Biomedical Imaging Applications Research Articles

Optical Performance of Quantum Dots and Their Applications in Biomedical Imaging

Quantum dots are nanomaterials which have attracted significant focus over the past few years because of their singular optical features. They have shown great potential in the field of bioimaging. This study delves into the photonic properties of quantum dots which include good luminescence stability and broad excitation spectra. Besides, the emission wavelength can be precisely controlled. These properties make them an excellent choice for bio-imaging. The usage of quantum dots in live organism imaging, such as pinpointing cell boundaries, tracking intracellular molecular dynamics, and early disease diagnosis, indicate the immense potential of quantum dots in biomedical realm. Through modifications on the surface of quantum dots, targeted imaging can be realized, which greatly improves the specificity and sensitivity of imaging. Nonetheless, the biosafety and long-term in vivo behavior of quantum dots still need to be further investigated. Overall, the light-based attributes of quantum dots have brought breakthroughs in bio-imaging technology. In addiiton, it would foretell a bright future for quantum dots in the biomedical field.

Enhanced Singlet Oxygen Generation in Aggregates of Naphthalene-Fused BODIPY and Its Application in Photodynamic Therapy.

Several reports are available on aggregation-induced emission and its applications in biomedical imaging and other material sciences. However, enhancement of singlet oxygen generation in nanoaggregates is rarely reported. Here, we report the synthesis of Naph-BODIPY Br2, which absorbs at 661 nm (monomer) with a high molar absorption coefficient. The presence of bromine promotes intersystem crossing, thereby enhancing the singlet oxygen quantum yield (ΦΔ ∼ 0.50 in methanol). In order to increase hydrophilicity, we developed Naph-BODIPY Br2 nanoaggregates (∼100 nm), which demonstrated aggregation-induced properties and exhibited a bathochromic shift with an absorption maximum at 757 nm. The bathochromic shift in the UV-vis spectra due to aggregation is corroborated by TD-DFT analysis. The computational data also confirm the presence of a low-lying triplet state, which enhances the generation of singlet oxygen, making it effective for photodynamic therapy. These aggregates showed excellent singlet oxygen generation in aqueous media, compared to their monomeric form and standard methylene blue. Their hydrophilic nature and high singlet oxygen generation enabled significant phototoxicity against human carcinoma cells with IC50 values of 4.06 ± 0.01 and 4.09 ± 0.1 μM, respectively, for MCF-7 and A549 cells upon 5 min exposure to light. Moreover, their phototoxicity further increases with an increasing exposure time of light for both cell lines. Notably, Naph-BODIPY Br2 nanoaggregates exhibited nearly zero dark cell toxicity and effectively induced apoptosis in cancer cells upon light activation, highlighting their potential as powerful photosensitizers for photodynamic cancer therapy.

High Quantum Yields and Biomedical Fluorescent Imaging Applications of Photosensitized Trivalent Lanthanide Ion-Based Nanoparticles.

In recent years, significant advances in enhancing the quantum yield (QY) of trivalent lanthanide (Ln3+) ion-based nanoparticles have been achieved through photosensitization, using host matrices or capping organic ligands as photosensitizers to absorb incoming photons and transfer energy to the Ln3+ ions. The Ln3+ ion-based nanoparticles possess several excellent fluorescent properties, such as nearly constant transition energies, atomic-like sharp transitions, long emission lifetimes, large Stokes shifts, high photostability, and resistance to photobleaching; these properties make them more promising candidates as next-generation fluorescence probes in the visible region, compared with other traditional materials such as organic dyes and quantum dots. However, their QYs are generally low and thus need to be improved to facilitate and extend their applications. Considerable efforts have been made to improve the QYs of Ln3+ ion-based nanoparticles through photosensitization. These efforts include the doping of Ln3+ ions into host matrices or capping the nanoparticles with organic ligands. Among the Ln3+ ion-based nanoparticles investigated in previous studies, this review focuses on those containing Eu3+, Tb3+, and Dy3+ ions with red, green, and yellow emission colors, respectively. The emission intensities of Eu3+ and Tb3+ ions are stronger than those of other Ln3+ ions; therefore, the majority of the reported studies focused on Eu3+ and Tb3+ ion-based nanoparticles. This review discusses the principles of photosensitization, several examples of photosensitized Ln3+ ion-based nanoparticles, and in vitro and in vivo biomedical fluorescent imaging (FI) applications. This information provides valuable insight into the development of Ln3+ ion-based nanoparticles with high QYs through photosensitization, with future potential applications in biomedical FI.

