Journal: Biomacromolecules

Article Title: Synthesis, Physicochemical Characterization, and Cytocompatibility of Bioresorbable, Dual-Gelling Injectable Hydrogels

doi: 10.1021/bm401413c

Figure Lengend Snippet: Viability of rat fibroblasts in in vitro cytocompatibility testing of TGM and hydrogel leachable products with 6 mol % DBA at 2 and 24 h. The first column corresponds to TGM leachables, and the second and third columns correspond to hydrogel leachables with P-1440 and P-2600 crosslinker, respectively. The top and bottom rows refer to 10 or 20 wt % hydrogels, respectively. Data are reported as means ± standard deviation for a sample size of n = 6. * and # indicate statistical significance (p<0.05) within and between timepoints, respectively.

Article Snippet: A rat fibroblast cell line (ATCC, CRL-1764) was chosen for the in vitro cytocompatibility tests.

Techniques: In Vitro, Standard Deviation

Journal: Biomacromolecules

Article Title: Synthesis, Physicochemical Characterization, and Cytocompatibility of Bioresorbable, Dual-Gelling Injectable Hydrogels

doi: 10.1021/bm401413c

Figure Lengend Snippet: Viability of rat fibroblasts in in vitro cytocompatibility testing of 6 mol % DBA-containing hydrogel degradation products. Rows correspond to the hydrogel TGM wt % (10 or 20 wt %), while columns refer to the PAMAM crosslinker used at a 1:1 amine:epoxy mol ratio (P-1440 or P-2600). Data are reported as means ± standard deviation for a sample size of n = 6. * and # indicate statistical significance (p<0.05) within and between timepoints, respectively.

Article Snippet: A rat fibroblast cell line (ATCC, CRL-1764) was chosen for the in vitro cytocompatibility tests.

Techniques: In Vitro, Standard Deviation

Journal: ACS Applied Materials & Interfaces

Article Title: Long-Term Controlled Growth Factor Release Using Layer-by-Layer Assembly for the Development of In Vivo Tissue-Engineered Blood Vessels

doi: 10.1021/acsami.2c05988

Figure Lengend Snippet: General overview of the cellular composition of the tissue capsule formed around implanted rods. (A) vWF staining for vascularization, (B) Ki67 for proliferating cells, (C) α-SMA for myofibroblast, (D) desmin for contractile smooth muscle cells, and (E) vimentin for fibroblast. The tissue capsules are mainly composed of fibroblasts and myofibroblasts. There are barely contractile smooth muscle cells present. All tissue capsules are well vascularized. Scale bar represents 50 μm.

Article Snippet: Adult rat dermal fibroblasts (aRDF, #R2320, ScienCell Research Laboratories) were cultured with a basic culture medium comprising DMEM (Gibco), fetal bovine serum (10%, Lonza), l -glutamine (2 mM, Gibco), and penicillin (100 U/mL) and streptomycin (100 mg/mL, Gibco). aRDF were expanded at an initial seeding density of 5000 cells/cm 2 in a culture medium and refreshed every 2–3 days.

Techniques: Staining, Capsules

Journal: ACS Applied Materials & Interfaces

Article Title: Long-Term Controlled Growth Factor Release Using Layer-by-Layer Assembly for the Development of In Vivo Tissue-Engineered Blood Vessels

doi: 10.1021/acsami.2c05988

Figure Lengend Snippet: (A) The number of cells (per 1000 μm 2 ) positively stained for α-smooth muscle actin is depicted, a differentiation marker for myofibroblasts. (B) The number of cells (per 1000 μm 2 ) stained positively with the desmin antibody is depicted, which stains the intermediate filament protein expressed in contractile smooth muscle cells. (C) The number of cells (per 1000 μm 2 ) positively stained for vimentin is depicted, which is an intermediate filament expressed in fibroblasts. The expressions of myofibroblasts, contractile smooth muscle cells, and fibroblasts were observed in the following conditions: control (no release), burst release (TGF-β1 and PDGF-BB), single layer-by-layer release (TGF-β1, PDGF-BB, and IGF-1), and dual layer-by-layer release (TGF-β1/IGF-1 and PDGF-BB/TGF-β1). Data was analyzed using ordinary one-way ANOVA followed by a post hoc analysis using Tukey’s test, and * indicates significance of P ≤ 0.05, ** P ≤ 0.01, *** P ≤ 0.001, and **** P ≤ 0.0001.

Article Snippet: Adult rat dermal fibroblasts (aRDF, #R2320, ScienCell Research Laboratories) were cultured with a basic culture medium comprising DMEM (Gibco), fetal bovine serum (10%, Lonza), l -glutamine (2 mM, Gibco), and penicillin (100 U/mL) and streptomycin (100 mg/mL, Gibco). aRDF were expanded at an initial seeding density of 5000 cells/cm 2 in a culture medium and refreshed every 2–3 days.

Techniques: Staining, Marker, Control