Specific Surface Plasmon Resonance Research Articles

6644 Glycosylation Patterns of the IgG Variable Region in Thyroglobulin Antibodies and Their Impact on Antigen Binding Affinity

Abstract Disclosure: S. Wang: None. Y. Cao: None. C. Zhao: None. C. Huang: None. K. Zhao: None. Y. Li: None. Y. Huang: None. Z. Ying: None. Y. Zhang: None. Y. Gao: None. Objective: Thyroglobulin antibodies (TgAb), key serological markers in Hashimoto's thyroiditis (HT) patients, are predominantly in immunoglobulin G (IgG) form. Prior research has highlighted the importance of increased glycosylation in TgAb IgG from HT patients. This study investigates the unique glycosylation patterns of F(ab')₂ fragments in TgAb IgG in HT patients, compared to healthy individuals. It focuses on how these patterns differ and their impact on binding to thyroglobulin (Tg). Exploring the role of N-glycosylation in the F(ab')₂ segment of TgAb IgG is crucial for understanding its effect on immune responses in HT, potentially unveiling key mechanisms of the disease. Methods: To assess serum TgAb levels in HT patients (n≥28), we used an electrochemiluminescence immunoassay, dividing patients into medium-level (mHT, n≥14) and high-level (hHT, n≥14) groups. TgAb IgG was isolated from serum of both HT and control groups (n = 14) using affinity chromatography. TgAb IgG was then cleaved with Ides enzyme to yield TgAb IgG F(ab’)2 and Fc fragments. The F(ab')2 fragment of TgAb IgG underwent MALDI-QIT-TOF-MS mass spectrometry for glycosylation profiling. Additionally, mixed TgAb IgG was separated using columns that recognize mannose and terminal sialic acid, yielding high mannose and high terminal sialic acid TgAb IgG. Different TgAb IgG glycoforms were prepared through enzymatic treatment with peptide-N-glycosidase F, β1-4 galactosidase, and α2-3,6,8 neuraminidase. The binding affinity of these TgAb IgG to Tg antigen was measured using Tg specific ELISA and surface plasmon resonance (SPR). Results: Using MALDI-TOF MS, we identified 22 IgG glycan types in both HT and control (Con) groups. In the hHT group, six glycan types (G0F, G1F, G2F, M5A1, A3G1F, A3F) were upregulated compared to Con, with statistical significance (p < 0.05). The mHT group showed increased levels of G1F and G2F compared to Con (p < 0.05). Between hHT and mHT, only A3F was significantly elevated (p < 0.05). Removal of N-glycosylation from IgG TgAb F(ab)2 reduced binding to Tg antigen. Presence of both mannose and terminal sialic acid in TgAb enhanced the binding to Tg. Conclusions: Most TgAb IgG in the variable region of HT patients contain N-glycans. The glycosylation patterns of TgAb IgG F(ab)2 in HT differ significantly from healthy controls, affecting antibody binding affinity. Our findings reveal the complex role of glycosylation patterns in TgAb IgG, providing new insights into HT pathogenesis and potential research directions. Presentation: 6/1/2024

Tightly and abundantly contacted Z-scheme heterojunction of Bi-modified TiO2/BiOCl: In-situ construction and boosting visible-light-driven purification of liquor brewing wastewater

The lower specific surface area and limited surface contact between BiOCl and TiO2 in composite fabricated by hybridization of TiO2 with BiOCl extremely hinder its catalytic performance. In this work, the area of interface contact between BiOCl and TiO2 was increased through the mediation of SiO2, and a Bi-modified ternary 0D/2D/2D TiO2/BiOCl Z-scheme heterojunction photocatalyst with large specific surface area (= 237.83 m2g−1) and surface plasmon resonance (SPR) effect was constructed in situ by ingeniously utilizing the reduction of carbon species generated during the calcination process. The results show that the COD removal rate of Bi/TBOC-10% for real liquor brewing wastewater (LBW) reaches 90.5% after 10 hours of visible light irradiation, which is 2.6 times and 2.1 times that of TiO2 and Degussa P25, respectively. The COD removal rate of the composite was reduced only by 8.9% after five cycles of performance test (50 h). Photoluminescence spectroscopy (PL), Transient Photocurrent Response (TPR), Electrochemical Impedance Spectroscopy (EIS) and BET characterization suggest that its excellent photocatalytic activity should be attributed to the Z-scheme heterojunction that broadens the light absorption range while retains strong oxidation-reduction active sites, the SPR effect that facilitates the separation and migration of photogenerated carriers, and high specific surface area of the composite that provides more active sites for the photodegradation reaction.

