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Abstract Photoactive agents based on natural products have attracted substantial attention in clinical applications because of their distinct biological activity, molecular structure multiformity, and low biotoxicity. Herein, we initially modify hypocrellin B (HB) with 1,2-diamino-2-methyl propane to form near-infrared (NIR) light (>700 nm)-responsive amino-substituted HB derivative (DPAHB). The DPAHB exhibit broad absorption (400–800 nm), NIR emission (maximum emission peak at 710 nm), and high singlet oxygen (1O 2) quantum yield (∼0.33) under NIR light (721 nm) irradiation. After self-assembly by using DPAHB with PEG-PLGA, the as-prepared nanovesicles (DPAHB NVs) retain efficient 1O 2 generation, more interestingly, show high photothermal conversion efficiency (∼0.24) under NIR light (721 nm) irradiation for synergistic photodynamic therapy (PDT) and photothermal therapy toward hypoxic tumor. The DPAHB NVs can not only be as a fluorescence/photoacoustic imaging agent but also exhibit an even stronger PDT efficiency than that of chlorin e6 (a widely used classic photosensitizer). In vitro and in vivo studies demonstrate that DPAHB NVs possess high photothermal stability, enhanced tumor accumulation, and suitable biodegradation rate, thus, show a highly promising clinical potential as a new photoactive agent for cancer therapy. [ABSTRACT FROM AUTHOR]

A novel phototheranostic platform based on tri -malonate derivative of fullerene C 70 (TFC 70 )/photosensitizer (Chlorin e6, Ce6) nanovesicles (FCNVs) has been developed for effective tumor imaging and treatment. The FCNVs were prepared from amphiphilic TFC 70 -oligo ethylene glycol -Ce6 molecules. The developed FCNVs possessed the following advantages: (i) high loading efficiency of Ce6 (up to ∼57 wt%); (ii) efficient absorption in near-infrared light region; (iii) enhanced cellular uptake efficiency of Ce6 in vitro and in vivo ; (iv) good biocompatibility and total clearance out from the body. These unique properties suggest that the as-prepared FCNVs could be applied as an ideal theranostic agent for simultaneous imaging and photodynamic therapy of tumor. This finding may provide a good solution to highly efficient phototheranostic applications based on fullerene derivatives fabricated nanostructures. [ABSTRACT FROM AUTHOR]

Organic molecules that are active in the near-infrared (NIR) bio-window for photo-to-heat energy-converting theranostics have attracted much attention in cancer therapy. However, current organic NIR-absorbing molecules are still suffering from the inefficient non-radiative decay or serious photobleaching under light irradiation. Herein, we design a convenient strategy to load a new kind of NIR-absorbing nonlinear optical (NLO) chromophore FTC-3f with the biocompatible polymer, methoxy poly(ethylene glycol)-poly(lactideco-glycolide) (mPEG-PLGA). The resulted FTC-3f/PLGA nanoparticles showed excellent stability, high photothermal conversion efficiency (∼51.11%) and good photoacoustic performance. Moreover, in vitro anticancer experiments demonstrated that the FTC-3f/PLGA nanoparticles possess a high PTT (photothermal therapy) efficiency under NIR laser irradiation. This work thus provides an insight into the exploration of versatile organic NIR-absorbing nanoparticles toward future practical PTT application. [Display omitted] • A new kind of FTC-3f chromophores were synthesized with a strong absorption in the spectral region of 600–1100 nm. • FTC-3f/PLGA nanoparticles possess high stability when dispersed in water, PBS solution and DMEM solution. • FTC-3f/PLGA shows a high photothermal conversion efficiency and excellent photoacoustic/photostability performance. • In vitro antitumor result revealed a high photothermal therapy efficiency under 750 nm NIR light irradiation. [ABSTRACT FROM AUTHOR]

Graphical abstract Highlights • Multifunctional liposomes with tumor targeted drug delivery and imaging. • Enhanced photoluminescence emission of carbon dots. • Enhanced anti-cancer efficacy of cinobufagin after loading into liposomes. Abstract Integrating the optical properties of near-infrared fluorescent carbon dots into liposomes may construct a multifunctional nano-system with the potential as a drug carrier, tracer and efficacy intensifier of the anticancer agent. In this study, the liposomes loaded with hydrophilic near-infrared carbon dots as a nano-carrier and tracer of lipophilic anticancer agent cinobufagin were developed. Prepared liposomes were characterized by particle size, morphology and entrapment efficiency. The drug release behavior, the tracer function, the anticancer effect and the side effect were investigated in vitro and in vivo. It was observed that the photoluminescence emission of carbon dots could be strongly enhanced up to 5 times by nano-liposomes. Due to this property, the bio-imaging of CDs + CB liposomes in vitro and in vivo could be clearly obtained. Our results also showed that the CDs + CB liposomes could be uptaken by cells (the lysosomes targeted) and delivered to the tumor site, and undoubtedly, the CDs + CB liposomes demonstrated sustained drug release, enhanced anticancer efficacy and low side effects in vivo. With the assistance of imaging function of CDs, the CDs + CB liposomes can easily display the distribution of drugs, which is very helpful for drug development and may open a novel avenue for drug delivery. [ABSTRACT FROM AUTHOR]

