A bi-functional nanofibrous composite membrane for wound healing applications.

Various wound dressings have been developed so far for wound healing, but most of them are ineffective in properly reestablishing the skin's structure, which increases infection risks and dehydration. Electrospun membranes are particularly interesting for wound dressing applications because they mimic the extracellular matrix of healthy skin. In this study, a potential wound healing platform capable of inducing synergistic antibacterial and antioxidation activities was developed by incorporating bio-active rosmarinic acid-hydroxyapatite hybrid (HAP-RA) with different contents (0.5, 1, and 1.5 wt.%) into the electrospun polyamide 6 (PA6) nanofibers. Then, polyethylene glycol (PEG) was introduced to the nanofibrous composite to improve the biocompatibility and biodegradability of the dressing. The results indicated that the hydrophilicity, water uptake, biodegradability, and mechanical properties of the obtained PA6/PEG/HAP-RA nanofibrous composite enhanced at 1 wt.% of HAP-RA. The nanofibrous composite had excellent antibacterial activity. The antioxidation potential of the samples was assessed in vitro. The MTT assay performed on the L929 cell line confirmed the positive effects of the nanofibrous scaffold on cell viability and proliferation. According to the results, the PA6/PEG/HAP-RA nanofibrous composite showed the desirable physiochemical and biological properties besides antibacterial and antioxidative capabilities, making it a promising candidate for further studies in wound healing applications.

Improving properties of platelet-rich fibrin scaffold with tannic acid for wound healing.

Platelet-rich fibrin (PRF), which is the rich source of growth factors, has been used as an efficient scaffold in tissue engineering and wound healing. In this study, tannic acid as a green cross-linker with different concentrations (0.5%, 1%, 5% and 10%) was used to improve the properties of PRF. The cross-linked gel scaffolds were evaluated by analyses such as scanning electron microscopy, Fourier transform infrared spectroscopy, swelling and degradation, mechanical strength, cell toxicity, cell adhesion and antibacterial test. The results showed that the scaffold structure changes by increasing cross-linker concentration. The swelling rate decreased from 49% to 5% for the samples without the cross-linker and with tannic acid (10%), respectively. The degradation percentage for the cross-linked samples was 8%, which showed a lower degradation rate than the non-cross-linked samples (63%). The mechanical strength of the scaffold with the cross-linker increased up to three times (Young's modulus for the non-cross linked and the cross-linked samples: 0.01 and 0.6 MPa, respectively). Cytotoxicity was not observed up to 10% cross-linker concentration. The cells proliferated well on the cross-linked scaffolds and also showed a good antibacterial effect. In general, tannic acid can improve the physical and mechanical properties of PRF without negatively affecting its biological properties.

Curing Kinetics Modeling of Epoxy Modified by Fully Vulcanized Elastomer Nanoparticles Using Rheometry Method.

In this study, the curing kinetics of epoxy nanocomposites containing ultra-fine full-vulcanized acrylonitrile butadiene rubber nanoparticles (UFNBRP) at different concentrations of 0, 0.5, 1 and 1.5 wt.% was investigated. In addition, the effect of curing temperatures was studied based on the rheological method under isothermal conditions. The epoxy resin/UFNBRP nanocomposites were characterized via Fourier transform infrared spectroscopy (FTIR). FTIR analysis exhibited the successful preparation of epoxy resin/UFNBRP, due to the existence of the UFNBRP characteristic peaks in the final product spectrum. The morphological structure of the epoxy resin/UFNBRP nanocomposites was investigated by both field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) studies. The FESEM and TEM studies showed UFNBRP had a spherical structure and was well dispersed in epoxy resin. The chemorheological analysis showed that due to the interactions between UFNBRP and epoxy resin, by increasing UFNBRP concentration at a constant temperature (65, 70 and 75 °C), the curing rate decreases at the gel point. Furthermore, both the curing kinetics modeling and chemorheological analysis demonstrated that the incorporation of 0.5% UFNBRP in epoxy resin matrix reduces the activation energy. The curing kinetic of epoxy resin/UFNBRP nanocomposite was best fitted with the Sestak-Berggren autocatalytic model.

Photo-induced green synthesis of bimetallic Ag/Pd nanoparticles decorated reduced graphene oxide/nitrogen-doped graphene quantum dots nanocomposite as an amperometric sensor for nitrite detection.

