Chemical Engineering / Kimya Mühendisliği

Permanent URI for this collectionhttps://hdl.handle.net/11147/14

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  • Article
    Citation - WoS: 12
    Citation - Scopus: 13
    Development of Agcl-Tio2 Xerogels Entrapped Antibacterial Polyacrylonitrile Membranes: the Effect of High Salinity Water on Silver Release, Antibiofouling and Antibacterial Efficacies
    (Elsevier Ltd., 2020) Uz, Metin; Yaşar Mahlıçlı, Filiz; Şeker, Erol; Alsoy Altınkaya, Sacide
    Silver-containing antibacterial membranes are commonly used to control biofouling during bacteria filtration. Unfortunately, fast and uncontrolled release of silver to water is a challenge since this causes mass accumulation of silver in water resources and insufficient long-term antimicrobial effect. To overcome these disadvantages, we propose to add AgCl-TiO2 xerogels (0–0.8 wt%) in the polyacrylonitrile membranes. The long-term silver retaining of the membranes was evaluated by measuring the silver release under filtration of deionized water in the absence and the presence of 1 M NaCl up to 5 days. The antibiofouling and the antibacterial efficacies were determined by measuring the changes in antibacterial activity and DI water flux of the membranes at the end of 5 days of E. coli filtration. The 0.2 wt% AgCl-TiO2 xerogel incorporated polyacrylonitrile membrane demonstrated a constant ~1 ?g of silver release/cm2 per filtration cycle after a total filtration of 0.05 L/cm2 with 1 M NaCl solution. Additionally, it showed antibacterial efficacy and ~100% recovery of deionized water flux by simple backwashing with water after having been used in many E. coli filtration cycles. Thus, this membrane could potentially be used up to ~5.8 years for 8000 h a year for the filtration of high salinity water. Statement of novelty: Silver-containing antibacterial membranes are commonly used to control biofouling during bacteria filtration. Uncontrolled release of silver from the membrane causes massive silver accumulation in water which in turn leads to contamination of water resources and threat to aquatic organisms. Although silver release is strongly influenced by the salinity of water, the release data was collected through filtration of pure DI water or tap water in literature. To overcome the shortcomings of the published studies, we propose to use AgCl-TiO2 xerogels in membranes due to low solubility of AgCl in water and measure the release by filtering high-salinity water. © 2020 Elsevier B.V.
  • Article
    Citation - WoS: 40
    Citation - Scopus: 47
    Gelatin-Based 3d Conduits for Transdifferentiation of Mesenchymal Stem Cells Into Schwann Cell-Like Phenotypes
    (Elsevier Ltd., 2017) Uz, Metin; Büyüköz, Melda; Sharma, Anup D.; Sakaguchi, Donald S.; Alsoy Altınkaya, Sacide; Mallapragada, Surya K.