The distance-dependent based sensing mechanism, such as fluorescence resonance energy transfer (FRET) and surface plasmon resonance (SPR) absorption of gold nanoparticles, has been used widely in visual detection. In this work, we report another distance-dependent detection method for nucleoside triphosphates (NTPs) based on carbon dots (CDs) ( 1 O 2 donor) and 9, 10-diphenylanthracene-2-boronic acid (DABA, 1 O 2 acceptor). The CDs can generate singlet oxygen ( 1 O 2 ) which allows diffusion within 200 nm. Thus, the distance between CDs and DABA decreased through binding of NTPs (<200 nm), leading to absorption changes of DABA under light irradiation due to 1 O 2 trapping. This sensing system (CDs@DABA) has high selectivity for the detection of NTPs due to the double molecular recognition and a linear response in the 0–80 μM concentration range was accomplished with the detection limit as low as 4.35 μM. [ABSTRACT FROM AUTHOR]

On base of the good optical properties of coumarin and fluorescein, we designed and synthesized two coumarin/fluorescein-fused fluorescent dyes ( CF dyes), which enlarged the emission wavelength and increased the Stokes shift of fluorescein moiety. The corresponding optical properties of CF dyes were investigated in detail. CF dyes could easily introduce other groups to design different functional molecules. CF dyes also exhibited rapid and sensitive responses to pH values in the range of 4.0–7.4 through the characterization of absorption and fluorescence spectra in buffer solution. More importantly, CF ethyl ester dye ( CFE dye) not only showed good cell membrane permeability and low cytotoxicity, but also had the ability to rapidly monitor mitochondrial pH changes in living cells. [ABSTRACT FROM AUTHOR]

A new water-soluble fluorescent probe 1 based on hemicyanine dye is designed for selective detection of glutathione (GSH). Probe 1 shows a tremendous colorimetric and ratiometric fluorescence response toward GSH with high selectivity over cysteine/homocysteine. After nucleophilic aromatic substitution reaction with GSH, probe 1 undergoes an intramolecular aldimine condensation that leads to forming a ring, which is accompanied by 107 and 41 nm red-shifts in the absorption and fluorescence spectra, respectively. Subsequent experiments in living cells indicate that probe 1 has a good photostability and response to mitochondrial GSH level in a ratiometric manner. [ABSTRACT FROM AUTHOR]

A novel fluorescent probe O-hNRSel based on tetralin-xanthene fused dye O-hNR was designed and synthesized by introducing 2,4-dinitrobenzenesulfonate functionality. This probe is able to detect selenocysteine (Sec) with rapid response time (2 min) and a large fluorescence enhancement at 624 nm (124-fold). O-hNRSel exhibited selective response to Sec over many other analy and high sensitivity with the detection limit as low as 17 nM. Furthermore, O-hNRSel has been used for fluorescent imaging of Sec in living cells with good biocompatibility. [ABSTRACT FROM AUTHOR]

The highly sensitive and rapid detection and distinction of gram-negative bacteria are essential for the early diagnosis and accurate medical treatment of bacterial infection. In this work, we investigated a new selective and sensitive method of detecting gram-negative bacteria based on a small molecule modified sensor chip by a laser scanning confocal imaging-surface plasmon resonance (LSCI-SPR) system. The small molecule (polymyxin B) strongly interacted with bacteria cell membrane. SPR signals changed with SYTO 9 stained bacteria concentrations, and fluorescence images were recorded at the same time. Results showed that Escherichia coli were distinguished clearly with a limit of detection (LOD) of 1.0 × 10 2 CFU/mL for Escherichia coli . Moreover, a good linear relationship was observed between bacteria concentrations and SPR signals from 1.0 × 10 2 CFU/mL to 1.0 × 10 6 CFU/mL with a linear coefficient R 2 of 0.99146. All these results indicated that this small-molecule modified sensor can be used for quantitative detection of known gram-negative bacteria and qualitative distinction of unknown gram-negative bacteria within 10 min each sample in real-time. [ABSTRACT FROM AUTHOR]

