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3.
<b>Figure 3.</b>  

Figure 3.  . Characterization of sutures made of random and aligned poly(ε-caprolactone) nanofibers. . From: Nanofiber-based sutures induce endogenous antimicrobial peptide.

(A) Photographs and scanning electron microscope images showing the morphology, surface structure and cross-section of sutures. (B) The strain–stress curves of sutures. (C) The break forces of sutures. These tests (n = 3) were repeated three times.
**p < 0.01.

Shixuan Chen, et al. Nanomedicine (Lond). 2017 Nov;12(21):2597-2609.
4.
<b>Figure 4.</b>  

Figure 4.  . Characterization of sutures made of poly(ε-caprolactone) aligned nanofibers and poly(ε-caprolactone)/F-127 co-axial aligned nanofibers. . From: Nanofiber-based sutures induce endogenous antimicrobial peptide.

(A) Photographs and scanning electron microscope images illustrating morphology, surface structure and cross-section of sutures made of PCL/F-127 co-axial nanofibers. (B) The strain–stress curves of sutures made of PCL nanofibers and PCL/F-127 co-axial nanofibers. (C) The break forces of sutures made of PCL nanofibers and PCL/F-127 co-axial nanofibers. These tests (n = 3) were repeated three times.
PCL: Poly(ε-caprolactone).

Shixuan Chen, et al. Nanomedicine (Lond). 2017 Nov;12(21):2597-2609.
5.
<b>Figure 5.</b>  

Figure 5.  . In vitro release profiles of 25-hydroxyvitamin D3 and FITC-dextran from sutures. . From: Nanofiber-based sutures induce endogenous antimicrobial peptide.

(A) The release profile of 25-hydroxyvitamin D3 alone loaded sutures (VD suture). (B) The release profiles of 25-hydroxyvitamin D3 and FITC-dextran (4.88 μg/ml) co-loaded sutures (VD + LC-dextran suture). (C) The release profiles of 25-hydroxyvitamin D3 and FITC-dextran (18.18 μg/ml) co-loaded sutures (VD + HC-dextran suture). These tests (n = 3) were repeated three times.

Shixuan Chen, et al. Nanomedicine (Lond). 2017 Nov;12(21):2597-2609.
6.
<b>Figure 6.</b>  

Figure 6.  . Cytotoxicity test of nanofiber sutures. . From: Nanofiber-based sutures induce endogenous antimicrobial peptide.

The proliferation of U937 (A), HL60 (B), keratinocytes (C) and dermal fibroblasts (D) after treatment with 1 mg/ml PCL sutures (control), 25-hydroxyvitamin D3 loaded PCL nanofiber sutures containing 100 μg/ml 25-hydroxyvitamin D3 (VD suture), 25-hydroxyvitamin D3 and peptide co-loaded PCL/pluronic F127 co-axial nanofiber sutures containing 100 μg/ml 25-hydroxyvitamin D3 and 4.88 μg/ml peptide (VD + LC-peptide suture), 25-hydroxyvitamin D3 and peptide co-loaded PCL/pluronic F127 co-axial nanofiber sutures containing 100 μg/ml 25-hydroxyvitamin D3 and 18.18 μg/ml peptide (VD + HC-peptide suture) for 1, 3 and 5 days. These tests (n = 3) were repeated three times.
PCL: Poly(ε-caprolactone).

Shixuan Chen, et al. Nanomedicine (Lond). 2017 Nov;12(21):2597-2609.
7.
<b>Figure 7.</b>  

Figure 7.  . Quantification of antimicrobial peptide LL-37 expression. . From: Nanofiber-based sutures induce endogenous antimicrobial peptide.

The LL-37 expression of U937 cells (A) and keratinocytes (B) after treatment with 1 mg/ml PCL sutures (control), 25-hydroxyvitamin D3 loaded PCL nanofiber sutures containing 100 μg/ml 25-hydroxyvitamin D3 (VD suture), 25-hydroxyvitamin D3 and peptide co-loaded PCL/pluronic F127 co-axial nanofiber sutures containing 100 μg/ml 25-hydroxyvitamin D3 and 4.88 μg/ml peptide (VD + LC-peptide suture), 25-hydroxyvitamin D3 and peptide co-loaded PCL/pluronic F127 co-axial nanofiber sutures containing 100 μg/ml 25-hydroxyvitamin D3 and 18.18 μg/ml peptide (VD + HC-peptide suture) for 1, 3 and 5 days. These tests (n = 3) were repeated three times.
PCL: Poly(ε-caprolactone).

Shixuan Chen, et al. Nanomedicine (Lond). 2017 Nov;12(21):2597-2609.

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