Green synthesis of silver nanoparticles using Houttuynia cordata Thunb rhizome extracts and their antibacterial potential against common foodborne pathogens

SummaryThe biological synthesis of functionalised nanoparticles using plant materials is considered more cost‐effective and eco‐friendly than chemical and physical methods. Hence, this study demonstrated the synthesis of silver nanoparticles (AgNPs) using Houttuynia cordata Thunb rhizome (HCR). The extract, prepared with distilled water, provided the required phytochemical components, such as flavonoids, terpenoids, phenols, proteins and other essential bio‐reducing agents. The AgNPs were exposed to reaction conditions, such as temperatures, pH values and AgNO3 concentrations, to identify the optimum synthesis condition and explore their impacts on particle size and antibacterial action against Gram‐positive (Staphylococcus aureus) and Gram‐negative (Salmonella enterica and Shigella dysenteriae) foodborne pathogens. The formation of AgNPs was indicated by specific surface plasmon resonance (SPR) intensity at 440–450 nm and colour changes under different reaction conditions. The structure and size distribution characterised by SEM and TEM revealed that the AgNPs exhibited a spherical‐shaped structure with irregular contours, regular distribution and aggregation. Although the average particle size ranged from 2 to 100 nm, relatively smaller sizes were detected at 10 mM (54.30), 80 °C (49.50 nm) and pH 6 (60.16 nm) conditions. The FTIR spectrum and EDX spectral signals affirmed the presence of reducing and stabilising agents in HCR extract, following the reduction of AgNPs from Ag+ to Ag0. AgNPs also exhibited excellent antibacterial activity against S. aureus, S. enterica and Sh. dysenteriae, indicating a broad spectrum for various applications in the food and pharmaceutical industries.

An Array SPRi Biosensor for the Determination of Follicle-Stimulating Hormone in Blood Plasma.

Follicle-stimulating hormone (FSH) regulates the development, growth, pubertal maturation and reproductive processes of the human body. The determination of serous FSH concentration is significant as an alternative to testicular biopsy in the case of boys suffering from cryptorchidism after orchidopexy, and as a means of determining the menopausal stage in women. The aim of this investigation is to develop a specific array surface plasmon resonance imaging (SPRi) biosensor for the determination of FSH in body liquids such as blood plasma, obtaining sufficient sensitivity to determine FSH at levels characteristic for that hormone in blood plasma, without any signal enhancement. The biosensor consists of a mouse monoclonal anti-FSH antibody attached to the gold surface of a chip via a cysteamine linker. Its linear response range is from 0.08 mIU mL-1 (LOQ) to 20 mIU mL-1, and well covers most of the range of FSH activities found in blood without dilution. The precision of measurement is between 3.2% and 13.1% for model samples, and between 3.7% and 5.6% for spiked plasma samples. Recoveries are in the range from 94% to 108%. The biosensor has good selectivity, and is validated by comparison with ECLE, with good agreement of the results.

A sensitive signal off photoelectrochemical aptasensor based on CuO nanosheets @Au nanoflowers for the detection of chloramphenicol

A signal off type photoelectrochemical (PEC) aptasensor was constructed for the sensitive detection of chloramphenicol based on CuO nanosheets (CuO NSs) and gold nanoflowers (Au NFs) modified indium tin oxide (ITO) electrode. CuO NSs was p-type photoactive semiconductor materials, which had narrow band gap and high absorption rate of visible light. After combining with Au NFs, the composite CuO NSs@Au NFs produced a strong cathodic photocurrent for the excellent electron conductivity, large specific surface area and Surface Plasmon Resonance effect (SPR) of Au NFs. At the same time, Au NFs provided a binding site for aptamer, which greatly improved the sensitivity of the constructed sensing platform. After the target chloramphenicol (CAP) was specifically captured by the aptamers on the electrode, the formed bioconjugates seriously hindered the transfer of electrons and the absorption of light and caused a reduced photocurrent. For the detection of CAP, this signal off type PEC aptasensor had a linear range of 5 pM-300 nM and a limit of detection of 49.9 fM (S/N = 3) with good stability, selectivity and reproducibility. Meanwhile, the method had satisfactory recovery results in the detection of CAP in real-life samples such as milk, tap water, honey and chloramphenicol eye drops.