Broadband and parallel multiple-order optical spatial differentiation enabled by Bessel vortex modulated metalens

Optical analog image processing technology is expected to provide an effective solution for high-throughput and real-time data processing with low power consumption. In various operations, optical spatial differential operations are essential in edge extraction, data compression, and feature classification. Unfortunately, existing methods can only perform low-order or selectively perform a particular high-order differential operation. Here, we propose and experimentally demonstrate a Bessel vortex modulated metalens composed of a single complex amplitude metasurface, which can perform multiple-order radial differential operations over a wide band by presetting the order of the corresponding Bessel vortex. This architecture further enables angle multiplexing to create multiple information channels that synchronously perform multi-order spatial differential operations, indicating the superiority of the proposed devices in parallel processing. Our approach may find various applications in artificial intelligence, machine vision, autonomous driving, and advanced biomedical imaging.

Monolayer MoS2 and WS2 for Vertical Circular‐ Polarized‐Light‐Emitting Diode: from Fundamental Understanding to Device Architecture

AbstractLight‐emitting diodes (LEDs) have revolutionized lighting and displays due to their numerous advantages over conventional lighting mechanisms. Moreover, the directional nature of luminescent materials has spurred significant advancements in the development of circularly polarized LEDs, which hold transformative potential for applications in biomedical imaging, liquid crystal displays, spintronics, and valleytronics. The performance of circularly polarized LEDs mainly depends on the emitter material, which is this study's focus. In particular, semiconducting‐phase 2D monolayer MoS2 and WS2 are attractive emitter‐material candidates owing to their bandgap versatility, high carrier mobility, high exciton binding energy, polarized‐light‐emission properties, and unique spin–valley coupling. Several works have examined the fundamental light‐emission properties of monolayer MoS2 and WS2 from the perspectives of optoelectronic concepts, material fabrication, and device construction. This paper presents approaches to control, tune, and enhance these properties of monolayer MoS2 and WS2. Possible guidelines for monolayer‐material synthesis (top‐down and bottom‐up approaches) and device engineering of vertically stacked MoS2 and WS2 are presented. Finally, the review considers the material topological characteristics, outlines the challenges and potential of monolayer MoS2 and WS2 for developing high‐performance commercial circularly polarized LED devices, and proposes a technological roadmap for leveraging other monolayer transition metal dichalcogenide systems in optoelectronic devices.

Micelles as nanocarriers of fluorescent and magnetic dendrimers for potential bimodal imaging applications

Bimodal magnetic-fluorescent materials that integrate magnetic and fluorescent properties have attracted significant attention due to their potential applications in biomedical imaging, biosensing, and therapeutic diagnosis. Tetra-amido-TEMPO 1, a compound that combines a fluorescent oligo(styryl)benzene dendrimer core with TEMPO radicals in its four branches was synthesized and used to form micelles with CTAB in water. DLS and Cryo-TEM techniques revealed the formation of micelles exhibiting a narrow particle size distribution, with an average hydrodynamic diameter ranging from 95 to 140 nm. After micellization, the ultraviolet-visible absorption and fluorescence emission intensities of micelles increased with tetra-amido-TEMPO concentration and EPR spectroscopy demonstrated consistent three-line spectra in the micelles, with the integrated area directly proportional to the amount of tetra-amido-TEMPO present. Besides, sufficient contrast enhancement in the proton T1 relaxation time-weighted magnetic resonance images in vitro proved their ability to act as magnetic resonance imaging (MRI) contrast agents. These tetra-amido-TEMPO/CTAB micelles offer an aqueous-compatible system for this bimodal fluorescent-magnetic molecule, showcasing proof of concept of their potential for biomedical applications.

MRI detection of free-contrast agent nanoparticles.

