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Pasteur Institute human foreskin fibroblasts hff cell lines
Human Foreskin Fibroblasts Hff 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/human+foreskin+fibroblasts+cell+line+(hff)/fibroblast+foreskin+human/10__1007_slash_s10876___025___02959___z-36-5-16
Average 86 stars, based on 1 article reviews
human foreskin fibroblasts hff cell lines - by Bioz Stars, 2026-10
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Related Articles

Activity Assay:

Article Title: Enhanced antimicrobial effects of carvacrol against methicillin-resistant Staphylococcus aureus strains using niosome formulations.
Article Snippet: The ntibiotic profile evaluated included cefoxitin (10 g), vanomycin (10 g), ciprofloxacin (5 g), penicillin (10 g), rythromycin (15 g), trimethoprim (12.5 g), amikacin 15 g), ampicillin (10 g), gentamicin (10 g), amoxicillin 10 g), chloramphenicol (15 g) and clindamycin (10 g). he S. aureus ATCC 25923 strain served as the positive conrol. ntimicrobial activity of carvacrol--niosomes ompared to the free drug easurement of MIC and MBC o evaluate the antibacterial efficacy of the arvacrol--niosome formulation and its free form, the tudy utilized minimum inhibitory concentration (MIC) and I F i PRESS za Mohammadi et al. inimum bactericidal concentration (MBC) procedures. herefore, the MIC assessment, conducted in accorance with CLSI standards, involved a microbroth dilution pproach and was executed in triplicate for precision. oncentrations spanning from 7.8 to 1000 g/ml were used o determine the MIC for the samples. ell culture and cell viability assay he human foreskin fibroblasts (HFF) cell line (NCBI461 ode) was sourced from the Pasteur Institute of Iran.

Article Title: Bioresponsive gingerol-loaded alginate-coated niosomal nanoparticles for targeting intracellular bacteria and cancer cells.
Article Snippet: The Human foreskin fibroblasts (HFF) cell line and MDA-MB-231 cell line were purchased from Pasteur Institute Cell Bank, Tehran, Iran.

Article Title: Green Synthesis and Bioactivity of Aliphatic N-Substituted Glycine Derivatives.
Article Snippet: The human foreskin fibroblasts (HFF) cell line was prepared from the Pasteur Institute of Iran, (Tehran, Iran).

Article Title: Chitosan -based nanoniosome for potential wound healing applications: Synergy of controlled drug release and antibacterial activity.
Article Snippet: This study aims to develop a niosomal platform which can delivery drugs such as tetracycline hydrochloride (TCH) to treat bacterial infections in wounds.. To this end, chitosan (CS) was used to obtain a controlled drug release and at the same time antibacterial activity.. By design of experiments the niosome encapsulated TCH (TCH-Nio) were optimized for their particle size and encapsulation efficiency, followed by analysis of the release profile of TCH and stability of TCH-Nio and TCH-Nio@CS.

Formulation:

Article Title: Enhanced antimicrobial effects of carvacrol against methicillin-resistant Staphylococcus aureus strains using niosome formulations.
Article Snippet: The ntibiotic profile evaluated included cefoxitin (10 g), vanomycin (10 g), ciprofloxacin (5 g), penicillin (10 g), rythromycin (15 g), trimethoprim (12.5 g), amikacin 15 g), ampicillin (10 g), gentamicin (10 g), amoxicillin 10 g), chloramphenicol (15 g) and clindamycin (10 g). he S. aureus ATCC 25923 strain served as the positive conrol. ntimicrobial activity of carvacrol--niosomes ompared to the free drug easurement of MIC and MBC o evaluate the antibacterial efficacy of the arvacrol--niosome formulation and its free form, the tudy utilized minimum inhibitory concentration (MIC) and I F i PRESS za Mohammadi et al. inimum bactericidal concentration (MBC) procedures. herefore, the MIC assessment, conducted in accorance with CLSI standards, involved a microbroth dilution pproach and was executed in triplicate for precision. oncentrations spanning from 7.8 to 1000 g/ml were used o determine the MIC for the samples. ell culture and cell viability assay he human foreskin fibroblasts (HFF) cell line (NCBI461 ode) was sourced from the Pasteur Institute of Iran.

Article Title: Bioresponsive gingerol-loaded alginate-coated niosomal nanoparticles for targeting intracellular bacteria and cancer cells.
Article Snippet: The Human foreskin fibroblasts (HFF) cell line and MDA-MB-231 cell line were purchased from Pasteur Institute Cell Bank, Tehran, Iran.

Article Title: Green Synthesis and Bioactivity of Aliphatic N-Substituted Glycine Derivatives.
Article Snippet: The human foreskin fibroblasts (HFF) cell line was prepared from the Pasteur Institute of Iran, (Tehran, Iran).

