Showing papers in "Nanomedicine Journal in 2019"
TL;DR: The present study aimed to develop a novel artificial bio-composite blood vessel using polymer-reinforced and bioceramic nanoparticles to be used in coronary artery bypassing in atherosclerosis as a soft tissue engineering procedure.
Abstract: Objective(s): Cardiovascular diseases (CVDs) are the leading cause of mortality in the elderly. A common medical procedure for the treatment of CVDs is the replacement of the blocked or narrowed arteries, which is currently the optimal vascular transplant associated with autograft transplantation. In general, the saphenous veins and radial arteries in the mammary gland are considered to be the selective vessels for vascular substitution. In many cardiac patients, artificial blood vessels (ABVs) are not used for several reasons, including the age of the patient, small size of the veins, previous impressions, and abnormally. Therefore, the consideration of vascular substitute demands is inevitable, especially regarding vascular transplantation with very small diameters and availability of proper alternatives. The present study aimed to develop a novel artificial bio-composite blood vessel using polymer-reinforced and bioceramic nanoparticles. Materials and Methods: The biomechanics and chemical properties of artificial vessels have been investigated to be used in coronary artery bypassing in atherosclerosis as a soft tissue engineering procedure. In this study, thermoplastic polyurethane (TPU) composed of nanocrystalline hydroxyapatite (HA) nanopowder was prepared using the extrusion technique to construct the ABVs. X-ray diffraction (XRD) and scanning electron microscopy (SEM) were used to investigate the optimum specimen. An important feature of the ABVs was the ability to find the elastic modulus, wettability, and porosity of the veins, which were assessed by fused deposition modeling and 3D printing. Results: The sample containing five wt% of HA had superior mechanical and biological features over the pure sample. Conclusion: According to the results, the narrowed arteries composed of TPU composite with nanocrystalline HA nanopowder had proper chemical stability and mechanical characteristics.
39 citations
TL;DR: The nanomaterials for vaccine application are focused intensively in poly(lactic-co-glycolic) acid, dendrimers, liposomes, nanogels and micelles which are the targeted antigen delivery system, and present high potential as a promising future strategy for DNA-based, bacterial and viral vaccines.
Abstract: Nanoparticles (NPs) are effective and safe adjuvants for antigen delivery in modern vaccinology. Biodegradable nanomaterials with suitable properties are frequently applied for conjugation or loading with antigens; they protect the antigens from degradation in vivo. NPs are applied as effective delivery system to facilitate antigen uptake by antigen presenting cells (APCs) and especially dendritic cells (DCs) both in vitro and in vivo. Using nanoparticles to target DCs is an effective method to deliver antigens and potent immunomodulators. Uptake of NPs by DCs enhances the intracellular process of antigens and the antigen presentation pathway by MHC class I and II molecules to induce both CD4+ and CD8+ T-cell responses. Liposome and polymer-based NPs are now extensively applied as effective adjuvants or immunomodulators in several types of vaccines. In this review, the nanomaterials for vaccine application are focused intensively in poly(lactic-co-glycolic) acid (PLGA), dendrimers, liposomes, nanogels and micelles which are the targeted antigen delivery system, and present high potential as a promising future strategy for DNA-based, bacterial and viral vaccines. Further advances in nanotechnology and molecular immunology techniques will enhance the success of targeting and lead to the next generation of nano-delivery systems.
16 citations
Journal Article•
TL;DR: The role of GNPs in improving radiotherapy efficiency as radiosensitizers is reviewed, with a focus on recent progresses in the field of gold nanostructures in cancer treatment and diagnosis.
Abstract: The application of nanotechnology in medicine involves using nanomaterials to develop novel therapeutic and diagnostic modalities. Given the unique physiochemical and optical properties of gold nanoparticle (GNP) such as good biocompatibility, nontoxic nature, surface properties and comparative stability, it has been widely studied in medicine, especially as a cancer theranostic agent. This review focuses on recent progresses in the field of gold nanostructures in cancer treatment and diagnosis. As far as cancer detection is concerned, several studies have indicated that GNPs can be used for X-ray, MR and optical imaging. With regard to cancer treatment, most studies have investigated the effect of GNPs in different treatment modalities like photothermal therapy, photodynamic therapy, sonodynamic therapy, drug delivery, and radiotherapy. In this paper, we have focused on reviewing the role of GNPs in improving radiotherapy efficiency as radiosensitizers. For optimization of parameters influencing the radiosensitization of GNPs, several studies have been undertaken in different scientific routes. We categorize these studies into three categories; Monte Carlo simulation, cellular studies and animal studies. Finally, according to findings reported by different researchers, the physical and biological mechanism of GNPs in generating radiosensitizing effect is discussed.
12 citations
TL;DR: In this paper, the natural bioactive hydroxyapatite scaffolds with nano-Diopside/Forstrite composite slurry was successfully synthesized to be used in tissue engineering applications.
Abstract: Objective(s): Scaffolds are considered as biological substitutes in bone defects which improve and accelerate the healing process of surrounding tissue. In recent years a major challenge in biomaterials is to produce porous materials with properties similar to bone tissue. In this study, the natural bioactive hydroxyapatite scaffolds with nano Diopside /Forstrite coating was successfully synthesized to be used in tissue engineering applications. Materials and Methods: The spongy part of bovine bone was cut and the subsequent sintering temperature was applied for fabrication of natural hydroxyapatite. Then the scaffolds were coated with 30 wt% nano-Diopside/Forstrite composite slurry. The scaffolds were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and energy-dispersive spectroscope (EDS).Results: In the present study, the mechanical properties of natural HA scaffold were improved when coated with a composite nmaed Diopside/Forstrite ceramic. The optimum properties were evaluated for the scaffolds containing 30 wt% composite ceramic coating. The pore size of the obtained scaffold was measured to be in the range of 300-400 nm. Compressive strength and porosity of the composite scaffold were approximately 1.5±0.2 MPa and 93±1.1 MPa, respectively.Conclusions: Based on the mechanical and bioactivity result, the natural bioactive hydroxyapatite scaffolds with nano Diopside /Forstrite coating showed improved mechanical properties, pore size, porosity content and apatite formation ability whcih can be a promising candidate for bone tissue engineering applications.