Carbon dots (CDs) have emerged as promising nanomaterials for bioimaging-guided photodynamic therapy (PDT). However, designing red-emissive CDs (RCDs) with tunable type I and type II reactive oxygen species (ROS) generation to simultaneously meet PDT applications in aerobic and hypoxic scenarios still remain major challenges. Herein, three types of RCDs with maximum emission at approximately 680 nm are successfully prepared. It is noteworthy that they exhibit the adjustable ROS production with equal superoxide anion (via type I PDT) and incremental singlet oxygen (via type II PDT). Detailed structural and optical characterizations along with theoretical calculation reveal that the unique type I/II ROS formation mainly depends on the core sizes and surface states of RCDs, which determine their identical redox potentials and tapering energy gaps between singlet- and triplet states, respectively. Additionally, due to the inherent mitochondria targeting capability, RCDs enable themselves to induce cell programmed death via activating mitochondrion-mediated apoptotic pathways. This work exploits the unprecedented RCDs with tunable type I and type II ROS generation that could ensure highly efficient tumor eradication both in vitro and in vivo, even under the harsh tumor microenvironment, providing a new prospect for CDs as nanophotosensitizers to conquer the limitations of single type PDT. Red emissive carbon dots with tunable reactive oxygen species generation are prepared to achieve highly efficient fluorescence imaging-guided type I/II photodynamic therapy via activating mitochondrion-mediated apoptotic pathways of cancer cells, providing a new prospect for carbon dots as nanophotosensitizers to conquer the limitations of single type PDT. [Display omitted] [ABSTRACT FROM AUTHOR]

A simple and general procedure is designed for in situ growth of gold nanoparticles (AuNPs) on hydrogen-bond supramolecular structures. The resulting nanocomposites are obtained via a one-pot synthetic method using chloroauric acid (HAuCl 4 ), sodium citrate, melamine (M) and cyanuric acid (CA) as precursors. At room temperature, melamine cyanurate (MCA) is formed immediately by M and CA through hydrogen bond self-assembly, possesses rich nitrogen content (49.4 wt%), and provides evenly dispersed and active sites to anchor and stabilize gold nanoparticles (AuNPs) as an ideal scaffold. The nanocomposites (AuNPs/MCA) exhibit high peroxidase-like activity that can catalyze the oxidation-reduction reaction of H 2 O 2 and peroxidase substrates over a broad pH range, including nearly neutral conditions (pH 5.0–7.4), as well as excellent stability. Combined with glucose oxidase (GO x ), AuNPs/MCA are successfully used for the quantitative determination of blood glucose via one-pot colorimetric assay. This study develops an economic approach for preparation of peroxidase mimetics with high catalytic activity at neutral pH, and well stability, expected to provide guidelines for other types of inorganic/supramolecule nanocomposites, and to broaden their applications in analytical chemistry and environmental science. [ABSTRACT FROM AUTHOR]

A fluorescent probe ( 1 ) for distinguishing amongst biothiols, including cysteine (Cys), homocysteine (Hcy) and glutathione (GSH), is developed based on different cascade reactions. The key design feature of fluorescent probe 1 is the integration of two potential reaction groups for the thiol and amino groups of biothiols in one molecule. By reacting with the halogen atom and α, β-unsaturated malonitrile in probe 1 , Cys, Hcy and GSH can generate a total of three main products with distinct photophysical properties. Probe 1 shows a strong fluorescence turn-on response to Cys with blue–green emission by using an excitation wavelength of 390 nm. At an excitation wavelength of 500 nm, probe 1 responds to GSH over Cys and Hcy and emits strong orange fluorescence. The discrimination of biothiols can be demonstrated by cell imaging experiments, indicating that probe 1 can be a useful tool for the selective imaging of Cys and GSH in living cells. [ABSTRACT FROM AUTHOR]

More and more attention has been paid to the design of new fluorescent imaging agents with good photostability and water solubility, especially those with emissions in the deep-red and near-infrared regions. In this work, we designed and synthesized four novel fluorescent dyes with deep-red or NIR fluorescence by hybridizing coumarin and pyronin moieties based on our previous work. Introduction of carboxylic acid in the dyes not only imparted the dyes with water solubility but also provided a versatile sensing platform for designing the fluorescent probes and sensors of biomolecules. The photophysical properties of these new dyes were investigated through absorption and fluorescence spectroscopy. Cell imaging experiments showed that esterification products could selectively stain lysosomes with good photostability, thereby indicating that they could be useful in the development of fluorescent probes for bioimaging. [ABSTRACT FROM AUTHOR]

