The Effects of Grape Seed Oligomeric Proanthocyanidin and Nisin on Dental Pulp Stem Cells.

Objective: This study aimed to evaluate the biological effects of "proanthocyanidin" (PA), and "nisin" (Ni), on dental pulp stem cells (DPSCs) and LPS-induced DPSCs as well as their antimicrobial effects against S. aureus and E. coli. Materials and methods: After characterization of DPSCs, cytotoxicity of PA and Ni on DPSCs were evaluated using a water-soluble tetrazolium salt (WST-1). The cytokines and chemokines released by DPSCs and the expression levels of IL-6, IL-8, and TNF alpha were detected with human Cytokine Array C5 and enzyme-linked immunosorbent assay (ELISA), respectively. The antibacterial activities of PA and Ni were tested using the drop plate method. Results: PA at 75 µg/ml increased cell viability, decreased TNF-α expression of DPSCs, did not show any cytotoxic effects on LPS-induced DPSCs, and also showed a tendency to decrease TNF-α expression. PA at 75 µg/ml exhibited higher expressions of TIMP-2, OPG, IL-7, and IL-8 in LPS-induced DPSCs compared to DPSCs. Ni at 100 µg/ml decreased TNF-α expression in DPSCs with no cytotoxic effects. It provided increased cell viability and a downregulation trend of TNF-α expression in LPS-induced DPSCs. Both Ni and PA provided strong antibacterial effects against S. aureus. Ni at 200µg/ml had strong antibacterial effects against E. coli without affecting negatively the viability of both DPSCs and LPS-induced DPSCs and showed anti-inflammatory activity by decreasing TNF-α expression. PA provided strong antibacterial effects against E. coli at 200 µg/ml but affected DPSCs viability negatively. Conclusion: PA and Ni at specific concentrations exhibited immunomodulatory activity on DPSCs and LPS-induced DPSCs without any cytotoxic effects and strong antibacterial effects on S. aureus.

Anti microbial corrosion properties of electrospun cellulose acetate nanofibers containing biogenic silver nanoparticles for copper coatings.

Nanofibers with inorganic nanoparticles are novel hybrid nanocomposites that have great potential in various areas. In the present study, cellulose acetate nanofibers (CA-Nf) loaded with biogenic silver nanoparticles were prepared and characterized. In situ synthesis of silver nanoparticles was accomplished using a bacteria free solution as a reducing agent. Nanofibers incorporated with silver nanoparticles were fabricated using the electrospinning technique. Upright microscopy and SEM micrographs depicted that the CA-Nf coatings consist of dense and compact entangled nanofibers that completely cover the copper surface. Corrosion measurements were performed by potentiodynamic polarization measurements and electrochemical impedance spectroscopy (EIS) techniques on the bare copper and CA-Nf and CA-Nf_5% AgNp coated copper surfaces in artificial seawater (ASW) and Escherichia coli ATCC 13883 inoculated solutions. Weight loss and electrochemical corrosion test results revealed that the CA-Nf-coated copper had greater corrosion resistance than bare copper. The additional electrospun CA-Nf_5% AgNp coating also had greater antibacterial behavior toward model biofilm bacterium Pseudomonas aeruginosa than uncoated copper specimens. Therefore, this nanofiber with AgNps was demonstrated as an efficient anticorrosive material in both corrosive and biocorrosive marine solutions.

Encapsulation of living bacteria in electrospun cyclodextrin ultrathin fibers for bioremediation of heavy metals and reactive dye from wastewater.

