Search Results (29)

In order to find a good candidate for Förster Resonance Energy Transfer (FRET)-mediated X-ray-induced photodynamic therapy (X-PDT) for the treatment of cancer, lanthanide (Ln)-based AGuIX nanoparticles (NPs) conjugated with Rose Bengal (RB) as a photosensitizer (PS) were synthesized. X-PDT overcomes the problem of the poor penetration of visible light into tissues, which limits the efficacy of PDT in the treatment of deep-seated tumors. It is essential to optimize FRET efficiency by maximizing the overlap integral between donor emission and acceptor absorption and lengthening the duration of the donor emission. In this study, we optimized energy transfer between a scintillator (Sc) as a donor and a PS as an acceptor. Terbium (Tb) and Gadolinium (Gd) as Scs and Rose RB as a PS were chosen. The study of energy transfer between Tb, Gd and RB in solution and chelated on AGuIX NPs proved to be FRET-like. RB was conjugated directly onto AGuIX NPs (i.e., AGuIX Ln@RB), and the use of a spacer arm (i.e., AGuIX Ln@spacer arm-RB) increased FRET efficiency. Singlet oxygen production by these NPs was observed under UV–visible illumination and X-ray irradiation. The in vitro bioassay demonstrated 52% cell death of U-251MG derived from human malignant glioblastoma multiforme at a concentration of 1 μM RB after illumination and irradiation (2 Gy, 320 kV, 10 mA, 3 Gy/min at 47 cm). In addition, the RB-coupled NRP-1-targeting peptide (i.e., K(RB)DKPPR) was conjugated onto AGuIX NPs by a thiol-maleimide click chemistry reaction, and an affinity in the nM range was observed. Full article

X-ray-induced photodynamic therapy (X-PDT) represents a promising new method of cancer treatment. A novel type of nanoscintillator based on cerium fluoride (CeF₃) nanoparticles (NPs) modified with flavin mononucleotide (FMN) has been proposed. A method for synthesizing CeF₃-FMN NPs has been developed, enabling the production of colloidal, spherical NPs with an approximate diameter of 100 nm, low polydispersity, and a high fluorescence quantum yield of 0.42. It has been demonstrated that CeF₃-FMN NPs exhibit pH-dependent radiation-induced redox activity when exposed to X-rays. This activity results in the generation of reactive oxygen species, which is associated with the scintillation properties of cerium and the transfer of electrons to FMN. The synthesized NPs have been demonstrated to exhibit minimal cytotoxicity towards normal cells (NCTC L929 fibroblasts) but are more toxic to tumor cells (epidermoid carcinoma A431). Concurrently, the synthesized NPs (CeF₃ and CeF₃-FMN NPs) demonstrate a pronounced selective radiosensitizing effect on tumor cells at concentrations of 10⁻⁷ and 10⁻³ M, resulting in a significant reduction in their clonogenic activity, increasing radiosensitivity for cancer cells by 1.9 times following X-ray irradiation at a dose of 3 to 6 Gy. In the context of normal cells, these nanoparticles serve the function of antioxidants, maintaining a high level of clonogenic activity. Functional nanoscintillators on the basis of cerium fluoride can be used as part of the latest technologies for the treatment of tumors within the framework of X-PDT. Full article

When exposed to X-rays, scintillators emit visible luminescence. X-ray-mediated optogenetics employs scintillators for remotely activating light-sensitive proteins in biological tissue through X-ray irradiation. This approach offers advantages over traditional optogenetics, allowing for deeper tissue penetration and wireless control. Here, we assessed the short-term safety and efficacy of candidate scintillator materials for neuronal control. Our analyses revealed that lead-free halide scintillators, such as Cs₃Cu₂I₅, exhibited significant cytotoxicity within 24 h and induced neuroinflammatory effects when injected into the mouse brain. In contrast, cerium-doped gadolinium aluminum gallium garnet (Ce:GAGG) nanoparticles showed no detectable cytotoxicity within the same period, and injection into the mouse brain did not lead to observable neuroinflammation over four weeks. Electrophysiological recordings in the cerebral cortex of awake mice showed that X-ray-induced radioluminescence from Ce:GAGG nanoparticles reliably activated 45% of the neuronal population surrounding the implanted particles, a significantly higher activation rate than europium-doped GAGG (Eu:GAGG) microparticles, which activated only 10% of neurons. Furthermore, we established the cell-type specificity of this technique by using Ce:GAGG nanoparticles to selectively stimulate midbrain dopamine neurons. This technique was applied to freely behaving mice, allowing for wireless modulation of place preference behavior mediated by midbrain dopamine neurons. These findings highlight the unique suitability of Ce:GAGG nanoparticles for X-ray-mediated optogenetics. The deep tissue penetration, short-term safety, wireless neuronal control, and cell-type specificity of this system offer exciting possibilities for diverse neuroscience applications and therapeutic interventions. Full article

