Background: Multiple drug-delivery systems obtained by loading nanoparticles (NPs) with different drugs that have different physicochemical properties present a promising strategy to achieve synergistic effects between drugs or overcome undesired effects. This study aims to develop a new NP by loading quercetin (Que) and valproic acid (VPA) into chitosan. In this context, our study investigated the antioxidant activities of chitosan NPs loaded with single and dual drugs containing Que against oxidative stress. Method: The synthesis of chitosan NPs loaded with a single (Que or VPA) and dual drug (Que and VPA), the characterization of the NPs, the conducting of in vitro antioxidant activity studies, and the analysis of the cytotoxicity and antioxidant activity of the NPs in human neuroblastoma SH-SY5Y cell lines were performed. Result: The NP applications that protected cell viability to the greatest extent against H₂O₂-induced cell damage were, in order, 96 µg/mL of Que-loaded chitosan NP (77.30%, 48 h), 2 µg/mL of VPA-loaded chitosan NP (70.06%, 24 h), 96 µg/mL of blank chitosan NP (68.31%, 48 h), and 2 µg/mL of Que- and VPA-loaded chitosan NP (66.03%, 24 h). Conclusion: Our study establishes a successful paradigm for developing drug-loaded NPs with a uniform and homogeneous distribution of drugs into NPs. Chitosan NPs loaded with both single and dual drugs possessing antioxidant activity were successfully developed. The capability of chitosan NPs developed at the nanometer scale to sustain cell viability in SH-SY5Y cell lines implies the potential of intranasal administration of chitosan NPs for future studies, offering protective effects in central nervous system diseases.

Nanostructured materials used have unique properties and many uses in nanotechnology. The most striking of these is using herbal compounds for the green synthesis of nanoparticles. Among the nanoparticle types used for green synthesis, gold nanoparticles (AuNPs) are used for cancer therapy due to their stable structure and non-cytotoxic. Lung cancer is the most common and most dangerous cancer worldwide in terms of survival and prognosis. In this study, Nasturtium officinale (L.) extract (NO), which contains biomolecules with antioxidant and anticancer effects, was used to biosynthesize AuNPs, and after their characterization, the effect of the green-synthesized AuNPs against lung cancer was evaluated in vitro. Ultraviolet‒visible (UV‒Vis) spectrophotometry, scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), multiple analysis platform (MAP), and Fourier transform infrared (FT-IR) spectroscopy analyses were performed to characterize the AuNPs prepared from the N. officinale plant extract. Moreover, the antioxidant activity, total phenolic and flavonoid contents and DNA interactions were examined. Additionally, A549 lung cancer cells were treated with 2–48 µg/mL Nasturtium officinale gold nanoparticles (NOAuNPs) for 24 and 48 h to determine the effects on cell viability. The toxicity of the synthesized NOAuNPs to lung cancer cells was determined by the 3-(4,5-dimethylthiazol-2-il)-2,5-diphenyltetrazolium bromide (MTT) assay, and the anticancer effect of the NOAuNPs was evaluated by apoptosis and cell cycle analyses using flow cytometry. The average size of the NPs was 56.4 nm. The intensities of the Au peaks from EDS analysis indicated that the AuNPs were synthesized successfully. Moreover, the in vitro antioxidant activities of the NO and NOAuNPs were evaluated; these materials gave values of 31.78 ± 1.71% and 31.62 ± 0.46%, respectively, in the 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay at 200 g/mL and values of 25.89 ± 1.90% and 33.81 ± 0.62%, respectively, in the 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) assay. The NO and NOAuNPs gave values of 0.389 ± 0.027 and 0.308 ± 0.005, respectively, in the ferrous ion reducing antioxidant capacity (FRAP) assay and values of 0.078 ± 0.009 and 0.172 ± 0.027, respectively, in the copper ion reducing antioxidant capacity (CUPRAC) assay. When the DNA cleavage activities of NO and the NOAuNPs were evaluated via hydrolysis, both samples cleaved DNA starting at a concentration of 25 g/mL in the cell culture analysis, while the nanoformulation of the NO components gave greater therapeutic and anticancer effects. We determined that the Au nanoparticles were not toxic to A549 cells. Moreover, after treatment with the half-maximal inhibitory concentration (IC50), determined by the MTT assay with A549 cells, we found that at 24 and 48 h, while the necrosis rates were high in cells treated with NO, the rates of apoptosis were greater in cells treated with NOAuNPs. Notably, for anticancer treatment, activating apoptotic pathways that do not cause inflammation is preferred. We believe that these results will pave the way for the use of NOAuNPs in in vitro studies of other types of cancer. In this study, AuNPs were successfully synthesized from N. officinale extract. The biosynthesized AuNPs exhibited toxicity to and apoptotic effects on A549 lung cancer cells. Based on these findings, we suggest that green-synthesized AuNPs are promising new therapeutic agents for lung cancer treatment. However, since this was an in vitro study, further research should be performed in in vivo lung cancer models to support our findings and to explain the mechanism of action at the molecular level.

