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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.
Tem Images, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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transmission electron microscope tem images  (JEOL)
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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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jem-2100 transmission electron microscope - by Bioz Stars, 2026-09
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transmission electron microscopy tem  (JEOL)
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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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transmission electron microscope tem  (JEOL)
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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.
Transmission Electron Microscope Tem, supplied by JEOL, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/transmission+electron+microscope+(tem/JEM-2100+Transmission+Electron+Microscope/pmc13123618-85-6-12
Average 99 stars, based on 1 article reviews
transmission electron microscope tem - by Bioz Stars, 2026-09
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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