White Light Irradiation Research Articles

Mitochondria-targeted NO donor enables synergistic NO and photodynamic therapies for effective inhibition of cancer cell proliferation and migration

Previously reported light-controlled nitric oxide donors are usually activated by blue or green light. The insufficient ability of short wavelength light to penetrate tissues and its potential phototoxicity to living organisms greatly restricted in vivo applications. This study presents the development of a novel mitochondria-targeted nitric oxide donor, R–NO, capable of controlled nitric oxide and photosensitizer release under white light irradiation in mitochondria. R–NO is capable of generating nitric oxide and R–NH, a novel photosensitizer that can produce O2•- upon irradiation with a single light source. In addition, the highly toxic ONOO− can be produced by the rapid reaction of nitric oxide and O2•-. Harnessing the synergistic effects of PDT, nitric oxide therapy and highly toxic ONOO−, the proliferation and migration of cancer cells can be significantly inhibited upon light irradiation with R–NO. Futhermore, our MTT experiments demonstrated that simultaneous producing of O2•- and nitric oxide in the same region is crucial for efficient cancer cell inhibition. These interesting findings underscore the enhanced synergistic effect achieved by combining PDT and NO therapy in a single molecule for cancer cell treatment.

Nanocluster-mediated electron–hole separation for efficient CO2 photoreduction

Poor capability of charge-holes separation and slower surface CO2 reaction kinetics hinder photocatalytic performance. Here, SnS2 atomic layer with Pt3Co alloy nanoclusters have been successfully prepared. Nanoclusters could be used as highly catalytic active sites, which not only facilitates the carrier separation and transport kinetics, but enriches electrons lowered the reaction barrier. As expected, the CO evolution rate of the champion SnS2/Pt3Co catalyst was 13.6 times higher than that of the original SnS2 catalyst under white light irradiation. In-situ DRIFTS identifies key intermediate in the photoreduction process. In-situ XPS and DFT calculation further verifies the electron transport direction and charge density distribution at the SnS2/Pt3Co interface. Our work uncovers the role of nanoclusters in carrier separation and transport as well as proton transport, opening new chances for obtaining efficient photoreduction CO2 property.

Cationic Conjugated Oligomers for Efficient and Rapid Antibacterial Photodynamic Therapy via Both Type I and Type II Pathways

Comprehensive SummaryRecently, photodynamic therapy (PDT) has attracted wide attention due to its less susceptibility to drug resistance, broad‐spectrum biocidal activity and biosafety in normal tissues. However, the traditional photosensitizers (PSs) face the disadvantage of poor therapeutic efficacy due to the requirement of an aerobic environment to generate 1O2 through Type ІI pathway. Herein, we designed and synthesized a novel cationic conjugated oligomer oligo(phenylene vinylene) (OPV) and studied its antibacterial photodynamic activity against both Gram‐negative Escherichia coli (E. coli) and Gram‐positive bacteria methicillin‐resistant Staphylococcus aureus (MRSA). Importantly, the OPV can rapidly produce reactive oxygen species (ROS) through double pathways, Type I and II mechanism under white light irradiation, and efficiently kill E. coli and MRSA at a nanomolar level. The dual type photosensitizing capability makes OPV promising for enhanced PDT to treat pathogens and tumors in complex environments.

Impact of green and blue-green light on the growth, pigment concentration, and fatty acid unsaturation in the microalga Monoraphidium braunii.

The spectral composition of light is an important factor for the metabolism of photosynthetic organisms. Several blue light-regulated metabolic processes have already been identified in the industrially relevant microalga Monoraphidium braunii. However, little is known about the spectral impact on this species' growth, fatty acid (FA), and pigment composition. In this study, M. braunii was cultivated under different light spectra (white light: 400-700 nm, blue light: 400-550 nm, green light: 450-600 nm, and red light: 580-700 nm) at 25°C for 96 h. The growth was monitored daily. Additionally, the FA composition, and pigment concentration was analyzed after 96 h. The highest biomass production was observed upon white light and red light irradiation. However, green light also led to comparably high biomass production, fueling the scientific debate about the contribution of weakly absorbed light wavelengths to microalgal biomass production. All light spectra (white, blue, and green) that comprised blue-green light (450-550 nm) led to a higher degree of FA unsaturation and a greater concentration of all identified pigments than red light. These results further contribute to the growing understanding that blue-green light is an essential trigger for maximized pigment concentration and FA unsaturation in green microalgae.

