Search Results (203)

The critical binding of quantum states in Screened Coulomb Potentials such as Yukawa/Debye, Hulthén, and ECSC (Exponential Cosine Screened Coulomb) potentials is of perennial interest and relevance in many fields of science, ranging from nuclear and particle physics; plasma physics, astrophysics, cosmology, and nuclear fusion; physical chemistry, condensed matter, and materials physics; to synthetic nanostructures and nanophotonics. The purpose of this paper is to heuristically explore two related mysteries, one new, the other more than 50 years old. The solutions to these mysteries have implications for a much broader class of potentials, those addressed by Klaus and Simon. In our recent paper we presented numerical calculations using the Phase Method (PM), which is accurate to 60 digits and to screening lengths $\mathcal{D}\le {10}^3$ au and l = 0–20 of the critical binding parameters for these potentials and, for Yukawa and ECSC, l = 0–12 to $\mathcal{D}\le {10}^5$ au, at 30 digits. In doing so, we discovered an anomalous period-40 sawtooth structure in the critical parameters of the ECSC potential that is not observed for the Yukawa potential. In this second paper, we quantitatively explain the origin and periodicity of this newly discovered structure. To do so, we use two complementary approaches: a “neoclassical” (NC) variant of conventional semiclassical phase-space quantization and the PM for very precise fully quantum calculations. The observed period-40 sawtooth structure is quantitatively explained in terms of a novel “tick-tock” mechanism. The periodicity is calculated in terms of the ratio of phase-space integrals for the primary and secondary potential wells. A quartic double-well potential is used as a simple model to further illustrate the tick-tock mechanism. Using the NC method, an approximate expression is derived to predict the locations of tick-tock glitches from higher-order wells; it is confirmed by a PM calculation up to $\mathcal{D}\le {10}^6$ au. The second mystery is a strangely linear dependence of the total number of bound states vs. screening length for both the Yukawa and ECSC potentials. Using the PM, we confirm and extend these empirical relations. We show, using the PM, that an approximate trivariate linear relation between the square root of the critical screening length $\sqrt{D_c}$, state number n, and angular momentum l applies to these potentials. This, plus a geometrical state accumulation argument, solve the second mystery. We show these properties derive from the scaling relation between screening length and coupling constant and, as such, are predicted to be applicable to the whole class of potentials. These results are expected to be of both theoretical interest and experimental relevance when interpreting spectra or calculating thermal properties. The significance of these results, and the applicability of these methods and conclusions to a vast array of related potentials, is briefly discussed. Full article

The thiourea grafting method can effectively improve the ability of activated carbon to recover chloroauric acid (AuCl₄⁻). Conventional grafting strategies rely on acyl halide reactions using reagents such as SOCl₂ and CH₂Cl₂, which suffer from instability and high toxicity. Herein, we propose a green grafting strategy for thiourea by activating carboxyl groups with EDC-HCl/NHS in acetonitrile, followed by the amidation reaction to obtain thiourea-modified carbon (AC-NCS). FT-IR and XPS analyses confirm the successful grafting of thiourea onto the activated carbon surface. Compared with pristine activated carbon, the adsorption capacity of AC-NCS is 104.8 mg/g, increased by 5.76 times. Furthermore, it maintains a recovery rate of 84.2% after three cycles. XPS and FT-IR further reveal that adsorption occurs on the thiourea sulfur atoms (C=S) and protonated primary amines(-NH₃⁺), and the recovery of chloroauric acid is achieved through a synergistic “reduction–electrostatic attraction” mechanism. This method reduces the dependence on highly toxic reagents and provides a promising approach for the efficient and green recovery of gold from secondary resources. Full article

Dopamine (DA) is essential for motor control, motivation, and cognition, and its dysregulation is associated with neurological and psychiatric disorders such as Parkinson’s disease, schizophrenia, and addiction. Accurate and selective DA quantification in complex biological matrices is important, but remains challenging because of coexisting interferents and the low physiological concentration of DA. Here, we report a disposable electrochemical DA sensor based on screen-printed carbon electrodes (SPCEs) modified with metal–organic framework-derived gold nanocomposites (MOFD-AuNCs). The optimal material, synthesized with a 60 min NaBH₄ reduction step (MOFD-AuNC-60), exhibited superior electron-transfer kinetics compared with materials prepared at other reduction times. A single coating of MOFD-AuNC-60 on SPCEs enabled DA oxidation at a low potential (~0.05 V) with high selectivity in the presence of ascorbic acid and uric acid. In undiluted porcine serum, the sensor exhibited a dynamic range of 2.5–500 nM with a calculated detection limit of 0.5 nM. In undiluted human serum, it exhibited a dynamic range of 5–100 nM with a calculated detection limit of 4.4 nM. The MOFD-AuNC-60/SPCEs further demonstrated excellent reproducibility (relative standard deviation, 3%) and stability (7.5% current loss over 7 days). These results demonstrate that the proposed sensor provides a disposable, robust, and reliable sensing platform for direct DA detection in undiluted serum, showing promise for practical applications. Full article