The present study introduces a novel nanocomposite based on reduced graphene oxide, nitrogen-doped graphene quantum dots, and palladium and silver nanoparticles (rGO/NGQD/AgPd) as an electrocatalyst toward nitrite oxidation reaction. Metal nanoparticles were prepared via a green one-pot photochemical reduction procedure utilizing UV light and NGQD simultaneously as a reducing and directing agent. Formation of the nanocomposite was thoroughly demonstrated by the FT-IR, XRD, Raman, XPS, FE-SEM, and TEM characterization tests. Various electrochemical tests evaluated the efficiency of the prepared sensing platform on the surface of a gold working electrode. Sensitivity and limit of detection (LOD) were calculated to be 0.854 µA.µM-1.cm-2 and 0.052 µM, respectively, from the chronoamperometry data. Finally, the proposed sensor was successfully applied for the determination of nitrite ions in river and mineral water samples as natural water sources.

Kinetic Modeling and Degradation Study of Liquid Polysulfide Resin-Clay Nanocomposite.

Kinetic modeling and degradation study of liquid polysulfide (LPS)/clay nanocomposite is possible through Ozawa-Flynn-Wall (OFW) and Kissinger methods. Comparing the results of these models with experimental data leads to provide an accurate degradation kinetic evaluation of these materials. To this aim, the morphology and distribution of clay nanoparticles (CNPs) within the LPS matrix were investigated using Field Emission Scanning Electron Microscopy (FESEM) and X-ray diffraction (XRD). To evaluate the interaction between the LPS and the CNPs, the Fourier transform infrared (FTIR) identification was utilized. Furthermore, to investigate the kinetics of degradation, the thermal gravimetric analysis (TGA) and derivative thermogravimetry (DTG) of the samples were used in the nitrogen atmosphere with the help of Kissinger and Ozawa-Flynn-Wall (OFW) models. The characterization results confirmed the homogenous dispersion of the CNPs into the LPS matrix. In addition, the presence of CNPs increased the thermal stability and activation energy (Ea) of the samples at different conversion rates. Moreover, the OFW method was highly consistent with the experimental data and provided an appropriate fit for the degradation kinetics.

Thermal Degradation Kinetics and Modeling Study of Ultra High Molecular Weight Polyethylene (UHMWP)/Graphene Nanocomposite.

The incorporation of nanofillers such as graphene into polymers has shown significant improvements in mechanical characteristics, thermal stability, and conductivity of resulting polymeric nanocomposites. To this aim, the influence of incorporation of graphene nanosheets into ultra-high molecular weight polyethylene (UHMWPE) on the thermal behavior and degradation kinetics of UHMWPE/graphene nanocomposites was investigated. Scanning electron microscopy (SEM) analysis revealed that graphene nanosheets were uniformly spread throughout the UHMWPE's molecular chains. X-Ray Diffraction (XRD) data posited that the morphology of dispersed graphene sheets in UHMWPE was exfoliated. Non-isothermal differential scanning calorimetry (DSC) studies identified a more pronounced increase in melting temperatures and latent heat of fusions in nanocomposites compared to UHMWPE at lower concentrations of graphene. Thermogravimetric analysis (TGA) and derivative thermogravimetric (DTG) revealed that UHMWPE's thermal stability has been improved via incorporating graphene nanosheets. Further, degradation kinetics of neat polymer and nanocomposites have been modeled using equations such as Friedman, Ozawa-Flynn-Wall (OFW), Kissinger, and Augis and Bennett's. The "Model-Fitting Method" showed that the auto-catalytic nth-order mechanism provided a highly consistent and appropriate fit to describe the degradation mechanism of UHMWPE and its graphene nanocomposites. In addition, the calculated activation energy (Ea) of thermal degradation was enhanced by an increase in graphene concentration up to 2.1 wt.%, followed by a decrease in higher graphene content.

Electrospinning of zein/propolis nanofibers; antimicrobial properties and morphology investigation.