9 citations
TL;DR: It is better to consider a combination of two methods as the treatment method, especially in tissue engineering and cell therapy, since bone marrow stromal cells were grown well on chitosan-nanofibers.
Abstract: Objective (s): Several methods have been proposed for repairing defects and damages, one of which is cell therapy. Bone marrow stromal cells seem to be suitable for this purpose. On the other hand, many biometric materials are used to improve and correct the defects in the body. Nanofibers are widely used in the medical industry, especially in tissue engineering, as scaffolds in wound healing and wound dressing. Chitosan/polyethylene oxide nanofibers can be a suitable replacement for routine wound coverages. Hence, this study was conducted to present a combination of these methods.Materials and Methods: Chitosan/polyethylene oxide nanofibers and thin films of chitosan were produced and optimized by electron microscopy, on which the bone marrow stromal cells were then cultivated. Interactions between the cells and these biomaterials were investigated through viability, morphology, immunocytochemistry and electron microscopy of cells after 6 days. All data were analyzed using Student’s t-test and one-way ANOVA tests in SPSS version 16. PResults: It seems that the high viscosity of chitosan prevents the formation of nanofibers, while chitosan/polyethylene oxide solutions with 80/20 and 90/10 ratios produce perfect, regular, bead free and non-toxic nanofibers with average diameter of 240±10 and 220±10 nm, respectively. The results of immunocytochemistry and viability showed that the cells had relatively high proliferation on the thin chitosan membranes, while the results of the electron microscopy showed that the morphology of cells was better on the nanofibers than on the thin membrane of chitosan.Conclusion: Since bone marrow stromal cells were grown well on chitosan-nanofibers, each of them alone was used in the therapeutic methods. It is better to consider a combination of two methods as the treatment method, especially in tissue engineering and cell therapy.
9 citations
TL;DR: Nanotechnology can be broadly employed in orthodontics to achieve better treatment including improved strength of utilized materials, more accurate positioning and reduced microorganisms.
Abstract: Objective (s): Nanotechnology has gained importance in recent years due to its ability in the enhancement of materials properties and other specifications such as antimicrobial properties. Nano-sized materials have been applied in various fields of dentistry. Nanotechnology can be employed in orthodontics to enhance the quality of treatment. In the current study, a comprehensive review is carried out on the applications of nanotechnology in orthodontics. Materials and Methods: In the first step, various databases such as Scopus, Google Scholar and Pubmed were searched by using appropriate keywords for the present study. Afterwards, the related resources were selected to be reviewed. Finally, the key findings of the reviewed studies were represented and summarized. Results: Based on the reviewed researches, nanotechnology is applicable in various aspects of orthodontics. By using nanotechnology, improved properties in mechanical and medical specifications are achievable. For instance, by using nano coating in archwires, the friction force between components can be reduced and facilitate its motion. In addition, adding some types of nano particles to the composites resulted in improvement in tensile and shear bond strength. Antimicrobial properties of specific nano particles such as silver makes them favorable for reducing microorganisms in orthodontics treatment. Moreover, nanotechnology can be used in nano-identation test to assess the tools employed in orthodontics. Conclusion: nanotechnology can be broadly employed in orthodontics to achieve better treatment including improved strength of utilized materials, more accurate positioning and reduced microorganisms.
9 citations
TL;DR: In this paper, the adsorption energy of Melphalan with fullerene C24 was evaluated at the B3LYP/6-31G (d) theoretical level.
Abstract: Objective (s): The present study aimed to assess the adsorption of fullerene C24 with Melphalan anticancer agent in a solvent phase (water) at the B3LYP/6-31G (d) theoretical level.Materials and Methods: Initially, the structures of Melphalan and fullerene complexes were optimized in four configurations. Afterwards, IR calculations and molecular orbital analysis were performed. In addition, some important parameters were assessed, including the adsorption energy, Gibbs free energy changes (ΔGad), enthalpy (ΔHad) variations, thermodynamic equilibrium constant, specific heat capacity, chemical hardness, energy gap, and electrophilicity. Results: According to the results, Gibbs free energy changes (ΔGad), enthalpy (ΔHad) variations, III-Isomer, and IV-Isomer were negatives at various temperatures, while for I-Isomer and II-Isomer were positives throughout the temperature range of 298.15-310.15 K.Conclusion: Since according to the obtained results for adsorption of Melphalan on the C24 in , III-Isomer, and IV-Isomer were spontaneous at various temperatures, while I-Isomer and II-Isomer were not spontaneous throughout the temperature range of 298.15-310.15 K.Conclusion: Since the adsorption of Melphalan with fullerene C24 is spontaneous. Moreover, the effects of temperature on thermodynamic parameters were investigated, and the calculated specific heat capacity values indicated that C24 could be utilized as a sensing material in the construction of thermal biosensors for Melphalan determination.
8 citations
TL;DR: Investigation of the antibacterial and anti-biofilm potential of the non-oxidized form of zinc nanoparticles prepared by a ‘green approach’ using the Lavandula vera extract demonstrated the production of spherical Zn NPs within the size range of 30-80 nanometers, however, further investigations are required.
Abstract: Objective(s): The present study aimed to investigate the antibacterial and anti-biofilm potential of the non-oxidized form of zinc nanoparticles (Zn NPs) prepared by a ‘green approach’ using the Lavandula vera extract with microwave irradiation.Materials and Methods: After synthesis of Zn NPs, the microdilution and disk diffusion methods was applied for antimicrobial evaluation followed by anti-biofilm activity measurement using crystal violet colorimetric assay procedure.Results: The obtained results demonstrated the production of spherical Zn NPs within the size range of 30-80 nanometers. The measured minimum inhibitory concentration of the Zn NPs and ZnSO4 against the biofilm-producing and clinically isolated pathogens of Staphylococcus aureus, Pseudomonas aeruginosa, and Proteus mirabilis was estimated to be more than 2560 µg/ml. In addition, a non-significant increase (P>0.05) was observed in the antibacterial activity against methicillin-resistant S. aureus after the addition of the Zn NPs (500 µg/disk) to the antibiotic discs containing tobramycin, erythromycin, tetracycline, azithromycin, and kanamycin compared to ZnSO4. On the other hand, the Zn NPs significantly decreased the biofilm formation of P. mirabilis compared to P. aeruginosa (P<0.05). Biofilm formation by S. aureus also reduced to 68.3±2.1% in the presence of the Zn NPs (640 µg/ml), which was considered significant compared to P. mirabilis and P. aeruginosa at the same concentration (P<0.05). Conclusion: To sum up, the biofilm inhibitory activity of Zn NPs at higher concentrations than 160 µg/ml against S. aureus and P. mirabilis was more significant compared to the inhibitory effects of ZnSO4. However, further investigations are required in order to determine the antibacterial and anti-biofilm mechanism of Zn NPs.
