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ir783  (MedChemExpress)


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    Structured Review

    MedChemExpress ir783
    Ir783, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ir783/product/MedChemExpress
    Average 93 stars, based on 2 article reviews
    ir783 - by Bioz Stars, 2026-06
    93/100 stars

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    (a) Cytotoxicity of HeLa cells incubated with free IR820, IR-T, and IR-DT at different concentrations (50, 100, 150, and 200 μg/mL) for 4 h. (b) NIR confocal laser scanning microscopic images of HeLa cells incubated with IR-DT nanoprobes. Scale bar = 50 μm. Excitation for the nanoprobes was 640 nm, excitation for HOCHEST was 405 nm. (c) Flow cytometric analysis of HeLa cells incubated with various concentrations (50, 100, 150, and 200 μg/mL) of <t>IR783,</t> IR-T nanoprobes, and IR-DT nanoprobes in aqueous dispersion, respectively.
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    (a) Cytotoxicity of HeLa cells incubated with free IR820, IR-T, and IR-DT at different concentrations (50, 100, 150, and 200 μg/mL) for 4 h. (b) NIR confocal laser scanning microscopic images of HeLa cells incubated with IR-DT nanoprobes. Scale bar = 50 μm. Excitation for the nanoprobes was 640 nm, excitation for HOCHEST was 405 nm. (c) Flow cytometric analysis of HeLa cells incubated with various concentrations (50, 100, 150, and 200 μg/mL) of <t>IR783,</t> IR-T nanoprobes, and IR-DT nanoprobes in aqueous dispersion, respectively.
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    (a) Cytotoxicity of HeLa cells incubated with free IR820, IR-T, and IR-DT at different concentrations (50, 100, 150, and 200 μg/mL) for 4 h. (b) NIR confocal laser scanning microscopic images of HeLa cells incubated with IR-DT nanoprobes. Scale bar = 50 μm. Excitation for the nanoprobes was 640 nm, excitation for HOCHEST was 405 nm. (c) Flow cytometric analysis of HeLa cells incubated with various concentrations (50, 100, 150, and 200 μg/mL) of <t>IR783,</t> IR-T nanoprobes, and IR-DT nanoprobes in aqueous dispersion, respectively.
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    Makoto USA Inc micelle-encapsulated ir783
    (a) Cytotoxicity of HeLa cells incubated with free IR820, IR-T, and IR-DT at different concentrations (50, 100, 150, and 200 μg/mL) for 4 h. (b) NIR confocal laser scanning microscopic images of HeLa cells incubated with IR-DT nanoprobes. Scale bar = 50 μm. Excitation for the nanoprobes was 640 nm, excitation for HOCHEST was 405 nm. (c) Flow cytometric analysis of HeLa cells incubated with various concentrations (50, 100, 150, and 200 μg/mL) of <t>IR783,</t> IR-T nanoprobes, and IR-DT nanoprobes in aqueous dispersion, respectively.
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    (a) Cytotoxicity of HeLa cells incubated with free IR820, IR-T, and IR-DT at different concentrations (50, 100, 150, and 200 μg/mL) for 4 h. (b) NIR confocal laser scanning microscopic images of HeLa cells incubated with IR-DT nanoprobes. Scale bar = 50 μm. Excitation for the nanoprobes was 640 nm, excitation for HOCHEST was 405 nm. (c) Flow cytometric analysis of HeLa cells incubated with various concentrations (50, 100, 150, and 200 μg/mL) of IR783, IR-T nanoprobes, and IR-DT nanoprobes in aqueous dispersion, respectively.

    Journal: ACS Omega

    Article Title: Theranostic Nanoprobes Assisted NIR-II Fluorescence Imaging for Efficient Angiography and Tumor Therapy

    doi: 10.1021/acsomega.5c01553

    Figure Lengend Snippet: (a) Cytotoxicity of HeLa cells incubated with free IR820, IR-T, and IR-DT at different concentrations (50, 100, 150, and 200 μg/mL) for 4 h. (b) NIR confocal laser scanning microscopic images of HeLa cells incubated with IR-DT nanoprobes. Scale bar = 50 μm. Excitation for the nanoprobes was 640 nm, excitation for HOCHEST was 405 nm. (c) Flow cytometric analysis of HeLa cells incubated with various concentrations (50, 100, 150, and 200 μg/mL) of IR783, IR-T nanoprobes, and IR-DT nanoprobes in aqueous dispersion, respectively.

    Article Snippet: For metabolic imaging, IR783 and IR-DT nanoprobes (200 μL, 2.7 mg/kg) were intravenously injected into mice and imaged at different time points (2, 4, 8, 24, 48, and 72 h) by using the NIR-II imaging system (MARS-Pathfinder) under 808 nm laser irradiation.

    Techniques: Incubation, Dispersion

    (a) In vivo NIR-II fluorescence imaging of IR-DT nanoprobes and IR783-treated nude mice at different time points (2 h, 4 h, 8 h, 24 h, 48 h, and 72 h). (b) Corresponding fluorescence intensity analysis at different time points in (a). (c) Corresponding quantitative fluorescence analysis of main organs in (d).

    Journal: ACS Omega

    Article Title: Theranostic Nanoprobes Assisted NIR-II Fluorescence Imaging for Efficient Angiography and Tumor Therapy

    doi: 10.1021/acsomega.5c01553

    Figure Lengend Snippet: (a) In vivo NIR-II fluorescence imaging of IR-DT nanoprobes and IR783-treated nude mice at different time points (2 h, 4 h, 8 h, 24 h, 48 h, and 72 h). (b) Corresponding fluorescence intensity analysis at different time points in (a). (c) Corresponding quantitative fluorescence analysis of main organs in (d).

    Article Snippet: For metabolic imaging, IR783 and IR-DT nanoprobes (200 μL, 2.7 mg/kg) were intravenously injected into mice and imaged at different time points (2, 4, 8, 24, 48, and 72 h) by using the NIR-II imaging system (MARS-Pathfinder) under 808 nm laser irradiation.

    Techniques: In Vivo, Fluorescence, Imaging