Gold Core Shell Research Articles

Metal–organic framework-based SERS chips enable in situ and sensitive detection of dissolved hydrogen sulfide in natural water: Towards a bring-back-chip mode for field analysis

Hydrogen sulfide (H2S) in natural water plays an important role in carbon and sulfur cycles in biosphere. Current detection protocol is complicated, which need to “bring back water” to lab followed by gas chromatograph analysis. In situ, field detection is still challenging. Herein, a portable, sensitive surface enhanced Raman scattering (SERS) chip was proposed for in situ H2S sampling and SERS signal stabilizing, enabling a “bring back chip” manner for lab analysis. The SERS chip was composed of single core-shell gold nanorod-ZIF-8 framework (Au NR@ZIF-8) nanoparticle. Relying on headspace adsorption, evaporated H2S was enriched in the ZIF-8 shell and then reacted with Au NR, resulting in the weakening of the Au-Br bond Raman peak (175 cm−1) and the appearance of the Au-S bond Raman peak (273 cm−1). The SERS signal reached equilibrium in 10 min. The detection range of H2S was 0.1–2000 μg/L and limit of detection was 0.098 μg/L. SERS signal was not interfered by normal volatile gases. Moreover, SERS signal of a reacted chip was stable at an ambient condition, allowing for in situ sampling and bring-back detection. The applicability of the chip was verified by dynamic H2S monitoring during artificial black-odor water evolution, and in-field quantitative analysis of H2S content in river water and sediment. Finally, the chip was sealed in a waterproof breathable membrane device, which realized the detection of vertical profiles of H2S in the river. This work provided a promising tool for field analysis of H2S in natural environments.

Ellagic acid-enhanced biocompatibility and bioactivity in multilayer core-shell gold nanoparticles for ameliorating myocardial infarction injury

BackgroundMyocardial infarction (MI) is the main contributor to most cardiovascular diseases (CVDs), and the available post-treatment clinical therapeutic options are limited. The development of nanoscale drug delivery systems carrying natural small molecules provides biotherapies that could potentially offer new treatments for reactive oxygen species (ROS)-induced damage in MI. Considering the stability and reduced toxicity of gold-phenolic core-shell nanoparticles, this study aims to develop ellagic acid-functionalized gold nanoparticles (EA-AuNPs) to overcome these limitations.ResultsWe have successfully synthesized EA-AuNPs with enhanced biocompatibility and bioactivity. These core-shell gold nanoparticles exhibit excellent ROS-scavenging activity and high dispersion. The results from a label-free imaging method on optically transparent zebrafish larvae models and micro-CT imaging in mice indicated that EA-AuNPs enable a favorable excretion-based metabolism without overburdening other organs. EA-AuNPs were subsequently applied in cellular oxidative stress models and MI mouse models. We found that they effectively inhibit the expression of apoptosis-related proteins and the elevation of cardiac enzyme activities, thereby ameliorating oxidative stress injuries in MI mice. Further investigations of oxylipin profiles indicated that EA-AuNPs might alleviate myocardial injury by inhibiting ROS-induced oxylipin level alterations, restoring the perturbed anti-inflammatory oxylipins.ConclusionsThese findings collectively emphasized the protective role of EA-AuNPs in myocardial injury, which contributes to the development of innovative gold-phenolic nanoparticles and further advances their potential medical applications.Graphical

A sensor platform based on SERS detection/janus textile for sweat glucose and lactate analysis toward portable monitoring of wellness status