In this work, for the first time, zein nanofiber mats loaded with ethanol extracts propolis (EEP) were successfully produced. Raw propolis was extracted by ethanol 70% and total flavonoid content was estimated by aluminum chloride colorimetric method. The anti-microbial activity of the EEP was investigated and compared with amoxicillin via zone of inhibition test against various microorganisms included gram-positive: Staphylococcus aureus, Staphylococcus epidermidis, gram-negative: Escherichia coli, Salmonella enterica, Pseudomonas aeruginosa and fungus: Candida albicans. The EEP showed activity only against gram-positive types and fungus, whereas no activity was observed against gram-negative types. Electrospun zein nanofiber was obtained from 70% ethanolic solutions included different content of zein, 15-40 wt.%. The SEM images revealed a smooth ribbon-like morphology for zein nanofibers without any beads in zein content more than 25 wt.%. As well, the SEM images of electrospun zein nanofibers containing different content of propolis (0-40 wt.% based on the zein content) disclosed the increase in the average size of fibers with propolis content from 264 to 419 nm. This increasing was more probably due to the reduction in ionic conductivity of zein solutions with propolis content. The proteinic nature of zein along with the antimicrobial activity and the herbal nature of the propolis make the obtained mats promising candidate for more evaluation in wound healing study.

Viscoelastic Properties of Human Tracheal Tissues.

The physiological performance of trachea is highly dependent on its mechanical behavior, and therefore, the mechanical properties of its components. Mechanical characterization of trachea is key to succeed in new treatments such as tissue engineering, which requires the utilization of scaffolds which are mechanically compatible with the native human trachea. In this study, after isolating human trachea samples from brain-dead cases and proper storage, we assessed the viscoelastic properties of tracheal cartilage, smooth muscle, and connective tissue based on stress relaxation tests (at 5% and 10% strains for cartilage and 20%, 30%, and 40% for smooth muscle and connective tissue). After investigation of viscoelastic linearity, constitutive models including Prony series for linear viscoelasticity and quasi-linear viscoelastic, modified superposition, and Schapery models for nonlinear viscoelasticity were fitted to the experimental data to find the best model for each tissue. We also investigated the effect of age on the viscoelastic behavior of tracheal tissues. Based on the results, all three tissues exhibited a (nonsignificant) decrease in relaxation rate with increasing the strain, indicating viscoelastic nonlinearity which was most evident for cartilage and with the least effect for connective tissue. The three-term Prony model was selected for describing the linear viscoelasticity. Among different models, the modified superposition model was best able to capture the relaxation behavior of the three tracheal components. We observed a general (but not significant) stiffening of tracheal cartilage and connective tissue with aging. No change in the stress relaxation percentage with aging was observed. The results of this study may be useful in the design and fabrication of tracheal tissue engineering scaffolds.

Novel carboxymethyl cellulose based nanocomposite membrane: Synthesis, characterization and application in water treatment.

Significant efforts have been made to develop composite membranes with high adsorption efficiencies for water treatment. In this study, a carboxymethyl cellulose-graft-poly(acrylic acid) membrane was synthesized in the presence of silica gel, which was used as an inorganic support. Then, different amounts of bentonite were introduced to the carboxymethyl cellulose (CMC) grafted networks as a multifunctional crosslinker, and nanocomposite membranes were prepared. The nanocomposite membranes were characterized using Fourier transform infrared spectroscopy, and scanning electron microscopy, which revealed their compositions and surface morphologies. The novel synthesized nanocomposite membranes were utilized as adsorbents for the removal of crystal violet (CV) and cadmium (Cd (II)) ions, which were selected as representatives of a dye and a heavy metal, respectively. We explored the effects of various parameters, such as time, pH, temperature, initial concentration of adsorbate solution and amount of adsorbent, on membrane adsorption capacity. Furthermore, the kinetic, adsorption isotherm models and thermodynamic were employed for the description of adsorption processes. The maximum adsorption capacities of membranes for CV and Cd (II) ions were found to be 546 and 781 mg g(-1), respectively. The adsorption of adsorbate ions by all types of nanocomposite membranes followed pseudo-second-order kinetic model and was best fit with the Freundlich adsorption isotherm. The results indicated that the synthesized nanocomposite membrane is an efficient adsorbent for the removal of cationic dye and metal contaminants from aqueous solution during water treatment.

Synthesis and evaluation of hydroponically alginate nanoparticles as novel carrier for intravenous delivery of propofol.

