Near-infrared Light Absorption Research Articles

Improved absorption of phosphates through interface junctions and photothermal–energy–storage capability of Ca(OH)2–[Co3O4–Co3(PO4)2]

Strong absorption in the full solar spectrum is required for efficient usage of solar energy. Near-infrared (NIR) light absorption mainly depends on surface plasmon resonance and a high density of free charge carriers (FCCs). However, increasing FCC density in semiconductors is still a challenge. In this work, we demonstrated that multitudinous S-scheme interface junctions can be constructed within nanoscale Co3O4–Co3(PO4)2, leading to enhanced light absorption of phosphates over the entire solar spectrum due to the increased FCC density and charge-carrier configurations. This absorber can also boost the photothermal performance of Ca(OH)2. The photothermal dehydration conversion of Ca(OH)2 is considerably improved (13.7 times). The reversibility of the photothermal hydration–dehydration cycles of Ca(OH)2 is improved by 39 times. This composite is promising for photothermal conversion and thermal energy storage in one-step.

Controllable preparation of lignin-based photothermal composites based on fractionation treatment

Using natural renewable lignin to prepare new photothermal materials can improve the value of lignin, reduce costs, and promote sustainable development. However, the heterogeneity of lignin is an important factor limiting the stability and tunability of lignin-based photothermal materials. In this paper, lignin after fractionation treatment was blended with the Polybutylene succinate (PBS) to obtain an environmental-friendly, tunable and multifunctional photothermal material. The modulation and enhancement of the compatibility, mechanical, thermal, and photothermal properties of PBS/Lignin composites were achieved by adjusting the structure of lignin. The abundant conjugated structure and high near-infrared (NIR) light absorption capability endowed the high molecular-weight lignin with 71.34 % photothermal conversion efficiency, which led to the maximum surface temperature of the as-prepared composite reached 291 °C under NIR light of 0.9 W/cm2. Meanwhile, the composite exhibited favorable light-triggered shape memory behavior (98.2 % fixation rate and 92.6 % recovery rate), effective light-controlled self-healing capability (91.6 % self-repairing efficiency), and significant photothermal antimicrobial activity (90.6 % inhibition of Escherichia coli, 88.1 % inhibition of Staphylococcus aureus) under the stimulation of NIR light. This study serves as a reference for regulating and enhancing the photothermal conversion efficiency of lignin and developing environmental-friendly photothermal materials.

Shining light on broad-spectrum responded NaYF4:Yb,Er,Tm@Bi@BiOI: Understanding the enhanced photodegradation performance of bisphenol A and mechanisms

This work reported a novel ternary heterogeneous photocatalyst NaYF4:Yb,Er,Tm@Bi@BiOI (NBEG-6h). NBEG-6h exhibits broad-spectrum absorption from ultraviolet to near-infrared. The elimination efficiency of BPA by NBEG-6h under simulated sunlight and near-infrared light irradiation was 88% (24 min) and 93.9% (160 min), respectively. It also has the universality of degrading various pollutants, good reusability and stability. The exceptional photocatalytic activity can be attributed to the absorption of near-infrared light by NaYF4:Yb,Er,Tm, which improves the total efficiency of sunlight utilization. The localized surface plasmon resonance effect of Bi nanoparticles enhances the light absorption performance of the heterostructure. Furthermore, combining Bi and BiOI accelerates carrier migration and improves the separation efficiency of photogenerated electron-hole pairs. h+, ·O2− and 1O2 play the pivotal roles during the photocatalytic process. This research offers new insights into the design, development, and mechanism understanding of full-spectrum-driven heterostructure photocatalysts. It provides an environmentally sustainable approach to the treatment of harmful organic pollutants.

Boosting the Efficiency of Perovskite/Organic Tandem Solar Cells via Enhanced Near-Infrared Absorption and Minimized Energy Losses.

The compatibility of perovskite and organic photovoltaic materials in solution processing provides a significant advantage in the fabrication of high-efficiency perovskite/organic tandem solar cells. However, additional recombination losses can occur during exciton dissociation in organic materials, leading to energy losses in the near-infrared region of tandem devices. Consequently, a ternary organic rear subcell is designed containing two narrow-bandgap non-fullerene acceptors to enhance the absorption of near-infrared light. Simultaneously, a unique diffusion-controlled growth technique is adopted to optimize the morphology of the ternary active layer, thereby improving exciton dissociation efficiency. This innovation not only broadens the absorption range of near-infrared light but also facilitates the generation and effective dissociation of excitons. Owing to these technological improvements, the power conversion efficiency (PCE) of organic solar cells increased to 19.2%. Furthermore, a wide-bandgap perovskite front subcell is integrated with a narrow-bandgap organic rear subcell to develop a perovskite/organic tandem solar cell. Owing to the reduction in near-infrared energy loss, the PCE of this tandem device significantly improved, reaching 24.5%.

