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human foreskin fibroblast cells  (ATCC)


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    ATCC human foreskin fibroblast cells
    Characteristics, cytotoxicity, and antioxidant activity of cannabidiol-loaded lipid nanoparticles (CBD/LNPs). ( A ) Morphology of CBD/LNPs as demonstrated by Transmission Electron Microscopy (TEM); ( B ) Cell viability relative to the control in <t>fibroblast-cultured</t> cells exposed to CBD/LNPs; ( C ) Radical oxidative stress levels induced by hydrogen peroxide exposure were measured by the fluorescent intensity of dichlorofluorescein (DCF) relative to the control group, referring to untreated cells exposed only to the medium without any treatment. The analysis was conducted in fibroblast cultures treated with CBD/LNPs. Data are expressed as mean ± SEM ( n = 4). * p < 0.05, ** p < 0.01, and *** p < 0.001 compared to the blank group.
    Human Foreskin Fibroblast Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human foreskin fibroblast cells/product/ATCC
    Average 97 stars, based on 1 article reviews
    human foreskin fibroblast cells - by Bioz Stars, 2025-03
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    1) Product Images from "Cannabidiol-Loaded Lipid Nanoparticles Incorporated in Polyvinyl Alcohol and Sodium Alginate Hydrogel Scaffold for Enhancing Cell Migration and Accelerating Wound Healing"

    Article Title: Cannabidiol-Loaded Lipid Nanoparticles Incorporated in Polyvinyl Alcohol and Sodium Alginate Hydrogel Scaffold for Enhancing Cell Migration and Accelerating Wound Healing

    Journal: Gels

    doi: 10.3390/gels10120843

    Characteristics, cytotoxicity, and antioxidant activity of cannabidiol-loaded lipid nanoparticles (CBD/LNPs). ( A ) Morphology of CBD/LNPs as demonstrated by Transmission Electron Microscopy (TEM); ( B ) Cell viability relative to the control in fibroblast-cultured cells exposed to CBD/LNPs; ( C ) Radical oxidative stress levels induced by hydrogen peroxide exposure were measured by the fluorescent intensity of dichlorofluorescein (DCF) relative to the control group, referring to untreated cells exposed only to the medium without any treatment. The analysis was conducted in fibroblast cultures treated with CBD/LNPs. Data are expressed as mean ± SEM ( n = 4). * p < 0.05, ** p < 0.01, and *** p < 0.001 compared to the blank group.
    Figure Legend Snippet: Characteristics, cytotoxicity, and antioxidant activity of cannabidiol-loaded lipid nanoparticles (CBD/LNPs). ( A ) Morphology of CBD/LNPs as demonstrated by Transmission Electron Microscopy (TEM); ( B ) Cell viability relative to the control in fibroblast-cultured cells exposed to CBD/LNPs; ( C ) Radical oxidative stress levels induced by hydrogen peroxide exposure were measured by the fluorescent intensity of dichlorofluorescein (DCF) relative to the control group, referring to untreated cells exposed only to the medium without any treatment. The analysis was conducted in fibroblast cultures treated with CBD/LNPs. Data are expressed as mean ± SEM ( n = 4). * p < 0.05, ** p < 0.01, and *** p < 0.001 compared to the blank group.

    Techniques Used: Antioxidant Activity Assay, Transmission Assay, Electron Microscopy, Control, Cell Culture

    Effects of cannabidiol-loaded lipid nanoparticles (CBD/LNPs) on wound healing in fibroblast-cultured cells. ( A ) Human dermal fibroblast cells were treated with 50 ppm CBD/LNPs or 100 ng/mL FGF (positive control). A scratch wound assay was monitored at 0, 24, and 48 h post-scratch and compared to untreated control cells. ( B ) Percentage of wound gap closure at 24 and 48 h, calculated relative to the initial scratch width (T 0 ). Data are expressed as mean ± SEM ( n = 3). *** p < 0.001 compared to the control group.
    Figure Legend Snippet: Effects of cannabidiol-loaded lipid nanoparticles (CBD/LNPs) on wound healing in fibroblast-cultured cells. ( A ) Human dermal fibroblast cells were treated with 50 ppm CBD/LNPs or 100 ng/mL FGF (positive control). A scratch wound assay was monitored at 0, 24, and 48 h post-scratch and compared to untreated control cells. ( B ) Percentage of wound gap closure at 24 and 48 h, calculated relative to the initial scratch width (T 0 ). Data are expressed as mean ± SEM ( n = 3). *** p < 0.001 compared to the control group.