Herein we report a wearable sweat sensor of a Janus fabric based on surface enhanced Raman scattering (SERS) technology, mainly detecting the two important metabolites glucose and lactate. Janus fabric is composed of electrospinning PU on a piece of medical gauze (cotton), working as the unidirectional moisture transport component (R = 1305%) to collect and transfer sweat efficiently. SERS tags with different structures act as the probe to recognize and detect the glucose and lactate in high sensitivity. Core-shell structured gold nanorods with DTNB inside (AuNRs@DTNB@Au) are used to detect lactate, while gold nanorods with MPBA (AuNRs@MPBA) are used to detect glucose. Through the characteristic SERS information, two calibration functions were established for the concentration determination of glucose and lactate. The concentrations of glucose and lactate in sweat of a 23 years volunteer during three-stage interval running are tested to be 95.5, 53.2, 30.5 μM and 4.9, 13.9, 10.8 mM, indicating the glucose (energy) consumption during exercise and the rapid accumulation of lactate at the early stage accompanied by the subsequent relief. As expected, this sensing system is able to provide a novel strategy for effective acquisition and rapid detection of essential biomarkers in sweat.

Designing and evaluation of a novel electrochemical biosensor based on carbon quantum dots and gold core-shell to detect and measure Human T-lymphotropic Virus-1 (HTLV-1) in clinical samples

The objective of this investigation is to introduce an innovative electrochemical biosensor that can swiftly detect HTLV-1 DNA targets without the need for nucleic acid amplification. The biosensor is equipped with a highly precise antisense DNA oligonucleotide. Additionally, we introduce a new core–shell material, CQDs@AuNPs, for the surface modification of glassy carbon electrodes. L-Cysteine is utilized as a conductive bridge to enhance the binding capabilities, electron transfer efficiency, and conductivity. The biosensor incorporates methylene blue (MB) as an electrochemical indicator with differential pulse voltammetry (DPV) technique, facilitating swift detection within a mere 20 min. Furthermore, it has been able to attain a detection limit of 0.7 aM and quantitation limit of 6 copies/µL with an impressive linear range spanning from 10 aM to 100 nM that displays a positive slope along with exhibiting a remarkably high correlation coefficient measuring at approximately 0.99.We tested the biosensor using 40 HTLV-1 DNA real clinical samples, comprising 30 positive and 10 negative samples, as determined by standard RT-PCR. The biosensor demonstrated a specificity of 96.67% and an exceptional sensitivity of 100%. Rigorous quantitative analysis and statistical techniques, including t-tests, cutoff value determination, receiver operating characteristic curves, and box diagrams, clearly differentiated between the positive and negative groups. These findings underscore the potential of our innovative biosensor as a rapid, precise, and cost-effective tool for early detection of HTLV-1, which holds promise for efficient management and control of the virus.

Multimodal Spectroscopy Assays for Advanced Nano-Optics Approaches by Tuning Nano-Tool Surface Chemistry and Metal-Enhanced Fluorescence

In this research work, different chemical modifications were applied to gold nanoparticles and their use in enhanced non-classical light emitters based on metal-enhanced fluorescence (MEF) was evaluated. In order to achieve this, gold core–shell nanoparticles with silica shells were modified via multilayered addition and the incorporation of a covalently linked laser dye to develop MEF. Their inter-nanoparticle interactions were evaluated by using additional silica shell multilayers and modified cyclodextrin macrocycles. In this manner, the sizes and chemical surface interactions on the multilayered nanoarchitectures were varied. These optical active nanoplatforms led to the development of different nanoassembly sizes and luminescence behaviors. Therefore, the interactions and nanoassembly properties were evaluated by using various spectroscopic and nanoimaging techniques. Highly dispersible gold core–shell nanoparticles with diameters of 50–60 nm showed improved colloidal dispersion that led to single ultraluminescent gold core–shell nanoparticles with MEF. Then, the addition of variable silica lengths produced increased interactions and consequent nanoaggregation. However, the silanized nanoparticles were easily dispersible after agitation or sonication. Thus, their sizes were proportional only to the diameter and the van de Waals interaction did not affect their sizes in bulk. Then, the covalent linking of different concentrations of modified cyclodextrins was applied to the chemical surfaces by incorporating additional hydroxyl groups from the glucose monomeric unities of cyclodextrins. In this manner, variable larger-sized and inter-branched grafted gold core–shell silica nanoparticles were generated. The ultraluminescent properties were conserved due to the non-optical activity of the cyclodextrins. However, they generated enhanced ultraluminescence phenomena. Laser fluorescence microscopy nanoimaging showed enhanced resolutions in comparison to non-grafted supramolecular gold core–shell nanoparticles. The differences in their interactions and the sizes of the nanoassemblies were explained by their single nanoparticle diameters and the interacting chemical groups on their nanosurfaces. While the varied luminescence emissions generated were tuned by plasmonics, enhanced plasmonic phenomena and light scattering properties were seen depending on the type of nanoassembly. Thus, optically active and non-optically active materials led to different optical properties in the bright field and enhanced the excited state within the electromagnetic near-field of the gold nanotemplates. In this manner, it was possible to achieve high sensitivity by varying the spacer lengths and optical properties. Therefore, further perspectives regarding the design of nano-tools composed of light for various applications were discussed.

