Hydroxyapatite-Gold Modified Screen-Printed Carbon Electrode for Selective SARS-CoV-2 Antibody Immunosensor.

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), or coronavirus disease 2019 (COVID-19), is still spreading worldwide; therefore, the need for rapid and accurate detection methods remains relevant to maintain the spread of this infectious disease. Electrochemical immunosensors are an alternative method for the rapid detection of the SARS-CoV-2 virus. Herein, we report the development of a screen-printed carbon electrode immunosensor using a hydroxyapatite-gold nanocomposite (SPCE/HA-Au) directly spray-coated with the immobilization receptor binding domain (RBD) Spike to increase the conductivity and surface electrode area. The HA-Au composite synthesis was optimized using the Box-Behnken method, and the resulting composite was characterized by UV-vis spectrophotometry, TEM-EDX, and XRD analysis. The specific interaction of RBD Spike with immunoglobulin G (IgG) antibodies was evaluated by differential pulse voltammetry and electrochemical impedance spectroscopy methods in a [Fe(CN)6]4-/3- solution redox system. The IgG was detected with a detection limit of 0.0561 pg mL-1, and the immunosensor had selectivity and stability of 103-122% and was stable until week 7 with the influence of storage conditions. Also, the immunosensor was tested using real samples from human serum, where the results were confirmed using the chemiluminescent microparticle immunoassay (CMIA) method and showed satisfactory results. Therefore, the developed electrochemical immunosensor can rapidly and accurately detect SARS-CoV-2 antibodies.

The Influence of Polyvinyl Alcohol Porogen Addition on the Nanostructural Characteristics of Hydroxyapatite.

Hydroxyapatite (HA) is a porous material widely developed in various research fields because of its high biodegradability, biocompatibility, and low toxicity. In this research, HA was synthesized using a hydrothermal method with chicken eggshells as a calcium source and various concentrations of polyvinyl alcohol as a porogen (2.5%, 5.0%, and 7.5% by wt). The structure and morphology of HA were determined by X-ray diffraction (XRD) and scanning electron microscope (SEM), respectively. HA was obtained with varying concentrations of polyvinyl alcohol (PVA) porogen according to Inorganic Crystal Structure Database (ICSD) standard. Based on analysis using a refinement method, changes in unit cell parameters (cell volume and lattice strain) of HA synthesized using PVA porogen compared to the standard, the chi square (χ2) and index of R values were relatively low, validating the acceptable of the data. In addition, HA [Ca10(PO4)6(OH)2] with hexagonal structure and the P63/m space group was successfully obtained. Morphological analysis of HA by SEM found that HA has a spherical shape, and the porosity of HA increases with increasing concentrations of polyvinyl alcohol. The highest porosity was obtained with an addition of 5.0 wt% of PVA porogen (HAP3), reaching 69.53%.

Evaluation of Structural Stability, Mechanical Properties, and Corrosion Resistance of Magnesia Partially Stabilized Zirconia (Mg-PSZ).

Nano Zirconia (ZrO2) has been used in dental implants due to having excellent mechanical properties and biocompatibility that match the requirements for the purpose. Zirconia undergoes phase transformation during heating: monoclinic (room temperature to 1170 °C), tetragonal (1170 °C to 2370 °C), and cubic (>2370 °C). Most useful mechanical properties can be obtained when zirconia is in a multiphase form or in partially stabilized zirconia (PSZ), which is achieved by adding small amounts of a metal oxide dopant, such as MgO (magnesia). This study aimed to synthesize nano Mg-PSZ from a local resource found in West Kalimantan, Indonesia, and examine its structural stability, biochemical stability, and mechanical properties. Nano Mg-PSZ was prepared from a zircon local to Indonesia, from West Kalimantan Province, MgSO4∙7H2O, and polyethylene glycol (PEG)-6000 was used as a template. The obtained t-ZrO2 after calcination at 800 °C was shown to be stable at room temperature. The highest percentage of the t-ZrO2 phase was obtained at Zr0.95Mg0.05O2 with a variation of 99.5%. The hardness of Mg-PSZ increased from 554 MPa for ZrO2 without MgO doping to 5266 MPa for ZrO2 with a doping of 10% MgO. An in vitro biodegradation test showed that the greater the concentration of MgO in doping the ZrO2, the greater the degradation resistance of Mg-PSZ in simulated body fluid (SBF) solution.