The integration of nanotechnology into biomedical imaging has significantly advanced diagnostic and theranostic capabilities. However, nanoparticle detection in imaging relies on functionalization with appropriate probes. In this work, a new approach to visualize free-label nanoparticles using MRI and MRS techniques is described, consisting of detecting by 1H CSI specific proton signals belonging to the components naturally present in most of the nanosystems used in preclinical and clinical research. Three different nanosystems, namely lipid-based micelles, liposomes, and perfluorocarbon-based nanoemulsions, were synthesized, characterized by high resolution NMR and then visualized by 1H CSI at 300 MHz. Subsequently the best 1H CSI performing system was administered to murine models of cancer to evaluate the possibility of tracking the nanosystem by looking at its proton associated signal. Furthermore, an in vitro comparison between 1H CSI and 19F MRI was carried out. The study successfully demonstrates the feasibility of detecting nanoparticles using MRI/MRS without probe functionalization, employing 1H CSI. Among the nanosystems tested, the perfluorocarbon-based nanoemulsion exhibited the highest SNR. Consequently, it was evaluated in vivo, where its detection was achievable within tumors and inflamed regions via 1H CSI, and in lymph nodes via PRESS. These findings present a promising avenue for nanoparticle imaging in biomedical applications, offering potential enhancements to diagnostic and theranostic procedures. This non-invasive approach has the capacity to advance imaging techniques and expand the scope of nanoparticle-based biomedical research. Further exploration is necessary to fully explore the implications and applications of this method.

Synthesis, Optical Spectroscopy, and Laser and Biomedical Imaging Application Potential of 2,4,6-Triphenylpyrylium Tetrachloroferrate and Its Derivatives.

Synthesis, optical spectroscopic properties, two-photon (TP) absorption-induced fluorescence, and laser and bioimaging application potentials of 2,4,6-triphenylpyrylium tetrachloroferrate (1),4-(4-methoxyphenyl)-2,6-diphenylpyrylium tetrachloroferrate (2), 2,6-bis(4-methoxyphenyl)-4-phenylpyrylium tetrachloroferrate (3), and 2,4,6-tris(4-methoxyphenyl)pyrylium tetrachloroferrate (4) are presented. The synthesis involves the conversion of pyrylium tosylates to pyrylium chlorides, followed by transformation into 1-4 on heating to reflux with FeCl3 in acetonitrile. They are characterized using 1H and 13C NMR spectra in CD3OD, and FTIR and Raman spectroscopic techniques. The salts dissolve in organic solvents and water (pH = 7 to 3) even at high concentrations (10-3 M). These solutions absorb light strongly from 500-300 nm. Solutions of 1, 3, and 4 fluoresce with high quantum yield in the 500-700 nm spectral range. Salts 1 and 4 exhibit fluorescence lifetime shortening, line width narrowing, and free-running laser action under intense pulsed laser excitation. Toxicity and cell imaging studies using human cancer cell lines reveal that salts 1 and 3 function as cellular fluorophores in vitro and have no adverse effects on cellular viability at nanomolar ranges. Furthermore, acetonitrile and methanol solutions of salts 1, 3, and 4 exhibit strong two-photon absorption-induced fluorescence, opening potential applications in biomedical imaging and microscopy.

Self‐Assembly of UiO‐66 on Conjugated Polyelectrolytes: Toward Enhanced Photophysical Properties

AbstractIn this study, the synthesis and characterization of the fluorescent metal–organic framework (MOF)‐polymer composites is reported based on zirconium‐based MOFs (UiO‐66 and UiO‐66(OH)₂) and a conjugated polyelectrolyte, poly(phenylene ethynylene) carboxylate (PPE‐CO₂‐108). The defect‐rich nature of these Zr‐MOFs facilitates strong interactions between the polyelectrolyte's carboxylic acid moieties and the open metal sites on the Zr clusters within the MOF nanoparticles. The composites are prepared by a simple impregnation approach, where MOF nanocrystals suspended in HEPES buffer are added to the polymeric solution under sonication for 10 min. The obtained MOF composites (i.e., UiO‐66‐CPE and UiO‐66 (OH)2‐CPE) are characterized using powder X‐ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), Brunauer‐Emmett‐Teller (BET) surface area, zeta potential measurements, and UV–vis spectroscopy. The characterization confirmed the homogeneous distribution of the MOF nanocrystals on the polymer as seen in the SEM images, and the interaction with PPE‐CO₂‐108 is confirmed by the decrease in the surface areas from 1050 to 590 m2 g−1 for UiO‐66‐CPE and from 500 to 137 m2 g−1, for UiO‐66(OH)2‐CPE. Fluorescence microscopy revealed strong fluorescence in the microparticles, confirming robust polymer‐MOF interaction. The composites also exhibit improved photostability of the conjugated polyelectrolyte, suggesting their potential for applications in biomedical imaging and other areas requiring stable and bright fluorescent systems.