Since bentonite can absorb neutrons and gamma rays without sacrificing structural integrity, it is frequently used as the main shielding material in many nuclear installations. Recently, there has been a trend toward enhancing the shielding qualities of bentonite by adding various chemicals. However, the majority of the added materials either require particular handling procedures or pose health risks. The availability of environmentally friendly additives would be wonderful. The addition of barite to bentonite composites greatly raises the density of the specimens. Additionally, the performance of bentonite–barite composites as radiation shielding materials is improved by adding various amounts of bulk and nano Bi₂O₃ as a filler (6%, 13%, and 20%). Energy dispersive X-ray analysis (EDX) was used to determine the chemical makeup of the produced specimens. The scanning electron microscopy (SEM) pictures showed the samples’ cross-sections’ porosity and homogeneity. ²⁴¹Am, ¹³³Ba, ¹³⁷Cs, and ⁶⁰Co are radioactive sources that emit energies of 59.53, 80.99, 356.01, 661.66, 1173.23, and 1332.5 keV, respectively, and the NaI (Tl) scintillation detector was used in this investigation. The area under the peak of the observed energy spectra was measured using the Genie 2000 program in both the specimen’s absence and presence. The coefficients for linear and mass attenuation were calculated. To determine the theoretical mass attenuation coefficients, the XCOM program was utilized and then compared to the corresponding experimental values. Various radiation shielding parameters dependent on the linear attenuation coefficient were computed for each studied composite. These parameters include the mean free path (MFP), half value layer (HVL), and tenth value layer (TVL). Also, the Z_eff and the EABF were determined for each specimen. According to the findings, bismuth oxide was added to bentonite–barite composites to reduce the transmitted flux through the specimens, which increased the LAC of the bentonite–barite composites. Furthermore, adding nanosized bismuth oxide particles increased the sample’s density and improved the material’s shielding properties. At a photon energy of 0.356 keV, the relative deviation (∆%) between the experimental nano- and micro values for Bi₂O₃ (20 wt%) was 12.1974, confirming that the nanoparticles increase attenuation efficiency. Full article

The application of a pulsed laser ablation technique for the generation of cerium-doped garnet nanoparticles in liquids is investigated. The morphological and optical properties of the obtained nanoparticles are demonstrated. Features introduced by the single crystals of Gd₃Al_2.4Ga_2.6O₁₂:Ce³⁺, Lu₃Al₅O₁₂:Ce³⁺, and Y₃Al_1.25Ga_3.75O₁₂:Ce³⁺ from which the nanoparticles are generated, as well as the parameters of a liquid media on the garnet nanoparticle generation are experimentally studied using TEM and UV-Vis spectroscopy methods. It is shown how the size, shape, and internal structure of the nanoparticles are related to the external laser ablation conditions, as well as to the laser melting processes of NPs in the colloidal solutions. This work provides important information about the generated nanoparticles, which can be used as building blocks for specially designed structures with predetermined optical properties. Full article