Rapid and Green Production of Mo2C Nanoparticles with High Photo‐Thermalization via Single‐Step Femtosecond‐Laser Irradiation

Photothermal cancer therapy demands nanomaterials with specific traits, including selective absorption of biotransparent near‐infrared (NIR) light, efficient light‐to‐heat conversion, biocompatibility, dispersibility, and prolonged temporal stability. These desirable properties are achieved by synthesizing Mo2C nanoparticles via an environmentally friendly femtosecond‐laser ablation method. Mo2C flakes are dispersed in water and treated with different laser powers for different durations. This process produces Mo2C nanoparticles in a single step in 10 min with water as the only additional material, forming stable colloidal solutions with no contaminants or hazardous waste. Structural and compositional characterization indicates laser‐induced amorphization of the nanoparticles, including gradual oxidation that enhances NIR light absorption. Notably, the Mo2C nanoparticle solution prepared using a 1.6‐W laser power in 10 min demonstrates photothermal conversion efficiencies exceeding 45% and 50% and temperature increases of 21 and 22 °C when illuminated with biotransparent 800 and 1064 nm NIR light, respectively. Furthermore, the solution exhibits exceptionally stable photothermal behavior over 6 months. These Mo2C nanoparticles, prepared by a rapid and clean laser manufacturing method, hold great promise for advancing photothermal therapy to combat cancer noninvasively.

Utilizing Carbon Nanomaterials for Enhanced Photothermal Therapy in Breast Cancer Treatment

Breast cancer is the most often diagnosed cancer in women and the second largest cause of cancer mortality worldwide. Photothermal therapy (PTT) has emerged as a viable cancer treatment that uses near-infrared (NIR) light-absorbing chemicals to selectively heat and destroy tumor cells while sparing healthy tissue. PTT has advantages such as high specificity, little invasiveness, and efficient tumor ablation. Recent advances include developing imageable photothermal agents to aid in therapy planning. This review focuses on the function of carbon nanoparticles in PTT, investigating their processes and advantages and analysing in vitro and in vivo investigations. Carbon nanomaterials like carbon nanotubes (CNTs) and graphene have a large surface area, great electrical conductivity, and biocompatibility, making them ideal for PTT. Carbon nanomaterials absorb NIR light, enabling deep tissue penetration and targeted heating of tumor tissues, resulting in necrosis and apoptosis. Carbon nanomaterials also increase tumor vascular permeability, which promotes chemotherapeutic drug accumulation and improves treatment results. Repurposing carbon nanomaterials for increased PTT is a potential method because of its capacity to target various pathways, select cytotoxicity against cancer cells, and synergistic effects with other anticancer drugs.

Magneto-Chiral Dichroism of Chiral Lanthanide Complexes in the Context of Richardson's Theory of Optical Activity.

Here we report on the Magneto-Chiral Dichroism (MChD) detected through visible and near-infrared light absorption of two enantiomeric pairs of ErIII and TmIII chiral complexes featuring a propeller-like molecular structure. The magnetic properties show typical features of isolated paramagnetic ions associated with 4I15/2 and 3H6 ground state terms. MChD spectroscopy shows high gMChD dissymmetry factors of ca. 0.12 T-1 and 0.05 T-1 (T=4.0 K and B=1.0 T) for ErIII and TmIII, respectively, associated with the magnetic-dipole allowed 4I13/2 ← 4I15/2 and 3H5 ← 3H6 transitions. MChD signals of the two complexes were detected up to room temperature and under magnetic fields up to 5.0 T. For the first time, the MChD results are discussed in the context of the Richardson theory of lanthanide optical activity and provide clear indications on the strongest MChD-active electronic transitions of lanthanide complexes.

Novel Synthesis Route of Plasmonic CuS Quantum Dots as Efficient Co-Catalysts to TiO2/Ti for Light-Assisted Water Splitting.

