فهرست مطالب
Iranian Journal of Materials science and Engineering
Volume:19 Issue: 2, Jun 2022
- تاریخ انتشار: 1401/03/16
- تعداد عناوین: 12
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Page 1
Green synthesis refers to the synthesis of nanoparticles using plants and microorganisms. It is preferred over conventional methods as its sustainable, eco-friendly, cost effective and rapid method. The phytochemicals and enzymes present in plants and microorganisms respectively acts as the reducing and capping agent for the synthesis of nanoparticles. Phytochemicals and enzymes have the ability to reduce precursor metal ions into nanoparticles. As the conventional methods involve the use of high energy and toxic chemicals which are harmful to both environment and organisms, these synthesis methods are discouraged. Of the nanoparticles, gold nanoparticles (AuNPs) and silver nanoparticles (AgNPs) have gained lots of attention owing to their multiple applications and less toxicity. In addition, various in-vitro studies have reported the antimicrobial activity of AgNPs and AuNPs against various microbes. This particular review portrays the methods of nanoparticles synthesis, components of green synthesis, mechanism of green synthesis, antimicrobial activity, other applications and various factors affecting the green synthesis of AgNPs and AuNPs.
Keywords: Green synthesis, Nanoparticles, AuNPs, AgNPs, Plants, Microorganisms, Antimicrobial activity -
Page 2
The success of a drug delivery system relies heavily on its interaction with cells from the target tissue. The range of applications for ibuprofen-loaded chitosan (ICH) films is widening, mainly due to the biodegradability of chitosan (CH) films and ibuprofen’s safety and versatility, with a particular interest in exploring it as neural drug delivery system. In this study, CH and 12% (w/w) ICH films were prepared through the solvent cast, and characterized regarding their physicochemical composition, surface and bulk morphology, drug release profile, and cell viability of primary neurons from the rat spinal cord. Fourier transform infrared spectroscopy (FTIR) analyses demonstrated that both groups had a similar composition. According to scanning electron microscopy (SEM) images, ibuprofen particles were entrapped on the surface and inside the polymeric matrix. In vitro drug release profile indicated that release starts as diffusion within the first hours, is best fitted by the Higuchi model, and continues for at least 30 days, in agreement with the Korsmeyer-Peppas model. Therefore, ibuprofen is first released through the diffusion process of the particles found on the surface and later through a combination of diffusion and erosion of the chitosan matrix. Regarding in vitro cell viability of primary neurons, CH and ICH extracts are non-toxic, as both groups displayed cell viability over 50%. ICH films are mildly reactive in neuronal cells, but do not cause severe cell death i.e., it allowed non-cytotoxic neuronal and glial differentiation. These findings enhanced our understanding of ICH films as a safe neural drug release system to be explored.
Keywords: Biomaterial, Chitosan, Ibuprofen, Drug Delivery System, Primary Neurons -
Page 3
In this paper, chemically-crosslinked gelatin/chitosan hydrogels containg zinc oxide nanoparticles (ZNPs), were loaded with curcumin (CUR), and their microstructural features, physical properties, curcumin entrapment efficiency, and drug release kinetics were evaluated using scanning electron microscopy (SEM), the liquid displacement method, and UV–Vis spectroscopy. The in vitro kinetics of drug release was also studied using First-order, Korsmeyer-Peppas, Hixon-Crowell, and Higuchi kinetic models. The SEM micrographs confirmed the formation of highly porous structures possessing well-defined, interconnected pore geometries. A significant reduction in the average pore sizes of the drug-loaded hydrogels was observed with the addition of ZNPs and CUR to the bare hydrogels. High value of drug loading efficiency (~ 72 %) and maximum drug release of about 50 % were obtained for the drug-loaded scaffolds. It was found that curcumin was transported via the non-Fickian diffusion mechanism. It was also shown that the kinetics of curcumin release was best described in order by Hixon-Crowell, Higuchi, and Korsmeyer-Peppas models, demonstrating that drug release was controlled by diffusion, degradation, and swelling of the drug carrier. However, lower degree of fitting was observed with First-order kinetic model.