Efficient Broadband Near‐Infrared Emitters in Lead‐Free Metal Halides with Record Photoluminescence Quantum Yield Under Blue Light Excitation

AbstractRealizing ultra‐efficient broadband near‐infrared (NIR) luminescence, especially under blue light excitation, remains an enormous challenge in lead‐free metal halides. Herein, the efficient NIR emission under blue light excitation is achieved in Sb3+‐doped 0D (ETPP)2ZnCl4xBr4‐4x (x = 0–1) (ETPP+ = (Ethyl)triphenylphosphonium) through coordination structure modulation and halogen substitution. Compared with the visible light emission of Sb(III)‐based compounds, the emission in Sb3+‐doped (ETPP)2ZnCl4xBr4‐4x shifts to the NIR region due to the large excited state lattice distortion. Parallelly, the excitation bands gradually shift from 376 to 450 nm as Br gradually replaces Cl, and the emission bands can further shift from 702 to 763 nm. Thus, the broadband NIR emission at 763 nm with a record luminous efficiency of 55.4% under 450 nm excitation can be achieved in Sb3+‐doped compounds. Moreover, the large‐scale synthesis technique of Sb3+‐doped (ETPP)2ZnBr4: NIR phosphors at room temperature is further developed and this compound exhibits impressive thermal and chemical‐stabilities. Finally, a high‐performance NIR light‐emitting‐diode is fabricated by combining a commercial blue chip and (ETPP)2ZnBr4:10%Sb3+ phosphors, which shows the most advanced photoelectric efficiency (17.8%) and output power (67.7 mW) in lead‐free metal halides. Thus, the as‐fabricated device is further demonstrated in the applications of night vision and biomedical imaging.

Efficient and Near-Zero Thermal Quenching Cr3+-Doped Garnet-Type Phosphor for High-Performance Near-Infrared Light-Emitting Diode Applications.

In recent years, near-infrared (NIR) phosphors have attracted great research interest due to their unique physical properties and broad application prospects. However, obtaining NIR phosphors with both high quantum efficiency and excellent thermal stability remains a great challenge. In this study, novel NIR Ca3Mg2ZrGe3O12:Cr3+ phosphors were successfully prepared using a high-temperature solid-phase method, and the structure and luminescent properties of the material were systematically investigated. Ca3Mg2ZrGe3O12:0.01Cr3+ emits NIR light in the range of 600 to 900 nm with a peak at 758 nm and a half-height width of 89 nm under the excitation of 457 nm blue light. NIR luminescence shows considerable quantum efficiency, and the internal quantum efficiency of the optimized sample is up to 68.7%. Remarkably, the Ca3Mg2ZrGe3O12:0.01Cr3+ phosphor exhibits a near-zero thermal quenching behavior, and the luminescence intensity of the sample at 250 °C maintains 92% of its intensity at room temperature. The mechanism of high thermal stability has been elucidated by calculating the Huang Kun factor and activation energy. Finally, NIR pc-LED devices prepared from Ca3Mg2ZrGe3O12:0.01Cr3+ phosphor with commercial blue LED chips have good performance, proving that this Ca3Mg2ZrGe3O12:0.01Cr3+ NIR phosphor has potential applications in night vision and biomedical imaging.

Medium optimization to improve growth and iron uptake by Bacillus tequilensis ASFS1 using fractional factorial designs