Red/NIR emissive aggregation-induced emission-active photosensitizers with strong donor-acceptor strength for image-guided photodynamic therapy of cancer.

Light-mediated therapies such as photodynamic therapy (PDT) are considered emerging cancer treatment strategies. However, there are still lots of defect with common photosensitizers (PSs), such as short emission wavelength, weak photostability, poor cell permeability, and low PDT efficiency. Therefore, it is very important to develop high-performance PSs. Recently, luminogens with aggregation-induced emission (AIE) characteristics and red/near-infrared (NIR) emissive have been reported as promising PSs for image-guided cancer therapy, due to them being able to prevent autofluorescence in physiological environments, their enhanced fluorescence in the aggregated state, and generation of reactive oxygen species (ROS). Herein, we developed PSs named TBTCPM and MTBTCPM with donor-acceptor (D-A) structures, strong red/NIR, excellent targeting specificities to good cell permeability, and high photostability. Interestingly, both of them can efficiently generate ROS under white light irradiation and possess excellent killing effect on cancer cells. This study, thus, not only demonstrates applications in cell image-guided PDT cancer therapy performances but also provides strategy for construction of AIEgens with long emission wavelengths.

Single-Pixel-Adjustable Structural Color Fabricated Using a Spatially Modulated Femtosecond Laser.

Structural colors provide a highly stable and ecofriendly dyeing mechanism. The ability to adjust structural colors by a single pixel enhances their flexibility and application range. However, achieving single-pixel control and dynamic adjustment of structural colors remain a challenge yet. In this study, we propose a coloring method involving microcurve surfaces fabricated using a spatially modulated femtosecond laser hybrid technology, which combines spatially modulated femtosecond laser-assisted wet etching and molding. The fabricated microcurve surface exhibits bright colors under white light irradiation, and the color of each pixel can be adjusted independently by changing the morphology of the modified region inside fused silica using a femtosecond laser. With the high flexibility of femtosecond laser fabrication, color lightness can be accurately controlled through the quantitative adjustment of the arrangement of microcurve surfaces in an array, and various color patterns can be fabricated through the programmable arrangement of different microcurve surfaces. Additionally, the color exhibits strong dynamic characteristics, that is, different colors correspond to different external forces.

Adjusting inter-semiconductor barrier height via crystal plane engineering: Crystalline face exposed single crystal cadmium sulfide augmentative S-scheme heterojunctions for efficiently photocatalytic hydrogen production

The design of crystalline face engineered photocatalysts can modulate the catalytic activity at the microscopic scale. The exposure ratio of (100), (002) and (101) crystal planes of CdS with visible light activity was adjusted by crystal plane engineering. Density functional theory (DFT) calculations and experiments show that the fully exposed (002) surface CdS-L (Leaf-like CdS) has excellent hydrogen evolution activity. The use of the interface heterojunction strategy can greatly mobilize the electron flow between CdS-L and CoS2 S-scheme heterojunction compound semiconductors by changing the potential barrier difference. The CoS2/CdS-L composite photocatalyst exhibits amazing hydrogen evolution activity under 5 W white light irradiation, and the hydrogen production rate can reach 19.22 mmol·g−1·h−1. The results of in situ radiation XPS tests and comparative experiments show that the catalysts with more exposed crystal planes on the basis of constructing S-scheme heterojunctions can provide more active sites and have stronger reactivity. The use of crystal facet engineering effect and interfacial heterojunction strategy lays the foundation for the structural design and large-scale application of highly active visible light catalysts.

Schottky-junction plasmonic nanocomposite: A non-hazardous excellent visible light photocatalyst for industrial waste management

A bio-compatible nanocomposite “Ag/Ag doped TiO2” with UV–Visible-NIR light gathering quality was synthesized by solvothermal method, followed by green synthesis method. Insertion of Ag+ ions into Ti2+ lattice sites in Ag doped TiO2 alters the n-type TiO2 semiconductor to p-type. Nanostructured doped TiO2 suffers high charge recombination loss in presence of trapped states, resulting 35 % photocatalytic efficiency. Ag decoration on p-type Ag doped TiO2 forms a Schottky barrier at metal-semiconductor junction, which reduces charge recombination loss by separating the photogenerated electron-hole (e-h) in two materials of the nanocomposite. These photogenerated charges create oxide and hydroxide super radicals in the aqueous system of photocatalyst, ensuing 80% degradation of SO dye under 50 min white light illumination. The nanocomposite also demonstrated good performance in degradation of industrial dyes like 50% Mordant Orange (MO) and 15% Direct Blue (DB) under 50 min white light irradiation. DFT analysis of the heterosystems supports absorptivity tuning of experimentally obtained nanocomposite. Moreover, the nanocomposite proved its non-toxicity to human cells, as it reveals <20% cell death with maximum dose (250 µg/ml) of the nanocomposite in cytotoxicity test. Hence, proper designing and synthesizing the nanocomposite explored an eco-friendly solar photocatalyst for industrial waste management.