Polymer composites were synthesized via melt mixing for radiation shielding in the healthcare sector. A polymethyl-methacrylate (PMMA) matrix was filled with Bi₂O₃ nanoparticles at 10%, 20%, 30%, and 40% weight percentages. The characterization of nanocomposites included their morphological, structural, and thermal properties, achieved using SEM, XRD, and TGA, respectively. The shielding properties for all synthesized samples including pristine PMMA were measured with gamma spectrometry using a NaI (Tl) scintillator detector spanning a wide range of energies and using different radioisotopes, namely Am-241 (59.6 keV), Co-57 (122.2 keV), Ra-226 (242.0), Ba-133 (80.99 and 356.02 keV), Cs-137 (661.6 keV), and Co-60 (1173.2 and 1332.5 keV). A substantial increase in the mass attenuation coefficients was obtained at low and medium energies as the filler weight percentage increased, with minor variations at higher gamma energies (1173 and 1332 keV). The mass attenuation coefficient decreased with increasing energy except under 122 keV gamma rays due to the K-absorption edge of bismuth (90.5 keV). At 40% loading of Bi₂O_3, the mass attenuation coefficient for the cesium ¹³⁷Cs gamma line at 662 keV reached the corresponding value for the toxic heavy element lead. The synthesized PMMA-Bi₂O₃ nanocomposites proved to be highly effective, lead-free, safe, and lightweight shielding materials for X- and gamma rays within a wide energy range (<59 keV to 1332 keV), making them of interest for healthcare applications. Full article

Photodynamic therapy (PDT), the use of light to excite photosensitive molecules whose electronic relaxation drives the production of highly cytotoxic reactive oxygen species (ROS), has proven an effective means of oncotherapy. However, its application has been severely constrained to superficial tissues and those readily accessed either endoscopically or laparoscopically, due to the intrinsic scattering and absorption of photons by intervening tissues. Recent advances in the design of nanoparticle-based X-ray scintillators and photosensitizers have enabled hybridization of these moieties into single nanocomposite particles. These nanoplatforms, when irradiated with diagnostic doses and energies of X-rays, produce large quantities of ROS and permit, for the first time, non-invasive deep tissue PDT of tumors with few of the therapeutic limitations or side effects of conventional PDT. In this review we examine the underlying principles and evolution of PDT: from its initial and still dominant use of light-activated, small molecule photosensitizers that passively accumulate in tumors, to its latest development of X-ray-activated, scintillator–photosensitizer hybrid nanoplatforms that actively target cancer biomarkers. Challenges and potential remedies for the clinical translation of these hybrid nanoplatforms and X-ray PDT are also presented. Full article

Inorganic scintillators are of great significance in the fields of medical CT, high-energy physics and industrial nondestructive testing. In this work, we confirm that the Pb₄Lu₃F₁₇: Re (Re = Tb, Eu, Sm, Dy, Ho) crystals are promising candidates for a new kind of scintillator. Detailed crystal structure information is obtained by the Rietveld refinement analysis. Upon X-ray irradiation, all these scintillators exhibited characteristic 4f-4f transitions. The Ce and Gd ions were verified to be useful for enhancing the scintillation intensity via introducing energy transfer processes. The integrated scintillation intensity of the Pb₄Lu₃F₁₇: Tb/Ce is about 16.8% of the commercial CsI (Tl) single crystal. Our results manifested that Pb₄Lu₃F₁₇: Re has potential application in X-ray detection and imaging. Full article

Cerenkov-induced photodynamic therapy (CR-PDT) with the use of Gallium-68 (⁶⁸Ga) as an unsealed radioactive source has been proposed as an alternative strategy to X-ray-induced photodynamic therapy (X-PDT). This new strategy still aims to produce a photodynamic effect with the use of nanoparticles, namely, AGuIX. Recently, we replaced Gd from the AGuIX@ platform with Terbium (Tb) as a nanoscintillator and added 5-(4-carboxyphenyl succinimide ester)-10,15,20-triphenylporphyrin (P1) as a photosensitizer (referred to as AGuIX@Tb-P1). Although Cerenkov luminescence from ⁶⁸Ga positrons is involved in nanoscintillator and photosensitizer activation, the cytotoxic effect obtained by PDT remains controversial. Herein, we tested whether free ⁶⁸Ga could substitute X-rays of X-PDT to obtain a cytotoxic phototherapeutic effect. Results were compared with those obtained with AGuIX@Gd-P1 nanoparticles. We showed, by Monte Carlo simulations, the contribution of Tb scintillation in P1 activation by an energy transfer between Tb and P1 after Cerenkov radiation, compared to the Gd-based nanoparticles. We confirmed the involvement of the type II PDT reaction during ⁶⁸Ga-mediated Cerenkov luminescence, id est, the transfer of photon to AGuIX@Tb-P1 which, in turn, generated P1-mediated singlet oxygen. The effect of ⁶⁸Ga on cell survival was studied by clonogenic assays using human glioblastoma U-251 MG cells. Exposure of pre-treated cells with AGuIX@Tb-P1 to ⁶⁸Ga resulted in the decrease in cell clone formation, unlike AGuIX@Gd-P1. We conclude that CR-PDT could be an alternative of X-PDT. Full article