Quantitative detection of alkaline phosphatase (ALP) activity is crucial in clinical diagnosis and bioanalysis. Herein, we have developed a highly sensitive electrochemiluminescence (ECL) biosensor that employs a biomimetic zirconia interface as its core sensing platform. The interface was constructed by immobilizing o-phosphorylethanolamine (PEA) onto zirconium oxide nanofilms (ZrO₂NFs), forming a surface rich in Zr-O-P bonds. This design mimics phosphate recognition and enzyme-triggered dephosphorylation processes, where ALP catalyzes the hydrolysis of these bonds, triggering a direct switch in the ECL signal from Ru(bpy)₃²⁺-loaded gold nanocage (Ru-AuNCs) emitters. This sensor achieves a wide linear range of 0.100–100 U/L and a low detection limit down to 0.0899 U/L. Its practical utility was validated through the accurate detection of ALP in fetal bovine serum samples, confirming high recovery and reliability. This strategy highlights the potential of biomimetic zirconia interfaces in developing robust biosensors for early disease diagnosis. Full article

Heavy metal mercury is one of the most significant and toxic environmental contaminants. Its inorganic form (Hg²⁺) and organic form (organic mercury, OrHg) can cause irreversible harm to human health and the ecological environment, and the latter is particularly prone to bioaccumulation and bioamplification in the food chain. Therefore, there is an urgent need for a rapid, reliable and specific detection of Hg²⁺ and OrHg to evaluate the potential risk for human health. Here, a novel label-free fluorescent sensing platform based on ssDNA aptamer (A_A-T7)-templated AuNCs was established for sensitive recognition and specific detection of Hg²⁺ and OrHg. In the presence of OrHg, the fluorescence of pure A_A-T7-templated AuNCs was visibly enhanced through forming Ag/AuNCs based on Ag⁰-doped AIEE effect. However, they were obviously quenched because of generating non-fluorescent Au/Ag/Hg ANPs via metallophilic interactions among Au³⁺, Ag⁺, and Hg²⁺ (5d¹⁰-4d¹⁰-5d¹⁰) when only Hg²⁺ existed. This fluorescent sensing platform could detect as low as 20.0 nM (4.0 ng Hg/g) and has a good linear detection range, with target concentrations ranging from 0.25 μM to 2.00 μM, recoveries of 98.0–108.0%, and RSD ≤ 5.0%. Low-toxic A_A-T7-templated AuNCs could be used for cytotoxicity analysis and intracellular fluorescent imaging. The method has been successfully applied to the determination of Hg²⁺ and OrHg in tap water, seawater and dried golden pomfret fish muscle samples, demonstrating promising prospects for the assay of mercury species in environmental samples and aquatic products to ensure human health and food safety. Full article

Background: Cancer is a major health concern that significantly impacts the global population. Selective chemotherapeutic delivery is needed to improve the efficacy of cancer therapy while minimizing side effects in healthy cells. This study investigated the potential of gold nanoclusters (AuNCs) functionalized with poly(amidoamine) dendrimers (PAMAM) and folic acid (FA) to selectively deliver doxorubicin (DOX) to cancer cells that express the folate receptor (FR). Methods: AuNC synthesis was confirmed via UV–visible and Fourier transform infrared spectroscopy, nanoparticle tracking analysis, and transmission electron microscopy. Folic acid (FA) was incorporated for cell surface receptor targeting, while the triphenylphosphonium cation (TPP⁺) was added to improve mitochondrial localization. Cytotoxicity (MTT), apoptosis, caspase 3/7, mitopotential, and oxidative stress assays were assessed using human MCF-7 (breast adenocarcinoma), HeLa (cervical carcinoma), Caco-2 (colon adenocarcinoma), MDA-MB-231 (epithelial breast cancer), and the embryonic kidney (HEK293) cells. Results: Favorable DOX loading (>78%), with more than 90% of the drug released at pH 4.5, was achieved. A dose-dependent increase in cytotoxicity was observed, with IC50 values lower in cancer cells than HEK293 cells, indicating selective toxicity and minimal off-target effects. Targeting nanocomplexes produced the best responses in the mitopotential, caspase, and oxidative stress assays in HeLa and MCF-7 cells. Conclusions: The improved cytotoxicity in cancer cells may be due to folate-receptor-mediated cellular uptake, as well as the mitochondrial uptake of TPP⁺ nanocomplexes. This highlighted the potential of the drug–AuNC nanocomplexes to limit systemic side effects, proposing a potential novel strategy for drug delivery to cancer cells. Full article