Many notable applications have been described for magnetic nanoparticles in delivery of diverse drugs and bioactive compounds into cells, magnetofection for the treatment of cancer, photodynamic therapy, photothermal therapy, and magnetic particle imaging (MPI). In response to the growing demand for magnetic nanoparticles for drug delivery or biomedical imaging applications, more effective and eco-friendly methodologies are required for large-scale biosynthesis of this nanoparticles. The major challenge in the large-scale biomedical application of magnetic nanoparticles lies in its low efficiency and optimization of nanoparticle production can address this issue. In the current study, a prediction model is suggested by the fractional factorial designs. The present study aims to optimize culture media components for improved growth and iron uptake of this strain. The result of optimization for iron uptake by the strain ASFS1 is to increase the production of magnetic nanoparticles by this strain for biomedical applications in the future. In the present study, design of experiment method was used to probe the effects of some key medium components (yeast extract, tryptone, FeSO4, Na2-EDTA, and FeCl3) on Fe content in biomass and dried biomass of strain ASFS1. A 25−1 fractional factorial design showed that Na2-EDTA, FeCl3, yeast extract-tryptone interaction, and FeSO4-Na2-EDTA interaction were the most parameters on Fe content in biomass within the experimented levels (p < 0.05), while yeast extract, FeCl3, and yeast extract-tryptone interaction were the most significant factors within the experimented levels (p < 0.05) to effect on dried biomass of strain ASFS1. The optimum culture media components for the magnetic nanoparticles production by strain ASFS1 was reported to be 7.95 g L−1 of yeast extract, 5 g L−1 of tryptone, 75 μg mL−1 of FeSO4, 192.3 μg mL−1 of Na2-EDTA and 150 μg mL−1 of FeCl3 which was theoretically able to produce Fe content in biomass (158 μg mL−1) and dried biomass (2.59 mg mL−1) based on the obtained for medium optimization. Using these culture media components an experimental maximum Fe content in biomass (139 ± 13 μg mL−1) and dried biomass (2.2 ± 0.2 mg mL−1) was obtained, confirming the efficiency of the used method.

A cost-effective field-programmable-gate-array-based pulse processor for biomedical imaging applications

ObjectiveThis paper presents the design and evaluation of a cost-effective, high-spatial resolution, multichannel, field-programmable gate array (FPGA)-based readout system for Positron Emission Tomography (PET) detectors suitable for clinical and pre-clinical work in cancer and other diseases. A key challenge in PET imaging is the precise measurement of the time of arrival and energy of gamma photons originating from positron annihilation, along with the position of interaction within the detector. These parameters enhance image quality by improving coincidence detection, excluding Compton-scattered photons, and improving system spatial resolution. We developed a 16-channel readout system using single silicon photomultiplier (SiPM) element readout for efficient and precise energy, time, and position measurements. Each channel incorporates an FPGA-based sigma-delta analog-to-digital converter (ΣΔ-ADC) and tapped delay line (TDL) based time-to-digital converter (TDC) for timing and energy estimation. Performance characterization of the system was performed through simulation, electronically generated waveform, and actual PET detector signals from three different single scintillation crystals of face dimensions 3 × 3 mm2 and depths of 5 and 20 mm coupled to a 3 × 3 mm2 SiPM. We also constructed and tested a modular PET detector with a 10x10 array of 1.2x1.2x14 mm³ LSO crystals coupled to a 4x4 SiPM array of 3 × 3 mm2 elements. Best energy resolution was 9.3% at the 511 KeV photopeak and best coincidence timing resolution (CTR) was 210 ± 3.5 ps. Our system balances cost-effectiveness with performance and contributes to developments in PET signal acquisition and detector technology.

Strategy to optimize the broadband near-infrared emission based on Eu2+-doped sulfureted garnet phosphors toward emerging spectroscopy applications

Eu2+-doped near-infrared (NIR) emitting phosphors, known for their high efficiency, broadband emission and spectral tunability, have gained much attention. However, achieving efficient NIR emission based on Eu2+ remains a challenge due to the co-existence of Eu3+, especially in materials (i.e. garnets and apatites) containing trivalent lanthanide cations. In this study, a Eu2+ doped sulfureted NIR-emitting garnet phosphor Ca3(Sc, Eu)2Si3(O, S)12: Eu2+ is successfully designed and synthesized. Notably, a strategy for regulating the initial valence state of dopants is proposed by using prepared EuS instead of the conventional Eu2O3 as raw material, enhancing the NIR emission by 135 %. Moreover, a sulfuration strategy is further introduced to enhance the NIR-emitting intensity and internal quantum efficiency by 192 % and 167.8 %, and to improve thermal stability by 154 % at 120 °C. The luminescence origin of the unusual broadband NIR emission is re-examined through chemical unit co-substitution strategy by introducing [Al3+Hf4+] to replace [Sc3+Si4+] ion pairs. Meanwhile, the spectral regulation and the performance optimization mechanism are systematically discussed. Finally, a green light pumped NIR LED device with a photoelectric efficiency of 9.43 %@100 mA and output power of 22.74 mW@100 mA is fabricated, showing remarkable potential in nondestructive testing and biomedical imaging applications.