Growth time dependency on the formation of gold nanobipyramids for efficient detection towards chlorpyrifos-based LSPR sensor

The structure of gold nanobipyramids (GNBPs) is very promising for specific Localized Surface Plasmon Resonance (LSPR) properties, and thus potentially to be used in various applications, especially in sensing. This work reported growth time dependency on the formation of GNBPs for application in LSPR sensors for chlorpyrifos detection. The study on the growth time found that GNBPs formation at the initial stage is dominated by elongation direction and its optimum growth time is 2 h. The optimum GNBPs with 106.32 ± 2.50 in length, 42.17 ± 0.82 in width and an aspect ratio of 2.55 ± 0.08 were implemented as a sensing material for direct and rapid localized surface plasmon resonance (LSPR) sensors to detect chlorpyrifos. The mechanism is based on the change in spectrum intensity and wavelength shift between GNBPs when tested in deionized water and chlorpyrifos solution. The change arises from molecular interaction between the targeted analyte and the sensing material and effectively changes the dielectric features of the medium. The presence of chlorpyrifos in the 1 – 100 mg/mL concentration range has been successfully detected. The proposed sensor offers better sensitivity as high as 1.22 times for transverse LSPR mode and 2.04 for longitudinal LSPR mode than the LSPR sensor based on gold nanosphericals. Moreover, the sensor stability and repeatability response showed a reliable performance for determining chlorpyrifos. Furthermore, this sensor also shows high selectivity towards chlorpyrifos compared to other organophosphate and organochlorine pesticides such as malathion, chlorothalonil, and triclopyr-butotyl.

Ganoderma lucidum-Mediated Green Synthesis of Silver Nanoparticles with Antimicrobial Activity.

"Green chemistry" is a simple and easily reproductible method that provides nanoparticles characterized by better stability and good dispersion in an aqueous solution. Nanoparticles can be synthesized by algae, bacteria, fungi, and plant extracts. Ganoderma lucidum is a commonly used medicinal mushroom with distinctive biological properties, such as antibacterial, antifungal, antioxidant, anti-inflammatory, anticancer, etc. In this study, aqueous mycelial extracts of Ganoderma lucidum were used to reduce AgNO3 to form silver nanoparticles (AgNPs). The biosynthesized nanoparticles were characterized by UV-visible spectroscopy, scanning electron microscopy (SEM), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) analysis. The maximum UV absorption was obtained at 420 nm, which represents the specific surface plasmon resonance band for biosynthesized silver nanoparticles. SEM images showed particles as predominantly spherical, while FTIR spectroscopic studies illustrated the presence of functional groups that can support the reducing of ion Ag+ to Ag(0). XRD peaks ratified the presence of AgNPs. The antimicrobial effectiveness of synthesized nanoparticles was tested against Gram-positive and Gram-negative bacterial and yeasts strains. The silver nanoparticles were effective against pathogens, inhibiting their proliferation, and thus reducing the risk to the environment and to public health.

Green synthesis of silver nanoparticles using Vernonia amygdalina plant extract and its antimicrobial activities

The green nanoparticles synthesis method from leaves extract revealed full an economical, sustainable and eco-friendly method. In this study, the leaf extract of Vernonia amygdalina was as a reducing and capping agent for the synthesis of silver nanoparticles (AgNPs). M/DW binary solvent was selected for its relatively better extraction performance than methanol, ethanol, distilled water and ethanol/distilled water. Furthermore, the effect of solvent ratio of M/DW, precursor concentration, ratio of silver nitrate (AgNO3) to plant extract, temperature, time and pH on the synthesis of AgNPs was carried out. Greenly synthesized Agents was confirmed using UV–Vis spectroscopy and characterized by XRD and FT-IR. Besides, its antimicrobial activities were also evaluated using agar diffusion techniques. The UV–Vis spectra showed specific Surface Plasmon Resonance (SPR) absorption peaks between 411 nm and 430 nm which revealed the formation of AgNPs during the synthesis. The nanoparticle synthesis was further confirmed by XRD analysis. Phytochemical screening test and FT-IR analysis of V. amygdalina leaves extract revealed the existence of phenolic, Tannin, saponins and flavonoid groups, which capped the nanoparticles during the synthesis. The antibacterial activities of the synthesized AgNPs were evaluated against Gram-positive bacteria (S. pyogenes and S. aureus) and Gram-negative bacteria (E. coli and P. aeruginosa) and higher inhibition zones were observed.