Current efforts to improve photodynamic therapy focus on nanomaterials that integrate deep tissue imaging with efficient reactive oxygen species generation. Gold nanoclusters (Au NCs) are promising alternatives to conventional photosensitizers due to their effective ROS production and enhanced biocompatibility when stabilized by a protein corona. However, both photosensitizers and Au NCs are typically activated by ultraviolet or visible light, which cannot penetrate deeper into tissues and is limited to superficial applications. Here, we report a near-infrared (NIR)-activated photodynamic nanoplatform based on core–shell upconverting nanoparticles (UCNPs; NaGdF₄:Yb³⁺,Er³⁺@NaGdF₄:Yb³⁺,Nd³⁺), functionalized with a protein corona containing bovine serum albumin-stabilized Au NCs (BSA–Au NCs) and photosensitizer chlorin e6 (Ce6). Spectroscopic data confirmed the formation of the UCNP-BSA–Au-Ce6 nanoplatform and demonstrated 32% energy transfer efficiency from UCNPs to Ce6, resulting in efficient reactive oxygen species generation under 808 nm irradiation. Cellular experiments confirmed the effective internalization and optimal biocompatibility of the nanoplatform in human breast cancer and healthy cells. Upon irradiation at 808 nm, the nanoplatform significantly reduced the viability of MDA-MB-231 cancer cells. These findings indicate that the UCNP-BSA–Au-Ce6 nanoplatform couples NIR activation with enhanced singlet oxygen production, providing a multifunctional platform for deep tissue imaging and NIR-activated photodynamic therapy. Full article

Fluorescent metal nanoclusters show great promise in heavy metal ion sensing. Herein, a bimetallic nanocluster (GSH-Au/Ag NCs) with orange fluorescence was synthesized through a facile one-pot method. The synthesized GSH-Au/Ag NCs displayed optimal excitation and emission peaks at 275 and 610 nm, respectively. The incorporation of silver can enhance the fluorescence of metal nanoclusters. The fluorescence of as-synthesized GSH-Au/Ag NCs can be significantly quenched by Hg²⁺ and Cu²⁺, and a “on–off” fluorescent probe was designed. The detection conditions, including pH and the concentration of the probe, were optimized. The respective detection limits for Hg²⁺ and Cu²⁺ ions under optimal detection conditions are estimated to be 40 nM and 33 nM, over the linear range of 100–1200 nM. Furthermore, a ratiometric fluorescent probe was prepared by mixing quinine sulfate and as-synthesized GSH-Au/Ag NCs. Hg²⁺ and Cu²⁺ can effectively quench the red fluorescence of GSH-Au/Ag NCs, whereas the blue fluorescence of quinine sulfate remains invariant. This leads to measurable changes in the RGB values of the resulting fluorescence images. The ratio (R/B) exhibits a linear relationship with the concentration of Hg²⁺ and Cu²⁺, enabling the determination of its concentration by analyzing RGB values in fluorescence images. This visual detection method significantly reduces both assay time and cost, making it suitable for on-site detection of heavy metal ions in water samples. Full article

In this work, a ratiometric fluorescent method for carbaryl detection is reported. We found that the combination of rapid hydrolysis of carbaryl and cetyltrimethylammonium bromide (CTAB) emulsification could significantly enhance the intrinsic weak blue fluorescence of carbaryl. By using red fluorescent glutathione-gold nanoculsters (GSH-Au NCs) as a reference signal, ratiometric detection of carbaryl within 3 min was successfully achieved. The method exhibited high sensitivity, with a linear response to carbaryl in the range from 1.0 to 70 ng/mL and an LOD of 0.05 ng/mL. The method was applied for detection of carbaryl in apple and cabbage samples, and recovery rates of 90~101% and 93~110%, respectively, were obtained. These results show that the proposed method for carbaryl detection has great potential for application in food sample monitoring. Full article

