is now also widely used in biomedical applications. However, several drawbacks limit the use of these techniques with standard optical devices like RGB cameras. The devices need to be calibrated and a a priori on the observed scene is often necessary. We propose a new method for estimating endmembers and their proportion automatically and without calibration of the acquisition device based on near separable non-negative matrix factorization. This method estimates the endmembers on spectra of absorbance changes presenting periodic events. This is very common in in vivo biomedical and medical optical imaging where hemodynamics dominate the absorbance fluctuations. We applied the method for identifying functional brain areas during neurosurgery using four different RGB cameras (an industrial camera, a smartphone and two surgical microscopes). Results obtained with the auto-calibration method were consistent with the intraoperative gold standards. Endmembers estimated with the auto-calibration method were similar to the calibrated endmembers used in the modified Beer-Lambert law. The similarity was particularly strong when both cardiac and respiratory periodic events were considered. This work can allow a widespread use of spectral imaging in the industrial or medical field.

Synthesis and In Vitro Evaluation of a HER2-Specific ImmunoSCIFI Probe.

Secondary Cerenkov-induced fluorescence imaging (SCIFI) is an emerging biomedical optical imaging modality that leverages Cerenkov luminescence, primarily generated by β-emitting radioisotopes, to excite fluorophores that offer near-infrared emissions with optimal tissue penetrance. Dual-functionalized immunoconjugates composed of an antibody, a near-infrared fluorophore, and a β-emitting radioisotope have potential utility as novel SCIFI constructs with high specificity for molecular biomarkers of disease. Here, we report the synthesis and characterization of [89Zr]Zr-DFO-trastuzumab-BOD665, a self-excitatory HER2-specific "immunoSCIFI" probe capable of yielding near-infrared fluorescence in situ without external excitation. The penetration depth of the SCIFI signal was measured in hemoglobin-infused optical tissue phantoms that indicated a 2.05-fold increase compared to 89Zr-generated Cerenkov luminescence. Additionally, the binding specificity of the immunoSCIFI probe for HER2 was evaluated in a cellular assay that showed significantly higher binding to SKBR3 (high HER2 expression) relative to MDA-MB-468 (low HER2) breast cancer cells based on measurements of total flux in the near-infrared region with external excitation blocked. Taken together, the results of this study indicate the potential utility of immunoSCIFI constructs for interrogation of molecular biomarkers of disease.

Technologies for depth scanning in miniature optical imaging systems [Invited

Biomedical optical imaging has found numerous clinical and research applications. For achieving 3D imaging, depth scanning presents the most significant challenge, particularly in miniature imaging devices. This paper reviews the state-of-art technologies for depth scanning in miniature optical imaging systems, which include two general approaches: 1) physically shifting part of or the entire imaging device to allow imaging at different depths and 2) optically changing the focus of the imaging optics. We mainly focus on the second group of methods, introducing a wide variety of tunable microlenses, covering the underlying physics, actuation mechanisms, and imaging performance. Representative applications in clinical and neuroscience research are briefly presented. Major challenges and future perspectives of depth/focus scanning technologies for biomedical optical imaging are also discussed.

Introducing Specific Iodine Ions in Perovskite-Based Nanocomplex to Cater for Versatile Biomedical Imaging and Tumor Radiotherapy.

Multimodal biomedical imaging and imaging-guided therapy have garnered extensive attention owing to the aid of nanoagents with the aim of further improving the therapeutic efficacy of diseases. The ability to engineer nanocomplexes (NCs) or control how they behave within an organism remains largely elusive. Here, a multifunctional nanoplatform is developed based on stabilized I-doped perovskite, CsPbBr3 -x Ix @SiO2 @Lip-c(RGD)2 (PSL-c(RGD)2 ) NCs. In particular, by regulating the amount of regular I- ions introduced, the fluorescence emission spectrum of perovskite-based NCs can be modulated well to match the requirement for biomedical optical imaging at the scale from molecule, cell to mouse; doping 125 I enables the nanoformulation to be competent for single-photon emission computed tomography (SPECT) imaging; the introduction of 131 I- imparts the NCs with the capability for radiotherapy. Through facile manipulation of specific iodine ions, this nanoplatform exhibits a remarkable ability to match multifunctional biomedical imaging and tumor therapy. In addition, their in vivo behavior can be manipulated by adjusting the thickness of the silica shell and the surface polarity for more practical applications. These experimental explorations offer a novel approach for engineering desirable multimodal NCs to simultaneously image and combat malignant tumors.

