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Pasteur Institute human dermal fibroblast hdf cell lines
Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal <t>fibroblast</t> cells <t>(HDF)</t>
Human Dermal Fibroblast Hdf Cell Lines, supplied by Pasteur Institute, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hdf+cell+line/dermal+fibroblasts+hdf+human/pmc12834894-112-5-14
Average 86 stars, based on 1 article reviews
human dermal fibroblast hdf cell lines - by Bioz Stars, 2026-10
86/100 stars

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1) Product Images from "Evaluation of the antivirulence and anticancer potential of green-synthesized silver/zinc oxide nanocomposites against methicillin-resistant Staphylococcus aureus and melanoma cells"

Article Title: Evaluation of the antivirulence and anticancer potential of green-synthesized silver/zinc oxide nanocomposites against methicillin-resistant Staphylococcus aureus and melanoma cells

Journal: Discover Nano

doi: 10.1186/s11671-026-04444-6

Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal fibroblast cells (HDF)
Figure Legend Snippet: Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal fibroblast cells (HDF)

Techniques Used: Synthesized

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Article Title: Dual loading of Nigella sativa oil-atorvastatin in chitosan-carboxymethyl cellulose nanogel as a transdermal delivery system.
Article Snippet: Both Nigella sativa oil and atorvastatin possess anti-inflammatory, immunomodulatory, antioxidant, and antibacterial properties that benefit wound healing.. In this work, chitosan–carboxymethyl cellulose was loaded on N. sativa oil to synthesize oil nanogel (ONG) which was later used to load with atorvastatin to obtain atorvastatin-oil nanogel (ATONG).. Evaluation of the particle size of ONG and ATONG proved the average of 172 and 193nm, and their surface charges were found to be 32.2 and 34.7mV, respectively.

Article Title: Enhanced in vitro wound healing of human dermal fibroblasts using nanohydroxyapatite synthesized from Elaeagnus Angustifolia and loaded with crocin
Article Snippet: .. hDF cell Line was purchased from the cell bank of Pasteur Institute of Iran and cultured in DMEM medium containing 10% fetal bovine serum and 1% antibiotics, including penicillin and streptomycin. ..

Modification:

Article Title: Dual loading of Nigella sativa oil-atorvastatin in chitosan-carboxymethyl cellulose nanogel as a transdermal delivery system.
Article Snippet: Both Nigella sativa oil and atorvastatin possess anti-inflammatory, immunomodulatory, antioxidant, and antibacterial properties that benefit wound healing.. In this work, chitosan–carboxymethyl cellulose was loaded on N. sativa oil to synthesize oil nanogel (ONG) which was later used to load with atorvastatin to obtain atorvastatin-oil nanogel (ATONG).. Evaluation of the particle size of ONG and ATONG proved the average of 172 and 193nm, and their surface charges were found to be 32.2 and 34.7mV, respectively.

other:

Article Title: Comparison between novel star-like redox-sensitive amphiphilic block copolymer and its linear counterpart copolymer as nanocarriers for doxorubicin.
Article Snippet: Linear and star-like redox-sensitive amphiphilic block copolymers have been studied as anticancer drug delivery systems.. However, few reports directly compared the properties of those two structures especially when they are used as nanocarriers for antitumor drugs.. To address this, a novel star-like copolymer and its linear counterpart were synthesized with a hydrophobic/redox-responsive/hydrophilic structure.

Article Title: Impacts of the Staphylococcal Enterotoxin H on the Apoptosis and lncRNAs in PC3 and ACHN
Article Snippet: ACHN (human renal cell adenocarcinoma), PC3 (human prostate adenocarcinoma cell line) and HDF (human dermal fibroblasts-normal) cell lines were purchased from the National Cell Bank of Iran (Pasteur Institute, Tehran, Iran).

Article Title: Inhibitory potency of the nettle lectin on neovascularization: a biomolecule for carbohydrate-mediated targeting of angiogenesis.
Article Snippet: The human umbilical vein endothelial cells (HUVEC), human dermal fibroblast (HDF), human normal breast (MCF-10 A), human brain cancer (U87 glioblastoma), human epidermoid carcinoma (A431), mouse normal adipose fibroblast-like (L929), and mouse breast tumor cells (4T1) cell lines were purchased from Pasteur Institute, Iran.



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Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal <t>fibroblast</t> cells <t>(HDF)</t>
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In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF <t>(CCD‐986Sk)</t> cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.
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In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF <t>(CCD‐986Sk)</t> cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.
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Pasteur Institute hdf normal fibroblast cell lines
In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF <t>(CCD‐986Sk)</t> cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.
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Image Search Results


Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal fibroblast cells (HDF)

Journal: Discover Nano

Article Title: Evaluation of the antivirulence and anticancer potential of green-synthesized silver/zinc oxide nanocomposites against methicillin-resistant Staphylococcus aureus and melanoma cells

doi: 10.1186/s11671-026-04444-6

Figure Lengend Snippet: Cell viability % efficiency of the green synthesized Ag/ZnO NCs. a Human malignant melanoma cells (A375), b Human dermal fibroblast cells (HDF)

Article Snippet: The human melanoma (A375) and human dermal fibroblast (HDF) cell lines, obtained from the Pasteur Institute (Tehran, Iran), were cultured in Roswell Park Memorial Institute (RPMI) 1640 medium supplemented with 10% fetal bovine serum (FBS), 100 U/mL penicillin G, and 100 μg/mL streptomycin.

Techniques: Synthesized

In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF (CCD‐986Sk) cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.

Journal: Advanced Healthcare Materials

Article Title: Skin‐Interfaced Therapeutic Patches for Wound Fluid Management and Transdermal Drug Delivery

doi: 10.1002/adhm.202504450

Figure Lengend Snippet: In vitro evaluation of wound healing enhancement effects of the integrated device. (a) Schematic representation of PDRN delivery via iontophoresis into the culture medium. (b) Fluorescence images of HDK (HaCaT) cells from different experimental groups captured at indicated time points. (c) Cell proliferation ratios of HDK cells from each group assessed at indicated time points. (d) Fluorescence images of HDF (CCD‐986Sk) cells and (e) corresponding proliferation ratios from each experimental group recorded at indicated time points. (f) Microscopic images showing scratch assays of HDK cells for each group at specific time intervals. (g) Quantitative analysis of scratch areas in HDK cells from each group across indicated time intervals. (h) Microscopic images of scratch assays performed on HDF cells and i) corresponding quantitative analysis of scratch areas from each group over time. Data represent means ± SD; n = 5. Statistical analysis was performed using one‐way ANOVA with Bonferroni‐corrected post‐hoc t ‐tests. Statistical significance: * p < 0.05, ** p < 0.01, *** p < 0.001.

Article Snippet: The HDF cell line CCD‐986Sk (RRID: CVCL_4200) was obtained from the Korean Cell Line Bank (KCLB, Seoul, South Korea) on August 2024 and was likewise confirmed to be free of contamination upon arrival.

Techniques: In Vitro, Fluorescence