Slot-Loaded Vivaldi Antenna for Biomedical Microwave Imaging Applications: Influence of Design Parameters on Antenna's Dimensions and Performances.

This paper demonstrates the design steps of a slot-loaded Vivaldi antenna for biomedical microwave imaging applications, showing the influence of the design parameters on the antenna's dimensions and performances. Several antenna miniaturization techniques were taken into consideration during the design: reduction in the electromagnetic wavelength by using a high-permittivity substrate material (relative permittivity ϵr=10.2), the placement of the antenna inside a coupling medium (ϵr=23), and the elongation of the current path by etching slots on each side of the radiator to reduce the antenna's lowest resonant frequency without increasing its physical dimensions. Moreover, an analysis of different antenna slot design scenarios was performed considering different slot lengths, inclination angles, positions, and numbers. Considering the frequency range of microwave imaging (i.e., about 500 MHz-5 GHz) and the array arrangement typical of microwave imaging, the best design was chosen. Finally, the antenna was fabricated and its performances in the coupling medium were characterized. The simulation and measurement results showed good agreement between each other. In comparison with literature antennas, the one developed in this work shows wide bandwidth and compact dimensions.

Advancements in Nanoporous Materials for Biomedical Imaging and Diagnostics.

This review explores the latest advancements in nanoporous materials and their applications in biomedical imaging and diagnostics. Nanoporous materials possess unique structural features, including high surface area, tunable pore size, and versatile surface chemistry, making them highly promising platforms for a range of biomedical applications. This review begins by providing an overview of the various types of nanoporous materials, including mesoporous silica nanoparticles, metal-organic frameworks, carbon-based materials, and nanoporous gold. The synthesis method for each material, their current research trends, and prospects are discussed in detail. Furthermore, this review delves into the functionalization and surface modification techniques employed to tailor nanoporous materials for specific biomedical imaging applications. This section covers chemical functionalization, bioconjugation strategies, and surface coating and encapsulation methods. Additionally, this review examines the diverse biomedical imaging techniques enabled by nanoporous materials, such as fluorescence imaging, magnetic resonance imaging (MRI), computed tomography (CT) imaging, ultrasound imaging, and multimodal imaging. The mechanisms underlying these imaging techniques, their diagnostic applications, and their efficacy in clinical settings are thoroughly explored. Through an extensive analysis of recent research findings and emerging trends, this review underscores the transformative potential of nanoporous materials in advancing biomedical imaging and diagnostics. The integration of interdisciplinary approaches, innovative synthesis techniques, and functionalization strategies offers promising avenues for the development of next-generation imaging agents and diagnostic tools with enhanced sensitivity, specificity, and biocompatibility.

Magneto-Luminescent Two-Dimensional Nanosheets of Gadolinium and Gold Nanocluster Assemblies with Surface Molecular Functionalization for White Light Emission.

We report the formation of photoluminescent two-dimensional (2D) crystalline nanosheet assemblies of gadolinium ions and ligand-stabilized gold nanoclusters (Gd-Au NCs). Transmission electron microscopy, selected area electron diffraction in conjunction with atomic force microscopy, and field-emission scanning electron microscopy analyses substantiated the 2D nature of Gd-Au NC nanosheets. The optical and magnetic properties of the nanosheets were investigated by photoluminescence measurements and vibrating-sample magnetometry analyses. The so-formed crystalline product was further utilized to generate a synchronous tricolor (orange, green, and blue) emission from a single excitation wavelength through an inorganic surface complexation reaction. The independent emissions were tunable after ligand functionalization by acetylsalicylic acid and fluorescein on the Gd-Au NC assembly. Interestingly, the assembled superstructure with augmented quantum yield led to white light emission at λexc ≈ 325 nm with CIE of (0.34, 0.33) and CRI value of >85 in the liquid phase. Furthermore, the ability to modulate the luminescence properties through the surface complexation of the 2D nanosheets of Au NCs may bring about new avenues toward applications in light-emitting devices, sensing, and biomedical imaging.

