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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
Human Dermal Fibroblasts, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
Vitro Cytotoxicity Assay Human Dermal Fibroblast Adult Hdfa Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
Hsf, supplied by ATCC, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
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hdfa  (ATCC)
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Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
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dermal fibroblasts hdfa  (ATCC)
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ATCC dermal fibroblasts hdfa
Effects of Epilobium dodonaei extracts on human dermal <t>fibroblast</t> (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).
Dermal Fibroblasts Hdfa, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hdfa/Primary+Dermal+Fibroblast%3B+Normal%2C+Human%2C+Adult/10__3892_slash_br__2026__2124-69-59-63
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Effects of Epilobium dodonaei extracts on human dermal fibroblast (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).

Journal: RSC Advances

Article Title: Harnessing the anti-inflammatory, skin-protective, and antioxidant potential of Epilobium dodonaei extracts using in vitro and in silico approaches

doi: 10.1039/d6ra01632d

Figure Lengend Snippet: Effects of Epilobium dodonaei extracts on human dermal fibroblast (HDF) cell proliferation by WST-1 analysis. (A) Effect of MeOH extract at concentrations of 25–100 µg mL −1 on HDF cell viability. (B) Proliferation profile of H 2 O extract in the same concentration range. The control group (HDF) was considered to have 100% viability. Data were presented as mean ± SD. Statistical significance was evaluated using GraphPad Prism software compared to the control group (ns: p > 0.05; *** p < 0.001; **** p < 0.0001).

Article Snippet: Also hTERT-immortalized normal human dermal fibroblasts (CRL-4066) were obtained from the American Type Culture Collection (ATCC, Manassas, VA, USA) and have been previously employed in our studies to ensure methodological consistency and reproducibility.

Techniques: Concentration Assay, Control, Software