    Techniques Used: Cell Culture, Positive Control, Scratch Wound Assay Assay, Control



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    Characteristics, cytotoxicity, and antioxidant activity of cannabidiol-loaded lipid nanoparticles (CBD/LNPs). ( A ) Morphology of CBD/LNPs as demonstrated by Transmission Electron Microscopy (TEM); ( B ) Cell viability relative to the control in fibroblast-cultured cells exposed to CBD/LNPs; ( C ) Radical oxidative stress levels induced by hydrogen peroxide exposure were measured by the fluorescent intensity of dichlorofluorescein (DCF) relative to the control group, referring to untreated cells exposed only to the medium without any treatment. The analysis was conducted in fibroblast cultures treated with CBD/LNPs. Data are expressed as mean ± SEM ( n = 4). * p < 0.05, ** p < 0.01, and *** p < 0.001 compared to the blank group.

    Journal: Gels

    Article Title: Cannabidiol-Loaded Lipid Nanoparticles Incorporated in Polyvinyl Alcohol and Sodium Alginate Hydrogel Scaffold for Enhancing Cell Migration and Accelerating Wound Healing

    doi: 10.3390/gels10120843

    Figure Lengend Snippet: Characteristics, cytotoxicity, and antioxidant activity of cannabidiol-loaded lipid nanoparticles (CBD/LNPs). ( A ) Morphology of CBD/LNPs as demonstrated by Transmission Electron Microscopy (TEM); ( B ) Cell viability relative to the control in fibroblast-cultured cells exposed to CBD/LNPs; ( C ) Radical oxidative stress levels induced by hydrogen peroxide exposure were measured by the fluorescent intensity of dichlorofluorescein (DCF) relative to the control group, referring to untreated cells exposed only to the medium without any treatment. The analysis was conducted in fibroblast cultures treated with CBD/LNPs. Data are expressed as mean ± SEM ( n = 4). * p < 0.05, ** p < 0.01, and *** p < 0.001 compared to the blank group.

    Article Snippet: Human foreskin fibroblast cells (ATCC SCRC-1041) were cultured in DMEM (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS) and 100 µg/mL streptomycin (Pen&Strep).

    Techniques: Antioxidant Activity Assay, Transmission Assay, Electron Microscopy, Control, Cell Culture

    Effects of cannabidiol-loaded lipid nanoparticles (CBD/LNPs) on wound healing in fibroblast-cultured cells. ( A ) Human dermal fibroblast cells were treated with 50 ppm CBD/LNPs or 100 ng/mL FGF (positive control). A scratch wound assay was monitored at 0, 24, and 48 h post-scratch and compared to untreated control cells. ( B ) Percentage of wound gap closure at 24 and 48 h, calculated relative to the initial scratch width (T 0 ). Data are expressed as mean ± SEM ( n = 3). *** p < 0.001 compared to the control group.

    Journal: Gels

    Article Title: Cannabidiol-Loaded Lipid Nanoparticles Incorporated in Polyvinyl Alcohol and Sodium Alginate Hydrogel Scaffold for Enhancing Cell Migration and Accelerating Wound Healing

    doi: 10.3390/gels10120843

    Figure Lengend Snippet: Effects of cannabidiol-loaded lipid nanoparticles (CBD/LNPs) on wound healing in fibroblast-cultured cells. ( A ) Human dermal fibroblast cells were treated with 50 ppm CBD/LNPs or 100 ng/mL FGF (positive control). A scratch wound assay was monitored at 0, 24, and 48 h post-scratch and compared to untreated control cells. ( B ) Percentage of wound gap closure at 24 and 48 h, calculated relative to the initial scratch width (T 0 ). Data are expressed as mean ± SEM ( n = 3). *** p < 0.001 compared to the control group.

    Article Snippet: Human foreskin fibroblast cells (ATCC SCRC-1041) were cultured in DMEM (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% fetal bovine serum (FBS) and 100 µg/mL streptomycin (Pen&Strep).

    Techniques: Cell Culture, Positive Control, Scratch Wound Assay Assay, Control