Behrooz Yahyaei

Magnetic iron oxide nanoparticles have attracted considerable attention in medical applications such as imaging and targeted drug delivery. In this study, biological magnetic iron nanoparticles were synthesized using Fusarium oxysporum and iron chloride. Their cytotoxicity was assessed using the MTT assay on ovarian cancer cells across ten stages. At stage 1, all treatment groups showed almost complete cancer cell death. To evaluate the magnetic responsiveness of the nanoparticles, cancer cells were exposed to a neodymium magnetic field in the presence and absence of nanoparticles, and intracellular iron concentration was measured using Inductively Coupled Plasma analysis. For in vivo assessment, 24 rats were divided into four groups and received intraperitoneal nanoparticle injections, with or without magnetic field exposure. The synthesized nanoparticles exhibited significant, dose‐dependent cytotoxicity. In later MTT assay stages, the nano‐drug group showed significantly lower cell viability compared to the free drug and nano‐carrier groups. Exposure to an electromagnetic field enhanced nanoparticle uptake into cells. Histological evaluation revealed no abnormal changes in healthy ovarian tissue. The biologically synthesized magnetic nanoparticles demonstrated effective, selective cytotoxicity against ovarian cancer cells, especially when combined with magnetic field exposure, while maintaining safety in healthy tissue.

Background/Objectives: Extracellular vesicles (EVs) are involved in cell-to-cell communication and delivery of signaling molecules and represent an interesting approach in targeted therapy. This project focused on EV-mediated facilitation and cell-specific delivery of effector antimiR molecules carried by biologically produced gold nanoparticles (AuNPs). Methods: First, we loaded EVs derived from cancer cells 4T1 with AuNPs-antimiR. The AuNPs were also decorated with or without transferrin (Tf) molecules. We examined parental cell-specific delivery of the AuNPs-Tf-antimiR within monocultures as well as co-cultures in vitro. Subsequently, we used autologous EVs containing AuNPs-Tf-antimiR to target tumor cells in a xenograft tumor model in vivo. Efficacy of the antimir transfer was assessed by qPCR and apoptosis assessment. Results: In vitro, EVs loaded with AuNPs-antimiR were internalized only by the parental cells and the AuNPs-antimiR transfer was successful and effective only in EVs that were decorated with Tf. We achieved effective delivery of the antimiR molecule into cancer cells in vivo, which was proved by specific silencing of the target oncogenic miRNA as well as induction of cancer cells apoptosis. Conclusions: EVs represent an interesting and potent way for targeted cargo delivery and personalized medicine. On the other hand, there are various safety and efficacy challenges that remain to be addressed.

Background and Objective: Ketamine, a derivative of phencyclidine, is utilized as an anesthetic agent in surgical procedures. Like other medications, it can be associated with various adverse effects on different organs in the body. This study was conducted to determine the effect of injectable ketamine on the histopathological changes in the ...

Nanotechnology and its byproducts are used increasingly considering its global nanotechnology market size and many applications in the health field. The aim of the present study was to investigate the effect of aerobic and anaerobic exercises on cellular uptake of nanoparticles in body tissues. Fusarium oxysporum was used to synthesize biological AgNPs in silver nitrate solution and UV–vis spectrophotometer; XRD and TEM were used to confirm production of nanoparticles. Moreover, 45 male Wistar rats were purchased and randomly divided into 9 equal groups including healthy control groups, aerobic preparation, anaerobic preparation, biological AgNPs, chemical AgNPs, biological AgNPs+aerobic preparation, biological AgNPs+anaerobic preparation, chemical AgNPs+ aerobic preparation, chemical AgNPs+anaerobic preparation. In order to induce aerobic and anaerobic preparation and to create tissue adaptations, male rats completed two types of aerobic and anaerobic protocols three sessions per week for 10 weeks. At the end of the study, sampling was done for histopathology study. The size and shape of AgNPs was 20–30 nm and spherical to polygonal, respectively. The results showed that anaerobic exercise was significantly effective in weight loss. The chemical nanoparticle group led to more intensive tissue degradation in all variables and there were no significant tissue changes in the aerobic, anaerobic, the biological nanoparticles + aerobic and anaerobic groups. It seems that biological AgNPs are more effective than chemical AgNPs on body tissues and chemical AgNPs lead to more tissue damage in most variables.Research Highlights: There were severe degradative histological effects in the chemical AgNPs groups compare biological AgNPs groups, in terms of most variables.