A Fully Integrated Miniaturized Optical Biosensor for Fast and Multiplexing Plasmonic Detection of High- and Low-Molecular-Weight Analytes.

Optical biosensors based on plasmonic sensing schemes combine high sensitivity and selectivity with label-free detection. However, the use of bulky optical components is still hampering the possibility of obtaining miniaturized systems required for analysis in real settings. Here, a fully miniaturized optical biosensor prototype based on plasmonic detection is demonstrated, which enables fast and multiplex sensing of analytes with high- and low molecular weight (80 000 and 582 Da) as quality and safety parameters for milk: a protein (lactoferrin) and an antibiotic (streptomycin). The optical sensor is based on the smart integration of: i) miniaturized organic optoelectronic devices used as light-emitting and light-sensing elements and ii) a functionalized nanostructured plasmonic grating for highly sensitive and specific localized surface plasmon resonance (SPR) detection. The sensor provides quantitative and linear response reaching a limit of detection of 10-4 refractive index units once it is calibrated by standard solutions. Analyte-specific and rapid (15 min long) immunoassay-based detection is demonstrated for both targets. By using a custom algorithm based on principal-component analysis, a linear dose-response curve is constructed which correlates with a limit of detection (LOD) as low as 3.7µg mL-1 for lactoferrin, thus assessing that the miniaturized optical biosensor is well-aligned with the chosen reference benchtop SPR method.

Selenite bioreduction with concomitant green synthesis of selenium nanoparticles by a selenite resistant EPS and siderophore producing terrestrial bacterium.

Environmental bacterial isolates play a very important role in bioremediation of metals and toxic metalloids. A bacterial strain with high selenite (SeO32-) tolerance and reducing capability was isolated from electronic waste dump site in Banaras Hindu University, Varanasi, India. Based on 16S rRNA sequencing and BLAST search, this bacterial isolate was identified as Bacillus paramycoides and designated as strain MF-14. It tolerated Sodium selenite up to 110 mM when grown aerobically in LB broth and reduced selenite into elemental selenium (Se0) significantly within 24h with concomitant biosynthesis of selenium nanoparticles as clearly revealed by brick red precipitate and specific surface plasmon resonance peak at 210nm using UV-Visible spectrophotometer. Scanning electron microscopy (SEM) analysis of this bacterial strain exposed to 1mM and 5 mM selenite also demonstrated morphological alterations as cell enlargement due to accumulation and bioprecipitation of elemental selenium (Se0). The FTIR analysis clearly demonstrated that functional groups present on the surface of biogenic selenium nanoparticles (SeNPs) play a significant role in the stabilization and capping of SeNPs. Furthermore, these SeNPs were characterized using spectroscopic analysis involving Dynamic light scattering, zeta potential, XPS, FTIR, XRD and Raman spectroscopy which clearly revealed particle size 10-700nm, amorphous nature, stability as well as it's oxidation state. The biochemical studies have demonstrated that membrane bound reductase enzyme may be responsible for significant reduction of selenite into elemental selenium. Therefore, we may employ Bacillus paramycoides strain MF-14 successfully for bioremediation of selenite contaminated environmental sites with concomitant green synthesis of SeNPs.

Oil mediated green synthesis of nano silver in the presence of surfactants for catalytic and food preservation application

Abstract The present study details the green synthesis of silver nanoparticles using clove oil as a reducing and stabilizing agent. Cationic, anionic, nonionic and zwitterionic surfactants were introduced to study the change in size, shape, and morphology of nanoparticles. The nanoparticles were characterized using different techniques. The nanoparticles had shown specific surface Plasmon resonance band with absorbance between 380 and 385 nm. The X-ray diffraction study revealed that the nanoparticles are composed of spherical cubic crystals with average size between 136 and 180 nm while Dynamic Laser scattering (DLS) studies revealed an effective diameter of 82 nm and polydispersity index of 0.005. Thermogravimetric analysis suggested that the particles are stable even at 600 °C. All the samples presented good antibacterial and antifungal efficacies against Staphylococcus aureus, Klebsiella pneumonia and Candida albicans and good catalytic activities for the degradation of fast green and Allura red dyes. Further, thin edible films of the nanoparticles were prepared using sodium alginate for food preservation. The films were coated on fruits and vegetables for extending their shelf life to cope with demand and supply gap.