Article Title: Chitosan -based nanoniosome for potential wound healing applications: Synergy of controlled drug release and antibacterial activity.
Article Snippet: This study aims to develop a niosomal platform which can delivery drugs such as tetracycline hydrochloride (TCH) to treat bacterial infections in wounds.. To this end, chitosan (CS) was used to obtain a controlled drug release and at the same time antibacterial activity.. By design of experiments the niosome encapsulated TCH (TCH-Nio) were optimized for their particle size and encapsulation efficiency, followed by analysis of the release profile of TCH and stability of TCH-Nio and TCH-Nio@CS.

Concentration Assay:

Article Title: Enhanced antimicrobial effects of carvacrol against methicillin-resistant Staphylococcus aureus strains using niosome formulations.
Article Snippet: The ntibiotic profile evaluated included cefoxitin (10 g), vanomycin (10 g), ciprofloxacin (5 g), penicillin (10 g), rythromycin (15 g), trimethoprim (12.5 g), amikacin 15 g), ampicillin (10 g), gentamicin (10 g), amoxicillin 10 g), chloramphenicol (15 g) and clindamycin (10 g). he S. aureus ATCC 25923 strain served as the positive conrol. ntimicrobial activity of carvacrol--niosomes ompared to the free drug easurement of MIC and MBC o evaluate the antibacterial efficacy of the arvacrol--niosome formulation and its free form, the tudy utilized minimum inhibitory concentration (MIC) and I F i PRESS za Mohammadi et al. inimum bactericidal concentration (MBC) procedures. herefore, the MIC assessment, conducted in accorance with CLSI standards, involved a microbroth dilution pproach and was executed in triplicate for precision. oncentrations spanning from 7.8 to 1000 g/ml were used o determine the MIC for the samples. ell culture and cell viability assay he human foreskin fibroblasts (HFF) cell line (NCBI461 ode) was sourced from the Pasteur Institute of Iran.

Article Title: Bioresponsive gingerol-loaded alginate-coated niosomal nanoparticles for targeting intracellular bacteria and cancer cells.
Article Snippet: The Human foreskin fibroblasts (HFF) cell line and MDA-MB-231 cell line were purchased from Pasteur Institute Cell Bank, Tehran, Iran.

Article Title: Green Synthesis and Bioactivity of Aliphatic N-Substituted Glycine Derivatives.
Article Snippet: The human foreskin fibroblasts (HFF) cell line was prepared from the Pasteur Institute of Iran, (Tehran, Iran).

Article Title: Chitosan -based nanoniosome for potential wound healing applications: Synergy of controlled drug release and antibacterial activity.
Article Snippet: This study aims to develop a niosomal platform which can delivery drugs such as tetracycline hydrochloride (TCH) to treat bacterial infections in wounds.. To this end, chitosan (CS) was used to obtain a controlled drug release and at the same time antibacterial activity.. By design of experiments the niosome encapsulated TCH (TCH-Nio) were optimized for their particle size and encapsulation efficiency, followed by analysis of the release profile of TCH and stability of TCH-Nio and TCH-Nio@CS.

Viability Assay:

Article Title: Enhanced antimicrobial effects of carvacrol against methicillin-resistant Staphylococcus aureus strains using niosome formulations.
Article Snippet: The ntibiotic profile evaluated included cefoxitin (10 g), vanomycin (10 g), ciprofloxacin (5 g), penicillin (10 g), rythromycin (15 g), trimethoprim (12.5 g), amikacin 15 g), ampicillin (10 g), gentamicin (10 g), amoxicillin 10 g), chloramphenicol (15 g) and clindamycin (10 g). he S. aureus ATCC 25923 strain served as the positive conrol. ntimicrobial activity of carvacrol--niosomes ompared to the free drug easurement of MIC and MBC o evaluate the antibacterial efficacy of the arvacrol--niosome formulation and its free form, the tudy utilized minimum inhibitory concentration (MIC) and I F i PRESS za Mohammadi et al. inimum bactericidal concentration (MBC) procedures. herefore, the MIC assessment, conducted in accorance with CLSI standards, involved a microbroth dilution pproach and was executed in triplicate for precision. oncentrations spanning from 7.8 to 1000 g/ml were used o determine the MIC for the samples. ell culture and cell viability assay he human foreskin fibroblasts (HFF) cell line (NCBI461 ode) was sourced from the Pasteur Institute of Iran.

Article Title: Bioresponsive gingerol-loaded alginate-coated niosomal nanoparticles for targeting intracellular bacteria and cancer cells.
Article Snippet: The Human foreskin fibroblasts (HFF) cell line and MDA-MB-231 cell line were purchased from Pasteur Institute Cell Bank, Tehran, Iran.

Article Title: Green Synthesis and Bioactivity of Aliphatic N-Substituted Glycine Derivatives.
Article Snippet: The human foreskin fibroblasts (HFF) cell line was prepared from the Pasteur Institute of Iran, (Tehran, Iran).