    In this study, gelatin-based 3D conduits with three different microstructures (nanofibrous, macroporous and ladder-like) were fabricated for the first time via combined molding and thermally induced phase separation (TIPS) technique for peripheral nerve regeneration. The effects of conduit microstructure and mechanical properties on the transdifferentiation of bone marrow-derived mesenchymal stem cells (MSCs) into Schwann cell (SC) like phenotypes were examined to help facilitate neuroregeneration and understand material-cell interfaces. Results indicated that 3D macroporous and ladder-like structures enhanced MSC attachment, proliferation and spreading, creating interconnected cellular networks with large numbers of viable cells compared to nanofibrous and 2D-tissue culture plate counterparts. 3D-ladder-like conduit structure with complex modulus of ∼0.4 × 106 Pa and pore size of ∼150 μm provided the most favorable microenvironment for MSC transdifferentiation leading to ∼85% immunolabeling of all SC markers. On the other hand, the macroporous conduits with complex modulus of ∼4 × 106 Pa and pore size of ∼100 μm showed slightly lower (∼65% for p75, ∼75% for S100 and ∼85% for S100β markers) immunolabeling. Transdifferentiated MSCs within 3D-ladder-like conduits secreted significant amounts (∼2.5 pg/mL NGF and ∼0.7 pg/mL GDNF per cell) of neurotrophic factors, while MSCs in macroporous conduits released slightly lower (∼1.5 pg/mL NGF and 0.7 pg/mL GDNF per cell) levels. PC12 cells displayed enhanced neurite outgrowth in media conditioned by conduits with transdifferentiated MSCs. Overall, conduits with macroporous and ladder-like 3D structures are promising platforms in transdifferentiation of MSCs for neuroregeneration and should be further tested in vivo. Statement of Significance This manuscript focuses on the effect of microstructure and mechanical properties of gelatin-based 3D conduits on the transdifferentiation of mesenchymal stem cells to Schwann cell-like phenotypes. This work builds on our recently accepted manuscript in Acta Biomaterialia focused on multifunctional 2D films, and focuses on 3D microstructured conduits designed to overcome limitations of current strategies to facilitate peripheral nerve regeneration. The comparison between conduits fabricated with nanofibrous, macroporous and ladder-like microstructures showed that the ladder-like conduits showed the most favorable environment for MSC transdifferentiation to Schwann-cell like phenotypes, as seen by both immunolabeling as well as secretion of neurotrophic factors. This work demonstrates the importance of controlling the 3D microstructure to facilitate tissue engineering strategies involving stem cells that can serve as promising approaches for peripheral nerve regeneration.
  • Article
    Citation - WoS: 44
    Citation - Scopus: 60
    Development of a Novel Strategy for Controlled Release of Lysozyme From Whey Protein Isolate Based Active Food Packaging Films
    (Elsevier Ltd., 2016) Pekşen Özer, Bahar Başak; Uz, Metin; Oymacı, Pelin; Alsoy Altınkaya, Sacide
    The purpose of this study is to develop a novel controlled release system based on pH-responsive polyacrylic acid (PAA)/lysozyme (LYS) complexes incorporated within a hydrophilic whey protein isolate (WPI) film matrix for active food packaging applications. Complex formation is simple under benign conditions that are suitable for preserving antimicrobial activity of the lysozyme. In addition, the pH-dependent charge density of complexes allowed a uniform distribution in the matrix. The properties of the complexes such as size, surface charge and hydrophilicity were varied by changing PAA/LYS ratio (0.1 and 0.3 w/w) and PAA molecular weight (2 kDa and 450 kDa). The effects of complex properties as well as mode of lysozyme incorporation into the films (100%-free, 50%-free+50%-PAA/LYS complex and 100%-PAA/LYS complex) on the LYS release rate, activity and antimicrobial efficacy of the films were investigated. The results have shown that ∼100% LYS loading into the complexes is possible regardless of PAA molecular weight or PAA/LYS ratio. Incorporating lysozyme into the film in complexed form extended its release time from less than 24 h up to 500 h and reduced its diffusivity from ∼10−9 to ∼10−13 cm2/s. The films including 50%-free-LYS+50%-PAA/LYS complex showed a 5.7 log reduction in bacterial population within 72 h whereas 100%-free-LYS containing film could not suppress Listeria innocua growth after 24 h. Overall, the results suggest that complexation of lysozyme with weak polyelectrolytes can be used as an effective strategy to achieve a long-lasting antimicrobial effect and that films prepared with such complexes have great potential as food packaging materials.
  • Conference Object
    Citation - Scopus: 3
    Characterization of Polysulfone Based Hemodialysis Membranes by Afm
    (Elsevier Ltd., 2012) Uz, Metin; Yaşar Mahlıçlı, Filiz; Polat, Mehmet; Alsoy Altınkaya, Sacide
    Most of the hemodialysis membrane materials are hydrophobic in nature and allow protein adsorption on the surface easily due to hydrophobic interaction between membrane surface and protein molecules when in contact with blood. Adsorbed proteins can affect platelet and leukocyte adhesion, and modulate the response of plasmatic reactions followed by the activation of different defense systems in blood (Sun et al. 2003).