Journal: Journal of materials chemistry. B

Article Title: Injectable biocompatible hydrogels with tunable strength based on crosslinked supramolecular polymer nanofibers.

doi: 10.1039/d4tb01873g

Figure Lengend Snippet: Fig. 11 Transmitted light microscopy images of L929 mouse fibroblast cells incubated on the BTP-C6 hydrogel for 72 hours: (a) image taken on the hydrogel, and (b) image of cells reseeded after 48 hours of incubation, collected from the top of the hydrogel. Optical magnification is 10 and the scale bar is 100 mm.

Article Snippet: L929 cells (CLS Cell Lines Service GmbH, Eppelheim, Germany) were cultured in TC-treated cell culture flasks (Greiner Bio-One International GmbH and Labsolute Th.

Techniques: Light Microscopy, Incubation

Journal: Journal of materials chemistry. B

Article Title: Injectable biocompatible hydrogels with tunable strength based on crosslinked supramolecular polymer nanofibers.

doi: 10.1039/d4tb01873g

Figure Lengend Snippet: Fig. 12 Relative metabolic activity (%) of L929 mouse fibroblast cells growing on the BTP-C6 hydrogel was determined using the PrestoBluet assay. The experiments were conducted as triplicate for four different passages represented as P1, P2, P3, and P4. The calculated mean values were depicted using lines.

Article Snippet: L929 cells (CLS Cell Lines Service GmbH, Eppelheim, Germany) were cultured in TC-treated cell culture flasks (Greiner Bio-One International GmbH and Labsolute Th.

Techniques: Activity Assay

Journal: International Journal of Nanomedicine

Article Title: h CeO 2 @CA-074Me Nanoparticles Alleviate Inflammation and Improve Osteogenic Microenvironment by Regulating the CTSB-NLRP3 Signaling Pathway

doi: 10.2147/IJN.S389156

Figure Lengend Snippet: Biocompatibility of h CeO 2 and h CeO 2 @CA-074Me NPs. ( A ) The 24, 48, and 72 h cytocompatibility of h CeO 2 NPs respectively. ( B ) The 24, 48, and 72 h cytocompatibility of h CeO 2 @CA-074Me NPs respectively. ( C ) Blood compatibility of h CeO 2 @CA-074Me NPs. (+) and (-) represent positive and negative controls, respectively. ( D ) Live/dead fluorescence staining images of L929 treated with h CeO 2 NPs for 24, 48, and 72 h. Scale bar: 100 μm. Data represent mean ± SD (n = 5; * represents significant differences. *p < 0.05, **P < 0.005, ***P < 0.0005, ****P < 0.0001).

Article Snippet: The L929 cell line was purchased from ScienCell (San Diego, CA, USA) and cultured in DMEM with 10% FBS, 10,000 U/mL penicillin, and 10 mg/mL streptomycin.

Techniques: Fluorescence, Staining

Journal: Polymers

Article Title: Antibacterial Chitosan Nanofiber Thin Films with Bacitracin Zinc Salt

doi: 10.3390/polym13071104

Figure Lengend Snippet: The cell viability of L929 fibroblasts after incubation with the thin films for 24 h (** p < 0.01).

Article Snippet: The cytotoxicity of the films was estimated from the viability of L929 fibroblasts (KAC Co., Ltd., Kyoto, Japan).

Techniques: Incubation

Journal: International Journal of Molecular Sciences

Article Title: Development and Functional Characterization of Recombinant Mussel Adhesive Protein for Anti-Oxidative and Anti-Aging Therapeutic Applications

doi: 10.3390/ijms262411947

Figure Lengend Snippet: NGT-M001 coacervate promotes cell attachment. NGT-M001 and NGT-M004 (each final 1 mg/mL) coacervate formation with 1% Hyaluronic acid, scale bar = 100 μm ( A ). Schematic of shown the coacervate 3D culture system and microscopic observation after MTT staining of L929 cell 3D cultures at various concentrations of NGT-M001, which exhibits excellent coacervate forming ability, scale bar = 300 μm ( B ).

Article Snippet: The L929 cell line (mouse fibroblast) was obtained from the Korean Cell Line Bank (KCLB; #10001, Seoul, Republic of Korea).

Techniques: Cell Attachment Assay, Staining