Facile Synthesis of Porous Ag Crystals as SERS Sensor for Detection of Five Methamphetamine Analogs.

Porous noble metal nanomaterials have attracted extensive attention due to their high specific surface area and surface plasmon resonance effect. However, it is difficult to form porous structures due to the high mobility and low reduction potential of noble metal precursors. In this article, we developed a facile method for preparing porous Ag with a controllable structure at room temperature. Two kinds of Ag crystals with different porous structures were successfully prepared by using AgCl cubes as sacrificial templates. Through the galvanic replacement reaction of Zn and AgCl, Ag crystals with a sponge-like porous structure were successfully prepared. Additionally, using NaBH4 as the reducing agent, we prepared granular porous Ag cubes by optimizing the amount of reducing agent. Both the sponge-like and granular porous Ag cubes have clean and accessible surfaces. In addition, we used the prepared two porous Ag cubes as substrate materials for SERS detection of five kinds of methamphetamine analogs. The experimental results show that the enhancement effect of granular porous Ag is better than that of sponge-like porous Ag. Furthermore, we probed the hot spot distribution of granular porous Ag by Raman mapping. By using granular porous Ag as the substrate material, we have achieved trace detection of 5 kinds of methamphetamine analogs including Ephedrine, Amphetamine, N-Methyl-1-(benzofuran-5-yl)propan-2-amine (5-MAPB), N-Methyl-1-(4-methoxyphenyl)propan-2-amine (PMMA) and N-Methyl-1-(4-fluorophenyl)propan-2-amine (4-FMA). Furthermore, to achieve qualitative differentiation of analogs with similar structures we performed density functional theoretical (DFT) calculations on the Raman spectra of the above analogs. The DFT calculations provided the vibrational frequencies, Raman activities, and normal mode assignment for each analog, enabling the qualitative differentiation of the above analogs.

Molecular study on the effect of dandelion leaf extract and silver nanoparticles in induced diabetic albino rats

The present study investigated the antidiabetic effects of dandelion leaf extract and silver nanoparticles on diabetic albino rats at molecular level, and compared with insulin. Silver nanoparticles were prepared by green chimestry method using dandelion leaf extract as capping and reducing agent, which reduced Silver nitrate (AgNO3) into silver nanoparticles. The morphology, size and crystalline structure, of silver nanoparticles are confirmed by ultraviolet, Scanning electron microscope technique, and X-ray diffraction respectively. The formation and stability of the reduced AgNPs in colloidal solution were detected and monitored by using UV-visible spectroscopy, and the absorption peak appear at 450 nm indicating the specific surface Plasmon resonance of AgNPs. The Scanning Electron Microscope showed that the AgNPs have spherical shape with aparticular size ranging from (13 to 28 )nm.The chemical characterization of synthesized AgNPs was tested using the X-ray diffraction technique, which shows that the average crystalline size was 16nm, and the synthesized silver nanoparticles have a polycrystalline structure. Application of nanoparticles in medicine is an attractive proposition. The present study included 35 female wistar albino rats weighting 200±20 grams.

Realization of specific localized surface plasmon resonance in Au-modified Ni nanoplasmonics for efficient detection

Monometallic nanostructures have gained tremendous research attentions owing to the ability of supporting surface plasmons and improving devices performance. However, the relatively inflexible localized surface plasmon resonance (LSPR) absorption peaks restrict the further development of monometallic plasmonics and relevantapplications. Herein, the bimetallic Au-Ni nanoparticles (NPs) with an ∼ 325 nm LSPR absorption peak were fabricated and decorated on polar GaN microwire (MW) array PDs via thin film thermal annealing approach. Compared with monometallic Au and Ni NPs, the bimetallic Au-Ni NPs can not only modulate LSPR absorption peak but also enhance absorptivity. Moreover, the bimetallic NPs/GaN MW array PDs demonstrated the maximum increase in responsivity than bare GaN under the resonance wavelength of 325 nm. Theimprovement in bimetallic NPs devices is correlated with the stronger light absorption, scattering and hot electron transfer at the GaN interface. This work presents a simply valid method for preparing the bimetallic Au-Ni NPs with tunable LSPR absorption peak, which can be helpful for realizing the energy-efficient optoelectronic device applications in most functional fields.