Cyclodextrins (CD) are cyclic oligosaccharides produced from the enzymatic degradation of starch as a white powder form; on the other hand, they can be transformed into ultrathin electrospun fiber form by electrospinning technique. The electrospun cyclodextrin fibers (CD-F) can be quite attractive materials to encapsulate bacteria for bioremediation purposes. For instance, CD-F not only serve as a carrier matrix but also it serves as a feeding source for the encapsulated bacteria. In the present study, we demonstrate a facile approach by encapsulation of bacteria into CD-F matrix for wastewater treatment application. The natural and non-toxic properties of CD-F render a better bacterial viability for fibrous biocomposite. The encapsulated bacteria in CD-F exhibit cell viability for more than 7days at 4°C storage condition. Furthermore, we have tested the bioremediation capability of bacteria/CD-F biocomposite for the treatment of heavy metals (Nickel(II) and Chromium(VI)) and textile dye (Reactive Black 5, RB5). The bacteria/CD-F biocomposite has shown removal efficiency of Ni(II), Cr(VI) and RB5 as 70±0.2%, 58±1.4% and 82±0.8, respectively. As anticipated, the pollutants removal capabilities of the bacteria/CD-F was higher compare to free bacteria since bacteria can use CD as an extra carbon source which promotes their growth rate. This study demonstrates that CD-F are suitable platforms for the encapsulation of bacterial cells to develop novel biocomposites that have bioremediation capabilities for wastewater treatment.

Bacteria immobilized electrospun polycaprolactone and polylactic acid fibrous webs for remediation of textile dyes in water.

In this study, preparation and application of novel biocomposite materials for textile dye removal which are produced by immobilization of specific bacteria onto electrospun nanofibrous webs are presented. A textile dye remediating bacterial isolate, Clavibacter michiganensis, was selected for bacterial immobilization, a commercial reactive textile dye, Setazol Blue BRF-X, was selected as the target contaminant, and electrospun polycaprolactone (PCL) and polylactic acid (PLA) nanofibrous polymeric webs were selected for bacterial integration. Bacterial adhesion onto nanofibrous webs was monitored by scanning electron microscopy (SEM) imaging and optical density (OD) measurements were performed for the detached bacteria. After achieving sufficient amounts of immobilized bacteria on electrospun nanofibrous webs, equivalent web samples were utilized for testing the dye removal capabilities. Both bacteria/PCL and bacteria/PLA webs have shown efficient remediation of Setazol Blue BRF-X dye within 48 h at each tested concentration (50, 100 and 200 mg/L), and their removal performances were very similar to the free-bacteria cells. The bacteria immobilized webs were then tested for five times of reuse at an initial dye concentration of 100 mg/L, and found as potentially reusable with higher bacterial immobilization and faster dye removal capacities at the end of the test. Overall, these findings suggest that electrospun nanofibrous webs are available platforms for bacterial integration and the bacteria immobilized webs can be used as starting inocula for use in remediation of textile dyes in wastewater systems.

Fast-Dissolving, Prolonged Release, and Antibacterial Cyclodextrin/Limonene-Inclusion Complex Nanofibrous Webs via Polymer-Free Electrospinning.

We have proposed a new strategy for preparing free-standing nanofibrous webs from an inclusion complex (IC) of a well-known flavor/fragrance compound (limonene) with three modified cyclodextrins (HPßCD, MßCD, and HPγCD) via electrospinning (CD/limonene-IC-NFs) without using a polymeric matrix. The experimental and computational modeling studies proved that the stoichiometry of the complexes was 1:1 for CD/limonene systems. MßCD/limonene-IC-NF released much more limonene at 37, 50, and 75 °C than HPßCD/limonene-IC-NF and HPγCD/limonene-IC-NF because of the greater amount of preserved limonene. Moreover, MßCD/limonene-IC-NF has released only 25% (w/w) of its limonene, whereas HPßCD/limonene-IC-NF and HPγCD/limonene-IC-NF released 51 and 88% (w/w) of their limonene in 100 days, respectively. CD/limonene-IC-NFs exhibited high antibacterial activity against E. coli and S. aureus. The water solubility of limonene increased significantly and CD/limonene-IC-NFs were dissolved in water in a few seconds. In brief, CD/limonene-IC-NFs with fast-dissolving character enhanced the thermal stability and prolonged the shelf life along with antibacterial properties could be quite applicable in food and oral care applications.