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

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.

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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 ◽

10.1515/epoly-2016-0304 ◽

2017 ◽

Vol 17 (5) ◽

pp. 363-371 ◽

Cited By ~ 14

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.

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In Vitro Cytotoxic Studies of Ultrafine TiO2/Graphene Oxide Sheet Nanocomposites in Human Alveolar Epithelial Cells

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.1051.353 ◽

2014 ◽

Vol 1051 ◽

pp. 353-362 ◽

Cited By ~ 1

Author(s):

Jing Gao ◽

Xue Shun Yuan ◽

Yu Wang ◽

Lin Cao ◽

Peng Yu Dong ◽

...

Keyword(s):

Graphene Oxide ◽

Photoelectron Spectroscopy ◽

Membrane Integrity ◽

A549 Cells ◽

Alveolar Epithelial Cells ◽

High Concentration ◽

X Ray ◽

Surface Areas ◽

Dose Dependent

The novel TiO2/graphene sheet (TiO2/GSs) nanocomposites were synthesized using graphene oxide sheets and TiCl3. All target composites were characterized by transmission electron microscopy (TEM), X-ray electron diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and energy dispersive X-ray spectra (EDX), and the surface areas were tested with the Brunauer-Emmett-Teller (BET) method. We studied the cytotoxicity of TiO2/GSs nanoparticles on A549 cells by examining the influence of TiO2/GSs on cell morphology and viability by methyl thiazolyl tetrazolium (MTT) assay. We also determined membrane integrity and apoptosis of A549 cells after different doses of TiO2/GSs exposure by LDH assay and flow cytometry. Assay of A549 cell viability showed regular reductions with a time-and dose-dependent tendency after exposure to pure TiO2, TiO2/4.2wt% GSs and TiO2/6wt% GSs for 24 hrs or 48 hrs. The LDH released and cellular apoptosis also had a dose-dependent effect, which was associated with the surface area of TiO2/4.2wt% GSs. Our results provide essential knowledge of the acceptable biocompatibility of TiO2/GSs nanocomposites, and only when cells were exposed at a high concentration (≥50 μg/mL), and for a prolonged period of time did TiO2/GSs nanoparticles exhibit minimal cytotoxicity against A549 cells.

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Functionalized Nano-graphene Oxide as Multi-modal Clinic for Effective Drug Delivery

International Journal of Pharmaceutical Sciences and Nanotechnology ◽

10.37285/ijpsn.2017.10.4.3 ◽

2017 ◽

Vol 10 (4) ◽

pp. 3768-3771

Author(s):

Soumitra Satapathi ◽

Rutusmita Mishra ◽

Manisha Chatterjee ◽

Partha Roy ◽

Somesh Mohapatra

Keyword(s):

Drug Delivery ◽

Graphene Oxide ◽

Cancer Cell ◽

High Surface ◽

High Surface Area ◽

Cancer Cell Line ◽

Xrd Analysis ◽

Graphene Derivatives ◽

Nano Graphene

Nano-materials based drug delivery modalities to specific organs and tissues has become one of the critical endeavors in pharmaceutical research. Recently, two-dimensional graphene has elicited considerable research interest because of its potential application in drug delivery systems. Here we report, the drug delivery applications of PEGylated nano-graphene oxide (nGO-PEG), complexed with a multiphoton active and anti-cancerous diarylheptanoid drug curcumin. Specifically, graphene-derivatives were used as nanovectors for the delivery of the hydrophobic anticancer drug curcumin due to its high surface area and easy surface functionalization. nGO was synthesized by modified Hummer’s method and confirmed by XRD analysis. The formation of nGO, nGO-PEG and nGO-PEG-Curcumin complex were monitored through UV-vis, IR spectroscopy. MTT assay and AO/EB staining found that nGO-PEG-Curcumin complex afforded highly potent cancer cell killing in vitro with a human breast cancer cell line MCF7.

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X-ray Photoelectron Spectroscopy Analysis of Chitosan–Graphene Oxide-Based Composite Thin Films for Potential Optical Sensing Applications

Polymers ◽

10.3390/polym13030478 ◽

2021 ◽

Vol 13 (3) ◽

pp. 478

Author(s):

Wan Mohd Ebtisyam Mustaqim Mohd Daniyal ◽

Yap Wing Fen ◽

Silvan Saleviter ◽

Narong Chanlek ◽

Hideki Nakajima ◽

...

