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tem images  (JEOL)


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    JEOL tem images
    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
    Tem Images, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 89788 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 99 stars, based on 89788 article reviews
    tem images - by Bioz Stars, 2026-05
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    Images

    1) Product Images from "Artificial mitochondria ameliorates osteoarthritis through restoring cellular energy metabolism homeostasis"

    Article Title: Artificial mitochondria ameliorates osteoarthritis through restoring cellular energy metabolism homeostasis

    Journal: Bioactive Materials

    doi: 10.1016/j.bioactmat.2026.02.028

    Characterization of CAMs. (a) TEM images of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
    Figure Legend Snippet: Characterization of CAMs. (a) TEM images of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.

    Techniques Used: Control, Zeta Potential Analyzer



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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Characterization of CAMs. (a) <t>TEM</t> <t>images</t> of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.
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    Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy <t>(TEM),</t> scale bar = 100 nm (up) and scanning electron <t>microscope</t> (SEM), scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.
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    Image Search Results


    Characterization of CAMs. (a) TEM images of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.

    Journal: Bioactive Materials

    Article Title: Artificial mitochondria ameliorates osteoarthritis through restoring cellular energy metabolism homeostasis

    doi: 10.1016/j.bioactmat.2026.02.028

    Figure Lengend Snippet: Characterization of CAMs. (a) TEM images of PF (PFA-only control nanoparticles) (left panel), PFMPCr CAMs (middle panel), and PFMPC/DS CAMs (right panel). Scale bar: 100 nm. (b) DLS particle size maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (c) Zeta potential maps of PF, PFMPCr CAMs, and PFMPCr/DS CAMs. (d) Maps of drug loading with different DS and PFMPCr mass ratios. (e) Motion trajectory of 10 randomly selected PF particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (f) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in PBS. (g) Motion trajectory of 10 randomly selected PFMPCr CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate. (h) Motion trajectory of 10 randomly selected PFMPCr/DS CAMs particles and their average velocity distribution in LPS-stimulated chondrocyte lysate.

    Article Snippet: The TEM images of the samples were captured using a JEOL JEM-2100 transmission electron microscope.

    Techniques: Control, Zeta Potential Analyzer

    Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron microscope (SEM), scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.

    Journal: Materials Today Bio

    Article Title: Macrophage exosome-engineered nanoplatform with pH-responsive ratiometric photoacoustic and NIR-II fluorescence imaging for guided photothermal immunotherapy of hepatocellular carcinoma

    doi: 10.1016/j.mtbio.2026.103058

    Figure Lengend Snippet: Synthesis and characterization of aCD47-CATE nanoplatform. (A) The preparation of aCD47-CATE nanoplatform. (B) UV-Vis absorption spectra of Croc under different pH. (C) The morphology of the aCD47-CATE nanostructure as visualized by transmission electron microscopy (TEM), scale bar = 100 nm (up) and scanning electron microscope (SEM), scale bar = 200 nm (down). (D) Changes in the zeta potential that occurred during the synthesis steps for both CATE and aCD47-CATE nanoplatform. Data are presented as mean ± SD (n = 3). (E) A characteristic high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) micrograph, presented alongside the associated elemental distribution maps for the aCD47-CATE nanoplatform. (F) NIR-II thermal images of the aCD47-CATE nanoplatform in a phantom under 1064 nm laser irradiation at different power densities (0.5, 1.0, 1.5, 2.0 W/cm 2 ) for 360 s. (G) Graphs depicting the temperature rise for the aCD47-CATE NPs under different laser power at 1064 nm laser irradiation. (H) Multiple heating cycles of aCD47-CATE nanoplatform under 1.0 W/cm 2 at 1064 nm laser irradiation.

    Article Snippet: Transmission electron microscope (TEM) images were captured with a JEOL JEM-2100, and Scanning Electron Microscope (SEM) images were obtained using a JEOL Model JSM-6490.

    Techniques: Transmission Assay, Electron Microscopy, Microscopy, Zeta Potential Analyzer, Irradiation