Electrochemical investigation of hydroxyapatite-lanthanum strontium cobalt ferrite composites (HA-LSCF) for SARS-CoV-2 aptasensors.

The hydroxyapatite-lanthanum strontium cobalt ferrite (HA-LSCF) composite showed a good response on a screen-printed carbon electrode (SPCE) electrochemical aptasensor to detect SARS-CoV-2. SPCE/HA-LSCF with a thiolated aptamer has a strong affinity for the SARS-CoV-2 spike RBD protein. This occurs due to the binding of -SH to the HA-positive region. In the presence of LSCF, which is conductive, an increase in electron transfer from the redox system [Fe(CN)6]3-/4- occurs. The interaction of the aptamer with the RBD protein can be observed based on the decrease in the electron transfer process. As a result, the developed biosensor is highly sensitive to the SARS-CoV-2 spike RBD protein with a linear range of 0.125 to 2.0 ng mL-1, a detection limit of 0.012 ng mL-1, and a quantification limit of 0.040 ng mL-1. The analytical application of the aptasensor demonstrates its feasibility in the analysis of saliva or swab samples.

Green Template-Mediated Synthesis of Biowaste Nano-Hydroxyapatite: A Systematic Literature Review.

Hydroxyapatite (HA) is a well-known calcium phosphate ingredient comparable to human bone tissue. HA has exciting applications in many fields, especially biomedical applications, such as drug delivery, osteogenesis, and dental implants. Unfortunately, hydroxyapatite-based nanomaterials are synthesized by conventional methods using reagents that are not environmentally friendly and are expensive. Therefore, extensive efforts have been made to establish a simple, efficient, and green method to form nano-hydroxyapatite (NHA) biofunctional materials with significant biocompatibility, bioactivity, and mechanical strength. Several types of biowaste have proven to be a source of calcium in forming HA, including using chicken eggshells, fish bones, and beef bones. This systematic literature review discusses the possibility of replacing synthetic chemical reagents, synthetic pathways, and toxic capping agents with a green template to synthesize NHA. This review also shed insight on the simple green manufacture of NHA with controlled shape and size.

Green Production of Zero-Valent Iron (ZVI) Using Tea-Leaf Extracts for Fenton Degradation of Mixed Rhodamine B and Methyl Orange Dyes.

The danger from the content of dyes produced by textile-industry waste can cause environmental degradation when not appropriately treated. However, existing waste-treatment methods have not been effective in degrading dyes in textile waste. Zero-valent iron (ZVI), which has been widely used for wastewater treatment, needs to be developed to acquire effective green production. Tea (Camellia sinensis) leaves contain many polyphenolic compounds used as natural reducing agents. Therefore, this study aims to synthesize ZVI using biological reducing agents from tea-leaf extract and apply the Fenton method to degrade the color mixture of rhodamine B and methyl orange. The results show that the highest polyphenols were obtained from tea extract by heating to 90 °C for 80 min. Furthermore, PSA results show that ZVI had a homogeneous size of iron and tea extract at a volume ratio of 1:3. The SEM-EDS results show that all samples had agglomerated particles. The ZVI 1:1 showed the best results, with a 100% decrease in the color intensity of the dye mixture for 60 min of reaction and a degradation percentage of 100% and 66.47% for rhodamine B and methyl orange from LC-MS analysis, respectively. Finally, the decrease in COD value by ZVI was 92.11%, higher than the 47.36% decrease obtained using Fe(II).

Enhanced adsorption capacity of activated carbon over thermal oxidation treatment for methylene blue removal: kinetics, equilibrium, thermodynamic, and reusability studies.