Photocatalytic synthesis of fluorescent and polarity-sensitive β-thiolated diketones for LDs-specific imaging

Fluorophores with easily tunable photophysical properties are highly desirable for bio-imaging. Herein, we develop a photocatalytic method for direct thiolation of β-diketone compounds with Rose Bengal as the photocatalyst under white light irradiation. The β-thiolated diketone compounds show a polarity-sensitive fluorescence emission and can be used for lipid droplets (LDs)-specific imaging with a high signal-to-noise ratio. We believe this photocatalytic method for direct preparation of fluorescent and polarity-sensitive β-thiolated diketones is promising for bioimaging applications.

Laser-Induced Graphene-based Flexible Substrate with Photothermal Conversion and Photoresponse Performance on Polyimide Film.

Graphene-based flexible electronic devices are widely used in photoelectric components and photodetectors. However, it remains a huge challenge to fabricate graphene-based flexible devices efficiently and economically. Compared with the flexible electronic devices made by combining the flexible film with metal and semiconductor materials, the graphene-based flexible substrate (GFS) can be efficiently and conveniently induced by laser direct writing on the flexible film. In this paper, the GFS with a resistance of as low as 15 Ω was successfully induced by CO2 laser on a polyimide (PI) film in one step, and the GFS surface covered with carbon nanoparticles (GFSC) with a resistance of 25 Ω was further induced by femtosecond (fs) laser reprocessing. Benefiting from the laser-induced porous graphene structure, the absorptivity of GFS is up to 90% in the wavelength range of 200-2000 nm. The formation of carbon nanoparticles on the GFSC surface further improves the absorptivity to 97.5% in a wide spectral range. Under white light irradiation of 1 sun, the surface temperature of GFS reaches 65.7 °C and that of GFSC is up to 70.8 °C within 2 min. Under the irradiation of a light-emitting diode (LED) with a central wavelength of 365 nm, the highest photoresponsivity of GFS and GFSC was 8.8 and 1.3 mA/W, respectively. The response time and recovery time of GFS are 8 and 7.3 s, and those of GFSC are 8.3 and 6.7 s, respectively. Importantly, GFSC has a more stable photoresponse performance due to the better electron capture and transfer capability of carbon nanoparticles. It is believed that GFS and GFSC have great application potential in flexible photodetectors and sensors.

Wet‐Chemical Etching and Delamination of MoAlB into MBene and Its Outstanding Photocatalytic Performance

AbstractMBenes are post‐MXene materials that contain boron in their structure instead of carbon and nitrogen. This unique composition offers an opportunity to explore the role of boron in the performance of 2D materials. However, wet‐chemical etching and delamination of the starting MoAlB phase are challenging due to the persistent bonding of aluminum atoms with their neighboring elements. Herein, it is overcome by processing MoAlB for 24, 48, and 72 h with an aqueous HCl/H2O2 solution. The time‐wise etching and delamination delivers individual single‐to‐few layered 48‐MBene flakes. The theoretical‐to‐experimental XRD analysis revealed the best‐delaminated 48‐MBene having Mo2B2 orthorhombic lattice arrangement. The presence of Mo oxide allows direct 1.2 eV and indirect 0.2 eV optical band gaps and outstanding photocatalytic activity in decomposing methylene blue as a model organic contaminant. The 48‐MBene photocatalyst achieves about 90% of MB decomposition under ultraviolet and simulated white light irradiation with three times faster kinetics outperforming even hybridized MXenes. In addition, 48‐MBene appeared best suited to utilize the full spectrum of visible light into reactive oxygen species. Conversely, 24‐MBene and 72‐MBene shows incomplete delamination or oxidation, hampering their photocatalytic activity. The obtained results open an experimental pathway to apply MBenes in environmental remediation.

