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Showing 6 results for Electrospinning

S. Nikbakht Katouli, A. Doostmohammadi, F. Esmaeili,
Volume 35, Issue 1 (6-2016)
Abstract

The aim of this study was to fabricate carbon nanotube (CNT) and bioactive glass nanoparticles (BG) (at levels of
5 and 10 wt%) incorporated electrospun chitosan (CS)/polyvinyl alcohol (PVA) nanofibers for potential neural tissue engineering applications.The morphology, structure, and mechanical properties of the formed electrospun fibrous mats were characterized using scanning electron microscopy (SEM) and mechanical testing, respectively. In vitro cell culture of embryonal carcinoma stem cells (P19) were seeded onto the electrospun scaffolds. The results showed that the incorporation of CNTs and BG nanoparticles did not appreciably affect the morphology of the CS/PVA nanofibers. The maximum tensile strength (7.9 MPa) was observed in the composite sample with 5 %wt bioactive glass nanoparticles. The results suggest that BG and CNT-incorporated CS/PVA nanofibrous scaffolds with small diameters, high porosity, and promoted mechanical properties can potentially provide many possibilities for applications in the fields of neural tissue engineering and regenerative medicine.


M. Shamsi, N. Nezafati, S. Zavareh, A. Zamanian,
Volume 35, Issue 1 (6-2016)
Abstract

Ternary (%mol) (64SiO2-31CaO-5P2O5) system of sol-gel derived bioactive glass fibers was prepared by electrospinning method. X-ray Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and nitrogen adsorption test (BET) analyses were performed to investigate the phase and chemical group of the composition, morphology of the surface and specific surface area of the fibers, respectively. SEM observations confirmed that the fibers were nano size. The amorphous nature and the presence of silanol groups in the composition were confirmed by XRD and FTIR, respectively. Apatite formation and biodegradability of the fibers were studied using various analyses after different days of soaking in simulated body fluid (SBF). The results affirmed the presence of apatite layers on the surface of the fibers. Cell culture evaluation indicated that MG-64 human osteoblast-like cells were attached and spread well on the surface. Furthermore, cell viability and cell growth demonstrated that the cells were grown and reproduced well on the fibers.


M. Mirhaj, M. Mahmoodi, A. Shybani,
Volume 36, Issue 4 (3-2018)
Abstract

In this research, keratin (Kr)/ poly caprolactone (PCL)/ hydroxyapatite (HA) scaffold was made by electrospinning method. Then, the effect of HA nanoparticles on properties of scaffold B (Kr 33%, PCL 50% and HA 17%) and scaffold A (Kr 40% and PCL 60%) were studied. The surface morphology, functional groups on the surface of samples, porosity, and specific surface area were evaluated by Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectrophotometer (FTIR), liquid displacement method, and BET test, respectively. The mean diameter of fibers in samples A and B was measured 184 nm and 108 nm, respectively. Results showed that the  specific surface area in scaffolds with HA nanoparticles was almost 2 times higher than that of the scaffold without HA. The biodegradability of scaffolds was examined in phosphate buffer solution (PBS) and the results showed an increase in the weight loss percentage of the scaffold B. The cell viability and adherence of osteosarcoma cell line (Saos-2) on the scaffold surface was observed via MTT assay and the results showed an increase in cell growth on PCL/Kr scaffolds with HA nanoparticles. Thus, scaffolds containing HA nanoparticles can be a good choice for tissue engineering applications.

M. Sohrabi, M. Abbasi, M. M Ansar,
Volume 38, Issue 1 (6-2019)
Abstract

In this study, using biodegradable polymers, nanofiberouse scaffolds were fabricated from the layer-by-layer electrospinning method, including two layer that poly (ε-caprolactone), polyvinylpyrrolidone deposited at first layer and poly (ε-caprolactone), polyvinyl alcohol , β-tricalcium phosphate at latter. After prepration of scaffolds, scanning electron microscopy (SEM), swelling, porosity, mechanical properties and biodegradability behavior in buffered saline phosphate solution were  studied. The results confirmed the bioactivity  and suitable mechanical properties of the layer-by-layer scaffold. The swelling increase with the addition of hydrophilic polymers and reache 811 ± 214 % in the layer-by-layer scaffold, which reveald a significant difference compared to pure PCL. The MTT test on the layer-by-layer scaffold, after 3, 5 and 7 days of rats bone marrow stem cells (rMSC) culture, showed the cell viability of above 80% moreover, cells morphology on the scafold indicated the optimal compatibility of  cells on the scaffold.

S. Torabi, S. Khorshidi, A. Karkhaneh,
Volume 39, Issue 2 (8-2020)
Abstract

For many years, dexamethasone has been used as an anti-inflammatory drug and is still one of the safest glucocorticoids for treating various diseases. Due to the wide range of the side effects of this drug, it is essential to find a suitable delivering system for reduction in dosage with increased effectiveness. Electrospinning is one of the fiber fabrication methods which is widely used to develop drug carriers due to its ability to load various drugs and biological components and control their release. In this research, neat poly (lactic acid) electrospun fibers and dexamethasone loaded fibers were prepared. To evaluate the effect of polymer concentration on morphology, mechanical properties and drug release profile of the resulting fibers, three polymer concentrations of 10%, 14% and 18% w/v were processed. Thereafter, 5% w/v dexamethasone was added to solutions. The scanning electron microscopy images were investigated to obtain the average diameter of fibers and the average area of pores in each sample. In neat samples, by moving from 10% to 18% composition, the average diameter of the fibers increased by 63.21%. However, in drug loaded samples this increased by 51/19%. After evaluating mechanical properties, an increase of 81/34% in Elastic modulus by moving from 10% to 18% composition was observed. Moreover, the ultimate strength increased by 68/021% when increasing the polymer concentration from 10 to 18%. Drug release from the electrospun samples was continued up to 7 days. Linear release was observed in 10% and 14% compositions. The drug release pattern of these samples was of zero order. Considering the importance of zero order release in different applications of dexamethasone, these delivering systems could be useful. The maximum drug release rate belonged to 14% composition (0.044 1/h).

S. S. Shafiei, M. Shavandi , Y. Nickakhtar ,
Volume 39, Issue 4 (2-2021)
Abstract

Tissue-engineering scaffolds provide biological and mechanical frameworks for cell adhesion, growth, and differentiation. Nanofibrous scaffolds mimic the native extracellular matrix (ECM) and play a significant role in formation and remodeling of tissues and/or organs . One way to mimic the desired properties of fibrous ECM is adding nanoparticles into the polymer matrix. In the current study, the uniform fibers of poly (ε-caprolactone) (PCL) enriched with different layered double hydroxide (LDH) contents (ranging from 0.1 wt.% to 10 wt.%) were successfully fabricated by electrospinning method. The LDH nano particles were randomly dispersed in the fibers, as confirmed by Energy Dispersive X-ray analysis (EDX). Scaffolds were analyzed from morphological, physical and mechanical view. Biological assessments of scaffolds in terms of cellular attachment and adipogenic differentiation of mouse adipose derived stem cells (mADSCs) were performed. The results showed that inclusion of LDH nanoparticles reduced the average fiber diameter and enhanced the tensile strength and elongation at break values of the PCL scaffold. The LDH-enriched electrospun PCL scaffolds had remarkable effects on cell adhesion. Moreover, a significant increase in adipogenic differentiation of mADSCs was observed. The PCL/LDH nanofibrous scaffolds showed great potential in application for soft tissue engineering.


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