Self-doped CuS nanoparticles (NPs) were successfully synthesized via microwave-assisted polyol process to act as co-catalysts to TiO2 nanofiber (NF)-based photoanodes to achieve higher photocurrents on visible light-assisted water electrolysis. The strategy adopted to perform the copper cation sulfidation in polyol allowed us to overcome the challenges associated with the copper cation reactivity and particle size control. The impregnation of the CuS NPs on TiO2 NFs synthesized via hydrothermal corrosion of a metallic Ti support resulted in composites with increased visible and near-infrared light absorption compared to the pristine support. This allows an improved overall efficiency of water oxidation (and consequently hydrogen generation at the Pt counter electrode) in passive electrolyte (pH = 7) even at 0 V bias. These low-cost and easy-to-achieve composite materials represent a promising alternative to those involving highly toxic co-catalysts.

Direct Laser Writing of Micro-Nano Filters Based on Three-Photon Polymerization.

Direct laser writing (DLW) enables the manufacturing of functional quantum dot (QD)-polymer nanostructures with the special performance desired for technological applications. However, most papers fabricate the QD-polymer photoresist based on the principle of two-photon polymerization using laser wavelengths of 750-800 nm, which cannot effectively fabricate the near-infrared QD-polymer photoresist with absorption wavelengths above 800 nm due to linear absorption. Moreover, most papers report a relatively low doping concentration of QDs. To address these issues, this study introduces three-photon DLW technology using a near-infrared 1035 nm laser to effectively avoid the linear absorption of the near-infrared PbS/CdS QD-polymer photoresist. Three kinds of QD-polymer photoresists with concentrations up to 150 mg mL-1 are prepared through surface modification of QDs. We demonstrate that three-photon DLW is feasible to fabricate high-concentration QD-polymer photoresist to produce micro/nano high-performance QD-polymer filters of visible and near-infrared light absorption. This study provides materials and process guidance for the fabrication and application of visible and near-infrared optical filters through three-photon DLW processing of various kinds of functional nanoparticles-polymer photoresist.

Dimension-matching crystallized linear conjugated polymer/graphitic carbon nitride heterojunctions for boosting visible/near-infrared light photocatalytic hydrogen production

Linear conjugated polymer photocatalysts remain suffer from insufficient near-infrared light absorption and poor photogenerated-carriers separation efficiency caused by twisted backbone, limiting their further application for photocatalytic water splitting to produce hydrogen energy. Herein, we first synthesized crystallized 2D poly(thiophene-co-nitrothiophene) (PN) with narrow band gap through direct (hetero) arylation polymerization (DHAP) method, then constructed dimension-matching PN/graphitic carbon nitride (CN) heterojunctions (PN/CN) with 2D/2D structure for visible/near-infrared light photocatalytic hydrogen production. The resulting 2D/2D heterojunctions exhibit excellent visible/near-infrared light absorption and photocatalytic activates. The ratio-optimized 15PN/CN shows boosting hydrogen production activity up to 11.73 mmol/hg−1 under visible/near-infrared light (λ > 420 nm) irradiation, which is ∼ 30-time and ∼ 46.9-time improvement than that of PN and CN separately. Notably, the apparent quantum yield (AQY) of 15PN/CN is calculated to be 2.35 % at 700 nm and 0.62 % at 800 nm. It is proved that the π − π interaction of dimension-matching heterojunctions between PN and CN facilitates electrons transfer from LUMO of PN to LUMO of CN. This study provides another new train of thought for reasonably developing dimension-matching polymer heterojunctions by manipulating crystallinity and band structure of linear conjugated polymers for efficient visible/near-infrared light photocatalytic hydrogen production.

Dramatically Enhancing Multiphoton Harvesting Metal-Organic Frameworks for NIR-II Photocatalysis through Functional Regulation of Octupolar Molecules.

The development of effective multiphoton absorption (MPA) materials for near-infrared (NIR) light-driven photocatalysis holds great significance. In this study, we incorporated two multibranched cyclometallated iridium(III) modules with varying degrees of conjugation onto MPA-inert metal-organic frameworks (MOFs) to active MPA performance. Subsequently, the MOFs were further modified with Co(II) and hyaluronic acid (HA) to fabricate MINCH and MISCH, respectively. By introducing octupolar molecules and expanding the conjugation, MISCH exhibited a larger MPA cross section for efficient NIR light absorption and improved carrier transfer, leading to outstanding NIR light-driven multiphoton photocatalytic hydrogen production. Moreover, the HA modification enabled MISCH to achieve specific multiphoton photocatalytic hydrogen therapy for cancer cells. This study provides valuable insights into constructing highly active MPA materials for NIR light-driven photocatalysis, presenting a potential platform for hydrogen therapy in tumor treatment.