Article Title: Chitosan -based nanoniosome for potential wound healing applications: Synergy of controlled drug release and antibacterial activity.
Article Snippet: This study aims to develop a niosomal platform which can delivery drugs such as tetracycline hydrochloride (TCH) to treat bacterial infections in wounds.. To this end, chitosan (CS) was used to obtain a controlled drug release and at the same time antibacterial activity.. By design of experiments the niosome encapsulated TCH (TCH-Nio) were optimized for their particle size and encapsulation efficiency, followed by analysis of the release profile of TCH and stability of TCH-Nio and TCH-Nio@CS.



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Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell <t>line</t> <t>HFF-1</t> as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)
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Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell <t>line</t> <t>HFF-1</t> as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)
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Cell compatibility of CoPc‐Lig NPs. A) Cell viability of <t>fibroblasts</t> (black bars) and keratinocytes (white bars) exposed to different concentrations of CoPc‐Lig NPs for 24 h. B) Confocal images showing cell internalization of CoPc‐Lig NPs (0.5 mg/mL) by fibroblasts and keratinocytes. The dark areas in brightfield images represent CoPc‐Lig NPs, while the fluorescence channels show cell nuclei (Blue), and cell cytoskeleton (green).
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Image Search Results


Journal: Archiv Der Pharmazie

Article Title: Spirooxindole 5‐(Trifluoromethyl)benzothiazole Hybrids: Synthesis, Crystal Structure, and Antioxidant Activity

doi: 10.1002/ardp.70343

Figure Lengend Snippet: Cytotoxic effects of the selected compounds on HFF‐1 cells.

Article Snippet: Human foreskin fibroblast cell line (HFF‐1, ATCC, SCRC‐1041) was used in the study.

Techniques:

Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)

Journal: BMC Cancer

Article Title: Targeting EpCAM expression via near-infrared fluorescent antibodies enables microscopic delineation of primary and recurrent HNSCC

doi: 10.1186/s12885-026-16172-2

Figure Lengend Snippet: Expression of EpCAM on cell lines of SCC-UADT, HNSCC-associated fibroblasts, and normal fibroblasts. A Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 (ESCC) and FaDu (HNSCC), the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody VU1D9 (high EpCAM-affinity) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu). B Representative histogram and quantitative data on the percentage of EpCAM-positive cells as well as on the expression level of EpCAM of the SCC-UADT cell lines KYSE-30 and FaDu, the HNSCC-associated fibroblast cell line CAF-4, and the normal fibroblast cell line HFF-1 as assessed by flow cytometry upon immunostaining with the AlexaFluor488-labeled anti-EpCAM antibody MT201 (intermediate EpCAM-affinity; clinically validated) (mean ± SEM for n = 4; * p < .05 vs. CAF; # p < .05 vs. HFF; § p < .05 vs. KYSE-30; & p < .05 vs. FaDu)

Article Snippet: Human foreskin fibroblast cell line HFF-1 was purchased from ATCC (Manassas, USA; SCRC-1041).

Techniques: Expressing, Flow Cytometry, Immunostaining, Labeling

Cell compatibility of CoPc‐Lig NPs. A) Cell viability of fibroblasts (black bars) and keratinocytes (white bars) exposed to different concentrations of CoPc‐Lig NPs for 24 h. B) Confocal images showing cell internalization of CoPc‐Lig NPs (0.5 mg/mL) by fibroblasts and keratinocytes. The dark areas in brightfield images represent CoPc‐Lig NPs, while the fluorescence channels show cell nuclei (Blue), and cell cytoskeleton (green).

Journal: Macromolecular Bioscience

Article Title: Lignin Nanoparticles Containing Cobalt‐Cyanine Complexes: Potential Multifunctional Platforms for Photoacoustic Imaging and Photothermal Treatment of Bacterial Biofilms in Chronic Wounds

doi: 10.1002/mabi.202500532

Figure Lengend Snippet: Cell compatibility of CoPc‐Lig NPs. A) Cell viability of fibroblasts (black bars) and keratinocytes (white bars) exposed to different concentrations of CoPc‐Lig NPs for 24 h. B) Confocal images showing cell internalization of CoPc‐Lig NPs (0.5 mg/mL) by fibroblasts and keratinocytes. The dark areas in brightfield images represent CoPc‐Lig NPs, while the fluorescence channels show cell nuclei (Blue), and cell cytoskeleton (green).

Article Snippet: Bacterial strains ( Staphylococcus aureus ATCC 6538 and Pseudomonas aeruginosa ATCC 9027) and human fibroblast cell line (ATCC‐SCRC‐1041, HFF‐1) were purchased from the American Type Culture Collection (ATCC LGC Standards, Italy).

Techniques: Fluorescence