Monitoring the concentration of doxorubicin (DOX) was critical for tumor treatment, but existing methods failed to cross cell membrane. Here, an electrochemical platform for intracellular DOX detection in MCF-7 cells based on membrane-permeation strategy was developed. A modified gold electrode was prepared via electrodepositing AuNPs and assembling SH-DNA. Concurrently, the silica nanosphere/gold nanocluster-circular transmembrane peptide (SiO₂/AuNCs-iRGD) composite nanoparticles with membrane permeability, tumor targeting, and imaging capability were synthesized. After co-incubation of SiO₂/AuNCs-iRGD with MCF-7 cells and DOX, followed by co-incubation with the DNA-modified electrode, intracellular DOX intercalated into the DNA backbone, and redox-generated electrons were transferred to the electrode to produce a concentration-correlated electrochemical signal. The modification of the electrode, the morphology of the composite nanoparticles and the detection process were characterized by means of SEM, TEM, CV, EIS, DPV, fluorescence spectroscopy and laser confocal imaging. Under the optimized conditions, the proposed method exhibited a wide detection range of 0.05–300 μmol/L, with a detection limit of 0.01 μmol/L. Moreover, the modified electrode demonstrated satisfactory regenerability, and the proposed method showed excellent reproducibility and stability. The development platform could offer a new strategy for real-time assessment of drug concentration within cultured breast cancer cells in vitro. Full article

This study reports the precise synthesis of red-emitting gold–silver bimetallic nanoclusters (Au-AgNCs) via a one-pot hydrothermal method using thiolactic acid as both the ligand and reducing agent. The Au-AgNCs possess an average diameter of 1.85 nm and exhibit strong fluorescence emission at 687 nm. Furthermore, they display notable assembly-induced emission enhancement (AIEE) properties. Upon assembly with bovine serum albumin (BSA), their fluorescence quantum yield significantly increases from 2.50% to 7.78%. Then Au-AgNCs@BSA assembly was employed as a ratiometric fluorescence sensor for the detection of chlortetracycline (CTC). In the presence of CTC, the original red emission of the assembly at 687 nm remained stable, while a new blue emission emerged at 420 nm and intensified progressively with CTC concentration. The ratio of the two emission intensities (I₄₂₀/I₆₈₇) exhibited an excellent linear correlation with CTC concentration over the range of 0.10 to 15 μM, with a limit of detection (LOD) of 20 nM. Notably, the sensor demonstrated exceptional selectivity for CTC, showing negligible response to common interfering substances such as metal ions, anions, amino acids, and crucially, other tetracycline antibiotics (tetracycline, oxytetracycline, and doxycycline). The practical applicability of the sensor was validated through the determination of spiked CTC in real water samples, achieving satisfactory recovery rates. In conclusion, this work accomplishes two key objectives: the development of novel AIEE-active Au-Ag bimetallic nanoclusters and the design of an efficient ratiometric sensing strategy. This approach enables the highly selective and sensitive detection of CTC, offering a promising tool for environmental monitoring. Full article

Mycobacterium tuberculosis (M. tuberculosis) relies on the thioredoxin (Trx)–thioredoxin reductase (TrxR) system to maintain intracellular redox homeostasis and to support Trx-dependent DNA synthesis and repair, making TrxR a potential target for anti-tuberculosis therapy. Gold nanoclusters have been reported to inhibit human TrxR and suppress tumor growth, suggesting that gold-based nanomaterials can modulate TrxR activity. In this study, we report a previously uncharacterized oxidized crystal structure of M. tuberculosis TrxR containing two dimers in the asymmetric unit and use this structure to investigate inhibition by a glutathione-coated gold nanocluster (GSH-AuNC). Biolayer interferometry and enzymatic assays show that GSH-AuNC binds directly to M. tuberculosis TrxR and efficiently inhibits its catalytic activity at the purified enzyme level. Molecular dynamics simulations indicate that GSH-AuNC can occupy a surface pocket proximal to the active site, providing a plausible structural basis for enzyme engagement. AlphaFold3 modeling of the M. tuberculosis TrxR-Trx heterodimeric complex defines the interaction interface required for productive electron transfer and provides a structural hypothesis for how GSH-AuNC disrupts this process. Together, these results provide structural and mechanistic insights into the biochemical modulation of M. tuberculosis TrxR by GSH-AuNC, while the antimycobacterial activity of GSH-AuNC remains to be evaluated in future studies. Full article

