Conventional Fluorophores Research Articles

Construction of Bovine Serum Albumin/AIE-Based Quaternary Complexes for Efficient Gene Transfection.

High transfection efficiency and superior cell imaging are required for cationic polymers-based gene delivery system to afford high therapeutic effect but its high toxicity and unstable cell imaging are easily ignored. In this study, cationic amino poly(glycerol methacrylate) derivative (PGMA-EDA) is used to incorporate bovine serum albumin (BSA) and aggregation-induced emission (AIE) molecular (tetraphenylethylene derivatives, TPE) as an efficient carrier for gene transfection and intracellular imaging. The obtained polymer/pDNA-TPE/BSA (PDTB) quaternary nanoparticles (NPs) not only exhibit efficient gene transfection but also show excellent biocompatibility. After inclusion of TPE/BSA (TB) NPs, BSA promoted dissociation of the complexes upon being protonated and the lipophilic TPE-reduced endosomal membrane stability, which enhanced endosomal escape of pDNA payload, finally resulting in an excellent gene transfection. On the other hand, less positive surface charge of PDTB NPs than that of the binary PD complexes, as well as the addition of biocompatible BSA, both factors contribute to the improved cell viability. Moreover, the AIE feature of TPE compared to aggregation-caused quenching character of conventional fluorophores enables the complex with stably tracking the delivery of pDNA into cancer cells. Therefore, the newly developed PDTB complexes may be a promising candidate vector for traceable, safe, and effective gene delivery.

Microsphere-based interferometric optical probe

Fluorescent optical probes have rapidly transformed our understanding of complex biological systems by providing specific information on biological targets in the natural living state. However, their utility is often limited by insufficient brightness, photostability, and multiplexing capacity. Here, we report a conceptually new optical probe, termed ‘reflectophore’, which is based on the spectral interference from a dielectric microsphere. Reflectophores are orders-of-magnitudes brighter than conventional fluorophores and are free from photobleaching, enabling practically unlimited readout at high fidelity. They also offer high-degree multiplexing, encoded in their optical size, which can be readily decoded through interferometric detection with nanoscale accuracy, even in turbid biological media. Furthermore, we showcase their biological applications in cellular barcoding and microenvironmental sensing of a target protein and local electric field.

Efficient Triplet-Triplet Annihilation Upconversion in an Electroluminescence Device with a Fluorescent Sensitizer and a Triplet-Diffusion Singlet-Blocking Layer.

Solid-state triplet-triplet annihilation upconversion (TTAUC) blue emission in an electroluminescence device (i.e., an organic light-emitting diode (OLED)) is demonstrated. A conventional green fluorophore, tris-(8-hydroxyquinoline)aluminum (Alq3 ), is employed as the sensitizer that generates 75% triplet under electrical pumping for the blue triplet-triplet annihilation emitter, 9,10-bis(2'-naphthyl) anthracene (ADN), with the heterojunction bilayer structure. The operation lifetime is elongated both for ADN blue (4.1x) and Alq3 green (34.8%) emission due to efficient use of excitons and separation of recombination and emission zone. To reduce the singlet quenching (SQ) of blue TTAUC signal by the Alq3 sensitizer with lower bandgap, 1-(2,5-dimethyl-4-(1-pyrenyl)phenyl)pyrene (DMPPP) is inserted between the Alq3 and ADN as a triplet-diffusion-and-singlet-blocking layer. DMPPP exhibits triplet energy close to Alq3 and higher than ADN, as well as higher singlet energy than both Alq3 and ADN. It allows triplet diffusion from Alq3 to ADN, but blocks the SQ of the blue TTAUC signal by Alq3 . 86.1% intrinsic efficiency of TTAUC is demonstrated in this trilayer (Alq3 /DMPPP/ADN) OLED.

Gold nanocluster fluorescence as an indicator for optical enzymatic nanobiosensors: choline and acetylcholine determination

Gold nanoclusters (AuNCs) have been covalently linked to a FAD-dependent enzyme, choline oxidase (AuNCs@ChOx), with the objective of using the AuNCs fluorescence at 700 nm for monitoring the enzymatic reaction. The linking methodology has been optimized to obtain oriented binding and as a result the structure of the enzyme changes leading to an enhancement of the intrinsic FAD fluorescence of the enzyme (at 525 nm). During the enzymatic reaction with choline, the AuNCs@ChOx fluorescence intensity at both wavelengths (700 nm and 525 nm) changes proportionally to the choline concentration and can be simultaneously monitored. The mechanism of the analytical signal has been studied and a combination of FRET and O2 quenching was found to be responsible for the changes. A mathematical equation is proposed for modelling the signal. The combination of AuNCs@ChOx with acetylcholinesterase permitted the determination of acetylcholine in a concentration range from 1·10−6 to 1·10-5 M and RSD = 4%. This new approach can potentially be applied to any other flavo-enzyme in order to both increase their FAD fluorescence properties and to move the fluorescence measurement to the NIR region. The biosensor is reversible and avoids the use of conventional fluorophores, which are prone to chemical degradation and present worse biocompatibility.