7 citations
TL;DR: In this article, the zinc selenide nanoparticles (ZnSe NPs) were prepared via green synthesis as a simple, fast, and eco-friendly method at an ambient temperature and various reaction pH (11, 12, and 13).
Abstract: Objective(s): In this study, zinc selenide nanoparticles (ZnSe NPs) were prepared via green synthesis as a simple, fast, and eco-friendly method at an ambient temperature and various reaction pH (11, 12, and 13). Also ZnSe NPs antibacterial activity was investigated.Materials and methods: The ZnSe NPs were characterized using instruments such as UV-Vis spectrophotometry within the range of 360-610 nanometers and transmission electron microscopy (TEM). The antimicrobial activity of various concentrations of ZnSe NPs (1, 2, 4, 8, 16, 32, 64, 128, 256, 512, and 1,024 μg/ml) was examined against Gram-positive bacteria (Staphylococcus epidermidis, Staphylococcus lugdunensis, Enterococcus faecalis, and Staphylococcus aureus), Gram-negative bacteria (Escherichia coli, Pseudomonas aeruginosa, and Enterobacter aerogenes), and Staphylococcus aureus biofilms using the broth microdilution MIC method.Results: The results of UV-Vis spectrum and TEM confirmed the successful synthesis of ZnSe NPs with the mean diameter of approximately 50 nanometers. According to the results of broth microdilution MIC method, there were differences in the resistance of the bacterial strains. In addition, Staphylococcus aureus biofilms were observed to be completely resistant to various concentrations of ZnSe NPs.Conclusion: It seems that synthesized ZnSe NPs can be capable of inhibiting growth of bacterial strains especially Gram-positive strains.
Keywords: Antimicrobial activity, Green chemistry, Nanoparticles, Zinc selenide
7 citations
TL;DR: According to the results, the PCL scaffolds that were modified by CH/GEL NPs/BG had the high potency to be used as bone tissue engineering scaffolds.
Abstract: Objective(s): The present study aimed to prepare polycaprolactone (PCL) scaffolds with high porosity and pore interconnectivity, in order to copy the microstructure of natural bones using the thermally induced phase separation (TIPS) technique. Materials and Methods: The scaffolds were coated with chitosan (CH), bioactive glass (BG), and gelatin nanoparticles (GEL NPs) and assessed using scanning electron microscopy and Fourier-transform infrared spectroscopy (FTIR). Results: The size of the prepared BG and GEL NPs was estimated to be 400 and 234 nanometers, respectively. The porosity and contact angle of PCL/CH/GEL NPs/BG was 74% and 72°, respectively. Weight loss and electron microscopy evaluations indicated the improved degradation rate of the scaffolds and spreading tendency of the cells on the scaffolds when modified as compared to the scaffolds that were purely obtained from PCL. In addition, the in-vitro studies revealed that the MG-63 cells cultured on the PCL/CH/GEL NPs/BG scaffolds showed improved cell proliferation more significantly compared to the scaffolds obtained from PCL, PCL/CH/GEL NPs, PCL/CH, and PCL/GEL NPs. Mechanical examinations also showed that PCL/CH/GEL/BG scaffolds had the highest mechanical strength compared to other groups (i.e., 4.66 Mpa). Cell viability was estimated to be 96.7%, and the alizarin red test indicated the significant improvement of mineralization in the PCL/CH/GEL NP group. Conclusion: According to the results, the PCL scaffolds that were modified by CH/GEL NPs/BG had the high potency to be used as bone tissue engineering scaffolds.
6 citations
TL;DR: Level of learning and memory, relative gene expression ratio of TRPV1, and the histological changes in the hippocampus were significantly different in the groups receiving silver NPs compared to the groups administered with RJ.
Abstract: Objective (s): Silver nanoparticles (NPs) have attracted considerable attention owing to their important properties, including antimicrobial and anti-oxidative stress effects. However, high concentrations of silver NPs have been reported to have toxic effects. The present study aimed to evaluate the modulatory and protective effects of royal jelly (RJ) against the harmful effects of silver NPs on hippocampal functions, such as learning and memory. Materials and Methods: This experimental study was conducted on 40 male Wistar rats. The animals were divided into four groups of 10, including the control group (no silver NPs and RJ), RJ group, silver NPs plus RJ, and silver NPs. Some functions of the hippocampus (e.g., learning and memory) were evaluated using Morris memory function tests for four consecutive days. In addition, the relative expression of TRPV1 was assessed using real-time polymerase chain reaction (RT-PCR). At the final stage, hippocampal tissues were collected for histological studies.Results: Levels of learning and memory, relative gene expression ratio of TRPV1, and the histological changes in the hippocampus were significantly different in the groups receiving silver NPs compared to the groups administered with RJ. Conclusion: According to the results, RJ may be the effective in the protection against the adverse effects of silver NPs and improve the function of the hippocampus.
TL;DR: The findings of the current research indicated that the synthesized HsAFr-DA complex was an optimal nanocarrier for the dual-targeted delivery of anticancer drugs.
