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Articles

Silver nanoparticles synthesized with Rumex hymenosepalus extracts: effective broad-spectrum microbicidal agents and cytotoxicity study

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Pages 1194-1206 | Received 04 Apr 2017, Accepted 07 Aug 2017, Published online: 21 Aug 2017

Figures & data

Figure 1. Flowchart diagram of the mechanism of synthesis of biogenic AgNPsC.

Figure 1. Flowchart diagram of the mechanism of synthesis of biogenic AgNPsC.

Figure 2. UV-Vis of AgNPsC after the washing process.

Figure 2. UV-Vis of AgNPsC after the washing process.

Figure 3. FT-IR spectra of AgNPsC (a) and Rh, RhA, and RhB (b).

Figure 3. FT-IR spectra of AgNPsC (a) and Rh, RhA, and RhB (b).

Figure 4. Typical TEM micrograph of the obtained AgNPsC (a), EDS of AgNPsC (b), and size distribution obtained by TEM (c).

Figure 4. Typical TEM micrograph of the obtained AgNPsC (a), EDS of AgNPsC (b), and size distribution obtained by TEM (c).

Figure 5. HRTEM of single AgNPsC (a), by fast Fourier transform plot (b), and integrated image from the FFT plot (c).

Figure 5. HRTEM of single AgNPsC (a), by fast Fourier transform plot (b), and integrated image from the FFT plot (c).

Figure 6. XR diffraction of AgNPsC (a) and high-resolution XPS spectrum of AgNPsC (b).

Figure 6. XR diffraction of AgNPsC (a) and high-resolution XPS spectrum of AgNPsC (b).

Figure 7. DPPH for RhA and RhB.

Figure 7. DPPH for RhA and RhB.

Table 1. The content of total polyphenols for Rh, RhA, and RhB.

Figure 8. Antibacterial activity of AgNPsC and Rh on E. coli ATCC25922 disc method (a), and well diffusion method with two different nanoparticle sizes (b) and (c).

Figure 8. Antibacterial activity of AgNPsC and Rh on E. coli ATCC25922 disc method (a), and well diffusion method with two different nanoparticle sizes (b) and (c).

Figure 9. Antibacterial activity of AgNPsC and Rh extract for S. aureus ATCC25923 disc method (a), and well diffusion method with two different sizes of nanoparticles (b) and (c).

Figure 9. Antibacterial activity of AgNPsC and Rh extract for S. aureus ATCC25923 disc method (a), and well diffusion method with two different sizes of nanoparticles (b) and (c).

Figure 10. Antibacterial activity of AgNPsC for RhA, and RhB for S. aureus ATCC 25923 (a). Only the inhibition over C. albicans by AgNPsC is shown (b) and E. coli 0157:H7 ATCC 43895 (c).

Figure 10. Antibacterial activity of AgNPsC for RhA, and RhB for S. aureus ATCC 25923 (a). Only the inhibition over C. albicans by AgNPsC is shown (b) and E. coli 0157:H7 ATCC 43895 (c).

Table 2. Inhibition halo of E. coli ATCC 25922 (Gram-negative) and S. aureus ATCC 25923 (Gram-positive) using AgNPsC and Rh by the well and disc diffusion methods.

Table 3. Inhibition halo of Gram-positive, Gram-negative, and yeast using AgNPsC.

Table 4. Inhibition halo of Gram-positive using fraction RhA and fraction RhB.

Figure 11. MTT assay for AgNPsC for PBMC.

Figure 11. MTT assay for AgNPsC for PBMC.

Figure 12. LD assay by monocytes of PBMC for Rh (a–c), RhA (e–g), RhB (i–k), and MTT assay for Rh (d), RhA (h), and RhB (l).

Figure 12. LD assay by monocytes of PBMC for Rh (a–c), RhA (e–g), RhB (i–k), and MTT assay for Rh (d), RhA (h), and RhB (l).

Figure 13. LD assay by monocytes of THP-1 for AgNPsC (a–c), positive control using AgNO3 (d,f), and TB test with AgNPsC over monocytes of THP-1 (g).

Figure 13. LD assay by monocytes of THP-1 for AgNPsC (a–c), positive control using AgNO3 (d,f), and TB test with AgNPsC over monocytes of THP-1 (g).
Supplemental material

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