scholarly journals Synergistic effects of retinoic acid and graphene oxide on the physicochemical and in-vitro properties of electrospun polyurethane scaffolds for bone tissue engineering

e-Polymers ◽  
2017 ◽  
Vol 17 (5) ◽  
pp. 363-371 ◽  
Author(s):  
Mohammad Mahdi Safikhani ◽  
Ali Zamanian ◽  
Farnaz Ghorbani
Keyword(s):  
Tissue Engineering ◽  
Graphene Oxide ◽  
Retinoic Acid ◽  
Synergistic Effects ◽  
Biological Properties ◽  
Electrospinning Process ◽  
Hard Tissue ◽  
Tissue Engineering Scaffolds ◽  
Sem Micrographs

AbstractTissue engineering scaffolds simulate extracellular matrixes (ECMs) to promote healing processes of damaged tissues. In this investigation, ECM were simulated by retinoic acid-loaded polyurethane-graphene oxide nanofibers to regenerate bone defects. Scanning electron microscopy (SEM) micrographs, Fourier transform infrared (FTIR) spectrum and X-ray diffraction (XRD) patterns proved the synthesis of graphene oxide (GO) nanosheets. SEM micrographs of nanofibers demonstrated through the formation of homogeneous and bead free fibrous scaffolds that the diameter of fibers were reduced by decreasing the applied voltage in an electrospinning process and the addition of GO. According to the results, the addition of GO to the polyurethane (PU) solution led to an increase in mechanical strength which is the most important parameter in the hard tissue repair. The GO-containing scaffolds showed an increased wettability, swelling, biodegradation and drug release level. Release behavior in nanocomposite scaffolds followed the swelling and biodegradation mechanisms, so osteogenic expression was possible by incorporating retinoic acid (RA) in PU-GO nanofibrous scaffolds. Biological evaluations demonstrated that composite scaffolds are biocompatible and support cellular attachment in which RA-loaded samples represented better cellular spreading. In brief, nanocomposite fibers showed desired that the physicochemical, mechanical and biological properties and synergic effects of GO and RA in osteogenic activity of MG-63 cells produced favorable constructs for hard tissue engineering applications.

scholarly journals Gradient Chitosan Hydrogels Modified with Graphene Derivatives and Hydroxyapatite: Physiochemical Properties and Initial Cytocompatibility Evaluation

2020 ◽  
Vol 21 (14) ◽  
pp. 4888
Author(s):  
Karolina Kosowska ◽  
Patrycja Domalik-Pyzik ◽  
Małgorzata Sekuła-Stryjewska ◽  
Sylwia Noga ◽  
Joanna Jagiełło ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
Mechanical Analysis ◽  
Biological Properties ◽  
Human Umbilical Cord ◽  
Tissue Engineering Scaffolds ◽  
X Ray ◽  
Chitosan Matrix ◽  
Graphene Derivatives

In this study, we investigated preparation of gradient chitosan-matrix hydrogels through a novel freezing–gelling–thawing method. The influence of three types of graphene family materials (GFM), i.e., graphene oxide (GO), reduced graphene oxide (rGO), and poly(ethylene glycol) grafted graphene oxide (GO-PEG), as well as hydroxyapatite (HAp) on the physicochemical and biological properties of the composite hydrogels was examined in view of their potential applicability as tissue engineering scaffolds. The substrates and the hydrogel samples were thoroughly characterized by X-ray photoelectron spectroscopy, X-ray diffractometry, infrared spectroscopy, digital and scanning electron microscopy, rheological and mechanical analysis, in vitro chemical stability and bioactivity assays, as well as initial cytocompatibility evaluation with human umbilical cord Wharton’s jelly mesenchymal stem cells (hUC-MSCs). We followed the green-chemistry approach and avoided toxic cross-linking agents, using instead specific interactions of our polymer matrix with tannic acid, non-toxic physical cross-linker, and graphene derivatives. It was shown that the most promising are the gradient hydrogels modified with GO-PEG and HAp.

Graphene oxide-enriched poly(ε-caprolactone) electrospun nanocomposite scaffold for bone tissue engineering applications

2016 ◽  
Vol 32 (3) ◽  
pp. 325-342 ◽  
Author(s):  
Sepideh Mohammadi ◽  
Seyedeh Sara Shafiei ◽  
Mitra Asadi-Eydivand ◽  
Mahmoud Ardeshir ◽  
Mehran Solati-Hashjin
Keyword(s):  
Tissue Engineering ◽  
Graphene Oxide ◽  
Average Diameter ◽  
Electrospinning Process ◽  
Graphene Oxide Nanosheets ◽  
Mg63 Cells ◽  
Graphene Oxide Nanosheet ◽  
Nanocomposite Scaffolds ◽  
Pure Poly