Abstract: Objective(s): Nanocarriers are drug delivery vehicles, which have attracted the attention of researchers in recent years, particularly in cancer treatment. The encapsulation of anticancer drugs using protein nanocages is considered to be an optimal approach to reducing drug side-effects and increasing the bioavailability of anticancer drugs. Epirubicin (EPR) is an active chemotherapeutic medication used in the treatment of breast cancer. However, the toxicity of this drug against normal cells is a considerable limitation in therapy. EPR toxicity could be reduced using nanocarriers and dual-targeted drug delivery. Dual-targeted drug delivery system was developed by the conjugation of dopamine (DA) with horse spleen apoferritin (HsAFr)-encapsulated EPR to overcome the limitations of chemotherapeutic EPR in breast cancer treatment. HsAFr-EPR-DA complexes could target the scavenger receptors, transferrin receptors 1, and DA receptors, which are overexpressed on breast cancer cells. Materials and Methods: UV-Visible, fluorescence, and circular dichroism (CD) spectroscopic techniques and transmission electronic microscope (TEM) have been applied to characterize HsAFr-EPR-DA complexes. In the present study, we utilized human breast cancer cell line (MCF-7), aiming to compare the cytotoxicity of HsAFr-EPR-DA complexes to free EPR. Results: The toxicity was measured using the MTT assay, which demonstrated that the dual-targeted nanocarrier (HsAFr-EPR-DA) enhanced cytotoxicity against MCF-7 more significantly compared to non-targeted nanocarriers.Conclusion: The findings of the current research indicated that the synthesized HsAFr-DA complex was an optimal nanocarrier for the dual-targeted delivery of anticancer drugs.
TL;DR: ZnO NPs had the potential to be a selective radiosensitizer for lung cancer radiotherapy under MV X-ray irradiation and some of the cytotoxic and genotoxic mechanisms in radiosensitization were elevated apoptosis induction and DNA damage levels.
Abstract: Objective(s): Semiconductor zinc oxide nanoparticles (ZnO NPs) have unique properties, such as inherent selectivity and photosensitization effects under ultraviolet (UV) radiation. ZnO NPs serve as promising anticancer agents. However, UV radiation limits their penetration into the body. In most clinical settings, it is essential to use high-energy photons in the treatment of deep-seated tumors. The present study aimed to evaluate the radiosensitization effects of ZnO NPs on human lung cancer cells under megavoltage (MV) X-ray irradiation. Materials and Methods: ZnO NPs with the mean diameter of seven nanometers were synthesized and characterized. The cytotoxicity and cellular uptake of ZnO NPs were evaluated in SKLC-6 lung cancer and MRC-5 normal lung cells using the 3-(4,5-dimethylthiazol-yl)-5(3-carboxymethoxyphenyl)-2H-tetrazolium (MTT) and inductively coupled plasma-mass spectrometry assays, respectively. In addition, the radiosensitization effects of ZnO NPs were investigated under MV irradiation using a clonogenic survival assay. Apoptosis induction and DNA damage were also evaluated using flow cytometry and cytokinesis-block micronucleus assay, respectively.Results: ZnO NPs were taken up and reduced the viability of the cancer cells at a higher rate compared to the normal cells. Moreover, ZnO NPs significantly enhanced the radiosensitivity of the cancer cells with the sensitizer enhancement ratios of 1.23 and 1.31 at the concentrations of 10 and 20 μg/ml, respectively. However, they had no significant effect on the radiosensitivity of the normal cells. Apoptosis induction and DNA damage also improved at a higher rate in the cancer cells compared to the normal cells with the combination of ZnO NPs with MV radiation.Conclusion: According to the results, ZnO NPs had the potential to be a selective radiosensitizer for lung cancer radiotherapy under MV X-ray irradiation. Some of the cytotoxic and genotoxic mechanisms in radiosensitization by ZnO NPs were elevated apoptosis induction and DNA damage levels.
TL;DR: The significance of this study lied in the fact that simulating microgravity can be a powerful physical cure for cancer therapy and open new horizons for the studies in the field of biology, biophysics, and medicine.
Abstract: Objective (s): Gravity could affect some system features and perform directly as an organizing field factor. Recent investigations have examined the titanium dioxide nanoparticles (TiO2 NPs) in biomedical applications, mostly in the cancer treatment field. This study aimed to evaluate the effects of simulated microgravity combined with TiO2 NPs in MDA-MB-231 cells proliferation for the first time. In other words, this study examined the utility of the microgravity environment in nano-therapy. Materials and Methods: The MDA-MB-231 human breast cancer cell line and TiO2 NPs were purchased. The 2D clinostat was applied for the simulation of the microgravity. The morphological studies, MTT cytotoxicity assay, Acridine orange/Ethidium bromide double staining studies and flow cytometry analysis were utilized.Results: The MTT assay, the morphological studies, Acridine orange/Ethidium bromide double staining studies and flow cytometry analysis confirmed the apoptosis-inducing effect of microgravity in combination with TiO2 NPs. The IC50 of simulated microgravity in the presence of TiO2 NPs was determined to be 130 µM. Furthermore, MDA-MB-231 cells exposed to microgravity adopted a different phenotype. Conclusion: Based on our observation, although the relative mechanisms need to be explored further, microgravity can strictly affect the TiO2 NPs effects on MDA-MB-231 cells. The significance of this study lied in the fact that simulating microgravity can be a powerful physical cure for cancer therapy and open new horizons for the studies in the field of biology, biophysics, and medicine.
TL;DR: The synergistic effects of combined ZnO NPs and 5-FU on MCF-7 human breast cancer cells were exerted via Bcl-2 inhibition and the up-regulation of p53 expression.
Abstract: Objective(s): The significant contribution of nanoparticles to cancer treatment has attracted therapeutic attention. The present study aimed to evaluate the synergistic effects of 5-fluorouracil (5-FU) and zinc oxide nanoparticles (ZnO NPs) as multimodal drug delivery on human breast cancer MCF-7 cells.Materials and Methods: In this in-vitro study, the impact of 5-FU and ZnO NPs in the single or combined forms was evaluated on cell viability, colony formation, apoptosis, p53 gene expression, and Bcl-2 signaling protein in MCF-7 breast cancer cell line using several techniques, such as MTT, clonogenic assay, flow cytometry, real-time quantitative polymerase chain reaction, and Western blot.Results: In this study, 5-FU combined with ZnO NPs showed synergistic effects against MCF-7 within 48 hours. In addition, the combination of 5-FU and ZnO NPs at the respective concentrations of 1 µM and 45 µg/ml exhibited significant apoptosis (79.53), p53 gene expression (3.6 folds), reduction of cell invasion (9.82), and plating efficiency (5), thereby leading to the significant reduction of cell viability (40±0.9) and decreased Bcl-2 anti-apoptotic protein relative to untreated control cells. Conclusion: According to the results, the synergistic effects of combined ZnO NPs and 5-FU on MCF-7 human breast cancer cells were exerted via Bcl-2 inhibition and the up-regulation of p53 expression.