Study on particle size and size distribution of gold nanoparticles by TEM and SAXS

Particle size and size distribution are two of the most vital parameters of nanomaterials since their physical properties as well as applications are highly dependent on these key factors. The objective of this work is to study the particle size and size distribution of gold nanoparticles (AuNPs), which were synthesized by a simple green synthesis in HAuCl4 and water-soluble chitosan solution (WSCS). Transmission electron microscope (TEM) and small-angle X-ray scattering (SAXS) techniques were carried out to determine the particle size, size distribution and polydispersity of AuNPs. The evidences from TEM and SAXS indicated that AuNPs can be formed in spherical shape with the size in the range of 10–30 nm. From TEM, the particle sizes of the AuNPs prepared in WSC, S at the concentration of 0.02 and 0.05 mg/mL containing 0.1 mM HAuCl4 were 20.5 ± 2.1 and 21.2 ± 1.8 nm, respectively. By increasing the concentration of HAuCl4 precursor up to 0.5 mM, AuNPs exhibited a slightly larger particle size (24.4 ± 2.2 nm). The particle size, size distribution and polydispersity of AuNPs observed by TEM and SAXS were in agreement. However, AuNPs sizes from SAXS were smaller than those from TEM because only the Au core of the AuNPs was detected by X-ray scattering. In addition, the chemical structure and specific surface plasmon resonance (SPR) absorption of AuNPs were well characterized by FTIR and UV-vis spectrophotometer. The FTIR results of AuNPs implied that the stabilization of AuNPs in the WSCS was due to electrostatic interaction and steric hindrance of C=O, C–O–C, –OH, –NH2 groups. By using WSCS at concentration 0.02 and 0.05 mg/mL, the SPR absorption bands were observed at 545 and 535 nm, respectively. The TEM and SAXS results of AuNPs in this study will provide an essential basis for synthesis of metallic nanoparticles for various applications in the future.

Bimetallic nanocomposite (Ag-Au, Ag-Pd, Au-Pd) synthesis using gum kondagogu a natural biopolymer and their catalytic potentials in the degradation of 4-nitrophenol

Bimetallic nanoparticles (BNPs) constitute two different metal elements and exhibit relatively superior mechanistic and catalytic efficacies owing to their synergistic functions over monometallic nanoparticles. In the present study various bimetallic Ag-Au, Ag-Pd, Au-Pd nanoparticles were synthesized using a natural biopolymer gum kondagogu (GK) as a reducing and capping agent, by a simple and cost-effective method. The synthesized BNPs when characterized using UV–vis spectroscopy revealed a specific surface plasmon resonance band (SPR) of each nanocomposite. The average particle size of Ag-Au, Ag-Pd, and Au-Pd BNPs was found to be 23 ± 10.3, 21 ± 7.6, and 23 ± 9.4 nm respectively based on transmission electron microscopy analysis. Surface morphology and functional groups on the gum matrix of GK-BNPs were analyzed by XRD and FT-IR respectively. The bimetallic nanocomposites were evaluated for their catalytic reduction of 4-nitrophenol (4-NP) to 4-aminophenol in the presence of NaBH4. The kinetic studies performed, depicted rate constants for Ag-Au, Ag-Pd, and Au-PdNPs as 0.31, 0.39, and 0.28 min−1 respectively. The catalytic efficiencies of three bimetallic nanocomposites were of the following order Ag-Pd > Ag-Au > Au-Pd. This study establishes the catalytic potentials of the three different bimetallic nanocomposites in the reduction of 4-NP an environmental pollutant, and the impact of their synergistic property.

Gold Nanomaterials and Bone/Cartilage Tissue Engineering: Biomedical Applications and Molecular Mechanisms.

Recently, as our population increasingly ages with more pressure on bone and cartilage diseases, bone/cartilage tissue engineering (TE) have emerged as a potential alternative therapeutic technique accompanied by the rapid development of materials science and engineering. The key part to fulfill the goal of reconstructing impaired or damaged tissues lies in the rational design and synthesis of therapeutic agents in TE. Gold nanomaterials, especially gold nanoparticles (AuNPs), have shown the fascinating feasibility to treat a wide variety of diseases due to their excellent characteristics such as easy synthesis, controllable size, specific surface plasmon resonance and superior biocompatibility. Therefore, the comprehensive applications of gold nanomaterials in bone and cartilage TE have attracted enormous attention. This review will focus on the biomedical applications and molecular mechanism of gold nanomaterials in bone and cartilage TE. In addition, the types and cellular uptake process of gold nanomaterials are highlighted. Finally, the current challenges and future directions are indicated.

