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Showing 3 results for Polycaprolactone

M. Akbari Taemeh, B. Akbari, J. Nourmohammadi,
Volume 37, Issue 3 (12-2018)
Abstract

In gradient scaffolds, changes in porosity, pore size or chemical composition occur gradually. Recently, different  methods have been applied to create gradient in the scaffolds, but they have some disadvantages such as high cost and control. The main purpose of this research was to fabricate porous gradient scaffolds by a novel, functional, simple, and low-cost method. Two homogenous scaffolds (Homog 1 and Homog 2) and two gradient scaffolds (Grad 1 and Grad 2) were fabricated and compared. Polycaprolactone scaffolds with the pore size gradient along the radial direction were fabricated by combining layer-by-layer assembly and porogen leaching techniques. Paraffin micro particles were used as porogen in two size ranges: 250 to 420 µm and 420 to 600 µm. The average pore size of Homog 1 and Homog 2 was 278.48 ± 11.23 µm and 417.79 ± 14.62, which were suitable for bone tissue engineering. The porosity of the samples was: Homog 1: 77.5 ± 1.25 %, Homog 2: 61.3 ± 3.5 %, Grad 1: 74 ± 0.5 % and Grad 2: 79.8 ± 4 %. It should be stated that the required porosity for cell survival and growth was above 70 %. Compressive strength at 80% strain and compressive modulus for Homog 1, Homog 2, Grad 1 and Grad 2 were 0.16 ± 0.16 MPa and 0.25 ± 0.11 MPa, 0.26 ± 0.20 MPa and 0.53 ± 0.34 MPa, 0.19 ± 0.34 MPa and 0.33 ± 0.43 MPa, 0.12 ± 0.28 MPa and 0.16 ± 0.51 MPa, respectively. The results showed that pore size gradient had a negligible effect on the mechanical properties of the scaffolds and using polycaprolactone (PCL) as the only material of scaffold was not appropriate. The structure of gradient scaffolds showed the radial pore size gradient with a good adhesion between layers without any detectable interface; the result of the compression test also confirmed it.

N. Poursharifi, D. Semnani, P. Soltani, S. Amanpour,
Volume 38, Issue 4 (1-2020)
Abstract

In this study, seven-layer nanofiber structures consisting of polycaprolactone/ chitosan polymers loaded with methotrexate and 5-fluorouracil anti-cancer drugs, for controlled drug delivery, were produced and evaluated. For this purpose, the second, fourth and sixth layers were loaded with drug and placed between the drug-free layers. The surface morphology of drug-free and drug-loaded nanofibers was investigated by scanning electron microscopy (SEM) and Fourier transform infrared spectrometry (FTIR) was used to study their chemical structure. The drug release rate in phosphate buffered saline (pH=7.4) and the released drug concentration were measured by spectrophotometry. Mechanical properties of single- and multi-layered samples were also investigated. SEM images showed formation of uniform and beadless fibers. FTIR spectrum confirmed presence of the drugs in the polymer mixture with no interaction. It was found that by increasing the chitosan content, a brittle structure with decreased elongation is formed. The release behavior of methotrexate and 5-Fluoracil drugs in neutral pH environment for 26 days was evaluated and the results exhibited a slow and sustained release.

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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