Keyword(s):

Thin Film ◽

Thin Films ◽

Graphene Oxide ◽

Photoelectron Spectroscopy ◽

Functional Group ◽

Optical Sensing ◽

Composite Thin Films ◽

Cobalt Ions ◽

X Ray ◽

Sensing Applications

In this study, X-ray photoelectron spectroscopy (XPS) was used to study chitosan–graphene oxide (chitosan–GO) incorporated with 4-(2-pyridylazo)resorcinol (PAR) and cadmium sulfide quantum dot (CdS QD) composite thin films for the potential optical sensing of cobalt ions (Co2+). From the XPS results, it was confirmed that carbon, oxygen, and nitrogen elements existed on the PAR–chitosan–GO thin film, while for CdS QD–chitosan–GO, the existence of carbon, oxygen, cadmium, nitrogen, and sulfur were confirmed. Further deconvolution of each element using the Gaussian–Lorentzian curve fitting program revealed the sub-peak component of each element and hence the corresponding functional group was identified. Next, investigation using surface plasmon resonance (SPR) optical sensor proved that both chitosan–GO-based thin films were able to detect Co2+ as low as 0.01 ppm for both composite thin films, while the PAR had the higher binding affinity. The interaction of the Co2+ with the thin films was characterized again using XPS to confirm the functional group involved during the reaction. The XPS results proved that primary amino in the PAR–chitosan–GO thin film contributed more important role for the reaction with Co2+, as in agreement with the SPR results.

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Synthesis, characterization and in vitro cytotoxicity study of Co and Ni ferrite nanoparticles prepared by sol-gel method

SN Applied Sciences ◽

10.1007/s42452-021-04709-y ◽

2021 ◽

Vol 3 (7) ◽

Author(s):

Alexandre Pancotti ◽

Dener Pereira Santos ◽

Dielly Oliveira Morais ◽

Mauro Vinícius de Barros Souza ◽

Débora R. Lima ◽

...

Keyword(s):

Photoelectron Spectroscopy ◽

Sol Gel ◽

Test Sample ◽

In Vitro Cytotoxicity ◽

Gel Method ◽

X Ray ◽

Sol Gel Method ◽

Transmission Electron ◽

Crystallite Sizes

AbstractIn this study, we report the synthesis and characterization of NiFe2O4 and CoFe2O4 nanoparticles (NPs) which are widely used in the biomedical area. There is still limited knowledge how the properties of these materials are influenced by different chemical routes. In this work, we investigated the effect of heat treatment over cytotoxicity of cobalt and niquel ferrites NPs synthesized by sol-gel method. Then the samples were studied using transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), Fourier Transform Infrared Spectroscopy Analysis (FTIR), and X-ray fluorescence (XRF). The average crystallite sizes of the particles were found to be in the range of 20–35 nm. The hemocompatibility (erythrocytes and leukocytes) was checked. Cytotoxicity results were similar to those of the control test sample, therefore suggesting hemocompatibility of the tested materials.

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Assessment of Titanate Nanolayers in Terms of Their Physicochemical and Biological Properties

Materials ◽

10.3390/ma14040806 ◽

2021 ◽

Vol 14 (4) ◽

pp. 806

Author(s):

Michalina Ehlert ◽

Aleksandra Radtke ◽

Katarzyna Roszek ◽

Tomasz Jędrzejewski ◽

Piotr Piszczek

Keyword(s):