Synthesis and characterization of Au@Ag/Ce-UIO-66 nanocomposite for highly sensitive detection of sulfadiazine residue

Antibiotic residue detection plays a key role in ensuring human health. However, rapid, reliable, and highly sensitive detection methods are still insufficient. To tackle this challenge, in this study, the Au@Ag/Ce-UIO-66, a nanocomposite material consisting of bimetallic gold core and silver shell (Au@Ag) introduced on the surface of Ce-UIO-66, was successfully synthesized. By meticulously regulating the exact concentration and volume of silver nitrate, we successfully generated an optimal matrix. This significantly enhanced the detection capability of the probe molecule CV to an impressive concentration of 10−9 M, with a remarkably low relative standard deviation of 7.54 %. The matrix exhibits excellent surface-enhanced Raman scattering (SERS) performance and stability, reaching adsorption equilibrium within 30 min. Moreover, employing this substrate enables the detection of sulfadiazine at concentrations as minimal as 2.5 μg/L, significantly surpassing the standards set by the European Union. Notably, the Raman spectral signal of sulfadiazine maintains stability across various pH conditions at a concentration of 10−5 M. Finally, the adsorption mechanism and enhancement mechanism between Au@Ag/Ce-UIO-66 and sulfadiazine were explored.

Cell membrane-targeted surface enhanced Raman scattering nanoprobes for the monitoring of hydrogen sulfide secreted from living cells

Hydrogen sulfide (H2S), an important gas signal molecule, participates in intercellular signal transmission and plays a considerable role in physiology and pathology. However, in-situ monitoring of H2S level during the processes of material transport between cells remains considerably challenging. Herein, a cell membrane-targeted surface-enhanced Raman scattering (SERS) nanoprobe was designed to quantitatively detect H2S secreted from living cells. The nanoprobes were fabricated by assembling cholesterol-functionalized DNA strands and dithiobis(phenylazide) (DTBPA) molecules on core-shell gold nanostars embedded with 4-mercaptoacetonitrile (4-MBN) (AuNPs@4-MBN@Au). Thus, three functions including cell-membrane targeted via cholesterol, internal standard calibration, and responsiveness to H2S through reduction of azide group in DTBPA molecules were integrated into the nanoprobes. In addition, the nanoprobes can quickly respond to H2S within 90 s and sensitively, selectively, and reliably detect H2S with a limit of detection as low as 37 nM due to internal standard-assisted calibration and reaction specificity. Moreover, the nanoprobes can effectively target on cell membrane and realize SERS visualization of dynamic H2S released from HeLa cells. By employing the proposed approach, an intriguing phenomenon was observed: the other two major endogenous gas transmitters, carbon monoxide (CO) and nitric oxide (NO), exhibited opposite effect on H2S production in living cells stimulated by related gas release molecules. In particular, the introduction of CO inhibited the generation of H2S in HeLa cells, while NO promoted its output. Thus, the nanoprobes can provide a robust method for investigating H2S-related extracellular metabolism and intercellular signaling transmission.