Ambient Processed rGO/Ti3CNTx MXene Thin Film with High Oxidation Stability, Photosensitivity, and Self-Cleaning Potential.

Solution-based processing offers advantages for producing thin films due to scalability, low cost, simplicity, and benignity to the environment. Here, we develop conductive and photoactivated self-cleaning reduced graphene oxide (rGO)/Ti3CNTx MXene thin films via spin coating under ambient conditions. The addition of a thin rGO layer on top of Ti3CNTx resulted in up to 45-fold improvement in the environmental stability of the film compared to the bare Ti3CNTx film. The optimized rGO/Ti3CNTx thin film exhibits an optical transmittance of 74% in the visible region of the spectrum and a sheet resistance of 19 kΩ/sq. The rGO/Ti3CNTx films show high rhodamine B discoloration activity upon light irradiation. Under UV irradiation, the electrically conductive MXene in combination with in situ formed semiconducting titanium oxide induces photogenerated charge carriers, which could potentially be used in photocatalysis. On the other hand, due to film transparency, white light irradiation can bleach the adsorbed dye via photolysis. This study opens the door for using MXene thin films as multifunctional coatings with conductive and potentially self-cleaning properties.

Modulating the Luminescence, Photosensitizing Properties, and Mitochondria-Targeting Ability of D-π-A-Structured Dihydrodibenzo[a,c]phenazines.

Herein, pyridinium and 4-vinylpyridinium groups are introduced into the VIE-active N,N'-disubstituted-dihydrodibenzo[a,c]phenazines (DPAC) framework to afford a series of D-π-A-structured dihydrodibenzo[a,c]phenazines in consideration of the aggregation-benefited performance of the DPAC module and the potential mitochondria-targeting capability of the resultant pyridinium-decorated DPACs (DPAC-PyPF6 and DPAC-D-PyPF6). To modulate the properties and elucidate the structure-property relationship, the corresponding pyridinyl/4-vinylpyridinyl-substituted DPACs, i.e., DPAC-Py and DPAC-D-Py, are designed and studied as controls. It is found that the strong intramolecular charge transfer (ICT) effect enables the effective separation of the highest occupied molecular orbital (HOMO) and the lowest unoccupied molecular orbital (LUMO) of DPAC-PyPF6 and DPAC-D-PyPF6, which is conducive to the generation of ROS. By adjusting the electron-accepting group and the π-bridge, the excitation, absorption, luminescence, photosensitizing properties as well as the mitochondria-targeting ability can be finely tuned. Both DPAC-PyPF6 and DPAC-D-PyPF6 display large Stokes shifts (70-222 nm), solvent-dependent absorptions and emissions, aggregation-induced emission (AIE), red fluorescence in the aggregated state (λem = 600-650 nm), aggregation-promoted photosensitizing ability with the relative singlet-oxygen quantum yields higher than 1.10, and a mitochondria-targeting ability with the Pearson coefficients larger than 0.85. DPAC-D-PyPF6 shows absorption maximum at a longer wavelength, slightly redder fluorescence and better photosensitivity as compared to DPAC-PyPF6, which consequently leads to the higher photocytotoxicity under the irradiation of white light as a result of the larger π-conjugation.

Photodynamic inactivation of a RNA-virus model using water-soluble β-octa-Substituted pyridinium-pyrazolyl phthalocyanines

Among the various groups of microorganisms, viruses have generally a greater capacity for mutation, especially RNA viruses, as was demonstrated by SARS-CoV2 virus mutations. This high mutation rate promotes the development of their resistance to traditional antivirals and establishes the resistance behaviour in virus populations, decreasing their susceptibility to these drugs. In this context, the photodynamic treatment appears as a potentially effective method against microorganisms and, considering its mode of action is not likely to lead to the development of resistance. In this work, two newly zinc(II) phthalocyanines (ZnPcs) bearing pyridinium-pyrazolyl groups (2a and 3a) were synthesized, characterized, and applied in photodynamic inactivation (PDI) of bacteriophage Φ6 (or Phage Phi6) as a RNA-virus model. These quaternized dyes were applied at different concentrations (from 5.0 to 20 μM, and under white light irradiation in the irradiance range between 50 and 150 mW/cm2) to test their efficiency for possible clinical or environmental applications. The results showed that the new cationic ZnPcs 2a and 3a efficiently inactivate the RNA-virus model (bacteriophage Φ6), even at the lowest tested irradiance. These compounds are thus promising photosensitizers to be used in various contexts.