Surface Modification ◽

Substrate Surface ◽

Biological Properties ◽

Structure Characterization ◽

Porous Coating ◽

Apatite Formation ◽

Sem Images ◽

Energy Dispersion Spectroscopy ◽

X Ray

The surface modification of titanium substrates and its alloys in order to improve their osseointegration properties is one of widely studied issues related to the design and production of modern orthopedic and dental implants. In this paper, we discuss the results concerning Ti6Al4V substrate surface modification by (a) alkaline treatment with a 7 M NaOH solution, and (b) production of a porous coating (anodic oxidation with the use of potential U = 5 V) and then treating its surface in the abovementioned alkaline solution. We compared the apatite-forming ability of unmodified and surface-modified titanium alloy in simulated body fluid (SBF) for 1–4 weeks. Analysis of the X-ray diffraction patterns of synthesized coatings allowed their structure characterization before and after immersing in SBF. The obtained nanolayers were studied using Raman spectroscopy, diffuse reflectance infrared Fourier transform spectroscopy (DRIFT), and scanning electron microscopy (SEM) images. Elemental analysis was carried out using X-ray energy dispersion spectroscopy (SEM EDX). Wettability and biointegration activity (on the basis of the degree of integration of MG-63 osteoblast-like cells, L929 fibroblasts, and adipose-derived mesenchymal stem cells cultured in vitro on the sample surface) were also evaluated. The obtained results proved that the surfaces of Ti6Al4V and Ti6Al4V covered by TiO2 nanoporous coatings, which were modified by titanate layers, promote apatite formation in the environment of body fluids and possess optimal biointegration properties for fibroblasts and osteoblasts.

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X-Ray Photoelectron Spectroscopy Study on Reduction of Graphene Oxide with Hydrazine Hydrate

Advanced Materials Research ◽

10.4028/www.scientific.net/amr.287-290.539 ◽

2011 ◽

Vol 287-290 ◽

pp. 539-543 ◽

Cited By ~ 5

Author(s):

Wen Shi Ma ◽

Jun Wen Zhou ◽

Xiao Dan Lin

Keyword(s):

Graphene Oxide ◽

Hydrazine Hydrate ◽

Photoelectron Spectroscopy ◽

Reduction Rate ◽

Reduction Reaction ◽

Chemical Compositions ◽

Total Oxygen ◽

Graphene Oxides ◽

X Ray ◽

Oxygen Groups

Graphene oxide was prepared through Hummers' method，then different reduced graphenes were prepared via reduction of graphene oxide with hydrazine hydrate for 1h、12h and 24h. X-ray photoelectron spectroscopy (XPS) was used for the characterization of graphene oxide and the reduced graphenes. The variation of the contents of carbon in carbon and oxygen functional groups and chemical compositions of graphene oxides were investigated through analysis the content of different carbon atoms in different reduced graphenes. The results showed that the reduction reaction was very fast in the first 1 h, the content of total oxygen bonded carbon atoms decreased from 83.6% to 22.1%, and then after the reduction rate became very slow. After 12h, the content of total oxygen bonded carbon atom is 19.56%, only 2.54% lower than that of 1h’s. At the same time, C-N was introduced in the graphene oxides; this increased the stereo-hindrance for hydrazine hydrate attacking the C-Oxygen groups, thus reduced the reduction rate. After reduction for 24h, there still exists 16.4% oxygen bonded carbon atoms and the total conversion ratio of graphene approaches 70%.

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Lactoferrin/Calcium Phosphate-Modified Porous Ti by Biomimetic Mineralization: Effective Infection Prevention and Excellent Osteoinduction

Materials ◽

10.3390/ma14040992 ◽

2021 ◽

Vol 14 (4) ◽

pp. 992

Author(s):

Song Chen ◽

Yuanli He ◽

Linna Zhong ◽

Wenjia Xie ◽

Yiyuan Xue ◽

...

Keyword(s):

Calcium Phosphate ◽

Photoelectron Spectroscopy ◽

Antibacterial Properties ◽

Biomimetic Mineralization ◽

Matrix Mineralization ◽

X Ray ◽

Porous Ti ◽

Potential Applications ◽

Modification Of Titanium

The surface modification of titanium (Ti) can enhance the osseointegration and antibacterial properties of implants. In this study, we modified porous Ti discs with calcium phosphate (CaP) and different concentrations of Lactoferrin (LF) by biomimetic mineralization and examined their antibacterial effects and osteogenic bioactivity. Firstly, scanning electron microscopy (SEM), the fluorescent tracing method, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), and the releasing kinetics of LF were utilized to characterize the modified Ti surface. Then, the antibacterial properties against S. sanguis and S. aureus were investigated. Finally, in vitro cytological examination was performed, including evaluations of cell adhesion, cell differentiation, extracellular matrix mineralization, and cytotoxicity. The results showed that the porous Ti discs were successfully modified with CaP and LF, and that the LF-M group (200 μg/mL LF in simulated body fluid) could mildly release LF under control. Further, the LF-M group could effectively inhibit the adhesion and proliferation of S. sanguis and S. aureus and enhance the osteogenic differentiation in vitro with a good biocompatibility. Consequently, LF-M-modified Ti may have potential applications in the field of dental implants to promote osseointegration and prevent the occurrence of peri-implantitis.