Nanozymes are artificial enzymes that mimic natural enzyme-like activities and show great promise for tumor catalytic therapy. However, new nanozymes with multiple catalytic activities for multifunctional nanotheranostic use remain challenging to design. Herein, for the first time, iron phthalocyanine (Fe(II)Pc) was assembled with poly(l -lactide-co-glycolide)-block-poly(ethylene glycol) to prepare an Fe(II)Pc assembly (denoted as Fe(II)Pc-A). The obtained Fe(II)Pc-A could be applied as a smart near-infrared (NIR) light-responsive nanotheranostic for simultaneous photoacoustic imaging-guided photothermal therapy. Notably, Fe(II)Pc-A possessed peroxidase, catalase, and oxidase mimicking activities, which could not only catalyze the conversion of intratumoral H 2 O 2 to •OH, but also degrade H 2 O 2 to generate O 2 and continuously catalyze the conversion of O 2 to cytotoxic O 2 •-. Impressively, the dual reactive oxygen species (ROS) generation of Fe(II)Pc-A was further remarkably enhanced by the endogenous acidity of the tumor microenvironment and the exogenous NIR light-responsive photothermal effect. Moreover, the O 2 self-supplying ability of Fe(II)Pc-A led to increased generation of O 2 •- for enhancing catalytic therapy in hypoxic tumor. These collective properties of Fe(II)Pc-A nanozyme enabled it to be a dual ROS generation accelerator for photothermally enhanced tumor catalytic therapy. Thus, a new type of high-performance nanozyme for multifunctional nanotheranostic use toward cancer was presented. Fe(II)Pc-derived nanozyme with three enzyme-mimicking activities as dual reactive oxygen species generation accelerator for photothermally enhanced tumor catalytic therapy was designed and prepared, thereby providing a new type of high-performance nanozyme for multifunctional nanotheranostic use toward cancer. [Display omitted] [ABSTRACT FROM AUTHOR]

Two asymmetrical benzoxanthene dyes (BP-1 and BP-2) were designed and synthesized by a convenient one-step procedure from naphthaldehyde and m -aminophenol precursors. These dyes showed long-wavelength absorption, near-infrared emission (>650 nm), and large Stokes shifts (>90 nm) because of the asymmetrical introduction of the benzene ring into the xanthene structure. BP-1 exhibited high fluorescence quantum yield in organic solvents, whereas BP-2 showed very weak fluorescence due to the photoinduced electron transfer of 9-substituted groups. Cell experiments indicated that BP-1 with crescent-shape structure showed lower cytotoxicity and higher photostability than BP-2 and could rapidly stain RNA in nucleoli at low concentration. [Display omitted] • Two asymmetrical benzoxanthene dyes were synthesized by a convenient one-step procedure. • The dyes showed long-wavelength absorption, near-infrared emission and large Stokes shifts. • BP-1 could stained RNA in nucleoli rapidly with low cytotoxicity and good photostability. • BP-2 showed a very weak fluorescence and cytotoxicity due to 9-substituted groups. [ABSTRACT FROM AUTHOR]

Efficient treatment of primary tumor and preventing cancer metastasis present intriguing alternatives to cancer therapy. Herein, for the first time, we reported the photo-triggered nano-gadofullerene (Gd@C 82 -Ala, abbreviated Gd-Ala) induced malignant tumor vascular disruption by shortening the light interval between Gd-Ala administration and light illumination, where oxygen in blood vessels was employed efficiently to produce cytotoxic reactive oxygen species (ROS). The produced ROS could not only destroy the tumor cells but also devastate the vascular endothelial cells corresponding to the loss of intercellular junctions and vessels disruption. Notably, the irradiated Gd-Ala could enhance dendritic cells (DCs) maturation, which further secreted tumor necrosis factor-α (TNF-α) and interleukin-12 (IL)-12, and then activated T lymphocytes by up-regulation of cluster of differentiation CD4+ and CD8+ T lymphocytes. Furthermore, the down-regulation of matrix metalloprotein 2 (MMP2) and MMP9 also reduce the rate of tumor metastasis. This work explored a new biomedical application of gadofullerene, thereby providing a smart carbon nanomaterial candidate for tumor ablation and inhibition of cancer metastasis. [ABSTRACT FROM AUTHOR]