TL;DR: In this paper, cetrimonium bromide (CTAB) was used as a surfactant at low (0.1 g), medium (1 g) and high concentrations (7 g), and the effects on the properties of the nanoparticles were investigated.
Abstract: Objective(s): The use of cationic surface-active agents (surfactant) in the synthesis of nanoparticles, with formation of micelle, can act as a template for the formation of meso-porous silica. Changes in the concentration of surfactants can affect the structures and properties of the resulting nanoparticles.Materials and Methods: Magnetite nanoparticles were prepared as cores using the coprecipitation method. Silica shells were formed on the prepared cores using sol-gel through the single-step process. During synthesis, cetrimonium bromide (CTAB) was used as a surfactant at low (0.1 g), medium (1 g), and high concentrations (7 g), and the effects on the properties of the nanoparticles were investigated. The core-shell nanoparticles were analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). In addition, the surface porosities of the nanoparticles were evaluated using the BET and BJH methods. The vibrating sample magnetometer (VSM) was also employed to assess the magnetic characteristics of the synthesized samples. Results: The results of XRD indicated that the nanoparticles were composed of magnetite and silica, while the SEM and TEM images confirmed the presence of uniform spherical particles with a core-shell structure. According to the results of the VSM tests, all nanoparticles showed super-paramagnetic behaviors. Moreover, the increased concentration of CTAB led to an increment in saturation magnetization (Ms), size, and volume of the surface pores, while the specific surface area of the nanoparticles decreased. Conclusion: According to the results, the properties of the silica shell could be adjusted in terms of pore characteristics and magnetic behavior by changing the concentration of the surfactant.
TL;DR: The results obtained in this study confirmed the efficacy of nanocurcumin as a radioprotective agent against radiation-induced mortality in mice and made this phytochemical as a potential radioprotsective agent in the radiotherapy setting and radiation accidents.
Abstract: Objective(s): Curcumin, a natural plant product, is commonly known as wonder drug of life, but the poor bioavailability of its free form has hindered its clinical development. The aim of the present study was to investigate the radioprotective effect of nanocurcumin on survival of mice under whole body X-ray irradiation. Materials and Methods: The Naval Medical Research Institute (NMRI) mice randomly assigned to separate groups and received nanocurcumin via oral gavage at different time points related to irradiation. The survival of mice was evaluated daily for 30 days post-irradiation and finally, the LD50/30 was calculated using Probit analysis. The 30-day survival curve was plotted using the Kaplan-Meier survival curve and the median survival of different subgroups was compared using log-rank test. The P-values less than 0.05 were considered significant. Results: Our results showed that the administration of oral nanocurcumin could effectively reduce the mortality rate in the irradiated mice. Five days pretreatment with nanocurcumin (4 mg/kg/day) induced maximum radioprotective effect. The LD50/30 was 7.18 Gray (Gy) (95% confidence interval [CI]: 6.59-7.77) and 8.78 Gy (95% CI: 8.14-9.50) for irradiation-only and the optimum nanocurcumin group (pre-irradiation group), respectively (dose reduction factor [DRF] = 1.22). Continued administration of nanocurcumin up to seven days post-irradiation resulted in no further radioprotection. Conclusions: The results obtained in this study confirmed the efficacy of nanocurcumin as a radioprotective agent against radiation-induced mortality in mice. The specific characteristics of nanocurcumin, such as non-toxicity, edibility, availability, make this phytochemical as a potential radioprotective agent in the radiotherapy setting and radiation accidents. Further clinical studies are highly recommended.
TL;DR: In this article, albumin-coated IONPs were prepared and the process was optimized using the response surface methodology (RSM) to achieve optimum loading of IOPs in albumin nanoparticles, and the resulting nanoparticles were characterized physicochemically by scanning electron microscopy (SEM), dynamic light scattering (DLS), inductively coupled plasma optical emission spectrometry (ICP-OES), Fourier transform infrared spectroscopy (FTIR), and vibrating sample magnetometer (VSM).
Abstract: Objective(s): Cancer diagnosis in its early stages of progress, can enhance the efficiency of treatment utilizing conventional therapy methods. Non-biocompatibility of iron oxide nanoparticles (IONPs) has made a big challenge against their usage as a contrast agent. Efficient coverage by biomolecules such as albumin can be a solution to overcome this problem. Herein, albumin-coated IONPs were prepared and the process was optimized using the response surface methodology (RSM) to achieve optimum loading of IONPs in albumin nanoparticles. Materials and Methods: IONPs were incorporated into bovine serum albumin nanoparticles (BSA NPs) matrix, to yield IONPs-BSA NPs. The resulting nanoparticles were characterized physicochemically by scanning electron microscopy (SEM), dynamic light scattering (DLS), inductively coupled plasma optical emission spectrometry (ICP-OES), Fourier transform infrared spectroscopy (FTIR) and vibrating sample magnetometer (VSM). The stability test was conducted over 6 months.Results: Under optimum conditions of 2.28 mg for iron weight and pH 9.21, loading of 7.76% was obtained for the spherical IONPs-BSA NPs with the size of 177±12 nm, PDI of 0.222±0.07 and zeta-potential of -36.4±2.3 mV. These findings revealed that more than 90% and 60% of the particles retained their size over four and six months of storage at 4 °C, respectively. In addition, non-cytotoxicity and hemocompatibility of IONPs-BSA NPs were verified in vitro thereby offering them as a biocompatible contrast agent for cancer diagnosis. Conclusion: The IONPs-BSA NPs developed in this study are promising to be further investigated and functionalized with a ligand to obtain a targetable MRI contrast agent for early cancer diagnosis.
