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Atomic force microscope

Manufactured by Veeco
Sourced in United States

The Atomic Force Microscope (AFM) is a high-resolution imaging and measurement tool designed to analyze the surface topography and properties of materials at the nanoscale level. It operates by using a sharp, nanometer-scale tip to scan the surface of a sample, detecting and mapping the interactions between the tip and the sample. The core function of the AFM is to provide detailed 3D surface images and quantitative measurements of various surface characteristics, such as roughness, adhesion, and stiffness.

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6 protocols using atomic force microscope

1

Characterization of Functionalized SWNTs

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The spectral, morphological, and electrical characteristics of SWNTs before and after being functionalized by MPs were investigated by atomic force microscopy (AFM), Raman, UV-Vis spectrometry, current-voltage (I-V), and field-effect transistor (FET) measurement. AFM images were obtained using an atomic force microscope (Veeco Innova, Santa Barbara, CA, USA). Raman spectra were measured with a Nicolet Almega XR Dispersive microscope with 532-nm laser excitation. The UV spectrum was acquired by a Beckman DU640 UV/Vis spectrophotometer (Beckman Coulter, Inc. USA). Electrical measurements were made using a semiconductor parameter analyzer (Keithley 2636, USA).
For FET measurements, the Si substrate was covered with gold film, which served as the base, and charged with a linear voltage ranging from −60 V to +20 V. The two gold electrodes etched on the SiO2 surface acted as the drain and source, to which a constant voltage (0.1 V) was applied. A dielectric layer of 100-nm thick SiO2 was used to separate the base from the source-drain.
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2

Comprehensive Characterization of Nanomaterials

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Scanning electron microscopy (SEM) images were recorded by an S-4800 field emission scanning electron microscope (Hitachi, Japan). Transmission electron microscopy (TEM) images were obtained on a JEM-1400 transmission electron microscope (JEOL, Japan). Atomic force microscopy (AFM) images were obtained on an atomic force microscope (Veeco, USA). Static water contact angles were measured using an OCA50 system (Dataphysics, Germany). Circular dichroism (CD) spectra were collected on the Chirascan spectropolarimeter. Isothermal titration calorimetry (ITC) was performed using a Nano calorimeter (Waters, TA Instruments, USA). FT-IR spectra were obtained from a Fourier transform infrared spectrometer (Nicolet IS10, Thermo Fisher). Zeta potential was detected on Malvern Zetasizer Nano-ZS90 (ZEN3590, UK). The UV−Vis absorption spectra were recorded on a Thermo Scientific NanoDrop 2000/2000C spectrophotometer. Fluorescence spectra were recorded on a HORIBA Scientific Fluoromax-4 spectrofluorometer.
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3

Multimodal Characterization of Nanomaterials

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TEM images and TEM-EDS images were obtained using a JEOL JEM-1010 and JEM-2100F, respectively. AFM images were obtained using a Veeco atomic force microscope. Raman spectroscopy measurements were carried out on a Dongwoo DM500i Raman spectrometer using green (514.5 nm) laser excitation. BET surface area and BJH pore size distributions were measured by using a Micromeritics Tristar 3000. XPS was carried out using a Kratos AXIS-HSi. Elemental analysis was performed using a Thermo Scientific Flash 2000 analyzer at NCIRF (National Center for Inter-university Research Facilities, Seoul National University, Korea).
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4

Atomic Force Microscopy of Extracellular Vesicles

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EV samples (1 µg protein) were diluted in a final volume of 200 µL PBS and 50 µL were adsorbed to freshly cleaved Ruby Muscovite mica (NanoAndMore GmbH, Germany) discs for 10 min. The discs were rinsed with deionized water and dried gently under nitrogen stream. Atomic force microscope (Veeco, Oyster Bay, NY, USA) in tapping mode and aluminum coated silicon probe tips (Mikromasch, Lady’s Island, SC, USA) were used for imaging. Topographic height, amplitude and phase images were recorded at 512 pixels × 512 pixels at a scanning rate of 1 Hz. Images were processed using NanoScope Image software (Veeco Metrology, NY, USA).
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5

Characterizing Surface Topography and Wettability

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The surface topography before and after coating with NPs was scanned by atomic force microscope (Veeco Instruments, Santa Barbara, CA, USA) under ambient conditions. The images were analyzed by using commercial Scanning Probe Image Processor (SPIP 6.0) software (Image Metrology ApS, Hørsholm, Denmark). Meanwhile, the water contact angle was analyzed with DSA100 drop shape analysis system (KRÜSS GmbH, Hamburg, Germany). The drop shape was photographed with a camera and the contact angle was calculated with the software provided by the manufacturer.
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6

Atomic Force Microscopy of Extracellular Vesicles

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First 50 µL of EV resuspension from healthy and cancer samples was added to a freshly cleaved muscovite mica surface (NanoAndMore GmbH, Wetzlar, Germany) for 10 min, washed with 2.5 mL of deionized water, and dried with nitrogen. Then, EVs were observed under an atomic force microscope (Veeco, Oyster Bay, NY, USA) in tapping mode with aluminum-coated silicon probe tips (HQ:NSC35/Al BS, Mikromasch, Lady’s Island, SC, USA). The height and amplitude of the samples were recorded at 512 pixels × 512 pixels at a scanning rate of 1 Hz and processed with NanoScope Image Software (v5.10, Veeco, Metrology, NY, USA).
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