High Photostability in Nonconventional Coumarins with Far-Red/NIR Emission through Azetidinyl Substitution

Replacement of electron-donating N,N-dialkyl groups with three- or four-membered cyclic amines (e.g., aziridine and azetidine, respectively) has been described as a promising approach to improve some of the drawbacks of conventional fluorophores, including low fluorescent quantum yields (ΦF) in polar solvents. In this work, we have explored the influence of azetidinyl substitution on nonconventional coumarin-based COUPY dyes. Two azetidine-containing scaffolds were first synthesized in four linear synthetic steps and easily transformed into far-red/NIR-emitting fluorophores through N-alkylation of the pyridine moiety. Azetidine introduction in COUPY dyes resulted in enlarged Stokes' shifts with respect to the N,N-dialkylamino-containing parent dyes, but the ΦF were not significantly modified in aqueous media, which is in contrast with previously reported observations in other fluorophores. However, azetidinyl substitution led to an unprecedented improvement in the photostability of COUPY dyes, and high cell permeability was retained since the fluorophores accumulated selectively in mitochondria and nucleoli of HeLa cells. Overall, our results provide valuable insights for the design and optimization of novel fluorophores operating in the far-red/NIR region, since we have demonstrated that three important parameters (Stokes' shifts, ΦF, and photostability) cannot be always simultaneously addressed by simply replacing a N,N-dialkylamino group with azetidine, at least in nonconventional coumarin-based fluorophores.

Imaging tissues and cells beyond the diffraction limit with structured illumination microscopy and Bayesian image reconstruction

BackgroundStructured illumination microscopy (SIM) is a family of methods in optical fluorescence microscopy that can achieve both optical sectioning and super-resolution effects. SIM is a valuable method for high-resolution imaging of fixed cells or tissues labeled with conventional fluorophores, as well as for imaging the dynamics of live cells expressing fluorescent protein constructs. In SIM, one acquires a set of images with shifting illumination patterns. This set of images is subsequently treated with image analysis algorithms to produce an image with reduced out-of-focus light (optical sectioning) and/or with improved resolution (super-resolution).FindingsFive complete, freely available SIM datasets are presented including raw and analyzed data. We report methods for image acquisition and analysis using open-source software along with examples of the resulting images when processed with different methods. We processed the data using established optical sectioning SIM and super-resolution SIM methods and with newer Bayesian restoration approaches that we are developing.ConclusionsVarious methods for SIM data acquisition and processing are actively being developed, but complete raw data from SIM experiments are not typically published. Publically available, high-quality raw data with examples of processed results will aid researchers when developing new methods in SIM. Biologists will also find interest in the high-resolution images of animal tissues and cells we acquired. All of the data were processed with SIMToolbox, an open-source and freely available software solution for SIM.

Core-Shell Structures of Upconversion Nanocrystals Coated with Silica for Near Infrared Light Enabled Optical Imaging of Cancer Cells.

Optical imaging of cancer cells using near infrared (NIR) light is currently an active area of research, as this spectral region directly corresponds to the therapeutic window of biological tissues. Upconversion nanocrystals are photostable alternatives to conventional fluorophores. In our work, we have prepared upconversion nanocrystals of NaYF4:Yb/Er and encapsulated them in silica to form core-shell structures. The as-prepared core-shell nanostructures have been characterized for their structure, morphology, and optical properties using X-ray diffraction, transmission electron microscopy coupled with elemental mapping, and upconversion luminescence spectroscopy, respectively. The cytotoxicity examined using cell viability assay indicated a low level of toxicity of these core-shell nanostructures. Finally, these core-shell nanostructures have been utilized as photostable probes for NIR light enabled optical imaging of human breast cancer cells. This work paves the way for the development of advanced photostable, biocompatible, low-toxic core-shell nanostructures for potential optical imaging of biological cells and tissues.