TL;DR: In this paper, a facile and ultrasensitive colorimetric aptasensor was reported for detection of oxytetracycline (OTC) in water and milk samples employing OTC-short aptamer and gold nanoparticles (AuNPs).
Abstract: Objective (s): In light of misuse of antibiotics in animal husbandry and their side effects on human health, there is an argent need to develop simple and rapid methods for determining the quantification of antibiotics in biological systems. Materials and Methods: In this work a facile and ultrasensitive colorimetric aptasensor was reported for detection of oxytetracycline (OTC) in water and milk samples employing OTC-short aptamer and gold nanoparticles (AuNPs). Results: In the presence of OTC, the interaction between OTC and its aptamer leads to the separation of OTC aptamer from the surface of AuNPs which is followed by the aggregation of AuNPs by salt, showing an evident color change from red to blue. On the contrary, in the absence of OTC, the attachment of aptamer on the surface of AuNPs can protect AuNPs against salt-induced aggregation with a wine-red color. The proposed aptasensor exhibits excellent sensitivity for detection of OTC with linear range between 20 to 2000 nM with limit of detection (LOD) as low as 10 nM. Furthermore, this strategy was applied to detect OTC in spiked milk samples and presented satisfying linear range from 25 to 1500 nM with the LOD of 20 nM. Conclusion: Owing to demonstrating appropriate sensitivity and selectivity, the designed biosensor can be considered as a promising tool to be applied in the field of biomedicine and food safety.
TL;DR: The results of CD200 silencing at the mRNA level revealed that the shRNA formulation could reduce the CD200 level in the cells of the patients by 3.2-6.06-fold relative to the cells transfected with non-effective, scrambled shRNA.
Abstract: Objective(s): ShRNA-mediated silencing strategy is considered to be a potent therapeutic approach. The present study aimed to assess the ability of the previously prepared polyethylenimine (PEI) derivative for the shRNA knock-down of the CD200 gene on the cells obtained from the patients with chronic lymphocytic leukemia (CLL). Materials and Methods: Since there are several investigations regarding the role of CD200 over-expression in the progression of several malignancies (e.g., CLL), polyplexes were prepared using succinylated PEI and the plasmid encoding anti-CD200 shRNA. The ability of the nanoparticles for CD200 silencing at the levels of protein and mRNA, as well as the apoptotic effects induced by unmodified PEI and its derivative, were evaluated. Results: Conjugation of succinic acid using the primary amines of PEI reduced the cell-induced toxicity of the polymer. Under such circumstances, 92.1% of the cells remained alive after treatment with the nanoparticles based on modified PEI. In addition, CD200 knock-down evaluations demonstrated a 50% reduction in the expression of the gene in the samples obtained from patients with CLL, while using the same formulation on the cells obtained from healthy donors decreased the CD200+ cells up to 10%. The results of CD200 silencing at the mRNA level revealed that the shRNA formulation could reduce the CD200 level in the cells of the patients by 3.2-6.06-fold relative to the cells transfected with non-effective, scrambled shRNA. Conclusion: Our findings supported the application of succinylated PEI for the down-regulation of the CD200 gene in the upcoming attempts to develop nano-carriers for gene therapy.
TL;DR: In this paper, the results of X-ray diffractometry (XRD) and scanning electron microscopy (SEM) confirmed the presence of nanoparticles on the nanocomposite surface.
Abstract: Objective(s): Antibacterial and antifungal nanocomposites are widely used in food packaging and pharmaceutical and medicine industries. Among the polymers of these nanocomposites, epoxy coatings are commonly used for health and industrial applications. The present study aimed to synthesize CuO nanoparticles using the chemical reduction method and characterized them by ultraviolet-visible (UV-Vis) spectroscopy and dynamic light scattering (DLS) analysis. Materials and Methods: The nanoparticles were synthesized with the mean size of 45 nanometers. Following that, the CuO/epoxy nanocomposite were prepared in three concentrations of 1%, 3%, and 5% of the CuO nanoparticles. The results of X-ray diffractometry (XRD) and scanning electron microscopy (SEM) confirmed the presence of nanoparticles on the nanocomposite surface. In addition, the disc-diffusion method was used to assess the antifungal properties of the nanocomposites. Results: The results of XRD and SEM confirmed the presence of CuO nanoparticles on the nanocomposite surface. The optimal nanocomposite concentration for the maximum antifungal activity was 3%.Conclusion: It seems that the CuO nanoparticles could be used to provide antifungal nanocomposites, which are applicable in medicine and food industries.
TL;DR: The use of silver nanoparticles can boost the serum levels of hepatic enzymes and increase liver tissue necrosis, as well, however, the silver cobalt nanoparticles did not change the levels of liver enzymes and liver tissue.
Abstract: Objective(s): This study aimed to compare impacts of silver nanoparticles and silver cobalt nanoparticles on the hepatic function tests and changes in liver tissues in adult male rats.Materials and Methods: This study was conducted on 49 adult male Wistar rats, each weighing approximately 180-220 gr. The rats were randomly assigned to seven groups of seven including one control group and six experimental groups. The experimental groups 1 and 2 respectively received 25 and 100 mg/kg of silver nanoparticles synthesized for 75 sec intraperitoneally for 14 days. Experimental group 3 received silver nanoparticles that were synthesized at 300 sec which were administered intraperitoneally in a 25 mg/kg dose for 14 days. The experimental groups 4 and 5 received silver cobalt nanoparticles, whereby silver nanoparticles were synthesized at 75 sec and were administered intraperitoneally in a 25 and 100 mg/kg dose for 14 days, respectively. Finally, experimental group 6 received a 25 mg/kg dose of silver cobalt nanoparticles, intraperitoneally for 14 days, with the silver nanoparticles synthesized for 300 sec. At the end of this period, the serum levels of hepatic enzymes, albumin, and total protein were measured and tissue changes were evaluated in this study.Results: The mean serum levels of AST, total protein, and albumin in the experimental groups 1 and 3 increased significantly compared to the control group. Similarly, the mean serum levels of ALT and ALP in the experimental group 3 showed a significant increase in comparison with the control group. The mean of liver weight in all experimental groups was significantly higher than the control group(P<0.05). Furthermore, the necrosis of the liver tissue was observed in the recipients of silver nanoparticles. However, liver necrosis was not observed in the groups receiving silver cobalt nanoparticles.Conclusion: The use of silver nanoparticles can boost the serum levels of hepatic enzymes and increase liver tissue necrosis, as well. However, the silver cobalt nanoparticles did not change the levels of hepatic enzymes and liver tissue.