Commercial lipid emulsion of propofol (CLE) has several drawbacks including pain on injection and emulsion instability. In this paper, a novel nanocarrier system is introduced to improve stability and solubility of the poorly soluble anesthetic drug, propofol, for intravenous administration. In this paper, alginate is modified using a facile method in which the carboxylic group of alginate is grafted to octanol. The octanol-grafted alginate (Alg-C8) is then employed to prepare nanoparticles which are subsequently used for encapsulation of propofol. The nanoparticles are analyzed for their pH, osmolarity, particle size, stability, morphology and sleep recovery and the results are compared with CLE as control. It is revealed that nanoparticles have the average particle size of 180 nm ± 1.2 and spherical morphology which is less than CLE while their pH, osmolarity and profile of release of formulated nanoparticles are similar to those of CLE. In addition, the results show good chemical and physical storage stability for the nanoparticles at room temperature for at least 6 months compared to CLE as control. The animal sleep recovery test on rats shows no significant difference in time of unconsciousness and recovery of the righting reflex between nanoparticles and CLE. It is concluded that encapsulated nanoparticles introduced here could be a promising clinical intravenous system for delivery of poorly soluble anesthetic propofol. In addition, this study provides an efficient and facile method for preparing a carrier system for water insoluble drugs.

Optimization of factors affecting hexavalent chromium removal from simulated electroplating wastewater by synthesized magnetite nanoparticles.

Hexavalent chromium is a mutagen and carcinogen that is of significant concern in water and wastewater. In the present study, magnetite nanoparticles (n-Mag) were investigated as a potential remediation technology for the decontamination of Cr (VI)-contaminated wastewater. Synthesized n-Mag was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), and BET-N2 technology. To screen and optimize the factors affecting Cr (VI) removal efficiency by synthesized nanoparticles, Plackett-Burman (PB) and Taguchi experimental designs were used respectively. The crystalline produced n-Mag was in the size range of 60-70 nm and had a specific surface area (SSA) of 31.55 m(2) g(-1). Results of PB design showed that the most significant factors affecting Cr (VI) removal efficiency were initial Cr (VI) concentration, pH, n-Mag dosage, and temperature. In a pH of 2, 20 mg L(-1) of Cr (VI) concentration, 4 g L(-1)of n-Mag, temperature of 40 °C, 220 rpm of shaking speed, and 60 min of contact time, the complete removal efficiency of Cr (VI) was achieved. Batch experiments revealed that the removal of Cr (VI) by n-Mag was consistent with pseudo-second order reaction kinetics. The competition from common coexisting ions such as NO3(-), SO4(2-), and Cl(-) were not considerable, unless in the higher concentration of SO4(2-). These results indicated that the readily synthesized magnetite nanoparticles have promising applications for the removal of Cr (VI) from aqueous solution.

Preparation of N,N-p-phenylene bismethacryl amide as a novel cross-link agent for synthesis and characterization of the core-shell magnetic molecularly imprinted polymer nanoparticles.

Novel magnetic molecularly imprinted nanoparticles (MMIPs) using N,N-p-phenylene bismethacryl amide as a cross linker and super paramagnetic core-shell nanoparticle as a supporter for use in controlled release were prepared by precipitation polymerization. Novel cross-linking agents were synthesized by the reaction of methacryloyl chloride with p-phenylenediamine. Then, the Fe3O4 nanoparticles were encapsulated with a SiO2 shell and functionalized with -CH=CH2 and MMIPs were further prepared by using methacrylic acid as a functional monomer, N,N-p-phenylene bismethacryl amide as a cross-linking agent and betamethasone as template. Magnetic non-MIPs were also prepared with the same synthesis procedure as with MMIPs only without the presence of the template. The obtained MMIPs were characterized by using transmission electron microscopy, Fourier transform infrared spectrum, X-ray diffraction, energy-dispersive X-ray spectroscopy, and the vibrating sample magnetometer. The performance of the MMIPs for the controlled release of betamethasone was assessed and results indicated that the magnetic MIPs also had potential applications in drug controlled release.

Photocatalytic activation of peroxydisulfate by UV-LED through rGO/g-C3N4/SiO2 nanocomposite for ciprofloxacin removal: Mineralization, toxicity, degradation pathways, and application for real matrix.