Multiplexed Surface Protein Detection and Cancer Classification Using Gap-Enhanced Magnetic-Plasmonic Core-Shell Raman Nanotags and Machine Learning Algorithm.

Cancer is the second leading cause of death attributed to disease worldwide. Current standard detection methods often rely on a single cancer marker, which can lead to inaccurate results, including false negatives, and an inability to detect multiple cancers simultaneously. Here, we developed a multiplex method that can effectively detect and classify surface proteins associated with three distinct types of breast cancer by utilizing gap-enhanced Raman scattering nanotags and machine learning algorithm. We synthesized anisotropic magnetic core-gold shell gap-enhanced Raman nanotags incorporating three different Raman reporters. These multicolor Raman nanotags were employed to distinguish specific surface protein markers in breast cancer cells. The acquired signals were deconvoluted and analyzed using classical least-squares regression to generate a surface protein profile and characterize the breast cancer cells. Furthermore, computational data obtained via finite-difference time-domain and discrete dipole approximation showed the amplification of the electric fields within the gap region due to plasmonic coupling between the two gold layers. Finally, a random forest classifier achieved an impressive classification and profiling accuracy of 93.9%, enabling effective distinguishing between the three different types of breast cancer cell lines in a mixed solution. With the combination of immunomagnetic multiplex target specificity and separation, gap-enhancement Raman nanotags, and machine learning, our method provides an accurate and integrated platform to profile and classify different cancer cells, giving implications for identification of the origin of circulating tumor cells in the blood system.

A core-shell structured AuNPs@ZnCo-MOF SERS substrate for sensitive and selective detection of thiram.

Surface-enhanced Raman scattering (SERS) enables pesticide residue monitoring to become facile and efficient. In this study, a core-shell structured gold nanoparticles@ZnCo metal-organic framework (AuNPs@ZnCo-MOF) SERS substrate was designed and successfully synthesized for efficient and selective detection of thiram. The bimetallic ZnCo-MOF shell can not only enrich the targeted molecules in the electromagnetic field because of its excellent absorptive capacity, but also act as a stabilized matrix for protecting the AuNPs from aggregation. The AuNPs@ZnCo-MOFs exhibited a high enhancement factor (EF) of 3.51 × 106 and a low detection limit of 1 × 10-7 mol L-1. Besides, the substrate material showed exceptional stability for up to 28 days at room temperature. The AuNPs@ZnCo-MOFs were used to detect thiram which displayed wide linearity (1 × 10-7 to 1 × 10-4 mol L-1) and high recoveries (83.45-99.61%). Moreover, the AuNPs@ZnCo-MOF SERS substrate exhibited excellent anti-interference ability and size selectivity for the target molecules. These indicate that the AuNPs@ZnCo-MOF substrate has great potential for the detection of thiram residues in practical applications.

Ultra-sensitive detection of tumor necrosis factor alpha based on silver-coated gold core shell and magnetically separated recognition of SERS aptamer sensors.

A highly sensitive tumor necrosis factor α (TNF-α) detection method based on a surface-enhanced Raman scattering (SERS) magnetic patch sensor is reported. Magnetic beads (MNPs) and core shells were used as the capture matrix and signaling probe, respectively. For this purpose, antibodies were immobilized on the surface of magnetic beads, and then Au@4-MBN@Ag core-shell structures coupled with aptamers and TNF-α antigen were added sequentially to form a sandwich immune complex. Quantitative analysis was performed by monitoring changes in the characteristic SERS signal intensity of the Raman reporter molecule 4-MBN. The results showed that the limit of detection (LOD) of the proposed method was 4.37 × 10-15 mg·mL-1 with good linearity (R2 = 0.9918) over the concentration range 10-12 to 10-5 mg·mL-1. Excellent assay accuracy was also demonstrated, with recoveries in the range 102% to 114%. Since all reactions occur in solution and are separated by magnetic adsorption of magnetic beads, this SERS-based immunoassay technique solves the kinetic problems of limited diffusion and difficult separation on solid substrates. The method is therefore expected to be a good clinical tool for the diagnosis of the inflammatory biomarker THF-α and in vivo inflammation screening.