TL;DR: According to the results, BMSCs could be differentiated into osteoblast-like cells in the presence of the chitosan/PEO nanofibers containing nano-hydroxyapatite.
Abstract: Objective(s): Design and construction of biocompatible and biodegradable scaffolds are among the main goals of tissue engineering. Recently, use of nano-hydroxyapatite as a bioactive bioceramic agent with high similarity to the mineral phase of the human bone tissue, in combination with biodegradable polymers and implant coatings has attracted the attention of researchers in the field of biomaterial sciences. The present study aimed to assess the differentiation of bone marrow stromal cells (BMSCs) in osteoblast-like cells on the chitosan/polyethylene oxide (PEO)/nano-hydroxyapatite scaffold in mature rats.Materials and Methods: Chitosan and PEO solution with the weight ratio of 80:20 and 70:30 were prepared, and 2% weight of nano-hydroxyapatite was added. Nanofibers were prepared using the electrospinning method, and the morphology was studied using scanning electron microscopy (SEM). Afterwards, the BMSCs of mature rats were cultured on nanofibers and differentiated by adding a differentiation medium. The survival of the differentiated cells was evaluated at the end of the first, second, and third week using acridine orange staining, and the morphology of the differentiated cells exposed to nanofibers was assessed using SEM. Results: The mean diameter of the nanofibers with the ratio of 80:20 was 150±17 nanometers. The differentiation of BMSCs into the osteoblast-like cells on nanofibers was confirmed using Alizarin red staining. The results indicated a significant decrease in the survival of the differentiated cells in the nanofiber groups by the end of the third week of differentiation compared to the control samples.Conclusion: According to the results, BMSCs could be differentiated into osteoblast-like cells in the presence of the chitosan/PEO nanofibers containing nano-hydroxyapatite.
TL;DR: MET- and IRI-loaded PLGA NPs may be a promising approach to treat GBM after a significant reduction in glutamate reuptake time compared with free drugs, blank NPs and cancer cells control groups.
Abstract: Objective(s): The present study was designed to evaluate of Metformin/Irinotecan-loaded poly-lactic-co-glycolic acid (PLGA) nanoparticles (NPs) effects on glutamate re-uptake time and receptor expression status in both glioblastoma multiforme (GBM) and cortex neuron cultures. The study was performed on glioblastoma cell line and primer cortex neuron.Materials and Methods: The re-uptake time and gene expression status of pure drugs and MET- or IRI-loaded-PLGA NPs on healthy neuron cells and U-87 MG cell line were investigated by using glutamate specific voltammetry electrodes technique and real time PCR. Results: Both MET and MET-PLGA NPs (1 and 2 mM) exhibited significant cytotoxicity on both U87MG and neuron cells. MET and MET-PLGA NPs (0.5 mM) showed lower cytotoxic effects on both cells. IRI and IRI-PLGA NPs (100 µM) had significant cytotoxic effects on both cell lines. Conclusion: All drug-loaded NPs caused a significant reduction in glutamate reuptake time compared with free drugs, blank NPs and cancer cells control groups. Consequently, MET- and IRI-loaded PLGA NPs may be a promising approach to treat GBM.
TL;DR: In this paper, alginate was conjugated to gadolinium/graphene oxide/alginate nanocomposite to form a nanomaterial to provide MRI contrast.
Abstract: Objective(s): Relevance between magnetic resonance imaging (MRI) relaxation rate and concentration of magnetic nanoparticles determines the capability of a nanomaterial to provide MRI contrast. In the present study, alginate was conjugated to gadolinium/graphene oxide nanocomposite to form gadolinium/graphene oxide/alginate nanocomposite, aiming to investigate its effect on the relevance between MRI longitudinal relaxation rate and paramagnetic gadolinium concentration.Materials and Methods: The physicochemical properties of the nanocomposite and its effect on the cell culture were investigated. Moreover, MRI longitudinal relaxation rates were determined based on the corresponding exponential curves, and the graph of their relevance with gadolinium concentration was plotted. Results: The average thickness and sheet size of the nanocomposite were three and 100 nanometers, respectively. The nanocomposite showed high cell viability, even at the relatively high concentration of 75 µg/ml. In addition, a linear correlation was observed between longitudinal relaxation rate and gadolinium concentration. Conclusion: According to the results, the linearity between gadolinium/graphene oxide/alginate nanocomposite and gadolinium concentration, which revealed a high slope, confirmed the potential of the nanocomposite to significantly improve the positive contrast of MR images.
TL;DR: Lactational exposure to AgNp may induce apoptosis via the intrinsic pathway in the offspring tissues of rats according to the results, but further investigation is required in order to document these findings.
Abstract: Objective(s): The adverse health effects of nanosilver (AgNp) on adult animal models have been well documented. However, data is scarce regarding the toxic effects of AgNp on sensitive developmental stages. The present study aimed to investigate the effects of maternal milk exposure to AgNp on apoptosis induction in the liver and brain of the offspring of rats. Materials and Methods: Lactating Wistar rats were intragastrically exposed to the vehicle (deionized water) or two doses of AgNp (25 and 100 mg/kg) for 21 days. Liver and brain samples were collected from the male pups of the mothers on postnatal day 21. The silver content and levels of caspase-8 and caspase-9 in the tissues were measured using the ICP-MS analysis and ELISA assay, respectively. For histopathological examinations, the tissue sections were stained using the hematoxylin-eosin (H&E) stain and examined by light microscopy.Results: A significant, dose-dependent increase was observed in the silver content of the liver and brain of the pups and maternal milk exposed to AgNp. In addition, the level of caspase-9 significantly increased in the liver and brain in the pups exposed to the high dose of AgNp (100 mg/kg-1), while no significant changes were observed in the level of caspase-8 in the experimental groups compared to the controls. Histopathological studies also demonstrated tissue damage in the liver and brain of the pups exposed to the high dose of AgNp. Conclusion: According to the results, lactational exposure to AgNp may induce apoptosis via the intrinsic pathway in the offspring tissues of rats. However, further investigation is required in order to document these findings.