Keywords: gelatin, chitosan, zinc oxide, curcumin, release kinetics -
Page 4
Single crystals of double crystalline block copolymers of poly(ethylene glycol) (PEG)-b-poly(ε-caprolactone) (PCL) and PEG-b-poly(L-lactide) (PLLA) were grown from dilute solution in homo- and mixed-brush systems. Crystallization behavior of biodegradable one end-restricted crystallizable PCL and PLLA chains in homo- and mixed-brush nanostructures were investigated. Chemical and physical circumstances of crystallizable brushes were altered. Physical environment was adjusted by amorphism/crystallinity and rigidity/flexibility of neighboring brushes. Chemical environment was manipulated by interaction and miscibility of various brushes. Distinct single crystals were grown with mixed-brushes of amorphous-crystalline (polystyrene (PS), poly(methyl methacrylate) (PMMA), PCL and PLLA, double crystalline (PCL/PLLA), and rod-crystalline polyaniline (PANI)/PCL or PLLA. Surrounding was only effective on hindrance or nucleation commencement of crystallization for crystallizable brushes and had no effect on crystallization features. Novel three-layer fully single crystalline nanostructures, whose characteristics were fixed via changing the crystallization temperature, were also developed. For long crystallizable tethers, crystallization increased both brush and substrate thicknesses.
Keywords: Restricted crystallizable chain, double crystalline block copolymer, single crystal -
Page 5
In this research, Gelatine (GEL)/ Chitosan (CH) wound dressing was prepared and irradiated with gamma rays from 60Co source for wound healing applications. GEL-CH composite characterization and functional properties were determined. The structural changes occurring after γ-irradiation at doses from 5 to 25 kGy were reported by physico-chemical techniques such as Electron Paramagnetic Resonance (EPR), Fourier Transform Infrared spectroscopy (FTIR), X-ray diffraction (XRD) and Electrochemical Impedance Spectroscopy (EIS) studies. The antioxidant capacity was studied using DPPH (1,1-diphenyl-2-picrylhydrazyl free radical) scavenging and the antibacterial activities of Staphylococcus aureus and Escherichia coli were observed using liquid medium. Results revealed that EPR spectroscopy of un-irradiated GEL-CH showed 2 paramagnetic centers correspond to g=2.077 and g= 2.079. After irradiation, no active centre was appeared. A dose-dependent decrease in the central signal intensity was detected, then the EPR signal intensity almost disappears at 20 kGy. Gamma rays caused a slight increase in ion conductivity. FTIR suggest a slightly crosslinking phenomenon at 20 kGy. The XRD analysis does not show peak indicating crystallinity between a range of 2θ (15–30°). Moreover, γ-irradiation elevated the Scavenging DPPH radical activity (0.75 ± 0.07%). Gamma rays did not affect the antibacterial activity of GEL-CH wound dressing against pathogenic bacteria. The innovative results showed that the required γ-radiation for sterilization was ranged from 5 to 25 kGy. It permits to improve the physico-chemical and biological properties and maintain the native structural integrity of the GEL/ COL wound dressing
Keywords: Gelatin, Chitosan, Wound Dressing, γ-irradiation, Electron Paramagnetic Resonance -
Page 6
Gelatin (GEL) is most extensively used in various fields, particularly in therapeutics and pharmaceuticals. GEL was extracted from goat skin using hot temperature extraction process and compared with that of commercial GEL. The physico-chemical characterization and functional properties were investigated by using temperature denaturation (Td), water-holding and fat-binding capacities (WHC and FBC), colour measurement and UV-light spectrum. In vitro biocompatibility was studied for the first time and was evaluated by blood coagulation index (BCI) and haemolytic tests for using as wounds dressing. The results revealed thermal stability of goat GEL at Td 37°C. WHC and FBC capacities represented 2.5 and 1.2 g/ml, respectively. The hunter colour spaces a*, b* and L* showed a -0.27, -1.97 and 25.23 values, respectively. UV-Vis absorption spectrum of the goat GEL showed a maximum absorption peak at 280 nm. The in vitro anticoagulant activities of extracting GEL were higher than 70% after incubation for one hour. After being in contact with red blood cells for 1 h, the haemolysis ratio increased from to 0.46 to 1.4 when the concentration of goat GEL increased from 1 to 50 mg/ml suggesting the safety of the tested samples. These results suggest that thromboresistivity and hemocompatibility of this biopolymer retained the biological activity of our samples for biomaterial applications. According to this, goat GEL successfully competes with, and significantly could be useful for substitution of bovine in wound healing.