Abstract 4113: A multimodal (PET/NIRF) smart probe for selectively identifying, grading, and visualizing astrocytic gliomas

Abstract Astrocytic gliomas are the most common glioma subtype and constitute the majority of all primary brain tumor types. The malignancy of an astrocytic glioma is classified into one of four grades (I-IV) based on its infiltrative and proliferative characteristics, wherein the extent of this diffuse tissue and depth of embedment into normal brain tissue correlates to the degree of difficulty in accurately identifying and directly visualizing the requisite tumor tissue for achieving its complete resection. To date, no single- or multimodal imaging agent can noninvasively identify intracranial gliomas or accurately distinguish its grade as well as facilitate the direct visualization of its diffuse and deeply-embedded tissue in real-time. The standard imaging modalities for lesion detection (MRI and CT) provide anatomical information which have limited application in the pre- and post-surgical setting for identifying and grading tumor types as well as in monitoring for early-stage and recurrent growth, thereby creating a critical gap in evaluating invasive brain tumors that these techniques cannot successfully fill. Positron emission tomography (PET) is the ideal imaging modality that could fill this gap due to its ability to report on biological processes with superior sensitivity. However, conventional PET probes for gliomas operate on ubiquitously-expressed targets which provide insufficient or unreliable contrast levels between tumor and normal brain tissue or amongst low-grade gliomas. The standard of care for treating brain tumors entails unguided surgical resection followed by a tailored radio- and/or chemotherapy regimen that depends on tumor type and grade. As such, the extent of surgical resection largely governs patient survival time. Fluorescence-guided surgery (FGS) improves maximal resection of tumor tissue while preserving eloquent brain tissue. Primarily 5-aminolevulinic acid (5-ALA) is used in the FGS of brain tumors. However, its fluorescent product emits at short wavelengths and operates via nonselective signal accumulation, which affords limited tissue penetration and false-positive demarcations. The advent of near-infrared fluorescence (NIRF)-guided surgery leverages conventional (nontargeted and/or unactivatable) NIR fluorophores for tumor tissue visualization at 10-fold greater penetration depths, but poorly delineate tumor margins due to generating minimal signal accumulation and high background. To these ends, we have worked to develop a PET/NIRF smart probe for noninvasively identifying and grading intracranial astrocytic gliomas as well as affording direct visualization of its diffuse and deeply-embedded tumor tissue upon its application to NIRF-guided surgery. The multimodal smart probe uses a molecular logic gate design strategy to target a select active enzyme that serves as a validated prognostic factor for astrocytic gliomas. Citation Format: Kenneth S. Hettie, Eben L. Rosenthal, Frederick T. Chin. A multimodal (PET/NIRF) smart probe for selectively identifying, grading, and visualizing astrocytic gliomas [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2018; 2018 Apr 14-18; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2018;78(13 Suppl):Abstract nr 4113.

Aggregation-Induced Emission (AIE) Dots: Emerging Theranostic Nanolights.

Theranostic nanolights refer to luminescent nanoparticles possessing both imaging and therapeutic functions. Their shape, size, surface functions, and optical properties can be precisely manipulated through integrated efforts of chemistry, materials, and nanotechnology for customized applications. When localized photons are used to activate both imaging and therapeutic functions such as photodynamic or photothermal therapy, these theranostic nanolights increase treatment efficacy with minimized damage to surrounding healthy tissues, which represents a promising noninvasive nanomedicine as compared to conventional theranostic approaches. As one of the most promising theranostic nanolights, organic dots with aggregation-induced emission (AIE dots) are biocompatible nanoparticles with a dense core of AIE fluorogens (AIEgens) and protective shells, whose sizes are in the range of a few to tens of nanometers. Different from conventional fluorophores that suffer from aggregation-caused quenching (ACQ) due to π-π stacking interaction in the aggregate state, AIEgens emit strongly as nanoaggregates due to the restriction of intramolecular motions. Through precise molecular engineering, AIEgens could also be designed to show efficient photosensitizing or photothermal abilities in the aggregate state. Different from ACQ dyes, AIEgens allow high loading in nanoparticles without compromised performance, which makes them the ideal cores for theranostic nanolights to offer high brightness for imaging and strong photoactivities for theranostic applications. In this Account, we summarize the recent advance of AIE dots and highlight their great potential as theranostic nanolights in biomedical applications. Starting from the design of AIEgens, the fabrication of AIE dots and their bioimaging applications are discussed. The exceptional advantages of superbrightness, high resistance to photobleaching, lack of emission intermittency, and excellent biocompatibility have made them reliable cross platform contrast agents for different imaging techniques such as confocal microscopy, multiphoton fluorescence microscopy, super-resolution nanoscopy, and light-sheet ultramicroscopy, which have been successfully applied for cell tracking, vascular disease diagnosis, and image-guided surgery. The integration of therapeutic functions with customized AIEgens has further empowered AIE dots as an excellent theranostic platform for image-guided phototherapy. Of particular interest is AIE photosensitizer dots, which simultaneously show bright fluorescence and high photosensitization, yielding superior performance to commercial photosensitizer nanoparticles in image-guided therapy. Further development in multiphoton excited photodynamic therapy has offered precise treatment with up to 5 μm resolution at 200 μm depth, while chemiexcited photodynamic therapy has completely eliminated the limitation of penetration depth to realize power-free imaging and therapy. With this Account, we hope to stimulate more collaborative research interests from different fields of chemistry, materials, biology, and medicine to promote translational research of AIE dots as the theranostic nanolights.