Label-free biomedical optical imaging.

Label-free optical imaging employs natural and nondestructive approaches for the visualisation of biomedical samples for both biological assays and clinical diagnosis. Currently, this field revolves around multiple broad technology-oriented communities, each with a specific focus on a particular modality despite the existence of shared challenges and applications. As a result, biologists or clinical researchers who require label-free imaging are often not aware of the most appropriate modality to use. This manuscript presents a comprehensive review of and comparison among different label-free imaging modalities and discusses common challenges and applications. We expect this review to facilitate collaborative interactions between imaging communities, push the field forward and foster technological advancements, biophysical discoveries, as well as clinical detection, diagnosis, and monitoring of disease.

Label-Free Imaging Techniques to Evaluate Metabolic Changes Caused by Toxic Liver Injury in PCLS.

Abuse with hepatotoxic agents is a major cause of acute liver failure. The search for new criteria indicating the acute or chronic pathological processes is still a challenging issue that requires the selection of effective tools and research models. Multiphoton microscopy with second harmonic generation (SHG) and fluorescence lifetime imaging microscopy (FLIM) are modern label-free methods of optical biomedical imaging for assessing the metabolic state of hepatocytes, therefore reflecting the functional state of the liver tissue. The aim of this work was to identify characteristic changes in the metabolic state of hepatocytes in precision-cut liver slices (PCLSs) under toxic damage by some of the most common toxins: ethanol, carbon tetrachloride (CCl4) and acetaminophen (APAP), commonly known as paracetamol. We have determined characteristic optical criteria for toxic liver damage, and these turn out to be specific for each toxic agent, reflecting the underlying pathological mechanisms of toxicity. The results obtained are consistent with standard methods of molecular and morphological analysis. Thus, our approach, based on optical biomedical imaging, is effective for intravital monitoring of the state of liver tissue in the case of toxic damage or even in cases of acute liver injury.

Mueller matrix polarization imaging and quantitative parameters analysis method.

Mueller matrix polarization imaging is a new biomedical optical imaging method that can generate both polarization and isotropic intensity images of structures of the biological tissue sample surface. In this paper, a Mueller polarization imaging system in the reflection mode is described for obtaining the Mueller matrix of the specimens. Diattenuation, phase retardation, and depolarization of the specimens are derived by using the conventional Mueller matrix polarization decomposition method and a newly proposed direct method. The results show that the direct method is more convenient and faster than the conventional decomposition method. The polarization parameter combination method is then presented in which any two of the diattenuation, phase retardation, and depolarization parameters are combined, and three new quantitative parameters are defined in order to reveal more detailed anisotropic structures. The images of in vitro samples are presented to demonstrate the capability of the parameters introduced.

Accounting for Polychromatic Light in Virtual Shack-Hartmann Wavefront Sensing

Virtual Shack-Hartmann wavefront sensing (vSHWS) has some significant advantages and is promising for aberration measurement in the field of biomedical optical imaging. The illumination sources used in vSHWS are almost broadband, but are treated as monochromatic sources (only using center wavelength) in current data processing, which may cause errors. This work proposed a data processing method to take into account the multiple wavelengths of the broadband spectrum, named multiple-wavelength centroid-weighting method. Its feasibility was demonstrated through a series of simulations. A wavefront generated with a set of statistical human ocular aberrations was used as the target wavefront to evaluate the performance of the proposed and current methods. The results showed that their performance was very close when used for the symmetrical, but the wavefront error of the proposed method was much smaller than that of the current method when used for the asymmetrical spectrum, especially for the broader spectrum. These results were also validated by using 20 sets of clinical human ocular aberrations including normal and diseased eyes. The proposed method and the obtained conclusions have important implications for the application of vSHWS.

Optical Biomedical Imaging Reveals Criteria for Violated Liver Regenerative Potential.