The development of X-ray-absorbing scintillating nanoparticles is of high interest for solving the short penetration depth problem of visible and infrared light in photodynamic therapy (PDT). Thus, these nanoparticles are considered a promising treatment for several types of cancer. Herein, gadolinium oxide nanoparticles doped with europium ions (Gd₂O₃:Eu³⁺) were obtained by using polyvinyl alcohol as a capping agent. Hybrid silica nanoparticles decorated with europium-doped gadolinium oxide (SiO₂-Gd₂O₃:Eu³⁺) were also prepared through the impregnation method. The synthesized nanoparticles were structurally characterized and tested to analyze their biocompatibility. X-ray diffraction, scanning electron microscopy, and transmission electron microscopy confirmed the high crystallinity and purity of the Gd₂O₃:Eu³⁺ particles and the homogeneous distribution of nanostructured rare earth oxides throughout the fumed silica matrix for SiO₂-Gd₂O₃:Eu³⁺. Both nanoparticles displayed stable negative ζ-potentials. The photoluminescence properties of the materials were obtained using a Xe lamp as an excitation source, and they exhibited characteristic Eu³⁺ bands, including at 610 nm, which is the most intense transition band of this ion. Cytotoxicity studies on mouse glioblastoma GL261 cells indicated that these materials appear to be nontoxic from 10 to 500 μg·mL⁻¹ and show a small reduction in viability in non-tumor cell lines. All these findings demonstrate their possible use as alternative materials in PDT. Full article

The development of cancer treatment techniques able to cure tumors located deep in the body is an urgent task for scientists and physicians. One of the most promising methods is X-ray-induced photodynamic therapy (X-PDT), since X-rays have unlimited penetration through tissues. In this work, octahedral iodide tungsten clusters, combining the properties of a scintillator and photosensitizer, are considered as a key component of nanosized polyurethane (pU) particles in the production of materials promising for X-PDT. Cluster-containing pU nanoparticles obtained here demonstrate bright photo- and X-ray-induced emission in both solid and water dispersion, great efficiency in the generation of singlet oxygen, and high sensitivity regarding photoluminescence intensity in relation to oxygen concentration. Additionally, incorporation of the cluster complex into the pU matrix greatly increases its stability against hydrolysis in water and under X-rays. Full article

Radiation (RT) remains the most frequently used treatment against cancer. The main limitation of RT is its lack of specificity for cancer tissues and the limited maximum radiation dose that can be safely delivered without damaging the surrounding healthy tissues. A step forward in the development of better RT is achieved by coupling it with other treatments, such as photodynamic therapy (PDT). PDT is an anti-cancer therapy that relies on the light activation of non-toxic molecules—called photosensitizers—to generate ROS such as singlet oxygen. By conjugating photosensitizers to dense nanoscintillators in hybrid architectures, the PDT could be activated during RT, leading to cell death through an additional pathway with respect to the one activated by RT alone. Therefore, combining RT and PDT can lead to a synergistic enhancement of the overall efficacy of RT. However, the involvement of hybrids in combination with ionizing radiation is not trivial: the comprehension of the relationship among RT, scintillation emission of the nanoscintillator, and therapeutic effects of the locally excited photosensitizers is desirable to optimize the design of the hybrid nanoparticles for improved effects in radio-oncology. Here, we discuss the working principles of the PDT-activated RT methods, pointing out the guidelines for the development of effective coadjutants to be tested in clinics. Full article