If trace amounts of antibiotics remain in the environment, they can lead to microbial pathogens becoming resistant to antibiotics and putting ecosystem health at risk. For instance, ciprofloxacin (CIP) can be found in surface and ground waters, suggesting that conventional water treatment technologies are ineffective at removing it. Now, a rGO/g-C3N4/SiO2 nanocomposite was synthesized in this study to activate peroxydisulfate (PDS) under UVA-LED irradiation. UVA-LED/rGO-g-C3N4-SiO2/PDS system performance was evaluated using Ciprofloxacin as an antibiotic. Particularly, rGO/g-C3N4/SiO2 showed superior catalytic activity for PDS activation to remove CIP. Operational variables, reactive species determination, and mechanisms were investigated. 0.85 mM PDS and 0.3 g/L rGO/g-C3N4/SiO2 eliminated 99.63% of CIP in 35 min and mineralized 59.78% in 100 min at pH = 6.18. By scavenging free radicals, bicarbonate ions inhibit CIP degradation. According to the trapping experiments, superoxide (O2•-) was the main active species rather than sulfate (SO4•-) and hydroxyl radicals (•OH). RGO/g-C3N4/SiO2 showed an excellent recyclable capability of up to six cycles. The UVA-LED/rGO-g-C3N4-SiO2/PDS system was also tested under real conditions. The system efficiency was reasonable. By calculating the synergistic factor (SF), this work highlights the benefit of combining composite, UVA-LED, and PDS. UVA-LED/rGO-g-C3N4-SiO2/PDS had also been predicted to be an eco-friendly process based on the results of the ECOSAR program. Consequently, this study provides a novel and durable nanocomposite with supreme thermal stability that effectively mitigates environmental contamination by eliminating antibiotics from wastewater.

Synthesis, characterization, and application of N-CNT/1-(2-Hydroxyethyl)-3-methylimidazolium dicyanamide as a green nanocatalyst for the sulfur removal from light oils.

Adsorptive desulfurization of light fuels is sustainable due to its ambient operation and reusability of exhausted adsorbents. In this study, 1-(2-hydroxyethyl)-3-methylimidazolium dicyanamide [HEMIM][DCA] IL was synthesized and utilized to modify N-doped carbon nanotubes (CNTs) to produce N-CNT/[HEMIM][DCA] as a green hybrid adsorbent. The adsorbent was characterized using XRD, FE-SEM, FTIR, BET, and TGA. It was indicated that the N-CNT treatment with [HEMIM][DCA] IL resulted in decreased crystallinity with the cubic and rod-shaped morphology and harsh surfaces and curved edges. The absence of shifts or variations in FTIR peaks of starting materials and N-CNT/[HEMIM][DCA] suggested that neither component was affected by chemical interactions. The adsorption capacity of N-CNT and N-CNT/[HEMIM][DCA] was 54.3 mg/g and for 83.6 mg/g for 50 ppm BT, respectively. Saturated with BT, the adsorbent's performance was decreased at high BT concentrations. The adsorption isotherms provided an understanding of interactions of BT with sorbent surface which follows the Langmuir model for N-CNT/[HEMIM][DCA] and N-CNT. The kinetics of BT adsorption on N-CNT/[HEMIM][DCA] was fitted with second-order kinetic model with the decreased adsorption ratio over time due to pore saturation. 25 % reduction of the adsorption capacity was obtained after two recycling cycles of the adsorbent (62.5 mg/g). N-CNT/[HEMIM][DCA] showed good recyclability and potential as a promising BT adsorbent.

Novel targeted delivery of quercetin for human hepatocellular carcinoma using starch/polyvinyl alcohol nanocarriers based hydrogel containing Fe2O3 nanoparticles.

The common adverse effects of chemotherapy are the reason for the use of effective, natural drugs and targeted administration to specific areas. On the one hand, Quercetin (QC) has positive effects as a natural anticancer agent. On the other hand, Fe2O3, as nanoparticles (NP) with clinical properties and high porosity, can be a suitable carrier for drug loading and controlled release. In this study, QC was encapsulated in a synthesized Fe2O3/Starch/Polyvinyl alcohol nanocarrier (Fe2O3/S/PVA NC). Characterization of the NC was done by Fourier transforms infrared spectroscopy (FTIR), X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), vibrating sample magnetometer (VSM), zeta potential and Dynamic light scattering (DLS). The percentage of drug loading (DLE) and encapsulation efficiency (EE) of QC in the NC containing Fe2O3 nanoparticles was 47 % and 86.50 %, respectively, while it was 36 % and 73 % in the NC without Fe2O3. QC profile release in acidic and natural mediums showed controlled release and pH dependency of the NC. Viability of L929 and HepG2 treated cells with the Fe2O3/S/PVA/QC was demonstrated by MTT staining which was in agreement with flow cytometry. The results show that Fe2O3/S/PVA is a suitable NC for the targeted delivery of QC as a drug against HepG2 cancer cells.