Ag@Au core–shell nanoparticle-based surface-enhanced Raman scattering coupled with chemometrics for rapid determination of chloramphenicol residue in fish

The alarming increase in drug-resistant bacteria in fish resulting from the misuse of antibiotics poses a significant threat to ecosystems and human health. Therefore, the development of a reliable approach for detecting antibiotic residues in fish is crucial. In this study, a rapid and simple method for detecting chloramphenicol (CAP) residue in tilapia was developed using surface-enhanced Raman scattering (SERS) combined with chemometric algorithms. Silver and gold core–shell nanoparticles (Ag@Au CSNPs) were used as SERS nanosensors to achieve strong signal amplification with an enhancement factor of 2.67 × 106. The results demonstrated that the variable combination population analysis-partial least square (VCPA-PLS) model combined with the standard normal variable transformation pretreatment method exhibited the best predictive performance with a detection limit of 1 × 10−5 µg/mL. Thus, an SERS technique was established based on Ag@Au CSNPs combined with VCPA-PLS to rapidly detect CAP in tilapia.

A point-of-care solid-phase colorimetric sensor based on the enzyme-induced metallization for ALP detection

Alkaline phosphatase (ALP) is a crucial biomarker for clinical diagnosis, which is closely related to the physiological homeostasis regulation process of human body. And the abnormal level of ALP is associated with numerous diseases, such as liver dysfunction, bone diseases, diabetes, and so on. In order to meet the demand of personalized healthcare, it is particularly important to develop a miniaturized point-of-care testing (POCT) device for ALP detection. Herein, a portable solid-phase colorimetric sensor based on enzyme-induced metallization signal amplification strategy was constructed for ALP detection. The AuNPs modified on the glass slides acted as crystal seeds, allowing Ag+ in the solution to be reduced and deposited on the surface of AuNPs, which further formed the gold core and silver shell (Au@Ag) complex and generated visual signals. The visual signals were recorded by a smartphone and quantified using open-source ImageJ software. Under the optimal conditions, the proposed method exhibited a good linear relationship from 2.0 to 16.0 pM, and the detection limit was as low as 0.9 pM. In addition, it was further successfully applied for ALP detection in non-transparent and complex samples (milk, different types of cells). A sensitive, low cost, rapid and convenient solid-phase sensor was developed for ALP detection, which was expected to provide a promising strategy for POCT devices.

Synthesis gold and jade type core shell structure Pt@Sn in deboronated MWW zeolite and its good performance for light alkane dehydrogenation

The Pt@Sn core–shell structure was generated in MWW zeolite catalysts prepared by atom-planting incorporated Sn and deposition–precipitation (DP) loaded Pt for direct dehydrogenation of ethane or propane and CO2 oxidative dehydrogenation. The introduced Sn species can immobilize cubic structure Pt nanoparticle with well dispersed particles by DP method through the charge’s attraction. The stronger charge transfer between Pt-Sn improves the catalyst activity for the C-H band breaking of alkane. The zeolite skeleton incoporated Sn formed Sn-O-Si bond and can be broken to be extracted from the zeolite structure as SnO2 under the dehydrogenation process. The extracted SnO2 in the ‘half-cup’ external supercage encapsulates the Pt nanoparticle and forms the gold and jade type core–shell structure, which reduces the Pt agglomeration and modifies the Pt nanoparticle crystal edge and corner active sites and reduced the C-C band cleavage to side products and coke formation, thus improving the dehydrogenation selectivity and stability.

Bi-coloured enhanced luminescence imaging by targeted switch on/off laser MEF coupling for synthetic biosensing of nanostructured human serum albumin.

