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A clean atmosphere should be provided as a right for human beings to live. The reality is that a significant proportion of the population is exposed to air pollution. This study presents an in-depth investigation into the spatio-temporal dynamics of PM2.5 concentrations in Ankara, Türkiye, spanning over three years. With particular emphasis on the impact of COVID-19 lockdown measures and local air quality management strategies, data from eight air pollution monitoring stations were analyzed. The findings indicate a significant reduction in PM2.5 levels during lockdown periods, with an average decrease of 18 % observed across the city. Implementing the Ankara Provincial Clean Air Action Plan further contributed to a 9.1 % decrease in PM2.5 concentrations in 2021, followed by an additional 6.6 % decrease in 2022 compared to 2020. The spatial distribution of PM2.5 concentrations reveals the influence of industrial and urban areas on pollution levels. Potential Source Contribution Function (PSCF) and Concentration-Weighted Trajectory (CWT) methods were employed to investigate the spatial and temporal variation of long-range transport source regions contributing to the PM2.5 levels in Ankara. PSCF and CWT analyses revealed a decreasing trend in anthropogenic contribution to PM2.5 from 2020 to 2022. The AirQ+ model was employed to predict the long-term mortality rates attributable to PM2.5 across different monitoring stations. Based on the estimations, all stations' average estimated attributable proportion is 9.8 % (3.3 %-27.8 %). The results depict varying trends in estimated mortality rates, emphasizing the importance of targeted interventions to mitigate the public health risks arising from exposure to polluted air. Overall, the results of this study show significant measures for the development of effective clean air quality strategies can effectively change the direction of the adverse impact of air pollution on public health.

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In order to find the spatial distribution characteristics of elemental (EC) and organic (OC) carbon in fine particles, daily PM2.5 aerosol samples were collected at two different stations, between July 2014 and September 2015 in Ankara, Turkey. Concentrations of OC ranged from 2.1 to 42 µg m-3 at urban station. These concentrations were higher than those obtained for suburban station whose values ranged from 1.3 to 15 µg m-3. Concentrations of EC ranged from 0.7 to 4.9 µg m-3 at the urban station. As in OC case, the corresponding levels were higher than those measured for suburban station. The associated EC levels ranged from 0.1 to 3.4 µg m-3 for the suburban station. Daily changes in the levels of EC were larger than the OC levels. OC/EC ratios were lower with lower monthly variability in summer and higher with lower monthly variability in winter at the urban site. Medium and weak correlations were obtained between EC and OC in the winter and summer seasons, respectively, at both stations. Secondary organic carbon (SOC) was an important component of OC in PM2.5 at the urban and suburban sites. The winter SOC level was higher than the summer SOC level at the urban site but slightly lower than the summer SOC level at the suburban site. Total carbon was apportioned using factor analysis for the eight carbon fraction data (OC1, OC2, OC3, OC4, EC1, EC2, EC3, and OP). The main sources of pollutants in the urban and suburban settings were from vehicular emissions, biomass and coal combustions, and road dust.

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Candida infections pose a serious public health threat due to increasing drug resistance. Azoles are first-line antifungal drugs for fungal infections. In this study, we tested an in-house azole collection incorporating naphthalene ring to find hits against planktonic and biofilm forms of resistant Candida spp. In the collection, potent derivatives were identified against the susceptible strains of Candida with minimum inhibitory concentration (MIC) values lower than those of the reference drug, fluconazole. MIC values of 0.125 µg/ml against C. albicans, 0.0625 µg/ml against C. parapsilosis, and 2 µg/ml against C. krusei, an intrinsically azole-resistant non-albicans Candida, were obtained. Some of the derivatives were highly active against fluconazole-resistant clinical isolate of C. tropicalis. Inhibition of C. albicans biofilms was also observed at 4 µg/ml similar as amphotericin B, the reference drug known for its antibiofilm activity. Through molecular docking studies, affinities and key interactions of the compounds with fungal lanosterol 14α-demethylase (CYP51), the target enzyme of azoles, were predicted. The interactions of imidazole with heme cofactor and of the naphthalene with Tyr118 were highlighted in line with the literature data. As a result, this study proves the importance of naphthalene for the antifungal activity of azoles against Candida spp. in both planktonic and biofilm forms.

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Azole antifungal drugs are commonly used in antifungal chemotherapy. Antibacterial effects of some topical antifungals, such as miconazole and econazole, have lately been revealed, which suggests a promising venue in antimicrobial chemotherapy. In this study, we tested an in-house azole collection with antifungal properties for their antibacterial activity to identify dual-acting hits using the broth microdilution method. The in vitro screen yielded a number of potent derivatives against gram-positive bacteria, Enterococcus faecalis and Staphylococcus aureus. Compound 73's minimum inhibitory concentration (MIC) value less than 1 µg/ml against S. aureus; however, none of the compounds showed noteworthy activity against methicillin-resistant S. aureus (MRSA). All the active compounds were found safe at their MIC values against the healthy fibroblast cells in the in vitro cytotoxicity test. Molecular docking studies of the most active compounds using a set of docking programs with flavohemoglobin (flavoHb) structure, the proposed target of the azole antifungals with antibacterial activity, presented striking similarities regarding the binding modes and interactions between the tested compounds and the antifungal drugs with crystallographic data. In addition to being noncytotoxic, the library was predicted to be drug-like and free of pan-assay interference compounds (PAINS). As a result, the current study revealed several potential azole derivatives with both antifungal and antibacterial activities. Inhibition of bacterial flavoHb was suggested as a possible mechanism of action for the title compounds.