Pancreatic function tests are used to determine the presence of chronic pancreatitis, particularly in the early stage of the disease. Chymotrypsin is an indicator of pancreatic function and is thus related to pancreatic diseases. However, these methods often require specific equipment and cannot always meet on-site analysis requirements. Consequently, a highly sensitive detection method needs to be developed. This research employed graphene oxide modified with NHS sensors and peptides (RRHFFGC: Arginine-Arginine-Histidine-Phenylalanine-Phenylalanine-Glycine-Cysteine) tagged with gold nanoclusters (Au NCs) for the detection of chymotrypsin. The N-Hydroxysuccinimide-(Polyethylene Glycol)₄-Dibenzocyclooctyne (NHS-PEG₄-DBCO) and graphene oxide (GO)-N₃ click reaction yielded GO-NHS material, appropriate for fluorescence quenching. The peptide chain was accurately broken with the introduction of chymotrypsin, and the Au NCs were situated far from the GO-NHS surface. The detection limit was 2.014 pg/mL. The results showed that the detection method had high sensitivity in comparison with the previous studies. This method is relevant to real samples due to its potential efficacy. Therefore, it is a promising method in the biomedical field. Full article

Co-reactants are essential in co-reactant-based electrochemiluminescence (ECL) systems because they generate reactive intermediates that can oxidize or reduce ECL luminophores, thereby driving ECL emission. In the context of ECL, gold nanoclusters (Au NCs) have emerged as innovative luminophores, owing to their tunable electronic structures and excellent biocompatibility. However, their efficiency in ECL applications is often compromised by challenges such as limited excited-state generation and non-radiative losses. To tackle these practical challenges, advanced co-reactant engineering strategies have been developed to improve the performance of Au NCs in ECL systems. This review begins with a brief overview of the mechanisms of ECL. Subsequently, a systematic overview of various co-reactant engineering strategies is presented, including: (1) using innovative co-reactants to replace traditional ones due to their lower toxicity and better biocompatibility; (2) applying co-reaction accelerators to reduce the onset potential and improve the production of reactive intermediates from co-reactants; (3) combining co-reactants with luminophores or creating integrated nanostructure assemblies of co-reactants, co-reaction accelerators, and luminophores to achieve shorter electron transfer paths and reduced energy loss for stable high-intensity ECL emission; (4) utilizing host-guest strategies that encapsulate co-reactants within cavities to stabilize radical intermediates and minimize environmental quenching. This review provides a comprehensive overview of recent developments in co-reactant engineering for Au NCs-based ECL systems, thereby encouraging further exploration and understanding of these systems and expanding their potential applications. Full article

Small interfering RNAs (siRNAs) have emerged as a powerful tool in the treatment of aggressive cancers. By exploiting and mimicking the natural gene regulation mechanism of RNA interference (RNAi), they allow for sequence-specific silencing of aberrant genes. siRNA-mediated knockdown of the inflammatory cytokine tumour necrosis factor-alpha (TNF-α) presents a novel therapy for triple-negative breast cancer (TNBC). This study investigated the potential of novel biomimetic glutathione-synthesised gold nanoclusters (AuNCs) as siRNA delivery vehicles. AuNCs were functionalized with biocompatible chitosan and polyethene glycol, and their interactions with siRNAs were investigated through binding studies. In vitro cytotoxicity and cellular uptake were conducted in the human breast cancer (MCF-7), TNBC (MDA-MB-231), and embryonic kidney (HEK293) cells, while the effect of anti-TNF-α siRNA nanocomplexes on biological processes, such as oxidative stress, apoptosis, and cell cycle distribution, was investigated using flow cytometry. UV–visible and Fourier transform infrared spectroscopy, as well as transmission electron microscopy, confirmed the synthesis and functionalization of the AuNCs. Functionalized AuNCs (FAuNC) effectively bound and condensed siRNA and protected against nuclease degradation. AuNCs facilitated efficient cellular uptake and were well-tolerated in vitro. Anti-TNF-α siRNA treatment of the MDA-MB-231 cells increased apoptosis and oxidative stress levels, and affected cell cycle distribution. Although the overall knockdown was low, these FAuNCs exhibited favorable physicochemical characteristics, low cytotoxicity and good cellular uptake in vitro, warranting further optimisation for improved delivery of therapeutic siRNAs. Full article