Cinclidotus fontinaloides (Hedw.) P. Beauv. and Palustriella commutata (Hedw.) Ochyra were used in this study. The chemical composition of mosses in the ethanol and water extract was determined using GC-MS and FT-IR. Antioxidant activities of moss extracts were tested by total phenol and ABTS methods. Trolox equivalent value (TEAC) of mosses was calculated as 26 ± 0.32 and 10 ± 0.22 mg/g. The amounts of the flavonoid compounds were calculated as mg gallic acid. Gallic acid equivalent value of mosses was calculated as 587 ± 0.55 and 496 ± 0.22 mg/g. The extracts antimicrobial activity was tested against Escherichia coli (ATCC 8739), Bacillus subtilis (ATCC 6633), Staphylococcus aureus (ATCC 6538), Pseudomonas aeruginosa (ATCC 10145) and Candida albicans (ATCC 10231). Significant antibacterial effect was observed for C. fontinaloides and P. commutata in ethanol extract. Total anthocyanin activities of C. fontinaloides and P. commutata were determined as 50 ± 0.17 and 144 ± 0.33 mg/L.

On Earth, atmosphere interact with crust and thus simultaneously monitoring of environmental pollution in both parts of the environment is important. Soil and rainwater samples were taken in different parts of Çanakkale, Turkey, in two seasons. Study sites laid along with the prevailing wind direction (from NE to SW) as wind has the potential to distribute pollutants emitted into the air throughout its path. The concentrations of selected elements were determined by Inductively Coupled Plasma-Mass Spectrometry (ICP-MS). Also, physical parameters such as pH, temperature, electrical conductivity of the rainwater and temperature and pH value of the soil samples were measured together with the meteorological parameters. Seasonal differences for the selected elements were insignificant in the soil samples (p>0.05), while some elements showed seasonal variations in the rainwater samples (p Pb > Mn> Cu> Cd > Ni> Cr in the rainwater samples and Mn > Zn > Cu > Pb > Cr > Ni > Co in the soil samples, respectively. The highest enrichments were found for Pb in the rainwater and As in the soil samples. Elevated As levels occurred in the samples can pose a great risk for public health and agriculture.

The study is an endoparasitic examination of chub mackerel (Scomber japonicus Houttuyn 1782), bogue (Boops boops Linnaeus 1758), horse mackerel (Trachurus trachurus Linnaeus 1758), sardine (Sardina pilchardus Walbaum 1792), and anchovy (Engraulis encrasicolus Linnaeus 1758) fish taken from Çanakkale fish state as an annual sampling between 01 September 2019- 01 September 2020. One thousand three hundred thirty-seven fishes were sampled. The external morphological examination of the fish brought to the laboratory was made, then the conditions of their visceral organs and their visceral structures were examined by dissection method. Nematodes collected alive from many parts of the body were kept in absolute (99.9%) ethanol. Parasites in ethanol were kept in glycerin for a few days before being examined under the microscope. Nematodes were first examined morphologically on a stereomicroscope and then under a light microscope for easy species identification. Classical detection methods have been used for species determination. As a result, among the individuals belonging to the Anisakidae family, Anisakis spp. L3 larval stage type 1 and type 2, Anisakis physeteris larval stage, Contracaecum larval stage, Hysterothylacium aduncum L3 larval stage were found. The density, abundance, and prevalence rates of the parasites in the infected fish are determined as a percentage.

The purpose of this investigation was to identify the presence of parasite infections and cystic formation in Scomber japonicus, Scomber scombrus, and Thunnus thynnus. Euryphorus brachypterus and Clavellisa scombri were identified from Thunnus thynnus and Scomber scombrus, respectively. Anisakis pegreffii was identified from Scomber japonicus and Scomber scombrus by using molecular methods. Additionally, Anisakis typical was determined from Scomber japonicus.