Keywords: goat gelatin, biocompatibility, natural polymer, wound dressing -
Page 7
Recently, using calcium phosphates and at the top of them, hydroxyapatite (HA) has been considered in medical and dental applications as an artificial biomaterial due to their chemical and structural similarity to the bodychr('39')s skeletal tissues such as bone and tooth. Because of reinforcement of hydroxyapatitechr('39')s mechanical and biological properties by substitution of OH- groups by F- ions to produce fluorapaptite (FA) has been proven, in this article synthesis methods, properties and medical applications of fluorapatite and its pros and cons in comparison with hydroxyapatite have been reviewed.
Keywords: Fluorapatite, Hydroxyapatite, Tissue engineering, Biomaterial, Biomedical application, Synthesis, characterization, Calcium phosphates -
Page 8
Biocompatible ceramics, commonly known as “bioceramics”, are an extremely versatile class of materials with a wide range of applications in modern medicine. Given the inorganic nature and physico-mechanical properties of most bioceramics, which are relatively close to the mineral phase of bone, orthopedics and dentistry are the preferred areas of usage for such biomaterials. Another clinical field where bioceramics play an important role is oculo-orbital surgery, a highly cross- and interdisciplinary medical specialty addressing to the management of injured eye orbit, with particular focus on the repair of orbital bone fractures and/or the placement of orbital implants following removal of a diseased eye. In the latter case, orbital implants are not intended for bone repair but, being placed inside the ocular cavity, have to be biointegrated in soft ocular tissues. This article reviews the state of the art of currently-used bioceramics in orbital surgery, highlighting the current limitations and the promises for the future in this field.
Keywords: Hydroxyapatite, Bioactive glass, Composites, Orbital floor, Orbital implants -
Page 9
In this study, for the first time, the Forsterite (Mg2SiO4) nanoparticles (NPs) with the size of about 25 nm were added to the phosphate-based electrolyte, and the characteristics and properties of the obtained plasma electrolytic oxidation (PEO) coating on AZ31 Mg alloy was investigated. The results of the potentiodynamic polarization measurements revealed that after one week of exposure to simulated body fluid (SBF) solution, the coating with Mg2SiO4 NPs possessed 12.30 kΩ cm2 polarization resistance, which was more than two times greater than that of the coating without NPs. The thicker coating layer, lower wettability, and also presence of Mg2SiO4 NPs inside the pores were responsible for enhanced corrosion protection in the Mg2SiO4 NPs incorporated coating. After three weeks of immersion in SBF solution, the in-vitro bioactivity test results indicated the ability of the NPs-containing coating to form apatite (Ca/P ratio of 0.92) was weaker than the coating without NPs (Ca/P ratio of 1.17). This could be attributed to the lower wettability of the coating with NPs and supports that the addition of the nanoparticles is not beneficial to the bioactivity performance of the coating.
Keywords: AZ31 Mg alloy, plasma electrolytic oxidation (PEO), Forsterite (Mg2SiO4), corrosion, bioactivity -
Page 10
Fabrication of fully optimized tissue-engineered materials in order to simulating the natural structure, and enhancing the biological properties of damaged tissue is one of the major challenges in biomedical engineering and regeneration medicine. Although polymeric based membranes have revealed noticeable advancements in bone regeneration, their mechanical stiffens, electrical conductivity and bioactivity need to be tolerated. Therefore, the present study is designed to generate a multifunctional biomaterial based on polylactic acid (PLA)/ polycaprolactone (PCL)/hydroxyapatite (HA) nanocomposite containing zinc oxide (ZnO) and Graphene (Gr) nanoparticles employing solvent casting combined with die cast techniques for using as absorbable joint implants in bone tissue regeneration. The physical, chemical, mechanical and biological properties of the produced nanocomposite biomaterials were analyzed in vitro. A detailed experimental evaluation between the nanocomposite coatings was carried out to shed light on the effect of ZnO and Gr nanoparticles on the properties. It was found that the nanocomposite contained 1% ZnO and 1% graphene with a Young's modulus of 1540.5 ± 169.426MPa and the pure sample had a Young's modulus of 1194.81±215.342MPa. The rate of elongation at break of the nanostructure contained 1% graphene was 5.1±0.816%. This value was 3.8±0.944% for the pure sample. The improvement in elongation at break is due to the presence of polycaprolactone in the polymer matrix. The optimal sample with 1% zinc oxide and 1% graphene had antibacterial properties more than other samples. Also, the survival rate of fibroblasts cell in the vicinity of the optimal matrix was significantly different from other samples. The obtained results revealed that the incorporation of the nanoparticles improved physico-chemical features and mechanical strength with enhanced biological properties and its anti-bacterial performance makes this material a promising candidate for further bone regeneration studies.