Tissue engineering aims at fabricating biological substitutes to improve, repair, and regenerate failing human tissues or organs. Designing a nanocomposite scaffolds with tailored properties that enhance the development of functional tissue can be an appropriate approach to achieve this purpose. In this study, the uniform and bead-free nanofibers of poly(ε-caprolactone) composited with different graphene oxide nanosheet contents (ranging from 0.5 to 2 wt%) were successfully fabricated through electrospinning process. A decrease in the average diameter of poly(ε-caprolactone) nanofibers was observed with the addition of graphene oxide nanosheets. Moreover, the nanocomposite scaffolds containing 2 wt% of graphene oxide nanosheets exhibited superior mechanical properties compared to that of pure poly(ε-caprolactone). Compared with pure poly(ε-caprolactone) scaffold, the degradation rate of poly(ε-caprolactone)-graphene oxide nanosheet nanofibers was enhanced, while the integrity of fibers was preserved. The presence of graphene oxide nanosheets in poly(ε-caprolactone) fibers promoted in vitro biomineralization, indicating bioactive features of the nanocomposite scaffolds. Compared to the pure one, nanocomposite fibers also showed better ability in protein adsorption. The in vitro cell culture studies showed that the addition of graphene oxide nanosheets did not diminish the biocompatibility of the electrospun poly(ε-caprolactone) nanofiber. Furthermore, the adhesion and proliferation of MG63 cells were increased. Altogether, the results demonstrated that electrospun poly(ε-caprolactone)-graphene oxide nanosheet nanofiber may be a suitable candidate for tissue engineering scaffold applications.

Compare of Electrospinning PLA and PLA/β-TCP Scaffold in Vitro

2005 ◽  
Vol 475-479 ◽  
pp. 2379-2382 ◽  
Author(s):  
Hong Song Fan ◽  
Xian Tao Wen ◽  
Yan Fei Tan ◽  
R. Wang ◽  
H.D. Cao ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Cell Proliferation ◽  
Calcium Phosphate ◽  
Composite Scaffold ◽  
Raw Materials ◽  
Electrospinning Process ◽  
Tissue Engineering Scaffolds ◽  
Biodegradable Composite ◽  
Spinning Process

In recent years, electrospinning process is gradually applied in producing tissue-engineering scaffold. In this study, we chose polylacticacid(PLA) and β-tertiary calcium phosphate(β-TCP) as raw materials to fabricate PLA/β-TCP biodegradable composite scaffold by electrospinning process. The characteristics of the scaffold and effect of the scaffolds to cell proliferation and cell adhesion was studied. Compare with pure PLA scaffold, blendingβ-TCP in the spinning process of the scaffold could improve the properties of the scaffold, especially the hydrophilicity and the proliferation and adhesion of cells, this means that the material is more potential to be used as tissue engineering scaffolds.

scholarly journals Influences of Molecular Weights on Physicochemical and Biological Properties of Collagen-Alginate Scaffolds

Marine Drugs ◽  
2021 ◽  
Vol 19 (2) ◽  
pp. 85 ◽  
Author(s):  
Truc Cong Ho ◽  
Jin-Seok Park ◽  
Sung-Yeoul Kim ◽  
Hoyeol Lee ◽  
Ju-Sop Lim ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Subcritical Water ◽  
Biological Properties ◽  
Ethanol Solution ◽  
Water Soluble ◽  
Potential Candidate ◽  
High Porosity ◽  
Engineering Applications ◽  
Molecular Weights

For tissue engineering applications, biodegradable scaffolds containing high molecular weights (MW) of collagen and sodium alginate have been developed and characterized. However, the properties of low MW collagen-based scaffolds have not been studied in previous research. This work examined the distinctive properties of low MW collagen-based scaffolds with alginate unmodified and modified by subcritical water. Besides, we developed a facile method to cross-link water-soluble scaffolds using glutaraldehyde in an aqueous ethanol solution. The prepared cross-linked scaffolds showed good structural properties with high porosity (~93%) and high cross-linking degree (50–60%). Compared with collagen (6000 Da)-based scaffolds, collagen (25,000 Da)-based scaffolds exhibited higher stability against collagenase degradation and lower weight loss in phosphate buffer pH 7.4. Collagen (25,000 Da)-based scaffolds with modified alginate tended to improve antioxidant capacity compared with scaffolds containing unmodified alginate. Interestingly, in vitro coagulant activity assay demonstrated that collagen (25,000 Da)-based scaffolds with modified alginate (C25-A63 and C25-A21) significantly reduced the clotting time of human plasma compared with scaffolds consisting of unmodified alginate. Although some further investigations need to be done, collagen (25,000 Da)-based scaffolds with modified alginate should be considered as a potential candidate for tissue engineering applications.

