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39 protocols using h 700

1

Characterization of Silver Nanoparticles

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The formations of silver nanoparticles were characterized by visual assessment as color changes of solution indicate the formation of nanoparticles. Reduction of pure silver ions were monitored by measuring UV-Vis spectra of the reaction mixture. UV-Vis spectra were measured using Hitachi, U-2800 spectrophotometer model UV- Visible double beam. For characterizing, absorption spectra of the samples were taken 200 to 700 nm. FTIR spectra were also performed and recorded with a Fourier Transform Infrared Spectrophotometer (IR Prestige-21, Shimadzu) in the range of 4000–500 cm−1 at a resolution of 4 cm−1. Size, shape and morphology of nanoparicles were determined by using Scanning Electron microscopy (2600SN Hitachi, Japan) from BCSIR, Bangladesh and Transmission Electron Microscopy (HITACHI H-700, Japan) from the Departmental laboratory of Applied Chemistry and Biochemistry, Kumamoto University, Japan.
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Characterization of ZnO Nanoparticles

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UV-Vis spectra of ZnO-NPs powders were measured using a Lambda 25 spectrophotometer (Perkin Elmer, Waltham, MA, USA) at wavelengths ranging from 200 to 800 nm. The X-ray diffraction data were recorded by PXRD (Philips, X’pert, Almelo, The Netherlands) at 40 kV and 30 mA from 2θ = 10° to 80° with nickel-filtered Cu (λ = 1.542 Å) at room temperature. The morphology and size of ZnO-NP samples were examined by using a Transmission Electron Microscope (TEM, Hitachi H-700, Tokyo, Japan) in 120 kV. The particle electrostatic charge was evaluated using the laser doppler electrophoresis technique, whereby 100 µL of the solution was diluted in 1.5 mL of water. Subsequently, it was poured into a Zetasizer-nano instrument cuvette (Malvern, UK); the results are stated as zeta potential (ZP). Photoluminescence (PL) spectra were recorded using a spectrophotometer (LS 55, Perkin–Elmer, Beaconsfield, UK) with an excitation wavelength of 320 nm.
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Comprehensive Characterization of ZnO Nanoparticles

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The ZnO NPs were characterized by PXRD (Philips, X’pert, Almelo, The Netherlands), at 40 kV and 30 mA from 2θ = 10° to 80° with nickel-filtered Cu (λ = 1.542 Å) at room temperature. FT-IR spectra of the samples were recorded over the range of 400–4000 cm−1 by a Model spectrum 100 series (Perkin Elmer, Waltham, MA, USA) FTIR spectrophotometer. UV-vis spectra of ZnO NPs powders were measured using a spectrophotometer (Lambda 25-Perkin Elmer) in wavelength between 200 and 800 nm. The morphology and size of ZnO-NP samples were examined by using a Transmission Electron Microscope (TEM, Hitachi H-700, Tokyo, Japan) in 120 kV. The particle electrostatic charge was evaluated using the laser doppler electrophoresis technique, whereby 100 µL of the solution was diluted in 1.5 mL of water. Then it was poured into a Zeta sizer-nano instrument cuvette (Malvern, UK); the results are stated as zeta potential (ZP). Concentration of Zn2+ ions before and after addition of extract was measured using Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) model Perkin Elmer 1000. Following Equation was used to calculate percentage yield (%Y) using initial concentration (IC) and final concentration (FC) of Zn2+ ions: %Y=IcFcIc×100%
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Isolation and Ultrastructural Analysis of Cardiomyocytes

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Primary ventricular cardiomyocytes were isolated from neonatal WT or CB2R KO mice and cultured at 37°C on glass coverslips overnight, followed by the treatments mentioned above. Cells were harvested and fixed overnight at 4°C in 2.5% glutaraldehyde in 0.1 M PBS, and then post-fixed in 1% buffered osmium tetroxide for 2 h. Specimens were processed in routine procedure and examined under a transmission electron microscope (H-700; Hitachi, Tokyo, Japan).
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5