To reduce the risk of post-hepatectomy liver failure in patients with hepatic pathologies, it is necessary to develop an approach to express the intraoperative assessment of the liver's regenerative potential. Traditional clinical methods do not enable the prediction of the function of the liver remnant. Modern label-free bioimaging, using multiphoton microscopy in combination with second harmonic generation (SHG) and fluorescence lifetime imaging microscopy (FLIM), can both expand the possibilities for diagnosing liver pathologies and for assessing the regenerative potential of the liver. Using multiphoton and SHG microscopy, we assessed the structural state of liver tissue at different stages of induced steatosis and fibrosis before and after 70% partial hepatectomy in rats. Using FLIM, we also performed a detailed analysis of the metabolic state of the hepatocytes. We were able to determine criteria that can reveal a lack of regenerative potential in violated liver, such as the presence of zones with reduced NAD(P)H autofluorescence signals. Furthermore, for a liver with pathology, there was an absence of the jump in the fluorescence lifetime contributions of the bound form of NADH and NADPH the 3rd day after hepatectomy that is characteristic of normal liver regeneration. Such results are associated with decreased intensity of oxidative phosphorylation and of biosynthetic processes in pathological liver, which is the reason for the impaired liver recovery. This modern approach offers an effective tool that can be successfully translated into the clinic for express, intraoperative assessment of the regenerative potential of the pathological liver of a patient.

Preface

International School of Photonics (ISP) was established in 1995 as a separate school under Cochin University of Science and Technology (CUSAT) with objectives of developing and establishing research activities in photonics and related fields. ISP offers a two-year MTech Programme in Optoelectronics and Laser Technology and Five-year Integrated Masters Programme in Photonics. Equiped with sophisticated research facilities, ISP also offers PhD in Photonics and related area.As a part of academic activities, ISP has been conducting a national level annual photonics workshop since its inception. This workshop gradually developed in to National Photonics Symposium (NPS) since 2017. NPS brings together leading scientists, academicians, industrialists and young researchers in India and aborad for fruitful interactions and active discussions on various aspects of photonics. Permanent venue of the conference is ISP, CUSAT, Cochin. In 2022, NPS was conducted as an International Conference on Recent Trends in Photonics (NPS 2022) in online mode during 27 February to 01 March. Virtual mode was preferred due to government restrictions in place due to COVID-19. NPS 2022 brought 12 invited speakers from India and abroad including one key note speaker and three plenary speakers. In addition to this, 21 contributed talks and 34 posters were also included for presentations. All invited talks were scheduled for one hour duration including the time for discussion. Contributed speakers were allotted 12 minutes for presentation and discussions. ZOOM Webinar was used for delivering the talks and Breakout Room facility in ZOOM Meetings was used for poster presentations. Dedicated sessions were arranged for industrial collaborators to present and discuss their latest research tools and equipment.The opening of NPS 2022 was marked by the keynote address of Prof. Franz X. Kärtner from the University of Hamburg, Germany. Prof. Kärtner talked about the latest experimental results and the implementation of electron and X-ray sources at DESY, Germany. There were three plenary talks covering various diverse areas of photonics research. Dr. Kazuhiko Maeda, an expert in the field of photocatalysis and energy, from the Tokyo Institute of Technology, Japan, talked bout artificial photosynthetic assemblies using layered materials. He also gave a general outlook on artificial photosynthesis, solar water splitting with recent developments, challenges and opportunities in the field. Another plenary speaker was Dr. Pablo Albella, from the University of Cantabria, Santander, Spain. Dr. Albella gave an elaborate account of the research activities in his research group in the area of dielectric nanoantennas for guiding light and heat at the nanoscale. The third plenary talk was delivered by Dr. V. M. Murukeshan, Director, Centre for Optical and Laser Engineering (COLE) at Nanyang Technological University, Singapore. Prof. Murugeshan’s talk focused at the research activities in his group on high resolution biomedical optical imaging of various tissues in human body.The invited speakers also included experts from various field of optics and photonics, Dr. Tatyana Sizyuk (Argonne National Laboratory, USA), Dr. Radhakrishna Prabhu (Robert Gordon University, Aberdeen, UK), Dr. Sonia Mary (The Jackson Laboratory, USA), Dr. Madhu V. (Technical University of Denmark, Denmark) and Dr. Swapna Nair (Central University of Kerala, India).Industrial sessions in NPS 2022 included two invited speakers and various contributed presentations from industries. Dr. Renilkumar Mudachathi, Chief Scientist at Motion Imager, Twente, The Netherlands gave an invited talk focused on various fabrication techniques for photonic and optoelectronic research and industry. Industry session was also marked by the interaction with Dr. Suresh Nair, IEEE India Council Chair, on the activities of IEEE and the industrial research related to optics and photonics. NPS 2022 also marked the celebration of National Science Day on 28 February, with a special lecture from Prof. G. Ravindra Kumar, TIFR, Mumbai. The lecture delivered on the development of ultraintense lasers and their application in research, was also open to the public.List of Committee members, NPS 2022 is available in this Pdf.