Enhanced delivery of doxorubicin for breast cancer treatment using pH-sensitive starch/PVA/g-C3N4 hydrogel.

This study introduces a starch/PVA/g-C3N4 nanocarrier hydrogel for pH-sensitive DOX delivery in breast cancer. DOX was loaded into the nanocarrier with 44.75 % loading efficiency and 88 % Entrapment Efficiency. The release of DOX from the starch/PVA/g-C3N4 hydrogel was pH-sensitive: DOX was released faster in the acidic environment pertinent to cancer tumors (with a pH level of 5.4) than in the surrounding regular tissue environment carrying a more neutral environment (pH 7.4). The release kinetics analysis, encompassing zero-order, first-order, Higuchi, and Korsmeyer-Peppas models, revealed significant fitting with the Higuchi model at both pH 5.4 (R2 = 0.99, K = 9.89) and pH 7.4 (R2 = 0.99, K = 5.70) levels. Finally, we found that hydrogel was less damaging to healthy cells and more specific to apoptotic cells than the drug's free form. The starch/PVA/g-C3N4 hydrogel had low toxicity for both normal cells and breast cancer cells, whereas DOX loaded into the starch/PVA/g-C3N4 hydrogel had higher toxicity for cancer cells than the DOX-only control samples, and led to specific high apoptosis for cancer cells. The study suggests that DOX can be loaded into a starch/PVA/g-C3N4 hydrogel to improve the specificity of the drug's release in cancer tumors or in vitro breast cancer cells.

Development of a novel Z-scheme CoxNi1-xTiO3/CdS (x = 0.5) photocatalyst for the efficient degradation of organic pollutants via a visible-light-driven photocatalytic process.

Herein, for the first time, we reported the synthesis of a novel Z-scheme CoxNi1-xTiO3/CdS (x = 0.5) heterojunction photocatalyst and the investigation of its visible-light-driven photocatalytic performance toward degradation of methylene blue (MB). The developed photocatalyst was structurally characterized by applying X-Ray diffraction analysis (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller (BET), differential reflectance spectroscopy (DRS), and photoluminescence (PL) techniques. The results indicated the formation of a highly porous structure with improved visible light adsorption capacity, favorable for the catalytic activity. At an optimum condition of 10 mg/L of MB and 300 mg/L of catalyst, the ternary photocatalyst demonstrated a MB removal efficiency of 99 % after 75 min of the treatment process. The radical trapping experiments unveiled that hydroxyl and superoxide radicals were two main reactive species formed under visible light, while the valance holes possessed an insignificant role. The synergetic impact of the CoxNi1-xTiO3 (x = 0.5) and CdS on the photodegradation of MB over the as-prepared CoxNi1-xTiO3/CdS (x = 0.5) photocatalyst through Z-scheme photocatalysis was indicated by the results of the mechanism studies. The percentage impact of the treatment time, MB concentration, the ratio of CoxNi1-xTiO3/CdS (x = 0.5), and the dosage of catalyst using analysis of the CCD modeling was obtained as 47.04, 16.67, 7.22 and 0.87 %, respectively. Furthermore, the as-synthesized photocatalyst possessed high recyclability and photostability with only a 3 % decline in activity after four repetitive cycles.

Electrospun nylon 6/hyaluronic acid/chitosan bioactive nanofibrous composite as a potential antibacterial wound dressing.

Hyaluronic acid (HA) and chitosan (CS), as natural biomaterials, display excellent biocompatibility and stimulate the growth and proliferation of fibroblasts. Furthermore, nylon 6 (N6) is a low-cost polymer with good compatibility with human tissues and high mechanical stability. In this study, HA and CS were applied to modify N6 nanofibrous mat (N6/HA/CS) for potential wound dressing. N6/HA/CS nanofibrous composite mats were developed using a simple one-step electrospinning technique at different CS concentrations of 1, 2, and 3 wt%. The results demonstrated that incorporating HA and CS into N6 resulted in increased hydrophilicity, as well as favorable physical and mechanical properties. In addition, the minimum inhibitory concentration and (MIC) optical density techniques were used to determine the antibacterial properties of N6/HA/CS nanofibrous composite mats, and the results demonstrated that the composites could markedly inhibit the growth of Gram-positive bacteria Staphylococcus aureus and Gram-negative bacteria Escherichia coli. Because of its superior mechanical properties, substantial antimicrobial effects, and hydrophilic surface, N6/HA/CS at 2 wt% of CS (N6/HA/CS2) was chosen as the most suitable nanofibrous mat. The swelling, porosity, gel content, and in vitro degradation studies imply that N6/HA/CS2 nanofibrous composite mat has proper moisture retention and biodegradability. Furthermore, the N6/HA/CS2 nanofibrous composite mat was discovered to be nontoxic to L929 fibroblast cells and to even improve cell proliferation. Based on the findings, this research offers a simple and rapid method for creating material that could be utilized as prospective wound dressings in clinical environments.