Intercomparison of optical scattering turbidity sensors for a wide range of suspended sediment types and concentrations

To monitor the effects of rapid changes in climate and land use on sediment export from erodible environments, it is crucial to accurately quantify highly fluctuating suspended sediment concentrations (SSCs) in contrasted river systems that drain small to mesoscale catchments. To this end, we investigate the turbidity-based quantification of SSCs in the range of 0.05–100 g/L through laboratory experiments performed with 7 different types of turbidity sensors and sediments from 10 watersheds. We find that measurements of scattered light from multiple angles may allow for: (1) an extended monitoring range with SSCs up to 10–100 g/L, where enhanced uncertainty may occur near the transition in the effective operational ranges of the underlying signals (typically somewhere in the range of 1–10 g/L); and/or (2) a slightly reduced sensitivity to sediment properties. The specific turbidity of the investigated sensors is inversely related to particle diameter (D10) for SSCs up to 1–5 g/L. Backscatter and combined-signal sensors also show a dependency on sediment colour (CIE a∗), which becomes particularly prominent at SSCs above 10 g/L. We relate this increase in colour dependency with SSC to the expected effect of cumulative near-infrared light absorption associated with multiple scattering. We discuss covarying physical properties of naturally occurring river sediment that can dampen or enhance measurement sensitivity and result in turbidity-based SSC rating curves that may strongly differ in magnitude and form from curves derived for industrially prepared material that is often used for sensor calibration. Although the differences in SSC per sensor among sediment types are generally less than one order of magnitude, the systematic errors and uncertainties associated with high SSCs are typically greater than one order of magnitude and may disproportionally affect the quantification of sediment loads during large-magnitude flow events.

Strong absorption of silica over full solar spectrum boosted by interfacial junctions and light–heat–storage of Mg(OH)2–(CrOx–SiO2)

Strong absorption of near-infrared (NIR) light is essential for efficient solar energy applications. NIR absorption primarily depends on the surface plasmon resonance of incident light with free charge carriers (FCCs). We demonstrated that S-scheme interfacial junctions (IJs) can substantially enhance FCC density, light-harvesting, photocurrent intensity, long lifetime of the charge carriers and photothermal effects, paving a way for novel light-material design. Abundant S–scheme IJs are constructed in CrOx–SiO2 nanoparticles, which increase the FCCs outstandingly and enhance light absorption exceptionally over the entire solar spectrum. IJs’ construction enables silica to harvest solar energy strongly. Doped with multifunctional CrOx–SiO2 nanoparticles, the photothermal-dehydration conversion and the stored heat of Mg(OH)2 can be improved by 7.0- and 5.1-times upon 30-min irradiation, respectively. The reversibility of the photothermal charge–discharge cycles of Mg(OH)2 improves 19.3 times. The thermal-storage kinetics is substantially improved owing to the reduction of the dehydration activation energy (−15.2 %). Mg(OH)2–CrOx–SiO2 composite is an excellent one-step system of light–heat–storage.

Supramolecular assembly of Polydopamine@Fe nanoparticles with near-infrared light-accelerated cascade catalysis applied for synergistic photothermal-enhanced chemodynamic therapy

Chemodynamic therapy (CDT) via Fenton-like reaction is greatly attractive owing to its capability to generate highly cytotoxic •OH radicals from tumoral hydrogen peroxide (H2O2). However, the antitumor efficacy of CDT is often challenged by the relatively low radical generation efficiency and the high levels of antioxidative glutathione (GSH) in tumor microenvironment. Herein, an innovative photothermal Fenton-like catalyst, Fe-chelated polydopamine (PDA@Fe) nanoparticle, with excellent GSH-depleting capability is constructed via one-step molecular assembly strategy for dual-modal imaging-guided synergetic photothermal-enhanced chemodynamic therapy. Fe(III) ions in PDA@Fe nanoparticles can consume the GSH overexpressed in tumor microenvironment to avoid the potential •OH consumption, while the as-produced Fe(II) ions subsequently convert tumoral H2O2 into cytotoxic •OH radicals through the Fenton reaction. Notably, PDA@Fe nanoparticles demonstrate excellent near-infrared light absorption that results in superior photothermal conversion ability, which further boosts above-mentioned cascade catalysis to yield more •OH radicals for enhanced CDT. Taken together with T1-weighted magnetic resonance imaging (MRI) contrast enhancement (r1 = 8.13 mM−1 s−1) and strong photoacoustic (PA) imaging signal of PDA@Fe nanoparticles, this design finally realizes the synergistic photothermal-chemodynamic therapy. Overall, this work offers a new promising paradigm to effectively accommodate both imaging and therapy functions in one well-defined framework for personalized precision disease treatment.