A novel and effective method to improve scintillation properties of glass-ceramics, such as intensity enhancement and decay-time shortening, is reported in this work. Compared with crystal scintillators, glass scintillators always have the problems of low efficiency and long decay; how to solve them has always been a scientific puzzle in the field of scintillation glass-ceramics. The plasma enhancement effect can be predicted to solve the above problems. Ag⁺ ions were diffused into glasses by ion exchange, and then Ag nanoparticles and CsPbBr₃ quantum dots were formed by heat treatment. The structure of the CsPbBr₃ perovskite consists of a series of shared corner PbBr₆ octahedra with Cs ions occupying the cuboctahedral cavities. By using Ag and the plasma resonance effect, the photoluminescence intensity of CsPbBr₃ quantum dot glasses was enhanced by 3 times, its radioluminescence intensity increased by 6.25 times, and its decay time was reduced by a factor of more than one. Moreover, the mechanism of photoluminescence and radioluminescence enhanced by Ag and plasma was discussed based on the experimental results and finite-difference time-domain method. We concluded that the increase in radioluminescence intensity was related to plasma enhancements and the energy exchange between Ag nanoclusters and CsPbBr₃ quantum dots. Doping Ag is a valid means to improve the scintillation luminescence of CsPbBr₃ quantum dot glasses, which can be applied in the field of scintillation. Full article

While there is great demand for effective, affordable radiation detectors in various applications, many commonly used scintillators have major drawbacks. Conventional inorganic scintillators have a fixed emission wavelength and require expensive, high-temperature synthesis; plastic scintillators, while fast, inexpensive, and robust, have low atomic numbers, limiting their X-ray stopping power. Formamidinium lead halide perovskite nanocrystals show promise as scintillators due to their high X-ray attenuation coefficient and bright luminescence. Here, we used a room-temperature, solution-growth method to produce mixed-halide FAPbX${}_3$ (X = Cl, Br) nanocrystals with emission wavelengths that can be varied between 403 and 531 nm via adjustments to the halide ratio. The substitution of bromine for increasing amounts of chlorine resulted in violet emission with faster lifetimes, while larger proportions of bromine resulted in green emission with increased luminescence intensity. By loading FAPbBr${}_3$ nanocrystals into a PVT-based plastic scintillator matrix, we produced 1 mm-thick nanocomposite scintillators, which have brighter luminescence than the PVT-based plastic scintillator alone. While nanocomposites such as these are often opaque due to optical scattering from aggregates of the nanoparticles, we used a surface modification technique to improve transmission through the composites. A composite of FAPbBr${}_3$ nanocrystals encapsulated in inert PMMA produced even stronger luminescence, with intensity 3.8× greater than a comparative FAPbBr${}_3$/plastic scintillator composite. However, the luminescence decay time of the FAPbBr${}_3$/PMMA composite was more than 3× slower than that of the FAPbBr${}_3$/plastic scintillator composite. We also demonstrate the potential of these lead halide perovskite nanocomposite scintillators for low-cost X-ray imaging applications. Full article

This work aimed to intensively study polypropylene samples (PP) embedded with micro- and nanoparticles of Bi₂O₃ for their application in radiation shielding. Samples were prepared by adding 10%, 20%, 30%, 40%, and 50% of Bi₂O₃ microparticles (mBi₂O₃) by weight, and adding 10% and 50% of Bi₂O₃ nanoparticles (nBi₂O₃), in addition to the control sample (pure polypropylene). The morphology of the prepared samples was tested, and also, the shielding efficiency of gamma rays was tested for different sources with different energies. The experimental LAC were determined using a NaI scintillation detector, the experimental results were compared with NIST-XCOM results, and a good agreement was noticed. The LAC values have been used to calculate some specific parameters, such as half value layer (HVL), mean free path (MFP), tenth value layer (TVL), and radiation protection efficiency (RPE), which are useful for discussing the shielding capabilities of gamma rays. The results of the shielding parameters show that the PP embedded with nBi₂O₃ gives better attenuation than its counterpart, PP embedded with mBi₂O₃, at all studied energies. Full article