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Double sided tape

Manufactured by Euromedex
Sourced in France

Double-sided tape is a flexible adhesive product with a sticky surface on both sides. It is designed to securely bond two surfaces together.

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6 protocols using double sided tape

1

Particle Size Analysis of ATIQCTPC

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To examine the particle size of ATIQCTPC, we also used SEM (50 kV; JEM-1230; JEOL). Lyophilized powders formed from aqueous ATIQCTPC (10−7 M, pH 7) were attached onto a copper plate with double-sided tape (Euromedex, Souffelweyersheim, France). On a JEOL JFC-1600 Auto Fine Coater, the specimens were coated with 20 nm gold–palladium. At 15 kV, 30 mA, and 200 mTorr (argon), the coater was operated for 60 s. The nanofeature and size distribution of the particles were visualized by examining >100 particles in randomly selected regions of the SEM alloy. Each measurement was performed with triplicate copper plates. The images were recorded on a 100–10,000× digitally enlarged imaging plate of Gatan Bioscan Camera Model 1792 with 20 eV energy windows.
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2

Visualizing MTCA-KKV Nanoparticle Morphology

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The shape and size of the nanoparticles of MTCA-KKV were visualized on scanning electron microscopy (SEM, S-4800, Hitachi, Tokyo, Japan) at 50 kV. For this purpose, the solution (10 μM, 0.1 μM and 1 nM) of MTCA-KKV in the ultrapure water of pH 6.8 was lyophilized and the powders were attached to the copper plate with double-sided tape (Euromedex, Strasbourg, France). Using Joel JFC-1600 Auto Fine Coater (JEOL, Japan) at 15 kV, 30 mA and 200 mTorr (argon) for 60 s the specimens were coated with 20 nm gold-palladium. The feature and size of the nanoparticles were identified by examining more than 100 species in randomly selected region on the SEM alloy. For each sample, triplicate grids were prepared and examined. To record 100–10,000× digitally enlarged SEM images, an imaging plate (Gatan Bioscan Camera Model 1792, Pleasanton, CA, USA) was used, and the energy window was 20 eV.
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3

Characterization of Lyophilized Nanoparticles

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The feature and diameter of the lyophilized powders from solutions of MSNS, MSNS-6MP and MSNS-6MP/CDDP in ultrapure water of pH 7.0 were examined by SEM (JEM-1230, JEOL, 50 kV), and were attached onto a copper plate with double-sided tape (Euromedex, Souffelweyersheim, France). On a JEOL JFC-1600 Auto Fine Coater, the copper plates were coated with 20 nm gold–palladium. At 15 kV, 30 mA and 200 mTorr (argon), the coater was operated for 60 s. By examining >100 particles in randomly selected regions on the SEM alloy, the feature and diameter distributions of the nanoparticles were visualized. Each measurement was performed with triplicate copper plates. The images were recorded on an imaging plate of Gatan Bioscan Camera Model 1792 (Gatan, Inc.) with 20 eV energy windows and at 100–10,000× digitally enlarged.
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4

Characterizing Nano-HMCEF Using SEM

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The shape and size of the nanospecies of HMCEF in solid state were measured by SEM (s-4800; Hitachi, Tokyo, Japan) at 50 kV. In brief, the lyophilized powders from 10−6 M solution of HMCEF in ultrapure water were attached to a copper plate with double-sided tape (Euromedex, Strasbourg, France). The specimens were coated with 20 nm gold–palladium using a Joel JFC-1600 Auto Fine Coater. The coater was operated at 15 kV, 30 mA and 200 mTorr (argon) for 60 s. The shape and size of the nanospecies on the SEM alloy were determined by examining >100 species in a randomly selected region. SEM images were recorded on an imaging plate (Gatan Bioscan Camera Model 1792) with 20 eV energy windows at 100–10,000× and were digitally enlarged. Each determination was performed with triplicate grids.
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5

Lyophilized IQCA-TAVV Powder Morphology

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The morphology and size of the lyophilized powders of IQCA-TAVV were imaged on an SEM (S-4800; Hitachi, Tokyo, Japan) at 15 kV. The SEM sample was prepared by fixing the lyophilized powders from a 10−8 M solution of IQCA-TAVV in ultrapure water onto the stub with double-sided tape (Euromedex, Strasbourg, France), which was then coated with 10-nm-thick gold–palladium by use of a Joel JFC-1600 auto fine coater (JEOL, Tokyo, Japan). The imaging conditions were 15 kV, 30 mA and 200 mTorr (argon) for 60 s. The randomly selected regions of the coater were viewed, and the morphology and size distribution of the lyophilized powders were recorded for over 100 species. Then 100–10,000× digitally enlarged lyophilized powders were recorded on the imaging plate (Gatan Bioscan Camera Model 1792) with 20 eV energy windows. Each imaging was performed with triplicate samples.
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6

SEM Analysis of Lyophilized Nanoparticles

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The shape and size of the nanospecies in lyophilized powders (from a solution of PZL318 in ultrapure water) were measured by scanning electron microscopy (SEM) (JEM-1230; JEOL) at 50 kV. The lyophilized powders were attached to a copper plate with double-sided tape (Euromedex, Souffelweyersheim, France). The specimens were coated with 20 nm gold–palladium using a JEOL JFC-1600 Auto Fine Coater. The coater was operated at 15 kV, 30 mA, and 200 mTorr (argon) for 60 seconds. The shape and size distributions of the nanoparticles were measured by examining >100 particles in randomly selected regions on the SEM alloy. All measurements were performed on triplicate grids. Images were recorded on an imaging plate (Gatan Bioscan Camera Model 1792; Gatan, Inc.) with 20 eV energy windows at 100–10,000×, and they were digitally enlarged.
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