The Decompositions of Fluorescent Defects and Pristine Structure in (6,5) Carbon Nanotubes Using Various Oxidants

Fluorescent quantum defects in single-wall carbon nanotubes (SWCNTs) are outstanding candidates as fluorophores for in vivo biomedical imaging applications such as image-guided surgeries and single-cell tracking. Their longer wavelength emission in the short-wave infrared penetrates biological tissues deeper than visible and NIR light. In addition, fluorescent quantum defects can enhance fluorescence brightness by a factor of ~9 compared to the pristine SWCNT emission. Besides their exceeding optical properties, the degradations of SWCNTs in biological and environmental systems are also of importance, but still not well understood yet. This study utilizes sodium hypochlorite (NaClO) and hydrogen peroxide (H2O2) to examine the chemical decompositions of pristine and defect-containing SWCNTs. We found that the oxidation rate of NaClO is ~5 times faster than that of H2O2, showing an obvious oxidant-dependent degradation kinetics. It is also worth mentioning that when using NaClO as the oxidant, the oxidation rate is significantly increased under acidic conditions, probably due to the increased concentration of hypochlorous acid (HOCl). In contrast, H2O2 prefers to oxidize the pristine structure. It is also found that SWCNT coating materials including SDS, SC, and ssDNA might protect the surface structures, especially the defects, from oxidant attacks. We believe our study will lead to a better understanding of the SWCNT degradation, providing valuable insights for future clinical applications.

A fibre-optic ultrasound sensor of simple fabrication.

The small size, high sensitivity, and immunity to electromagnetic interference of fibre-optic ultrasound sensors make them highly attractive for applications in biomedical imaging and metrology. Typically, such sensors rely on optically resonant structures, such as Fabry-Perot cavities, that require elaborate fabrication techniques. Here, an alternative fibre-optic ultrasound sensor is presented that comprises a simple deformable and reflective structure that was deposited using simple dip-coating. Interrogation with a laser Doppler vibrometer demonstrated how this sensor achieved a sensitivity, signal-to-noise ratio, and noise-equivalent pressure that outperformed piezoelectric hydrophones, whilst offering a highly miniature form factor, turn-key operation, and simple fabrication.

Erythrocyte nano-ghosts with dual optical and magnetic resonance characteristics.

Fluorescent organic dyes provide imaging capabilities at cellular and sub-cellular levels. However, a common problem associated with some of the existing dyes such as the US FDA-approved indocyanine green (ICG) is their weak fluorescence emission. Alternative dyes with greater emission characteristics would be useful in various imaging applications. Complementing optical imaging, magnetic resonance (MR) imaging enables deep tissue imaging. Nano-sized delivery systems containing dyes with greater fluorescence emission as well as MR contrast agents present a promising dual-mode platform with high optical sensitivity and deep tissue imaging for image-guided surgical applications. We have engineered a nano-sized platform, derived from erythrocyte ghosts (EGs), with dual near-infrared fluorescence and MR characteristics by co-encapsulation of a brominated carbocyanine dye and gadobenate dimeglumine (Gd-BOPTA). We have investigated the use of three brominated carbocyanine dyes (referred to as BrCy106, BrCy111, and BrCy112) with various degrees of bromination, structural symmetry, and acidic modifications for encapsulation by nano-sized EGs (nEGs) and compared their resulting optical characteristics with nEGs containing ICG. We find that asymmetric dyes (BrCy106 and BrCy112) with one dibromobenzene ring offer greater fluorescence emission characteristics. For example, the relative fluorescence quantum yield ( ) for nEGs fabricated using of BrCy112 is -fold higher than nEGs fabricated using the same concentrations of ICG. The dual-mode nEGs containing BrCy112 and Gd-BOPTA show a nearly twofold increase in their as compared with their single optical mode counterpart. Cytotoxicity is not observed upon incubation of SKOV3 cells with nEGs containing BrCy112. Erythrocyte nano-ghosts with dual optical and MR characteristics may ultimately prove useful in various biomedical imaging applications such as image-guided tumor surgery where MR imaging can be used for tumor staging and mapping, and fluorescence imaging can help visualize small tumor nodules for resection.