One dimensional magneto-optical nanocomplex from silver nanoclusters and magnetite nanorods containing ordered mesocages for sensitive detection of PD-L1

Programmed death ligand 1 (PD-L1) is a typical immune checkpoint protein, whose up-regulation on the membrane of different tumor cells inhibits the immune response of T cells and leads to the escape of tumor cells. In this work, we designed a facile and highly specific surface plasmon resonance (SPR) biosensor to detect PD-L1 in human plasma based on magnetite nanorods containing ordered mesocages (MNOM) and silver nanoclusters (AgNCs). Magneto-optical nanocomplex MNOM@AgNCs with superior magneto-optical properties and high signal-to-noise ratio were fabricated to improve the detection sensitivity owing to the high specific surface area of MNOM and excellent localized SPR of AgNCs. The PD-L1 Antibody on the surface of gold chip and the PD-L1 aptamer on MNOM@AgNCs could realize dual selective recognition of PD-L1, providing the specificity of the sensor and reducing non-specific binding. The SPR sensor showed a good linear range of PD-L1 from 10 ng/mL to 300 ng/mL with the detection limit of 3.29 ng/mL. The practical performance of this immunosensing platform had been successfully verified by clinical samples which included healthy donors and cancer patients. Based on the analysis, the developed immunosensor provided a new strategy for point-of-care detection of PD-L1 and could be used as clinical companion diagnosis of PD-1/PD-L1 inhibitor therapy.

Green synthesis of multifunctional carbon coated copper oxide nanosheets and their photocatalytic and antibacterial activities

The studies of metal oxides in environmental remediation of chemical and biological pollutants are gaining colossal importance. Herein, we report the facile synthesis of multifunctional copper oxide nanosheets (CuO NS) using an aqueous extract of Rhazya stricta. The phytochemical investigation of R. stricta indicated the presence of saponins, tannins, and reducing sugars, responsible for the reduction and stabilization of CuO NS. A UV–Visible spectrophotometer initially confirmed the fabrication of CuO NS with specific Surface Plasmon Resonance at 294 nm. Field Emission Scanning Electron Microscopy (FE-SEM), Fourier-transform infrared spectroscopy FTIR, and XRD were further used to characterize the CuO NS. The obtained CuO NS were poly-dispersed with an average size of 20 nm. Interestingly these particles were aligned together in 3D cubical sheets layered above each other via self-assembly. The as-synthesized CuO NS showed enhanced antibacterial potential (17.63 mm, overall mean inhibition zone) in comparison to the known antibiotics (11.51 mm, overall mean inhibition zone) against both Solanaceous crop's wilt-causing bacteria (Ralstonia solanacearum and Clavibacter michiganensis). Furthermore, the appreciable photocatalytic potential of CuO NS has also been observed, causing 83% degradation of methylene blue (MB) upon solar irradiation. The synthesis methodology is devoid of any toxic waste or by-products. It could be used to produce eco-friendly CuO nanomaterial for industrial uses.

Bio-fabricated bioactive arisaema triphyllum aqueous extract-loaded nano-ZnO particles improve the nursing care of esophageal cancer

Metal nanoparticles, synthesized using phyto-constituents, are one of the most economical and environmentally friendly materials. Biogenic zinc oxide nanoparticles (ZnONPs) obtained from Arisaema triphyllum plant extract were synthesized and characterized using UV-visible spectroscopy, XRD, TEM, and EDX. The presence of various plant extracts and the zinc oxide capping of ZnONPs was confirmed using UV-visible spectroscopy, further confirming the existence of ZnO in the 400–430 nm region based on its specific surface plasmon resonance. XRD patterns showed ZnONP-centered cubic crystalline assembly, while electron microscopy showed that the formation of spherical ZnONPs varied from ∼10 nm to 15 nm in diameter. Strong ZnONPs bands were established, as verified by EDX. The anticancer properties of ZnONPs prepared with different extracts were evaluated using esophageal cancer cells. High levels of anticancer activity against the two esophageal cancer cell lines, EC109 and TE8, were observed. The morphological changes of the esophageal cancer cells were evaluated using AO-EB and nuclear staining biochemical methods. Hemolysis assays with human erythrocytes showed excellent bio-compatibility with ZnONPs. To the best of our knowledge, this is the first study to report the use of A. triphyllum-loaded biogenic ZnONPs against esophageal cancer cells.