A collection of 105 discrete AuNPs were randomly selected from the HR-TEM images to measure the average diameter. The two most abundant diameters were 4 ~ 5 and 7 ~ 8 nm, which Entinostat mw accounted for 19% of the total (Figure 2D). Clear lattice fringes further confirmed the crystalline structure of the EW-AuNPs (Figure 2B,C). We previously obtained spherical EW-AuNPs with the diameter of 6.70 ± 2.69 nm using a green synthesis route with different reaction conditions [16]. Figure 2 HR-TEM images of the EW-AuNPs. The scale bar represents (A) 50 nm, (B) 5 nm, and (C) 5 nm. (D) Size histogram. Anticoagulant activity via aPTT assay

The EW-AuNPs reinforced or enhanced the anticoagulant activity of heparin by aPTT assay when the combination find more of EW-AuNPs and heparin was used for treatment (Figure 3). The clotting times of the negative (deionized water) and positive (heparin) controls were 44.1 and 50.8 s, respectively (Figure 3 parts A and B). No GF120918 significant anticoagulant activities were noted in the extract (47.2 s, Figure 3 part C), the EW-AuNPs (44.8 s, Figure 3 part D), or in heparin combined with the extract (50.9 s, Figure 3 part E). However, when heparin and the EW-AuNPs were combined, the clotting time was extended to 60.4 s (Figure 3 part F), which corresponds to an increase of 118.9% and 134.8% over the clotting times of the same concentrations of the positive control

(heparin) and the EW-AuNPs, respectively. Figure 3 Anticoagulant activity according to the aPTT assay. The values in parentheses indicate the final concentrations of each component in the assay. (A) Negative control (deionized water), (B) positive control (heparin, 0.02 U/mL), (C) the extract (0.03%), (D) the EW-AuNPs (0.03% EW and 60 μM HAuCl4 · 3H2O), (E) a combination of heparin (0.02 U/mL) with sample (C), and (F) a combination of heparin (0.02 U/mL) with sample (D). AFM images Casein kinase 1 As depicted in Figure 4A, the obtained AuNPs were primarily spherical. This result is consistent with the HR-TEM images presented in Figure 2. Following an ultracentrifugation/resuspension process, the pellets (EW-AuNPs) were redispersed in deionized water and examined via AFM. The 2-D

and 3-D images demonstrated that cubic and block-shaped AuNPs were also present as minor components (Figure 4B,C,D,E). Cross-sectional analysis further confirmed the block shape of the AuNPs (Figure 4F). Figure 4 AFM images of the EW-AuNPs. (A) 3-D height image (500 nm × 500 nm), (B) 2-D height image (2.5 μm × 2.5 μm), (C) 2-D amplitude error image (2.5 μm × 2.5 μm), (D) 3-D amplitude error image (2.5 μm × 2.5 μm), (E) 3-D height image (2.5 μm × 2.5 μm), and (F) cross-sectional analysis of both the length (line a-b) and the width (line c-d) from B. FE-SEM images When we imaged the cubic and block-shaped AuNPs via FE-SEM, these shapes appeared in a line that resembled fish bones (Figure 5A). A more detailed examination revealed cubic and block-shaped anisotropic particles.