Photo-to-Thermal Conversion Harnessing Low-Energy Photons Renders Efficient Solar CO2 Reduction.

Efficient photocatalytic solar CO2 reduction presents a challenge because visible-to-near-infrared (NIR) low-energy photons account for over 50% of solar energy. Consequently, they are unable to instigate the high-energy reaction necessary for dissociating C═O bonds in CO2. In this study, we present a novel methodology leveraging the often-underutilized photo-to-thermal (PTT) conversion. Our unique two-dimensional (2D) carbon layer-embedded Mo2C (Mo2C-Cx) MXene catalyst in black color showcases superior near-infrared (NIR) light absorption. This enables the efficient utilization of low-energy photons via the PTT conversion mechanism, thereby dramatically enhancing the rate of CO2 photoreduction. Under concentrated sunlight, the optimal Mo2C-C0.5 catalyst achieves CO2 reduction reaction rates of 12000-15000 μmol·g-1·h-1 to CO and 1000-3200 μmol·g-1·h-1 to CH4. Notably, the catalyst delivers solar-to-carbon fuel (STF) conversion efficiencies between 0.0108% to 0.0143% and the STFavg = 0.0123%, the highest recorded values under natural sunlight conditions. This innovative approach accentuates the exploitation of low-frequency, low-energy photons for the enhancement of photocatalytic CO2 reduction.

Interaction between polydopamine-based IONPs and human serum albumin (HSA): a spectroscopic analysis with cytotoxicity impact

Iron oxide nanoparticles (IONPs) have been extensively explored in biomedicine, bio-sensing, hyperthermia, and drug/gene delivery, attributed to their versatile and tunable properties. However, owing to its numerous applications, the functionalization of IONPs with appropriate materials is in demand. To achieve optimal functionalization of IONPs, polydopamine (PDA) was utilized due to its ability to provide a superior functionalized surface, near-infrared light absorption, and adhesive nature to customize desired functionalized IONPs. This notion of involving PDA led to the successful synthesis of magnetite-PDA nanoparticles, where PDA is surface-coated on magnetite (Fe3O4@PDA). The Fe3O4@PDA nanoparticles were characterized using techniques like TEM, FESEM, PXRD, XPS, VSM, and FTIR, suggesting PDA’s successful attachment with magnetite crystal structure retention. Human serum albumin (HSA), the predominant protein in blood plasma, interacts with the delivered nanoparticles. Therefore, we have employed various spectroscopic techniques, along with cytotoxicity, to inspect the effect of Fe3O4@PDA NPs on the stability and structure of HSA. The structural alterations were examined using circular dichroism (CD) and synchronous fluorescence spectroscopy (SFS). It has been observed that there are no structural perturbations in the secondary structure of the HSA protein after interaction with Fe3O4@PDA. Studies using steady-state fluorescence revealed that the inherent fluorescence intensities of HSA were suppressed after interaction with Fe3O4@PDA. In addition, temperature-dependent fluorescence measurements suggested that the type of quenching consists of both static and dynamic quenching simultaneously. A cytotoxicity study in Drosophila melanogaster larvae revealed no cytotoxic effects but did show a minor genotoxic effect only at higher concentrations.

Photothermal Depth Profiling of Gelatin-Stabilised Gold Nanorods-Trastuzumab Conjugate as a Potential Breast Cancer Photothermal Agent

Gold nanorods (AuNRs) are powerful photothermal agents (PTAs) in cancer treatment due to their near-infrared laser light absorption ability. However, the cytotoxicity of AuNRs caused by the presence of cationic surfactants often used and their lack of specificity affect their application in photothermal therapy. Thus, we herein developed a bioconjugate obtained from the functionalisation of AuNRs to gelatin (Gel@AuNRs), followed by the conjugation of the as-synthesised material to a breast cancer antibody, trastuzumab (Trast-Gel@AuNRs) to address these issues. The optical and structural characterization of the as-synthesized indicated no significant changes in the optical properties of AuNRs after their functionalisation with gelatin and conjugation with the antibody. The photothermal profiling of the as-synthesised materials showed that AuNRs still have an excellent photothermal conversion efficiency (PCE) after their functionalisation (20%) and their conjugation to an antibody (19%). In addition, the In vitro photothermal depth response showed that Trast-Gel@AuNRs is a promising photothermal agent for HER2-positive breast cancer treatment.Graphical