Imaging and detection of long-lived fluorescence probes in presence of highly emissive and scattering background.

Optical biomedical imaging and diagnostics is a rapidly growing field that provides both structural and functional information with uses ranging from fundamental to practical clinical applications. Nevertheless, imaging/visualizing fluorescence objects with high spatial resolution in a highly scattering and emissive biological medium continues to be a significant challenge. A fundamental limiting factor for imaging technologies is the signal-to-background ratio (SBR). For a long time to improve the SBR, we tried to improve the brightness of fluorescence probes. Many novel fluorophores with improved brightness (almost reaching the theoretical limit), redshifted emission, highly improved photostability, and biocompatibility greatly helped advance fluorescence detection and imaging. However, autofluorescence, scattering of excitation light, and Raman scattering remain fundamental limiting problems that drastically limit detection sensitivity. Similarly, significant efforts were focused on reducing the background. High-quality sample purification eliminates the majority of autofluorescence background and in a limited confocal volume allows detection to reach the ultimate sensitivity to a single molecule. However, detection and imaging in physiological conditions does not allow for any sample (cells or tissue) purification, forcing us to face a fundamental limitation. A significant improvement in limiting background can be achieved when fluorophores with a long fluorescence lifetime are used, and time-gated detection is applied. However, all long-lived fluorophores present low brightness, limiting the potential improvement. We recently proposed to utilize multipulse excitation (burst of pulses) to enhance the relative signal of long-lived fluorophores and significantly improve the SBR. Herein, we present results obtained with multipulse excitation and compare them with standard single-pulse excitation. Subtraction of images obtained with a single pulse from those obtained with pulse burst (differential image) highly limits background and instrumental noise resulting in more specific/sensitive detection and allows to achieve greater imaging depth in highly scattering media, including skin and tissue.

Broadband Coherent Mid-Infrared Supercontinuum Generation in All-Chalcogenide Microstructured Fiber With All-Normal Dispersion

We demonstrated numerically the generation of broadband, coherent supercontinuum (SC) spectra in the mid-infrared region using dispersion-engineered all-chalcogenide microstructured fibers (MOFs). The 1-cm-long hexagonal fiber can be made with Ge11.5As24S64.5 glass as a low-refractive-index material embedded in a Ge11.5As24Se64.5 glass matrix. By optimizing the structural parameters, we determined a broad and flat all-normal-dispersion characteristic up to 14 μm. A highly coherent broadband SC with an intensity greater than −3 dB in the range from 5973 to 8695 nm is obtained when the fiber is pumped by a 7 μm laser with pulse duration of 50 fs and peak power of 6 kW. Flat-top SC of −30 dB level can be observed utilizing identical pump pulse parameters, covering wavelengths from 3823 to 13577 nm (>1.5 octaves). This broadband coherent MIR SC source can be applied in frequency metrology, optical coherence tomography, biomedical imaging, and few-cycle pulse compression.

