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sdio–do3a  (Eppendorf AG)


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    Structured Review

    Eppendorf AG sdio–do3a
    Physical Properties of <t> SDIO–DO3A </t> in Comparison to Those of DIO–DO3A
    Sdio–Do3a, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sdio–do3a/product/Eppendorf AG
    Average 90 stars, based on 1 article reviews
    sdio–do3a - by Bioz Stars, 2026-04
    90/100 stars

    Images

    1) Product Images from "Quantitative Assessment of Binding Affinities for Nanoparticles Targeted to Vulnerable Plaque"

    Article Title: Quantitative Assessment of Binding Affinities for Nanoparticles Targeted to Vulnerable Plaque

    Journal: Bioconjugate chemistry

    doi: 10.1021/acs.bioconjchem.5b00144

    Physical Properties of  SDIO–DO3A  in Comparison to Those of DIO–DO3A
    Figure Legend Snippet: Physical Properties of SDIO–DO3A in Comparison to Those of DIO–DO3A

    Techniques Used: Comparison, Zeta Potential Analyzer



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    Representative T 2 ∗ -weighted MRI and histological staining of mouse brains from different imaging groups. (a) T 2 ∗ -weighted MR images in each row represent MRI scans at different time points from the same animal in that group. The second row is an animal that did not receive intracerebral injection, only intravenous <t>SDIO</t> injection. The other three rows are animals that underwent TNF- α intracerebral injections. From left to right, column 1 represents images after TNF- α injection, but before IV injection of contrast agent, the rest of the columns of MRI represent time points after intravenous injection of stated contrast agent (except for row 1, these animals were not injected with contrast agents). Red arrows denote the needle tracks and regions highlighted by contrast agents. (b–i) Histological evaluation of the same animals as shown in (a): (b, c) TNF- α only; (d, e) IV-SDIO only; (f, g) TNF- α + IV-SDIO; (h, i) TNF- α + IV-DIO. Blue arrows in (b), (f), and (h) denote small cavities in the brain that were observed. Images (c), (e), (g), and (i) show magnification of Iba-1 and iron staining of selected areas (red square) from images (b), (d), (f), and (h). Activated microglia at inflammation sites were stained brown by Iba-1 antibody, while iron oxide nanoparticles accumulated in the vicinity region were stained blue by Perls' Prussian blue. Scale bars represent 200 µ m.
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    Representative T 2 ∗ -weighted MRI and histological staining of mouse brains from different imaging groups. (a) T 2 ∗ -weighted MR images in each row represent MRI scans at different time points from the same animal in that group. The second row is an animal that did not receive intracerebral injection, only intravenous <t>SDIO</t> injection. The other three rows are animals that underwent TNF- α intracerebral injections. From left to right, column 1 represents images after TNF- α injection, but before IV injection of contrast agent, the rest of the columns of MRI represent time points after intravenous injection of stated contrast agent (except for row 1, these animals were not injected with contrast agents). Red arrows denote the needle tracks and regions highlighted by contrast agents. (b–i) Histological evaluation of the same animals as shown in (a): (b, c) TNF- α only; (d, e) IV-SDIO only; (f, g) TNF- α + IV-SDIO; (h, i) TNF- α + IV-DIO. Blue arrows in (b), (f), and (h) denote small cavities in the brain that were observed. Images (c), (e), (g), and (i) show magnification of Iba-1 and iron staining of selected areas (red square) from images (b), (d), (f), and (h). Activated microglia at inflammation sites were stained brown by Iba-1 antibody, while iron oxide nanoparticles accumulated in the vicinity region were stained blue by Perls' Prussian blue. Scale bars represent 200 µ m.
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    Image Search Results


    Physical Properties of  SDIO–DO3A  in Comparison to Those of DIO–DO3A

    Journal: Bioconjugate chemistry

    Article Title: Quantitative Assessment of Binding Affinities for Nanoparticles Targeted to Vulnerable Plaque

    doi: 10.1021/acs.bioconjchem.5b00144

    Figure Lengend Snippet: Physical Properties of SDIO–DO3A in Comparison to Those of DIO–DO3A

    Article Snippet: To label the particles with 111 In 3+ , SDIO–DO3A (1.6 mg) was dissolved in 100 μ L of 0.2 M, pH 5.5, sodium acetate–acetic acid buffer solution in a 1.5 mL Eppendorf vial.

    Techniques: Comparison, Zeta Potential Analyzer

    Representative T 2 ∗ -weighted MRI and histological staining of mouse brains from different imaging groups. (a) T 2 ∗ -weighted MR images in each row represent MRI scans at different time points from the same animal in that group. The second row is an animal that did not receive intracerebral injection, only intravenous SDIO injection. The other three rows are animals that underwent TNF- α intracerebral injections. From left to right, column 1 represents images after TNF- α injection, but before IV injection of contrast agent, the rest of the columns of MRI represent time points after intravenous injection of stated contrast agent (except for row 1, these animals were not injected with contrast agents). Red arrows denote the needle tracks and regions highlighted by contrast agents. (b–i) Histological evaluation of the same animals as shown in (a): (b, c) TNF- α only; (d, e) IV-SDIO only; (f, g) TNF- α + IV-SDIO; (h, i) TNF- α + IV-DIO. Blue arrows in (b), (f), and (h) denote small cavities in the brain that were observed. Images (c), (e), (g), and (i) show magnification of Iba-1 and iron staining of selected areas (red square) from images (b), (d), (f), and (h). Activated microglia at inflammation sites were stained brown by Iba-1 antibody, while iron oxide nanoparticles accumulated in the vicinity region were stained blue by Perls' Prussian blue. Scale bars represent 200 µ m.

    Journal: Contrast Media & Molecular Imaging

    Article Title: In Vivo MRI of Functionalized Iron Oxide Nanoparticles for Brain Inflammation

    doi: 10.1155/2018/3476476

    Figure Lengend Snippet: Representative T 2 ∗ -weighted MRI and histological staining of mouse brains from different imaging groups. (a) T 2 ∗ -weighted MR images in each row represent MRI scans at different time points from the same animal in that group. The second row is an animal that did not receive intracerebral injection, only intravenous SDIO injection. The other three rows are animals that underwent TNF- α intracerebral injections. From left to right, column 1 represents images after TNF- α injection, but before IV injection of contrast agent, the rest of the columns of MRI represent time points after intravenous injection of stated contrast agent (except for row 1, these animals were not injected with contrast agents). Red arrows denote the needle tracks and regions highlighted by contrast agents. (b–i) Histological evaluation of the same animals as shown in (a): (b, c) TNF- α only; (d, e) IV-SDIO only; (f, g) TNF- α + IV-SDIO; (h, i) TNF- α + IV-DIO. Blue arrows in (b), (f), and (h) denote small cavities in the brain that were observed. Images (c), (e), (g), and (i) show magnification of Iba-1 and iron staining of selected areas (red square) from images (b), (d), (f), and (h). Activated microglia at inflammation sites were stained brown by Iba-1 antibody, while iron oxide nanoparticles accumulated in the vicinity region were stained blue by Perls' Prussian blue. Scale bars represent 200 µ m.

    Article Snippet: Four milligrams of SDIO was dissolved in 150 μ L of injectable saline in a 1.5 mL Eppendorf vial and vortexed for 5 seconds to obtain a uniform solution.

    Techniques: Staining, Imaging, Injection, IV Injection