In this communication luminescent bioconjugated human serum albumin nanostructures (HSA NPs) with tiny ultraluminescent gold core-shell silica nanoparticles (Au@SiO2-Fl) were designed with enhanced bi-coloured luminescence properties. The HSA NPs were obtained from Human Serum Albumin free (HSA free) through the desolvation method, and Au@SiO2-Fl, through modified Turkevich and Störber methods. In this manner, porous HSA Nanostructures of 150.0-200nm and Au@SiO2-Fl 45.0nm final diameters were obtained. Both methodologies and structures were conjugated to obtain modified Nanocomposites based on tiny gold cores of 15nm surrounded with well spatial Nanostructured architectures of HSA (d15 Au@SiO2-Fl-HSA) that generated variable nanopatterns depending on the modified methodology of synthesis applied within colloidal dispersions. Therefore, three methodologies of non-covalent conjugation were developed. In optimal conditions, through Transmission Electronic Microscopy (TEM), well resolved multilayered nano-architectures with a size 190.0-200nm in average with variable contrast depending of the focused nanomaterial within the nanocomposite were shown. Optimized nanoarchitecture was based on a template tiny gold core-shell surrounded by nanostructured HSA NPs (d15 Au@SiO2-Fl-HSA). In this manner, the NanoImaging generated by laser fluorescence microscopy permitted to record improved optical properties and functionalities, such as: (i) enhanced ultraluminescent d15 Au@SiO2-Fl-HSA composites in comparison to individual components based on Metal Enhanced Fluorescence (MEF); (ii) diminished photobleaching; (iii) higher dispersibility; (iv) higher resolution of single bright nano-emitters of 210.0nm sizes; and (v) enhanced bi-coloured Bio-MEF coupling with potential non-classical light delivery towards other non-optical active biostructures for varied applications. The characterization of these nanocomposites allowed the comparison, evaluation and discussion focused on new properties generated and functionalities based on the incorporation of different types of tuneable materials. In this context, the biocompatibility, Cargo confined spaces, protein-based materials, optical transparent could be highlighted, as well as optical active materials. Thus, the potential applications of nanotechnology to both nanomedicine and nano-pharmaceutics were discussed.

Thermal Behavior of Silver–Gold Core–Shell Nanocubes: In Situ X-ray Diffraction and In Situ Electron Microscopy (SEM and TEM)

Thermal Behavior of Silver–Gold Core–Shell Nanocubes: In Situ X-ray Diffraction and In Situ Electron Microscopy (SEM and TEM)

Thermal-Induced Convective Flow around Core–Shell Gold Nanodimers under Continuous-Wave Laser Irradiation: Implications for Nanofluidics

Thermal-Induced Convective Flow around Core–Shell Gold Nanodimers under Continuous-Wave Laser Irradiation: Implications for Nanofluidics

Precise tuning of silica pore length and pore diameter on silica-encapsulated gold core–shell nanoparticles and catalytic impact

The ability to individually tune the pore length and pore diameter of silica-encapsulated gold core–shell nanoparticles (CSNPs) via a seeded encapsulation method is demonstrated and their impact on catalysis determined. Reducing the solvent volume during the shell growth phase resulted in CSNPs with shells of increasing thickness from 75 nm to 202 nm, following a linear relationship. The addition of 1, 3, 5-triisopropylbenzene (TIB) during synthesis increased the average pore diameter from 25 Å to 32 Å by swelling the pore template, swelling further to 38 Å when adding both TIB and n-decane. By decoupling the gold core reduction and silica condensation stages, gold core diameters were largely unaffected by silica growth reaction conditions. This was achieved by encapsulating CTAB-stabilized nanoparticles rather than reducing and stabilizing the nanoparticles during silica condensation. When used to catalyze solvent-free benzyl alcohol oxidation, it was found that CSNPs with increasing shell thicknesses demonstrated increased formation of the desirable aldehyde product, holding the undesired ester product yield constant. In contrast, CSNPs with increasing pore diameter exhibit increased formation of both aldehyde and ester products unselectively. These results—uniquely observed through the parametric isolation of pore length and diameter—suggest the reactant concentration at the pore wall due to hydrogen bonding, forming concentric “microphases” within the pores.