Strategies to Overcome the Limitations of AIEgens in Biomedical Applications

AbstractMotivated by the demand for high‐performance tools for biomedical applications, numerous new luminescent nanomaterials with advanced functionalities are synthesized in recent years. Conventional fluorophores generally suffer from the notorious aggregation‐caused quenching effect that deteriorates their practical performance. The recently emerged fluorogens with aggregation‐induced emission (AIE) characteristics (AIEgen) have generated a new avenue for biomedical applications due to their unique optical properties, flexible designability, and multifunctional potential. However, the inherent characteristics of AIEgens, including short wavelength absorption, broad emission, and aggregation‐dependent brightness indirectly limit their practical performance in the biomedical field. Here, the recent development of AIEgens for biomedical applications is summarized and novel strategies to overcome their limitations are proposed. Furthermore, the strategies and guidelines for the rational design of AIEgens, preparation of water‐dispersible AIE nanoparticles, and selection of the excitation/emission methods, which enable AIEgens to be useful in a broader range of biomedical applications, are discussed.

Varied Length Stokes Shift BODIPY-Based Fluorophores for Multicolor Microscopy

Multicolor microscopy tools necessary to localize and visualize the complexity of subcellular systems are limited by current fluorophore technology. While commercial fluorophores cover spectral space from the ultraviolet to the near infrared region and are optimized for conventional bandpass based fluorescence microscopy, they are not ideal for highly multiplexed fluorescence microscopy as they tend to have short Stokes shifts, restricting the number of fluorophores that can be detected in a single sample to four to five. Herein, we synthesized a library of 95 novel boron-dipyrromethene (BODIPY)-based fluorophores and screened their photophysical, optical and spectral properties for their utility in multicolor microscopy. A subset of our BODIPY-based fluorophores yielded varied length Stokes shifts probes, which were used to create a five-color image using a single excitation with confocal laser scanning microscopy for the first time. Combining these novel fluorophores with conventional fluorophores could facilitate imaging in up to nine to ten colors using linear unmixing based microscopy approaches.

Tricarbocyanine N-triazoles: the scaffold-of-choice for long-term near-infrared imaging of immune cells in vivo.

Herein tricarbocyanine N-triazoles are first described as a rationally-designed near-infrared (NIR) structure overcoming the brightness and photostability limitations of tricarbocyanines for long-term in vivo imaging. The straightforward synthetic approach and the wide availability of alkynes makes this strategy a versatile methodology for the preparation of highly stable N-substituted tricarbocyanines. Furthermore, we validated CIR38M as a non-transferable marker to monitor the fate of therapeutic T cells non-invasively in vivo, showing enhanced performance over conventional NIR fluorophores (i.e. DiR, IR800CW and indocyanine green) as well as compatibility with human cells for translational studies. CIR38M is able to track over time smaller numbers of T cells than current NIR agents, and to visualise antigen-driven accumulation of immune cells at specific sites in vivo. This chemical technology will improve longitudinal imaging studies to assess the efficacy of cell-based immunotherapies in preclinical models and in human samples.