This study recognized biologically produced gold nanoparticles (AuNP) as multiple cargo carriers with a perspective of drugs delivery into specialized tumor cells in vivo. Paclitaxel (PTX), transferrin, and antimiR-135b were conjugated with AuNPs and their uptake by mouse tumor cells in an induced breast cancer model was investigated. Each of the above-mentioned molecules was conjugated to the AuNPs separately as well as simultaneously, loading efficiency of each cargo was assessed, and performance of the final product (FP) was assessed. After tumor induction in BALB/c mice, sub-IC50 doses of FP as well as control AuNPs, PTX, and PBS were administered in vivo. Round AuNPs were prepared using Fusarium oxysporum and exhibited size of 13 ± 1.3 nm and zeta potential of -35.8 ± 1.3 mV. The cytotoxicity of individual conjugates and FP were tested by MTT assay in breast tumor cells 4T1 and non-tumor fibroblasts NIH/3T3 cells. The conjugation of the individual molecules with AuNPs was confirmed and FP (size of 54 ± 14 nm and zeta potential of -31.9 ± 2.08 mV) showed higher 4T1-specific toxicity in vitro when compared to control conjugates. After in vivo application of the FP, TEM analyses proved presence of AuNPs in the tumor cells. Hematoxylin and eosin staining of the tumor tissue revealed that the FP group exhibited the highest amounts of inflammatory, necrotic, and apoptotic cells in contrast to control groups. Finally, qPCR results showed that FP could transfect and suppress miR-135b expression in vivo, confirming the tumor-targeting properties of FP. The capacity of biologically produced gold nanoparticles to conjugate with multiple decorative molecules while remaining their stability and effective intracellular uptake makes them promising alternative strategy superior to current drug carriers.

Silver nanoparticles (SNPs) can be produced by active and inactive forms of biomass, but their properties have not been compared. Recent research is attempting to reveal their differences in shape, size, amount, antibacterial activity, cytotoxicity, and apoptosis induction. The biomass of Fusarium oxysporum was divided into four groups and pretreated in the following devices: room temperature (RT) and refrigerator (for preparation of active biomass forms), autoclave, and hot air oven (for preparation of inactive biomass forms). Samples were floated in ddH₂O, and SNPs were produced after the addition of 0.1699 g/L AgNO₃ in the ddH₂O solution. SNP production was confirmed by visible spectrophotometry, transmission electron microscopy (TEM) and X-ray diffraction (XRD). SNPs were washed, and their concentration was determined by measuring atomic emission spectroscopy with inductively coupled plasma (ICP-OES). For antibacterial activity, the plate-well diffusion method was used. MTT and Annexin V-FITC/propidium iodide assays were used for cytotoxicity and apoptosis induction, respectively. The maximum absorbance peaks for SNPs pretreated in RT, refrigerator, autoclave, and hot air oven were 404, 402, 412, and 412 nm, respectively. The SNPs produced were almost the same shape and size, and the XRD results confirmed the presence of SNPs in all samples. Due to the differences in the type of bacterial strains used, the SNPs produced showed some differences in their antibacterial activity. The MTT assay showed that the amounts of SNPs in their IC₅₀ dose based on the results of ICP-OES were 0.40, 0.45, 0.66, and 0.44 ppm for the samples pretreated in the hot air oven, autoclave, and refrigerator, and RT, respectively. The apoptosis induction results showed that the biologically engineered SNPs induced more apoptosis (about 34.25%) and less necrosis (about 13.25%). In conclusion, the type and activity of SNPs produced by the active and inactive forms of fungal biomass did not change. Therefore, use of the inactive form of biomass in the future to avoid environmental contamination is reccommended.

Introduction: Ketamine is a popular drug for use in various populations, including pregnant women. Of note, the high prevalence of ketamine use may cause disorders, especially in the nervous system. This study aimed to investigate the effect of repeated short-term and long-term anesthesia with ketamine on balance behavior and cerebellar tissue ...

The aim of this study was to compare the effect of vegetable oils and animal oils on the reproductive system of male rats.This study was a random and observational study conducted on 36 male rats w...

Introduction: Today, due to the increasing application of silver nanoparticles in medical products, it is necessary to pay attention to the user's safety. There are three methods, namely, chemical, physical, and biological, used for the production of nanoparticles. Although the first two methods might introduce health hazards, the latter is hypothetically safe. In this study, we examined the histopathological changes in the cerebellum of neonatal Wistar rats induced by injection of toxic and nontoxic doses of silver nanoparticles, which were produced by green synthetic method and were compared with chemical silver nanoparticles.Methods: This study was a laboratory interventional study performed on 25 Wistar rats in the Animal Laboratory of Islamic Azad University of Shahrood. These rats were divided into five groups of the control group, the group with nonpoisonous injection of chemical nanoparticles, the group with nonpoisonous injection of biological nanoparticles, the group with injection of poisonous chemical nanoparticles, and the group with injection of poisonous biological nanoparticles. The rats were impregnated by the males of the same race and the cerebellum of their offspring was studied after birth.Results: We found that the injection of nonpoisonous chemical nanoparticles caused hyperemia, inappropriate size, and dark cytoplasm in some Purkinje cells. Also, injection of poisonous chemical nanoparticles caused hyperemia and cellular dispersion in the molecular layer, caused abnormal shapes, and reduced the number of cells in Purkinje cells. However, injection of poisonous and nonpoisonous biological nanoparticles did not alter cerebellum cells nor did it cause any inflammation or hyperemia.Conclusion: In contrast with chemical nanoparticles, biological nanoparticles have less significant effect on the cerebellum cells.