Evaporative self-assembling bioconcentrators onto superhydrophobic micropyramidal arrays as rapid and intelligent blood cancer filtering platforms

Harnessing the power of artificial intelligence (AI) for rapid and accurate cancer diagnosis is invaluable for medical practice, but technically challenging due to the low sensitivity and low selectivity of traditional bio-analytical methods. Here, we explored an AI-driven filtering method integrated with a plasmonic bioconcentrator for rapid, sensitive, and accurate blood cancer diagnosis. The bioconcentrator were sequentially dual-assembled by sequentially depositing multi-walled carbon nanotubes and core-shell gold silicon dioxide nanoparticles onto a laser-fabricated superhydrophobic surface with micropyramidal arrays. The laser spectroscopic sensing technique, nanoparticle-enhanced laser-induced breakdown spectroscopy, was applied to obtain the fingerprint information of serum samples from four types blood cancers and one health control. Furthermore, the principal component analysis and support vector machine algorithms were performed to discriminate the serum samples for AI-driven filtering. The results demonstrated that the integration of AI-driven filtering with bioconcentrator enabled sensitive and accurate diagnosis of blood cancers with several minutes. Rapid, cost-effective, and personalized cancer treatment could be envisioned by the AI-driven cancer filtering with the plasmonic bioconcentrator.

Au NBPs@ZIF‑67 nanoprobe based single-particle glutathione assay by dark-field microscopy

Abnormal level of glutathione (GSH) was usually related to some physiological and pathological diseases. Thus, developing an intelligent probe for the quantification of GSH was of great significance. Here, we proposed a general, simple, and rapid in situ synthesis strategy for preparing a novel plasmonic core-shell nanoprobe gold nanobipyramids@zeolitic imidazolate framework-67 (Au NBPs@ZIF-67) to realize the quantification of GSH in human serum sample at the single particle level. Mechanism research showed that the Co2+ (the metal node of ZIF-67) would be reduced by GSH, which resulted in the breakdown of ZIF-67 in the presence of GSH, and the scattering color of the nanoprobe would change from green to red under dark-field microscopy. Tricolor (RGB) analysis exhibited that the R/G value was linearly related to the concentration of GSH in the range of 0.01–1 μM (R2 = 0.999) and the detection limit was 5.7 nM. Besides, this GSH sensing strategy exhibited high selectivity, which demonstrated a satisfactory recovery in human serum sample. This work provided a general method of synthesizing a type of intelligent core-shell scattering nanoprobe and the single particle detection strategy indicated promising application under the biological milieu.

Translocation and fate of nanospheres in pheochromocytoma cells following exposure to synchrotron-sourced terahertz radiation.

The routes by which foreign objects enter cells is well studied; however, their fate following uptake has not been explored extensively. Following exposure to synchrotron-sourced (SS) terahertz (THz) radiation, reversible membrane permeability has been demonstrated in eukaryotic cells by the uptake of nanospheres; nonetheless, cellular localization of the nanospheres remained unclear. This study utilized silica core-shell gold nanospheres (AuSi NS) of diameter 50 ± 5 nm to investigate the fate of nanospheres inside pheochromocytoma (PC 12) cells following SS THz exposure. Fluorescence microscopy was used to confirm nanosphere internalization following 10 min of SS THz exposure in the range 0.5-20 THz. Transmission electron microscopy followed by scanning transmission electron microscopy energy-dispersive spectroscopic (STEM-EDS) analysis was used to confirm the presence of AuSi NS in the cytoplasm or membrane, as single NS or in clusters (22% and 52%, respectively), with the remainder (26%) sequestered in vacuoles. Cellular uptake of NS in response to SS THz radiation could have suitable applications in a vast number of biomedical applications, regenerative medicine, vaccines, cancer therapy, gene and drug delivery.