Electrospun nanofibers using ß-cyclodextrin grafted chitosan macromolecules loaded with indomethacin as an innovative drug delivery system.

Electrospun nanofibers, as an innovative drug delivery system, provide selective, effective, and safe drug release. The present study aimed to fabricate nanofibers based on ß-cyclodextrin grafted chitosan (ß-CD-g-CS) macromolecules with incorporated drug via the blend electrospinning technique. The grafting of ß-CD onto chitosan (CS) was confirmed by FT-IR, 1H NMR, TGA, XRD, and EDX analysis. Indomethacin was encapsulated in the ß-CD-g-CS matrix as blend nanofibers using electrospinning in presence of polyvinyl alcohol (PVA). The SEM images revealed nanofibers with diameters at the nanoscale. The unique features of ß-CD-g-CS/PVA as drug delivery system were investigated using indomethacin as a model drug molecule. Controlled release of indomethacin from nanofibers was studied in PBS solution by measuring the absorbance by UV-Vis spectrophotometer. The drug release profile exhibited that the rate of drug release can be tailored by polymer type and changing the drug/polymer ratio. The physicomechanical properties of the developed nanofibers were analyzed by tensile strength and water contact angle. The results demonstrated that ß-CD-g-CS revealed enhanced wettability as well as favorable physicomechanical properties. In addition, the growth rate of the L929 cells on the CS and ß-CD-g-CS nanofibers was not significantly inhibited and even improved cell proliferation. These findings indicated that ß-CD-g-CS nanofibers could be appropriate as a smart drug delivery system for sustained release of indomethacin as an anti-inflammatory medicine in the wound healing and tissue engineering approaches in orthopedic applications.

A green approach for preparation of polyacrylic acid/starch incorporated with titanium dioxide nanocomposite as a biocompatible platform for curcumin delivery to breast cancer cells.

Curcumin (Cur) is a polyphenolic hydrophobic molecule with several biological uses, including cancer therapy. However, its widespread use in cancer treatment faces limitations due to its low solubility in acidic and neutral conditions, rapid removal from the circulatory system, and poor bioavailability. In order to overcome these challenges, a biocompatible and pH-sensitive carrier nanoplatform was designed for the specific delivery of curcumin to breast cancer cells. This nanocomposite containing polyacrylic acid (PAA), starch, and titanium dioxide (TiO2) was synthesized with a specific morphology through the water-in-oil-in-water green emulsification strategy. The nanocomposite structure was confirmed by Fourier transform infrared (FT-IR), X-ray diffraction (XRD), dynamic light scattering (DLS), zeta potential, and field-emission scanning electrom microscopy (FE-SEM) imaging tests. The mean particle size of 151 nm for the PAA-Starch-TiO2 nanocomposite ensures specific entry into cancer cells and minimal damage to healthy cells. Loading efficiency (LE) and encapsulation efficiency (EE) for curcumin obtained 49.50 % and 87.25 %, which are desirable for a carrier nanoplatform. Compared to the physiological medium, the in-vitro release of curcumin was higher in the acidic conditions in all time intervals, which indicates the possibility of targeted drug release from the PAA-Starch-TiO2 nanocomposite around the tumor tissue. Furthermore, for better understanding of the release mechanism, the cumulative release data in both media were fitted with common mathematical kinetic models. Cytotoxicity tests against the MCF-7 cell line were performed using in vitro MTT and flow cytometry tests. The results showed that the PAA-Starch-TiO2 carrying Cur was more effective through increasing the bioavailability and controlled release of the drug compared to the free Cur. Also, the death of cancer cells in the presence of this nanocomposite compared to free Cur occurred mainly through the induction of apoptosis, which indicates the programmed death of cancer cells and the high efficiency of the designed nanocarrier.