Keywords: polylactic acid, hydroxyapatite, graphene, zinc oxide, polylactic acid -
Page 11
Sodium alginate (SA), brown seaweed algae, and Lignosulphonic acid (LS), a plant product, are biodegradable polymers extensively investigated for drug-controlled release. The Hydroxychloroquine sulphate (HCQ) drug, an antimalarial drug, was extensively used in the initial periods of COVID situations. The HCQ drug release from SALS beads is investigated for its control release in a simulated medium (pH1.2 and pH7.4) using different crosslinking agents such as Calcium chloride, Barium chloride and Aluminum chloride. The HCQ release has better controlled in Barium crosslinked beads. They are found to be relatively intact and stable and release the drug for more than 180 minutes in the simulated medium. Further drug entrapment studies prove very high for Ba crosslinked SALS beads. Whereas Aluminum crosslinked beads showed, inferior crosslinking and drug retention in beads is very low and starts degrading in simulated fluids. Drug release kinetics were analyzed using various kinetic model equations to discuss the order of reaction and drug-polymer mechanism. FT-IR investigations of beads show chemical interactions between crosslinking ion and alginate blends.
Keywords: Sodium alginate, Swelling, Drug entrapment, Crosslinking -
Page 12
Neoplastic cells have co-opted inflammatory receptors and signaling molecules that potentiate inflammation. Activated inflammatory pathways lead to neo-angiogenesis, lymph-angiogenesis, immunosuppression, tumor growth, proliferation and metastasis. This cancer-sustaining inflammation is a critical target to arrest cancer growth. Multiple drug resistance, high cost, low oral bioavailability and serious side effects have rendered conventional cytotoxic chemotherapeutics less impressive. The aim of this research was to achieve cancer debulking and proliferation prevention by limiting ‘cancer-sustaining’ tumor niche inflammation through non-conventional oral approach employing anti-inflammatory agents and avoiding conventional cytotoxic agents. Synergistic anti-inflammatory agents, i.e. celecoxib as selective COX-2 inhibitor and montelukast as cysteinyl leukotriene receptor antagonist, were selected. Silver nanoparticles (AgNPs) were used as nanocarriers because of their efficient synergistic anti-neoplastic effects and excellent oral drug delivery potential. Specifically, selected drugs were co-conjugated onto AgNPs. Synthesized nanoparticles were then surface-modified with poly(vinyl alcohol) to control particle size, avoid opsonization/preferred cellular uptake and improve dispersion. Surface plasmon resonance analysis, particle size analysis, DSC, TGA, XRD, FTIR and LIBS analysis confirmed the successful conjugation of drugs and efficient polymer coating with high loading efficiency. In-vitro, the nanoparticles manifested best and sustained release in moderately acidic (pH 4.5) milieu enabling passive tumor targeting potential. In-vivo, synthesized nanoparticles exhibited efficient dose-dependent anti-inflammatory activity reducing the dose up to 25-fold. The formulation also manifested hemo-compatibility, potent anti-denaturation activity and dose-dependent in-vitro and in-vivo anti-cancer potential against MCF-7 breast cancer and Hep-G2 liver cancer cell lines in both orthotopic and subcutaneous xenograft cancer models. The anti-inflammatory nanoparticles manifested tumor specific release potential exhibiting selective cytotoxicity at cancerous milieu with slightly acidic environment and activated inflammatory pathways. The formulation displayed impressive oral bioavailability, sustained release, negligible cytotoxicity against THLE-2 normal human hepatocytes, low toxicity (high LD50) and wide therapeutic window. Results suggest promise of developed nanomaterials as hemo-compatible, potent, cheaper, less-toxic oral anti-inflammatory and non-conventional anti-cancer agents.
Keywords: Nanoparticles, Anti-cancer, Anti-inflammatory, Non-conventional chemotherapy, Drug delivery