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Ternary Composite of Molybdenum Disulfide-Graphene Oxide-Polyaniline for Supercapacitor

Journal of The Electrochemical Society ◽

10.1149/1945-7111/ac3f1e ◽

2021 ◽

Author(s):

Ke Qu ◽

Yuqi Bai ◽

Miao Deng

Keyword(s):

Graphene Oxide ◽

Molybdenum Disulfide ◽

Photoelectron Spectroscopy ◽

Electrochemical Impedance ◽

Light Emitting Diode ◽

Rate Capability ◽

Energy Storage And Conversion ◽

Carbon Paper ◽

Power Sources ◽

X Ray

Abstract The ever-increasing need for small and lightweight power sources for use in portable or wearable electronic devices has spurred the development of supercapacitors as a promising energy storage and conversion system. In this work, a simple, facile and easy-to-practice method has been developed to employ carbon paper (CP) as the support to coat molybdenum disulfide (MoS2) and graphene oxide (GO), followed by electrodeposition of polyaniline (PANI) to render CP/MoS2-GO-PANI. The preparation parameters, such as amounts of MoS2, GO and number of aniline electropolymerization cycles, have been optimized to render CP/MoS2-GO-PANI the best capacitive performance. The as-prepared optimal CP/MoS2-GO-PANI is characterized by X-ray powder diffraction, scanning electron microscopy, energy-dispersive spectroscopy, and X-ray photoelectron spectroscopy. The supercapacitive properties of CP/MoS2-GO-PANI as an electrode have been evaluated electrochemically via cyclic voltammetry, galvanostatic charge/discharge, and electrochemical impedance spectroscopy testing. CP/MoS2-GO-PANI delivers a specific capacitance of 255.1 F/g at 1.0 A/g and exhibits excellent rate capability under larger current densities. Moreover, a symmetrical supercapacitor is assembled and three are connected in series to power a light-emitting diode for ~15 minutes, demonstrating the promising application potential of CP/MoS2-GO-PANI-based supercapacitor.

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Facile one pot microbe-mediated in situ synthesis and antibacterial activity of reduced graphene oxide-silver nanocomposite

Nanotechnology ◽

10.1088/1361-6528/ac4521 ◽

2021 ◽

Author(s):

Ashwini Patil

Keyword(s):

Antibacterial Activity ◽

Graphene Oxide ◽

Zeta Potential ◽

Reduced Graphene Oxide ◽

In Vitro Dissolution ◽

Size Analysis ◽

X Ray ◽

Reduced Graphene

Abstract The present research deals with the development of a novel bioinspired in situ fabrication of reduced graphene oxide (rGO)-silver nanoparticle (AgNPs) nanocomposite (rGO@AgNCs) using microbes namely Pseudomonas aeruginosa (PA) and Staphylococcus aureus (SA). The fabricated rGO@AgNCs were characterized using Ultraviolet-visible (UV) spectroscopy, Fourier-transform infrared spectroscopy (FTIR), particle size analysis, polydispersity index (PDI), zeta potential analysis, energy dispersive X-ray analysis (EDAX), Raman spectroscopy, powder X-ray diffraction (PXRD), high-resolution transmission electron microscopy (HR-TEM) analysis, etc. Furthermore, the rGO@AgNCs-PA and rGO@AgNCs-SA interaction with serum protein, pH stability study, and in vitro dissolution of AgNPs were also performed. The research findings of the proposed study demonstrated the simultaneous reduction of graphene oxide (GO) and AgNPs and the formation of rGO@AgNCs in the presence of microbes. The in vitro dissolution studies of rGO@AgNCs composites showed better AgNPs dissolution with controlled release and offered remarkable matrix integrity throughout the dissolution period. The size and stability of rGO@AgNCs-PA and rGO@AgNCs-SA had no significant changes at physiological pH 7.4. A minimal decrease in the zeta potential of rGO@AgNCs was observed, which may be due to the weak interaction of nanocomposites and albumin. The antibacterial application of the synthesized nanocomposite was evaluated against a pathogenic mastitis-forming bacterium. The obtained results suggested an admirable antibacterial activity of synthesized nanocomposites against the tested microbes. This knowledge will assist the scientific fraternity in designing novel antibacterial agents with enhanced antibacterial activity against various veterinary pathogens in near future.

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