Colloidal carbon dots based highly stable luminescent solar concentrators

Luminescent solar concentrators (LSCs) can serve as large-area sunlight collectors for photovoltaic (PV) cells, reducing the cost of PV generated power. Typical LSCs consist of optical waveguides doped with highly emissive fluorophores e.g. quantum dots (QDs) or dyes/polymers which are required to exhibit high optical efficiency and long-term stability. Compared to conventional fluorophores, carbon dots (C-dots) have superior advantages of non-toxicity, environmental friendliness, low-cost and simple preparation using abundant carbon based feedstock. Here, we demonstrate large-area LSCs (up to 100cm2) using colloidal C-dots. Two types of LSCs were fabricated by either incorporating oil-soluble oleylamine-treated C-dots into photo-polymerized poly(lauryl methacrylate) (PLMA) or spin-coating the water-soluble C-dots/polyvinylpyrrolidone (PVP) mixture on the glass substrate. LSCs based on C-dots/PLMA exhibit a quantum efficiency of 4% (geometric (G) factor of 38) and an optical efficiency of 1.1% (100cm2, G factor of 12.5) of tandem thin-film LSCs based on C-dots/PVP was achieved under one sun illumination. This performance is comparable to those of LSCs based on inorganic QDs with similar G factor. The LSCs based on C-dots are highly air-stable without any noticeable variation in photoluminescence under ultraviolet illumination (1.3W/cm2) for over 12h.

Fluorescence brightness and photostability of individual copper (I) oxide nanocubes

Conventional organic fluorophores lose their ability to fluoresce after repeated exposure to excitation light due to photobleaching. Therefore, research into emerging bright and photostable nanomaterials has become of great interest for a range of applications such as bio-imaging and tracking. Among these emerging fluorophores, metal oxide-based nanomaterials have attracted significant attention as a potential multifunctional material with photocatalytic and angeogenisis abilities in addition to fluorescnce applications. However, most of these applications are highly dependent on size, morphology, and chemo-physical properties of individual particles. In this manuscript, we present a method to study the intrinsic optical characteristics of individual copper (I) oxide (Cu2O) nanocubes. When excited at 520 nm using only 11 µW excitation power (1.7 W/cm2), individual nanocubes were observed to emit light with peak wavelengths ~760 nm which is conveniently within the near-infrared 1 (NIR1) biological window where tissue autofluorescence is minimal. Bright and photostable fluorescence was observed with intensities up to 487 K counts/s under constant illumination for at least 2 minutes with a brightness approximately four times higher than the autofluorescence from a fixed cumulus-oocyte complex. With near-IR emission, high fluorescence brightness, and outstanding photostability, Cu2O nanocubes are attractive candidates for long-term fluorescent bioimaging applications.

Tuning Enhancement Efficiency of Multiple Emissive Centers in Graphene Quantum Dots by Core-Shell Plasmonic Nanoparticles.

Graphene quantum dots (GQDs) are emerging luminescent nanomaterials for energy, bioimaging, and optoelectronic applications. However, unlike conventional fluorophores, GQDs contain multiple emissive centers that result in a complex interaction with external electromagnetic fields. Here we utilize core-shell plasmonic nanoparticles to simultaneously enhance and modulate the photoluminescence (PL) intensities and spectral profiles of GQDs. By analyzing the spectral profiles, we show that the emissive centers are highly influenced by the proximity to the metal particles. Under optimal spacer thickness of 25 nm, the overall PL displays a four-fold enhancement compared with a pristine GQD. However, detailed lifetime measurements indicate the presence of midgap states that act as the bottleneck for further enhancement. Our results offer new perspectives for fundamental understanding and new design of functional luminescent materials (e.g., GQDs, graphene oxide, carbon dots) for imaging, sensing, and light harvesting.

Polyelectrolyte induced controlled assemblies for the backbone of robust and brilliant Raman tags.

Near-field and far-field optical properties of plasmonic materials can be tailored by coupling the existing structures. However, fabricating 3D coupled structures in the solution by molecular linkers may suffer from low yield, low stability (particle aggregates), long reaction time, complex surface modification or multiple purification steps. In this report, stable 3D plasmonic core-satellite assemblies (CSA) with a ~1 nm interior gap accompanied by high field enhancement (|E/Einc|>200) are formed in a few seconds through a single polyelectrolyte linker layer. In addition, by covalently binding different reporter molecules and core particles, three distinct RamSSan tags based on this CSA backbone are demonstrated and compared with conventional fluorophores in terms of stability. This general assembly method can be applied to any type of colloidal particles carrying stable surface charge, even non-plasmonic nanoparticles. It will facilitate the development of various robust Raman tags for multiplexed biomedical imaging/sensing by efficiently combining constituent particles of differing size/shape/composition. The CSA backbone with an embedded high field not only makes the brightness of Raman tags more comparable to the fluorophores and can also be utilized in the platform of molecule-light quantum strong coupling.