Seeing is believing: Efficiency evaluation of multifunctional ionic-dependent AIEgens for tuberculosis

Tuberculosis (TB), caused by Mycobacterium tuberculosis (Mtb), remains a significant public health threat with high rates of infection and mortality. Rapid and reliable theranostics of TB are essential to control transmission and shorten treatment duration. In this study, we report two cationic aggregation-inducing emission luminogens (AIEgens) named TTVP and TTPy, which have different functional charged moieties, to investigate their potential for simultaneous tracing and photodynamic therapy in TB infection. TTVP and TTPy exhibit intrinsic positive charges, excellent water solubility, and near-infrared (NIR) emission. Based on ionic-function relationships, TTVP, with more positive charges, demonstrates a stronger binding affinity to Mycobacterium marinum (M.m), (a close genetic relative of Mtb), compared to TTPy. Both TTVP and TTPy exhibit high efficiency in generating reactive oxygen species (ROS) when exposed to white light irradiation, enabling effective photodynamic killing of M.m in vitro. Additionally, we achieved long-term, real-time, noninvasive, continuous tracing, and evaluated therapeutic performance in vivo. Notably, TTVP outperformed TTPy in intracellular killing of M.m, suggesting a possible correlation between the labeling and photodynamic killing abilities of AIEgens. These findings provide valuable insights and a design basis for cationic AIEgens in TB research, offering potential advancements in TB theranostics.

Synthesis and cis-trans kinetics of an azobenzene-based molecular switch for light-responsive silica surfaces

Light-responsive materials design is an attractive research field that stimulates demand for the synthesis of novel molecular photoswitches. The novel photoswitches should be capable of being attached to a desired surface in order to provide it with light-responsive properties. The switchback to its ground state is expected to be gradual, with the possibility of acceleration. This study presents a comprehensive description of a chemical route to a molecular photoswitch based on an azobenzene derivative with a trifluoromethoxy group and a long alkyl chain. The photoswitch is capable of modifying submicrometer silica particles and silicon wafers as models of curved and flat surfaces, respectively. The thermal relaxation times of the synthesized azobenzene were studied in three different solvents: ethanol, chloroform, and toluene. The results reveal a significantly delayed relaxation process lasting for several days. This observation is found to be related to the polarity of the solvents used. To characterize the extensive thermal relaxation process, a methodology including the use of white-light pulses to accelerate cis-trans isomerization is suggested. The white light spectrum used in pulses affects thermal relaxation but does not alter the relaxation time extrapolated to zero. The density of the photoswitch molecules attached to particles varies from 0.7 to 1.7 molecules/nm2 as the initial amount of azobenzene in the reaction increases. Surface-attached photoswitches demonstrate reversible cis-trans isomerization behavior when exposed to UV and white light irradiation. A 14° contact angle change is observed when flat surfaces modified with photoswitches are irradiated with UV light.

Poly(vinyl alcohol) antibacterial films containing cross‐linked chitosan‐citric and photosensitive curcumin

AbstractComposite films PVA‐CS‐Curx (x = 0, 0.01, 0.06 and 0.12%) were successfully obtained by using vacuum‐drying at 80°C. The occurrence of nonenzymatic browning and cross‐linking of chitosan‐citric improved the thermal stability, water‐resistance, and mechanical property of films. Under the same humidity, the oxygen permeability of PVA‐CS‐Curx showed the dependence of test temperature and curcumin concentration (P &lt; 0.05). Relative to other films, the oxygen permeability (10−14 cc μm cm−2 s−1 Pa−1) of PVA‐CS‐Cur0.12 was 3.47 ± 0.55, 4.72 ± 0.94, and 7.29 ± 0.45 at 23, 30, and 40°C, respectively, showing gentle upward trend as temperature increased. Under white light irradiation, excellent antibacterial capability of PVA‐CS‐Curx demonstrated that polycationic chitosan‐citric complex and curcumin immobilized in films played the roles as synergistic antibacterial agents. Upon white irradiation of 20 min at 60 mW cm−2, the bactericidal rate of PVA‐CS‐Cur0.12 reached to 94.0 ± 3.09%. The excellent decontamination in meat preservation endowed films with the possibility in application of food decontamination.