Activated carbon (AC) is an effective and inexpensive adsorbent material for dye removal, but it cannot always be used repeatedly. Furthermore, the adsorbed dyes with toxicity usually remain on its surface. In this study, a thermal air oxidation process was used to modify the surface of AC and decompose adsorbed methylene blue (MB). The behavior of this process on spent AC was investigated using TGA-DTA, while the degradation of MB before and after the regeneration process was analyzed using a carbon, hydrogen, nitrogen, sulfur (CHNS) analyzer. It was discovered that thermal air oxidation could promote the formation of oxygenated functional groups on AC produced from steam-activated carbon coconut shell (SACCS), which when treated at 350 °C (denoted as SACCS-350), demonstrated an adsorption capacity 2.8 times higher than the non-air-oxidized AC (SACCS). The key parameters for the MB adsorption of SACCS and SACCS-350, such as kinetics, equilibrium, and thermodynamics, were compared. Moreover, the SACCS-350 could be reused at least 3 times for the adsorption of MB. Based on these results, thermal air oxidation treatment could successfully improve the adsorption performance of AC and regenerate spent AC through a reasonable and environmentally friendly process compared to other regeneration methods.

Highly enhanced electrical properties of lanthanum-silicate-oxide-based SOFC electrolytes with co-doped tin and bismuth in La9.33-x Bi x Si6-y Sn y O26.

Solid oxide fuel cells (SOFCs) are one of the most promising clean energy sources to be developed. However, the operating temperature of SOFCs is currently still very high, ranging between 1073 and 1273 K. Reducing the operating temperature of SOFCs to intermediate temperatures in between 773 and 1073 K without decreasing the conductivity value is a challenging research topic and has received much attention from researchers. The electrolyte is one of the components in SOFCs which has an important role in reducing the operating temperature of the SOFC compared to the other two fuel cell components, namely the anode and cathode. Therefore, an electrolyte that has high conductivity at moderate operating temperature is needed to obtain SOFC with medium operating temperature as well. La9.33Si6O26 (LSO) is a potential electrolyte that has high conductivity at moderate operating temperatures when this material is modified by doping with metal ions. Here, we report a modification of the structure of the LSO by partial substitution of La with Bi3+ ions and Si with Sn4+, which forms La9.33-x Bi x Si6-y Sn y O26 with x = 0.5, 1.0, 1.5, and y = 0.1, 0.3, 0.5, in order to obtain an electrolyte of LSO with high conductivity at moderate operating temperatures. The addition of Bi and Sn as dopants has increased the conductivity of the LSO. Our work indicated highly enhanced electrical properties of La7.83Bi1.5Si5.7Sn0.3O26 at 873 K (1.84 × 10-2 S cm-1) with considerably low activation energy (E a) of 0.80 eV comparing to pristine La9.33Si6O26 (0.08 × 10-2 S cm-1).

A novel hydrothermal synthesis of nanohydroxyapatite from eggshell-calcium-oxide precursors.

Hydroxyapatite (HA) is a material that has been widely applied to replace the damaged bone as a bone implant. Different types of HA have been successfully synthesized by a hydrothermal method based on calcium oxide (CaO) which was originated from chicken eggshells and diammonium hydrogen phosphate (DHP)/(NH4)2HPO4 as their precursors. We present a novel approach to the hydrothermal synthesis of HA form eggshells as a new precursor via a one-step synthesis method. The influence of temperature was also observed to study the effect on the crystallinity, purity, and morphology of obtained HAs. The synthesis was carried out at two different temperatures, 200 °C (HA-200) and 230 °C (HA-230) for 48 h respectively. The structures, purities, and morphologies of hydroxyapatite were analyzed by X-ray Diffraction (XRD), Fourier Transform Infra-Red (FTIR), and Scanning Electron Microscopy- Energy Dispersive Spectroscopy (SEM-EDS), and Transmission electron microscopy (TEM). The XRD patterns show the HA main phase indicated the purity of 96.5% for HA-200 and 99.5% for HA-230. The TEM micrograph suggested a hexagonal-like of HA with an average particle size of 92.61 nm. Hexagonal-like of HAs are suitable for bone implants and further application.