Recent advances in near infrared upconverting nanomaterials for targeted photodynamic therapy of cancer

Photodynamic therapy (PDT) is a well-established treatment of cancer that uses the toxic reactive oxygen species, including singlet oxygen (1O2), generated by photosensitiser (PS) drugs following irradiation of a specific wavelength to destroy the cancerous cells and tumours. Visible light is commonly used as the excitation source in PDT, which is not ideal for cancer treatment due to its reduced tissue penetration, and thus inefficiency to treat deep-lying tumours. Additionally, these wavelengths exhibit elevated autofluorescence background from the biological tissues which hinders optical biomedical imaging. An alternative to UV–Vis irradiation is the use of near infrared (NIR) excitation for PDT. This can be achieved using upconverting nanoparticles (UCNPs) functionalised with photosensitiser drugs where UCNPs can be used as an indirect excitation source for the activation of PS drugs yielding to the production of singlet 1O2 following NIR excitation. The use of nanoparticles for PDT is also beneficial due to their tumour targeting capability, either passively via the enhanced permeability and retention (EPR) effect or actively via stimuli-responsive targeting and ligand-mediated targeting (i.e. using recognition units that can bind specific receptors only present or overexpressed on tumour cells). Here, we review recent advances in NIR upconverting nanomaterials for PDT of cancer with a clear distinction between those reported nanoparticles that could potentially target the tumour due to accumulation via the EPR effect (passive targeting) and nanoparticle-based systems that contain targeting agents with the aim of actively target the tumour via a molecular recognition process.

One-pot synthesis of efficient multifunctional nitrogen-doped carbon dots with efficient yellow fluorescence emission for detection of hypochlorite and thiosulfate.

CD-based ratiometric fluorescence probes are of great significance for visual detection, but accomplishing this goal is still a particularly challenging task. Herein, nitrogen-doped carbon dots (NCDs) with bright yellow fluorescence were easily manufactured via a one-pot hydrothermal method for visual detection of hypochlorite (ClO-) and thiosulfate (S2O32-) under UV light irradiation. The as-prepared NCDs demonstrate favorable water solubility, excellent biocompatibility, superior optical properties and low cytotoxicity. Strikingly, the fluorescence of the NCDs could be quenched with ClO-. Based on these results, an original fluorescent nanoprobe was constructed for the highly discriminating recognition of ClO- by oxidation of the amino groups on their surface to nitro groups. The assay covered the ranges from 0.067 to 19.33 μM and 24 to 98 μM with a limit of detection (S/N = 3) of as low as 0.013 μM. Remarkably, a growing peak appears at 537 nm and the emission at 492 nm shrinks with the introduction of S2O32-, which demonstrates ratiometric fluorescence emission characteristics (F537nm/F492nm) in the range of 6.6-100 μM with a limit of detection (S/N = 3) of as low as 0.78 μM. In addition, the fluorescence color of the NCDs also changes (yellow-green-blue) after adding various ClO- concentrations. The fluorescence color of the NCDs-ClO- also changes (blue-green-yellow) after adding various S2O32- concentrations. This excellent ratiometric fluorescence probe was successfully further used for nuclear imaging. Accordingly, an easy-to-prepare paper-based sensor to identify ClO- and S2O32- was fabricated, which demonstrated their adaptability for in situ on-site testing. This research further opens up new opportunities for the development of efficient yellow fluorescent probes based on NCDs nanomaterials for visual detection, biomarking, and biomedical optical imaging.

Facile synthesis of multifunctional carbon dots with 54.4% orange emission for label-free detection of morin and endogenous/exogenous hypochlorite

Carbon dots with long-wavelength emission (orange to red), high quantum yield (QY) and good biocompatibility are of great significance for biomedical applications, but achieving this is still a highly challenging task. In this work, multifunctional carbon dots with 54.4% orange emission (O-CDs) were prepared through one-pot solvothermal treatment of nileblueasulphate and citric acid as precursor for label-free recognition of morin and endogenous/exogenous hypochlorite (ClO-) and bioimaging in cellular and zebrafish. Morin can quench the luminescence of O-CDs by static quenching (SQ). The linear range is 5–125 μM and LOD is 0.84 μM. ClO- reduce the photoluminescence intensity of O-CDs via SQ. The linear range is 2.5–90 μM and LOD was 0.46 μM. In addition, The obtained O-CDs have successfully realized the monitoring of morin and endogenous/ exogenous ClO- in living cells and zebrafish owing to its superior biocompatibility, exceptional photostability and lower toxicity. This work opens up a novel opportunity for the development of long-wavelength emission multifunctional nanomaterial with high quantum yield based on CDs for biosensing, biolabeling and biomedical optical imaging.

Introduction to Special Biomedical Optical Imaging Issue

Introduction to Special Biomedical Optical Imaging Issue