Size distribution of MS was determined using a LS 13 320 Laser Diffraction Particle Size Analyzer (Beckman Coulter, USA). Samples (1 mg) of either unloaded-MS or LTB4 -loaded MS was dispersed in 0.4 mL of purified sterile water and then analyzed at 25 °C. Zeta potential of MS was determined using a Zetasizer Nano (Malvern Instruments, England). Each sample was prepared dispersing 1 mg of unloaded-MS or LTB4-loaded MS in 0.4 mL of purified water containing 10 mM NaCl and then analyzed at 25 °C. Morphology of MS samples was assessed by scanning electron microscopy (SEM) using a FEI Inspect S 50 scanning microscope (FEI; Oregon, USA).
Inspect s 50 scanning microscope
Manufactured by Thermo Fisher Scientific
Sourced in United States
The Inspect S 50 is a scanning electron microscope (SEM) designed for high-resolution imaging of samples. It provides detailed surface information and analysis of materials at the micro- and nanoscale. The Inspect S 50 is capable of magnifications up to 300,000x and offers a range of analytical functions for various applications.
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Lab products found in correlation
4 protocols using inspect s 50 scanning microscope
1
Characterization of MS Particles
2
Characterization of Microparticle Size, Zeta Potential, and Morphology
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Size distribution of MS was determined using a LS 13 320 Laser Diffraction Particle Size Analyzer (Beckman Coulter, USA). Samples (1 mg) of either unloaded-MS or LTB4 -loaded MS was dispersed in 0.4 mL of purified sterile water and then analyzed at 25 °C. Zeta potential of MS was determined using a Zetasizer Nano (Malvern Instruments, England). Each sample was prepared dispersing 1 mg of unloaded-MS or LTB4-loaded MS in 0.4 mL of purified water containing 10 mM NaCl and then analyzed at 25 °C. Morphology of MS samples was assessed by scanning electron microscopy (SEM) using a FEI Inspect S 50 scanning microscope (FEI; Oregon, USA).
3
Characterization of Lipid-based Microparticles
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Size distribution of MS was determined using a LS 13 320 Laser Diffraction Particle Size Analyzer (Beckman Coulter, USA). Samples (1 mg) of either unloaded-MS or LTB 4 -loaded MS was dispersed in 0.4 mL of purified sterile water and then analyzed at 25 °C. Zeta potential of MS was determined using a Zetasizer Nano (Malvern Instruments, England). Each sample was prepared was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission.
The copyright holder for this preprint (which this version posted May 24, 2020. ; https://doi.org/10.1101/2020.05.22.111633 doi: bioRxiv preprint 6 dispersing 1 mg of unloaded-MS or LTB 4 -loaded MS in 0.4 mL of purified water containing 10 mM NaCl and then analyzed at 25 °C. Morphology of MS samples was assessed by scanning electron microscopy (SEM) using a FEI Inspect S 50 scanning microscope (FEI; Oregon, USA).
The copyright holder for this preprint (which this version posted May 24, 2020. ; https://doi.org/10.1101/2020.05.22.111633 doi: bioRxiv preprint 6 dispersing 1 mg of unloaded-MS or LTB 4 -loaded MS in 0.4 mL of purified water containing 10 mM NaCl and then analyzed at 25 °C. Morphology of MS samples was assessed by scanning electron microscopy (SEM) using a FEI Inspect S 50 scanning microscope (FEI; Oregon, USA).
4
Characterization of Polymeric Microspheres
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Size distribution of MS was determined using a LS 13 320 Laser Diffraction Particle Size Analyzer (Beckman Coulter, Inc., Atlanta, GA, USA). Samples (1 mg) of either unloaded-MS or PGE 2 -loaded MS was dispersed in 0.4 mL of purified sterile water and then analyzed at 25 °C. Zeta potential of MS was determined using a Zetasizer Nano (Malvern Instruments, England). Each sample was prepared dispersing 1 mg of unloaded-MS or PGE 2 -loaded MS in 0.4 mL of purified water containing 10 mM NaCl and then analyzed at 25 °C. Morphology of MS samples was assessed by scanning electron microscopy (SEM) using a FEI Inspect S 50 scanning microscope (FEI; Oregon, USA).
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