Comprehensive Characterization of WSe2-PVP NPs

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The surface morphology was analyzed via a TEM (H‐700, Hitachi, Ltd., Tokyo, Japan). Meanwhile, energy dispersive spectrometer was performed to measure surface elements of WSe2‐PVP NPs. Chemical state analysis of samples was characterized using XRD (X'Pert Pro, Netherlands). The chemical bonds and functional groups of synthetic WSe2‐PVP NPs were characterized using FT‐IR spectral (Nicolet 8700, Thermo Nicolet, Madison, USA) and Raman spectra (Jobin‐Yvon, Horiba Group, France). The XPS measurement equipment was conducted to analyze the chemical composition of the synthetic WSe2‐PVP NPs.
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6

Visualizing Lipid Emulsion Characteristics

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TEM was used to visualize the shapes and characteristics of lipid emulsions and to confirm the Dz by dynamic light scattering. Samples were prepared by the conventional negative-staining method. Lipid-based emulsions were placed on carbon-coated copper grids and negatively stained with 2% (w/v) phosphotungstic acid for several minutes at room temperature, and dried in air. Grids bearing lipid emulsions were measured with a transmission electron microscope (Hitachi H-700, Tokyo, Japan).
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7

Nanoparticle Characterization by TEM and Zetasizer

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The morphology of PBCA and CTS- or CG-coated nanoparticles was observed by transmission electron microscopy (H-700; Hitachi, Japan) using a negative-staining method. Particle size, size distribution, and the zeta potential of the nanoparticles were determined with a Zetasizer (3000HS, Malvern Instruments, Malvern, UK).
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8

Ultrastructural Tissue Preparation

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The specimens were fixed in 2% glutaraldehyde and 2% paraformaldehyde and then treated with 1% osmium tetroxide for 1 h. The wound skin samples were subsequently embedded in Epon and processed for TEM (HITACHI H-700).
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9

Characterization of ZnO Nanoparticles

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The crystal structure of ZnO-NPs were analyzed by PXRD (Philips, X’pert, Cu Kα) in the 2θ range between (2–80°) at room temperature. FTIR spectra of the samples were recorded by FTIR spectrometer (Perkin-Elmer 1725X, Waltham, MA, USA), with a resolution of 4.0 cm−1 at wavenumber range from 400 to 4000 cm−1. The UV-Visible absorption of powder samples were examined by UV-Vis spectrophotometer (a Lambda 25-Perkin Elmer, Waltham, MA, USA) in the range of 200–800 nm. Transmission electron microscope (HITACHI H-700, Tokyo, Japan) with an acceleration voltage of 120 kV was applied to study size and morphology of the ZnO-NPs. TEM samples were prepared by depositing a few drops of the sample suspension on a copper grid followed with drying at room temperature. The morphology of samples were further observed using FESEM (JSM-6360LA, Eindhoven, The Netherlands). The small amounts of powder samples were mounted on a metal stub using carbon tape and then gold-coated using a sputter coater. The particle sizes and the zeta potentials of ZnO-NPs were analyzed by photon correlation spectroscopy and laser Doppler anemometry, respectively, with a Zetasizer, Nano ZS (Malvern Instruments Ltd., Malvern, UK) at room temperature.
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10

TEM Imaging of ZnO Nanoparticles

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ZnO-NPs were imaged using TEM (H-700, Hitachi Ltd., Tokyo, Japan) at an accelerated voltage of 80 kv using a negative staining method following our previously published protocol [2 (link),7 (link)]. Briefly, the sample was diluted (1:50) with double-distilled water and then a drop of the diluted sample was applied to a mesh copper grid coated with a carbon film and was left to dry for 5 min. After this, a drop of the phospho-tungstic acid solution (2% w/w) was added to the grid for 50 s and the excess liquid was removed using filter paper. The grid was left to air-dry in advance of imaging. TEM imaging was performed for the identification of the sample’s uniformity, shape, size, and presence of any aggregation.
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