Investigation of synergistic effects of inductive and conductive factors in gelatin-based cryogels for bone tissue engineering

2016 ◽  
Vol 4 (10) ◽  
pp. 1827-1841 ◽  
Author(s):  
Han-Tsung Liao ◽  
K. T. Shalumon ◽  
Kun-Hung Chang ◽  
Chialin Sheu ◽  
Jyh-Ping Chen
Keyword(s):  
Tissue Engineering ◽  
Bone Tissue Engineering ◽  
Bone Tissue ◽  
Synergistic Effects

Gelatin cryogels modified with nHAP and BMP-2 could provide cues to promote the osteogenesis of ADSCs in vitro and in vivo.

Preparation, Characterization and In Vitro Release Kinetics of Vancomycin Carried β-TCP/Chitosan Composite Microspheres Used as Bone Tissue Engineering Scaffolds

2012 ◽  
Vol 512-515 ◽  
pp. 1821-1825
Author(s):  
Lin Zhang ◽  
Xue Min Cui ◽  
Qing Feng Zan ◽  
Li Min Dong ◽  
Chen Wang ◽  
...  
Keyword(s):  
Tissue Engineering ◽  
Release Kinetics ◽  
In Vitro Release ◽  
Cross Linking ◽  
Tissue Engineering Scaffolds ◽  
Composite Microspheres ◽  
Chitosan Composite ◽  
Vitro Release

A novel microsphere scaffolds composed of chitosan and β-TCP containing vancomycin was designed and prepared. The β-TCP/chitosan composite microspheres were prepared by solid-in-water-in-oil (s/w/o) emulsion cross-linking method with or without pre-cross-linking process. The mode of vancomycin maintaining in the β-TCP/chitosan composite microspheres was detected by Fourier transform infrared spectroscopy (FTIR). The in vitro release curve of vancomycin in simulated body fluid (SBF) was estimated. The results revealed that the pre-cross-linking prepared microspheres possessed higher loading efficiency (LE) and encapsulation efficiency (EE) especially decreasing the previous burst mass of vancomycin in incipient release. These composite microspheres got excellent sphere and well surface roughness in morphology. Vancomycin was encapsulated in composite microspheres through absorption and cross-linking. While in-vitro release curves illustrated that vancomycin release depond on diffusing firstly and then on the degradation ratio later. The microspheres loading with vancomycin would be to restore bone defect, meanwhile to inhibit bacterium proliferation. These bioactive, degradable composite microspheres have potential applications in 3D tissue engineering of bone and other tissues in vitro and in vivo.

scholarly journals Effects of novel retinoid X receptor-selective ligands on myeloid leukemia differentiation and proliferation in vitro

Blood ◽  
1996 ◽  
Vol 87 (5) ◽  
pp. 1977-1984 ◽  
Author(s):  
M Kizaki ◽  
MI Dawson ◽  
R Heyman ◽  
E Elster ◽  
R Morosetti ◽  
...  
Keyword(s):  
Retinoic Acid ◽  
Clonal Growth ◽  
Myeloid Leukemia ◽  
Target Genes ◽  
Synergistic Effects ◽  
Leukemic Cells ◽  
Acute Myeloid Leukemia Cells ◽  
Differentiation And Proliferation ◽  
Acute Myeloid

The biologic effects of retinoids such as all-trans-retinoic acid (ATRA) and 9-cis-retinoic acid on proliferation and differentiation of hematopoietic cells are mediated by binding and activating two distinct families of transcription factors: the retinoic acid receptors (RARs) and the retinoid X receptors (RXRs). The RARs require heterodimerization with RXRs; in addition, RXRs can form homodimers, which can bind to DNA response elements that are either distinct or the same as those bound by the RAR/RXR heterodimers. Therefore, the two retinoid pathways provide sequences that are specific for effective DNA binding and activation of target genes. We have developed several series of novel synthetic retinoids that selectively interact with RXR/RXR homodimers and RAR/RXR heterodimers. We show here that SR11236 and SR11246, which are RXR-selective analogs, had little ability to inhibit clonal growth and induce differentiation of leukemic cells (HL- 60 cells and fresh acute myeloid leukemia cells). However, SR11249, SR11256, and LGD1069, which activated both RXR/RXR homodimers and RAR/RXR heterodimers, could inhibit clonal growth and induce differentiation of HL-60 cells as well as leukemic cells from patients, including those with acute promyelocytic leukemia (APL). This is similar to results observed with RAR/RXR-specific ligands. Interestingly, the combination of ATRA and either SR11249, SR11256, or LGD1069 showed synergistic effects in inducing differentiation of HL-60 cells. A retinoid (SR11238) with strong anti-AP-1 activity that did not activate the RARs and RXRs for gene transcription from the response element TREpal was inactive in our assay systems, suggesting that the antiproliferative effects of retinoids on leukemic cells is not mediated by inhibiting the AP-1 pathway. We conclude that the RAR/RXR pathway is more important than RXR/RXR pathway for differentiation and proliferation of acute myeloid leukemic cells, and certain retinoids or combination of retinoids with both RAR and RXR specificities may synergistically enhance the differentiation activity of ATRA, which may be relevant in several clinical situations.

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