A scalable method for fabricating monolithic perovskite/silicon tandem solar cells based on low-cost industrial silicon bottom cells

Tandem solar cells composed of perovskite and silicon (PVSK/Si TSCs) exhibit significant potential for improving the power conversion efficiency (PCE) and reducing the levelized cost of electricity. Currently, most tandem cells demonstrating high efficiencies utilize costly float zone (FZ) silicon wafers, which pose limitations for large-scale production due to their high expense. This study presents a scalable approach for manufacturing perovskite/silicon tandem solar cells using industrial silicon bottom cells. We employ a double-layer intrinsic amorphous silicon passivation layer to enhance the carrier lifetime of the bottom silicon cell. Additionally, we introduce a novel indium oxide doped with transition metals (IMO) transparent electrode to enhance near-infrared (NIR) light absorption. To achieve silicon bottom cells with a polished front surface, we utilize a cost-effective and time-saving saw damage etching process. The perovskite absorber is then deposited on the polished surface using slot-die coating. Furthermore, we coat the perovskite absorber with a mixed solution of FAI and mF-PEAI via slot-die coating to eliminate excess PbI2 on the surface and passivate surface defects. Through the integration of top and bottom sub-cells, we obtained a PCE exceeding 24.22 % from a 5 cm × 5 cm TSCs device (with an aperture area of 3.8 cm × 3.8 cm) and a PCE of 28.68 % from a 2.5 cm × 2.5 cm TSCs device (with an aperture area of 1 cm × 1 cm).

Nonionizing diagnostic imaging modalities for visualizing health and pathology of periodontal and peri-implant tissues.

Radiographic examination has been an essential part of the diagnostic workflow in periodontology and implant dentistry. However, radiographic examination unavoidably involves ionizing radiation and its associated risks. Clinicians and researchers have invested considerable efforts in assessing the feasibility and capability of utilizing nonionizing imaging modalities to replace traditional radiographic imaging. Two such modalities have been extensively evaluated in clinical settings, namely, ultrasonography (USG) and magnetic resonance imaging (MRI). Another modality, optical coherence tomography (OCT), has been under investigation more recently. This review aims to provide an overview of the literature and summarize the usage of USG, MRI, and OCT in evaluating health and pathology of periodontal and peri-implant tissues. Clinical studies have shown that USG could accurately measure gingival height and crestal bone level, and classify furcation involvement. Due to physical constraints, USG may be more applicable to the buccal surfaces of the dentition even with an intra-oral probe. Clinical studies have also shown that MRI could visualize the degree of soft-tissue inflammation and osseous edema, the extent of bone loss at furcation involvement sites, and periodontal bone level. However, there was a lack of clinical studies on the evaluation of peri-implant tissues by MRI. Moreover, an MRI machine is very expensive, occupies much space, and requires more time than cone-beam computed tomography (CBCT) or intraoral radiographs to complete a scan. The feasibility of OCT to evaluate periodontal and peri-implant tissues remains to be elucidated, as there are only preclinical studies at the moment. A major shortcoming of OCT is that it may not reach the bottom of the periodontal pocket, particularly for inflammatory conditions, due to the absorption of near-infrared light by hemoglobin. Until future technological breakthroughs finally overcome the limitations of USG, MRI and OCT, the practical imaging modalities for routine diagnostics of periodontal and peri-implant tissues remain to be plain radiographs and CBCTs.

A near-infrared naphthalocyanine photosensitizer with superior light absorption and renal clearance for type-I photodynamic and photothermal combination therapy

Currently, it is still a challenge to develop an organic photosensitizer (PS) with outstanding near-infrared absorption, low O2 dependence, precise tumor targeting and rapid clearance through the kidney to improve the overall outcome of phototherapy. In this study, we have designed an organic PS (NcPB) with an excellent near-infrared light absorption through a refined molecular strategy. Meanwhile, NcPB was assembled into nanoparticles with different sizes (NanoNcPB-1 and NanoNcPB-0) by a supramolecular modulation strategy. As the results, the nanoparticle with an ultra-small size (NanoNcPB-1) generated a large number of superoxide anion (O2•−) in a low-O2-dependent manner and release plenty of heat. Furthermore, the results of in vivo experiments demonstrated that NanoNcPB-1 actively accumulated in tumor tissues and showed a 92% tumor inhibition after photodynamic and photothermal combination therapy. More importantly, NanoNcPB-1 could be rapidly cleared from the body of mice via the renal pathway, which alleviates potential side effects of prolonged retention of PS in the circulation.