Key parameters for enhancing visible-light-driven photocatalytic activity of ZnS nanoparticle

The use of pharmaceuticals is increasing rapidly as the industrialization of the pharmaceutical industry progresses. Accordingly, antibiotics discharged into wastewater are attracting attention as emerging pollutants that aggravate water pollution. The spread of antibiotic-resistant bacteria that cause clinically infectious diseases is also a global challenge. In this study, ZnS nanoparticles were synthesized using a simple hydrothermal process and applied to the photocatalytic degradation of antibiotic tetracycline and the photocatalytic inactivation of high-strength multidrug-resistant bacteria (Klebsiella pneumonia and Staphylococcus aureus) and total coliforms under visible light irradiation. The prepared nanomaterial was characterized using a range of analytical techniques to confirm the properties of the ZnS nanoparticles. The photocatalytic activities of nanoparticles were investigated with various parameters, such as catalyst dose, type and intensity of light, antibiotic concentration, and pH. Among them, the type of light (white light) and pH were the most important factors affecting the photocatalytic activity of ZnS nanoparticles. The basic pH condition (pH 10) improved the photocatalytic reaction activity (k = 0.0318 min−1, R2 = 0.9653), approximately 30 times more than acidic conditions (pH 3) and approximately 3.3 times more than neutral conditions (pH 7). The total coliforms in wastewater effluent were completely inactivated within 30 min of reaction time using white light irradiation (80 mW/cm2). The scavenger experiment revealed that the reactive oxygen species appeared in the order of O2·− > ·OH > h+. The reusability studies showed that the ZnS nanoparticles were very stable and retained more than 94% of their catalytic capacity after five cycles.

Procedural Promotion of Wound Healing by Graphene-Barium Titanate Nanosystem with White Light Irradiation.

Wound healing is a continuous and complex process that comprises multiple phases including hemostasis, inflammation, multiplication (proliferation) and remodeling. Although a variety of nanomaterials have been developed to control infection and accelerate wound healing, most of them can only promote one phase but not multiple phases, resulting in lower efficient healing. Although various formulations such as nitric oxide releasing wound dressings were developed for dual action, the nanostructure synthesis and the encapsulation process were complex. Here, we report on the design of graphene-barium titanate nanosystem to procedural promote the wound healing process. The antibacterial effect was assessed in Gram-negative Escherichia coli bacteria (E. coli) and Gram-positive Staphylococcus aureus bacteria (S. aureus), the cell proliferation and migration experiment was investigated in mouse embryonic fibroblast (NIH-3T3) cells, and the wound healing effect was analyzed in female BALB/c mice with infected skin wound on the back. Results showed that graphene-barium titanate nanosystem could generate abundant ROS to kill both E. coli and S. aureus. The growth curves, bacterial viability, colony number formation and scanning electron microscopy (SEM) images of E. coli and S. aureus all confirmed the antibacterial effect. Cell Counting Kit-8 (CCK-8) assay displayed that GBT possesses great biocompatibility. EdU assay showed that GBT plus white light irradiation significantly promoted the proliferation and migration of NIH-3T3 cells. Scratch assay found that GBT could achieve a fast scratch closure compared to the control. In vivo wound healing effect indicates that GBT can accelerate wound repair procedure. GBT nanocomposite is capable of programmatically accelerating wound healing through multiple stages, including production of a large amount of ROS after white light exposure to effectively kill E. coli and S. aureus to prevent wound infection and as a scaffold to accelerate fibroblast proliferation and migration to the wound to accelerate wound healing.

Precise Molecular Engineering of Type I Photosensitizer with Aggregation-Induced Emission for Image-Guided Photodynamic Eradication of Biofilm.

Biofilm-associated infections exert more severe and harmful attacks on human health since they can accelerate the generation and development of the antibiotic resistance of the embedded bacteria. Anti-biofilm materials and techniques that can eliminate biofilms effectively are in urgent demand. Therefore, we designed a type I photosensitizer (TTTDM) with an aggregation-induced emission (AIE) property and used F-127 to encapsulate the TTTDM into nanoparticles (F-127 AIE NPs). The NPs exhibit highly efficient ROS generation by enhancing intramolecular D-A interaction and confining molecular non-radiative transitions. Furthermore, the NPs can sufficiently penetrate the biofilm matrix and then detect and eliminate mature bacterial biofilms upon white light irradiation. This strategy holds great promise for the rapid detection and eradication of bacterial biofilms.