TL;DR: In this paper, a comprehensive review of the applications of nano-based materials, technologies, and methods used in restorative dentistry is presented, where the appropriate references regarding the research subject were assessed, and findings were collected to achieve a comprehensive study.
Abstract: Nanotechnology has various applications in restorative dentistry in order to achieve reliable treatment outcomes. The present study aimed to comprehensively review the studies focused on the applications of nano-based materials, technologies, and methods used in restorative dentistry. Related articles were retrieved via searching in databases such as PubMed, Google Scholar, and Scopus. Afterwards, the appropriate references regarding the research subject were assessed, and findings were collected to achieve a comprehensive review study. According to the obtained results, the utilization of nanotechnology in restorative dentistry could yield beneficial outcomes. The dispersion of nano-sized structures in restorative materials could enhance mechanical properties such as diametral and flexural strength and fracture toughness. However, the improvement of the mentioned mechanical properties depends on the type of the nano-sized materials, their content, and type of the additional materials used along with nano-based restorative materials.
TL;DR: Although improved activity of the CN-AuNPs-PEG encapsulating was achieved but its cytotoxicity still is a limitation, the AuNPs were crystalline in nature.
Abstract: Objective(s): Drug delivery is an engineering technology to control the release and delivery of therapeutic agents to target organs, tissues, and cells. Metallic nanoparticles, such as gold nanoparticles (AuNPs) have exceptional properties which enable efficient drug transport into different cell types with reduced side effects and cytotoxicity to other tissues.Materials and Methods: AuNPs were synthesized by adopting the Turkevich method to reduce tetra chloroauric (III) acid (HAuCl4) solution with sodium citrate. A factorial design of 24 was used to investigate the influence of temperature, stirring speed, and the volume of citrate and gold salt on the size of AuNPs synthesis. The produced chemical-AuNPs (CN-AuNPs) were characterized using ultraviolet-visible spectroscopy and dynamic light scattering (DLS) which was conjugated with polyethylene glycol (PEG) loaded with chloroquine diphosphate. The latter were characterized with transmission electron microscopy (TEM), Energy dispersive x-ray spectroscopy (EDS), selected area electron diffraction (SAED) patterns and Fourier transmission infrared spectroscopy. The antimalarial activities of the three formulations were tested on Plasmodium-infected mice. Moreover, the evaluation of curative potentials of the formulations was carried out via parasite counts. The anemic and pathological conditions of nano-encapsulation were investigated for their cytotoxicity level. Results: The CN-AuNPs show surface plasmon resonance absorption ranging from 526 to 529 nm with smaller particle size at the lower citrate volume. The TEM image of CN-AuNPs with polyethylene glycol (PEG) and CN-AuNPs-PEG encapsulated with chloroquine diphosphate revealed spherical shape with EDS showing the appearance of gold (Au) at 2.0, 2.1, and 9.9 KeV. The SAED also revealed that the AuNPs were crystalline in nature. The in vitro time-dependent encapsulation release showed an extension of time release, compared to CN-AuNPs-PEG with parasitemia clearance at the same level of cytotoxicity. Conclusion: Therefore, although improved activity of the CN-AuNPs-PEG encapsulating was achieved but its cytotoxicity still is a limitation.
TL;DR: The results indicated that the fabricated MAGIC-f gel could be recommended as a suitable tool for three dimensional dosimetric investigations at high energy radiotherapy procedures wherein GNPs are used.
Abstract: Objective(s): Normoxic MAGIC-f polymer gels are established dosimeters used for three dimensional dose quantifications in radiotherapy. Nanoparticles with high atomic number such as gold are novel radiosensitizers used to enhance doses delivered to tumors. The aim of this study was to investigate the effect of gold nanoparticles (GNPs) in enhancing percentage depth doses (PDDs) within the MAGIC-f gel exposed to linear accelerator (linac) high energy photon beams. Materials and Methods: The MAGIC-f gel was fabricated based on its standard composition with some modifications. The PDDs in tubes containing the gel were calculated by using a common Monte Carlo code (Geant4) followed by experimental verifications. Then, GNPs with an average diameter of 15 nm and a concentration of 0.1 mM were embedded in the gel, poured into falcon tubes and irradiated with 18 MeV beams of an Elekta linac. Finally, similar experimental and Monte Carlo (MC) calculations were made to determine the effect of using GNPs on some dosimetric parameters of interest.Results: The results of experimental measurements and simulated MC calculations showed a dose enhancement factor (DEF) of 1.12±0.08 and 1.13±0.04, respectively due to the use of GNPs when exposed to 18 MeV linac energies.Conclusion: The results indicated that the fabricated MAGIC-f gel could be recommended as a suitable tool for three dimensional dosimetric investigations at high energy radiotherapy procedures wherein GNPs are used.
TL;DR: According to the results, PVP-grafted SPIONs could be preferred positive contrast agents with specific imaging parameters and have the potential application for early cancer diagnosis and perfusion measurements.
Abstract: Objective(s): The present study aimed to evaluate the capability of synthesized and modified superparamagnetic iron oxide nanoparticles (SPIONs) as the positive contrast agent in magnetic resonance imaging (MRI) by investigating the effect of repetition time (TR) on the MRI signal intensity. Materials and Methods: SPIONs were synthesized using the co-precipitation method, and their surface was successfully modified with biocompatible poly (N-vinylpyrrolidone) (PVP). The effect of TR on the signal intensity (SI) of the PVP-grafted SPIONs was assessed in the spin-echo T1-weighted MRI images. Results: The results indicated the maximum SI at the concentration of 400 µmol Fe/l with the TR of 800-2,200 milliseconds. Moreover, the maximum SI was observed at the concentration of 75 µmol Fe/l, where TR was within the range of 2,900-6,400 milliseconds. Conclusion: According to the results, in addition to their capability as negative MRI contrast agents, PVP-grafted SPIONs could be preferred positive contrast agents with specific imaging parameters and have the potential application for early cancer diagnosis and perfusion measurements.