Fluorescent Sensors Based on Aggregation-Induced Emission: Recent Advances and Perspectives.

Fluorescent sensors with advantages of excellent sensitivity, rapid response, and easy operation are emerging as powerful tools in environmental monitoring, biological research, and disease diagnosis. However, conventional fluorophores featured with π-planar structures usually suffer from serious self-quenching in the aggregated state, poor photostability, and small Stokes' shift. In contrast to conventional aggregation-caused quenching (ACQ) fluorophores, the newly emerged aggregation-induced emission fluorogens (AIEgens) are featured with high emission efficiency in the aggregated state, which provide unique opportunities for various sensing applications with advantages of high signal-to-noise ratio, strong photostability, and large Stokes' shift. In this review, we will first briefly give an introduction of the AIE concept and the turn-on sensing principles. Then, we will discuss the recent examples of AIE sensors according to types of analytes. Finally, we will give a perspective on the future developments of AIE sensors. We hope this review will inspire more endeavors to devote to this emerging world.

Azo-Based Fluorogenic Probes for Biosensing and Bioimaging: Recent Advances and Upcoming Challenges.

The use of nonfluorescent azo dyes as dark quenchers in activatable optical bioprobes based on the Förster resonance energy transfer (FRET) mechanism and designed to target a wide range of enzymes has been established for over two decades. The key value of the azo moiety (-N=N-) to act as an efficient "ON-OFF" switch of fluorescence once introduced within the core structure of conventional organic-based fluorophores (mainly fluorescent aniline derivatives) has recently been exploited in the development of alternative reaction-based small-molecule probes based on the "profluorescence" concept. These unprecedented "azobenzene-caged" fluorophores are valuable tools for the detection of a wide range of reactive (bio)analytes. This review highlights the most recent and relevant advances made in the design and biosensing/bioimaging applications of azo-based fluorogenic probes. Emphasis is also placed on relevant achievements in the synthesis of bioconjugatable/biocompatible azo dyes used as starting building blocks in the rational and rapid construction of these fluorescent chemodosimeters. Finally, a brief glimpse of possible future biomedical applications (theranostics) of these "smart" azobenzene-based molecular systems is presented.

Luminescent Probes for Sensitive Detection of pH Changes in Live Cells through Two Near-Infrared Luminescence Channels.

Two water-soluble near-infrared luminescent probes, which possess both conventional intense Stokes fluorescence and unique single-photon frequency upconversion luminescence (FUCL), were developed for sensitive and selective detection of pH changes in live cells. The water solubility and biocompatibility of these probes were achieved by introducing mannose residues through 2,2'-(ethylenedioxy)diethylamine tethered spacers to a near-infrared conventional fluorescence (CF) and FUCL organic fluorophore. At a pH higher than 7.4, the probes have ring-closed spirocyclic lactam structures, thus are colorless and nonfluorescent. Nevertheless, they sensitively respond to acidic pH values, with a drastic structural change to ring-opened spirocyclic lactam forms, which cause significant absorbance increases at 714 nm. Correspondingly, their near-infrared CF and FUCL intensities at 740 nm are also significantly enhanced when excited by 690 and 808 nm, respectively. The probes hold a variety of advantages such as high sensitivity, excellent reversibility and selectivity to pH over metal ions, low cellular autofluorescence background interference, good cell membrane permeability and photostability, as well as low cytotoxicity. Our results have successfully proven that these probes can visualize intracellular lysosomal pH changes in live cells by monitoring both near-infrared CF and FUCL changes.

Aggregation-induced emission probes for cancer theranostics

Conventional cancer therapy usually suffers from poor treatment efficiency and adverse effects. To improve the treatment efficiency, it is critical to precisely diagnose specific cancer types and monitor the therapy process in situ. Fluorescence imaging has the advantages of high sensitivity and easy operation, but conventional fluorophores suffer from aggregation-caused quenching (ACQ), and therefore, their applications for imaging or diagnosis are severely impeded. By contrast, aggregation-induced emission (AIE) probes have significant advantages in terms of excellent photostability and a lack of self-quenching, and can be conveniently incorporated into theranostic platforms by combining them with various therapeutic modalities. Here, we discuss and summarize the recent advances in the development of AIE probes for cancer theranostics.